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Sample records for photoelectrochemical cells based

  1. Photoelectrochemical cells

    NASA Astrophysics Data System (ADS)

    Nozik, A. J.

    1980-02-01

    The application of photoelectrochemical systems based on photoactive semiconducting electrodes to the problem of solar energy conversion and chemical synthesis is discussed. Three types of cells are described: electrochemical photovoltaic cells (wherein optical energy is converted into electrical energy); photoelectrolysis cells (wherein optical energy is converted into chemical free energy); and photocatalytic cells (wherein optical energy provides the activation energy for exoergic chemical reactions). The critical semiconductor electrode properties for these cells are the band gap, the flat-band potential, and the photoelectrochemical stability. No semiconductor electrode material is yet known for which all three parameters are simultaneously optimized. An interesting configurational variation of photoelectrolysis cells, labelled 'photochemical diodes', is described. These diodes comprise cells that have been collapsed into monolithic particles containing no external wires. Recent advances in several areas of photoelectrochemical systems are also described.

  2. Apollony photonic sponge based photoelectrochemical solar cells.

    PubMed

    Ramiro-Manzano, Fernando; Atienzar, Pedro; Rodriguez, Isabelle; Meseguer, Francisco; Garcia, Hermenegildo; Corma, Avelino

    2007-01-21

    We have developed a quasi-fractal colloidal crystal to localize efficiently photons in a very broad optical spectral range; it has been applied to prepare dye sensitized photoelectrochemical solar (PES) cells able to harvest very efficiently photons from the ultraviolet (UV) and the visible (VIS) regions of the solar spectrum.

  3. Photoelectrochemical cell

    DOEpatents

    Rauh, R. David; Boudreau, Robert A.

    1983-06-14

    A photoelectrochemical cell comprising a sealed container having a light-transmitting window for admitting light into the container across a light-admitting plane, an electrolyte in the container, a photoelectrode in the container having a light-absorbing surface arranged to receive light from the window and in contact with the electrolyte, the surface having a plurality of spaced portions oblique to the plane, each portion having dimensions at least an order of magnitude larger than the maximum wavelength of incident sunlight, the total surface area of the surface being larger than the area of the plane bounded by the container, and a counter electrode in the container in contact with the electrolyte.

  4. Nanocomposite Photoelectrochemical Cells

    NASA Technical Reports Server (NTRS)

    Narayan, Sri R.; Kindler, Andrew; Whitacre, Jay F.

    2007-01-01

    Improved, solid-state photoelectrochemical cells for converting solar radiation to electricity have been proposed. (In general, photoelectrochemical cells convert incident light to electricity through electrochemical reactions.) It is predicted that in comparison with state-of-the-art photoelectrochemical cells, these cells will be found to operate with greater solar-to-electric energy-conversion efficiencies.

  5. A plasticized polymer-electrolyte-based photoelectrochemical solar cell

    SciTech Connect

    Mao, D.; Ibrahim, M.A.; Frank, A.J.

    1998-01-01

    A photoelectrochemical solar cell based on an n-GaAs/polymer-redox-electrolyte junction is reported. Di(ethylene glycol) ethyl ether acrylate containing ferrocene as a redox species and benzoin methyl ether as a photoinitiator is polymerized in situ. Propylene carbonate is used as a plasticizer to improve the conductivity of the polymer redox electrolyte. For thin (1 {micro}m) polymer electrolytes, the series resistance of the cell is negligible. However, the short-circuit photocurrent density of the cell at light intensities above 10 mW/cm{sup 2} is limited by mass transport of redox species within the polymer matrix. At a light intensity of 70 mW/cm{sup 2}, a moderate light-to-electrical energy conversion efficiency (3.1%) is obtained. The interfacial charge-transfer properties of the cell in the dark and under illumination are studied.

  6. Photoelectrochemical Solar Cells.

    ERIC Educational Resources Information Center

    McDevitt, John T.

    1984-01-01

    This introduction to photoelectrochemical (PEC) cells reviews topics pertaining to solar energy conversion and demonstrates the ease with which a working PEC cell can be prepared with n-type silicon as the photoanode and a platinum counter electrode (both immersed in ethanolic ferrocene/ferricenium solutions). Experiments using the cell are…

  7. Tris(hydroxymethyl)aminomethane photooxidation on titania based photoanodes and its implication for photoelectrochemical biofuel cells

    NASA Astrophysics Data System (ADS)

    Filipiak, Marcin S.; Zloczewska, Adrianna; Grzeskowiak, Piotr; Lynch, Robert; Jönsson-Niedziolka, Martin

    2015-09-01

    In many photoelectrochemical biofuel cells tris(hydroxymethyl)aminomethane (TRIS) is used a buffer. We show that TRIS can be readily photooxidised on titania electrodes. Combining a titania nanotube photoanode in a TRIS buffer with an air-breathing enzymatic biocathode we construct a relatively efficient photoelectrochemical biofuel cell using the TRIS buffer as fuel. This shows both the prospect of using air-breathing bio-cathodes in this kind of cells, but more importantly, shows the need for caution when using TRIS as buffer in photoelectrochemical applications.

  8. Superlattice photoelectrodes for photoelectrochemical cells

    SciTech Connect

    Nozik, A.J.

    1985-07-03

    The application of superlattice semiconductors as photoelectrodes in photoelectrochemical energy conversion processes is described. The invention is comprised of a multiple quantum well, or superlattice, semiconductor positioned on a plate and encapsulated in an insulation material, except the top surface, which is left exposed. An opening in insulation exposes a portion of the plate. When the photoelectrochemical cell is immersed in a liquid electrolyte and exposed to solar radiation, a redox reaction occurs, producing gases such as hydrogen and oxygen from a water electrolyte, which bubble off the cathode and anode portions of the cell. (LEW)

  9. Specific of a photocurrent in GaN-based photoelectrochemical cell

    NASA Astrophysics Data System (ADS)

    Marchenko, O. N.; Ermakov, I. A.; Puzyk, M. V.; Kovalev, D. S.; Ivanova, S. A.; Papchenko, B. P.; Usikov, A. S.; Chernyakov, A. E.

    2016-08-01

    An influence of various parameters of a photoelectrochemical cell (PECC) having a GaN working electrode on the photocurrent was studied. Type of the aqua electrolyte (alkaline (KOH)-, neutral salt (Na2SO4)- and acid (H2SO4)- based electrolytes) influences on transient time for the photocurrent stabilization. A transient time for the photo current stabilization was observed under illumination by the UV LED light sources. The shortest transient time and the highest photocurrent were observed in the alkaline-based electrolyte (∼0.5M KOH) with n- GaN working electrodes (ND-NA =(3-5)×1016 cm-3). PECC with electrolytes based on sodium sulfate and sulfuric acid demonstrated longer transient time (up to ten minutes) for the photocurrent stabilization and smaller photocurrent.

  10. Automatic illumination compensation device based on a photoelectrochemical biofuel cell driven by visible light.

    PubMed

    Yu, You; Han, Yanchao; Xu, Miao; Zhang, Lingling; Dong, Shaojun

    2016-04-28

    Inverted illumination compensation is important in energy-saving projects, artificial photosynthesis and some forms of agriculture, such as hydroponics. However, only a few illumination adjustments based on self-powered biodetectors that quantitatively detect the intensity of visible light have been reported. We constructed an automatic illumination compensation device based on a photoelectrochemical biofuel cell (PBFC) driven by visible light. The PBFC consisted of a glucose dehydrogenase modified bioanode and a p-type semiconductor cuprous oxide photocathode. The PBFC had a high power output of 161.4 μW cm(-2) and an open circuit potential that responded rapidly to visible light. It adjusted the amount of illumination inversely irrespective of how the external illumination was changed. This rational design of utilizing PBFCs provides new insights into automatic light adjustable devices and may be of benefit to intelligent applications.

  11. Automatic illumination compensation device based on a photoelectrochemical biofuel cell driven by visible light

    NASA Astrophysics Data System (ADS)

    Yu, You; Han, Yanchao; Xu, Miao; Zhang, Lingling; Dong, Shaojun

    2016-04-01

    Inverted illumination compensation is important in energy-saving projects, artificial photosynthesis and some forms of agriculture, such as hydroponics. However, only a few illumination adjustments based on self-powered biodetectors that quantitatively detect the intensity of visible light have been reported. We constructed an automatic illumination compensation device based on a photoelectrochemical biofuel cell (PBFC) driven by visible light. The PBFC consisted of a glucose dehydrogenase modified bioanode and a p-type semiconductor cuprous oxide photocathode. The PBFC had a high power output of 161.4 μW cm-2 and an open circuit potential that responded rapidly to visible light. It adjusted the amount of illumination inversely irrespective of how the external illumination was changed. This rational design of utilizing PBFCs provides new insights into automatic light adjustable devices and may be of benefit to intelligent applications.Inverted illumination compensation is important in energy-saving projects, artificial photosynthesis and some forms of agriculture, such as hydroponics. However, only a few illumination adjustments based on self-powered biodetectors that quantitatively detect the intensity of visible light have been reported. We constructed an automatic illumination compensation device based on a photoelectrochemical biofuel cell (PBFC) driven by visible light. The PBFC consisted of a glucose dehydrogenase modified bioanode and a p-type semiconductor cuprous oxide photocathode. The PBFC had a high power output of 161.4 μW cm-2 and an open circuit potential that responded rapidly to visible light. It adjusted the amount of illumination inversely irrespective of how the external illumination was changed. This rational design of utilizing PBFCs provides new insights into automatic light adjustable devices and may be of benefit to intelligent applications. Electronic supplementary information (ESI) available. See DOI: 10.1039/c6nr00759g

  12. Photoelectrochemical and photovoltaic characteristics of amorphous-silicon-based tandem cells as photocathodes for water splitting.

    PubMed

    Ziegler, Jürgen; Kaiser, Bernhard; Jaegermann, Wolfram; Urbain, Félix; Becker, Jan-Philipp; Smirnov, Vladimir; Finger, Friedhelm

    2014-12-15

    In this study amorphous silicon tandem solar cells are successfully utilized as photoelectrodes in a photoelectrochemical cell for water electrolysis. The tandem cells are modified with various amounts of platinum and are combined with a ruthenium oxide counter electrode. In a two-electrode arrangement this system is capable of splitting water without external bias with a short-circuit current of 4.50 mA cm(-2). On the assumption that no faradaic losses occur, a solar-to-hydrogen efficiency of 5.54% is achieved. In order to identify the relevant loss processes, additional three-electrode measurements were performed for each involved half-cell.

  13. Photoelectrochemical based direct conversion systems

    SciTech Connect

    Kocha, S.; Arent, D.; Peterson, M.

    1995-09-01

    The goal of this research is to develop a stable, cost effective, photoelectrochemical based system that will split water upon illumination, producing hydrogen and oxygen directly, using sunlight as the only energy input. This type of direct conversion system combines a photovoltaic material and an electrolyzer into a single monolithic device. We report on our studies of two multifunction multiphoton photoelectrochemical devices, one based on the ternary semiconductor gallium indium phosphide, (GaInP{sub 2}), and the other one based on amorphous silicon carbide. We also report on our studies of the solid state surface treatment of GaInP{sub 2} as well as our continuing effort to develop synthetic techniques for the attachment of transition metal complexes to the surface of semiconductor electrodes. All our surface studies are directed at controlling the interface energetics and forming stable catalytic surfaces.

  14. Photoelectrochemical cells including chalcogenophosphate photoelectrodes

    NASA Technical Reports Server (NTRS)

    Reichman, B.; Byvik, C. E. (Inventor)

    1984-01-01

    Photoelectrochemical cells employing chalcogenophosphate (MPX3) photoelectrodes are described where M is selected from the group of transition metal series of elements beginning with scandium (atomic number 21) through germanium (atomic number 32) yttrium (atomic number 39) through antimony (atomic number 51) and lanthanum (atomic number 57) through polonium (atomic number 84); P is phosphorus; and X is selected from the chalogenide series consisting of sulfur, selenium, and tellurium. These compounds have bandgaps in the desirable range from 2.0 eV to 2.2 eV for the photoelectrolysis of water and are stable when used as photoelectrodes for the same.

  15. Photoelectrochemical cells - Conversion of intense optical energy

    NASA Technical Reports Server (NTRS)

    Wrighton, M. S.; Ellis, A. B.; Kaiser, S. W.

    1976-01-01

    Conversion of optical energy to chemical energy and/or electrical energy using wet photoelectrochemical cells is described. Emphasis is on (1) the photoelectrolysis of H2O to H2 and O2 using cells having n-type semiconductor photoelectrodes fabricated from TiO2, SnO2, SrTiO3, KTaO3, and KTa(0.77)Nb(0.23)O3, and (2) the conversion of light to electrical energy using CdSe- and CdS-based cells with polysulfide electrolytes.

  16. Electrochemical photovoltaic and photoelectrochemical storage cells based on II-VI polycrystalline thin film materials

    SciTech Connect

    Wallace, W.L.

    1983-06-01

    Research on electrochemical photovoltaic cells incorporating thin film CdSe and CdSe /SUB x/ Te /SUB 1-x/ photoanodes has progressed to the point where efficiencies of up to 7% can be achieved on small area electrodes using a polysulfide electrolyte. Higher efficiencies can be obtained in alternate electrolytes in significantly less stable systems. The major limitations on cell efficiency are associated with the open circuit voltage and fill factor. At present, the most promising photoelectrochemical storage system is an in situ three electrode cell which consists of an n-CdSe /SUB x/ Te /SUB 1-x/ photoanode and CoS counterelectrode in a sulfide/polysulfide electrolyte and a Sn/SnS storage electrode isolated in an aqueous sulfide electrolyte.

  17. Numerical algorithms based on Galerkin methods for the modeling of reactive interfaces in photoelectrochemical (PEC) solar cells

    NASA Astrophysics Data System (ADS)

    Harmon, Michael; Gamba, Irene M.; Ren, Kui

    2016-12-01

    This work concerns the numerical solution of a coupled system of self-consistent reaction-drift-diffusion-Poisson equations that describes the macroscopic dynamics of charge transport in photoelectrochemical (PEC) solar cells with reactive semiconductor and electrolyte interfaces. We present three numerical algorithms, mainly based on a mixed finite element and a local discontinuous Galerkin method for spatial discretization, with carefully chosen numerical fluxes, and implicit-explicit time stepping techniques, for solving the time-dependent nonlinear systems of partial differential equations. We perform computational simulations under various model parameters to demonstrate the performance of the proposed numerical algorithms as well as the impact of these parameters on the solution to the model.

  18. Superlattice photoelectrodes for photoelectrochemical cells

    DOEpatents

    Nozik, Arthur J.

    1987-01-01

    A superlattice or multiple-quantum-well semiconductor is used as a photoelectrode in a photoelectrochemical process for converting solar energy into useful fuels or chemicals. The quantum minibands of the superlattice or multiple-quantum-well semiconductor effectively capture hot-charge carriers at or near their discrete quantum energies and deliver them to drive a chemical reaction in an electrolyte. The hot-charge carries can be injected into the electrolyte at or near the various discrete multiple energy levels quantum minibands, or they can be equilibrated among themselves to a hot-carrier pool and then injected into the electrolyte at one average energy that is higher than the lowest quantum band gap in the semiconductor.

  19. CdS/CdSe quantum dot shell decorated vertical ZnO nanowire arrays by spin-coating-based SILAR for photoelectrochemical cells and quantum-dot-sensitized solar cells.

    PubMed

    Zhang, Ran; Luo, Qiu-Ping; Chen, Hong-Yan; Yu, Xiao-Yun; Kuang, Dai-Bin; Su, Cheng-Yong

    2012-04-23

    A CdS/CdSe composite shell is assembled onto the surface of ZnO nanowire arrays with a simple spin-coating-based successive ionic layer adsorption and reaction method. The as-prepared photoelectrode exhibit a high photocurrent density in photoelectrochemical cells and also generates good power conversion efficiency in quantum-dot-sensitized solar cells.

  20. Solar energy conversion in photoelectrochemical cells with semiconductor electrodes

    NASA Astrophysics Data System (ADS)

    Pleskov, Yu. V.

    in recent years the semiconductor/electrolyte interface has been attracting much attention in connection with the search for effective ways of utilizing solar energy. This review systematizes information on photoelectrochemical cells, both for production of hydrogen by water photoelectrolysis and for electric power generation in “liquid-junction solar cells.” Special attention is given to integral characteristics of photoelectrochemical cells. The main difficulties in practical realization of the conversion process and some possible methods of surmounting them are formulated.

  1. Anionic structure-dependent photoelectrochemical responses of dye-sensitized solar cells based on a binary ionic liquid electrolyte.

    PubMed

    Hao, Feng; Lin, Hong; Liu, Yizhu; Li, Jianbao

    2011-04-14

    Room temperature ionic liquids (RTILs) have been used as electrolytes to investigate the anionic structure dependence of the photoelectrochemical responses of dye-sensitized solar cells (DSCs). A series of RTILs with a fixed cation structure coupling with various anion structures are employed, in which 1-methyl-3-propylimidazolium iodide (PMII) and I(2) are dissolved as redox couples. It is found that both the diffusivity of the electrolyte and the photovoltaic performance of the device show a strong dependence on the fluidity of the ionic liquids, which is primarily altered by the anion structure. Further insights into the structure-dependent physical properties of the employed RTILs are discussed in terms of the reported van der Waals radius, the atomic charge distribution over the anion backbones, the interaction energy of the anion and cation, together with the existence of ion-pairs and ion aggregates. Particularly, both the short-circuit photocurrent and open-circuit voltage exhibit obvious fluidity dependence. Electrochemical impedance and intensity-modulated photovoltage/photocurrent spectroscopy analysis further reveal that increasing the fluidity of the ionic liquid electrolytes could significantly decrease the diffusion resistance of I(3)(-) in the electrolyte, and retard the charge recombination between the injected electrons with triiodide in the high-viscous electrolyte, thus improving the electron diffusion length in the device, as well as the photovoltaic response. However, the variation of the electron diffusion coefficients is trivial primarily due to the effective charge screening of the high cation concentration.

  2. Solar-to-Chemical Energy Conversion with Photoelectrochemical Tandem Cells.

    PubMed

    Sivula, Kevin

    2013-01-01

    Efficiently and inexpensively converting solar energy into chemical fuels is an important goal towards a sustainable energy economy. An integrated tandem cell approach could reasonably convert over 20% of the sun's energy directly into chemical fuels like H2 via water splitting. Many different systems have been investigated using various combinations of photovoltaic cells and photoelectrodes, but in order to be economically competitive with the production of H2 from fossil fuels, a practical water splitting tandem cell must optimize cost, longevity and performance. In this short review, the practical aspects of solar fuel production are considered from the perspective of a semiconductor-based tandem cell and the latest advances with a very promising technology - metal oxide photoelectrochemical tandem cells - are presented.

  3. Integrated photoelectrochemical cell and system having a liquid electrolyte

    DOEpatents

    Deng, Xunming; Xu, Liwei

    2010-07-06

    An integrated photoelectrochemical (PEC) cell generates hydrogen and oxygen from water while being illuminated with radiation. The PEC cell employs a liquid electrolyte, a multi-junction photovoltaic electrode, and a thin ion-exchange membrane. A PEC system and a method of making such PEC cell and PEC system are also disclosed.

  4. Integrating a dual-silicon photoelectrochemical cell into a redox flow battery for unassisted photocharging.

    PubMed

    Liao, Shichao; Zong, Xu; Seger, Brian; Pedersen, Thomas; Yao, Tingting; Ding, Chunmei; Shi, Jingying; Chen, Jian; Li, Can

    2016-05-04

    Solar rechargeable flow cells (SRFCs) provide an attractive approach for in situ capture and storage of intermittent solar energy via photoelectrochemical regeneration of discharged redox species for electricity generation. However, overall SFRC performance is restricted by inefficient photoelectrochemical reactions. Here we report an efficient SRFC based on a dual-silicon photoelectrochemical cell and a quinone/bromine redox flow battery for in situ solar energy conversion and storage. Using narrow bandgap silicon for efficient photon collection and fast redox couples for rapid interface charge injection, our device shows an optimal solar-to-chemical conversion efficiency of ∼5.9% and an overall photon-chemical-electricity energy conversion efficiency of ∼3.2%, which, to our knowledge, outperforms previously reported SRFCs. The proposed SRFC can be self-photocharged to 0.8 V and delivers a discharge capacity of 730 mAh l(-1). Our work may guide future designs for highly efficient solar rechargeable devices.

  5. Research on photoelectrochemical cells based on CdSe, CdSe/sub 1-x/Te/sub x/ and other photoelectrode materials

    SciTech Connect

    Wallace, W L

    1984-05-01

    Research on electrochemical photovoltaic cells incorporating thin film n-CdSe and n-CdSe/sub 1-x/Te/sub x/ photoanodes has resulted in efficiencies up to 7.5% using small area electrodes in polysulfide electrolytes. Efficiencies close to 10% can be achieved using alternate electrolytes in significantly less stable systems. The major limitations on the efficiency of II-VI photoelectrochemical cells are associated with the open circuit voltage and the fill factor. Research on CuInSe/sub 2/ electrochemical photovoltaic cells has resulted in efficiencies up to 11.7% using single crystal n-CuInSe/sub 2/ photoanodes in aqueous electrolytes. The n-CuInSe/sub 2/ surface and the electrolyte have been optimized to produce a highly stable semiconductor/electrolyte junction. A review will also be given on the status of photoelectrochemical storage cell research. In situ photoelectrochemical measurement techniques have been used to probe the semiconductor/electrolyte interface and have been used to support the characterization of semiconductor materials for solid state photovoltaic applications.

  6. Optimization of amorphous silicon double junction solar cells for an efficient photoelectrochemical water splitting device based on a bismuth vanadate photoanode.

    PubMed

    Han, Lihao; Abdi, Fatwa F; Perez Rodriguez, Paula; Dam, Bernard; van de Krol, Roel; Zeman, Miro; Smets, Arno H M

    2014-03-07

    A photoelectrochemical water splitting device (PEC-WSD) was designed and fabricated based on cobalt-phosphate-catalysed and tungsten-gradient-doped bismuth vanadate (W:BiVO4) as the photoanode. A simple and cheap hydrogenated amorphous silicon (a-Si:H) double junction solar cell has been used to provide additional bias. The advantage of using thin film silicon (TF-Si) based solar cells is that this photovoltaic (PV) technology meets the crucial requirements for the PV component in PEC-WSDs based on W:BiVO4 photoanodes. TF-Si PV devices are stable in aqueous solutions, are manufactured by simple and cheap fabrication processes and their spectral response, voltage and current density show an excellent match with the photoanode. This paper is mainly focused on the optimization of the TF-Si solar cell with respect to the remaining solar spectrum transmitted through the W:BiVO4 photoanode. The current matching between the top and bottom cells is studied and optimized by varying the thickness of the a-Si:H top cell. We support the experimental optimization of the current balance between the two sub-cells with simulations of the PV devices. In addition, the impact of the light induced degradation of the a-Si:H double junction, the so-called Staebler-Wronski Effect (SWE), on the performance of the PEC-WSD has been studied. The light soaking experiments on the a-Si:H/a-Si:H double junctions over 1000 hours show that the efficiency of a stand-alone a-Si:H/a-Si:H double junction cell is significantly reduced due to the SWE. Nevertheless, the SWE has a significantly smaller effect on the performance of the PEC-WSD.

  7. A photoelectrochemical-thermal hydrogen producing cycle involving a semiconductor liquid junction cell

    NASA Astrophysics Data System (ADS)

    Gissler, W.

    A photoelectrochemical-thermal hydrogen producing cycle is proposed involving a semiconductor liquid junction solar cell. In contrast with direct photoelectrolysis, the proposal is based upon a photoelectrochemical oxidation or reduction of the n- or p-type semiconductor electrode respectively in an aqueous electrolyte. In subsequent thermal reaction steps the water splitting process is completed, and the semiconductor electrode is regenerated. The advantage of the method is that semiconductors of band gap energies which are well matched to the solar spectrum can be used and correspondingly high solar energy conversion efficiencies can be obtained. The drawback is that the electrode regeneration process is in general quite complicated. The method is demonstrated by using a trigonal selenium electrode which allows a relatively simple regeneration. First experimental results on the photoelectrochemical reaction step are reported.

  8. Photoelectrochemical Cell of Hybrid Regioregular POLY(3-HEXYLTHIOPHENE-2,5-DIYL) and Molybdenum Disulfide Film

    NASA Astrophysics Data System (ADS)

    Abdelmola, Fatmaelzahraa M.; Ram, Manoj K.; Takshi, Arash; Stafanakos, Elias; Kumar, Ashok; Goswami, D. Yogi

    The photoelectrochemical cell attracts attention worldwide due to conversion of optical energy into electricity, production of hydrogen through water splitting and use in photodetector and photo-sensor applications. We have been working on the photochemical cell based on regioregular polyhexylthiophenes hybrid-structured films for photoelectrochemical and photovoltaic applications. This paper discusses the hybrid film studies on regioregular poly(3-hexylthiophene-2,5-diyl) (P3HT) with 2D molybdenum disulfide (MoS2) for photoelectrochemical cell. The hybrid P3HT/MoS2 films deposited over indium tin oxide (ITO)-coated glass plate or n-type silicon substrates were characterized using FTIR, UV/vis, electrochemical and scanning electron microscopy (SEM) techniques. The optical measurements showed a higher absorption magnitude with low reflection properties of P3HT/MoS2 hybrid films revealing a superior photocurrent compared to both P3HT and MoS2 films. The P3HT/MoS2 hybrid-based photoelectrochemical cell yielded a short-circuit current (Isc) of 183.16μAṡcm‑2, open-circuit voltage (Voc) of 0.92V, fill factor (FF) of 25% and power conversion efficiency (η) of 0.18% under the light intensity of 242Wṡm‑2. The estimated power conversion efficiency and fill factor are comparable to organic-based photovoltaic devices.

  9. Double junction photoelectrochemical solar cells based on Cu2ZnSnS4/Cu2ZnSnSe4 thin film as composite photocathode

    NASA Astrophysics Data System (ADS)

    Zhu, L.; Qiang, Y. H.; Zhao, Y. L.; Gu, X. Q.

    2014-02-01

    A solvothermal method was used to synthesize Cu2ZnSnS4 (CZTS) and Cu2ZnSnSe4 (CZTSe) nanoparticles. CZTS/CZTSe bilayer films have been fabricated via a layer-by-layer blade coating process on the fluorine dope tin oxide (FTO) substrates. We converted conventional dye-sensitized solar cells (DSSCs) into double junction photoelectrochemical solar cells with the replacement of the Pt-coated counter electrode with the as-prepared films as composite photocathodes. Compared with conventional DSSCs, the cells show an increased short circuit current and power conversion efficiency.

  10. Photoelectrochemical based direct conversion systems for hydrogen production

    SciTech Connect

    Khaselev, O.; Bansal, A.; Kocha, S.; Turner, J.A.

    1998-08-01

    With an eye towards developing a photoelectrochemical system for hydrogen production using sunlight as the only energy input, two types of systems were studied, both involving multijunction devices. One set of cells consisted of a-Si triple junctions and the other a GaInP{sub 2}/GaAs tandem cell combination. Additional investigations were carried out on semiconductor surface modifications to move semiconductor band edges to more favorable energetic positions.

  11. The n-CdSe photoelectrochemical cell: wavelength-dependent photostability

    SciTech Connect

    Rubin, H.D.; Arent, D.J.; Bocarsly, A.B.

    1985-02-01

    Much recent work has focused on Fe(CN)/sub 6/ /SUP 4-/3-/ as a stabilizing electrolyte for n-CdX(X=S,Se) based photoelectrochemical cells (1-5). Prior studies performed in this laboratory (6) showed that irradiation of n-CdS in an electrolyte containing Fe(CN)/sub 6/ /SUP 4-/3-/ can lead to formation of a surface layer of (Cd /SUP II/ Fe /SUP II/III/ (CN)/sub 6/) /SUP 2-/1-/ . In the presence of the appropriate cations, this layer was associated with improved cell output parameters. These studies have now been extended to include the n-CdSe system. In this letter we wish to report an unprecedented wavelength dependence of the n-CdSe photoelectrochemical cell.

  12. Solar energy conversion in a photoelectrochemical biofuel cell.

    PubMed

    Hambourger, Michael; Kodis, Gerdenis; Vaughn, Michael D; Moore, Gary F; Gust, Devens; Moore, Ana L; Moore, Thomas A

    2009-12-07

    A photoelectrochemical biofuel cell has been developed which incorporates aspects of both an enzymatic biofuel cell and a dye-sensitized solar cell. Photon absorption at a porphyrin-sensitized n-type semiconductor electrode gives rise to a charge-separated state. Electrons and holes are shuttled to appropriate cathodic and anodic catalysts, respectively, allowing the production of electricity, or a reduced fuel, via the photochemical oxidation of a biomass-derived substrate. The operation of this device is reviewed. The use of alternate anodic redox mediators provides insight regarding loss mechanisms in the device. Design strategies for enhanced performance are discussed.

  13. Luminescent Photoelectrochemical Cells. 6. Spatial Aspects of the Photoluminescence and Electroluminescence of Cadmium Selenide Electrodes.

    DTIC Science & Technology

    1981-10-06

    NO. 8 Luminescent Photoelectrochemical Cells. 6. Spatial Aspects of the Photoluminescence and Electroluminescence of Cadmium Selenide Electrodes by...Photoelectrochemistry; photoluminescence; electroluminescence; cadmium selenide electrodes 20. ABSTRACT (Continue. on reverse aide flnocosee7 and...REPORT A PERIOD COVERED Luminescent Photoelectrochemical Cells. 6.1 1 Spatial Aspects of the Photoluminescence and Elect roluminescence of Cadmium

  14. Photoelectrochemical based direct conversion systems for hydrogen production

    SciTech Connect

    Kocha, S.; Peterson, M.; Arent, D.

    1996-10-01

    Photon driven, direct conversion systems consist of a light absorber and a water splitting catalyst as a monolithic system; water is split directly upon illumination. This one-step process eliminates the need to generate electricity externally and subsequently feed it to an electrolyzer. These configurations require only the piping necessary for transport of hydrogen to an external storage system or gas pipeline. This work is focused on multiphoton photoelectrochemical devices for production of hydrogen directly using sunlight and water. Two types of multijunction cells, one consisting of a-Si triple junctions and the other GaInP{sub 2}/GaAs homojunctions, were studied for the photoelectrochemical decomposition of water into hydrogen and oxygen from an aqueous electrolyte solution. To catalyze the water decomposition process, the illuminated surface of the device was modified either by addition of platinum colloids or by coating with ruthenium dioxide. These colloids have been characterized by gel electrophoresis.

  15. Visible light to electrical energy conversion using photoelectrochemical cells

    NASA Technical Reports Server (NTRS)

    Wrighton, Mark S. (Inventor); Ellis, Arthur B. (Inventor); Kaiser, Steven W. (Inventor)

    1983-01-01

    Sustained conversion of low energy visible or near i.r. light (>1.25 eV) to electrical energy has been obtained using wet photoelectrochemical cells where there are no net chemical changes in the system. Stabilization of n-type semi-conductor anodes of CdS, CdSe, CdTe, GaP, GaAs and InP to photoanodic dissolution is achieved by employing selected alkaline solutions of Na.sub.2 S, Na.sub.2 S/S, Na.sub.2 Se, Na.sub.2 Se/Se, Na.sub.2 Te and Na.sub.2 Te/Te as the electrolyte. The oxidation of (poly) sulfide, (poly)selenide or (poly)telluride species occurs at the irradiated anode, and reduction of polysulfide, polyselenide or polytelluride species occurs at the dark Pt cathode of the photoelectrochemical cell. Optical to electrical energy conversion efficiencies approaching 15% at selected frequencies have been observed in some cells. The wavelength for the onset of photocurrent corresponds to the band gap of the particular anode material used in the cell.

  16. Solar-rechargeable battery based on photoelectrochemical water oxidation: Solar water battery.

    PubMed

    Kim, Gonu; Oh, Misol; Park, Yiseul

    2016-09-15

    As an alternative to the photoelectrochemical water splitting for use in the fuel cells used to generate electrical power, this study set out to develop a solar energy rechargeable battery system based on photoelectrochemical water oxidation. We refer to this design as a "solar water battery". The solar water battery integrates a photoelectrochemical cell and battery into a single device. It uses a water oxidation reaction to simultaneously convert and store solar energy. With the solar water battery, light striking the photoelectrode causes the water to be photo-oxidized, thus charging the battery. During the discharge process, the solar water battery reduces oxygen to water with a high coulombic efficiency (>90%) and a high average output voltage (0.6 V). Because the reduction potential of oxygen is more positive [E(0) (O2/H2O) = 1.23 V vs. NHE] than common catholytes (e.g., iodide, sulfur), a high discharge voltage is produced. The solar water battery also exhibits a superior storage ability, maintaining 99% of its specific discharge capacitance after 10 h of storage, without any evidence of self-discharge. The optimization of the cell design and configuration, taking the presence of oxygen in the cell into account, was critical to achieving an efficient photocharge/discharge.

  17. Solar-rechargeable battery based on photoelectrochemical water oxidation: Solar water battery

    PubMed Central

    Kim, Gonu; Oh, Misol; Park, Yiseul

    2016-01-01

    As an alternative to the photoelectrochemical water splitting for use in the fuel cells used to generate electrical power, this study set out to develop a solar energy rechargeable battery system based on photoelectrochemical water oxidation. We refer to this design as a “solar water battery”. The solar water battery integrates a photoelectrochemical cell and battery into a single device. It uses a water oxidation reaction to simultaneously convert and store solar energy. With the solar water battery, light striking the photoelectrode causes the water to be photo-oxidized, thus charging the battery. During the discharge process, the solar water battery reduces oxygen to water with a high coulombic efficiency (>90%) and a high average output voltage (0.6 V). Because the reduction potential of oxygen is more positive [E0 (O2/H2O) = 1.23 V vs. NHE] than common catholytes (e.g., iodide, sulfur), a high discharge voltage is produced. The solar water battery also exhibits a superior storage ability, maintaining 99% of its specific discharge capacitance after 10 h of storage, without any evidence of self-discharge. The optimization of the cell design and configuration, taking the presence of oxygen in the cell into account, was critical to achieving an efficient photocharge/discharge. PMID:27629362

  18. Solar-rechargeable battery based on photoelectrochemical water oxidation: Solar water battery

    NASA Astrophysics Data System (ADS)

    Kim, Gonu; Oh, Misol; Park, Yiseul

    2016-09-01

    As an alternative to the photoelectrochemical water splitting for use in the fuel cells used to generate electrical power, this study set out to develop a solar energy rechargeable battery system based on photoelectrochemical water oxidation. We refer to this design as a “solar water battery”. The solar water battery integrates a photoelectrochemical cell and battery into a single device. It uses a water oxidation reaction to simultaneously convert and store solar energy. With the solar water battery, light striking the photoelectrode causes the water to be photo-oxidized, thus charging the battery. During the discharge process, the solar water battery reduces oxygen to water with a high coulombic efficiency (>90%) and a high average output voltage (0.6 V). Because the reduction potential of oxygen is more positive [E0 (O2/H2O) = 1.23 V vs. NHE] than common catholytes (e.g., iodide, sulfur), a high discharge voltage is produced. The solar water battery also exhibits a superior storage ability, maintaining 99% of its specific discharge capacitance after 10 h of storage, without any evidence of self-discharge. The optimization of the cell design and configuration, taking the presence of oxygen in the cell into account, was critical to achieving an efficient photocharge/discharge.

  19. Integrating a dual-silicon photoelectrochemical cell into a redox flow battery for unassisted photocharging

    PubMed Central

    Liao, Shichao; Zong, Xu; Seger, Brian; Pedersen, Thomas; Yao, Tingting; Ding, Chunmei; Shi, Jingying; Chen, Jian; Li, Can

    2016-01-01

    Solar rechargeable flow cells (SRFCs) provide an attractive approach for in situ capture and storage of intermittent solar energy via photoelectrochemical regeneration of discharged redox species for electricity generation. However, overall SFRC performance is restricted by inefficient photoelectrochemical reactions. Here we report an efficient SRFC based on a dual-silicon photoelectrochemical cell and a quinone/bromine redox flow battery for in situ solar energy conversion and storage. Using narrow bandgap silicon for efficient photon collection and fast redox couples for rapid interface charge injection, our device shows an optimal solar-to-chemical conversion efficiency of ∼5.9% and an overall photon–chemical–electricity energy conversion efficiency of ∼3.2%, which, to our knowledge, outperforms previously reported SRFCs. The proposed SRFC can be self-photocharged to 0.8 V and delivers a discharge capacity of 730 mAh l−1. Our work may guide future designs for highly efficient solar rechargeable devices. PMID:27142885

  20. General Characterization Methods for Photoelectrochemical Cells for Solar Water Splitting.

    PubMed

    Shi, Xinjian; Cai, Lili; Ma, Ming; Zheng, Xiaolin; Park, Jong Hyeok

    2015-10-12

    Photoelectrochemical (PEC) water splitting is a very promising technology that converts water into clean hydrogen fuel and oxygen by using solar light. However, the characterization methods for PEC cells are diverse and a systematic introduction to characterization methods for PEC cells has rarely been attempted. Unlike most other review articles that focus mainly on the material used for the working electrodes of PEC cells, this review introduces general characterization methods for PEC cells, including their basic configurations and methods for characterizing their performance under various conditions, regardless of the materials used. Detailed experimental operation procedures with theoretical information are provided for each characterization method. The PEC research area is rapidly expanding and more researchers are beginning to devote themselves to related work. Therefore, the content of this Minireview can provide entry-level knowledge to beginners in the area of PEC, which might accelerate progress in this area.

  1. Photoelectrolysis of water at high current density - Use of laser light excitation of semiconductor-based photoelectrochemical cells

    NASA Technical Reports Server (NTRS)

    Wrighton, M. S.; Bocarsley, A. B.; Bolts, J. M.

    1978-01-01

    In the present paper, some results are given for UV laser light irradiation of the photoanode (SnO2, SrTiO3, or TiO2) in a cell for the light-driven electrolysis of H2O, at radiation intensities of up to 380 W/sq cm. The properties of the anode material are found to be independent of light intensity. Conversion of UV light to stored chemical energy in the form of 2H2/O2 from H2O was driven at a rate of up to 30 W/sq cm. High O2 evolution rates at the irradiated anodes without changes in the current-voltage curves are attributed to the excess oxidizing power associated with photogenerated holes. A test for this sort of hypothesis for H2 evolution at p-type materials is proposed.

  2. Development of photoelectrochemical cells based on compound semiconductors and nonaqueous electrolytes. Semiannual report, May 1, 1981-October 31, 1981

    SciTech Connect

    Rauh, R. D.

    1982-03-01

    A reproducible procedure for chemical bath deposition (CBD) of CdSe has been documented in detail, allowing a consistent production of photoelectrode yielding 5.5 to 6.5% conversion efficiency in alkaline polysulfide electrolyte (employing a tungsten halogen lamp/KG-2 filter solar simulated light source). The CBD films of n-CdSe on Ti have achieved an efficiency of approx. 10% under both solar simulated and real sunlight conditions using an Fe(CN)/sub 6//sup -3///sup -4/ electrolyte at pH 13. For an initial current density of 16 mA/cm/sup 2/ (approx. 80 mW/cm/sup 2/ illumination), a decrease of approx. 25% is observed after 3 hours illumination. Research was completed on developing a stable Cu/sup +///sup +2/ redox electrolyte in CH/sub 3/CN, which contains excess Cl/sup -/, to promote photochemical stability. For poly-n-GaAs, best results were obtained for electrolytes containing approx. 0.5M Cucl, 0.05M CuCl/sub 2/, 1M tetrabutylammonium chloride, viz: at 80 mW/cm/sup 2/, j/sub sc/ = 19 mA/cm/sup 2/, V/sub oc/ = 0.74V, P/sub max/ = 3.78 mW/cm/sup 2/, ff = 0.27 and eta = 4.8% (eta = 8.1% at 8 mW/cm/sup 2/ irradiation). Five encapsulated sealed cells have been tested with 15 cm/sup 2/ photoelectrodes comprised of CBD CdSe on Ti. The cells are frontwall illuminated with various configurations for ion flow to the rear-placed Ni/CoS electrode. For one design, an efficiency of 4.3% was achieved under 63 mW/cm/sup 2/ real solar illumination. Laser spot scanning has been developed as a technique for evaluation of both large area geometrical effects and microscopic photoelectrode morphological effects on the performance of PECs.

  3. A Photoelectrochemical Solar Cell: An Undergraduate Experiment.

    ERIC Educational Resources Information Center

    Boudreau, Sharon M.; And Others

    1983-01-01

    Preparation and testing of a cadmium selenide photoelectrical solar cell was introduced into an environmental chemistry course to illustrate solid state semiconductor and electrochemical principles. Background information, procedures, and results are provided for the experiment which can be accomplished in a three- to four-hour laboratory session…

  4. Iron Pyrite/Titanium Dioxide Photoanode for Extended Near Infrared Light Harvesting in a Photoelectrochemical Cell

    PubMed Central

    Wang, Di-Yan; Li, Cheng-Hung; Li, Shao-Sian; Kuo, Tsung-Rong; Tsai, Chin-Ming; Chen, Tin-Reui; Wang, Ying-Chiao; Chen, Chun-Wei; Chen, Chia-Chun

    2016-01-01

    The design of active and stable semiconducting composites with enhanced photoresponse from visible light to near infrared (NIR) is a key to improve solar energy harvesting for photolysis of water in photoelectrochemical cell. In this study, we prepared earth abundant semiconducting composites consisting of iron pyrite and Titanium oxide as a photoanode (FeS2/TiO2 photoanode) for photoelectrochemical applications. The detailed structure and atomic compositions of FeS2/TiO2 photoanode was characterized by high-resolution transmission electron microscopy (HRTEM), energy-dispersive X-ray spectroscopy (EDS), powder X-ray diffraction (XRD), inductively coupled plasma with atomic emission spectroscopy (ICPAES) and Raman spectroscopy. Through the proper sulfurization treatment, the FeS2/TiO2 photoanode exhibited high photoresponse from visible light extended to near infrared range (900 nm) as well as stable durability test for 4 hours. We found that the critical factors to enhance the photoresponse are on the elimination of surface defect of FeS2 and on the enhancement of interface charge transfer between FeS2 and TiO2. Our overall results open a route for the design of sulfur-based binary compounds for photoelectrochemical applications. PMID:26852670

  5. Controlled synthesis of vertically aligned hematite on conducting substrate for photoelectrochemical cells: nanorods versus nanotubes.

    PubMed

    Mao, Aiming; Shin, Kahee; Kim, Jung Kyu; Wang, Dong Hwan; Han, Gui Young; Park, Jong Hyeok

    2011-06-01

    This paper describes two different processes to synthesize vertically aligned hematite nanorod and nanotube arrays, respectively, on a conductive substrate by the electrochemical deposition method with the help of an anodized aluminum oxide nanotemplate. The two types of nanostructured hematite were used as the photoanode for photoelectrochemical cells. The hematite nanotubes exhibited much higher photoelectrochemical activity than the hematite nanorods, including an improved photocurrent density, more negative onset potential, better photon harvesting, and better charge carrier transfer ability. The observed behavior may offer new information to enhance the photocatalytic ability of hematite, which is considered to be one of the best photoanode materials in the research field of photoelectrochemical cells.

  6. Stable organic-inorganic hybrid multilayered photoelectrochemical cells

    NASA Astrophysics Data System (ADS)

    Park, Sun-Young; Kim, Min-gyeong; Jung, Jaehoon; Heo, Jinhee; Hong, Eun Mi; Choi, Sung Mook; Lee, Joo-Yul; Cho, Shinuk; Hong, Kihyon; Lim, Dong Chan

    2017-02-01

    The production of hydrogen from water via solar energy conversion has attracted immense attention as a potential solution for addressing energy supply issues. We demonstrated a stable and efficient organic-inorganic hybrid photoelectrochemical (H-PEC) cell. Modifying the surface energy and structure of the organic photoactive layer using multi-functional nanomaterials including -OH-modified NiO nanoparticles and reduced graphene oxide (RGO) led to a 2.8-fold enhancement of the water splitting performance in a single junction H-PEC cell. The enhanced performance was attributed to the i) improved water-wettability, ii) enhanced charge extraction property by band-edge alignment, and iii) the catalytic effect of the introduced NiO-OH nanoparticles. In addition, because of the effects of the RGO layer preventing water penetration and photo-corrosion during the oxidation of water, a distinguishable long-term stability was achieved from the H-PEC cell with an RGO capping layer. The best performance was obtained from the organic-inorganic hybrid multi-junction PEC cells consisting of the WO3 photo-anode (activated under UV irradiation) and the H-PEC cell (activated under visible light irradiation). The H-PEC cell with a WO3 photo-anode exhibited significantly enhanced stability and performance by a factor of 11.6 higher than photocurrent of the single H-PEC cell.

  7. Conversion of sunlight into electrical power and photoassisted electrolysis of water in photoelectrochemical cells

    SciTech Connect

    Heller, A.

    1981-05-01

    The development of photoelectrochemical solar cells based on semiconductor liquid junctions is discussed. Over the past 6 years, the efficiency of solar energy conversion has increased from < 1% to 12%, and the operational life of these cells has increased from hours to months. Understanding the chemistry of surfaces and grain boundaries has made it possible to manipulate the position of the surface and grain boundary states and thus reduce losses due to electron-hole recombination. Cells exhibiting approx. 12% efficiency of conversion are: (1) chemisorbed Ru/sup 3 +/ ions on n-GaAs photoanodes; (2) diffused Ru/sup 3 +/ and Pb/sup 2 +/ into grain boundaries of polycrystalline n-GaAs films on graphite; (3) p-InP/VCl/sub 3/-VCl/sub 2/-HCl/C cell; and (4) p-InP(Ru)/HCl-KCl/Pt cell. Photoassisted electrolysis of water for conversion of solar energy to hydrogen using the last mentioned photoelectrochemical cell represents the most efficient system for solar energy conversion. 61 references are cited. (BLM)tic stainless steel is required to prevent stress corrosion cracking byd stuffs contamination in the USSR takes place in the framework of variations observed in separate countries of northern hemisphere.

  8. Application of ZnO/graphene and S6 aptamers for sensitive photoelectrochemical detection of SK-BR-3 breast cancer cells based on a disposable indium tin oxide device.

    PubMed

    Liu, Fang; Zhang, Yan; Yu, Jinghua; Wang, Shaowei; Ge, Shenguang; Song, Xianrang

    2014-01-15

    ZnO/graphene (ZnO/G) composite and S6 aptamer were employed to sensitive photoelectrochemical (PEC) strategy for the specific detection of SK-BR-3 cancer cells based on a portable indium tin oxide microdevice. ZnO/G composite was synthesized using a facile ultrasonic method, and then applied to improve the PEC performance due to the unique hollow structure of ZnO naospheres and the superior properties of graphene. Subsequently, S6 aptamer was applied to this specific detection of SK-BR-3 cancer cells. And the concentration of SK-BR-3 cells was measured with a low detection limit of 58 cells mL(-1) and a wide linear range of 1×10(2)-1×10(6) cells mL(-1), through the decrease in photocurrent intensity resulting from the increase in steric hindrances when specifically recognized with S6 aptamers. Excellent discrimination against target and analogous cells was demonstrated, indicating the high selectivity of the proposed cell sensor. Our work also demonstrated a sensitive, stable and low cytotoxicity approach for early and accurate detection of cancer cells.

  9. Wire Array Solar Cells: Fabrication and Photoelectrochemical Studies

    NASA Astrophysics Data System (ADS)

    Spurgeon, Joshua Michael

    Despite demand for clean energy to reduce our addiction to fossil fuels, the price of these technologies relative to oil and coal has prevented their widespread implementation. Solar energy has enormous potential as a carbon-free resource but is several times the cost of coal-produced electricity, largely because photovoltaics of practical efficiency require high-quality, pure semiconductor materials. To produce current in a planar junction solar cell, an electron or hole generated deep within the material must travel all the way to the junction without recombining. Radial junction, wire array solar cells, however, have the potential to decouple the directions of light absorption and charge-carrier collection so that a semiconductor with a minority-carrier diffusion length shorter than its absorption depth (i.e., a lower quality, potentially cheaper material) can effectively produce current. The axial dimension of the wires is long enough for sufficient optical absorption while the charge-carriers are collected along the shorter radial dimension in a massively parallel array. This thesis explores the wire array solar cell design by developing potentially low-cost fabrication methods and investigating the energy-conversion properties of the arrays in photoelectrochemical cells. The concept was initially investigated with Cd(Se, Te) rod arrays; however, Si was the primary focus of wire array research because its semiconductor properties make low-quality Si an ideal candidate for improvement in a radial geometry. Fabrication routes for Si wire arrays were explored, including the vapor-liquid-solid growth of wires using SiCl4. Uniform, vertically aligned Si wires were demonstrated in a process that permits control of the wire radius, length, and spacing. A technique was developed to transfer these wire arrays into a low-cost, flexible polymer film, and grow multiple subsequent arrays using a single Si(111) substrate. Photoelectrochemical measurements on Si wire array

  10. Self-powered sensing platform equipped with Prussian blue electrochromic display driven by photoelectrochemical cell.

    PubMed

    Wang, Yanhu; Gao, Chaomin; Ge, Shenguang; Zhang, Lina; Yu, Jinghua; Yan, Mei

    2017-03-15

    By incorporating the Prussian Blue (PB) electrochromic display as cathode, a solar-driven photoelectrochemical (PEC) cell was constructed through combining sandwich-structured graphite-like carbon nitride (g-C3N4)-Au-branched-titanium dioxide (B-TiO2) nanorods as photoanode for self-powered hydrogen peroxide (H2O2) sensing, which exhibits both direct photoelectrochemical and electrochromic response. The gold nanoparticles (Au NPs) sandwiched between the B-TiO2 nanorods and the g-C3N4 layer served as electron relay as well as plasmonic photosensitizer to enhance the solar-to-chemical energy conversion efficiency. Owing to the effective disproportionation of H2O2 and specific recognition of mannose on cell surface, concanavalin-A conjugated porous AuPd alloy nanoparticles were introduced as the catalytically active nanolabels promoting generation of hydroxyl radicals (·OH). Based on the cleavage of DNA with the participation of ·OH radicals generated by the decomposition of H2O2 under the catalysis of AuPd alloy result in the disassembly of cancer cells to achieve further signal enhancement. The multiple-signal-output sensing response not only provides a promising strategy for different analytical purposes based on novel stimuli-responsive materials, but also enhances the reliability in the analyte detection.

  11. Quantum-dots-based photoelectrochemical bioanalysis highlighted with recent examples.

    PubMed

    Zhang, Nan; Zhang, Ling; Ruan, Yi-Fan; Zhao, Wei-Wei; Xu, Jing-Juan; Chen, Hong-Yuan

    2017-03-07

    Photoelectrochemical (PEC) bioanalysis is a newly developed methodology that provides an exquisite route for innovative biomolecular detection. Quantum dots (QDs) are semiconductor nanocrystals with unique photophysical properties that have attracted tremendous attentions among the analytical community. QDs-based PEC bioanalysis comprises an important research hotspot in the field of PEC bioanalysis due to its combined advantages and potentials. Currently, it has ignited increasing interests as demonstrated by increased research papers. This review aims to cover the most recent advances in this field. With the discussion of recent examples of QDs-PEC bioanalysis from the literatures, special emphasis will be placed on work reporting on fundamental advances in the signaling strategies of QDs-based PEC bioanalysis from 2013 to now. Future prospects in this field are also discussed.

  12. Enzyme-catalyzed biocathode in a photoelectrochemical biofuel cell

    NASA Astrophysics Data System (ADS)

    Yang, Jing; Hu, Donghua; Zhang, Xiaohuan; Wang, Kunqi; Wang, Bin; Sun, Bo; Qiu, Zhidong

    2014-12-01

    A novel double-enzyme photoelectrochemical biofuel cell (PEBFC) has been developed by taking glucose dehydrogenase (GDH) and horseradish peroxidase (HRP) as the enzyme of the photoanode and biocathode to catalyze the oxidation of glucose and the reduction of oxygen. A H2-mesoporphyrin IX is used as a dye for a TiO2 film electrode to fabricate a photoanode. The horseradish peroxidase (HRP) is immobilized on a glassy carbon (GC) electrode to construct a biocathode which is used to catalyze the reduction of oxygen in the PEBFC for the first time. The biocathode exhibits excellent electrocatalytic activity in the presence of O2. The performances of the PEBFC are obtained by current-voltage and power-voltage curves. The short-circuit current density (Isc), the open-circuit voltage (Voc), maximum power density (Pmax), fill factor (FF) and energy conversion efficiency (η) are 439 μA cm-2, 678 mV, 79 μW cm-2, 0.39 and 0.016%, respectively, and the incident photon-to-collected electron conversion efficiency (IPCE) is 32% at 350 nm. The Isc is higher than that of the PEBFC with Pt cathode, and the Voc is higher than that of the dye-sensitized solar cell or the enzyme-catalyzed biofuel cell operating individually, which demonstrates that the HRP is an efficient catalyst for the biocathode in the PEBFC.

  13. Polyoxymetalate liquid-catalyzed polyol fuel cell and the related photoelectrochemical reaction mechanism study

    NASA Astrophysics Data System (ADS)

    Wu, Weibing; Liu, Wei; Mu, Wei; Deng, Yulin

    2016-06-01

    A novel design of liquid catalyzed fuel cell (LCFC), which uses polyoxometalates (POMs) as the photocatalyst and charge carrier has been reported previously. In this paper, the adaptability of biomass fuels (e.g., glycerol and glucose) to the LCFC and corresponding cell performance were studied in detail here. An interesting finding that greatly differs from conventional fuel cell is that high molecular weight fuels rather than small molecule fuels (e.g., methanol and ethylene glycol) are favored by the novel LCFC with respect to the power densities. The power output of LCFC strongly depends on the number and structure of hydroxyl groups in the biomass fuels. The evidence of UV-Vis and 1H NMR spectra shows that the preassociation between POM and alcohol fuels, which determines the photoelectrochemical reaction pathway of POM, is enhanced as the number of hydroxyl increases. Experimental results also demonstrate that more hydroxyl groups in the molecules lead to faster photoelectrochemical reaction between POM and fuels, higher reduction degree of POM, and further higher power output of LCFC. Our study reveals that biomass-based polyhydroxyl compounds such as starch, hemicellulose and cellulose are potential high-performance fuels for LCFC.

  14. Photoelectrochemical storage cell with n-CdSe and p-CdTe electrodes

    SciTech Connect

    Gerritsen, H.J.; Ruppel, W.

    1984-09-01

    Charge and energy storage is presented for a photoelectrochemical cell, in which in a CdSO4 electrolyte one electrode, n-CdSe, is photodecomposed under illumination, and the other electrode, p-CdTe, is photoelectroplated by Cd. These processes lead to a galvanic cell with Se on CdSe as one electrode, and Cd on CdTe as the other electrode. The discharge products, when the cell is discharged in the dark, are the original photosensitive semiconductors. Each of these photosensitive electrodes, as well as their combined performance, is discussed, together with the source of irreversibilities for this method of photoelectrochemical energy conversion. 15 references.

  15. Ultrasensitive Photoelectrochemical Biosensing of Cell Surface N-Glycan Expression Based on the Enhancement of Nanogold-Assembled Mesoporous Silica Amplified by Graphene Quantum Dots and Hybridization Chain Reaction.

    PubMed

    Ge, Shenguang; Lan, Feifei; Liang, Linlin; Ren, Na; Li, Li; Liu, Haiyun; Yan, Mei; Yu, Jinghua

    2017-03-01

    An ultrasensitive photoelectrochemical (PEC) biosensor for N-glycan expression based on the enhancement of nanogold-assembled mesoporous silica nanoparticles (GMSNs) was fabricated, which also combined with multibranched hybridization chain reaction (mHCR) and graphene quantum dots (GQDs). In this work, the localized surface plasmon resonance, mHCR and GQDs-induced signal amplification strategies were integrated exquisitely and applied sufficiently. In the fabrication, after porous ZnO spheres immobilized on the Au nanorod-modified paper working electrode were sensitized by CdTe QDs, the GMSNs were assembled on the CdTe QDs. Then the photocurrent efficiency was improved by the sensitization of the CdTe QDs and the localized surface plasmon resonance of GMSNs. Successively, the products of mHCR with multiple biotins for multiple horseradish peroxidase binding and multiple branched arms for capturing the target cells were attached on the as-prepared electrode. The chemiluminescent (CL) emission with the aid of horseradish peroxidase served as an inner light source to excite photoactive materials for simplifying the instrument. Furthermore, the aptamer could capture the cancer cells by its highly efficient cell recognition ability, which avoided the conventional routing cell counting procedures. Meanwhile, the GQDs served as the signal amplication strategy, which was exerted in the process of N-glycan evaluation because the competitive absorption of exciting light and consumption of H2O2 served as the electron donor of the PEC system and the oxidant of the luminol-based CL system. This judiciously engineered biosensor offered a promising platform for the exploration of N-glycan-based physiological processes.

  16. Photoelectrochemical investigation of ultrathin film iron oxide solar cells prepared by atomic layer deposition.

    SciTech Connect

    Klahr, B. M.; Martinson, A. B. F.; Hamann, T. W.

    2011-01-01

    Atomic layer deposition was used to grow conformal thin films of hematite with controlled thickness on transparent conductive oxide substrates. The hematite films were incorporated as photoelectrodes in regenerative photoelectrochemical cells employing an aqueous [Fe(CN){sub 6}]{sup 3-/4-} electrolyte. Steady state current density versus applied potential measurements under monochromatic and simulated solar illumination were used to probe the photoelectrochemical properties of the hematite electrodes as a function of film thickness. Combining the photoelectrochemical results with careful optical measurements allowed us to determine an optimal thickness for a hematite electrode of {approx}20 nm. Mott-Schottky analysis of differential capacitance measurements indicated a depletion region of {approx}17 nm. Thus, only charge carriers generated in the depletion region were found to contribute to the photocurrent.

  17. Photoelectrochemical Investigation of Ultrathin Film Iron Oxide Solar Cells Prepared by Atomic Layer Deposition

    SciTech Connect

    Klahr, Benjamin M.; Martinson, Alex B.F.; Hamann, Thomas W.

    2010-12-02

    Atomic layer deposition was used to grow conformal thin films of hematite with controlled thickness on transparent conductive oxide substrates. The hematite films were incorporated as photoelectrodes in regenerative photoelectrochemical cells employing an aqueous [Fe(CN)6]3-/4- electrolyte. Steady state current density versus applied potential measurements under monochromatic and simulated solar illumination were used to probe the photoelectrochemical properties of the hematite electrodes as a function of film thickness. Combining the photoelectrochemical results with careful optical measurements allowed us to determine an optimal thickness for a hematite electrode of ~20 nm. Mott-Schottky analysis of differential capacitance measurements indicated a depletion region of ~17 nm. Thus, only charge carriers generated in the depletion region were found to contribute to the photocurrent.

  18. Photoelectrochemical investigation of ultrathin film iron oxide solar cells prepared by atomic layer deposition.

    PubMed

    Klahr, Benjamin M; Martinson, Alex B F; Hamann, Thomas W

    2011-01-04

    Atomic layer deposition was used to grow conformal thin films of hematite with controlled thickness on transparent conductive oxide substrates. The hematite films were incorporated as photoelectrodes in regenerative photoelectrochemical cells employing an aqueous [Fe(CN)(6)](3-/4-) electrolyte. Steady state current density versus applied potential measurements under monochromatic and simulated solar illumination were used to probe the photoelectrochemical properties of the hematite electrodes as a function of film thickness. Combining the photoelectrochemical results with careful optical measurements allowed us to determine an optimal thickness for a hematite electrode of ∼20 nm. Mott-Schottky analysis of differential capacitance measurements indicated a depletion region of ∼17 nm. Thus, only charge carriers generated in the depletion region were found to contribute to the photocurrent.

  19. Photostable p-type dye-sensitized photoelectrochemical cells for water reduction.

    PubMed

    Ji, Zhiqiang; He, Mingfu; Huang, Zhongjie; Ozkan, Umit; Wu, Yiying

    2013-08-14

    A photostable p-type NiO photocathode based on a bifunctional cyclometalated ruthenium sensitizer and a cobaloxime catalyst has been created for visible-light-driven water reduction to produce H2. The sensitizer is anchored firmly on the surface of NiO, and the binding is resistant to the hydrolytic cleavage. The bifunctional sensitizer can also immobilize the water reduction catalyst. The resultant photoelectrode exhibits superior stability in aqueous solutions. Stable photocurrents have been observed over a period of hours. This finding is useful for addressing the degradation issue in dye-sensitized photoelectrochemical cells caused by desorption of dyes and catalysts. The high stability of our photocathodes should be important for the practical application of these devices for solar fuel production.

  20. Metal-free organic sensitizers for use in water-splitting dye-sensitized photoelectrochemical cells

    PubMed Central

    Swierk, John R.; Méndez-Hernández, Dalvin D.; McCool, Nicholas S.; Liddell, Paul; Terazono, Yuichi; Pahk, Ian; Tomlin, John J.; Oster, Nolan V.; Moore, Thomas A.; Moore, Ana L.; Gust, Devens; Mallouk, Thomas E.

    2015-01-01

    Solar fuel generation requires the efficient capture and conversion of visible light. In both natural and artificial systems, molecular sensitizers can be tuned to capture, convert, and transfer visible light energy. We demonstrate that a series of metal-free porphyrins can drive photoelectrochemical water splitting under broadband and red light (λ > 590 nm) illumination in a dye-sensitized TiO2 solar cell. We report the synthesis, spectral, and electrochemical properties of the sensitizers. Despite slow recombination of photoinjected electrons with oxidized porphyrins, photocurrents are low because of low injection yields and slow electron self-exchange between oxidized porphyrins. The free-base porphyrins are stable under conditions of water photoelectrolysis and in some cases photovoltages in excess of 1 V are observed. PMID:25583488

  1. Reaction kinetics and product distributions in photoelectrochemical cells. Report on research activities, March 15, 1991--March 14, 1994

    SciTech Connect

    Koval, C.A.

    1993-09-01

    Semiconductor/liquid junction solar cells, also called photoelectrochemical cells (PEC), represent a versatile way to use solar energy. Photon energy can be used to make electricity and chemical fuels or can be used as an alternative to thermal activation energy in photocatalytic cells. Two fundamental processes associated with photoelectrochemical solar energy conversion were investigated experimentally: (i) Reactions of `hot` electrons, and (ii) Electrode kinetics at 2-dimensional materials.

  2. Wire-supported CdSe nanowire array photoelectrochemical solar cells.

    PubMed

    Zhang, Luhui; Shi, Enzheng; Li, Zhen; Li, Peixu; Jia, Yi; Ji, Chunyan; Wei, Jinquan; Wang, Kunlin; Zhu, Hongwei; Wu, Dehai; Cao, Anyuan

    2012-03-14

    Previous fiber-shaped solar cells are based on polymeric materials or dye-sensitized wide band-gap oxides. Here, we show that efficient fiber solar cells can be made from semiconducting nanostructures (e.g. CdSe) with smaller band-gap as the light absorption material. We directly grow a vertical array of CdSe nanowires uniformly around a core metal wire and make the device by covering the top of nanowires with a carbon nanotube (CNT) film as the porous transparent electrode. The CdSe-CNT fiber solar cells show power conversion efficiencies of 1-2% under AM 1.5 illumination after the nanowires are infiltrated with redox electrolyte. We do not use a secondary metal wire (e.g. Pt) as in conventional fiber-shaped devices, instead, the end part of the CNT film is condensed into a conductive yarn to serve as the secondary electrode. In addition, our CdSe nanowire-based photoelectrochemical fiber solar cells maintain good flexibility and stable performance upon rotation and bending to large angles.

  3. High-performance silicon nanowire array photoelectrochemical solar cells through surface passivation and modification.

    PubMed

    Wang, Xin; Peng, Kui-Qing; Pan, Xiao-Jun; Chen, Xue; Yang, Yang; Li, Li; Meng, Xiang-Min; Zhang, Wen-Jun; Lee, Shuit-Tong

    2011-10-10

    Nanowire solar cells: Pt nanoparticle (PtNP) decorated C/Si core/shell nanowire photoelectrochemical solar cells show high conversion efficiency of 10.86 % and excellent stability in aggressive electrolytes under 1-sun AM 1.5 G illumination. Superior device performance is achieved by improved surface passivation of the nanowires by carbon coating and enhanced interfacial charge transfer by PtNPs.

  4. Porous copper zinc tin sulfide thin film as photocathode for double junction photoelectrochemical solar cells.

    PubMed

    Dai, Pengcheng; Zhang, Guan; Chen, Yuncheng; Jiang, Hechun; Feng, Zhenyu; Lin, Zhaojun; Zhan, Jinhua

    2012-03-21

    Porous copper zinc tin sulfide (CZTS) thin film was prepared via a solvothermal approach. Compared with conventional dye-sensitized solar cells (DSSCs), double junction photoelectrochemical cells using dye-sensitized n-type TiO(2) (DS-TiO(2)) as the photoanode and porous p-type CZTS film as the photocathode shows an increased short circuit current, external quantum efficiency and power conversion efficiency.

  5. Low-toxic Ag2S quantum dots for photoelectrochemical detection glucose and cancer cells.

    PubMed

    Zhang, Xiaoru; Liu, Mingshuai; Liu, Hongxia; Zhang, Shusheng

    2014-06-15

    A new photoelectrochemical (PEC) biosensor was developed using low-toxic Ag2S QDs as photoelectrochemically active species. Energy levels of Ag2S and Ag2Se QD were compared to explain their differences in the PEC performance. The preparation condition of Ag2S QD was optimized and its structure characterization was measured. Then the developed photoelectric active interface was used to detect glucose and MCF-7 cancer cell and showed the good sensitivity and specificity. Under optimal condition, detection limits of 3.2 × 10(-5)M for glucose and 98 cells/mL for MCF-7 cell were achieved. Thus, the prepared Ag2S QD could serve as an excellent and promising photoelectric active material in the PEC biosensor.

  6. Fluorescent gold nanoclusters based photoelectrochemical sensors for detection of H2O2 and glucose.

    PubMed

    Zhang, Jianxiu; Tu, Liping; Zhao, Shuang; Liu, Guohua; Wang, Yangyun; Wang, Yong; Yue, Zhao

    2015-05-15

    In this work, low-toxicity fluorescent gold nanoclusters (AuNCs) based photoelectrochemical sensors were developed for H2O2 and glucose detection. Herein, the processes used to fabricate the sensors and the photoelectrochemical performances of the sensors under different conditions were presented. Based on the energy band levels of the AuNCs and electron tunneling processes, a detailed photoelectrochemical sensing model was given. The designed sensors were then used for H2O2 and glucose detection without any extra modification of the AuNCs or complex enzyme immobilization. The results demonstrate that the AuNCs allow for H2O2 sensing based on their capacity for both fluorescence and catalysis. Indeed, it was observed that H2O2 was catalyzed by the AuNCs and reduced by photoinduced electrons derived from excited AuNCs. Furthermore, an enhancement in photocurrent amplitude followed the increase in the concentrations of H2O2 and glucose. The effects of the types of ligands surrounding the AuNCs and the applied potential on the output photocurrent were well studied to optimize the measurement conditions. The sensitivity and LOD of MUA-AuNCs at -500 mV were 4.33 nA/mM and 35 μM, respectively. All experimental results indicated that AuNCs could not only serve as a promising photoelectrical material for building the photoelectrochemical biosensors but as catalysts for H2O2 sensing.

  7. A solid oxide photoelectrochemical cell with UV light-driven oxygen storage in mixed conducting electrodes.

    PubMed

    Walch, Gregor; Rotter, Bernhard; Brunauer, Georg Christoph; Esmaeili, Esmaeil; Opitz, Alexander Karl; Kubicek, Markus; Summhammer, Johann; Ponweiser, Karl; Fleig, Jürgen

    2017-01-28

    A single crystalline SrTiO3 working electrode in a zirconia-based solid oxide electrochemical cell is illuminated by UV light at temperatures of 360-460 °C. In addition to photovoltaic effects, this leads to the build-up of a battery-type voltage up to more than 300 mV. After switching off UV light, this voltage only slowly decays. It is caused by UV-induced oxygen incorporation into the mixed conducting working electrode and thus by changes of the oxygen stoichiometry δ in SrTiO3-δ under UV illumination. These changes of the oxygen content could be followed in time-dependent voltage measurements and also manifest themselves in time-dependent resistance changes during and after UV illumination. Discharge currents measured after UV illumination reveal that a large fraction of the existing oxygen vacancies in SrTiO3 become filled under UV light. Additional measurements on cells with TiO2 thin film electrodes show the broader applicability of this novel approach for transforming light into chemical energy and thus the feasibility of solid oxide photoelectrochemical cells (SOPECs) in general and of a "light-charged oxygen battery" in particular.

  8. A solid oxide photoelectrochemical cell with UV light-driven oxygen storage in mixed conducting electrodes

    PubMed Central

    Walch, Gregor; Rotter, Bernhard; Brunauer, Georg Christoph; Esmaeili, Esmaeil; Opitz, Alexander Karl; Kubicek, Markus; Summhammer, Johann; Ponweiser, Karl

    2017-01-01

    A single crystalline SrTiO3 working electrode in a zirconia-based solid oxide electrochemical cell is illuminated by UV light at temperatures of 360–460 °C. In addition to photovoltaic effects, this leads to the build-up of a battery-type voltage up to more than 300 mV. After switching off UV light, this voltage only slowly decays. It is caused by UV-induced oxygen incorporation into the mixed conducting working electrode and thus by changes of the oxygen stoichiometry δ in SrTiO3–δ under UV illumination. These changes of the oxygen content could be followed in time-dependent voltage measurements and also manifest themselves in time-dependent resistance changes during and after UV illumination. Discharge currents measured after UV illumination reveal that a large fraction of the existing oxygen vacancies in SrTiO3 become filled under UV light. Additional measurements on cells with TiO2 thin film electrodes show the broader applicability of this novel approach for transforming light into chemical energy and thus the feasibility of solid oxide photoelectrochemical cells (SOPECs) in general and of a “light-charged oxygen battery” in particular. PMID:28261480

  9. Photoelectrochemical cell having photoanode with thin boron phosphide coating as a corrosion resistant layer

    DOEpatents

    Baughman, Richard J.; Ginley, David S.

    1984-01-01

    A surface prone to corrosion in corrosive environments is rendered anticorrosive by CVD growing a thin continuous film, e.g., having no detectable pinholes, thereon, of boron phosphide. In one embodiment, the film is semiconductive. In another aspect, the invention is an improved photoanode, and/or photoelectrochemical cell with a photoanode having a thin film of boron phosphide thereon rendering it anitcorrosive, and providing it with unexpectedly improved photoresponsive properties.

  10. High efficiency single-crystal CdSe photoelectrochemical solar cell and an associated loss mechanism

    SciTech Connect

    Frese, K.W. Jr.

    1982-02-01

    The conversion efficiency of a n-CdSe (1120) photoelectrochemical solar cell was found to be 12.4% in alkaline K/sub 3/Fe(CN)/sub 6//K/sub 4/Fe(CN)/sub 6/ electrolyte. The pH of the electrolyte is critical for observing high efficiency and stable photocurrent. A selenium corrosion layer acts as a light filter to block the photocurrent.

  11. Solid-state dye-sensitized solar cells fabricated by coupling photoelectrochemically deposited poly(3,4-ethylenedioxythiophene) (PEDOT) with silver-paint on cathode.

    PubMed

    Manseki, Kazuhiro; Jarernboon, Wirat; Youhai, You; Jiang, Ke-Jian; Suzuki, Kazuharu; Masaki, Naruhiko; Kim, Yukyeong; Xia, Jiangbin; Yanagida, Shozo

    2011-03-21

    A PEDOT-based dye-sensitized solar cell (DSC) is successfully improved by coupling photoelectrochemically deposited PEDOT layer with an Ag paste-paint on the cathode. With a 9.3 μm thick mesoscopic nanocrystalline TiO(2) film, a maximum cell performance of 3.2% with relatively high V(oc) of around 780 mV is achieved.

  12. An investigation on the photoelectrochemical properties of dye-sensitized solar cells based on graphene-TiO2 composite photoanodes

    NASA Astrophysics Data System (ADS)

    Zhu, Menghua; Li, Xin; Liu, Weiwei; Cui, Ying

    2014-09-01

    The graphene-TiO2 nanocomposite has been prepared by mixing graphene oxide (GO) and tetra-n-butyl titanate (TBT) followed by the facile hydrothermal process when the reduction of GO to reduced graphene oxide (RGO) and the hydrolysis of TBT to TiO2 happen. Characterization of the graphene-TiO2 nanostructures is investigated in detail by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and Raman spectroscopy. A dye-sensitized solar cell (DSSC) based on graphene-TiO2 composite photoelectrode exhibits a high energy conversion efficiency of 4.28%, compared with a DSSC based on pure TiO2 photoelectrode (3.11%), accompanied by an increment in both short-circuit photocurrent density and open-circuit voltage. The significant enhancement in performance of DSSC is investigated through intensity-modulated photovoltage spectroscopy, intensity-modulated photocurrent spectroscopy, and electrochemical impedance spectroscopy. It is found that the incorporation of two-dimensional graphene nanosheets in the TiO2 electrodes is the key factor leading to the improved photogenerated electron transfer ability and reduced charge recombination.

  13. Nanostructured photoelectrochemical solar cell for nitrogen reduction using plasmon-enhanced black silicon

    NASA Astrophysics Data System (ADS)

    Ali, Muataz; Zhou, Fengling; Chen, Kun; Kotzur, Christopher; Xiao, Changlong; Bourgeois, Laure; Zhang, Xinyi; Macfarlane, Douglas R.

    2016-04-01

    Ammonia (NH3) is one of the most widely produced chemicals worldwide. It has application in the production of many important chemicals, particularly fertilizers. It is also, potentially, an important energy storage intermediate and clean energy carrier. Ammonia production, however, mostly uses fossil fuels and currently accounts for more than 1.6% of global CO2 emissions (0.57 Gt in 2015). Here we describe a solar-driven nanostructured photoelectrochemical cell based on plasmon-enhanced black silicon for the conversion of atmospheric N2 to ammonia producing yields of 13.3 mg m-2 h-1 under 2 suns illumination. The yield increases with pressure; the highest observed in this work was 60 mg m-2 h-1 at 7 atm. In the presence of sulfite as a reactant, the process also offers a direct solar energy route to ammonium sulfate, a fertilizer of economic importance. Although the yields are currently not sufficient for practical application, there is much scope for improvement in the active materials in this cell.

  14. Nanostructured photoelectrochemical solar cell for nitrogen reduction using plasmon-enhanced black silicon

    PubMed Central

    Ali, Muataz; Zhou, Fengling; Chen, Kun; Kotzur, Christopher; Xiao, Changlong; Bourgeois, Laure; Zhang, Xinyi; MacFarlane, Douglas R.

    2016-01-01

    Ammonia (NH3) is one of the most widely produced chemicals worldwide. It has application in the production of many important chemicals, particularly fertilizers. It is also, potentially, an important energy storage intermediate and clean energy carrier. Ammonia production, however, mostly uses fossil fuels and currently accounts for more than 1.6% of global CO2 emissions (0.57  Gt in 2015). Here we describe a solar-driven nanostructured photoelectrochemical cell based on plasmon-enhanced black silicon for the conversion of atmospheric N2 to ammonia producing yields of 13.3 mg m−2 h−1 under 2 suns illumination. The yield increases with pressure; the highest observed in this work was 60 mg m−2 h−1 at 7 atm. In the presence of sulfite as a reactant, the process also offers a direct solar energy route to ammonium sulfate, a fertilizer of economic importance. Although the yields are currently not sufficient for practical application, there is much scope for improvement in the active materials in this cell. PMID:27093916

  15. Realizing InGaN monolithic solar-photoelectrochemical cells for artificial photosynthesis

    SciTech Connect

    Dahal, R.; Pantha, B. N.; Li, J.; Lin, J. Y.; Jiang, H. X.

    2014-04-07

    InGaN alloys are very promising for solar water splitting because they have direct bandgaps that cover almost the whole solar spectrum. The demonstration of direct solar-to-fuel conversion without external bias with the sunlight being the only energy input would pave the way for realizing photoelectrochemical (PEC) production of hydrogen by using InGaN. A monolithic solar-PEC cell based on InGaN/GaN multiple quantum wells capable to directly generate hydrogen gas under zero bias via solar water splitting is reported. Under the irradiation by a simulated sunlight (1-sun with 100 mW/cm{sup 2}), a 1.5% solar-to-fuel conversion efficiency has been achieved under zero bias, setting a fresh benchmark of employing III-nitrides for artificial photosynthesis. Time dependent hydrogen gas production photocurrent measured over a prolonged period (measured for 7 days) revealed an excellent chemical stability of InGaN in aqueous solution of hydrobromic acid. The results provide insights into the architecture design of using InGaN for artificial photosynthesis to provide usable clean fuel (hydrogen gas) with the sunlight being the only energy input.

  16. Realizing InGaN monolithic solar-photoelectrochemical cells for artificial photosynthesis

    NASA Astrophysics Data System (ADS)

    Dahal, R.; Pantha, B. N.; Li, J.; Lin, J. Y.; Jiang, H. X.

    2014-04-01

    InGaN alloys are very promising for solar water splitting because they have direct bandgaps that cover almost the whole solar spectrum. The demonstration of direct solar-to-fuel conversion without external bias with the sunlight being the only energy input would pave the way for realizing photoelectrochemical (PEC) production of hydrogen by using InGaN. A monolithic solar-PEC cell based on InGaN/GaN multiple quantum wells capable to directly generate hydrogen gas under zero bias via solar water splitting is reported. Under the irradiation by a simulated sunlight (1-sun with 100 mW/cm2), a 1.5% solar-to-fuel conversion efficiency has been achieved under zero bias, setting a fresh benchmark of employing III-nitrides for artificial photosynthesis. Time dependent hydrogen gas production photocurrent measured over a prolonged period (measured for 7 days) revealed an excellent chemical stability of InGaN in aqueous solution of hydrobromic acid. The results provide insights into the architecture design of using InGaN for artificial photosynthesis to provide usable clean fuel (hydrogen gas) with the sunlight being the only energy input.

  17. Experimenting with photoelectrochemical cells in drinking straws: practical aids for learning about solar energy in school or at home

    NASA Astrophysics Data System (ADS)

    Appleyard, S. J.

    2008-05-01

    Photoelectrochemical cells using dye-sensitized ZnO with a Cu2+/Fe2+/Fe3+ electrolyte can be easily made at home or in a school classroom with household chemicals and other readily available materials. The cells, which are made with wire housed within plastic drinking straws, have open-circuit voltages of 0.5-0.7 V and short-circuit currents of about 0.5-2.5 mA cm-2. Step-by-step instructions are provided on how to construct the photoelectrochemical cells, as are suggestions about how to use the cells to explore some concepts associated with utilizing solar energy.

  18. Solar-driven photoelectrochemical probing of nanodot/nanowire/cell interface.

    PubMed

    Tang, Jing; Zhang, Yueyu; Kong, Biao; Wang, Yongcheng; Da, Peimei; Li, Jun; Elzatahry, Ahmed A; Zhao, Dongyuan; Gong, Xingao; Zheng, Gengfeng

    2014-05-14

    We report a nitrogen-doped carbon nanodot (N-Cdot)/TiO2 nanowire photoanode for solar-driven, real-time, and sensitive photoelectrochemical probing of the cellular generation of H2S, an important endogenous gasotransmitter based on a tunable interfacial charge carrier transfer mechanism. Synthesized by a microwave-assisted solvothermal method and subsequent surface chemical conjugation, the obtained N-Cdot/TiO2 nanowire photoanode shows much enhanced photoelectrochemical photocurrent compared with pristine TiO2 nanowires. This photocurrent increase is attributed to the injection of photogenerated electrons from N-Cdots to TiO2 nanowires, confirmed by density functional theory simulation. In addition, the charge transfer efficiency is quenched by Cu(2+), whereas the introduction of H2S or S(2-) ions resets the charge transfer and subsequently the photocurrent, thus leading to sensitive photoelectrochemical recording of the H2S level in buffer and cellular environments. Moreover, this N-Cdot-TiO2 nanowire photoanode has been demonstrated for direct growth and interfacing of H9c2 cardiac myoblasts, with the capability of interrogating H2S cellular generation pathways by vascular endothelial growth factor stimulation as well as inhibition.

  19. Converting environmentally hazardous materials into clean energy using a novel nanostructured photoelectrochemical fuel cell

    SciTech Connect

    Gan, Yong X.; Gan, Bo J.; Clark, Evan; Su, Lusheng; Zhang, Lihua

    2012-09-15

    Highlights: ► A photoelectrochemical fuel cell has been made from TiO{sub 2} nanotubes. ► The fuel cell decomposes environmentally hazardous materials to produce electricity. ► Doping the anode with a transition metal oxide increases the visible light sensitivity. ► Loading the anode with a conducting polymer enhances the visible light absorption. -- Abstract: In this work, a novel photoelectrochemical fuel cell consisting of a titanium dioxide nanotube array photosensitive anode and a platinum cathode was made for decomposing environmentally hazardous materials to produce electricity and clean fuel. Titanium dioxide nanotubes (TiO{sub 2} NTs) were prepared via electrochemical oxidation of pure Ti in an ammonium fluoride and glycerol-containing solution. Scanning electron microscopy was used to analyze the morphology of the nanotubes. The average diameter, wall thickness and length of the as-prepared TiO{sub 2} NTs were determined. The photosensitive anode made from the highly ordered TiO{sub 2} NTs has good photo-catalytic property, as proven by the decomposition tests on urea, ammonia, sodium sulfide and automobile engine coolant under ultraviolet (UV) radiation. To improve the efficiency of the fuel cell, doping the TiO{sub 2} NTs with a transition metal oxide, NiO, was performed and the photosensitivity of the doped anode was tested under visible light irradiation. It is found that the NiO-doped anode is sensitive to visible light. Also found is that polyaniline-doped photosensitive anode can harvest photon energy in the visible light spectrum range much more efficiently than the NiO-doped one. It is concluded that the nanostructured photoelectrochemical fuel cell can generate electricity and clean fuel by decomposing hazardous materials under sunlight.

  20. Photoluminescence and Raman spectroscopy of photoelectrochemical solar cells

    SciTech Connect

    Garuthara, R.K.A.

    1986-01-01

    The CdSe/polysulfide system was studied in order to produce low-cost liquid-junction solar cells. Three basic area were investigated: (1) space-charge-layer effects, (2) aging of photoanodes due to slow chemical changes on electrode surface, and (3) the effect of photoetching and the impurity centers in photoanodes. Relaxation spectrum analysis, photoluminescence, modulated photoluminescence, and Raman spectroscopy were utilized to study these areas. The potential distribution at the interface of n-type CdSe/polysulfide was examined. At reverse bias and at electrode potential, the modulated photoluminescence is described by the dead layer model. The electrical characterization of the interface, based on modulated photoluminescence, agrees with the relaxation spectrum-analysis measurements. The slow chemical changes on the CdSe/polysulfide liquid-junction solar cells, as a function of aging procedures, were studied using photoluminescence and Raman spectroscopy. For the first time, it is reported that cells do age under open-circuit conditions. The effect of photoetching on single crystal n-type CdSe was investigated, using photoluminescence spectroscopy. A blue-shift is observed in the photoluminescence spectrum of crystals when the doping density is decreased.

  1. Photoelectrochemical cells for the production of hydrogen and hydrogen peroxide via photoredox reactions

    SciTech Connect

    Neumann-Spallart, M.; Kalyanasundaram, K.

    1982-07-08

    The performance of various dye-sensitized photoredox systems leading to either water reduction on Br/sup -/ oxidation has been examined in photoelectrochemical cells. In the first part, we consider visible-light-induced H/sub 2/ evolution sensitized by dues such as Ru(bpy)/sub 3//sup 2 +/, water soluble zinc prophyrin (zinc tetrakis(4-N-methylpyridyl)porphyrin, ZnTMPyP), proflavin, and phenosafranine. Various factors such as the oxidative vs reductive cycle, the role of relay and its concentration, etc., in relation to photoelectrochemical cells are examined. A quantitative analysis and a kinetic model for the current-potential curves in cells involving photoredox reactions (systems involving oxidative quenching) is presented. Later, the cell system C/Ru(bpy)/sub 3//sup 2 +/,MV/sup 2 +/,O/sub 2/ parallel HBr/C is examined in detail, where photoinduced oxygen reduction to H/sub 2/O/sub 2/ is coupled to bromide oxidation. For all the cell systems examined, there is good agreement between the observed photocurrents and photopotentials with those deduced from the intersection of the individual i-e curves. 8 figures, 2 tables.

  2. Tin doped indium oxide core—TiO2 shell nanowires on stainless steel mesh for flexible photoelectrochemical cells

    NASA Astrophysics Data System (ADS)

    Hong Noh, Jun; Ding, Bo; Soo Han, Hyun; Seong Kim, Ju; Hoon Park, Jong; Baek Park, Sang; Suk Jung, Hyun; Lee, Jung-Kun; Sun Hong, Kug

    2012-02-01

    Photoanode architecture is built on highly conductive tin doped indium oxide (ITO) nanowires (NWs) on a flexible stainless steel mesh (SSM). ITO nanowires were coated with the atomic layer deposition grown TiO2 layer and the photoelectrochemical performance of the stainless steel mesh based photoanode were examined as a function of wire-length and shell-thickness. The photoanode consisting of 20 μm-long nanowire core and 36 nm thick shell increased the photocurrent of the testing cell by 4 times, compared to a reference cell. This enhanced photochemical activity is attributed to higher light harvesting efficiency of nanowire arrays and suppressed charge recombination of core-shell structure.

  3. A Simple Photoelectrochemical Cell Using Fe+++/Fe++(aq) As Redox Couple

    NASA Astrophysics Data System (ADS)

    Saxena, Vibha; Koiry, S. P.; Veerender, P.; Vasundhara, Aswal, D. K.; Gupta, S. K.; Shivran, Neelam; Mula, S.; Chattopadhyay, S.; Yakhmi, J. V.

    2010-12-01

    We report a simple photoelectrochemical cell (PEC) using a derivative of borondipyrromethane (BODIPY), that is, (4,4-difluoro-1,3,5,7,8-pentamethyl-2,6-diethyl-4-bora-3a,4a-diaza-s-indecene) as dye sensitizer and an aqueous electrolyte containing Ferric/ferrous redox couple (F+++/Fe++). Under white light illumination of intensity ˜1 mW/cm2, the open circuit voltage and short-circuit current of the PEC was found to be respectively, 180 mV and 1.3 μA/cm2.

  4. Efficient and stable photoelectrochemical cells constructed with WSe2 and MoSe2 photoanodes

    NASA Astrophysics Data System (ADS)

    Kline, G.; Kam, K.; Canfield, D.; Parkinson, B. A.

    1981-03-01

    Single crystals of n-WSe2 and n-MoSe2 were grown and employed as the photoanode in a regenerative photoelectrochemical cell with an iodide/triiodide electrolyte. Solar to electrical power conversion efficiencies of 10.2 and 9.4% were achieved on selected crystals of WSe2 and MoSe2, respectively. Products of a photocorrosion reaction from a MoSe2 electrode could not be detected in the electrolyte after one month of continuous operation. The photocurrent spectra and optimization of the electrolyte are also discussed.

  5. Photoelectrochemical and Electrochemical Characterization of Sub-Micro-Gram Amounts of Organic Semiconductors Using Scanning Droplet Cell Microscopy

    PubMed Central

    2014-01-01

    A model organic semiconductor (MDMO-PPV) was used for testing a modified version of a photoelectrochemical scanning droplet cell microscope (PE-SDCM) adapted for use with nonaqueous electrolytes and containing an optical fiber for localized illumination. The most attractive features of the PE-SDCM are represented by the possibility of addressing small areas on the investigated substrate and the need of small amounts of electrolyte. A very small amount (ng) of the material under study is sufficient for a complete electrochemical and photoelectrochemical characterization due to the scanning capability of the cell. The electrochemical behavior of the polymer was studied in detail using potentiostatic and potentiodynamic investigations as well as electrochemical impedance spectroscopy. Additionally, the photoelectrochemical properties were investigated under illumination conditions, and the photocurrents found were at least 3 orders of magnitude higher than the dark (background) current, revealing the usefulness of this compact microcell for photovoltaic characterizations. PMID:25101149

  6. Experimenting with Photoelectrochemical Cells in Drinking Straws: Practical Aids for Learning about Solar Energy in School or at Home

    ERIC Educational Resources Information Center

    Appleyard, S. J.

    2008-01-01

    Photoelectrochemical cells using dye-sensitized ZnO with a Cu[superscript 2+]/Fe[superscript 2+]/Fe[superscript 3+] electrolyte can be easily made at home or in a school classroom with household chemicals and other readily available materials. The cells, which are made with wire housed within plastic drinking straws, have open-circuit voltages of…

  7. Solar water splitting in a molecular photoelectrochemical cell

    PubMed Central

    Alibabaei, Leila; Brennaman, M. Kyle; Norris, Michael R.; Kalanyan, Berç; Song, Wenjing; Losego, Mark D.; Concepcion, Javier J.; Binstead, Robert A.; Parsons, Gregory N.; Meyer, Thomas J.

    2013-01-01

    Artificial photosynthesis and the production of solar fuels could be a key element in a future renewable energy economy providing a solution to the energy storage problem in solar energy conversion. We describe a hybrid strategy for solar water splitting based on a dye sensitized photoelectrosynthesis cell. It uses a derivatized, core–shell nanostructured photoanode with the core a high surface area conductive metal oxide film––indium tin oxide or antimony tin oxide––coated with a thin outer shell of TiO2 formed by atomic layer deposition. A “chromophore–catalyst assembly” 1, [(PO3H2)2bpy)2Ru(4-Mebpy-4-bimpy)Rub(tpy)(OH2)]4+, which combines both light absorber and water oxidation catalyst in a single molecule, was attached to the TiO2 shell. Visible photolysis of the resulting core–shell assembly structure with a Pt cathode resulted in water splitting into hydrogen and oxygen with an absorbed photon conversion efficiency of 4.4% at peak photocurrent. PMID:24277806

  8. Solar water splitting in a molecular photoelectrochemical cell.

    PubMed

    Alibabaei, Leila; Brennaman, M Kyle; Norris, Michael R; Kalanyan, Berç; Song, Wenjing; Losego, Mark D; Concepcion, Javier J; Binstead, Robert A; Parsons, Gregory N; Meyer, Thomas J

    2013-12-10

    Artificial photosynthesis and the production of solar fuels could be a key element in a future renewable energy economy providing a solution to the energy storage problem in solar energy conversion. We describe a hybrid strategy for solar water splitting based on a dye sensitized photoelectrosynthesis cell. It uses a derivatized, core-shell nanostructured photoanode with the core a high surface area conductive metal oxide film--indium tin oxide or antimony tin oxide--coated with a thin outer shell of TiO2 formed by atomic layer deposition. A "chromophore-catalyst assembly" 1, [(PO3H2)2bpy)2Ru(4-Mebpy-4-bimpy)Rub(tpy)(OH2)](4+), which combines both light absorber and water oxidation catalyst in a single molecule, was attached to the TiO2 shell. Visible photolysis of the resulting core-shell assembly structure with a Pt cathode resulted in water splitting into hydrogen and oxygen with an absorbed photon conversion efficiency of 4.4% at peak photocurrent.

  9. Electrochemical, Electrochemiluminescence, and Photoelectrochemical Aptamer-Based Nanostructured Sensors for Biomarker Analysis

    PubMed Central

    Ravalli, Andrea; Voccia, Diego; Palchetti, Ilaria; Marrazza, Giovanna

    2016-01-01

    Aptamer-based sensors have been intensively investigated as potential analytical tools in clinical analysis providing the desired portability, fast response, sensitivity, and specificity, in addition to lower cost and simplicity versus conventional methods. The aim of this review, without pretending to be exhaustive, is to give the readers an overview of recent important achievements about electrochemical, electrochemiluminescence, and photoelectrochemical aptasensors for the protein biomarker determination, mainly cancer related biomarkers, by selected recent publications. Special emphasis is placed on nanostructured-based aptasensors, which show a substantial improvement of the analytical performances. PMID:27490578

  10. Electrochemical, Electrochemiluminescence, and Photoelectrochemical Aptamer-Based Nanostructured Sensors for Biomarker Analysis.

    PubMed

    Ravalli, Andrea; Voccia, Diego; Palchetti, Ilaria; Marrazza, Giovanna

    2016-08-02

    Aptamer-based sensors have been intensively investigated as potential analytical tools in clinical analysis providing the desired portability, fast response, sensitivity, and specificity, in addition to lower cost and simplicity versus conventional methods. The aim of this review, without pretending to be exhaustive, is to give the readers an overview of recent important achievements about electrochemical, electrochemiluminescence, and photoelectrochemical aptasensors for the protein biomarker determination, mainly cancer related biomarkers, by selected recent publications. Special emphasis is placed on nanostructured-based aptasensors, which show a substantial improvement of the analytical performances.

  11. Ternary Cd(Se,Te) alloy semiconductors - Synthesis, material characterization, and high-efficiency photoelectrochemical cells

    NASA Astrophysics Data System (ADS)

    Levy-Clement, C.; Triboulet, R.; Rioux, J.; Etcheberry, A.; Licht, S.

    1985-12-01

    High-quality Cd(Se,Te) in two compositions was synthesized using the modified Bridgman technique. The Se-rich crystals had the hexagonal structure, while the Te-rich phase consisted of crystals with cubic packing. Their quality could be gauged from high-electron mobility and low resistivity, which suited the purpose of their synthesis, i.e., for high-efficiency photoelectrochemical cells. Photoelectrochemical etching was employed, which resulted in a heavily pitted surface with the density of the etch pits exceeding 10 to the 9th/sq cm. Quantum efficiency of the semiconductor/aqueous polysulfide interface increased considerably after photoetching. Solar-to-electrical conversion efficiencies in excess of 12 percent were obtained. Photoluminenscence spectrum was measured for the two crystals prior to and after photoetching. The emission maximum is near the calculated band gap. The decline in the luminescence intensity, after photoetching, is attributed to the corrugation of the surface and the reduced density of the donor state near the semiconductor surface, which increases the thickness of the space-charge layer (dead layer model).

  12. Electrolyte Concentration Effect of a Photoelectrochemical Cell Consisting of TiO 2 Nanotube Anode

    DOE PAGES

    Ren, Kai; Gan, Yong X.; Nikolaidis, Efstratios; ...

    2013-01-01

    The photoelectrochemical responses of a TiO 2 nanotube anode in ethylene glycol (EG), glycerol, ammonia, ethanol, urea, and Na 2 S electrolytes with different concentrations were investigated. The TiO 2 nanotube anode was highly efficient in photoelectrocatalysis in these solutions under UV light illumination. The photocurrent density is obviously affected by the concentration change. Na 2 S generated the highest photocurrent density at 0, 1, and 2 V bias voltages, but its concentration does not significantly affect the photocurrent density. Urea shows high open circuit voltage at proper concentration and low photocurrent at different concentrations. Externally applied bias voltage ismore » also an important factor that changes the photoelectrochemical reaction process. In view of the open circuit voltage, EG, ammonia, and ethanol fuel cells show the trend that the open circuit voltage (OCV) increases with the increase of the concentration of the solutions. Glycerol has the highest OCV compared with others, and it deceases with the increase in the concentration because of the high viscosity. The OCV of the urea and Na 2 S solutions did not show obvious concentration effect.« less

  13. Tunable Syngas Production from CO2 and H2 O in an Aqueous Photoelectrochemical Cell.

    PubMed

    Chu, Sheng; Fan, Shizhao; Wang, Yongjie; Rossouw, David; Wang, Yichen; Botton, Gianluigi A; Mi, Zetian

    2016-11-07

    Syngas, the mixture of CO and H2 , is a key feedstock to produce methanol and liquid fuels in industry, yet limited success has been made to develop clean syngas production using renewable solar energy. We demonstrated that syngas with a benchmark turnover number of 1330 and a desirable CO/H2 ratio of 1:2 could be attained from photoelectrochemical CO2 and H2 O reduction in an aqueous medium by exploiting the synergistic co-catalytic effect between Cu and ZnO. The CO/H2 ratio in the syngas products was tuned in a large range between 2:1 and 1:4 with a total unity Faradaic efficiency. Moreover, a high Faradaic efficiency of 70 % for CO was acheived at underpotential of 180 mV, which is the lowest potential ever reported in an aqueous photoelectrochemical cell. It was found that the combination of Cu and ZnO offered complementary chemical properties that lead to special reaction channels not seen in Cu, or ZnO alone.

  14. The Kinetics of Recombination in the N-Silicon Photoelectrochemical Cell

    NASA Astrophysics Data System (ADS)

    Rosenbluth, Mary Louise

    In order to understand fundamental conduction processes in semiconductor/liquid junctions, the current -voltage characteristics and electron recombination mechanisms of the n-silicon/methanol-dimethylferrocene-dimethylferricenium photoelectrochemical cell were studied. Variations of the open circuit photovoltage are consistent with bulk recombination/diffusion kinetics. Photovoltages were first order in photocurrent density, and dopant density and hole diffusion length of the silicon. The diode quality factor was 1.05 +/- 0.1. The activation barrier for carrier recombination, obtained from plots of open circuit voltage vs. temperature, was 1.1-1.2 eV. The kinetics of the electron recombination mechanism were not dependent on redox molecule concentrations or solution pH, indicating that electron transfer at the interface is not rate determining. Optimization of the silicon and solution parameters yielded a 10% efficient solar cell using mirror-finished electrodes, with an open-circuit voltage of 670 millivolts at 20.0 mA/cm^2 photocurrent density. If the surface was matte -etched, the efficiency was 12.1%. The open-circuit voltages for these devices are among the highest observed for n -silicon surface barrier devices at these intensities. Surface recombination velocity measurements in-situ reveal a beneficial negative shift in flatband with photoelectrochemical treatment of the surface, but no significant decrease in the surface state concentration. Also, studies on the kinetics of electron current in the n-silicon/methanol photoelectrochemical cell vs. redox potential are reported for a redox potential range where the bucking current is influenced by electron transfer at the interface. The redox potential was varied by changing both the formal potential (by changing the redox molecule) and the Nernstian cell potential (by changing redox couple concentrations). For a particular redox molecule, the open circuit voltage depended only on the redox potential

  15. Electrochemical and photoelectrochemical nano-immunesensing using origami paper based method.

    PubMed

    Hasanzadeh, Mohammad; Shadjou, Nasrin

    2016-04-01

    Patterned paper has characteristics that lead to miniaturized assays that run by capillary action with small volumes of fluids. These methods suggest a path for the development of simple, inexpensive, and portable diagnostic assays that can be useful in remote settings, where simple immunoassays are becoming increasingly important for detecting disease and monitoring health. Incorporation of nanomaterials plays a major role in sensing probe immobilization and detection sensitivity of paper-based devices. Nanomaterial properties, such as increased surface area, have aided with signal amplification and lower detection limits. This review focuses on application of nanomaterials as signal amplification elements on origami paper-based electro-analytical devices for immune biomarkers detection with a brief introduction about various fabrication techniques and designs, biological and detection methods. In this review, we comprehensively summarize the selected latest research articles from 2013 to May 2015 on application of nanomaterials in various types of origami paper based electrochemical and photoelectrochemical immunosensors. The review breaks into two parts. The first part devotes to the development and applications of nanomaterials in electrochemical immunesensing. The second part provides an overview of recent origami paper based photoelectrochemical immunosensors.

  16. ZnO nanoflower-based photoelectrochemical DNAzyme sensor for the detection of Pb2+.

    PubMed

    Zhang, Bintian; Lu, Lili; Hu, Qichang; Huang, Feng; Lin, Zhang

    2014-06-15

    Lead contamination is now widespread, and exposure to lead may cause adverse effects on human beings. In this study, a photoelectrochemical sensor based on flower-like ZnO nanostructures was developed for Pb(2+) detection, using a Pb(2+)-dependent DNAzyme as the recognition unit and a double-strand DNA intercalator, Ru(bpy)2(dppz)(2+) (bpy=2,2'-bipyridine, dppz=dipyrido[3,2-a:2',3'-c] phenazine) as the photoelectrochemical signal reporter. The ZnO nanoflower was fabricated on an indium tin oxide (ITO) electrode by the convenient hydrothermal decomposition method. The morphology and photoelectrochemical property of the ZnO nanoflowers were characterized by SEM, XRD and photocurrent measurements. DNAzyme-substrate duplex was assembled on an ITO/ZnO electrode through electrostatic adsorption. In the presence of Pb(2+), RNA-cleavage activity of the DNAzyme was activated and its substrate strand was cleaved, resulting in the release of Ru(bpy)2(dppz)(2+) from the DNA film and the concomitant photocurrent decrease. The detection principle was verified by fluorescence measurements. Under the optimized conditions, a linear relationship between photocurrent and Pb(2+) concentration was obtained over the range of 0.5-20 nM, with a detection limit of 0.1 nM. Interference from other common metal ions was found negligible. Applicability of the sensor was demonstrated by analyzing lead level in human serum and Pb(2+) spiked water samples. This facile and economical sensor system showed high sensitivity and selectivity, thus can be potentially applied for on-site monitoring of lead contaminant.

  17. A new photoelectrochemical test cell and its use for a combined two-electrode and three-electrode approach to cell testing

    NASA Astrophysics Data System (ADS)

    Esposito, Daniel V.; Goue, Ouloide Y.; Dobson, Kevin D.; McCandless, Brian E.; Chen, Jingguang G.; Birkmire, Robert W.

    2009-12-01

    This paper describes the design, assembly, and operation of a photoelectrochemical (PEC) test cell that is relatively easy to construct and well suited for testing photoelectrode/counterelectrode combinations in a reproducible manner. The design of the cell permits measurements to be made in both two-electrode and three-electrode arrangements. The benefits of conducting both two-electrode and three-electrode measurements are illustrated using data obtained from the new test cell for a PEC system based on a polysulfide electrolyte, CdSe0.8Te0.2 photoanode, and tungsten monocarbide counterelectrode. It is shown that linear sweep voltammograms measured in three-electrode mode can be used to describe current transients recorded in a two-electrode cell modified by the addition of a reference electrode.

  18. Synthesis of titanium dioxide nanotubes from thin film on silicon wafer for photoelectrochemical cell

    NASA Astrophysics Data System (ADS)

    Chappanda Nanaiah, Karumbaiah

    TiO2 is an extensively studied material due to its nontoxic, environmental friendly, corrosion-resistant nature and wide band gap (~3 eV). TiO2 nanotubes (T-NTs) synthesized via electrochemical anodization have been studied extensively, with particular focus on their electrical and optical properties. The advantage of T-NT is the large surface area to volume ratio. T-NT has been used to demonstrate many applications such as sensors and energy harvesting. These applications have traditionally been demonstrated via T-NT synthesized on Ti foil. However, there is currently no commercially available T-NT- based device, which may be due to a lack of fabrication techniques, to make such devices on a large scale. One of the requirements for fabricating compact T-NT- based devices is the need for a stable and planar substrate. The titanium foils commonly used for T-NT synthesis are mechanically flexible, making them more prone to bending, limiting the integration of T-NT with microfabrication techniques. Here, we present the synthesis of T-NT on Si wafer at room temperature from direct current (D.C.) sputtered as well as e-beam evaporated thin Ti film. Hundred nm SiO2 was used to electrically isolate the T-NT from the substrate. We demonstrate integration of the synthesis of T-NT with photolithography, which is one of the most important requirements for scaling up a T-NT-based device. The T-NT was stable up to 500°C, which is required for improved charge transport. The T-NT was 1.4 times longer than the thickness of the Ti film, showing selective electric field-assisted etching of Ti by the electrolyte. We also report site-specific and patterned growth of the T-NT. The effect of properties of thin films such as grain size, residual stress and density on the morphology of T-NT was studied to improve the stability and quality of the T-NT. We demonstrate the synthesis of TiO2-WO 3 composite nanotubes for photoelectrochemical cells with up to a 40% increase in photocurrent in

  19. Stable N-CuInSe.sub.2 /iodide-iodine photoelectrochemical cell

    DOEpatents

    Cahen, David; Chen, Yih W.

    1985-01-01

    In a photoelectrochemical solar cell, stable output and solar efficiency in excess of 10% are achieved with a photoanode of n-CuInSe.sub.2 electrode material and an iodine/iodide redox couple used in a liquid electrolyte. The photoanode is prepared by treating the electrode material by chemical etching, for example in Br.sub.2 /MeOH; heating the etched electrode material in air or oxygen; depositing a surface film coating of indium on the electrode material after the initial heating; and thereafter again heating the electrode material in air or oxygen to oxidize the indium. The electrolyte is treated by the addition of Cu.sup.+ or Cu.sup.2+ salts and In.sup.3+ salts.

  20. Stable n-CuInSe/sub 2/iodide-iodine photoelectrochemical cell

    DOEpatents

    Cahen, D.; Chen, Y.W.

    1984-09-20

    In a photoelectrochemical solar cell, stable output and solar efficiency in excess of 10% are achieved with a photoanode of n-CuInSe/sub 2/ electrode material and an iodine/iodide redox couple used in a liquid electrolyte. The photoanode is prepared by treating the electrode material by chemical etching, for example in Br/sub 2//MeOH; heating the etched electrode material in air or oxygen; depositing a surface film coating of indium on the electrode material after the initial heating; and thereafter again heating the electrode material in air or oxygen to oxidize the indium. The electrolyte is treated by the addition of Cu/sup +/ or Cu/sup 2 +/ salts and in In/sup 3 +/ salts.

  1. Chemical bath deposition of thin film cadmium selenide for photoelectrochemical cells

    SciTech Connect

    Boudreau, R.A.; Raugh, R.D.

    1983-02-01

    Chemical bath deposition provides an attractive, low cost method of producing cadmium chalcogenide thin films. Intimate contact between the bath solution and the substrate material permits uniform deposition on substrates of complex geometry, presently difficult with spray pyrolysis, vacuum evaporation, or electrodeposition techniques. For CdSe, rigorous control of deposition conditions promotes the formation of a hexagonal, specularly reflecting deposit rather than a less desirable sphalerite (cubic) powdery deposit. Scanning electron microscopy reveals a small grained layered plate morphology similar to that produced by the evaporation method. Specularly reflecting CdSe films can be formed over large area substrates at a thickness optimal for their use as photoelectrochemical cells (PEC). Employing polysulfide as the redox couple, conversion efficiencies as high as 6.8% have been achieved in the authors' laboratory for these films using a tungstenhalogen white light source.

  2. Bio-Photoelectrochemical Solar Cells Incorporating Reaction Center and Reaction Center Plus Light Harvesting Complexes

    NASA Astrophysics Data System (ADS)

    Yaghoubi, Houman

    Harvesting solar energy can potentially be a promising solution to the energy crisis now and in the future. However, material and processing costs continue to be the most important limitations for the commercial devices. A key solution to these problems might lie within the development of bio-hybrid solar cells that seeks to mimic photosynthesis to harvest solar energy and to take advantage of the low material costs, negative carbon footprint, and material abundance. The bio-photoelectrochemical cell technologies exploit biomimetic means of energy conversion by utilizing plant-derived photosystems which can be inexpensive and ultimately the most sustainable alternative. Plants and photosynthetic bacteria harvest light, through special proteins called reaction centers (RCs), with high efficiency and convert it into electrochemical energy. In theory, photosynthetic RCs can be used in a device to harvest solar energy and generate 1.1 V open circuit voltage and ~1 mA cm-2 short circuit photocurrent. Considering the nearly perfect quantum yield of photo-induced charge separation, efficiency of a protein-based solar cell might exceed 20%. In practice, the efficiency of fabricated devices has been limited mainly due to the challenges in the electron transfer between the protein complex and the device electrodes as well as limited light absorption. The overarching goal of this work is to increase the power conversion efficiency in protein-based solar cells by addressing those issues (i.e. electron transfer and light absorption). This work presents several approaches to increase the charge transfer rate between the photosynthetic RC and underlying electrode as well as increasing the light absorption to eventually enhance the external quantum efficiency (EQE) of bio-hybrid solar cells. The first approach is to decrease the electron transfer distance between one of the redox active sites in the RC and the underlying electrode by direct attachment of the of protein complex

  3. Harvesting hydrogen gas from air pollutants with an un-biased gas phase photo-electrochemical cell.

    PubMed

    Verbruggen, Sammy W; Van Hal, Myrthe; Bosserez, Tom; Rongé, Jan; Hauchecorne, Birger; Martens, Johan A; Lenaerts, Silvia

    2017-02-08

    The concept of an all-gas-phase photo-electrochemical cell (PEC) producing hydrogen gas from volatile organic contaminated gas and light is presented. Without applying any external bias, organic contaminants are degraded and hydrogen gas is produced in separate electrode compartments. The system works most efficiently with organic pollutants in inert carrier gas. In the presence of oxygen gas, the cell performs less efficiently but still significant photocurrents are generated, showing the cell can be run on organic contaminated air. The purpose of this study is to demonstrate new application opportunities of PEC technology and to encourage further advancement toward photo-electrochemical remediation of air pollution with the attractive feature of simultaneous energy recovery and pollution abatement.

  4. Bismuth sulfide nanoflakes and nanorods as high performance photodetectors and photoelectrochemical cells

    NASA Astrophysics Data System (ADS)

    Chao, Junfeng; Xing, Shumin; Zhao, Yanchun; Gao, Suling; Song, Qinghua; Guo, Lixia; Wang, Di; Zhang, Tingliang

    2016-11-01

    Flake-like and rod-like bismuth sulfide nanostructures were synthesized via a facile polyol refluxing process. The rigid photodetectors based on both nanomaterials have the features of linear photocurrent characteristics and good sensitivity. Especially, the rigid bismuth sulfide nanoflakes photodetector has fast response time of 0.5 s and recovery time of 0.7 s. The flexible photodetectors were then fabricated on PET substrate, and this caused both the response time and the recovery time to increase by a factor of ∼2.5. Moreover, the photoelectrochemical (PEC) devices exhibited photosensitivity with the features of rapid response and recovery time, high on/off ratio and stable switching cycle performance. Our results imply that the two types of bismuth sulfide nanomaterials are prospective candidates for next generation photodetectors and optoelectronic switches.

  5. Electrochemical synthesis of nanoporous tungsten carbide and its application as electrocatalysts for photoelectrochemical cells.

    PubMed

    Kang, Jin Soo; Kim, Jin; Lee, Myeong Jae; Son, Yoon Jun; Jeong, Juwon; Chung, Dong Young; Lim, Ahyoun; Choe, Heeman; Park, Hyun S; Sung, Yung-Eun

    2017-03-16

    Photoelectrochemical (PEC) cells are promising tools for renewable and sustainable solar energy conversion. Currently, their inadequate performance and high cost of the noble metals used in the electrocatalytic counter electrode have postponed the practical use of PEC cells. In this study, we report the electrochemical synthesis of nanoporous tungsten carbide and its application as a reduction catalyst in PEC cells, namely, dye-sensitized solar cells (DSCs) and PEC water splitting cells, for the first time. The method employed in this study involves the anodization of tungsten foil followed by post heat treatment in a CO atmosphere to produce highly crystalline tungsten carbide film with an interconnected nanostructure. This exhibited high catalytic activity for the reduction of cobalt bipyridine species, which represent state-of-the-art redox couples for DSCs. The performance of tungsten carbide even surpassed that of Pt, and a substantial increase (∼25%) in energy conversion efficiency was achieved when Pt was substituted by tungsten carbide film as the counter electrode. In addition, tungsten carbide displayed decent activity as a catalyst for the hydrogen evolution reaction, suggesting the high feasibility for its utilization as a cathode material for PEC water splitting cells, which was also verified in a two-electrode water photoelectrolyzer.

  6. Silicon microhole arrays architecture for stable and efficient photoelectrochemical cells using ionic liquids electrolytes

    NASA Astrophysics Data System (ADS)

    Shen, Xiaojuan; Chen, Ling; Li, Junnan; Zhao, Jie

    2016-06-01

    Silicon microhole arrays (SiMHs) structure is constructed and fabricated by a low-cost maskless anodic etching process, which is applied as the photoanode for the silicon photoelectrochemical (PEC) cells. The depths of silicon microhole arrays can be independently controlled by the etching time. The light-scattering properties are also investigated. Additionally, surface morphology analysis show that large hole diameters of SiMHs is very favourable for the full-filling of ionic liquids electrolyte. Therefore, better electrochemical contact as well as high ionic conductivity of the ionic liquids electrolyte renders the PEC SiMHs solar cells to exhibit more excellent performance. After optimization, the maximum PCE could be achieved at 4.04% for the SiMHs cell. The performance of the SiMHs cell is highly comparable to that of silicon nanowires cell. More importantly, the liquid-state electrolyte is confined in the unique microhole structure, which can obviously prevent the leakage of the ionic liquids electrolyte, resulting in much better long-term stability than the reference devices. These preliminary results validate the concept of interpenetrating networks with semiconductor structure/ILs junction to develop stable and efficient PEC cells.

  7. Controlled synthesis of GaN-based nanowires for photoelectrochemical water splitting applications

    NASA Astrophysics Data System (ADS)

    Ebaid, Mohamed; Kang, Jin-Ho; Ryu, Sang-Wan

    2017-01-01

    Photoelectrochemical (PEC) water splitting using semiconductor materials as light absorbers have been extensively studied. Several semiconducting materials have been proposed, such as TiO2, ZnO, and GaN. Because the efficiency of PEC water splitting is dependent on visible light absorption, the ability to tune the bandgap of GaN by alloying with In makes it advantageous over other wide bandgap semiconductors. The fabrication of GaN-based materials with nanoscale geometry offers more merit for their use in PEC water splitting. In this review, we provide an overview of the recent progress made in the synthesis and application of GaN-based nanomaterials in PEC water splitting. The outstanding challenges and the future prospects of this field will also be addressed.

  8. A miniature photoelectrochemical sensor based on organic electrochemical transistor for sensitive determination of chemical oxygen demand in wastewaters.

    PubMed

    Liao, Jianjun; Lin, Shiwei; Zeng, Min; Yang, Yue

    2016-05-01

    A three-electrode configuration is often required in the conventional photoelectrochemical measurements. Nevertheless, one common drawback is the reference electrode and the counter electrode used in the measurements, which has been proved to be an impediment for the miniaturization. In this study, a simple, cost-effective and miniature photoelectrochemical sensor based on high sensitive organic electrochemical transistor (OECT) is developed and used for the determination of chemical oxygen demand (COD) in wastewaters. The devices show detection limit down to 0.01 mg/L COD, which is two orders of magnitude better than that of the conventional photoelectrochemical method. The excellent sensing performance can be contributed to the novel sensing mechanism of OECT devices. That is, the devices are sensitive to the potential changes induced by the photoelectrochemical reaction on TiO2 nanotube arrays gate electrodes. Real sample analyses are also carried out. The results demonstrate that the measured COD values using the OECT devices and the standard dichromate methods are in a good agreement. Since the proposed sensor is constructed on a miniature transistor, it is expected that the device shows a promising application on the integrated COD monitoring platform.

  9. Photoelectrochemical corrosion of GaN-based p-n structures

    NASA Astrophysics Data System (ADS)

    Fomichev, A. D.; Kurin, S. Yu; Ermakovi, I. A.; Puzyk, M. V.; Usikov, A. S.; Helava, H.; Nikiforov, A.; Papchenko, B. P.; Makarov, Yu N.; Chernyakov, A. E.

    2016-08-01

    Direct water photoelectrolysis using III-N materials is a promising way for hydrogen production. GaN/AlGaN based p-n structures were used in a photoelectrochemical process to investigate the material etching (corrosion) in an electrolyte. At the beginning, the corrosion performs through the top p-type layers via channels associated with threading defects and can penetrate deep into the structure. Then, the corrosion process occurs in lateral direction in n- type layers forming voids and cavities in the structure. The lateral etching is due to net positive charges at the AlGaN/GaN interfaces arising because of spontaneous and piezoelectric polarization in the structure and positively charged ionized donors in the space charge region of the p-n junction.

  10. Photoelectrochemical cell for simultaneous electricity generation and heavy metals recovery from wastewater.

    PubMed

    Wang, Dawei; Li, Yi; Li Puma, Gianluca; Lianos, Panagiotis; Wang, Chao; Wang, Peifang

    2017-02-05

    The feasibility of simultaneous recovery of heavy metals from wastewater (e.g., acid mining and electroplating) and production of electricity is demonstrated in a novel photoelectrochemical cell (PEC). The photoanode of the cell bears a nanoparticulate titania (TiO2) film capped with the block copolymer [poly(ethylene glycol)-b-poly(propylene glycol)-b-poly(ethylene glycol)] hole scavenger, which consumed photogenerated holes, while the photogenerated electrons transferred to a copper cathode reducing dissolved metal ions and produced electricity. Dissolved silver Ag(+), copper Cu(2+), hexavalent chromium as dichromate Cr2O7(2-) and lead Pb(2+) ions in a mixture (0.2mM each) were removed at different rates, according to their reduction potentials. Reduced Ag(+), Cu(2+) and Pb(2+) ions produced metal deposits on the cathode electrode which were mechanically recovered, while Cr2O7(2-) reduced to the less toxic Cr(3+) in solution. The cell produced a current density Jsc of 0.23mA/cm(2), an open circuit voltage Voc of 0.63V and a maximum power density of 0.084mW/cm(2). A satisfactory performance of this PEC for the treatment of lead-acid battery wastewater was observed. The cathodic reduction of heavy metals was limited by the rate of electron-hole generation at the photoanode. The PEC performance decreased by 30% after 9 consecutive runs, caused by the photoanode progressive degradation.

  11. Electron transfer kinetics in water-splitting dye-sensitized photoelectrochemical cells

    NASA Astrophysics Data System (ADS)

    Swierk, John R.

    Water-splitting dye-sensitized photoelectrochemical (WS-DSPECs) cells utilize molecular sensitizers absorbed on mesoporous TiO2 electrodes to harvest visible light, inject photoexcited electrons into the conduction band of TiO2, and finally transfer holes across the TiO2 surface to water oxidation catalysts, which in turn oxidize water to give molecular oxygen and four protons. Within the TiO2 layer photoinjected electrons are transported to a transparent conductor back contact and from there to a dark cathode to reduce protons to molecular hydrogen. WS-DSPECs offer several advantages for alternative solar fuels systems: the use of low-cost materials, tunable molecular sensitizers, and relaxed catalytic turnover requirements to name a few. Despite these advantageous features, power conversion efficiencies in WS-DSPECs are generally low. Broadly, this thesis explores the fundamental electron transfer processes that control the efficiency of these cells. Chapter 1 presents a survey of the previous literature and individually considers each component of a WS-DSPEC (water oxidation catalyst, sensitizers, electrode materials, redox mediators, and overall system design). Chapter 2 presents a novel method of preparing a WS-DSPEC that utilizes crystalline IrO2 nanoparticles directly sintered to TiO2 as a water oxidation catalyst and describes a previously unknown electron-scavenging pathway by IrO2. Chapter 3 explores how electron trapping by and proton intercalation into TiO2 controls the photoelectrochemical performance of WS-DSPECs. Chapter 4 characterizes how electron recombination with the oxidized sensitizer and electron scavenging by the IrO 2 catalyst combine to limit the concentration of conduction band electrons and by extension photocurrent in WS-DSPECs. Chapter 5 demonstrates the use of the first totally organic sensitizers for light driven water-splitting and explores how the molecular and electronic structure of a sensitizer affects the electron transfer

  12. Light Harvesting Proteins for Solar Fuel Generation in Bioengineered Photoelectrochemical Cells

    PubMed Central

    Ihssen, Julian; Braun, Artur; Faccio, Greta; Gajda-Schrantz, Krisztina; Thöny-Meyer, Linda

    2014-01-01

    The sun is the primary energy source of our planet and potentially can supply all societies with more than just their basic energy needs. Demand of electric energy can be satisfied with photovoltaics, however the global demand for fuels is even higher. The direct way to produce the solar fuel hydrogen is by water splitting in photoelectrochemical (PEC) cells, an artificial mimic of photosynthesis. There is currently strong resurging interest for solar fuels produced by PEC cells, but some fundamental technological problems need to be solved to make PEC water splitting an economic, competitive alternative. One of the problems is to provide a low cost, high performing water oxidizing and oxygen evolving photoanode in an environmentally benign setting. Hematite, α-Fe2O3, satisfies many requirements for a good PEC photoanode, but its efficiency is insufficient in its pristine form. A promising strategy for enhancing photocurrent density takes advantage of photosynthetic proteins. In this paper we give an overview of how electrode surfaces in general and hematite photoanodes in particular can be functionalized with light harvesting proteins. Specifically, we demonstrate how low-cost biomaterials such as cyanobacterial phycocyanin and enzymatically produced melanin increase the overall performance of virtually no-cost metal oxide photoanodes in a PEC system. The implementation of biomaterials changes the overall nature of the photoanode assembly in a way that aggressive alkaline electrolytes such as concentrated KOH are not required anymore. Rather, a more environmentally benign and pH neutral electrolyte can be used. PMID:24678669

  13. Layered transition metal thiophosphates /MPX3/ as photoelectrodes in photoelectrochemical cells

    NASA Astrophysics Data System (ADS)

    Byvik, C. E.; Smith, B. T.; Reichman, B.

    1982-10-01

    Layered crystals of the transition metal thiophosphates were synthesized and characterized for use as photoelectrodes in photoelectrochemical cells. Crystals incorporating tin and manganese show n-type response while those with iron and nickel show p-type response. These materials have a measured indirect bandgap of about 2.1 eV. They show ability to photoelectrolyze water in acid solutions with onset potentials which change in a Nernstian way as the PH of the solution changes. The onset potential is near zero volts versus a saturated calomel electrode at pH 2. At n-type crystals, oxygen could be evolved upon irradiation at underpotentials of 850 mV and at p-type crystals, hydrogen could be evolved at underpotentials of 400 mV, indicating a net gain in energy conversion. All crystals were unstable in basic solution. Liquid junction photovoltaic cells in iodide-triiodide acid solution using these layered materials were also constructed and found to have low efficiences.

  14. Detection of esophageal cancer cell by photoelectrochemical Cu2O/ZnO biosensor (Conference Presentation)

    NASA Astrophysics Data System (ADS)

    Hsu, Chao-Hsin; Chu, Cheng-Hsun; Chen, Weichung; Wu, I.-Chen; Wu, Ming Tsang; Kuo, Chie-Tong; Tsiang, Raymond Chien-Chao; Wang, Hsiang-Chen

    2016-03-01

    We have demonstrated a Cu2O/ZnO nanorods (NRs) array p-n heterostructures photoelectrochemical biosensor. The electrodeposition of Cu2O at pH 12 acquired the preferably (111) lattice planes, resulting in the largest interfacial electric field between Cu2O and ZnO, which finally led to the highest separation efficiency of photogenerated charge carriers. High verticality ZnO nanorods by seed layer and thermal annealing assist the hydrothermal growth. The optimized Cu2O/ZnO NRs array p-n heterostructures exhibited enhanced PEC performance, such as elevated photocurrent and photoconversion efficiency, as well as excellent sensing performance for the sensitive detection of four strains of different races and different degree of cancer cell which made the device self-powered. We got spectral response characteristics and operating wavelength range of biosensor, and to verify the biological characteristics of cancer cells wafer react with different stages of cancer characterized by a cancer measured reaction experiment.

  15. Light harvesting proteins for solar fuel generation in bioengineered photoelectrochemical cells.

    PubMed

    Ihssen, Julian; Braun, Artur; Faccio, Greta; Gajda-Schrantz, Krisztina; Thöny-Meyer, Linda

    2014-01-01

    The sun is the primary energy source of our planet and potentially can supply all societies with more than just their basic energy needs. Demand of electric energy can be satisfied with photovoltaics, however the global demand for fuels is even higher. The direct way to produce the solar fuel hydrogen is by water splitting in photoelectrochemical (PEC) cells, an artificial mimic of photosynthesis. There is currently strong resurging interest for solar fuels produced by PEC cells, but some fundamental technological problems need to be solved to make PEC water splitting an economic, competitive alternative. One of the problems is to provide a low cost, high performing water oxidizing and oxygen evolving photoanode in an environmentally benign setting. Hematite, α-Fe2O3, satisfies many requirements for a good PEC photoanode, but its efficiency is insufficient in its pristine form. A promising strategy for enhancing photocurrent density takes advantage of photosynthetic proteins. In this paper we give an overview of how electrode surfaces in general and hematite photoanodes in particular can be functionalized with light harvesting proteins. Specifically, we demonstrate how low-cost biomaterials such as cyanobacterial phycocyanin and enzymatically produced melanin increase the overall performance of virtually no-cost metal oxide photoanodes in a PEC system. The implementation of biomaterials changes the overall nature of the photoanode assembly in a way that aggressive alkaline electrolytes such as concentrated KOH are not required anymore. Rather, a more environmentally benign and pH neutral electrolyte can be used.

  16. Photoelectrochemical biofuel cell using porphyrin-sensitized nanocrystalline titanium dioxide mesoporous film as photoanode.

    PubMed

    Wang, Kunqi; Yang, Jing; Feng, Ligang; Zhang, Yuwei; Liang, Liang; Xing, Wei; Liu, Changpeng

    2012-02-15

    Electrical energy generated directly from sunlight and biomass solution with a Photoelectrochemical Biofuel Cell (PEBFC) was investigated. The PEBFC consisted of a meso-tetrakis(4-carboxyphenyl)porphyrin (TCPP)-sensitized nanocrystalline titanium dioxide (TiO(2)) mesoporous film (NTDMF) as the photoanode and platinum black as the cathode. The interaction between TCPP sensitizer and NTDMF was evaluated by X-ray photoelectron spectra and FT-IR absorption spectra, indicating that the TCPP sensitizer was adsorbed on the NTDMF by bridging or bidentate coordinate bonds. The spectroscopic properties of pure TCPP ethanol solution and TCPP-sensitized NTDMF were obtained by UV-vis absorption spectra, demonstrating that the characteristic absorption peaks of TCPP on NTDMF displayed slight red shift compared with pure TCPP ethanol solution. The performances of the PEBFC were obtained by photocurrent-photovoltage characteristic curves. The open-circuit photovoltage (V(oc)), the short-circuit photocurrent (I(sc)) and the maximum power density (P(max)) was 0.74 V, 69.96 μA and 33.94 μWcm(-2) at 0.45 V, respectively. The fill factor (FF) was 0.19 and the incident photo-to-current efficiency (IPCE) was 36.0% at 436 nm. The results demonstrated that the TCPP was an appropriate photosensitizer for PEBFC.

  17. Improved Photoelectrochemical Cell Performance of Tin Oxide with Functionalized Multiwalled Carbon Nanotubes-Cadmium Selenide Sensitizer.

    PubMed

    Bhande, Sambhaji S; Ambade, Rohan B; Shinde, Dipak V; Ambade, Swapnil B; Patil, Supriya A; Naushad, Mu; Mane, Rajaram S; Alothman, Z A; Lee, Soo-Hyoung; Han, Sung-Hwan

    2015-11-18

    Here we report functionalized multiwalled carbon nanotubes (f-MWCNTs)-CdSe nanocrystals (NCs) as photosensitizer in photoelectrochemical cells, where f-MWCNTs were uniformly coated with CdSe NCs onto SnO2 upright standing nanosheets by using a simple electrodeposition method. The resultant blended photoanodes demonstrate extraordinary electrochemical properties including higher Stern-Volmer constant, higher absorbance, and positive quenching, etc., caused by more accessibility of CdSe NCs compared with pristine SnO2-CdSe photoanode. Atomic and weight percent changes of carbon with f-MWCNTs blending concentrations were confirmed from the energy dispersive X-ray analysis. The morphology images show a uniform coverage of CdSe NCs over f-MWCNTs forming a core-shell type structure as a blend. Compared to pristine CdSe, photoanode with f-MWCNTs demonstrated a 257% increase in overall power conversion efficiency. Obtained results were corroborated by the electrochemical impedance analysis. Higher scattering, more accessibility, and hierarchical structure of SnO2-f-MWCNTs-blend-CdSe NCs photoanode is responsible for higher (a) electron mobility (6.89 × 10(-4) to 10.89 × 10(-4) cm(2) V(-1) S(1-)), (b) diffusion length (27 × 10(-6)),

  18. In situ generated AgBr-enhanced ZnO nanorod-based photoelectrochemical aptasensing via layer-by-layer assembly.

    PubMed

    Li, Jing; Tu, Wenwen; Li, Hongbo; Bao, Jianchun; Dai, Zhihui

    2014-02-28

    A robust aptasensor for Ag(+) was proposed for the first time using an enhanced ZnO nanorod-based photoelectrochemistry by in situ generated AgBr via layer-by-layer assembly. This work opens up new avenues for application of one-dimensional ZnO nanorod arrays in photoelectrochemical sensing. Additionally, the strategy of employing in situ generated narrow-bandgap semiconductors paves a new way for photoelectrochemical sensing.

  19. Solar-Energy-Driven Photoelectrochemical Biosensing Using TiO2 Nanowires.

    PubMed

    Tang, Jing; Li, Jun; Da, Peimei; Wang, Yongcheng; Zheng, Gengfeng

    2015-08-03

    Photoelectrochemical sensing represents a unique means for chemical and biological detection, with foci of optimizing semiconductor composition and electronic structures, surface functionalization layers, and chemical detection methods. Here, we have briefly discussed our recent developments of TiO2 nanowire-based photoelectrochemical sensing, with particular emphasis on three main detection mechanisms and corresponding examples. We have also demonstrated the use of the photoelectrochemical sensing of real-time molecular reaction kinetic measurements, as well as direct interfacing of living cells and probing of cellular functions.

  20. Target-induced nano-enzyme reactor mediated hole-trapping for high-throughput immunoassay based on a split-type photoelectrochemical detection strategy.

    PubMed

    Zhuang, Junyang; Tang, Dianyong; Lai, Wenqiang; Xu, Mingdi; Tang, Dianping

    2015-09-15

    Photoelectrochemical (PEC) detection is an emerging and promising analytical tool. However, its actual application still faces some challenges like potential damage of biomolecules (caused by itself system) and intrinsic low-throughput detection. To solve the problems, herein we design a novel split-type photoelectrochemical immunoassay (STPIA) for ultrasensitive detection of prostate specific antigen (PSA). Initially, the immunoreaction was performed on a microplate using a secondary antibody/primer-circular DNA-labeled gold nanoparticle as the detection tag. Then, numerously repeated oligonucleotide sequences with many biotin moieties were in situ synthesized on the nanogold tag via RCA reaction. The formed biotin concatamers acted as a powerful scaffold to bind with avidin-alkaline phosphatase (ALP) conjugates and construct a nanoenzyme reactor. By this means, enzymatic hydrolysate (ascorbic acid) was generated to capture the photogenerated holes in the CdS quantum dot-sensitized TiO2 nanotube arrays, resulting in amplification of the photocurrent signal. To elaborate, the microplate-based immunoassay and the high-throughput detection system, a semiautomatic detection cell (installed with a three-electrode system), was employed. Under optimal conditions, the photocurrent increased with the increasing PSA concentration in a dynamic working range from 0.001 to 3 ng mL(-1), with a low detection limit (LOD) of 0.32 pg mL(-1). Meanwhile, the developed split-type photoelectrochemical immunoassay exhibited high specificity and acceptable accuracy for analysis of human serum specimens in comparison with referenced electrochemiluminescence immunoassay method. Importantly, the system was not only suitable for the sandwich-type immunoassay mode, but also utilized for the detection of small molecules (e.g., aflatoxin B1) with a competitive-type assay format.

  1. Nano-structure ZnO/Cu2O photoelectrochemical and self-powered biosensor for esophageal cancer cell detection.

    PubMed

    Wu, I-Chen; Weng, Yu-Hsin; Lu, Ming-Yen; Jen, Chun-Ping; Fedorov, Vladimir E; Chen, Wei Chung; Wu, Ming Tsang; Kuo, Chie-Tong; Wang, Hsiang-Chen

    2017-04-03

    The p-n heterojunction photoelectrochemical biosensor, which comprises a p-type Cu2O film formed by electrochemical deposition and n-type ZnO nanorods formed by the hydrothermal method, is prone to photoelectrochemical reactions and self-powered. Four types of human esophageal cancer cells (ECCs) were detected by this biosensor without requiring an extra bias voltage. The measured photocurrent values of high invasion capacity cancer cells was consistently 2 times higher than those measured by a slight invasion capacity cancer cells. The response time, which was about 0.5 s, allowed repeated measurement.

  2. Effect of ion-chelating chain lengths in thiophene-based monomers on in situ photoelectrochemical polymerization and photovoltaic performances.

    PubMed

    Song, In Young; Kim, Minjun; Park, Taiho

    2015-06-03

    We synthesized thiophene-based monomers (bis-EDOTs) with different ethylene glycol oligomer (EGO) lengths (TBO3, TBO4, and TBO5) and investigated their polymerization characteristics during photoelectrochemical polymerization (PEP) at the surfaces of dye (D205)-sensitized TiO2 nanocrystalline particles. During the PEP reaction, monomers were expected to diffuse toward neighboring dyes through the growing polymer layers to enable continuous chain growth. We found that the less bulky monomer (TBO3) formed a more compact polymer layer with a high molecular weight. Its diffusion to the active sites through the resulting growing polymer layer was, therefore, limited. We deployed layers of the polymers (PTBO3, PTBO4, and PTBO5) in iodine-free solid-state hybrid solar cells to investigate the lithium ion chelating properties of the polymers as a function of the number of oxygen atoms present in the EGOs. PTBO4 and PTBO5 were capable of chelating lithium ions, yielding a photovoltaic performance that was 142% of the performance obtained without the polymer layers (3.0→5.2%).

  3. Copper-based ternary and quaternary semiconductor nanoplates: templated synthesis, characterization, and photoelectrochemical properties.

    PubMed

    Wu, Xue-Jun; Huang, Xiao; Qi, Xiaoying; Li, Hai; Li, Bing; Zhang, Hua

    2014-08-18

    Two-dimensional (2D) copper-based ternary and quaternary semiconductors are promising building blocks for the construction of efficient solution-processed photovoltaic devices at low cost. However, the facile synthesis of such 2D nanoplates with well-defined shape and uniform size remains a challenge. Reported herein is a universal template-mediated method for preparing copper-based ternary and quaternary chalcogenide nanoplates, that is, CuInS2, CuIn(x)Ga(1-x)S2, and Cu2ZnSnS4, by using a pre-synthesized CuS nanoplate as the starting template. The various synthesized nanoplates are monophasic with uniform thickness and lateral size. As a proof of concept, the Cu2ZnSnS4 nanoplates were immobilized on a Mo/glass substrate and used as semiconductor photoelectrode, thus showing stable photoelectrochemical response. The method is general and provides future opportunities for fabrication of cost-effective photovoltaic devices based on 2D semiconductors.

  4. Visible photoelectrochemical water splitting into H2 and O2 in a dye-sensitized photoelectrosynthesis cell

    DOE PAGES

    Alibabaei, Leila; Sherman, Benjamin D.; Norris, Michael R.; ...

    2015-04-27

    A hybrid strategy for solar water splitting is exploited here based on a dye-sensitized photoelectrosynthesis cell (DSPEC) with a mesoporous SnO2/TiO2 core/shell nanostructured electrode derivatized with a surface-bound Ru(II) polypyridyl-based chromophore–catalyst assembly. The assembly, [(4,4’-(PO3H2)2bpy)2Ru(4-Mebpy-4’-bimpy)Ru(tpy)(OH2)]4+ ([RuaII-RubII-OH2]4+, combines both a light absorber and a water oxidation catalyst in a single molecule. It was attached to the TiO2 shell by phosphonate-surface oxide binding. The oxide-bound assembly was further stabilized on the surface by atomic layer deposition (ALD) of either Al2O3 or TiO2 overlayers. Illumination of the resulting fluorine-doped tin oxide (FTO)|SnO2/TiO2|-[RuaII-RubII-OH2]4+(Al2O3 or TiO2) photoanodes in photoelectrochemical cells with a Pt cathode andmore » a small applied bias resulted in visible-light water splitting as shown by direct measurements of both evolved H2 and O2. The performance of the resulting DSPECs varies with shell thickness and the nature and extent of the oxide overlayer. Use of the SnO2/TiO2 core/shell compared with nanoITO/TiO2 with the same assembly results in photocurrent enhancements of ~5. In conclusion, systematic variations in shell thickness and ALD overlayer lead to photocurrent densities as high as 1.97 mA/cm2 with 445-nm, ~90-mW/cm2 illumination in a phosphate buffer at pH 7.« less

  5. Visible photoelectrochemical water splitting into H2 and O2 in a dye-sensitized photoelectrosynthesis cell

    PubMed Central

    Alibabaei, Leila; Sherman, Benjamin D.; Norris, Michael R.; Brennaman, M. Kyle; Meyer, Thomas J.

    2015-01-01

    A hybrid strategy for solar water splitting is exploited here based on a dye-sensitized photoelectrosynthesis cell (DSPEC) with a mesoporous SnO2/TiO2 core/shell nanostructured electrode derivatized with a surface-bound Ru(II) polypyridyl-based chromophore–catalyst assembly. The assembly, [(4,4’-(PO3H2)2bpy)2Ru(4-Mebpy-4’-bimpy)Ru(tpy)(OH2)]4+ ([RuaII-RubII-OH2]4+, combines both a light absorber and a water oxidation catalyst in a single molecule. It was attached to the TiO2 shell by phosphonate-surface oxide binding. The oxide-bound assembly was further stabilized on the surface by atomic layer deposition (ALD) of either Al2O3 or TiO2 overlayers. Illumination of the resulting fluorine-doped tin oxide (FTO)|SnO2/TiO2|-[RuaII-RubII-OH2]4+(Al2O3 or TiO2) photoanodes in photoelectrochemical cells with a Pt cathode and a small applied bias resulted in visible-light water splitting as shown by direct measurements of both evolved H2 and O2. The performance of the resulting DSPECs varies with shell thickness and the nature and extent of the oxide overlayer. Use of the SnO2/TiO2 core/shell compared with nanoITO/TiO2 with the same assembly results in photocurrent enhancements of ∼5. Systematic variations in shell thickness and ALD overlayer lead to photocurrent densities as high as 1.97 mA/cm2 with 445-nm, ∼90-mW/cm2 illumination in a phosphate buffer at pH 7. PMID:25918426

  6. Cyclometalated iridium complex-based label-free photoelectrochemical biosensor for DNA detection by hybridization chain reaction amplification.

    PubMed

    Li, Chunxiang; Wang, Hongyang; Shen, Jing; Tang, Bo

    2015-04-21

    Photoactive material is the most crucial factor which intimately determines analytical performances of the photoelectrochemical sensor. On the basis of the high affinity of dipyrido [3,2-a:2',3'-c] phenazine (dppz) with DNA helix, a novel photoactive intercalator, [(ppy)2Ir(dppz)](+)PF6(-)(ppy = 2-phenylpyridine and dppz = dipyrido [3,2-a:2',3'-c] phenazine) was prepared and characterized by UV-vis absorption spectroscopy, fluorescence spectroscopy, and cyclic voltammetry. The photoelectrochemical properties of the as-prepared iridium(III) complex immobilized on the ITO electrode was investigated. Either cathodic or anodic photocurrent generation can be observed when triethanolamine (TEOA) or dissolved O2 is used as a sacrificial electron donor/acceptor, respectively. The probable photocurrent-generation mechanisms are speculated. A highly sensitive iridium(III) complex-based photoelectrochemical sensor was proposed for DNA detection via hybridization chain reaction (HCR) signal amplification. Under optimal conditions, the biosensor was found to be linearly proportional to the logarithm of target DNA concentration in the range from 0.025 to 100 pmol L(-1) with a detection limit of 9.0 fmol L(-1) (3σ). Moreover, the proposed sensor displayed high selectivity and good reproducibility, demonstrating efficient and stable photoelectric conversion ability of the Ir(III) complex.

  7. In situ-generated nano-gold plasmon-enhanced photoelectrochemical aptasensing based on carboxylated perylene-functionalized graphene.

    PubMed

    Li, Jing; Tu, Wenwen; Li, Hongbo; Han, Min; Lan, Yaqian; Dai, Zhihui; Bao, Jianchun

    2014-01-21

    A novel in situ-generated nanogold plasmon-enhanced photoelectrochemical aptasensor for Hg(2+) ions was fabricated using a perylene-3,4,9,10-tetracarboxylic acid/graphene (PTCA-GR) heterojunction. The fabricated photoelectrochemical aptasensor was based on thymine-Hg(2+)-thymine coordination chemistry and the plasmonic near-field absorption enhancement effect of the subsequent specific catalytic formation of nanogold. The energetic electrons from the surface plasmons of the nanogold were injected into the LUMO orbit of the organic PTCA semiconductor and then rapidly transferred to the electrode through GR due to the possible Hg(2+)-DNA molecular wires following irradiation with the visible light (λ > 450 nm) and at a bias voltage of 0.2 V. The fabricated aptasensor was linear in its response to the concentration of Hg(2+) ions in the range of 5-500 pmol L(-1), with a detection limit of 2 pmol L(-1). The presence of up to 200-fold greater concentrations of other common metal ions did not interfere with the detection of Hg(2+) ions in an aqueous system, and the results corresponded well with those obtained by ICP-MS. This novel plasmon-enhanced photoelectrochemical aptasensor exhibited good performance with its high sensitivity, good selectivity, low cost, and portable features. The strategy of the localized surface plasmon resonance through the in situ generation of noble metal nanoparticles paves the way for improvements in PEC aptasensor performance.

  8. Photoelectrochemical sensing of 4-chlorophenol based on Au/BiOCl nanocomposites.

    PubMed

    Yan, Pengcheng; Xu, Li; Xia, Jiexiang; Huang, Yan; Qiu, Jingxia; Xu, Qian; Zhang, Qi; Li, Huaming

    2016-08-15

    The Au/BiOCl composites have been prepared by a facile one-pot ethylene glycol (EG) assisted solvothermal reaction in the presence of ionic liquid 1-hexadecyl-3-methylimidazolium chloride ([C16mim]Cl). During the synthesis procedure, the [C16mim]Cl has been used as Cl source, solvent of this system, and dispersing agent to effectively disperse Au on the surface of BiOCl. The as-prepared samples have been systematically characterized by multiple instruments to investigate the structure, morphology, and photoelectrochemical properties. According to the photoelectrochemical data, the Au/BiOCl composites exhibit better photoelectrochemical performance toward the detection of 4-chlorophenol than that of the pure BiOCl. The photocurrent response of Au/BiOCl modified electrode is high and stable under light irradiation. The proposed Au/BiOCl modified electrode shows a wide linear response ranging from 0.16 to 20mgL(-1) with detection limit of 0.05mgL(-1). It indicates a dramatically promising application of bismuth oxyhalides in photoelectrochemical detection. It will be expected that the present study may be lightly extended to the monitor of other organic pollutants by photoelectrochemical detection of the Au/BiOCl composites.

  9. Luminescent photoelectrochemical cells. 6. Spatial aspects of the photoluminescence and electroluminescence of cadmium selenide electrodes

    SciTech Connect

    Streckert, H.H.; Tong, J.; Ellis, A.B.

    1982-01-27

    Samples of single-crystal, n-type CdSe emit when excited with ultraband gap excitation. The emission band (lambda/sub max/ approx. = 720 nm) is near the band gap of CdSe (approx. 1.7 eV); its energy, decay time, and temperature dependence are consistent with its description as edge emission. Photoluminescence (PL) spectra can be dependent on excitation wavelength and show evidence of self-absorption effects: PL spectra obtained with 457.9-nm excitation are broadened in the high-energy portion of the band relative to spectra obtained with more deeply penetrating 632.9-nm excitation. Measured PL efficiencies, theta/sub r/, are approx.10/sup -4/ in air at 295 K. When CdSe is used as the photoanode of photoelectrochemical cells employing aqueous polychalcogenide electrolytes, emission is quenched by the passage of photocurrent resulting from ultraband gap excitation. Electroluminescence (EL) can be observed from CdSe when the semiconductor is used as a dark cathode in aqueous, alkaline peroxydisulfate electrolyte. The EL spectrum is similar to the PL spectrum, suggesting the involvement of a common emissive excited state. Differences in the breadths of the spectra, however, indicate that, on average, EL is produced nearer to the semiconductor-electrolyte interface than PL under comparable experimental conditions. Measured EL efficiencies, theta/sub EL/, approaching 10/sup -3/ at -1.50 V vs SCE are comparable to PL efficiencies measured at this potential in hydroxide solution and provide evidence that the emissive excited state can be efficiently populated in an EL experiment; these lower-limit estimates of theta/sub EL/ and theta/sub r/ decline in passing to potentials near the onset of EL, approx.-0.9 V vs SCE. Spatial features of these comparisons are discussed.

  10. Semiconductor-based photoelectrochemical water splitting at the limit of very wide depletion region

    SciTech Connect

    Liu, Mingzhao; Lyons, John L.; Yan, Danhua H.; Hybertsen, Mark S.

    2015-11-23

    In semiconductor-based photoelectrochemical (PEC) water splitting, carrier separation and delivery largely relies on the depletion region formed at the semiconductor/water interface. As a Schottky junction device, the trade-off between photon collection and minority carrier delivery remains a persistent obstacle for maximizing the performance of a water splitting photoelectrode. Here, it is demonstrated that the PEC water splitting efficiency for an n-SrTiO3 (n-STO) photoanode is improved very significantly despite its weak indirect band gap optical absorption (α < 10⁴ cm⁻¹), by widening the depletion region through engineering its doping density and profile. Graded doped n-SrTiO3 photoanodes are fabricated with their bulk heavily doped with oxygen vacancies but their surface lightly doped over a tunable depth of a few hundred nanometers, through a simple low temperature re-oxidation technique. The graded doping profile widens the depletion region to over 500 nm, thus leading to very efficient charge carrier separation and high quantum efficiency (>70%) for the weak indirect transition. As a result, this simultaneous optimization of the light absorption, minority carrier (hole) delivery, and majority carrier (electron) transport by means of a graded doping architecture may be useful for other indirect band gap photocatalysts that suffer from a similar problem of weak optical absorption.

  11. Semiconductor-based photoelectrochemical water splitting at the limit of very wide depletion region

    DOE PAGES

    Liu, Mingzhao; Lyons, John L.; Yan, Danhua H.; ...

    2015-11-23

    In semiconductor-based photoelectrochemical (PEC) water splitting, carrier separation and delivery largely relies on the depletion region formed at the semiconductor/water interface. As a Schottky junction device, the trade-off between photon collection and minority carrier delivery remains a persistent obstacle for maximizing the performance of a water splitting photoelectrode. Here, it is demonstrated that the PEC water splitting efficiency for an n-SrTiO3 (n-STO) photoanode is improved very significantly despite its weak indirect band gap optical absorption (α < 10⁴ cm⁻¹), by widening the depletion region through engineering its doping density and profile. Graded doped n-SrTiO3 photoanodes are fabricated with their bulkmore » heavily doped with oxygen vacancies but their surface lightly doped over a tunable depth of a few hundred nanometers, through a simple low temperature re-oxidation technique. The graded doping profile widens the depletion region to over 500 nm, thus leading to very efficient charge carrier separation and high quantum efficiency (>70%) for the weak indirect transition. As a result, this simultaneous optimization of the light absorption, minority carrier (hole) delivery, and majority carrier (electron) transport by means of a graded doping architecture may be useful for other indirect band gap photocatalysts that suffer from a similar problem of weak optical absorption.« less

  12. Photoelectrochemical sensor for pentachlorophenol on microfluidic paper-based analytical device based on the molecular imprinting technique.

    PubMed

    Sun, Guoqiang; Wang, Panpan; Ge, Shenguang; Ge, Lei; Yu, Jinghua; Yan, Mei

    2014-06-15

    Combining microfluidic paper-based analytical device (μ-PAD) and the molecular imprinting technique, a visible light photoelectrochemical (PEC) sensing platform for the detection of pentachlorophenol (PCP) was established on gold nanoparticles (AuNPs) decorated paper working electrode using polypyrrole-functionalized ZnO nanoparticles. Ascorbic acid (AA) was exploited as an efficient and nontoxic electron donor for scavenging photogenerated holes under mild solution medium and facilitating the generation of stable photocurrent. The microfluidic molecular imprinted polymer-based PEC analytical origami device is developed for the detection of PCP in the linear range from 0.01 ng mL(-1) to 100 ng mL(-1) with a low detection limit of 4 pg mL(-1). This disposable microfluidic PEC origami device would provide a new platform for sensitive, specific, and multiplex assay in public health, environmental monitoring, and the developing world.

  13. Self-deposition of Pt nanoparticles on graphene woven fabrics for enhanced hybrid Schottky junctions and photoelectrochemical solar cells.

    PubMed

    Kang, Zhe; Tan, Xinyu; Li, Xiao; Xiao, Ting; Zhang, Li; Lao, Junchao; Li, Xinming; Cheng, Shan; Xie, Dan; Zhu, Hongwei

    2016-01-21

    In this study, we demonstrated a self-deposition method to deposit Pt nanoparticles (NPs) on graphene woven fabrics (GWF) to improve the performance of graphene-on-silicon solar cells. The deposition of Pt NPs increased the work function of GWF and reduced the sheet resistance of GWF, thereby improving the power conversion efficiency (PCE) of graphene-on-silicon solar cells. The PCE (>10%) was further enhanced via solid electrolyte coating of the hybrid Schottky junction in the photoelectrochemical solar cells. These results suggest that the combination of self-deposition of Pt NPs and solid-state electrolyte coating of graphene-on-silicon is a promising way to produce high performance graphene-on-semiconductor solar cells.

  14. Nano-architecture based photoelectrochemical water oxidation efficiency enhancement by CdS photoanodes

    NASA Astrophysics Data System (ADS)

    Pareek, Alka; Kim, Hyun Gyu; Paik, Pradip; Joardar, Joydip; Borse, Pramod H.

    2017-02-01

    In the present work, 2D nanostructuring has been utilized to impart an efficiency improvement to the hexagonal phase CdS films for the photoelectrochemical (PEC) cells those were deposited by spray pyrolysis technique. By controlling the aerosol droplet- size, population and impingement time during the spray pyrolysis deposition, various nano-features viz. randomly aligned nanorods, nanotubes and nanowires of CdS has been demonstrated for the first time. A growth mechanism has been proposed to predict the temporal evolution of the nanostructures. The prominent nanoscale structures show improved optical properties in the visible range of solar spectrum. The structural studies validate the morphological differences of nanostructures in terms of the texture coefficient analysis as well as 2D micro x-ray diffraction imaging. Electrochemical characterization is carried out to understand the effect of nanostructuring on the PEC performance of the CdS photoanodes in the sulphide (0.1 M Na2S  +  0.02 M Na2SO3) electrolyte at applied bias of 0.2 V (versus SCE). The evolution of morphology from randomly aligned rods to nanowire is responsible for improved photocurrent (3.5 times). CdS film morphology can be tuned to nanotubes, nano- rose buds and nanorod bunches even by doping Zn2+ ions in CdS lattice. Nano-structuring of doped CdS has shown enhanced performance of the photoanodes. The nanotubes structures yielded highest photocurrent density of 1.6 mA cm‑2. Whereas modifying the 2D-nanostructured CdS film by simple MoO3 spray coating yields the photocurrent enhancement to 2.1 mA cm‑2.

  15. Electricity generation and pollutant degradation using a novel biocathode coupled photoelectrochemical cell.

    PubMed

    Du, Yue; Feng, Yujie; Qu, Youpeng; Liu, Jia; Ren, Nanqi; Liu, Hong

    2014-07-01

    The photoelectrochemical cell (PEC) is a promising tool for the degradation of organic pollutants and simultaneous electricity recovery, however, current cathode catalysts suffer from high costs and short service lives. Herein, we present a novel biocathode coupled PEC (Bio-PEC) integrating the advantages of photocatalytic anode and biocathode. Electrochemical anodized TiO2 nanotube arrays fabricated on Ti substrate were used as Bio-PEC anodes. Field-emission scanning electron microscope images revealed that the well-aligned TiO2 nanotubes had inner diameters of 60-100 nm and wall-thicknesses of about 5 nm. Linear sweep voltammetry presented the pronounced photocurrent output (325 μA/cm(2)) under xenon illumination, compared with that under dark conditions. Comparing studies were carried out between the Bio-PEC and PECs with Pt/C cathodes. The results showed that the performance of Pt/C cathodes was closely related with the structure and Pt/C loading amounts of cathodes, while the Bio-PEC achieved similar methyl orange (MO) decoloration rate (0.0120 min(-1)) and maximum power density (211.32 mW/m(2)) to the brush cathode PEC with 50 mg Pt/C loading (Brush-PEC, 50 mg). The fill factors of Bio-PEC and Brush-PEC (50 mg) were 39.87% and 43.06%, respectively. The charge transfer resistance of biocathode was 13.10 Ω, larger than the brush cathode with 50 mg Pt/C (10.68 Ω), but smaller than the brush cathode with 35 mg Pt/C (18.35 Ω), indicating the comparable catalytic activity with Pt/C catalyst. The biocathode was more dependent on the nutrient diffusion, such as nitrogen and inorganic carbon, thus resulting in relatively higher diffusion resistance compared to the brush cathode with 50 mg Pt/C loading that yielded similar MO removal and power output. Considering the performance and cost of PEC system, the biocathode was a promising alternative for the Pt/C catalyst.

  16. An ultrasensitive and universal photoelectrochemical immunoassay based on enzyme mimetics enhanced signal amplification.

    PubMed

    Wang, Guang-Li; Shu, Jun-Xian; Dong, Yu-Ming; Wu, Xiu-Ming; Li, Zai-Jun

    2015-04-15

    An ultrasensitive photoelectrochemical (PEC) immunoassay based on signal amplification by enzyme mimetics was fabricated for the detection of mouse IgG (as a model protein). The PEC immunosensor was constructed by a layer-by-layer assembly of poly (diallyldimethylammonium chloride) (PDDA), CdS quantum dots (QDs), primary antibody (Ab1, polyclonal goat antimouse IgG), and the antigen (Ag, mouse IgG) on an indium-tin oxide (ITO) electrode. Then, the secondary antibody (Ab2, polyclonal goat antimouse IgG) combined to a bio-bar-coded Pt nanoparticle(NP)-G-quadruplex/hemin probe was used for signal amplification. The bio-bar-coded Pt NP-G-quadruplex/hemin probe could catalyze the oxidation of hydroquinone (HQ) using H2O2 as an oxidant, demonstrating its intrinsic enzyme-like activity. High sensitivity for the target Ag was achieved by using the bio-bar-coded probe as signal amplifier due to its high catalytic activity, a competitive nonproductive absorption of hemin and the steric hindrance caused by the polymeric oxidation products of HQ. For most important, the oxidation product of HQ acted as an efficient electron acceptor of the illuminated CdS QDs. The target Ag could be detected from 0.01pg/mL to 1.0ng/mL with a low detection limit of 6.0fg/mL. The as-obtained immunosensor exhibited high sensitivity, good stability and acceptable reproducibility. This method might be attractive for clinical and biomedical applications.

  17. Photoelectrochemical water splitting for hydrogen production with metal oxide (hematite and cupric oxide) based photocatalysts

    NASA Astrophysics Data System (ADS)

    Tang, Houwen

    Solar hydrogen is one ideal energy source to replace fossil fuel, as it is sustainable and environmentally friendly. Solar hydrogen can be generated in a number of ways. Photoelectrochemical (PEC) water splitting is one of the most promising methods for solar-to-chemical energy conversion. In this research project, metal oxide-based photocatalysts, especially hematite (α-Fe 2O3) and cupric oxide (CuO), were investigated for use as electrodes in PEC water splitting for solar hydrogen production. In our research project of hematite-based electrodes, we started with the incorporation of transition metal, particularly titanium (Ti), in hematite thin films to modify the valence and conduction band edges of hematite. We found that Ti impurities improve the electron conductivity of hematite and consequently lead to significantly enhanced photocurrents. We further investigated the Ti and Mg co-alloyed hematite. In this case, Ti is the donor and Mg is the acceptor in hematite. The co-alloying approach enhanced the solubility of Mg and Ti, which led to reduced electron effective mass and therefore increased electron mobility. Also, co-alloying tunes the carrier density and therefore allows the optimization of electrical conductivity. The densities of charged defects were found to be reduced, and therefore carrier recombinations were reduced. As a result, the Ti and Mg co-alloyed hematite thin films exhibited much improved performance in PEC water splitting as compared to pure hematite thin films. For the study of cupric oxide-based electrodes, we first investigated the possibility of reducing the electrode corrosion of cupric oxide in aqueous solutions by incorporating Ti as an electrode corrosion inhibitor. We found that Ti alloying can enhance the stability of cupric oxide in base solutions at the cost of reducing its crystallinity and optical absorption, and consequently lowering its photon-to-electron conversion efficiency. In order to balance the stability and the

  18. Enhanced carrier collection efficiency in hierarchical nano-electrode for a high-performance photoelectrochemical cell

    NASA Astrophysics Data System (ADS)

    Hien, Truong Thi; Van Lam, Do; Kim, Chunjoong; Vuong, Nguyen Minh; Quang, Nguyen Duc; Kim, Dahye; Chinh, Nguyen Duc; Hieu, Nguyen Minh; Lee, Seung-Mo; Kim, Dojin

    2016-12-01

    The photoelectrochemical properties of CdS-sensitized ZnO nanorods grown on Pt-coated WO3 nanoplates are investigated to evaluate their effectiveness in hydrogen production. WO3 nanonanoplates are synthesized on glass substrates, followed by atomic layer deposition of Pt thin films as the terminal electrode to efficiently collect the photo-carriers generated from the ZnO/CdS absorption layers. Optimization of the fabrication process for the 3D hierarchical structure is performed, and the morphology and its effect on the photoelectrochemical performance of the electrodes are carefully studied using scanning electron microscopy, x-ray diffraction, and measurements of the photocurrent density and photo-conversion efficiencies. The enhanced PEC performance is elucidated by the 3D hierarchical geometry of the electrode. The optimized electrode shows a photocurrent density of ∼ 13 mA cm-2 and a conversion efficiency of ∼8.0% at -0.83 V (vs. SCE) in 0.5 M Na2S solution under the illumination of simulated solar light.

  19. A photoelectrochemical immunosensor for detection of α-fetoprotein based on Au-ZnO flower-rod heterostructures

    NASA Astrophysics Data System (ADS)

    Han, Zhizhong; Luo, Min; Chen, Li; Chen, Jinghua; Li, Chunyan

    2017-04-01

    In this work, a novel label free photoelectrochemical (PEC) immunosensor has been developed for the detection of α-fetoprotein (AFP). The immunosensor was based on Au-ZnO flower-rods (FRs) heterostructure, where Au nanoparticles (NPs) were firstly electrodeposited by cyclic voltammetry methods. Scanning electron microscopy (SEM), X-ray diffraction (XRD), Mott-Schottky plot (MS), UV-vis diffuse reflectance spectrum and fluorescence emission spectrum were used for the characterizations of Au-ZnO FRs. The results demonstrated that Au NPs not only obviously enhanced the visible light absorption of ZnO FRs due to surface plasmon resonance (SPR) but also improved the separation of photo-generated electron-hole pairs. Therefore, the photocurrent of Au-ZnO FRs was increased under simulated sunlight. The photocurrent was reduced after the specific antibody-antigen immune reaction. And the photocurrent decrement was linear with the logarithm of AFP antigen concentration in the range from 0.005 ng mL-1 to 50 ng mL-1 with a low detection limit of 0.56 pg mL-1 (S/N = 3). The PEC immunosensor also exhibited high anti-interference property and acceptable stability. This work would provide a promising photoelectrochemical strategy for the detection of other proteins in clinical diagnosis.

  20. Dye-sensitized polyoxometalate for visible-light-driven photoelectrochemical cells.

    PubMed

    Gao, Junkuo; Miao, Jianwei; Li, Yongxin; Ganguly, Rakesh; Zhao, Yang; Lev, Ovadia; Liu, Bin; Zhang, Qichun

    2015-08-28

    A simple and facile one-step method for the synthesis of an organic dye-functionalized polyoxometalate (POM) hybrid with visible-light photo-response was reported. The POM hybrid was fully characterized via single crystal XRD, powder XRD, FTIR and elemental analysis. The reaction of the organic dye with inorganic salts gave the dye-functionalized POM (MoBB3), in which the POM cluster was formed in situ. The electronic absorption peak of this hybrid was successfully extended beyond 680 nm. Photoelectrochemical measurement indicated that MoBB3 was photoresponsive under visible-light illumination, suggesting that it is an n-type (electron conductive) semiconducting material. This result might offer a method for the design of novel organic dye-functionalized POMs for photoelectric applications.

  1. C=C π bond modified graphitic carbon nitride films for enhanced photoelectrochemical cell performance.

    PubMed

    Bian, Juncao; Xi, Lifei; Li, Jianfu; Xiong, Ze; Huang, Chao; Lange, Kathrin; Tang, Jinyao; Shalom, Menny; Zhang, Rui-Qin

    2017-03-08

    Applications of graphitic carbon nitride (g-CN) in photoelectrochemical and optoelectronic devices are still hindered due to the difficulties in synthesis of g-CN films with tunable chemical, physical and catalytic properties. Herein we present a general method to alter the electronic and photoelectrochemical properties of g-CN films by annealing. We found that N atoms can be removed from the g-CN networks after annealing treatment. Assisted by theoretical calculations, we confirm that upon appropriate N removal, the adjacent C atoms will form new C=C π bonds. Detailed calculations demonstrate that the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) are localized at the structure unit with C=C π bonds and the electrons are more delocalized. Valence band X-ray photoelectron spectroscopy spectra together with the absorption spectra unveil that the structure changes result in the alteration of the g-CN energy levels and position of band edges. Our results show that the photocurrent density of the annealed g-CN film is doubled compared with the pristine one, thanks to the better charge separation and transport within the film induced by the new C=C π bonds. An ultrathin TiO2 film (2.2 nm) is applied as stabilizer and the photocurrent density is kept at 0.05 mA/cm2 at 1.23 V vs. reversible hydrogen electrode after two-cycle stability assessment. This work enables the applications of g-CN films in many electronic and optoelectronic devices.

  2. One-dimensional Fe2O3/TiO2 photoelectrode and investigation of its photoelectric properties in photoelectrochemical cell

    NASA Astrophysics Data System (ADS)

    Song, Xi-Ming; Zhou, Xin; Yuan, Chunxue; Zhang, Yu; Tong, Qiang; Li, Ying; Cui, Luxia; Liu, Daliang; Zhang, Wei

    2017-03-01

    We reported a novel Fe2O3/rutile TiO2 nanorod (NR) arrays with the heterogeneous structure for photoelectrochemical (PEC) cells, which were fabricated on fluorine-doped tin oxide glass (FTO) substrates that serve as model architecture via a hydrothermal method. Fe2O3 was revealed as an inexpensive and eco-friendly semiconductor sensitizer to make TiO2 respond to visible light. By using this photoanode, the photoelectric conversion and water splitting properties of PEC cells based on the one-dimensional (1D) Fe2O3/TiO2 heterostructures were investigated in detail under simulated sunlight. Meanwhile, the optimization of photovoltaic performance was also achieved by regulating the amount of Fe2O3. The open circuit voltage and short circuit current of the Fe2O3/TiO2 solar cell can reach 0.435 V and 1.840 mA/cm2, respectively. In addition, theoretical analysis of the photoelectric effect is preliminarily explored on the basis of the flat band potential results.

  3. Photoelectrochemical lab-on-paper device based on molecularly imprinted polymer and porous Au-paper electrode.

    PubMed

    Wang, Panpan; Sun, Guoqiang; Ge, Lei; Ge, Shenguang; Yu, Jinghua; Yan, Mei

    2013-09-07

    In this work, microfluidic paper-based analytical device (μ-PAD) was applied in a photoelectrochemical (PEC) method and thus a truly low-cost, simple, portable, and disposable microfluidic PEC origami device (μ-PECOD) was demonstrated. The molecular imprinting technique was introduced into microfluidic paper-based analytical devices (μ-PADs) through electropolymerization of molecular imprinted polyaniline (MPANI) in a novel Au nanoparticle (AuNP)-modified paper working electrode (Au-PWE). This is fabricated through the growth of an AuNP layer on the surfaces of cellulose fibers in the PWE. Under visible light irradiation, MPANI can generate the photoelectric transition from the highest occupied molecular orbital (HOMO) to the lowest unoccupied molecular orbital (LUMO), delivering the excited electrons to the AuNPs, and then to the carbon working electrode. Simultaneously, it is believed that a positively charged hole of MPANI that took part in the oxidation process was consumed by ascorbic acid (AA) to promote the amplifying photocurrent response. On the basis of this novel MPANI-Au-PWE and the principle of origami, a microfluidic molecular imprinted polymer (MIP)-based photoelectrochemical analytical origami device (μ-MPECOD), comprised of an auxiliary tab and a sample tab, is developed for the detection of heptachlor in the linear range from 0.03 nmol L(-1) to 10.0 nmol L(-1) with a low detection limit of 8.0 pmol L(-1). The selectivity, reproducibility, and stability of this μ-MPECOD are investigated. This μ-MPECOD would provide a new platform for high-throughput, sensitive, specific, and multiplex assay in public health, environmental monitoring, and the developing world.

  4. Morphology, structural and optical properties of iron oxide thin film photoanodes in photoelectrochemical cell: Effect of electrochemical oxidation

    NASA Astrophysics Data System (ADS)

    Maabong, Kelebogile; Machatine, Augusto G.; Hu, Yelin; Braun, Artur; Nambala, Fred J.; Diale, Mmantsae

    2016-01-01

    Hematite (α-Fe2O3) is a promising semiconductor as photoanode in solar hydrogen production from photoelectrolysis of water due to its appropriate band gap, low cost and high electrochemical stability in aqueous caustic electrolytes. Operation of such photoanode in a biased photoelectrochemical cell constitutes an anodization with consequent redox reactions at the electrode surface. α-Fe2O3 thin film photoanodes were prepared by simple and inexpensive dip coating method on fluorine doped tin oxide (FTO) glass substrate, annealed in air at 500 °C for 2 h, then electrochemically oxidized (anodized) in 1 M KOH at 500 mV for 1 min in dark and light conditions. Changes in structural properties and morphology of α-Fe2O3 nanoparticles films were investigated by XRD, Raman spectroscopy and a high resolution FE-SEM. The average grain size was observed to increase from 57 nm for pristine samples to 73 and 77 nm for anodized samples in dark and light respectively. Broadening and red shift in Raman spectra in anodized samples may be attributed to lattice expansion upon oxidation. The UV-visible measurements revealed enhanced absorption in the photoanodes after the treatment. The findings suggest that the anodization of the photoelectrode in a biased cell causes not only changes of the molecular structure at the surface, but also changes in the crystallographic structure which can be detected with x-ray diffractometry.

  5. An All-vanadium Continuous-flow Photoelectrochemical Cell for Extending State-of-charge in Solar Energy Storage.

    PubMed

    Wei, Zi; Shen, Yi; Liu, Dong; Liu, Fuqiang

    2017-04-04

    Greater levels of solar energy storage provide an effective solution to the inherent nature of intermittency, and can substantially improve reliability, availability, and quality of the renewable energy source. Here we demonstrated an all-vanadium (all-V) continuous-flow photoelectrochemical storage cell (PESC) to achieve efficient and high-capacity storage of solar energy, through improving both photocurrent and photocharging depth. It was discovered that forced convective flow of electrolytes greatly enhanced the photocurrent by 5 times comparing to that with stagnant electrolytes. Electrochemical impedance spectroscopy (EIS) study revealed a great reduction of charge transfer resistance with forced convective flow of electrolytes as a result of better mass transport at U-turns of the tortuous serpentine flow channel of the cell. Taking advantage of the improved photocurrent and diminished charge transfer resistance, the all-V continuous-flow PESC was capable of producing ~20% gain in state of charge (SOC) under AM1.5 illumination for ca. 1.7 hours without any external bias. This gain of SOC was surprisingly three times more than that with stagnant electrolytes during a 25-hour period of photocharge.

  6. Glassy carbon/multi walled carbon nanotube/cadmium sulphide photoanode for light energy storage in vanadium photoelectrochemical cell

    NASA Astrophysics Data System (ADS)

    Peimanifard, Zahra; Rashid-Nadimi, Sahar

    2015-12-01

    The aim of this study is utilizing the artificial photosynthesis, which is an attractive and challenging theme in the photoelectrocatalytic water splitting, to charge the vanadium redox flow battery (VRFB). In this work multi walled carbon nanotube/cadmium sulphide hybrid is employed as a photoanode material to oxidize VO2+ to VO2+ for charging the positive vanadium redox flow battery's half-cell. Characterization studies are also described using the scanning electron microscopic-energy-dispersive X-ray spectroscopy (SEM-EDS), inductively coupled plasma atomic emission spectroscopy (ICP-AES) and UV-Visible methods. The phtoelectrochemical performance is characterized by cyclic voltammetry and chronoamperometry. Applied bias photon-to-current efficiency (ABPE) is achieved for both two and three-electrode configurations. The glassy carbon/multi walled carbon nanotube/cadmium sulphide yields high maximum ABPE of 2.6% and 2.12% in three and two-electrode setups, respectively. These results provide a useful guideline in designing photoelectrochemical cells for charging the vanadium redox flow batteries by sunlight as a low cost, free and abundant energy source, which does not rely on an external power input.

  7. BiOI/TiO2-nanorod array heterojunction solar cell: Growth, charge transport kinetics and photoelectrochemical properties

    NASA Astrophysics Data System (ADS)

    Wang, Lingyun; Daoud, Walid A.

    2015-01-01

    A series of BiOI/TiO2-nanorod array photoanodes were grown on fluorine-doped tin oxide (FTO) glass using a simple two-step solvothermal/hydrothermal method. The effects of the hydrothermal process, such as TiO2 nanorod growth time, BiOI concentration and the role of surfactant, polyvinylpyrrolidone (PVP), on the growth of BiOI, were investigated. The heterojunctions were characterized by X-ray diffraction, UV-vis absorbance spectroscopy and scanning electron microscopy. The photoelectrochemical properties of the as-grown junctions, such as linear sweep voltammetry (LSV) behavior, photocurrent response and incident photon-to-electron conversion efficiency (IPCE) under Xenon lamp illumination, are presented. The cell with BiOI/TiO2 (PVP) as photoanode can reach a short current density (Jsc) of 0.13 mA/cm2 and open circuit voltage (Voc) of 0.46 V vs. Ag/AgCl under the irradiation of a 300 W Xenon lamp. Compared to bare TiO2, the IPCE of BiOI/TiO2 (PVP) increased 4-5 times at 380 nm. Furthermore, the charge transport kinetics within the heterojunction is also discussed.

  8. Investigation of photoconversion efficiency of Cu and Ni doped TiO2 thin film in photoelectrochemical cell

    NASA Astrophysics Data System (ADS)

    Mohamed, Norani Muti; Bashiri, Robabeh; Kait, Chong Fai; Sufian, Suriati; Khatani, Mehboob

    2016-11-01

    This paper presents the investigation on the optimal primary preparation parameters of Cu-Ni bimetallic supported TiO2 photocatalyst on photoconversion efficiency in photoelectrochemical cell (PEC). Three preparation parameters including, water, acid and copper dopant to Titanium tetraisopropoxide molar ratio was investigated. The single and combined impacts of these variables were examined by applying central composite design (CCD) from a response surface method (RSM). Quadratic polynomial regression models were proposed for the analysis of variance (ANOVA) to fit the experimental data in CCD. There was a good agreement in the linear relationship between the experimental and predicted values where model was fitted with high coefficient of determination value of 0.98. Data analysis had demonstrated that water and copper loading were two more effective parameters on the photoconversion efficiency compared to acid. The water molar ratio of 16, acid ratio of 3, and Cu loading of 7 mol % were the optimal preparation parameters with maximum efficiency of 3.72% at potential -0.109 V.

  9. N-doped TiO2 based visible light activated label-free photoelectrochemical biosensor for detection of Hg(2+) through quenching of photogenerated electrons.

    PubMed

    Han, Qianqian; Wang, Kewei; Xu, Lijun; Yan, Xiang; Zhang, Kunchi; Chen, Xing; Wang, Qinglin; Zhang, Lan; Pei, Renjun

    2015-06-21

    A novel photoelectrochemical (PEC) biosensor was fabricated based on N-doped TiO2 for the detection of Hg(2+) through the quenching of photogenerated electrons. The N-doped TiO2 was synthesized by a sol-gel method with urea and tetrabutyl titanate as the N and Ti sources. Compared with the undoped TiO2, the N-doped TiO2 showed an enhanced photocurrent response under visible light (λ > 420 nm). The sensing surface was functionalized with 5'-amino-modified T-rich oligonucleotides. The photoelectrochemical biosensor bound Hg(2+) on the surface by a highly specific T-Hg(2+)-T recognition. Hg(2+) on the surface of the N-doped TiO2 film withdrew the photogenerated electrons and decreased the recorded current signal. The dynamic linear range for Hg(2+) has been determined to be as low as 2-6 μM.

  10. A highly selective photoelectrochemical biosensor for uric acid based on core-shell Fe3O4@C nanoparticle and molecularly imprinted TiO2.

    PubMed

    Zhang, Chunjing; Si, Shihui; Yang, Zhengpeng

    2015-03-15

    Combining the surface modification and molecular imprinting technique, a novel photoelectrochemical sensing platform with excellent photochemical catalysis and molecular recognition capabilities was established for the detection of uric acid based on the magnetic immobilization of Fe3O4@C nanoparticles onto magnetic glassy carbon electrode (MGCE) and modification of molecularly imprinted TiO2 film on Fe3O4@C. The developed biosensor was highly sensitive to uric acid in solutions, with a linear range from 0.3 to 34µM and a limit of detection of 0.02μM. Furthermore, the biosensor exhibited outstanding selectivity while used in coexisting systems containing various interferents with high concentration. The practical application of the biosensor was also realized for the selective detection of uric acid in spiked samples. The study made a successful attempt in the development of highly selective and sensitive photoelectrochemical biosensor for urine monitoring.

  11. Performance predictions for solar-chemical converters based on photoelectrochemical I-V curves

    SciTech Connect

    Luttmer, J.D.; Trachtenberg, I.

    1985-06-01

    Texas Instruments' solar energy system contains a solar-chemical converter (SCC) which converts solar energy into chemical energy via the electrolysis of hydrobromic acid (HBr) into hydrogen (H/sub 2/) and bromine (Br/sub 2/). Previous predictions of SCC performance have employed electrical dry-probe data and a computer simulation model to predict the H/sub 2/ generation rates. The method of prediction described here makes use of the photoelectrochemical Icurves to determine the ''wet'' probe parameters of V /SUB oc/ J /SUB sc/ FF, and efficiency for anodes and cathodes. The advantages of this technique over the dry-probe/computer simulation method are discussed. A comparison of predicted and measured H/sub 2/ generation rates is presented. Solar to chemical efficiencies of 8.6% have been both predicted and measured for the electrolysis of 48% HBr to hydrogen and bromine by a full anode/cathode array. Individual cathode solar to hydrogen efficiencies of 9.5% have been obtained.

  12. Photoelectrodes based upon Mo:BiVO4 inverse opals for photoelectrochemical water splitting.

    PubMed

    Zhou, Min; Bao, Jian; Xu, Yang; Zhang, Jiajia; Xie, Junfeng; Guan, Meili; Wang, Chengliang; Wen, Liaoyong; Lei, Yong; Xie, Yi

    2014-07-22

    BiVO4 has been regarded as a promising material for photoelectrochemical water splitting, but it suffers from a major challenge on charge collection and utilization. In order to meet this challenge, we design a nanoengineered three-dimensional (3D) ordered macro-mesoporous architecture (a kind of inverse opal) of Mo:BiVO4 through a controllable colloidal crystal template method with the help of a sandwich solution infiltration method and adjustable post-heating time. Within expectation, a superior photocurrent density is achieved in return for this design. This enhancement originates primarily from effective charge collection and utilization according to the analysis of electrochemical impedance spectroscopy and so on. All the results highlight the great significance of the 3D ordered macro-mesoporous architecture as a promising photoelectrode model for the application in solar conversion. The cooperating amplification effects of nanoengineering from composition regulation and morphology innovation are helpful for creating more purpose-designed photoelectrodes with highly efficient performance.

  13. Self-Powered Photoelectrochemical Biosensor Based on CdS/RGO/ZnO Nanowire Array Heterostructure.

    PubMed

    Zhao, Kun; Yan, Xiaoqin; Gu, Yousong; Kang, Zhuo; Bai, Zhiming; Cao, Shiyao; Liu, Yichong; Zhang, Xiaohui; Zhang, Yue

    2016-01-13

    A CdS/reduced graphene oxide (RGO)/ZnO nanowire array (NWAs) heterostructure is designed, which exhibits enhanced photoelectrochemical (PEC) activity compared to pure ZnO, RGO/ZnO, and CdS/ZnO. The enhancement can be attributed to the synergistic effect of the high electron mobility of ordered 1D ZnO NWAs, extended visible-light absorption of CdS nanocrystals, and the formed type II band alignment between them. Moreover, the incorporation of RGO further promotes the charge carrier separation and transfer process due to its excellent charge collection and shuttling characteristics. Subsequently, the CdS/RGO/ZnO heterostructure is successfully utilized for the PEC bioanalysis of glutathione at 0 V (vs Ag/AgCl). The self-powered device demonstrates satisfactory sensing performance with rapid response, a wide detection range from 0.05 mm to 1 mm, an acceptable detection limit of 10 μm, as well as certain selectivity, reproducibility, and stability. Therefore, the CdS/RGO/ZnO heterostructure has opened up a promising channel for the development of PEC biosensors.

  14. Metal-based anode for high performance bioelectrochemical systems through photo-electrochemical interaction

    NASA Astrophysics Data System (ADS)

    Liang, Yuxiang; Feng, Huajun; Shen, Dongsheng; Long, Yuyang; Li, Na; Zhou, Yuyang; Ying, Xianbin; Gu, Yuan; Wang, Yanfeng

    2016-08-01

    This paper introduces a novel composite anode that uses light to enhance current generation and accelerate biofilm formation in bioelectrochemical systems. The composite anode is composed of 316L stainless steel substrate and a nanostructured α-Fe2O3 photocatalyst (PSS). The electrode properties, current generation, and biofilm properties of the anode are investigated. In terms of photocurrent, the optimal deposition and heat-treatment times are found to be 30 min and 2 min, respectively, which result in a maximum photocurrent of 0.6 A m-2. The start-up time of the PSS is 1.2 days and the maximum current density is 2.8 A m-2, twice and 25 times that of unmodified anode, respectively. The current density of the PSS remains stable during 20 days of illumination. Confocal laser scanning microscope images show that the PSS could benefit biofilm formation, while electrochemical impedance spectroscopy indicates that the PSS reduce the charge-transfer resistance of the anode. Our findings show that photo-electrochemical interaction is a promising way to enhance the biocompatibility of metal anodes for bioelectrochemical systems.

  15. Photoelectrochemical characteristics of dye-sensitized solar cells incorporating innovative and inexpensive materials

    NASA Astrophysics Data System (ADS)

    Harlow, Lisa Jean

    The use of energy is going to continue to increase rapidly due to population and economic advances occurring throughout the world. The most widely used energies produce carbon dioxide during their combustion and have finite limits on how much of these resources are available. A strong push to utilizing renewable energy is necessary to keep up with the demand. The only renewable energy that has unlimited supply is solar. Our goal is to find cost-effective alternatives to historically the most extensively used materials in dye-sensitized solar cells. In order to rely on efficiency changes coinciding with the introduction of a new component, a standard baseline of performance is necessary to establish. A reproducible fabrication procedure composed of standard materials was instituted; the efficiency parameters exhibited a less than 10% standard deviation for any set of solar cells. Any modifications to the cell components would be apparent in the change in efficiency. Our cell modifications focused on economical alternatives to the electrolyte, the counter electrode and the chromophore. Solution-based electrolytes were replaced with a non-volatile ionic liquid, 1-methyl-3-propylimidazolium iodide, and then a poly(imidazole-functionalized) silica nanoparticle. Solid-state electrolytes reduce or prevent leakage and could ease manufacturing in large-scale devices. Platinum has been the counter electrode catalyst primarily used with the iodide/triiodide redox couple, but is a rare metal making it rather costly. We reduce platinum loading by introducing a novel counter electrode that employs platinum nanoparticles embedded on a graphene nanoplatelet paper. The highly conductive carbon base also negates the use of the expensive conductive substrate necessary for the platinum catalyst, further reducing cost. We also study the differences in transitioning from ruthenium polypyridyls to iron-based chromophores in dye-sensitized solar cells. Iron introduces low-lying ligand

  16. Photoelectrochemical enzymatic biosensors.

    PubMed

    Zhao, Wei-Wei; Xu, Jing-Juan; Chen, Hong-Yuan

    2017-06-15

    Enzymatic biosensors have been valuable bioanalytical devices for analysis of diverse targets in disease diagnosis, biological and biomedical research, etc. Photoelectrochemical (PEC) bioanalysis is a recently emerged method that promptly becoming a subject of new research interests due to its attractive potential for future bioanalysis with high sensitivity and specificity. PEC enzymatic biosensors integrate the inherent sensitivities of PEC bioanalysis and the selectivity of enzymes and thus share their both advantages. Currently, PEC enzymatic biosensors have become a hot topic of significant research and the recent impetus has grown rapidly as demonstrated by increased research papers. Given the pace of advances in this area, this review will make a thorough discussion and survey on the fundamentals, sensing strategies, applications and the state of the art in PEC enzymatic biosensors, followed by future prospects based on our own opinions. We hope this work could provide an accessible introduction to PEC enzymatic biosensors for any scientist.

  17. Platelike WO3 sensitized with CdS quantum dots heterostructures for photoelectrochemical dynamic sensing of H2O2 based on enzymatic etching.

    PubMed

    Wang, Yanhu; Gao, Chaomin; Ge, Shenguang; Yu, Jinghua; Yan, Mei

    2016-11-15

    A platelike tungsten trioxide (WO3) sensitized with CdS quantum dots (QDs) heterojunction is developed for solar-driven, real-time, and selective photoelectrochemical (PEC) sensing of H2O2 in the living cells. The structure is synthesized by hydrothermally growing platelike WO3 on fluorine doped tin oxide (FTO) and subsequently sensitized with CdS QDs. The as-prepared WO3-CdS QDs heterojunction achieve significant photocurrent enhancement, which is remarkably beneficial for light absorption and charge carrier separation. Based on the enzymatic etching of CdS QDs enables the activation of quenching the charge transfer efficiency, thus leading to sensitive PEC recording of H2O2 level in buffer and cellular environments. The results indicated that the proposed method will pave the way for the development of excellent PEC sensing platform with the quantum dot sensitization. This study could also provide a new train of thought on designing of self-operating photoanode in PEC sensing, promoting the application of semiconductor nanomaterials in photoelectrochemistry.

  18. Highly Enhanced Photoelectrochemical Water Oxidation Efficiency Based on Triadic Quantum Dot/Layered Double Hydroxide/BiVO 4 Photoanodes

    SciTech Connect

    Tang, Yanqun; Wang, Ruirui; Yang, Ye; Yan, Dongpeng; Xiang, Xu

    2016-08-03

    The water oxidation half-reaction is considered to be a bottleneck for achieving highly efficient solar-driven water splitting due to its multiproton-coupled four-electron process and sluggish kinetics. Herein, a triadic photoanode consisting of dual-sized CdTe quantum dots (QDs), Co-based layered double hydroxide (LDH) nanosheets, and BiVO4 particles, that is, QD@LDH@BiVO4, was designed. Two sets of consecutive Type-II band alignments were constructed to improve photogenerated electron-hole separation in the triadic structure. The efficient charge separation resulted in a 2-fold enhancement of the photocurrent of the QD@LDH@BiVO4 photoanode. A significantly enhanced oxidation efficiency reaching above 90% in the low bias region (i.e., E < 0.8 V vs RHE) could be critical in determining the overall performance of a complete photoelectrochemical cell. The faradaic efficiency for water oxidation was almost 90%. The conduction band energy of QDs is -1.0 V more negative than that of LDH, favorable for the electron injection to LDH and enabling a more efficient hole separation. The enhanced photon-to-current conversion efficiency and improved water oxidation efficiency of the triadic structure may result from the non-negligible contribution of hot electrons or holes generated in QDs. Such a band-matching and multidimensional triadic architecture could be a promising strategy for achieving high-efficiency photoanodes by sufficiently utilizing and maximizing the functionalities of QDs.

  19. Probing the structural flexibility of MOFs by constructing metal oxide@MOF-based heterostructures for size-selective photoelectrochemical response

    NASA Astrophysics Data System (ADS)

    Zhan, Wenwen; He, Yue; Guo, Jiangbin; Chen, Luning; Kong, Xiangjian; Zhao, Haixia; Kuang, Qin; Xie, Zhaoxiong; Zheng, Lansun

    2016-07-01

    It is becoming a challenge to achieve simpler characterization and wider application of flexible metal organic frameworks (MOFs) exhibiting the gate-opening or breathing behavior. Herein, we designed an intelligent MOF-based system where the gate-opening or breathing behavior of MOFs can be facially visualized in solution. Two types of metal oxide@MOF core-shell heterostructures, ZnO@ZIF-7 and ZnO@ZIF-71, were prepared using ZnO nanorods as self-sacrificial templates. The structural flexibility of both the MOFs can be easily judged from the distinct molecular-size-related formation modes and photoelectrochemical performances between the two ZnO@ZIF heterostructures. Moreover, the rotational dynamics of the flexible parts of ZIF-7 were studied by analyzing the intrinsic physical properties, such as dielectric constants, of the structure. The present work reminds us to pay particular attention to the influences of the structural flexibility of MOFs on the structure and properties of MOF-involved heterostructures in future studies.It is becoming a challenge to achieve simpler characterization and wider application of flexible metal organic frameworks (MOFs) exhibiting the gate-opening or breathing behavior. Herein, we designed an intelligent MOF-based system where the gate-opening or breathing behavior of MOFs can be facially visualized in solution. Two types of metal oxide@MOF core-shell heterostructures, ZnO@ZIF-7 and ZnO@ZIF-71, were prepared using ZnO nanorods as self-sacrificial templates. The structural flexibility of both the MOFs can be easily judged from the distinct molecular-size-related formation modes and photoelectrochemical performances between the two ZnO@ZIF heterostructures. Moreover, the rotational dynamics of the flexible parts of ZIF-7 were studied by analyzing the intrinsic physical properties, such as dielectric constants, of the structure. The present work reminds us to pay particular attention to the influences of the structural flexibility of

  20. Biomolecule-free, selective detection of o-diphenol and its derivatives with WS2/TiO2-based photoelectrochemical platform.

    PubMed

    Ma, Weiguang; Wang, Lingnan; Zhang, Nan; Han, Dongxue; Dong, Xiandui; Niu, Li

    2015-01-01

    Herein, a novel photoelectrochemical platform with WS2/TiO2 composites as optoelectronic materials was designed for selective detection of o-diphenol and its derivatives without any biomolecule auxiliary. First, catechol was chosen as a model compound for the discrimination from resorcinol and hydroquinone; then several o-diphenol derivatives such as dopamine, caffeic acid, and catechin were also detected by employing this proposed photoelectrochemical sensor. Finally, the mechanism of such a selective detection has been elaborately explored. The excellent selectivity and high sensitivity should be attributed to two aspects: (i) chelate effect of adjacent double oxygen atoms in the o-diphenol with the Ti(IV) surface site to form a five/six-atom ring structure, which is considered as the key point for distinction and selective detection. (ii) This selected WS2/TiO2 composites with proper band level between WS2 and TiO2, which could make the photogenerated electron and hole easily separated and results in great improvement of sensitivity. By employing such a photoelectrochemical platform, practical samples including commercial clinic drugs and human urine samples have been successfully performed for dopamine detection. This biomolecule-free WS2/TiO2 based photoelectrochemical platform demonstrates excellent stability, reproducibility, remarkably convenient, and cost-effective advantages, as well as low detection limit (e.g., 0.32 μmol L(-1) for dopamine). It holds great promise to be applied for detection of o-diphenol kind species in environment and food fields.

  1. Facile fabrication of an aptasensor for thrombin based on graphitic carbon nitride/TiO2 with high visible-light photoelectrochemical activity.

    PubMed

    Fan, Dawei; Guo, Cuijuan; Ma, Hongmin; Zhao, Di; Li, Yina; Wu, Dan; Wei, Qin

    2016-01-15

    A novel aptasensor for thrombin with high visible-light activity was facilely fabricated based on graphitic carbon nitride/TiO2 (g-C3N4/TiO2) photoelectrochemical (PEC) composite. Crystallization of TiO2 nanoparticles (NPs) and their strong interaction with g-C3N4 sheet were confirmed by high-resolution transmission electron microscope (HR-TEM), both of which contributed to the high photocurrent intensity under visible-light irradiation. Carboxyl functionalized thrombin aptamers were first successfully bound to the g-C3N4/TiO2 modified electrode as proven by photoelectrochemical test and electrochemical impedance spectroscopy (EIS) analysis. Ascorbic acid was utilized as the electron donor for scavenging photo-generated holes and inhibiting light driven electron-hole pair recombination. The specific recognition between thrombin aptamer and thrombin led to the linear decrease of photocurrent with the increase of logarithm of thrombin concentration in the range of 5.0×10(-13)molL(-1) to 5.0×10(-9)molL(-1) with a detection limit of 1.2×10(-13)molL(-1). This proposed low-cost, convenient and sensitive aptasensor showed promising applications in biosensor and photoelectrochemical analysis.

  2. A novel multi-amplification photoelectrochemical immunoassay based on copper(II) enhanced polythiophene sensitized graphitic carbon nitride nanosheet.

    PubMed

    Li, Rongxia; Liu, Yixin; Li, Xiaojian; Zhang, Sen; Wu, Dan; Zhang, Yong; Wei, Qin; Du, Bin

    2014-12-15

    A new sandwich photoelectrochemical (PEC) sensing strategy was proposed for the first time based on the increasing photocurrent of water-soluble polythiophene sensitized g-C3N4 nanosheet (PT-Cl/g-C3N4) in the presence of copper(II) (Cu(2+)), which was doped on the surface of titanium dioxide as labels for multi-amplification. Herein, the photoactive films of PT-Cl/g-C3N4 is employed as the photoactive antibody (Ab1) immobilization matrix for the subsequent sandwich-type antibody-antigen affinity interactions. Upon the presence of antigen (Ag), greatly enhanced photocurrent could be triggered in the PEC platform by the labels of second antibody (Ab2) of Cu(2+) doped titanium dioxide (Cu(2+)-TiO2). As a result of the multi-amplification in this Cu(2+)-TiO2 enhanced PT-Cl/g-C3N4-based PEC immunoassay, it possesses excellent analytical performance. The antigen could be detected from 0.01 pg mL(-1) to 100.0 ng mL(-1) with a detection limit of 5 fg mL(-1). This work opens up g-C3N4 nanosheet applied in PEC sensing. More importantly, the strategy of specific positive effect of Cu(2+) on the photocurrent of g-C3N4 opens an alternative horizon for PEC sensing.

  3. Photoelectrochemical measurements at Hydrogen Solar

    NASA Astrophysics Data System (ADS)

    Wijayantha, K. G. U.

    2006-08-01

    Recent progress in nanotechnology has stimulated research in the area of advanced materials and resulted in the development of a new class of nano structured materials. These materials are finding uses in a wide range of applications including photoelectrochemical water splitting using Tandem Cells TM. . This is a novel concept designed to generate hydrogen by splitting water under direct sunlight [1]. A Tandem Cell TM consists of two photocells which are connected optically in series, each containing a nanostructured semiconductor photoelectrode (Fig. 1). The Tandem Cell TM is a low cost alternative to solar water splitting configurations proposed by others and Hydrogen Solar is currently in the process of developing the technology.

  4. A novel bismuth oxychloride-graphene hybrid nanosheets based non-enzymatic photoelectrochemical glucose sensing platform for high performances.

    PubMed

    Gopalan, A I; Muthuchamy, N; Lee, K P

    2017-03-15

    A novel non-enzymatic photoelectrochemical (PEC) glucose sensor was first constructed based on the unique two-dimensional (2D) bismuth oxychloride-graphene nanohybrid sheets (BiOCl-G NHS). We have utilized a facile hydrothermal approach for the preparation of BiOCl-G NHS. Results from cyclic voltammetric and differential pulse voltammetric measurements revealed that the BiOCl-G NHS electrode is capable of generating photocurrent for glucose when its surface is irradiated with a light source (wavelength=365nm). The photocurrents produced for the presence of glucose at the bias potential of +0.50V showed a linear dependence on glucose concentration in the range between 0.5 and 10mM and had a detection limit of 0.22mM. The PEC detection of glucose at BiOCl-G NHS was not influenced by the presence of other common interfering species. The glucose levels, as determined by the BiOCl-G NHS sensor, agreed well with those obtained by the commercial glucometers. This novel non-enzymatic PEC glucose sensor exhibited good performances, such as a wider concentration range (500µM-10mM), high sensitivity (1.878µMmM(-1)cm(-2) (500µM-2mM) and 127.2µMmM(-1)cm(-2) (2mM-10mM)), good selectivity, reproducibility (RSD=2.4%) and applicability to real sample (human serum).

  5. A label-free photoelectrochemical aptasensor based on nitrogen-doped graphene quantum dots for chloramphenicol determination.

    PubMed

    Liu, Yong; Yan, Kai; Okoth, Otieno Kevin; Zhang, Jingdong

    2015-12-15

    A photoelectrochemical (PEC) sensing platform for chloramphenicol (CAP) detection was constructed using nitrogen-doped graphene quantum dots (N-GQDs) as transducer species and label-free aptamer as biological recognition element. N-GQDs, synthesized via a facile one-step hydrothermal method, were explored to achieve highly efficient photon-to-electricity conversion under visible light irradiation. The obtained N-GQDs were characterized by transmission electron microscopy (TEM), which displayed a narrow size distribution with a mean diameter of 2.14 nm. The X-ray photoelectron spectroscopic (XPS) and Fourier transform infrared spectroscopic (FT-IR) analysis confirmed that nitrogen was successfully doped in GQDs. The UV-visible absorption spectra indicated that nitrogen doping obviously enhanced the absorption of GQDs in visible light region. As a result, the PEC activity of GQDs was promoted by nitrogen doping. Additionally, the π-conjugated structure of N-GQDs provided an excellent platform for aptamer immobilization via π-π stacking interaction. Such an aptamer/N-GQDs based sensor showed a linear PEC response to CAP concentration in the range of 10-250 nM with a detection limit (3 S/N) of 3.1 nM. The developed PEC aptasensor exhibited high sensitivity and selectivity, good reproducibility and high stability.

  6. Visible light photoelectrochemical aptasensor for adenosine detection based on CdS/PPy/g-C3N4 nanocomposites.

    PubMed

    Liu, Yixin; Ma, Hongmin; Zhang, Yong; Pang, Xuehui; Fan, Dawei; Wu, Dan; Wei, Qin

    2016-12-15

    In this work, a label-free photoelectrochemical (PEC) aptasensor was developed for adenosine detection based on CdS/PPy/g-C3N4 nanocomposites. The CdS/g-C3N4 heterojunction effectively prevented the photogenerated charges recombination of g-C3N4 and self-photocorrosion processes of CdS, improving photo-to-current conversion efficiency. The introduced polypyrrole (PPy) nanoparticles could lead to a more effective separation of photogenerated charges, thus resulting in a further increasing of photocurrent. The CdS/PPy/g-C3N4 was firstly employed as the photoactive materials for fabrication of aptasensor, and SH-aptamer was then adsorbed on the CdS/PPy/g-C3N4 modified electrodes through S-Cd bond. With increasing of adenosine concentration, the photocurrent decreased as the formation of SH-aptamer-adenosine bioaffinity complexes. Under optimal conditions, the PEC aptasensor had a sensitive response to adenosine in a linear range of 0.3nmolL(-1) to 200nmolL(-1) with a detection limit of 0.1nmolL(-1). Besides, the as-proposed aptasensor has also been applied in human serum samples analysis. The aptasensor exhibits high sensitivity and good stability, thus opening up a new promising PEC platform for some other small molecules analysis.

  7. A competitive photoelectrochemical immunosensor based on a CdS-induced signal amplification strategy for the ultrasensitive detection of dexamethasone

    PubMed Central

    Wang, Xueping; Yan, Tao; Li, Yan; Liu, Yixin; Du, Bin; Ma, Hongmin; Wei, Qin

    2015-01-01

    A novel photoelectrochemical immunosensor based on the competitive strategy is proposed for the specific detection of dexamethasone (DXM). Graphitic carbon nitride coupled with bismuth sulfide are used as the sensing matrix for the immobilization of BSA-DXM on the electrode surface, while cadmium sulfide functionalized titanium dioxide (TiO2@CdS) is used as the photoelectric active labels of anti-DXM. Due to the perfect matching of energy levels between TiO2 and CdS, the in situ prepared composite labels show excellent photocurrent response under visible lights. The competitive binding of DXM in sample solutions and BSA-DXM on the electrode surface reduces the specific attachment of labels to the electrode, resulting in a decrease of the photocurrent intensity. Greatly enhanced sensitivity is achieved after the optimization of the detection conditions. Under the optimal detection condition, the well-designed immunosensor for DXM exhibits a low detection limit of 2 pg∙mL−1. Additionally, the proposed immunoassay system shows high specificity, good reproducibility and acceptable stability, which is also expected to become a promising platform for the detection of other small molecules. PMID:26648409

  8. Photoelectrochemical hydrogen production

    SciTech Connect

    Rocheleau, R.; Misra, A.; Miller, E.

    1998-08-01

    A significant component of the US DOE Hydrogen Program is the development of a practical technology for the direct production of hydrogen using a renewable source of energy. High efficiency photoelectrochemical systems to produce hydrogen directly from water using sunlight as the energy source represent one of the technologies identified by DOE to meet this mission. Reactor modeling and experiments conducted at UH provide strong evidence that direct solar-to-hydrogen conversion efficiency greater than 10% can be expected using photoelectrodes fabricated from low-cost, multijunction (MJ) amorphous silicon solar cells. Solar-to-hydrogen conversion efficiencies as high as 7.8% have been achieved using a 10.3% efficient MJ amorphous silicon solar cell. Higher efficiency can be expected with the use of higher efficiency solar cells, further improvement of the thin film oxidation and reduction catalysts, and optimization of the solar cell for hydrogen production rather than electricity production. Hydrogen and oxygen catalysts developed under this project are very stable, exhibiting no measurable degradation in KOH after over 13,000 hours of operation. Additional research is needed to fully optimize the transparent, conducting coatings which will be needed for large area integrated arrays. To date, the best protection has been afforded by wide bandgap amorphous silicon carbide films.

  9. Excellent graphitic carbon nitride nanosheets-based photoelectrochemical platform motivated by Schottky barrier and LSPR effect and its sensing application.

    PubMed

    Dai, Hong; Zhang, Shupei; Li, Yilin; Lin, Yanyu

    2015-05-21

    A visible light responsive photocatalytic hybrid with excellent photoelectrochemical activity was first fabricated via the self-assembly of Au nanorods onto poly(l-cysteine) modified graphitic carbon nitride nanosheets. Herein, layered structural graphitic carbon nitride nanosheets with a proper band gap, high stability, and nontoxicity, as a photoactive material, demonstrate a high photocatalytic activity. Furthermore, the incorporation of multifunctional Au nanorods gave the hybrid a Schottky barrier and localized surface plasmonic resonance, which considerably enhanced the separation of the photo-excited electrons and holes, resulting in increased photoelectrochemical performance. As a proof of concept, mercapto-beta-cyclodextrin as a bionic recognition device was introduced into the hybrid to selectively detect naringin on the basis of the dramatic decreasing of photocurrent. The visible-light driven photoelectrochemical sensor exhibited excellent analytical performance, including high sensitivity, good selectivity and wide linear range from 1 × 10(-4) to 1 × 10(-10) M.

  10. Visible-light driven photoelectrochemical immunosensor for insulin detection based on MWCNTs@SnS2@CdS nanocomposites.

    PubMed

    Liu, Yixin; Zhang, Yifeng; Wu, Dan; Fan, Dawei; Pang, Xuehui; Zhang, Yong; Ma, Hongmin; Sun, Xu; Wei, Qin

    2016-12-15

    In this work, a label-free photoelectrochemical (PEC) immunosensor was developed for ultrasensitive detection of insulin based on MWCNTs@SnS2@CdS nanocomposites. As graphene-like 2D nanomaterial, SnS2 nanosheets loaded on the conducting framework of multi-walled carbon nanotubes (MWCNTs) were adopted for the construction of immunosensor for the first time, providing a favorable substrate for in-situ growth of CdS nanocrystal that had suitable band structure matching well with SnS2. The well-matched band structure of these two metal sulfides effectively inhibited the recombination of photogenerated electron-hole pairs, thus improving the photo-to-current conversion efficiency. Besides, the introduction of MWCNTs facilitated electron transfer across the surface of electrodes, leading to a further increment of photocurrent. The as constructed label-free PEC immunosensor based on MWCNTs@SnS2@CdS nanocomposites exhibited excellent PEC performance for the detection of insulin. The concentrations of insulin could be directly detected based on the decrement of photocurrent that was brought by the increased steric hindrances due to the formation of antigen-antibody immunocomplexes. Under the optimal conditions, the PEC immunosensor had a sensitive response to insulin in a linear range of 0.1pgmL(-1) to 5ngmL(-1) with a detection limit of 0.03pgmL(-1). Meanwhile, good stability and selectivity were achieved as well. The design and fabrication of this PEC immunosensor based on MWCNTs@SnS2@CdS nanocomposites not only provided an ideal platform for the detection of insulin, but also opened up a new avenue for the development of immunosensor for some other biomarkers analysis.

  11. Multifunctional reduced graphene oxide trigged chemiluminescence resonance energy transfer: Novel signal amplification strategy for photoelectrochemical immunoassay of squamous cell carcinoma antigen.

    PubMed

    Zhang, Yan; Sun, Guoqiang; Yang, Hongmei; Yu, Jinghua; Yan, Mei; Song, Xianrang

    2016-05-15

    Herein, a photoelectrochemical (PEC) immunoassay is constructed for squamous cell carcinoma antigen (SCCA) detection using zinc oxide nanoflower-bismuth sulfide (Bi2S3) composites as photoactive materials and reduced graphene oxide (rGO) as signal labels. Horseradish peroxidase is used to block sites against nonspecific binding, and then participated in luminol-based chemiluminescence (CL) system. The induced CL emission is acted as an inner light source to excite photoactive materials, simplifying the instrument. A novel signal amplification strategy is stem from rGO because of the rGO acts as an energy acceptor, while luminol serves as a donor to rGO, triggering the CL resonance energy transfer phenomenon between luminol and rGO. Thus, the efficient CL emission to photoactive materials decreases. Furthermore, the signal amplification caused by rGO labeled signal antibodies is related to photogenerated electron-hole pairs: perfect matching of energy levels between rGO and Bi2S3 makes rGO a sink to capture photogenerated electrons from Bi2S3; the increased steric hindrance hinders the electron donor to the surface of Bi2S3 for reaction with the photogenerated holes. On the basis of the novel signal amplification strategy, the proposed immunosensor exhibits excellent analytical performance for PEC detection of SCCA, ranging from 0.8 pg mL(-1) to 80 ng mL(-1) with a low detection limit of 0.21 pg mL(-1). Meanwhile, the designed signal amplification strategy provides a general format for future development of PEC assays.

  12. DNA sequence functionalized with heterogeneous core-satellite nanoassembly for novel energy-transfer-based photoelectrochemical bioanalysis.

    PubMed

    Zhu, Yuan-Cheng; Xu, Fei; Zhang, Nan; Zhao, Wei-Wei; Xu, Jing-Juan; Chen, Hong-Yuan

    2017-05-15

    This work reports the use of compositionally heterogeneous asymmetric Ag@Au core-satellite nanoassembly functionalized with DNA sequence as unique signaling nanoprobes for the realization of new energy-transfer-based photoelectrochemical (PEC) immunoassay of prostate- specific antigen (PSA). Specifically, the Ag@Au asymmetric core-satellite nanoassemblies (Ag@Au ACS) were fabricated on a two-dimensional glass substrate by a modified controlled assembly technique, and then functionalized with DNA sequences containing PSA aptamers as signaling nanoprobes. Then, the sandwich complexing between the PSA, its antibodies, and the signaling nanoprobes was performed on a CdS QDs modified indium tin oxide (ITO) electrode. The single stranded DNA can server as a facile mediator that place the Ag@Au ACS in proximity of CdS QDs, stimulating the interparticle exciton-plasmon interactions between Ag@Au ACS and CdS QDs and thus quenching the excitonic states in the latter. Since the damping effect is closely related to the target concentration, a novel energy-transfer-based PEC bioanalysis could be achieved for the sensitive and specific PSA assay. The developed biosensor displayed a linear range from 1.0×10(-11)gmL(-1) to 1.0×10(-7)gmL(-1) and the detection limit was experimentally found to be of 0.3×10(-13)gmL(-1). This strategy used the Ag@Au ACS-DNA signaling nanoprobes and overcame the deficiency of short operating distance of the energy transfer process for feasible PEC immunoassay. More significantly, it provided a way to couple the plasmonic properties of the Ag NPs and Au NPs in a single PEC bioanalytical system. We expected this work could inspire more interests and further investigations on the advanced engineering of the core-satellite or other judiciously designed nanostructures for new PEC bioanalytical uses with novel properties.

  13. Assessing the utility of bipolar membranes for use in photoelectrochemical water-splitting cells.

    PubMed

    Vargas-Barbosa, Nella M; Geise, Geoffrey M; Hickner, Michael A; Mallouk, Thomas E

    2014-11-01

    Membranes are important in water-splitting solar cells because they prevent crossover of hydrogen and oxygen. Here, bipolar membranes (BPMs) were tested as separators in water electrolysis cells. Steady-state membrane and solution resistances, electrode overpotentials, and pH gradients were measured at current densities relevant to solar photoelectrolysis. Under forward bias conditions, electrodialysis of phosphate buffer ions creates a pH gradient across a BPM. Under reverse bias, the BPM can maintain a constant buffer pH on both sides of the cell, but a large membrane potential develops. Thus, the BPM does not present a viable solution for electrolysis in buffered electrolytes. However, the membrane potential is minimized when the anode and cathode compartments of the cell contain strongly basic and acidic electrolytes, respectively.

  14. Photoelectrochemical batteries for efficient energy recovery.

    PubMed

    Han, Lei; Guo, Shaojun; Xu, Miao; Dong, Shaojun

    2014-11-11

    Herein we propose novel photoelectrochemical fuel cells (PEFCs) by the introduction of a solid-state Ag2O/Ag cathode (here also term as photoelectrochemical battery). Due to the superior electrochemical properties of Ag2O/Ag, the maximum power density of our PEFCs can reach 0.94 mW cm(-2) upon UV illumination. Furthermore, our PEFCs have stable cycle operation and can be undertaken in a single chamber without an ion-exchange membrane. Most importantly, we demonstrate that our PEFCs can be adopted to degrade the methyl orange (MO) dye with a decomposition percentage of 72.5% within 30 min during the PEFC process.

  15. Experimental and Computational Studies on the Design of Dyes for Water-splitting Dye-sensitized Photoelectrochemical Tandem Cells

    NASA Astrophysics Data System (ADS)

    Mendez-Hernandez, Dalvin D.

    Solar energy is a promising alternative for addressing the world's current and future energy requirements in a sustainable way. Because solar irradiation is intermittent, it is necessary to store this energy in the form of a fuel so it can be used when required. The light-driven splitting of water into oxygen and hydrogen (a useful chemical fuel) is a fascinating theoretical and experimental challenge that is worth pursuing because the advance of the knowledge that it implies and the availability of water and sunlight. Inspired by natural photosynthesis and building on previous work from our laboratory, this dissertation focuses on the development of water-splitting dye-sensitized photoelectrochemical tandem cells (WSDSPETCs). The design, synthesis, and characterization of high-potential porphyrins and metal-free phthalocyanines with phosphonic anchoring groups are reported. Photocurrents measured for WSDSPETCs made with some of these dyes co-adsorbed with molecular or colloidal catalysts on TiO2 electrodes are reported as well. To guide in the design of new molecules we have used computational quantum chemistry extensively. Linear correlations between calculated frontier molecular orbital energies and redox potentials were built and tested at multiple levels of theory (from semi-empirical methods to density functional theory). Strong correlations (with r2 values > 0.99) with very good predictive abilities (rmsd < 50 mV) were found when using density functional theory (DFT) combined with a continuum solvent model. DFT was also used to aid in the elucidation of the mechanism of the thermal relaxation observed for the charge-separated state of a molecular triad that mimics the photo-induced proton coupled electron transfer of the tyrosine-histidine redox relay in the reaction center of Photosystem II. It was found that the inclusion of explicit solvent molecules, hydrogen bonded to specific sites within the molecular triad, was essential to explain the observed

  16. Polymer blends for use in photoelectrochemical cells for conversion of solar energy to electricity

    DOEpatents

    Skotheim, Terje

    1986-01-01

    There is disclosed a polymer blend of a highly conductive polymer and a solid polymer electrolyte that is designed to achieve better charge transfer across the conductive film/polymer electrolyte interface of the electrochemical photovoltaic cell. The highly conductive polymer is preferably polypyrrole or poly-N-p-nitrophenylpyrrole and the solid polymer electrolyte is preferably polyethylene oxide or polypropylene oxide.

  17. Polymer blends for use in photoelectrochemical cells for conversion of solar energy to electricity

    DOEpatents

    Skotheim, T.

    1984-09-28

    There is disclosed a polymer blend of a highly conductive polymer and a solid polymer electrolyte that is designed to achieve better charge transfer across the conductive film/polymer electrolyte interface of the electrochemical photovoltaic cell. The highly conductive polymer is preferably polypyrrole or poly-N-p-nitrophenylpyrrole and the solid polymer electrolyte is preferably polyethylene oxide or polypropylene oxide.

  18. Photoelectrochemical hydrogen production

    SciTech Connect

    Rocheleau, R.E.; Miller, E.; Zhang, Z.

    1995-09-01

    The large-scale production of hydrogen utilizing energy provided by a renewable source to split water is one of the most ambitious long-term goals of the U.S. Department of Energy`s Hydrogen Program. Photoelectrochemical devices-direct photoconversion systems utilizing a photovoltaic-type structure coated with water-splitting catalysts-represent a promising option to meet this goal. Direct solar-to-chemical conversion efficiencies greater than 7% and photoelectrode lifetimes of up to 30 hours in 1 molar KOH have been demonstrated in our laboratory using low-cost, amorphous-silicon-based photoelectrodes. Loss analysis models indicate that the DOE`s goal of 10% solar-to-chemical conversion can be met with amorphous-silicon-based structures optimized for hydrogen production. In this report, we describe recent progress in the development of thin-film catalytic/protective coatings, improvements in photoelectrode efficiency and stability, and designs for higher efficiency and greater stability.

  19. Photoelectrochemical, photophysical and morphological studies of electrostatic layer-by-layer thin films based on poly(p-phenylenevinylene) and single-walled carbon nanotubes.

    PubMed

    Almeida, L C P; Zucolotto, V; Domingues, R A; Atvars, T D Z; Nogueira, A F

    2011-11-01

    The preparation of multilayer films based on poly(p-phenylenevinylene) (PPV) and carboxylic-functionalized single-walled carbon nanotubes (SWNT-COOH) by electrostatic interaction using the layer-by-layer (LbL) deposition method is reported herein. The multilayer build-up, monitored by UV-Vis and photoluminescence (PL) spectroscopies, displayed a linear behavior with the number of PPV and SWNT-COOH layers deposited that undergo deviation and spectral changes for thicker films. Film morphology was evaluated by AFM and epifluorescence microscopies showing remarkable changes after incorporation of SWNT-COOH layers. Films without SWNT show roughness and present dispersed grains; films with SWNT-COOH layers are flatter and some carbon nanotube bundles can be visualized. The photoinduced charge transfer from the conducting polymer to SWNT-COOH was analyzed by PL quenching either by the decrease of the emission intensity or by the presence of dark domains in the epifluorescence micrographs. Photoelectrochemical characterization was performed under white light and the films containing SWNT-COOH displayed photocurrent values between 2.0 μA cm(-2) and 7.5 μA cm(-2), as the amount of these materials increases in the film. No photocurrent was observed for the film without carbon nanotubes. Photocurrent generation was enhanced and became more stable when an intermediate layer of PEDOT:PSS was interposed between the active layer and the ITO electrode, indicating an improvement in hole transfer to the contacts. Our results indicate that these multilayer films are promising candidates as active layers for organic photovoltaic cells.

  20. I-III-VI2 (Copper Chalcopyrite-based) Materials for Use in Hybrid Photovoltaic/Photoelectrochemical Water-Splitting Devices

    NASA Astrophysics Data System (ADS)

    Kaneshiro, Jess Masao Makana

    This project, in an effort to improve upon basic crystalline silicon photovoltaic energy conversion, proposes both an alternative material and an alternative method of solar energy conversion. The sun, responsible for giving us life of all kinds, is capable of giving us more. Photovoltaic energy, derived from the conversion of solar energy to electrical energy, can be a very efficient process. Unfortunately, it is often produced at a location and time where we are unable to use it immediately, necessitating transmission or storage of this converted energy; both imposing energy losses and costs. Furthermore, the typical use of crystalline silicon for this process is hindered by supply and fabrication cost issues. Photoelectrochemical (PEC) water-splitting offers an alternative energy-transport mechanism in the form of evolved hydrogen gas. Untethered by aging power lines and insufficient energy distribution technology, hydrogen gas offers new methods to store and transport converted solar energy to be used in fuel cells or hydrogen combustion engines representing a sustainable, clean and completely carbon-free energy cycle. PEC water-splitting also allows the use of a variety of new semiconductor materials like the I-III-VI2 copper chalcopyrite based material class capable of displacing our reliance on crystalline silicon used to harness the sun's power. Capable of photocurrents as high as 20mA/cm 2, a device utilizing this material demonstrates 4.35% solar-to-hydrogen conversion efficiency. Material durability is also documented, achieving 420 hours of sustained water-splitting representing 4.6 years of operation.

  1. Routes to Ultrahigh Efficiency Photovoltaic and Photoelectrochemical Devices

    SciTech Connect

    Eisler, Carissa; Lloyd, John; Flowers, Cris; Darbe, Sunita; Warmann, Emily; Verlage, Erik; Fountaine, Kate; Hu, Shu; Lewis, Nathan; Atwater, Harry

    2014-10-15

    We discuss ‘full spectrum’ photovoltaic modules that leverage low-cost III-V compound semiconductor cells, efficient optics and unconventional fabrication/assembly methods, and discuss advances in photoelectrochemical water-splitting with high efficiency.

  2. Visible photoelectrochemical water splitting into H2 and O2 in a dye-sensitized photoelectrosynthesis cell

    SciTech Connect

    Alibabaei, Leila; Sherman, Benjamin D.; Norris, Michael R.; Brennaman, M. Kyle; Meyer, Thomas J.

    2015-04-27

    A hybrid strategy for solar water splitting is exploited here based on a dye-sensitized photoelectrosynthesis cell (DSPEC) with a mesoporous SnO2/TiO2 core/shell nanostructured electrode derivatized with a surface-bound Ru(II) polypyridyl-based chromophore–catalyst assembly. The assembly, [(4,4’-(PO3H2)2bpy)2Ru(4-Mebpy-4’-bimpy)Ru(tpy)(OH2)]4+ ([RuaII-RubII-OH2]4+, combines both a light absorber and a water oxidation catalyst in a single molecule. It was attached to the TiO2 shell by phosphonate-surface oxide binding. The oxide-bound assembly was further stabilized on the surface by atomic layer deposition (ALD) of either Al2O3 or TiO2 overlayers. Illumination of the resulting fluorine-doped tin oxide (FTO)|SnO2/TiO2|-[RuaII-RubII-OH2]4+(Al2O3 or TiO2) photoanodes in photoelectrochemical cells with a Pt cathode and a small applied bias resulted in visible-light water splitting as shown by direct measurements of both evolved H2 and O2. The performance of the resulting DSPECs varies with shell thickness and the nature and extent of the oxide overlayer. Use of the SnO2/TiO2 core/shell compared with nanoITO/TiO2 with the same assembly results in photocurrent enhancements of ~5. In conclusion, systematic variations in shell thickness and ALD overlayer lead to photocurrent densities as high as 1.97 mA/cm2 with 445-nm, ~90-mW/cm2 illumination in a phosphate buffer at pH 7.

  3. Brown seaweed pigment as a dye source for photoelectrochemical solar cells

    NASA Astrophysics Data System (ADS)

    Calogero, Giuseppe; Citro, Ilaria; Di Marco, Gaetano; Armeli Minicante, Simona; Morabito, Marina; Genovese, Giuseppa

    2014-01-01

    Chlorophylls based-dyes obtained from seaweeds represent attractive alternatives to the expensive and polluting pyridil based Ru complexes because of their abundance in nature. Another important characteristic is that the algae do not subtract either cropland or agricultural water, therefore do not conflict with agro-food sector. This pigment shows a typical intense absorption in the UV/blue (Soret band) and a less intense band in the red/near IR (Q band) spectral regions and for these reasons appear very promising as sensitizer dyes for DSSC. In the present study, we utilized chlorophylls from samples of the brown alga Undaria pinnatifida as sensitizer in DSSCs. The dye, extracted by frozen seaweeds and used without any chemical purification, showed a very good fill factor (0.69). Even the photelectrochemical parameters if compared with the existent literature are very interesting.

  4. Photoelectrochemical Hydrogen Production

    SciTech Connect

    Hu, Jian

    2013-12-23

    The objectives of this project, covering two phases and an additional extension phase, were the development of thin film-based hybrid photovoltaic (PV)/photoelectrochemical (PEC) devices for solar-powered water splitting. The hybrid device, comprising a low-cost photoactive material integrated with amorphous silicon (a-Si:H or a-Si in short)-based solar cells as a driver, should be able to produce hydrogen with a 5% solar-to-hydrogen conversion efficiency (STH) and be durable for at least 500 hours. Three thin film material classes were studied and developed under this program: silicon-based compounds, copper chalcopyrite-based compounds, and metal oxides. With the silicon-based compounds, more specifically the amorphous silicon carbide (a-SiC), we achieved a STH efficiency of 3.7% when the photoelectrode was coupled to an a-Si tandem solar cell, and a STH efficiency of 6.1% when using a crystalline Si PV driver. The hybrid PV/a-SiC device tested under a current bias of -3~4 mA/cm{sup 2}, exhibited a durability of up to ~800 hours in 0.25 M H{sub 2}SO{sub 4} electrolyte. Other than the PV driver, the most critical element affecting the photocurrent (and hence the STH efficiency) of the hybrid PV/a-SiC device was the surface energetics at the a-SiC/electrolyte interface. Without surface modification, the photocurrent of the hybrid PEC device was ~1 mA/cm{sup 2} or lower due to a surface barrier that limits the extraction of photogenerated carriers. We conducted an extensive search for suitable surface modification techniques/materials, of which the deposition of low work function metal nanoparticles was the most successful. Metal nanoparticles of ruthenium (Ru), tungsten (W) or titanium (Ti) led to an anodic shift in the onset potential. We have also been able to develop hybrid devices of various configurations in a monolithic fashion and optimized the current matching via altering the energy bandgap and thickness of each constituent cell. As a result, the short

  5. Photoelectrochemical detection of alpha-fetoprotein based on ZnO inverse opals structure electrodes modified by Ag2S nanoparticles.

    PubMed

    Jiang, Yandong; Liu, Dali; Yang, Yudan; Xu, Ru; Zhang, Tianxiang; Sheng, Kuang; Song, Hongwei

    2016-12-06

    In this work, a new photoelectrochemical biosensor based on Ag2S nanoparticles (NPs) modified macroporous ZnO inverse opals structure (IOs) was developed for sensitive and rapid detection of alpha fetal protein (AFP). Small size and uniformly dispersed Ag2S NPs were prepared using the Successive Ionic Layer Adsorption And Reaction (SILAR) method, which were adsorbed on ZnO IOs surface and frame work as matrix for immobilization of AFP. The composite structure of ZnO/Ag2S expanded the scope of light absorption to long wavelength, which can make full use of the light energy. Meanwhile, an effective matching of energy levels between the conduction bands of Ag2S and ZnO are beneficial to the photo-generated electrons transfer. The biosensors based on FTO (fluorine-doped tinoxide) ZnO/Ag2S electrode showed enough sensitivity and a wide linear range from 0.05 ng/mL to 200 ng/mL with a low detection limit of 8 pg/mL for the detection of AFP. It also exhibited high reproducibility, specificity and stability. The proposed method was potentially attractive for achieving excellent photoelectrochemical biosensor for detection of other proteins.

  6. Photoelectrochemical detection of alpha-fetoprotein based on ZnO inverse opals structure electrodes modified by Ag2S nanoparticles

    PubMed Central

    Jiang, Yandong; Liu, Dali; Yang, Yudan; Xu, Ru; Zhang, Tianxiang; Sheng, Kuang; Song, Hongwei

    2016-01-01

    In this work, a new photoelectrochemical biosensor based on Ag2S nanoparticles (NPs) modified macroporous ZnO inverse opals structure (IOs) was developed for sensitive and rapid detection of alpha fetal protein (AFP). Small size and uniformly dispersed Ag2S NPs were prepared using the Successive Ionic Layer Adsorption And Reaction (SILAR) method, which were adsorbed on ZnO IOs surface and frame work as matrix for immobilization of AFP. The composite structure of ZnO/Ag2S expanded the scope of light absorption to long wavelength, which can make full use of the light energy. Meanwhile, an effective matching of energy levels between the conduction bands of Ag2S and ZnO are beneficial to the photo-generated electrons transfer. The biosensors based on FTO (fluorine-doped tinoxide) ZnO/Ag2S electrode showed enough sensitivity and a wide linear range from 0.05 ng/mL to 200 ng/mL with a low detection limit of 8 pg/mL for the detection of AFP. It also exhibited high reproducibility, specificity and stability. The proposed method was potentially attractive for achieving excellent photoelectrochemical biosensor for detection of other proteins. PMID:27922086

  7. A sensitive photoelectrochemical biosensor for AFP detection based on ZnO inverse opal electrodes with signal amplification of CdS-QDs.

    PubMed

    Xu, Ru; Jiang, Yandong; Xia, Lei; Zhang, Tianxiang; Xu, Lin; Zhang, Shuang; Liu, Dali; Song, Hongwei

    2015-12-15

    In this work, ZnO inverse opals structure (IOs) based photoelectrochemical (PEC) electrode was fabricated for alpha-fetoprotein (AFP) detection. Then, the uniform CdS quantum dots (QDs) were hydrothermally synthesized, which allowed the binding of AFP and glucose oxidase (GOD) on CdS QDs, forming the AFP-CdS-GOD composite. The competitive immunosensor of AFP and the AFP-CdS-GOD composite with anti-AFP antibodies (Ab) immobilized on FTO (fluorine-doped tin oxide) /ZnO IOs electrode was successfully applied to the detection of AFP. GOD could catalyze glucose to produce hydrogen peroxide (H2O2) acting as an electron donor to scavenge photogenerated holes in the valence band of CdS QDs, reducing the recombination of electrons and holes of CdS QDs. Also the effective energy level matching between the conduction bands of CdS QDs and ZnO widened the range of light absorption, allowing for electron injection from excited CdS QDs to ZnO upon visible light irradiation, which enhanced the photocurrent. The results show that the immunosensor of AFP possesses a large linear detection range of 0.1-500 ng/ml with a detection limit of 0.01 ng/ml. It also exhibits excellent anti-interference property and acceptable stability. This work provides a promising method for achieving excellent photoelectrochemical biosensor detection of other proteins.

  8. Photo-enhanced salt-water splitting using orthorhombic Ag8SnS6 photoelectrodes in photoelectrochemical cells

    NASA Astrophysics Data System (ADS)

    Cheng, Kong-Wei; Tsai, Wei-Tseng; Wu, Yu-Hsuan

    2016-06-01

    Orthorhombic Ag8SnS6 photoelectrodes are prepared on various substrates via reactive sulfurization using the radio-frequency magnetron sputtering of silver-tin metal precursors. Evaluations of the photoelectrochemical performances of Ag8SnS6 photoelectrodes with various levels of silver content are carried out in various aqueous solutions. X-ray diffraction patterns and Hall measurements of samples after a three-stage sulfurization process show that all samples are the pure orthorhombic Ag8SnS6 phase with n-type conductivity. The energy band gaps, carrier concentrations, and mobilities of samples on glass substrates are 1.31-1.33 eV, 7.07 × 1011-8.52 × 1012 cm-3, and 74.9-368 cm2 V-1 s-1, respectively, depending on the [Ag]/[Ag+Sn] molar ratio in samples. The highest photoelectrochemical performances of orthorhombic Ag8SnS6 photoelectrodes in aqueous 0.35 M Na2S + 0.25 M K2SO3 and 0.5 M NaCl solutions are respectively 2.09 and 2.5 mA cm-2 at an applied voltages of 0.9 and 1.23 V vs. a reversible hydrogen electrode under light irradiation with a light intensity of 100 mW cm-2 from a 300-W Xe lamp.

  9. Nanoparticulate Dye-Semiconductor Hybrid Materials Formed by Electrochemical Self-Assembly as Electrodes in Photoelectrochemical Cells

    NASA Astrophysics Data System (ADS)

    Nonomura, Kazuteru; Loewenstein, Thomas; Michaelis, Esther; Kunze, Peter; Schiek, Manuela; Reemts, Jens; Yoshie Iwaya, Mirian; Wark, Michael; Rathousky, Jiri; Al-Shamery, Katharina; Kittel, Achim; Parisi, Jürgen; Wöhrle, Dieter; Yoshida, Tsukasa; Schlettwein, Derck

    2009-08-01

    Dye-sensitized zinc oxide thin films were prepared, characterized and optimized for applications as photoelectrochemically active electrodes. Conditions were established under which crystalline thin films of ZnO with a porous texture were formed by electrochemically induced crystallization controlled by structure-directing agents (SDA). Dye molecules were adsorbed either directly as SDA during this preparation step or, preferably, following desorption of a SDA. The external quantum efficiency (IPCE) could thereby be increased significantly. Particular emphasis was laid on dye molecules that absorb in the red part of the visible spectrum. Model experiments under ultrahigh vacuum (UHV) conditions with dye molecules adsorbed on defined crystal planes of single crystals aimed at a deeper understanding of the coupling of the chromophore electronic π-system within molecular aggregates and to the semiconductor surface. Detailed photoelectrochemical kinetic measurements were used to characterize and optimize the electrochemically prepared dye-sensitized ZnO films. Parallel electrical characterization in vacuum served to distinguish between contributions of charge transport within the ZnO semiconductor matrix and the ions of the electrolyte in the pore system of the electrode.

  10. Fabrication of CuInS2 films from electrodeposited Cu/In bilayers: effects of preheat treatment on their structural, photoelectrochemical and solar cell properties.

    PubMed

    Lee, Sun Min; Ikeda, Shigeru; Yagi, Tetsuro; Harada, Takashi; Ennaoui, Ahmed; Matsumura, Michio

    2011-04-14

    Polycrystalline CuInS(2) films were fabricated by sulfurization of electrodeposited Cu and In metallic precursor films in a Cu-rich composition at 520 °C in H(2)S (5% in Ar). Structural analyses revealed that the adherence of the thus-formed CuInS(2) film to the Mo substrate was strongly dependent on heating profiles of the Cu/In bilayer film: a CuInS(2) film with poor adherence having many crevices was formed when the Cu/In bilayer film was heated monotonously from room temperature to 520 °C in Ar within 25 min followed by sulfurization, whereas CuInS(2) films with good adherence were obtained when the Cu/In films were pretreated at 110 °C in Ar for 10-60 min just before increasing the temperature up to 520 °C for sulfurization. It was also clarified that the CuInS(2) film obtained without 110 °C pretreatment had pinholes inside the film, whereas the CuInS(2) films formed after 110 °C pretreatment showed no notable pinholes. Photoelectrochemical responses of these CuInS(2) films in an electrolyte solution containing Eu(III) indicated that the CuInS(2) films obtained after 110 °C pretreatment had higher external quantum efficiency (EQE) values than those of films obtained without 110 °C pretreatment, mainly due to better adherence of 110 °C pretreated CuInS(2) films to the Mo substrate than the CuInS(2) film obtained without 110 °C pretreatment. The performance of solar cells with an Al:ZnO/Zn(S,O)/CdS/CuInS(2)/Mo structure also depended on the structural characteristics of the CuInS(2) films, i.e., preliminary conversion efficiencies of ca. 5% were obtained for devices based on the CuInS(2) films obtained after 110 °C pretreatment, whereas the device prepared by the CuInS(2) film without 110 °C pretreatment showed the conversion efficiency less than 1.5%.

  11. Enhancing the photoelectrochemical water splitting characteristics of titanium and tungsten oxide based materials via doping and sensitization

    NASA Astrophysics Data System (ADS)

    Gakhar, Ruchi

    To better utilize solar energy for clean energy production, efforts are needed to overcome the natural diurnal variation and the diffuse nature of sunlight. Photoelectrochemical (PEC) hydrogen generation by water splitting is a promising approach to harvest solar energy. Hydrogen gas is a clean and high energy capacity fuel. However, the solar-to-hydrogen conversion efficiency is determined mainly by the properties of the materials employed as photoanodes. Improving the power-conversion efficiency of PEC water splitting requires the design of inexpensive and efficient photoanodes that have strong visible light absorption, fast charge separation, and lower charge recombination rate. In the present study, PEC characteristics of various semiconducting photoelectrodes such as TiO2, WO3 and CuWO4 were investigated. Due to the inherent wide gap, such metal oxides absorb only ultraviolet radiation. Since ultraviolet radiation only composes of 4% of the sun's spectrum, the wide band gap results in lower charge collection and efficiency. Thusto improve optical absorption and charge separation, it is necessary to modify the band gap with low band gap materials.The two approaches followed for modification of band gap are doping and sensitization. Here, TiO2 and WO3 based photoanodes were sensitized with ternary quatum dots, while doping was the primary method utilized to investigate the modification of the band gap of CuWO4. The first part of this dissertation reports the synthesis of ternary quantum dot - sensitized titania nanotube array photoelectrodes. Ternary quantum dots with varying band gaps and composition (MnCdSe, ZnCdSe and CdSSe) were tethered to the surface of TiO2 nanotubes using succcessive ionic layer adsorption and reaction (SILAR) technique. The stoichiometry of ternary quantum dots was estimated to beMn0.095Cd0.95Se, Zn0.16Cd0.84Se and CdS0.54Se0.46. The effect of varying number of sensitization cycles and annealing temperature on optical and

  12. An ultrasensitive photoelectrochemical nucleic acid biosensor

    PubMed Central

    Gao, Zhiqiang; Tansil, Natalia C.

    2005-01-01

    A simple and ultrasensitive procedure for non-labeling detection of nucleic acids is described in this study. It is based on the photoelectrochemical detection of target nucleic acids by forming a nucleic acid/photoreporter adduct layer on an ITO electrode. The target nucleic acids were hybridized with immobilized oligonucleotide capture probes on the ITO electrode. A subsequent binding of a photoreporter—a photoactive threading bis-intercalator consisting of two N,N′-bis(3-propyl-imidazole)-1,4,5,8-naphthalene diimides (PIND) linked by a Ru(bpy)22+ (bpy = 2,2′-bipyridine) complex (PIND–Ru–PIND)—allowed for photoelectrochemical detection of the target nucleic acids. The extremely low dissociation rate of the adduct and the highly reversible photoelectrochemical response under visible light illumination (490 nm) make it possible to conduct nucleic acid detection, with a sensitivity enhancement of four orders of magnitude over voltammetry. These results demonstrate for the first time the potential of photoelectrochemical biosensors for PCR-free ultrasensitive detection of nucleic acids. PMID:16061935

  13. Ratiometric fluorescence, electrochemiluminescence, and photoelectrochemical chemo/biosensing based on semiconductor quantum dots

    NASA Astrophysics Data System (ADS)

    Wu, Peng; Hou, Xiandeng; Xu, Jing-Juan; Chen, Hong-Yuan

    2016-04-01

    Ratiometric fluorescent sensors, which can provide built-in self-calibration for correction of a variety of analyte-independent factors, have attracted particular attention for analytical sensing and optical imaging with the potential to provide a precise and quantitative analysis. A wide variety of ratiometric sensing probes using small fluorescent molecules have been developed. Compared with organic dyes, exploiting semiconductor quantum dots (QDs) in ratiometric fluorescence sensing is even more intriguing, owing to their unique optical and photophysical properties that offer significant advantages over organic dyes. In this review, the main photophysical mechanism for generating dual-emission from QDs for ratiometry is discussed and categorized in detail. Typically, dual-emission can be obtained either with energy transfer from QDs to dyes or with independent dual fluorophores of QDs and dye/QDs. The recent discovery of intrinsic dual-emission from Mn-doped QDs offers new opportunities for ratiometric sensing. Particularly, the signal transduction of QDs is not restricted to fluorescence, and electrochemiluminescence and photoelectrochemistry from QDs are also promising for sensing, which can be made ratiometric for correction of interferences typically encountered in electrochemistry. All these unique photophysical properties of QDs lead to a new avenue of ratiometry, and the recent progress in this area is addressed and summarized here. Several interesting applications of QD-based ratiometry are presented for the determination of metal ions, temperature, and biomolecules, with specific emphasis on the design principles and photophysical mechanisms of these probes.

  14. Cadmium Sulphide-Reduced Graphene Oxide-Modified Photoelectrode-Based Photoelectrochemical Sensing Platform for Copper(II) Ions.

    PubMed

    Ibrahim, I; Lim, H N; Huang, N M; Pandikumar, A

    2016-01-01

    A photoelectrochemical (PEC) sensor with excellent sensitivity and detection toward copper (II) ions (Cu2+) was developed using a cadmium sulphide-reduced graphene oxide (CdS-rGO) nanocomposite on an indium tin oxide (ITO) surface, with triethanolamine (TEA) used as the sacrificial electron donor. The CdS nanoparticles were initially synthesized via the aerosol-assisted chemical vapor deposition (AACVD) method using cadmium acetate and thiourea as the precursors to Cd2+ and S2-, respectively. Graphene oxide (GO) was then dip-coated onto the CdS electrode and sintered under an argon gas flow (50 mL/min) for the reduction process. The nanostructured CdS was adhered securely to the ITO by a continuous network of rGO that also acted as an avenue to intensify the transfer of electrons from the conduction band of CdS. The photoelectrochemical results indicated that the ITO/CdS-rGO photoelectrode could facilitate broad UV-visible light absorption, which would lead to a higher and steady-state photocurrent response in the presence of TEA in 0.1 M KCl. The photocurrent decreased with an increase in the concentration of Cu2+ ions. The photoelectrode response for Cu2+ ion detection had a linear range of 0.5-120 μM, with a limit of detection (LoD) of 16 nM. The proposed PEC sensor displayed ultra-sensitivity and good selectivity toward Cu2+ ion detection.

  15. Plasmon enhanced photoelectrochemical sensing of mercury (II) ions in human serum based on Au@Ag nanorods modified TiO₂ nanosheets film.

    PubMed

    Zhang, Yong; Shoaib, Anwer; Li, Jiaojiao; Ji, Muwei; Liu, Jiajia; Xu, Meng; Tong, Bin; Zhang, Jiatao; Wei, Qin

    2016-05-15

    Taking advantages of the monodisperse TiO2 nanosheets (NSs) with high active crystal face exposure and the tunable localized surface plasmon resonance (LSPR) properties of Au@Ag nanorods (NRs), this study demonstrated that TiO2 NSs film with trace amount of Au@Ag NRs modification possess a strong enhancement of photocurrent response, which was remarkably inhibited with the addition of mercury (II) ions (Hg(2+)). Based on the selective decrease of photocurrent with the addition of Hg(2+), a simple photoelectrochemical (PEC) sensor has been assembled. The PEC sensor exhibits wide linear range (0.01-10nM), low detection limit (2.5 pM), satisfying selectivity, reproducibility and acceptable stability for Hg(2+) detection. The feasibility of this method for practical application in human serum has been evaluated and the result was satisfactory. This PEC sensing method would provide a potential application for Hg(2+) detection in clinical diagnosis.

  16. Higher-efficiency photoelectrochemical electrodes of titanium dioxide-based nanoarrays sensitized simultaneously with plasmonic silver nanoparticles and multiple metal sulfides photosensitizers

    NASA Astrophysics Data System (ADS)

    Guo, Keying; Liu, Zhifeng; Han, Jianhua; Zhang, Xueqi; Li, Yajun; Hong, Tiantian; Zhou, Cailou

    2015-07-01

    This paper describes a novel design of high-efficiency photoelectrochemical water splitting electrode, i.e., ordered TiO2 nanorod arrays (NRs) sensitized simultaneously with noble metal (Ag), binary metal sulfides (Ag2S) and ternary metal sulfides (Ag3CuS2) multiple photosensitizers for the first time. The TiO2/Ag/Ag2S/Ag3CuS2 NRs heterostructure is successfully synthesized through successive ion layer adsorption and reaction (SILAR) and a simple ion-exchange process based on ionic reaction mechanism. On the basis of an optimal quantity of Ag, Ag2S and Ag3CuS2 nanoparticles, such TiO2/Ag/Ag2S/Ag3CuS2 NRs exhibit a higher photoelectrochemical activity ever reported for TiO2-based nanoarrays in PEC water splitting, the photocurrent density is up to 9.82 mA cm-2 at 0.47 V versus Ag/AgCl, respectively. This novel architecture is able to increase electron collection efficiency and suppress carrier recombination via (i) a higher efficiency of light-harvesting through these multiple photosensitizers (Ag, Ag2S and Ag3CuS2); (ii) the efficient separation of photo-induced electrons and holes due to the direct electrical pathways; (iii) the surface plasmon resonance (SPR) effect of Ag nanoparticles, which enhances the efficient charge separation and high carrier mobility. This work is useful to explore feasible routes to further enhance the performance of oxide semiconductors for PEC water splitting to produce clean H2 energy.

  17. Cadmium Sulphide-Reduced Graphene Oxide-Modified Photoelectrode-Based Photoelectrochemical Sensing Platform for Copper(II) Ions

    PubMed Central

    Ibrahim, I; Lim, H. N; Huang, N. M; Pandikumar, A

    2016-01-01

    A photoelectrochemical (PEC) sensor with excellent sensitivity and detection toward copper (II) ions (Cu2+) was developed using a cadmium sulphide-reduced graphene oxide (CdS-rGO) nanocomposite on an indium tin oxide (ITO) surface, with triethanolamine (TEA) used as the sacrificial electron donor. The CdS nanoparticles were initially synthesized via the aerosol-assisted chemical vapor deposition (AACVD) method using cadmium acetate and thiourea as the precursors to Cd2+ and S2-, respectively. Graphene oxide (GO) was then dip-coated onto the CdS electrode and sintered under an argon gas flow (50 mL/min) for the reduction process. The nanostructured CdS was adhered securely to the ITO by a continuous network of rGO that also acted as an avenue to intensify the transfer of electrons from the conduction band of CdS. The photoelectrochemical results indicated that the ITO/CdS-rGO photoelectrode could facilitate broad UV-visible light absorption, which would lead to a higher and steady-state photocurrent response in the presence of TEA in 0.1 M KCl. The photocurrent decreased with an increase in the concentration of Cu2+ ions. The photoelectrode response for Cu2+ ion detection had a linear range of 0.5–120 μM, with a limit of detection (LoD) of 16 nM. The proposed PEC sensor displayed ultra-sensitivity and good selectivity toward Cu2+ ion detection. PMID:27176635

  18. Determination of photo conversion efficiency of nanotubular titanium oxide photo-electrochemical cell for solar hydrogen generation

    NASA Astrophysics Data System (ADS)

    Raja, K. S.; Mahajan, V. K.; Misra, M.

    Anodized and annealed titanium oxide nanotubes show enhanced photo activity and can be used as photo anodes for water electrolysis in hydrogen generation. Application of an external potential to the photo anode is required for enhancement of the photocurrent. This additional electrical energy input complicates the photo conversion efficiency calculation. In this investigation, the photo-electrochemical behavior of anodized titanium oxide nanotubular arrays have been characterized in various electrolytes. Increase in the applied potential increased the photocurrent under illumination with visible light. A simple experimental method for calculating the photo conversion efficiency has been proposed. According to this method, the potential difference between the photo anode and cathode is measured with and without light illumination. The product of the photocurrent and the increase in potential due to light irradiation is considered as the net power output. The photocurrent and the conversion efficiency increased with increase in the pH of the electrolyte. TiO 2 nanotubular arrays annealed at 350 °C for 6 h in nitrogen atmosphere showed a maximum photo conversion efficiency of ∼4% in 1 M KOH electrolyte and ∼3% in 3.5 wt.% sodium chloride solution. The results indicate that nanotubular TiO 2 can be potentially used for the photo electrolysis of seawater to generate hydrogen.

  19. Wavelength-resolved simultaneous photoelectrochemical bifunctional sensor on single interface: A newly in vitro approach for multiplexed DNA monitoring in cancer cells.

    PubMed

    Zheng, Yingning; Liang, Wenbin; Yuan, Yali; Xiong, Chengyi; Xie, Shunbi; Wang, Haijun; Chai, Yaqin; Yuan, Ruo

    2016-07-15

    Currently, the photoelectrochemical (PEC) strategies can just achieve single analyte detection on a single interface with limited detection efficiency. It is highly valuable but full of challenge to develop a PEC biosensor for multiple analytes evaluation on a single interface. For this point, the wavelength-selective photoactive materials, which could generate separated photocurrents under excitation lights with certain wavelengths, were mainly important to overcome this challenge. Herein, these wavelength-selective photoactive materials were successfully synthesized and served as signal indicators to construct a novel PEC biosensor for multiple analytes evaluation on a single interface for the first time. Moreover, an enzyme-assisted target recycling amplification strategy was introduced for ultrasensitive monitoring. As a result, the proposed PEC biosensor showed excellent analytical performance for both oral cancer (ORVOA 1) gene and p53 gene down to attomolar level. In addition, the fabricated PEC biosensor was employed to evaluate ORVOA 1 gene and p53 gene in Hela cells. This assay has laid the foundation for fabrication of simple, ultrasensitive and economical PEC diagnostic devices to detect multiple analytes in cells, which paved a new avenue for early diagnosis of cancer with higher efficiency and accuracy.

  20. Si microwire array photoelectrochemical cells: Stabilized and improved performances with surface modification of Pt nanoparticles and TiO2 ultrathin film

    NASA Astrophysics Data System (ADS)

    Yan, Jimu; Wu, Shaolong; Zhai, Xiongfei; Gao, Xiang; Li, Xiaofeng

    2017-02-01

    To achieve the semiconductor photoelectrochemical (PEC) cells targeting the industry applications with commercial competitiveness, high efficiency and good stability are requisite properties. To improve the PEC response, the vertically-aligned silicon microwire arrays (SiMWAs) modified with isolated Pt nanoparticles (PtNPs) and conformal TiO2 ultrathin film (TiO2/Pt@SiMWAs) are fabricated and examined in this study. The modified system shows the significantly enhanced responses and operation stability, that is, an enhancement of ∼30.0% in saturation photocurrent density (Jsat), a cathodic shift of ∼0.85 V (relative to the bare SiMWAs) in applied potential for Jsat, and an attenuation ratio of the photocurrent <1.5% during 1800-sec-continuous operation in an aqueous electrolyte. The underlying mechanisms are attributed to: (1) PtNPs concentrate the incident photons, promote the photo-carrier separation, and catalyze the chemical reaction at the photoelectrode-electrolyte interfaces; (2) conformal TiO2 ultrathin film protects the SiMWAs from photo-oxidation/corrosion as well as suppresses the surface recombination. Our results indicate a feasible route for the practical applications of oxidizable and corrodible semiconductor micro-/nanostructures in the fields of PEC solar cells, water splitting, photodegradation, and so on.

  1. Semiconducting materials for photoelectrochemical energy conversion

    NASA Astrophysics Data System (ADS)

    Sivula, Kevin; van de Krol, Roel

    2016-02-01

    To achieve a sustainable society with an energy mix primarily based on solar energy, we need methods of storing energy from sunlight as chemical fuels. Photoelectrochemical (PEC) devices offer the promise of solar fuel production through artificial photosynthesis. Although the idea of a carbon-neutral energy economy powered by such ‘artificial leaves’ is intriguing, viable PEC energy conversion on a global scale requires the development of devices that are highly efficient, stable and simple in design. In this Review, recently developed semiconductor materials for the direct conversion of light into fuels are scrutinized with respect to their atomic constitution, electronic structure and potential for practical performance as photoelectrodes in PEC cells. The processes of light absorption, charge separation and transport, and suitable energetics for energy conversion in PEC devices are emphasized. Both the advantageous and unfavourable aspects of multinary oxides, oxynitrides, chalcogenides, classic semiconductors and carbon-based semiconductors are critically considered on the basis of their experimentally demonstrated performance and predicted properties.

  2. Correlation of electrical and physical properties of photoanode with hydrogen evolution in enzymatic photo-electrochemical cell

    NASA Astrophysics Data System (ADS)

    Bae, Sanghyun; Kang, Junwon; Shim, Eunjung; Yoon, Jaekyung; Joo, Hyunku

    2008-05-01

    In this study, the electrical and physical properties, including the current density, open-circuit voltage, morphology and crystalline structure, of an anodized TiO2 electrode on a titanium foil are correlated with the hydrogen production rate in an enzymatic photo-electrochemical system. The effect of light intensity at ca. 74 and ca. 146 mW cm-2 on the properties is also examined. Anodizing (20 V; bath temperature 5 °C; anodizing time 45 min) and subsequent annealing (350-850 °C for 5 h) of the Ti foils in an O2 atmosphere led to the formation of a tube-shaped, or a compact layered, TiO2 film on the Ti substrate depending on the annealing temperature. The annealing temperature has a similar effect on the properties of the sample and the hydrogen evolution rate. The generated electrical value, the chronoamperometry (CA), is +13 to -229 and +13 to -247 μA for light intensities of ca. 74 and ca. 146 mW cm-2, while the corresponding open-circuit voltage (OCV) is in the range of -41 to -687 and -144 to 738 mV, respectively. In the absence of light (dark), the CA is 13-29 μA and the OCV is +258 to -126 mW cm-2. The trend in the electrical properties for the different samples is well matched with the rate of hydrogen evolution. The samples with higher activities (450, 550, and 650 °C) have similar X-ray diffraction (XRD) patterns, which clearly indicates that the samples showing the highest evolution rate are composed of both anatase and rutile, while those showing a lower evolution rate are made of either anatase or rutile. Increasing the intensity of the irradiated light causes a remarkable enhancement in the rate of hydrogen production from 71 to 153 μmol h-1 cm-2.

  3. Comparison of silatrane, phosphonic acid, and carboxylic acid functional groups for attachment of porphyrin sensitizers to TiO2 in photoelectrochemical cells.

    PubMed

    Brennan, Bradley J; Llansola Portolés, Manuel J; Liddell, Paul A; Moore, Thomas A; Moore, Ana L; Gust, Devens

    2013-10-21

    A tetra-arylporphyrin dye was functionalized with three different anchoring groups used to attach molecules to metal oxide surfaces. The physical, photophysical and electrochemical properties of the derivatized porphyrins were studied, and the dyes were then linked to mesoporous TiO2. The anchoring groups were β-vinyl groups bearing either a carboxylate, a phosphonate or a siloxy moiety. The siloxy linkages were made by treatment of the metal oxide with a silatrane derivative of the porphyrin. The surface binding and lability of the anchored molecules were studied, and dye performance was compared in a dye-sensitized solar cell (DSSC). Transient absorption spectroscopy was used to study charge recombination processes. At comparable surface concentration, the porphyrin showed comparable performance in the DSSC, regardless of the linker. However, the total surface coverage achievable with the carboxylate was about twice that obtainable with the other two linkers, and this led to higher current densities for the carboxylate DSSC. On the other hand, the carboxylate-linked dyes were readily leached from the metal oxide surface under alkaline conditions. The phosphonates were considerably less labile, and the siloxy-linked porphyrins were most resistant to leaching from the surface. The use of silatrane proved to be a practical and convenient way to introduce the siloxy linkages, which can confer greatly increased stability on dye-sensitized electrodes with photoelectrochemical performance comparable to that of the other linkers.

  4. A Photoelectrochemical Solar Cell Consisting of a Cadmium Sulfide Photoanode and a Ruthenium-2,2'-Bipyridine Redox Shuttle in a Non-aqueous Electrolyte.

    PubMed

    Kageshima, Yosuke; Kumagai, Hiromu; Minegishi, Tsutomu; Kubota, Jun; Domen, Kazunari

    2015-06-26

    A photoelectrochemical (PEC) cell consisting of an n-type CdS single-crystal electrode and a Pt counter electrode with the ruthenium-2,2'-bipyridine complex [Ru(bpy)3](2+/3+) as the redox shuttle in a non-aqueous electrolyte was studied to obtain a higher open-circuit voltage (V(OC)) than the onset voltage for water splitting. A V(OC) of 1.48 V and a short-circuit current (I(SC)) of 3.88 mA cm(-2) were obtained under irradiation by a 300 W Xe lamp with 420-800 nm visible light. This relatively high voltage was presumably due to the difference between the Fermi level of photo-irradiated n-type CdS and the redox potential of the Ru complex at the Pt electrode. The smooth redox reaction of the Ru complex with one-electron transfer was thought to have contributed to the high V(OC) and I(SC). The obtained V(OC) was more than the onset voltage of water electrolysis for hydrogen and oxygen generation, suggesting prospects for application in water electrolysis.

  5. Control of dark current in photoelectrochemical (TiO2/I--I3-)) and dye-sensitized solar cells.

    PubMed

    Ito, Seigo; Liska, Paul; Comte, Pascal; Charvet, Raphaël; Péchy, Peter; Bach, Udo; Schmidt-Mende, Lukas; Zakeeruddin, Shaik Mohammed; Kay, Andreas; Nazeeruddin, Mohammad K; Grätzel, Michael

    2005-09-14

    The ruthenium complex bis-tetrabutylammonium cis-dithiocyanato-N,N'-bis-2,2'-bipyridine-4-carboxylic acid, 4'-carboxylate ruthenium(II), N-719, was found to block the dark current of dye sensitized solar cells (DSC), based on mesoporous TiO2 films deposited on a F-doped tin oxide electrode and the effect was compared to surface treatment by TiCl4 and the introduction of a compact TiO2 blocking layer.

  6. Matrix-assisted laser desorption/ionization mass spectrometric analysis of poly(3,4-ethylenedioxythiophene) in solid-state dye-sensitized solar cells: comparison of in situ photoelectrochemical polymerization in aqueous micellar and organic media.

    PubMed

    Zhang, Jinbao; Ellis, Hanna; Yang, Lei; Johansson, Erik M J; Boschloo, Gerrit; Vlachopoulos, Nick; Hagfeldt, Anders; Bergquist, Jonas; Shevchenko, Denys

    2015-04-07

    Solid-state dye-sensitized solar cells (sDSCs) are devoid of such issues as electrolyte evaporation or leakage and electrode corrosion, which are typical for traditional liquid electrolyte-based DSCs. Poly(3,4-ethylenedioxythiophene) (PEDOT) is one of the most popular and efficient p-type conducting polymers that are used in sDSCs as a solid-state hole-transporting material. The most convenient way to deposit this insoluble polymer into the dye-sensitized mesoporous working electrode is in situ photoelectrochemical polymerization. Apparently, the structure and the physicochemical properties of the generated conducting polymer, which determine the photovoltaic performance of the corresponding solar cell, can be significantly affected by the preparation conditions. Therefore, a simple and fast analytical method that can reveal information on polymer chain length, possible chemical modifications, and impurities is strongly required for the rapid development of efficient solar energy-converting devices. In this contribution, we applied matrix-assisted laser desorption/ionization mass spectrometry (MALDI MS) for the analysis of PEDOT directly on sDSCs. It was found that the PEDOT generated in aqueous micellar medium possesses relatively shorter polymeric chains than the PEDOT deposited from an organic medium. Furthermore, the micellar electrolyte promotes a transformation of one of the thiophene terminal units to thiophenone. The introduction of a carbonyl group into the PEDOT molecule impedes the growth of the polymer chain and reduces the conductivity of the final polymer film. Both the simplicity of sample preparation (only application of the organic matrix onto the solar cell is needed) and the rapidity of analysis hold the promise of making MALDI MS an essential tool for the physicochemical characterization of conducting polymer-based sDSCs.

  7. Electrochemical and photoelectrochemical oxidation of 5-hydroxymethylfurfural to 2,5-furandicarboxylic acid and 2,5-diformylfuran

    DOEpatents

    Choi, Kyoung-Shin; Cha, Hyun Gil

    2017-03-21

    Electrochemical and photoelectrochemical cells for the oxidation of 5-hydroxymethylfurfural to 2,5-furandicarboxylic acid and/or 2,5-diformylfuran are provided. Also provided are methods of using the cells to carry out the electrochemical and photoelectrochemical oxidation of 5-hydroxymethylfurfural to 2,5-furandicarboxylic acid and/or 2,5-diformylfuran.

  8. TiO 2 nano-porous photoelectrochemical cells (PECs) sensitized with mixed cationic/anionic dye systems: Role of the second cationic fluorescent dye on the photocurrent enhancement

    NASA Astrophysics Data System (ADS)

    Jayaweera, P. M.; Rajapaksha, R. M. S. P.; Tennakone, K.

    2005-08-01

    Bromopyrogallol red (BPR), an anionic dye material was used in nano-porous photoelectrochemical cells as the sensitizer in conjunction with a fluorescent cationic dye, rhodamineB (RhB) and acridine orange (AO). The overlap between absorption and emission spectra of BPR/RhB and the formation of a strong associated complex influences the photoelectron transfer rate to be enhanced and to produce enhanced photovoltaic properties. Fluorescence quenching studies indicate that photoexcited cationic dye materials deactivate efficiently by BPR following different mechanisms. FTIR and rR spectroscopic evidences suggest that the electrostatic interaction of fluorescent cationic dye takes place from the -SO3- group of the BPR molecule.

  9. Ag nanoclusters could efficiently quench the photoresponse of CdS quantum dots for novel energy transfer-based photoelectrochemical bioanalysis.

    PubMed

    Zhang, Ling; Sun, Yue; Liang, Yan-Yu; He, Jian-Ping; Zhao, Wei-Wei; Xu, Jing-Juan; Chen, Hong-Yuan

    2016-11-15

    Herein the influence of ultrasmall Ag nanoclusters (Ag NCs) against CdS quantum dots (QDs) in a photoelectrochemical (PEC) nanosystem was exploited for the first time, based on which a novel PEC bioanalysis was successfully developed via the efficient quenching effect of Ag NCs against the CdS QDs. In a model system, DNA assay was achieved by using molecular beacon (MB) probes anchored on a CdS QDs modified electrode, and the MB probes contain two segments that can hybridize with both target DNA sequence and the label of DNA encapsulated Ag NCs. After the MB probe was unfolded by the target DNA sequence, the labels of oligonucleotide encapsulated Ag NCs would be brought in close proximity to the CdS QDs electrode surface, and efficient photocurrent quenching of QDs could be resulted from an energy transfer process that originated from NCs. Thus, by monitoring the attenuation in the photocurrent signal, an elegant and sensitive PEC DNA bioanalysis could be accomplished. The developed biosensor displayed a linear range from 1.0pM to 10nM and the detection limit was experimentally found to be of 0.3pM. This work presents a feasible signaling principle that could act as a common basis for general PEC bioanalysis development.

  10. Photoelectrochemical Properties of Graphene and Its Derivatives

    PubMed Central

    Adán-Más, Alberto; Wei, Di

    2013-01-01

    Graphene and its derivatives combine a numerous range of supreme properties that can be useful in many applications. The purpose of this review is to analyse the photoelectrochemical properties of pristine graphene, graphene oxide (GO) and reduced graphene oxide (rGO) and their impact on semiconductor catalysts/quantum dots. The mechanism that this group of materials follows to improve their performance will be cleared by explaining how those properties can be exploited in several applications such as photo-catalysts (degradation of pollutants) and photovoltaics (solar cells). PMID:28348339

  11. Hybrid heterojunction and photoelectrochemistry solar cell based on silicon nanowires and double-walled carbon nanotubes.

    PubMed

    Shu, Qinke; Wei, Jinquan; Wang, Kunlin; Zhu, Hongwei; Li, Zhen; Jia, Yi; Gui, Xuchun; Guo, Ning; Li, Xinming; Ma, Chaoran; Wu, Dehai

    2009-12-01

    A hybrid solar cell model composed of a heterojunction cell and a photoelectrochemical (PEC) cell has been proposed and characterized. In the hybrid cell, a thin film of double-walled carbon nanotubes forms a heterojunction with the silicon nanowire (SiNW) array and also functions as the transparent counter electrode of the PEC cell. The cell performance can be readily tuned by controlling the SiNW density. Under AM 1.5G illumination, a power conversion efficiency of 1.29%, higher than those reported for SiNW array-based PEC cells, has been obtained.

  12. A generalized in situ electrodeposition of Zn doped CdS-based photoelectrochemical strategy for the detection of two metal ions on the same sensing platform.

    PubMed

    Zhang, Yong; Ma, Hongmin; Wu, Dan; Li, Rongxia; Wang, Xueping; Wang, Yaoguang; Zhu, Wenjuan; Wei, Qin; Du, Bin

    2016-03-15

    An efficient strategy for the sensitive detection of Cd(2+) and Cu(2+) on the same sensing platform was first developed based on the photocurrents generated from the electrodeposited Zn doped CdS (CdZnS) film. The enhancement of the photocurrents, which was directly obtained from the in situ electrodeposited CdZnS on ITO with the gradual addition of Cd(2+), was used an indicator for the content of Cd(2+) with theoretical and technical simplicity. Moreover, the electrodeposited CdZnS was further applied to sensing of Cu(2+) based on the interaction between Cu(2+) and S(2-) by immersing the hetero-structural film electrode into a Cu(2+)-containing sample for an appropriate time, leading to decrease the photocurrent of CdZnS. The decrease extent of photocurrent was depended on the concentration of Cu(2+) in the sample solution. Due to the sensitivity of the photoelectrochemical (PEC) sensor was enhanced obviously through the doping of Zn, the present electrodeposited PEC method demonstrated acceptable linear range of 10(-9)-10(-2)M and 10(-8)-10(-4)M, with low detection limit down to 0.35 nM and 3 nM for Cd(2+) and Cu(2+) respectively, which were lower than the Environmental Protection Agency (EPA) and World Health Organization (WHO) guidelines. The proposed CdZnS-based PEC strategy achieved two metal ions detection on the same sensing platform, which had positive and significant effect on solving the common problems, such as time-consuming, high cost, complex operation and high detection limit in the detection of metal ions. In addition, the proposed PEC device was further successfully applied to an assay of Cd(2+) and Cu(2+) in water sample.

  13. Photoelectrochemical aptasensor for the sensitive and selective detection of kanamycin based on Au nanoparticle functionalized self-doped TiO2 nanotube arrays.

    PubMed

    Xin, Yanmei; Li, Zhenzhen; Zhang, Zhonghai

    2015-11-04

    In this communication, a new photoelectrochemical aptasensor with Au nanoparticle functionalized self-doped TiO2 nanotube arrays (Au/SD-TiO2 NTs) as the core sensing unit and aptamers as the recognition unit was set up to accomplish the sensitive and selective detection of kanamycin with the lowest detection limit of 0.1 nM.

  14. Plasmonic AuNP/g-C3N4 Nanohybrid-based Photoelectrochemical Sensing Platform for Ultrasensitive Monitoring of Polynucleotide Kinase Activity Accompanying DNAzyme-Catalyzed Precipitation Amplification.

    PubMed

    Zhuang, Junyang; Lai, Wenqiang; Xu, Mingdi; Zhou, Qian; Tang, Dianping

    2015-04-22

    A convenient and feasible photoelectrochemical (PEC) sensing platform based on gold nanoparticles-decorated g-C3N4 nanosheets (AuNP/g-C3N4) was designed for highly sensitive monitoring of T4 polynucleotide kinase (PNK) activity, using DNAzyme-mediated catalytic precipitation amplification. To realize our design, the AuNP/g-C3N4 nanohybrid was initially synthesized through in situ reduction of Au(III) on the g-C3N4 nanosheets, which was utilized for the immobilization of hairpin DNA1 (HP1) on the sensing interface. Thereafter, a target-induced isothermal amplification was automatically carried out on hairpin DNA2 (HP2) in the solution phase through PNK-catalyzed 5'-phosphorylation accompanying formation of numerous trigger DNA fragments, which could induce generation of hemin/G-quadruplex-based DNAzyme on hairpin DNA1. Subsequently, the DNAzyme could catalyze the 4-chloro-1-naphthol (4-CN) oxidation to produce an insoluble precipitation on the AuNP/g-C3N4 surface, thereby resulting in the local alternation of the photocurrent. Experimental results revealed that introduction of AuNP on the g-C3N4 could cause a ∼100% increase in the photocurrent because of surface plasmon resonance-enhanced light harvesting and separation of photogenerated e-/h+ pairs. Under the optimal conditions, the percentage of photocurrent decrement (ΔI/I0, relative to background signal) increased with the increasing PNK activity in a dynamic working range from 2 to 100 mU mL(-1) with a low detection limit (LOD) of 1.0 mU mL(-1). The inhibition effect of adenosine diphosphate also received a good performance in PNK inhibitor screening research, thereby providing a useful scheme for practical use in quantitative PNK activity assay for life science and biological research.

  15. Gold nanrods plasmon-enhanced photoelectrochemical aptasensing based on hematite/N-doped graphene films for ultrasensitive analysis of 17β-estradiol.

    PubMed

    Du, Xiaojiao; Dai, Liming; Jiang, Ding; Li, Henan; Hao, Nan; You, Tianyan; Mao, Hanping; Wang, Kun

    2017-05-15

    It remains a vital task to establish ultrasensitive sensing interfaces for detection of target analytes to meet the demands of modern analysis. Herein, a highly sensitive turn-on photoelectrochemical (PEC) platform for trace 17β-estradiol (E2) assay was developed based on Au nanrods (AuNRs) with surface plasmon resonance (SPR) properties induced signal amplification. Specifically, a ternary hybrid was prepared by integrating hematite (α-Fe2O3) nanocrystals and N-doped graphene (NG) with AuNRs, which further served as highly efficient photoactive species. Subsequently, a PEC sensing platform was fabricated based on the specific binding of E2 and its aptamer. On such a sensor, the capture of E2 molecules by aptamers led to increased photocurrent. This was attributed to that the specific recognition reaction between E2 and aptamer resulted in the conformational change of the aptamers and complete dissociation of some aptamers on the PEC sensing interface. It can be confirmed by the electrochemical impedance spectroscopy (EIS) results. This process decreased the steric hindrances between the electrode surface and solution and thus increased the photocurrent response. Under the optimal conditions, the as-prepared PEC aptasensor exhibited superb analytical performances for detection of E2 in the range from 1×10(-15)M to 1×10(-9)M with a detection limit of 3.3×10(-16)M. The aptasensor manifested outstanding selectivity towards E2 when other endocrine disrupting compounds with similar structure coexisted. Furthermore, the aptasensor was successfully applied for the determination of E2 in milk powder. The present strategy provides a potential way to boost the activity of photoactive materials and improve the sensitivity of PEC biosensor.

  16. Production of electricity and hydrogen by photocatalytic degradation of organic wastes in a photoelectrochemical cell: the concept of the Photofuelcell: a review of a re-emerging research field.

    PubMed

    Lianos, Panagiotis

    2011-01-30

    The present review aims to give to a researcher who has no experience with Photofuelcells all necessary basic knowledge to join the field without much trouble and to give to an experienced researcher a handy manual of reference. The author has dealt with the principal matters related with the design of a photoelectrochemical cell and the factors that affect efficient production of electricity by photocatalytic degradation of (principally) organic and (secondarily) inorganic waste materials. A large portion of the paper is devoted to the review of materials used for making a photoanode since most of the accomplished research is on this exact matter. The paper also briefly reviews the materials used to make the rest of the components of the cell as well as the models of cell efficiency and photodegradation procedures during cell operation.

  17. Photoelectrochemical molecular comb

    DOEpatents

    Thundat, Thomas G [Knoxville, TN; Ferrell, Thomas L [Knoxville, TN; Brown, Gilbert M [Knoxville, TN

    2012-02-07

    A method, system, and apparatus are provided for separating molecules, such as biomolecules. The method, system, and apparatus utilize an electrochemical cell having at least two electrodes, one electrode comprising a photo-sensitive material capable of generating a photopotential. Molecules are moved through an electrolyte medium between the at least two electrodes based upon localized photopotentials.

  18. Photoelectrochemical molecular comb

    DOEpatents

    Thundat, Thomas G.; Ferrell, Thomas L.; Brown; Gilbert M.

    2007-05-01

    A method, system, and apparatus are provided for separating molecules, such as biomolecules. The method, system, and apparatus utilize an electrochemical cell having at least to electrodes, one electrode comprising a photo-sensitive material capable of generating a photopotential. Molecules are moved through an electrolyte medium between the at least two electrodes based upon localized photopotentials.

  19. Polymer blends for use in photoelectrochemical cells for conversion of solar energy to electricity and methods for manufacturing such blends

    DOEpatents

    Skotheim, T.

    A polymer blend is disclosed of a highly conductive polymer and a solid polymer electrolyte that is designed to achieve better charge transfer across the conductive film/polymer electrolyte interface of the electrochemical photovoltaic cell. The highly conductive polymer is preferably polypyrrole or poly-N-p-nitrophenylpyrrole and the solid polymer electrolyte is preferably polyethylene oxide or polypropylene oxide.

  20. Polymer blends for use in photoelectrochemical cells for conversion of solar energy to electricity and methods for manufacturing such blends

    DOEpatents

    Skotheim, Terje

    1984-01-01

    There is disclosed a polymer blend of a highly conductive polymer and a solid polymer electrolyte that is designed to achieve better charge transfer across the conductive film/polymer electrolyte interface of the electrochemical photovoltaic cell. The highly conductive polymer is preferably polypyrrole or poly-N-p-nitrophenylpyrrole and the solid polymer electrolyte is preferably polyethylene oxide or polypropylene oxide.

  1. Photoelectrochemical fabrication of spectroscopic diffraction gratings

    NASA Technical Reports Server (NTRS)

    Rauh, R. David; Carrabba, Michael M.; Nguyen, Nguyet M.

    1986-01-01

    Photoelectrochemical etching was demonstrated as a means of fabricating a variety of periodic structures in semiconductors. The semiconductor is used as an electrode in an electrochemical cell, and is in contact with a liquid electrolyte. When the crystal is held at a positive voltage and illuminated, etching occurs in only the illuminated regions to a depth proportional to the illumination intensity and exposure time. In Phase 1, it was determined that diffraction gratings could be produced in gallium arsenide crystals by this method, using either a scanned focused laser beam or by uniform illumination of a ruling mask defined in metal or photoresist on the crystal surface. The latter approach was determined to produce V-grooves if the mask is oriented along certain crystallographic directions. These V-grooves were produced with an exceedingly smooth crystal morphology due to the highly controllable nature of the process and the mild electrolytes involved. The results form the basis for photoelectrochemical fabrication of deep, low pitch Eschelle gratings for use in high orders in NASA spectrographic instrumentation such as the Space Telescope Imaging Spectrograph.

  2. Photo-electrochemical and physical characterizations of a new single crystal POM-based material. Application in photocatalysis

    NASA Astrophysics Data System (ADS)

    Meziani, D.; Abdmeziem, K.; Bouacida, S.; Trari, M.

    2016-12-01

    A new inorganic-organic hybrid material [(H2pip)3][α-PW12O40]2·4H2O, prepared by hydrothermal method, was structurally characterized by single-crystal X-ray diffraction. The compound based on a Keggin-type polyoxotungstate and piperazine (pip) displays a hybrid framework built from two (α-Keggin)3- polyoxoanions and three (H2pip)2+ hydrogen-bonded fragments, forming 3-D supramolecular architecture. The diffuse reflectance spectrum shows two optical transitions directly (3.27 eV) and indirectly (3.12 eV) allowed. The electrical conductivity follows an exponential law, indicating a semiconducting comportment with activation energy of 14 meV. The Mott-Schottky characteristic, plotted in Na2SO4 (0.5 M) solution indicates n-type conduction with a flat band potential of -0.084 VSCE and electrons density of 4.24 × 1018 cm-3. As application, the photo-degradation of methylene blue (MB) upon UV irradiation was successfully achieved by OH• radicals. The improved activity is attributed to the potentials closeness of the valence and conduction bands with the radical levels.

  3. Unassisted photoelectrochemical water splitting exceeding 7% solar-to-hydrogen conversion efficiency using photon recycling.

    PubMed

    Shi, Xinjian; Jeong, Hokyeong; Oh, Seung Jae; Ma, Ming; Zhang, Kan; Kwon, Jeong; Choi, In Taek; Choi, Il Yong; Kim, Hwan Kyu; Kim, Jong Kyu; Park, Jong Hyeok

    2016-06-21

    Various tandem cell configurations have been reported for highly efficient and spontaneous hydrogen production from photoelectrochemical solar water splitting. However, there is a contradiction between two main requirements of a front photoelectrode in a tandem cell configuration, namely, high transparency and high photocurrent density. Here we demonstrate a simple yet highly effective method to overcome this contradiction by incorporating a hybrid conductive distributed Bragg reflector on the back side of the transparent conducting substrate for the front photoelectrochemical electrode, which functions as both an optical filter and a conductive counter-electrode of the rear dye-sensitized solar cell. The hybrid conductive distributed Bragg reflectors were designed to be transparent to the long-wavelength part of the incident solar spectrum (λ>500 nm) for the rear solar cell, while reflecting the short-wavelength photons (λ<500 nm) which can then be absorbed by the front photoelectrochemical electrode for enhanced photocurrent generation.

  4. Limiting photocurrent analysis of a wide channel photoelectrochemical flow reactor

    NASA Astrophysics Data System (ADS)

    Davis, Jonathan T.; Esposito, Daniel V.

    2017-03-01

    The development of efficient and scalable photoelectrochemical (PEC) reactors is of great importance for the eventual commercialization of solar fuels technology. In this study, we systematically explore the influence of convective mass transport and light intensity on the performance of a 3D-printed PEC flow cell reactor based on a wide channel, parallel plate geometry. Using this design, the limiting current density generated from the hydrogen evolution reaction at a p-Si metal–insulator–semiconductor (MIS) photocathode was investigated under varied reactant concentration, fluid velocity, and light intensity. Additionally, a simple model is introduced to predict the range of operating conditions (reactant concentration, light intensity, fluid velocity) for which the photocurrent generated in a parallel plate PEC flow cell is limited by light absorption or mass transport. This model can serve as a useful guide for the design and operation of wide-channel PEC flow reactors. The results of this study have important implications for PEC reactors operating in electrolytes with dilute reactant concentrations and/or under high light intensities where high fluid velocities are required in order to avoid operation in the mass transport-limited regime.

  5. Ultrasensitive photoelectrochemical immunoassay for matrix metalloproteinase-2 detection based on CdS:Mn/CdTe cosensitized TiO2 nanotubes and signal amplification of SiO2@Ab2 conjugates.

    PubMed

    Fan, Gao-Chao; Han, Li; Zhu, Hua; Zhang, Jian-Rong; Zhu, Jun-Jie

    2014-12-16

    An ultrasensitive photoelectrochemical sandwich immunoassay was developed to detect matrix metalloproteinase-2 (MMP-2, antigen, Ag) based on CdS:Mn/CdTe cosensitized TiO2 nanotubes (TiO2-NTs) and signal amplification of SiO2@Ab2 conjugates. Specifically, the TiO2-NTs electrode was first deposited with CdS:Mn by successive ionic layer adsorption and reaction technique and then further coated with CdTe quantum dots (QDs) via the layer-by-layer method, forming TiO2-NTs/CdS:Mn/CdTe cosensitized structure, which was employed as a matrix to immobilize capture MMP-2 antibodies (Ab1); whereas, SiO2 nanoparticles were coated with signal MMP-2 antibodies (Ab2) to form SiO2@Ab2 conjugates, which were used as signal amplification elements via the specific antibody-antigen immunoreaction between Ag and Ab2. The ultrahigh sensitivity of this immunoassay derived from the two major reasons as below. First, the TiO2-NTs/CdS:Mn/CdTe cosensitized structure could adequately absorb the light energy, dramatically promote electron transfer, and effectively inhibit the electron-hole recombination, resulting in significantly enhanced photocurrent intensity of the sensing electrode. However, in the presence of target Ag, the immobilized SiO2@Ab2 conjugates could evidently increase the steric hindrance of the sensing electrode and effectively depress the electron transfer, leading to obviously decreased photocurrent intensity. Accordingly, the well-designed photoelectrochemical immunoassay exhibited a low detection limit of 3.6 fg/mL and a wide linear range from 10 fg/mL to 500 pg/mL for target Ag detection. Meanwhile, it also presented good reproducibility, specificity, and stability and might open a new promising platform for the detection of other important biomarkers.

  6. Photoelectrochemical conversion of toluene to methylcyclohexane as an organic hydride by Cu2ZnSnS4-based photoelectrode assemblies.

    PubMed

    Wang, Peng; Minegishi, Tsutomu; Ma, Guijun; Takanabe, Kazuhiro; Satou, Yasushi; Maekawa, Shunsuke; Kobori, Yoshihiro; Kubota, Jun; Domen, Kazunari

    2012-02-08

    Direct photoelectrochemical conversion of toluene (TL) to methylcyclohexane (MC) with water has been examined as an organic hydride conversion using light irradiation. The production of MC from TL was observed on Pt/CdS/Cu(2)ZnSnS(4)/Mo photoelectrodes with anion-type ionomer membrane assemblies. A cathodic photocurrent was observed below 0.7 V vs RHE (V(RHE)) in 0.1 M Na(2)SO(4)/NaOH (pH 9.5) aqueous solution, and an apparent photocurrent density of 0.5 mA cm(-2) was obtained at 0 V(RHE) under the irradiation of a 300 W Xe lamp with a 420 nm cutoff filter. The yield of MC was measured by gas chromatography, and an 88% faradaic efficiency was estimated. This study suggests the possibility of direct energy conversion from solar energy to MC as an energy carrier of organic hydrides.

  7. Sensitizers for Aqueous-Based Solar Cells.

    PubMed

    Li, Chun-Ting; Lin, Ryan Yeh-Yung; Lin, Jiann T

    2017-03-02

    Aqueous dye-sensitized solar cells (DSSCs) are attractive due to their sustainability, the use of water as a safe solvent for the redox mediators, and their possible applications in photoelectrochemical water splitting. However, the higher tendency of dye leaching by water and the lower wettability of dye molecules are two major obstacles that need to be tackled for future applications of aqueous DSSCs. Sensitizers designed for aqueous DSSCs are discussed based on their functions, such as modification of the molecular skeleton and the anchoring group for better stability against dye leaching by water, and the incorporation of hydrophilic entities into the dye molecule or the addition of a surfactant to the system to increase the wettability of the dye for more facile dye regeneration. Surface treatment of the photoanode to deter dye leaching or improve the wettability of the dye molecule is also discussed. Redox mediators designed for aqueous DSSCs are also discussed. The review also includes quantum-dot-sensitized solar cells, with a focus on improvements in QD loading and suppression of interfacial charge recombination at the photoanode.

  8. Photoelectrochemical Immunosensor for Detection of Carcinoembryonic Antigen Based on 2D TiO2 Nanosheets and Carboxylated Graphitic Carbon Nitride

    PubMed Central

    Wang, Huan; Wang, Yaoguang; Zhang, Yong; Wang, Qi; Ren, Xiang; Wu, Dan; Wei, Qin

    2016-01-01

    Carcinoembryonic antigen (CEA) was used as the model, an ultrasensitive label-free photoelectrochemical immunosensor was developed using 2D TiO2 nanosheets and carboxylated graphitic carbon nitride (g-C3N4) as photoactive materials and ascorbic acid as an efficient electron donor. 2D TiO2 nanosheets was sythsized by surfactant self-assembly method and proved to have higher photoelectrochemical signals than TiO2 nanoparticles. Firstly, carboxylated g-C3N4 could be attached to 2D TiO2 nanosheets through the bond formed between carboxyl group of carboxylated g-C3N4 and TiO2. And the photocurrent of g-C3N4/TiO2 drastically enhances compared to carboxylated g-C3N4 and TiO2. Then, antibody of CEA was bonded to TiO2 through the dentate bond formed between carboxyl group of anti-CEA and TiO2, leading to the decrease of the photocurrents. As proven by PEC experiments and electrochemical impedance spectroscopy (EIS) analysis, the fabrication process of the immunosensor is successful. Under the optimal conditions, the intensity decreased linearly with CEA concentration in the range of 0.01~10 ng/mL. The detection limit is 2.1 pg/mL. The work provides an effective method for the detection of tumor markers and can be extended for the application in food safety and environmental monitoring analysis. PMID:27263659

  9. Novel catalysts and photoelectrochemical system for solar fuel production

    NASA Astrophysics Data System (ADS)

    Zhang, Yan

    Solar fuel production from abundant raw chemicals such as CO2 and water is highly desired as a clean renewable energy solution for the future. Developing photoelectrochemical cells is viewed as a promising approach to realize this energy conversion and storage process. Efficient and robust oxygen evolution catalyst made from non-precious materials remains a major challenge for such a system. This thesis basically consists of three parts of work, including studies on enhancing the photocatalytic oxygen evolution activity of cobalt-based spinel nanoparticles by manganese3+ substitution, in situ formation of cobalt oxide nanocubanes as highly active catalyst for photocatalytic oxygen evolution reaction, and development of a photoanode-driven photoelectrochemical cell for CO2 reduction with water. The first part of this thesis work devotes efforts in the development and study on cobalt and other transition metal oxide based oxygen evolution catalyst. Photocatalytic oxygen evolution is a critical step for solar fuel production from abundant sources. It poses a significant challenge because it requires an efficient catalyst to bridge the one-electron photon capture process with the four-electron oxygen reaction. Among all the metal oxides, Co3O4 spinel exhibits a high activity as an oxygen evolution catalyst. The results of this work demonstrate that the photocatalytic oxygen evolution activity of Co3O4 spinel can be further enhanced by substituting Co with Mn in the spinel structure. Using a facile hydrothermal approach, Co3O4 spinel nanoparticles as well as Mn-substituted and Ni-substituted Co3O4 spinel nanoparticles with a typical particle size of 5-7 nm were successfully synthesized. The morphology and crystal structures of the as-synthesized nanoparticle catalysts have been carefully examined using various structural characterization techniques, including powder x-ray diffraction (PXRD), transmission electron microscope (TEM), gas adsorption, and x-ray absorption

  10. Integrated photoelectrochemical energy storage: solar hydrogen generation and supercapacitor.

    PubMed

    Xia, Xinhui; Luo, Jingshan; Zeng, Zhiyuan; Guan, Cao; Zhang, Yongqi; Tu, Jiangping; Zhang, Hua; Fan, Hong Jin

    2012-01-01

    Current solar energy harvest and storage are so far realized by independent technologies (such as solar cell and batteries), by which only a fraction of solar energy is utilized. It is highly desirable to improve the utilization efficiency of solar energy. Here, we construct an integrated photoelectrochemical device with simultaneous supercapacitor and hydrogen evolution functions based on TiO(2)/transition metal hydroxides/oxides core/shell nanorod arrays. The feasibility of solar-driven pseudocapacitance is clearly demonstrated, and the charge/discharge is indicated by reversible color changes (photochromism). In such an integrated device, the photogenerated electrons are utilized for H(2) generation and holes for pseudocapacitive charging, so that both the reductive and oxidative energies are captured and converted. Specific capacitances of 482 F g(-1) at 0.5 A g(-1) and 287 F g(-1) at 1 A g(-1) are obtained with TiO(2)/Ni(OH)(2) nanorod arrays. This study provides a new research strategy for integrated pseudocapacitor and solar energy application.

  11. Photoelectrochemical hydrogen production

    SciTech Connect

    Rocheleau, R.E.; Miller, E.; Misra, A.

    1996-10-01

    The large-scale production of hydrogen utilizing energy provided by a renewable source to split water is one of the most ambitious long-term goals of the U.S. Department of Energy`s Hydrogen Program. One promising option to meet this goal is direct photoelectrolysis in which light absorbed by semiconductor-based photoelectrodes produces electrical power internally to split water into hydrogen and oxygen. Under this program, direct solar-to-chemical conversion efficiencies as high as 7.8 % have been demonstrated using low-cost, amorphous-silicon-based photoelectrodes. Detailed loss analysis models indicate that solar-to-chemical conversion greater than 10% can be achieved with amorphous-silicon-based structures optimized for hydrogen production. In this report, the authors describe the continuing progress in the development of thin-film catalytic/protective coatings, results of outdoor testing, and efforts to develop high efficiency, stable prototype systems.

  12. Synthesis and characterization of Cd{sub 0.7}Pb{sub 0.3}Se thin films for photoelectrochemical solar cell

    SciTech Connect

    Delekar, S.D.; Patil, M.K.; Jadhav, B.V.; Sanadi, K.R.; Hankare, P.P.

    2010-03-15

    Optimum composition Cd{sub 0.7}Pb{sub 0.3}Se thin films have been deposited using the chemical bath containing cadmium sulfate octahydrate, lead nitrate, tartaric acid, potassium hydroxide, ammonia, and sodium selenosulfate onto fluorine-doped tin oxide glass substrate. The various deposition parameters such as composition of reactive bath, pH of the solution, deposition temperature, deposition time, speed of rotation, etc. have been optimized for obtaining good quality film. X-ray diffraction studies revealed the polycrystalline nature of sample with the solid solution of lead (II) ions in CdSe host lattice, having a hexagonal phase structure. Scanning electron micrograph suggested that the grains were non-uniformly distributed over the substrate surface. Film composition was determined by atomic absorption spectroscopy as well as energy dispersive X-ray atomic spectroscopy. Optical absorption data showed the presence of direct transition with energy band gap 1.80 eV for the deposited thin films. The dark specific conductance of Cd{sub 0.7}Pb{sub 0.3}Se thin films was found to the order of 10{sup -6} ({omega} cm){sup -1} having n-type semiconducting nature. Photoelectrochemical characterization was carried out using sulfide/polysulfide electrolyte with 1.401% efficiency. (author)

  13. Chemically Modified Metal Oxide Nanostructure for Photoelectrochemical Water Splitting

    NASA Astrophysics Data System (ADS)

    Wang, Gongming

    Hydrogen gas is chemical fuel with high energy density, and represents a clean, renewable and carbon-free burning fuel, which has the potential to solve the more and more urgent energy crisis in today's society. Inspired by natural photosynthesis, artificial photosynthesis to generate hydrogen energy has attracted a lot of attentions in the field of chemistry, physics and material. Photoelectrochemical water splitting based on semiconductors represents a green and low cost method to generate hydrogen fuel. However, the current overall efficiency of solar to hydrogen is quite low, due to some intrinsic limitations such as bandgap, diffusion distance, carrier lifetime and photostability of semiconductors. Although nanostructured semiconductors can improve their photoelectrochemical water splitting performance to some extent, by increasing electrolyte accessible area and shortening minority carrier diffusion distance, nanostructure engineering cannot change their intrinsic electronic properties. Recent development in chemically modified nanostructures such as surface catalyst decoration, element doping, plasmonic modification and interfacial hetero-junction design have led to significant advancement in the photoelectrochemical water splitting, by improving surface reaction kinetics and charge separation, transportation and collection efficiency. In this thesis, I will give a detailed discussion on the chemically modified metal oxide nanostructures for photoelectrocemical hydrogen generation, with a focus on the element doping, hydrogen treatment and catalyst modification. I have demonstrated nitrogen doping on ZnO and Ti doping on hematite can improve their photoelectrochemical performance. In addition, we found hydrogen treatment is a general and effective method to improve the photocatalytic performance, by increasing their carrier desities. Hydrogen treatment has been demonstrated on TiO2, WO3 and BiVO4. In the end, we also used electrochemical catalyt to modify

  14. Photoelectrochemical water-splitting systems

    SciTech Connect

    Turner, J.A.; Kocha, S.S.

    1995-10-01

    Photochemical water-splitting is the process where an illuminated semiconductor is used to decompose water into its components, hydrogen and oxygen. Light, incident on a semiconductor electrode, splits water directly. A one-step monolithic system such as this eliminates the need to generate electricity externally and subsequently feed it to an electrolyser. Combining the electrolyser with the PV system eliminates one of the high cost components of a PV-electrolysis hydrogen generation system. Since external wiring is not used, only the piping necessary for the transport of hydrogen to an external storage system or gas pipeline is required. This paper will discuss the current technical status of direct conversion photoelectrochemical (PEC) water-splitting systems.

  15. Light addressable photoelectrochemical cyanide sensor

    SciTech Connect

    Licht, S.; Myung, N.; Sun, Y.

    1996-03-15

    A sensor is demonstrated that is capable of spatial discrimination of cyanide with use of only a single stationary sensing element. Different spatial regions of the sensing element are light activated to reveal the solution cyanide concentration only at the point of illumination. In this light addressable photoelectrochemical (LAP) sensor the sensing element consists of an n-CdSe electrode immersed in solution, with the open-circuit potential determined under illumination. In alkaline ferro-ferri-cyanide solution, the open-circuit photopotential is highly responsive to cyanide, with a linear response of (120 mV) log [KCN]. LAP detection with a spatial resolution of {+-}1 mm for cyanide detection is demonstrated. The response is almost linear for 0.001-0.100 m cyanide with a resolution of 5 mV. 38 refs., 7 figs., 1 tab.

  16. Photoelectrochemical reduction of CO{sub 2} by silicate rock powders

    SciTech Connect

    Ohta, Kiyohisa; Ohguchi, Youko; Kaneco, Satoshi; Mizuno, Takayuki

    1999-06-01

    The reduction in CO{sub 2} emissions by photoelectrochemical conversion of the CO{sub 2} to formic acid and methanol using silicate rock (andesite) powders suspended in water is presented. For photoelectrochemical reduction of CO{sub 2}, a homemade cell with a platinum and a copper electrode was used. 0.1 M KHCO{sub 3} solution was used as the electrolyte. In the photoelectrochemical reduction of CO{sub 2} with a copper cathode in the catholyte dispersing andesite powder, mainly formic acid, methanol, methane, ethylene, carbon monoxide, and hydrogen were produced. Consequently, it was found that this method using a copper electrode was effective for formic acid and methanol formations from carbon dioxide.

  17. Enhanced photoelectrochemical aptasensing platform for TXNDC5 gene based on exciton energy transfer between NCQDs and TiO2 nanorods

    PubMed Central

    Pang, Xuehui; Wang, Lin; Ma, Hongmin; Zhang, Yong; Pan, Jihong; Chen, Yao; Du, Bin; Wei, Qin

    2016-01-01

    The over expression of thioredoxin domain-containing protein 5 (TXNDC5) can promote the growth of castration-resistant prostate cancer (CRPC). A novel highly sensitive photoelectrochemical (PEC) aptsensor was developed for the detection of TXNDC5 by using the nanohybrids (TiO2 NRs/NCQDs) of nitrogen-doped carbon quantum dots (NCQDs) and TiO2 nanorods as the photo-to-electron conversion medium. TiO2 NRs/NCQDs nanohybrids were prepared by controlling the experimental condition. TiO2 NRs were self-assembled to form the nanopores with good photocurrent conversion efficiency. NCQDs possessed carboxyl groups (−COOH) and amino groups (−NH2) in the preparation process. −COOH and −NH2 groups played important roles for anchoring the capture probes (5′ primer and 3′ primer) through covalent binding. The ultrasensitive and stable detection for TXNDC5 was achieved by the specific recognition between the capture probes and the targets. The fabricated aptsensor showed excellent performance with a wide linear range (0.5 fmol/L ∼ 10 nmol/L) and a low detection limit of 0.1 fmol/L. This kind of aptsensor would provide a potential application for TXNDC5. PMID:26777976

  18. Fabricating photoelectrochemical aptasensor for selectively monitoring microcystin-LR residues in fish based on visible light-responsive BiOBr nanoflakes/N-doped graphene photoelectrode.

    PubMed

    Du, Xiaojiao; Jiang, Ding; Dai, Liming; Zhou, Lei; Hao, Nan; Qian, Jing; Qiu, Baijing; Wang, Kun

    2016-07-15

    The presence of microcystins in fish has been augmenting the risk of toxicity to animal and human health. Herein, a selective and sensitive method for detecting microcystin-LR (MC-LR) in fish samples by integrating the photoelectrochemical (PEC) technique and the specific recognition ability of aptamer was developed. Specifically, as an efficient PEC transducer, the BiOBr nanoflakes/N-doped graphene p-n heterojunction electrode was utilized as the aptamer immobilization platform via the π-π stacking interaction, which would be a biosensor enabling the convenient and exquisite PEC analysis. Subsequently, the PEC response of constructed aptasensor was specific binding to MC-LR. Other isoforms did not interfere with the detection process, and thus, it could be applied for the highly selective determination of MC-LR level. Under the optimized condition, the PEC signal versus the logarithm of the MC-LR concentration was in good linear relationship ranging from 0.1pM to 100nM with detection limit about 0.03pM. The constructed method was employed to analyze fish samples collected from the local supermarket. The overall analytical recovery of MC-LR in the fish matrices ranged from 97.8 to 101.6%, with relative standard deviation (RSD) of 2.52-5.14%, implying it would have great potential in farm product analysis.

  19. Particulate photocatalyst sheets for Z-scheme water splitting: advantages over powder suspension and photoelectrochemical systems and future challenges.

    PubMed

    Wang, Qian; Hisatomi, Takashi; Katayama, Masao; Takata, Tsuyoshi; Minegishi, Tsutomu; Kudo, Akihiko; Yamada, Taro; Domen, Kazunari

    2017-02-06

    Water splitting using semiconductor photocatalysts has been attracting growing interest as a means of solar energy based conversion of water to hydrogen, a clean and renewable fuel. Z-scheme photocatalytic water splitting based on the two-step excitation of an oxygen evolution photocatalyst (OEP) and a hydrogen evolution photocatalyst (HEP) is a promising approach toward the utilisation of visible light. In particular, a photocatalyst sheet system consisting of HEP and OEP particles embedded in a conductive layer has been recently proposed as a new means of obtaining efficient and scalable redox mediator-free Z-scheme solar water splitting. In this paper, we discuss the advantages and disadvantages of the photocatalyst sheet approach compared to conventional photocatalyst powder suspension and photoelectrochemical systems through an examination of the water splitting activity of Z-scheme systems based on SrTiO3:La,Rh as the HEP and BiVO4:Mo as the OEP. This photocatalyst sheet was found to split pure water much more efficiently than the powder suspension and photoelectrochemical systems, because the underlying metal layer efficiently transfers electrons from the OEP to the HEP. The photocatalyst sheet also outperformed a photoelectrochemical parallel cell during pure water splitting. The effects of H(+)/OH(-) concentration overpotentials and of the IR drop are reduced in the case of the photocatalyst sheet compared to photoelectrochemical systems, because the HEP and OEP are situated in close proximity to one another. Therefore, the photocatalyst sheet design is well-suited to efficient large-scale applications. Nevertheless, it is also noted that the photocatalytic activity of these sheets drops markedly with increasing background pressure because of reverse reactions involving molecular oxygen under illumination as well as delays in gas bubble desorption. It is shown that appropriate surface modifications allow the photocatalyst sheet to maintain its water

  20. Semiconductor wire array structures, and solar cells and photodetectors based on such structures

    SciTech Connect

    Kelzenberg, Michael D.; Atwater, Harry A.; Briggs, Ryan M.; Boettcher, Shannon W.; Lewis, Nathan S.; Petykiewicz, Jan A.

    2014-08-19

    A structure comprising an array of semiconductor structures, an infill material between the semiconductor materials, and one or more light-trapping elements is described. Photoconverters and photoelectrochemical devices based on such structure also described.

  1. Production of Hydrogen for Clean and Renewable Source of Energy for Fuel Cell Vehicles

    SciTech Connect

    Deng, Xunming; Ingler, William B, Jr.; Abraham, Martin; Castellano, Felix; Coleman, Maria; Collins, Robert; Compaan, Alvin; Giolando, Dean; Jayatissa, Ahalapitiya. H.; Stuart, Thomas; Vonderembse, Mark

    2008-10-31

    This was a two-year project that had two major components: 1) the demonstration of a PV-electrolysis system that has separate PV system and electrolysis unit and the hydrogen generated is to be used to power a fuel cell based vehicle; 2) the development of technologies for generation of hydrogen through photoelectrochemical process and bio-mass derived resources. Development under this project could lead to the achievement of DOE technical target related to PEC hydrogen production at low cost. The PEC part of the project is focused on the development of photoelectrochemical hydrogen generation devices and systems using thin-film silicon based solar cells. Two approaches are taken for the development of efficient and durable photoelectrochemical cells; 1) An immersion-type photoelectrochemical cells (Task 3) where the photoelectrode is immersed in electrolyte, and 2) A substrate-type photoelectrochemical cell (Task 2) where the photoelectrode is not in direct contact with electrolyte. Four tasks are being carried out: Task 1: Design and analysis of DC voltage regulation system for direct PV-to-electrolyzer power feed Task 2: Development of advanced materials for substrate-type PEC cells Task 3: Development of advanced materials for immersion-type PEC cells Task 4: Hydrogen production through conversion of biomass-derived wastes

  2. Nitrogen and cobalt co-doped zinc oxide nanowires - Viable photoanodes for hydrogen generation via photoelectrochemical water splitting

    NASA Astrophysics Data System (ADS)

    Patel, Prasad Prakash; Hanumantha, Prashanth Jampani; Velikokhatnyi, Oleg I.; Datta, Moni Kanchan; Hong, Daeho; Gattu, Bharat; Poston, James A.; Manivannan, Ayyakkannu; Kumta, Prashant N.

    2015-12-01

    Photoelectrochemical (PEC) water splitting has been considered as a promising and environmentally benign approach for efficient and economic hydrogen generation by utilization of solar energy. Development of semiconductor materials with low band gap, high photoelectrochemical activity and stability has been of particular interest for a viable PEC water splitting system. In this study, Co doped ZnO, .i.e., (Zn0.95Co0.05)O nanowires (NWs) was selected as the composition for further co-doping with nitrogen by comparing solar to hydrogen efficiency (SHE) of ZnO NWs with that of various compositions of (Zn1-xCox)O NWs (x = 0, 0.05, 0.1). Furthermore, nanostructured vertically aligned Co and N-doped ZnO, .i.e., (Zn1-xCox)O:N NWs (x = 0.05) have been studied as photoanodes for PEC water splitting. An optimal SHE of 1.39% the highest reported so far to the best of our knowledge for ZnO based photoanodes was obtained for the co-doped NWs, (Zn0.95Co0.05)O:N - 600 NWs generated at 600 °C in ammonia atmosphere. Further, (Zn0.95Co0.05)O:N-600 NWs exhibited excellent photoelectrochemical stability under illumination compared to pure ZnO NWs. These promising results suggest the potential of (Zn0.95Co0.05)O:N-600 NWs as a viable photoanode in PEC water splitting cell. Additionally, theoretical first principles study conducted explains the beneficial effects of Co and N co-doping on both, the electronic structure and the band gap of ZnO.

  3. Nanoscale connectivity in a TiO2/CdSe quantum dots/functionalized graphene oxide nanosheets/Au nanoparticles composite for enhanced photoelectrochemical solar cell performance.

    PubMed

    Narayanan, Remya; Deepa, Melepurath; Srivastava, Avanish Kumar

    2012-01-14

    hierarchical rapid electron transfer model can be adapted to other nanostructures as well, as they can favorably impact photoelectrochemical performance.

  4. Metal-free hybrids of graphitic carbon nitride and nanodiamonds for photoelectrochemical and photocatalytic applications.

    PubMed

    Zhou, Li; Zhang, Huayang; Guo, Xiaochen; Sun, Hongqi; Liu, Shaomin; Tade, Moses O; Wang, Shaobin

    2017-05-01

    Graphitic carbon nitride (g-C3N4) has been considered as a metal-free, cost-effective, eco-friendly and efficient catalyst for various photoelectrochemical applications. However, compared to conventional metal-based photocatalysts, its photocatalytic activity is still low because of the low mobility of carriers restricted by the polymer nature. Herein, a series of hybrids of g-C3N4 (GCN) and nanodiamonds (NDs) were synthesized using a solvothermal method. The photoelectrochemical performance and photocatalytic efficiency of the GCN/NDs were investigated by means of the generation of photocurrent and photodegradation of methylene blue (MB) solutions under UV-visible light irradiations. In this study, the sample of GCN/ND-33% derived from 0.1g GCN and 0.05g NDs displayed the highest photocatalytic activity and the strongest photocurrent density. The mechanism of enhanced photoelectrochemical and photocatalytic performances was also discussed.

  5. Ultrasensitive sandwich-type photoelectrochemical immunosensor based on CdSe sensitized La-TiO2 matrix and signal amplification of polystyrene@Ab2 composites.

    PubMed

    Fan, Dawei; Ren, Xiang; Wang, Haoyuan; Wu, Dan; Zhao, Di; Chen, Yucheng; Wei, Qin; Du, Bin

    2017-01-15

    A novel and sensitive sandwich-type photoelectrochemical (PEC) sensor was fabricated using signal amplification strategy for the quantitative detection of the prostate specific antigen (PSA). CdSe nanoparticles (NPs) sensitized lanthanum-doped titanium dioxide (La-TiO2) composites were used to bind the primary antibodies (Ab1). The doping of lanthanum promoted the visible light absorption of TiO2 and remarkably enhanced the photocurrent. Moreover, 0.3%La-TiO2 displayed the highest photocurrent in the La-TiO2 composites, which was twice as much as that of undoped TiO2. Carboxyl modified CdSe NPs were assembled onto La-TiO2 composites via the dentate binding between -COOH and Ti atom in TiO2 NPs, which dramatically promoted the photocurrent intensity by approximately 2.1 times. Carboxyl functionalized polystyrene (PS) microspheres were coated with the secondary antibodies (Ab2). Owing to the better insulation property and steric hindrance of the prepared polystyrene@Ab2 (PS@Ab2) composites, the significant reduction of the photocurrent signal was achieved after the specific immune recognition. Under the optimum experimental conditions, the fabricated PEC sensor realized ultrasensitive detection of PSA in the range of 0.05-100pgmL(-1) with a detection limit of 17fgmL(-1). Moreover, this well-designed PEC immunoassay exhibited ideal reproducibility, stability, and selectivity, which is a promising platform for the detection of other important tumor targets.

  6. Critical Research for Cost-Effective Photoelectrochemical Production of Hydrogen

    SciTech Connect

    Xu, Liwei; Deng, Xunming; Abken, Anka; Cao, Xinmin; Du, Wenhui; Vijh, Aarohi; Ingler, William; Chen, Changyong; Fan, Qihua; Collins, Robert; Compaan, Alvin; Yan, Yanfa; Giolando, Dean; Turner, John

    2014-10-29

    The objective of this project is to develop critical technologies required for cost-effective production of hydrogen from sunlight and water using a-Si triple junction solar cell based photo-electrodes. In this project, Midwest Optoelectronics, LLC (MWOE) and its collaborating organizations utilize triple junction a-Si thin film solar cells as the core element to fabricate photoelectrochemical (PEC) cells. Triple junction a-Si/a-SiGe/a-SiGe solar cell is an ideal material for making cost-effective PEC system which uses sun light to split water and generate hydrogen. It has the following key features: 1) It has an open circuit voltage (Voc ) of ~ 2.3V and has an operating voltage around 1.6V. This is ideal for water splitting. There is no need to add a bias voltage or to inter-connect more than one solar cell. 2) It is made by depositing a-Si/a-SiGe/aSi-Ge thin films on a conducting stainless steel substrate which can serve as an electrode. When we immerse the triple junction solar cells in an electrolyte and illuminate it under sunlight, the voltage is large enough to split the water, generating oxygen at the Si solar cell side (for SS/n-i-p/sunlight structure) and hydrogen at the back, which is stainless steel side. There is no need to use a counter electrode or to make any wire connection. 3) It is being produced in large rolls of 3ft wide and up to 5000 ft long stainless steel web in a 25MW roll-to-roll production machine. Therefore it can be produced at a very low cost. After several years of research with many different kinds of material, we have developed promising transparent, conducting and corrosion resistant (TCCR) coating material; we carried out extensive research on oxygen and hydrogen generation catalysts, developed methods to make PEC electrode from production-grade a-Si solar cells; we have designed and tested various PEC module cases and carried out extensive outdoor testing; we were able to obtain a solar to hydrogen conversion efficiency (STH

  7. Photoelectrochemical Reduction of CO2 Coupled to Water Oxidation Using a Photocathode With a Ru(II)-Re(I) Complex Photocatalyst and a CoOx/TaON Photoanode.

    PubMed

    Sahara, Go; Kumagai, Hiromu; Maeda, Kazuhiko; Kaeffer, Nicolas; Artero, Vincent; Higashi, Masanobu; Abe, Ryu; Ishitani, Osamu

    2016-10-02

    Photoelectrochemical CO2 reduction activity of a hybrid photocathode, based on a Ru(II)-Re(I) supramolecular metal complex photocatalyst immobilized on a NiO electrode (NiO-RuRe) was confirmed in an aqueous electrolyte solution. Under half-reaction conditions, the NiO-RuRe photocathode generated CO with high selectivity, and its turnover number for CO formation reached 32 based on the amount of immobilized RuRe. A photoelectrochemical cell comprising a NiO-RuRe photocathode and a CoOx/TaON photoanode showed activity for visible-light-driven CO2 reduction using water as a reductant to generate CO and O2, with the assistance of an external electrical (0.3 V) and chemical bias (0.10 V) produced by a pH difference. This is the first example of a molecular and semiconductor photocatalyst hybrid-constructed photoelectrochemical cell for visibl-light-driven CO2 reduction using water as a reductant.

  8. Photoelectrochemical Behavior of Chlorophyll a in Thin Films

    DTIC Science & Technology

    2000-01-01

    UNCLASSIFIED Defense Technical Information Center Compilation Part Notice ADPO 11829 TITLE: Photoelectrochemical Behavior of Chlorophyll a in Thin...comprise the compilation report: ADPO11800 thru ADP011832 UNCLASSIFIED PHOTOELECTROCHEMICAL BEHAVIOR OF CHLOROPHYLL a IN THIN FILMS LAURA TUGULEA Faculty of...Physics-University of Bucharest P. O.Box Mg-1, Bucharest-Magurele 76900 Romania Abstract The photoelectrochemical behavior of chlorophyll a species

  9. A Novel Photoelectrochemical Biosensor for Tyrosinase and Thrombin Detection

    PubMed Central

    Chen, Jiexia; Liu, Yifan; Zhao, Guang-Chao

    2016-01-01

    A novel photoelectrochemical biosensor for step-by-step assay of tyrosinase and thrombin was fabricated based on the specific interactions between the designed peptide and the target enzymes. A peptide chain with a special sequence which contains a positively charged lysine-labeled terminal, tyrosine at the other end and a cleavage site recognized by thrombin between them was designed. The designed peptide can be fixed on surface of the CdTe quantum dots (QDs)-modified indium-tin oxide (ITO) electrode through electrostatic attraction to construct the photoelectrochemical biosensor. The tyrosinase target can catalyze the oxidization of tyrosine by oxygen into ortho-benzoquinone residues, which results in a decrease in the sensor photocurrent. Subsequently, the cleavage site could be recognized and cut off by another thrombin target, restoring the sensor photocurrent. The decrease or increase of photocurrent in the sensor enables us to assay tyrosinase and thrombin. Thus, the detection of tyrosinase and thrombin can be achieved in the linear range from 2.6 to 32 μg/mL and from 4.5 to 100 μg/mL with detection limits of 1.5 μg/mL and 1.9 μg/mL, respectively. Most importantly, this strategy shall allow us to detect different classes of enzymes simultaneously by designing various enzyme-specific peptide substrates. PMID:26805846

  10. Photoelectrochemical Water Systems for H2 Production (Presentation)

    SciTech Connect

    Turner, J. A.; Deutsch, T.; Head, J.; Vallett, P.

    2007-05-17

    This Photoelectrochemical Water Systems for Hydrogen Production presentation by the National Renewable Energy Laboratory's John Turner was given at the DOE Hydrogen Program's 2007 Annual Merit Review.

  11. Dye-sensitized PS-b-P2VP-templated nickel oxide films for photoelectrochemical applications

    PubMed Central

    Massin, Julien; Bräutigam, Maximilian; Kaeffer, Nicolas; Queyriaux, Nicolas; Field, Martin J.; Schacher, Felix H.; Popp, Jürgen; Chavarot-Kerlidou, Murielle; Dietzek, Benjamin; Artero, Vincent

    2015-01-01

    Moving from homogeneous water-splitting photocatalytic systems to photoelectrochemical devices requires the preparation and evaluation of novel p-type transparent conductive photoelectrode substrates. We report here on the sensitization of polystyrene-block-poly-(2-vinylpyridine) (PS-b-P2VP) diblock copolymer-templated NiO films with an organic push–pull dye. The potential of these new templated NiO film preparations for photoelectrochemical applications is compared with NiO material templated by F108 triblock copolymers. We conclude that NiO films are promising materials for the construction of dye-sensitized photocathodes to be inserted into photoelectrochemical (PEC) cells. However, a combined effort at the interface between materials science and molecular chemistry, ideally funded within a Global Artificial Photosynthesis Project, is still needed to improve the overall performance of the photoelectrodes and progress towards economically viable PEC devices. PMID:26052420

  12. Flash photoelectrochemical studies of transient electrode processes important in solar energy conversion. Progress report, May 1, 1980-April 30, 1981

    SciTech Connect

    Perone, S. P.

    1980-12-01

    The program objectives related to pulsed laser irradiation of semiconductor/liquid junction photoelectrochemical cells were: (1) detect and characterize transient photoproducts due to electrode and/or solution photoelectrolysis at the interface; (2) obtain time-resolved photoelectrolysis data indicative of charge transfer rates; (3) obtain photoelectrochemical measurements related to electron-hole recombination rates subsequent to pulsed laser irradiation; (4) utilize complementary spectroscopic methods for characterizing transient photoprocesses at the semiconductor/electrolyte interface; (5) characterize the dynamics of super-sensitizer interactions with sensitizing dyes adsorbed at the interface; and (6) direct observation of surface state photoelectrolysis processes. Progress is reported. (WHK)

  13. Efficiency limits for photoelectrochemical water-splitting

    PubMed Central

    Fountaine, Katherine T.; Lewerenz, Hans Joachim; Atwater, Harry A.

    2016-01-01

    Theoretical limiting efficiencies have a critical role in determining technological viability and expectations for device prototypes, as evidenced by the photovoltaics community's focus on detailed balance. However, due to their multicomponent nature, photoelectrochemical devices do not have an equivalent analogue to detailed balance, and reported theoretical efficiency limits vary depending on the assumptions made. Here we introduce a unified framework for photoelectrochemical device performance through which all previous limiting efficiencies can be understood and contextualized. Ideal and experimentally realistic limiting efficiencies are presented, and then generalized using five representative parameters—semiconductor absorption fraction, external radiative efficiency, series resistance, shunt resistance and catalytic exchange current density—to account for imperfect light absorption, charge transport and catalysis. Finally, we discuss the origin of deviations between the limits discussed herein and reported water-splitting efficiencies. This analysis provides insight into the primary factors that determine device performance and a powerful handle to improve device efficiency. PMID:27910847

  14. Efficiency limits for photoelectrochemical water-splitting

    NASA Astrophysics Data System (ADS)

    Fountaine, Katherine T.; Lewerenz, Hans Joachim; Atwater, Harry A.

    2016-12-01

    Theoretical limiting efficiencies have a critical role in determining technological viability and expectations for device prototypes, as evidenced by the photovoltaics community's focus on detailed balance. However, due to their multicomponent nature, photoelectrochemical devices do not have an equivalent analogue to detailed balance, and reported theoretical efficiency limits vary depending on the assumptions made. Here we introduce a unified framework for photoelectrochemical device performance through which all previous limiting efficiencies can be understood and contextualized. Ideal and experimentally realistic limiting efficiencies are presented, and then generalized using five representative parameters--semiconductor absorption fraction, external radiative efficiency, series resistance, shunt resistance and catalytic exchange current density--to account for imperfect light absorption, charge transport and catalysis. Finally, we discuss the origin of deviations between the limits discussed herein and reported water-splitting efficiencies. This analysis provides insight into the primary factors that determine device performance and a powerful handle to improve device efficiency.

  15. Clean TiO2 nanocuboid film tightly attached on a conductive substrate for highly efficient photoelectrochemical water splitting

    NASA Astrophysics Data System (ADS)

    Meng, Ming; Liu, Kuili; Gan, Zhixing; Zhang, Xiantu; Zhang, Honghui; Sun, Xianke; Zhou, Xiaodong; Chen, Yuanyuan; Feng, Yamin

    2016-12-01

    Anatase TiO2 film consisting of nanocuboids with co-exposed {1 0 1}, {0 0 1} and {1 0 0} facets have been successfully synthesized via thermally annealing amorphous anodized TiO2 nanotube arrays in ambient fluorine. When employed as a photoanode material in photoelectrochemical water splitting, the film of the clean TiO2 nanocuoboids yields a photocurrent density of up to 0.65 mA cm-2 at 0.22 V versus the Ag/AgCl electrode with Faradic efficiency of 100% and exhibits excellent stability, which can be attributed to enhanced photogenerated charge separation and transport to the collecting electrode. This film could also potentially be used for other facet-related applications such as TiO2 based dye-sensitized solar cells, sensors and lithium batteries.

  16. Integrated Photoelectrochemical Solar Energy Conversion and Organic Redox Flow Battery Devices.

    PubMed

    Li, Wenjie; Fu, Hui-Chun; Li, Linsen; Cabán-Acevedo, Miguel; He, Jr-Hau; Jin, Song

    2016-10-10

    Building on regenerative photoelectrochemical solar cells and emerging electrochemical redox flow batteries (RFBs), more efficient, scalable, compact, and cost-effective hybrid energy conversion and storage devices could be realized. An integrated photoelectrochemical solar energy conversion and electrochemical storage device is developed by integrating regenerative silicon solar cells and 9,10-anthraquinone-2,7-disulfonic acid (AQDS)/1,2-benzoquinone-3,5-disulfonic acid (BQDS) RFBs. The device can be directly charged by solar light without external bias, and discharged like normal RFBs with an energy storage density of 1.15 Wh L(-1) and a solar-to-output electricity efficiency (SOEE) of 1.7 % over many cycles. The concept exploits a previously undeveloped design connecting two major energy technologies and promises a general approach for storing solar energy electrochemically with high theoretical storage capacity and efficiency.

  17. Novel nanostructure zinc zirconate, zinc oxide or zirconium oxide pastes coated on fluorine doped tin oxide thin film as photoelectrochemical working electrodes for dye-sensitized solar cell.

    PubMed

    Hossein Habibi, Mohammad; Askari, Elham; Habibi, Mehdi; Zendehdel, Mahmoud

    2013-03-01

    Zinc zirconate (ZnZrO(3)) (ZZ), zinc oxide (ZnO) (ZO) and zirconium oxide (ZrO(2)) (ZRO) nano-particles were synthesized by simple sol-gel method. ZZ, ZO and ZRO nano-particles were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD) and UV-Vis diffuse reflectance spectrum (DRS). Nanoporous ZZ, ZO and ZRO thin films were prepared doctor blade technique on the fluorine-doped tin oxide (FTO) and used as working electrodes in dye sensitized solar cells (DSSC). Their photovoltaic behavior were compared with standard using D35 dye and an electrolyte containing [Co(bpy)(3)](PF(6))(2), [Co(pby)(3)](PF(6))(3), LiClO(4), and 4-tert-butylpyridine (TBP). The properties of DSSC have been studied by measuring their short-circuit photocurrent density (Jsc), open-circuit voltage (VOC) and fill factor (ff). The application of ZnZrO(3) as working electrode produces a significant improvement in the fill factor (ff) of the dye-sensitized solar cells (ff=56%) compared to ZnO working electrode (ff=40%) under the same condition.

  18. Ultrasensitive photoelectrochemical immunoassay for CA19-9 detection based on CdSe@ZnS quantum dots sensitized TiO2NWs/Au hybrid structure amplified by quenching effect of Ab2@V(2+) conjugates.

    PubMed

    Zhu, Hua; Fan, Gao-Chao; Abdel-Halim, E S; Zhang, Jian-Rong; Zhu, Jun-Jie

    2016-03-15

    A novel, enhanced photoelectrochemical immunoassay was established for sensitive and specific detection of carbohydrate antigen 19-9 (CA19-9, Ag). In this protocol, TiO2 nanowires (TiO2NWs) were first decorated with Au nanoparticles to form TiO2NWs/Au hybrid structure, and then coated with CdSe@ZnS quantum dots (QDs) via the layer-by-layer method, producing TiO2NWs/Au/CdSe@ZnS sensitized structure, which was employed as the photoelectrochemical matrix to immobilize capture CA19-9 antibodies (Ab1); whereas, bipyridinium (V(2+)) molecules were labeled on signal CA19-9 antibodies (Ab2) to form Ab2@V(2+) conjugates, which were used as signal amplification elements. The TiO2NWs/Au/CdSe@ZnS sensitized structure could adequately absorb light energy and dramatically depress electron-hole recombination, resulting in evidently enhanced photocurrent intensity of the immunosensing electrode. While target Ag were detected, the Ab2@V(2+) conjugates could significantly decrease the photocurrent detection signal because of strong electron-withdrawing property of V(2+) coupled with evident steric hindrance of Ab2. Thanks to synergy effect of TiO2NWs/Au/CdSe@ZnS sensitized structure and quenching effect of Ab2@V(2+) conjugates, the well-established photoelectrochemical immunoassay exhibited a low detection limit of 0.0039 U/mL with a wide linear range from 0.01 U/mL to 200 U/mL for target Ag detection. This proposed photoelectrochemical protocol also showed good reproducibility, specificity and stability, and might be applied to detect other important biomarkers.

  19. Enhanced photoelectrochemical activity of a hierarchical-ordered TiO₂ mesocrystal and its sensing application on a carbon nanohorn support scaffold.

    PubMed

    Dai, Hong; Zhang, Shupei; Hong, Zhensheng; Li, Xiuhua; Xu, Guifang; Lin, Yanyu; Chen, Guonan

    2014-07-01

    A ternary hybrid was developed through interaction between a hierarchical-ordered TiO2 and a thiol group that was obtained by in situ chemical polymerization of L-cysteine on the carbon nanohorn (CNH) superstructure modified electrode. Herein, unique-ordered TiO2 superstructures with quasi-octahedral shape that possess high crystallinity, high porosity, oriented subunit alignment, very large specific surface area, and superior photocatalytic activity were first introduced as a photosensitizer element in the photoelectrochemical determination. Additionally, the assembly of hierarchical-structured CNHs was used to provide an excellent electron-transport matrix to capture and transport an electron from excited anatase to the electrode rapidly, hampering the electron-hole recombination effectively, resulting in improved photoelectrochemical response and higher photocatalytic activity in the visible light region. Owing to the dependence of the photocurrent signal on the concentration of electron donor, 4-methylimidozal, which can act as a photogenerated hole scavenger, an exquisite photoelectrochemical sensor was successfully fabricated with a wide linear range from 1 × 10(-4) to 1 × 10(-10) M, and the detection limit was down to 30 pM. The low applied potential of 0.2 V was beneficial to the elimination of interference from other reductive species that coexisted in the real samples. More importantly, the mesocrystal was first introduced in the fabricating of a biosensor, which not only opens up a new avenue for biosensors manufactured based on mesocrystal materials but also provides beneficial lessons in the research fields ranging from solar cells to photocatalysis.

  20. Broad Spectrum Photoelectrochemical Diodes for Solar Hydrogen Generation

    SciTech Connect

    Grimes, Craig A.

    2014-11-26

    Under program auspices we have investigated material chemistries suitable for the solar generation of hydrogen by water photoelectrolysis. We have built upon, and extended, our knowledge base on the synthesis and application of TiO2 nanotube arrays, a material architecture that appears ideal for water photoelectrolysis. To date we have optimized, refined, and greatly extended synthesis techniques suitable for achieving highly ordered TiO2 nanotube arrays of given length, wall thickness, pore diameter, and tube-to-tube spacing for use in water photoelectrolysis. We have built upon this knowledge based to achieve visible light responsive, photocorrosion stable n-type and p-type ternary oxide nanotube arrays for use in photoelectrochemical diodes.

  1. Luminescent Photoelectrochemical Cells. 2. Doped Cadmium Sulfide Photoelectrodes as Probes of Excited-State Processes Which Influence Optical to Electrical Energy Conversion.

    DTIC Science & Technology

    1980-08-12

    with the maximum quantum efficiency for electron flow in the external circuit. Emission from band gap edge 514.5-nm excitation is mor sensitive to... electron transfer are shown by open-circuit photopotential measurements to be comparable for undoped CdS and 100 ppm CdS:Te. Results bearing on the...based, for example, on energy transfer across the semiconductor-electrolyte interface. Second, the data obtained should allow an assessment of the band

  2. Photoelectrochemical generation of hydrogen and electricity from hydrazine hydrate using BiVO4 electrodes.

    PubMed

    Pilli, Satyananda Kishore; Summers, Kodi; Chidambaram, Dev

    2015-06-07

    This study demonstrates solar driven oxidation of hydrazine hydrate and the simultaneous production of hydrogen and electricity in photoelectrochemical cells and photofuel cells, respectively, using a visible light active molybdenum doped BiVO4 photoelectrode. The developed photoelectrodes exhibited tremendous efficiency towards anodic oxidation of hydrous hydrazine with continuous and stable hydrogen evolution at the Pt cathode under benign pH and zero bias conditions. Significantly, the photofuel cell containing hydrazine hydrate fuel has generated electricity with a high open circuit potential of 0.8 V. The presence of bicarbonate ions in the electrolyte has played a significant role in enhancing the kinetics of photoelectrochemical oxidation of hydrazine and improved the hydrogen and electricity generation efficiency thus avoiding the integration of an oxidation electrocatalyst. In addition, molybdenum doped BiVO4 as a possible photoelectrochemical hydrazine sensor has been investigated and the electrode photocurrent was found to be linearly dependent on the concentration of the hydrazine hydrate in the range of 20-90 mM with a correlation coefficient of 0.9936.

  3. All-in-One Derivatized Tandem p(+)n-Silicon-SnO2/TiO2 Water Splitting Photoelectrochemical Cell.

    PubMed

    Sheridan, Matthew V; Hill, David J; Sherman, Benjamin D; Wang, Degao; Marquard, Seth L; Wee, Kyung-Ryang; Cahoon, James F; Meyer, Thomas J

    2017-04-12

    Mesoporous metal oxide film electrodes consisting of derivatized 5.5 μm thick SnO2 films with an outer 4.3 nm shell of TiO2 added by atomic layer deposition (ALD) have been investigated to explore unbiased water splitting on p, n, and p(+)n type silicon substrates. Modified electrodes were derivatized by addition of the water oxidation catalyst, [Ru(bda)(4-O(CH2)3PO3H2)-pyr)2], 1, (pyr = pyridine; bda = 2,2'-bipyridine-6,6'-dicarboxylate), and chromophore, [Ru(4,4'-PO3H2-bpy) (bpy)2](2+), RuP(2+), (bpy = 2,2'-bipyridine), which form 2:1 RuP(2+)/1 assemblies on the surface. At pH 5.7 in 0.1 M acetate buffer, these electrodes with a fluorine-doped tin oxide (FTO) back contact under ∼1 sun illumination (100 mW/cm(2); white light source) perform efficient water oxidation with a photocurrent of 1.5 mA/cm(2) with an 88% Faradaic efficiency (FE) for O2 production at an applied bias of 600 mV versus RHE ( ACS Energy Lett. , 2016 , 1 , 231 - 236 ). The SnO2/TiO2-chromophore-catalyst assembly was integrated with the Si electrodes by a thin layer of titanium followed by an amorphous TiO2 (Ti/a-TiO2) coating as an interconnect. In the integrated electrode, p(+)n-Si-Ti/a-TiO2-SnO2/TiO2|-2RuP(2+)/1, the p(+)n-Si junction provided about 350 mV in added potential to the half cell. In photolysis experiments at pH 5.7 in 0.1 M acetate buffer, bias-free photocurrents approaching 100 μA/cm(2) were obtained for water splitting, 2H2O → 2H2 + O2. The FE for water oxidation was 79% with a hydrogen efficiency of ∼100% at the Pt cathode.

  4. Optimization of conditions for hydrogen production from anodized TiO2 nanotube-based photoelectrochemical cells.

    PubMed

    Hong, Won Sung; Park, Jong Hyeok; Han, Gui Young

    2009-12-01

    The photocatalytic splitting of water into H2 and O2 using semiconductors has received much attention, especially in terms of its potential application to the direct production of H2 as a clean energy source. In this study, the H2 yield increased with increasing reactor temperature, but the TiO2 nanotube arrays collapsed after prolonged operation at temperatures over 75 degrees C. We found that aqueous Na2SO3 reagent was the best hole scavenger of the different aqueous solutions examined. Using the optimum temperatures and electrolytes, we conducted an experiment to produce H2 from solutions with different pH values, and found that acidic conditions were better in terms of the amount of H2 produced. The results obtained allowed us to identify the optimal temperature, electrolyte and pH conditions required to produce H2 by photochemically splitting water.

  5. Manipulation of charge transfer and transport in plasmonic-ferroelectric hybrids for photoelectrochemical applications

    PubMed Central

    Wang, Zhijie; Cao, Dawei; Wen, Liaoyong; Xu, Rui; Obergfell, Manuel; Mi, Yan; Zhan, Zhibing; Nasori, Nasori; Demsar, Jure; Lei, Yong

    2016-01-01

    Utilizing plasmonic nanostructures for efficient and flexible conversion of solar energy into electricity or fuel presents a new paradigm in photovoltaics and photoelectrochemistry research. In a conventional photoelectrochemical cell, consisting of a plasmonic structure in contact with a semiconductor, the type of photoelectrochemical reaction is determined by the band bending at the semiconductor/electrolyte interface. The nature of the reaction is thus hard to tune. Here instead of using a semiconductor, we employed a ferroelectric material, Pb(Zr,Ti)O3 (PZT). By depositing gold nanoparticle arrays and PZT films on ITO substrates, and studying the photocurrent as well as the femtosecond transient absorbance in different configurations, we demonstrate an effective charge transfer between the nanoparticle array and PZT. Most importantly, we show that the photocurrent can be tuned by nearly an order of magnitude when changing the ferroelectric polarization in PZT, demonstrating a versatile and tunable system for energy harvesting. PMID:26753764

  6. Manipulation of charge transfer and transport in plasmonic-ferroelectric hybrids for photoelectrochemical applications

    NASA Astrophysics Data System (ADS)

    Wang, Zhijie; Cao, Dawei; Wen, Liaoyong; Xu, Rui; Obergfell, Manuel; Mi, Yan; Zhan, Zhibing; Nasori, Nasori; Demsar, Jure; Lei, Yong

    2016-01-01

    Utilizing plasmonic nanostructures for efficient and flexible conversion of solar energy into electricity or fuel presents a new paradigm in photovoltaics and photoelectrochemistry research. In a conventional photoelectrochemical cell, consisting of a plasmonic structure in contact with a semiconductor, the type of photoelectrochemical reaction is determined by the band bending at the semiconductor/electrolyte interface. The nature of the reaction is thus hard to tune. Here instead of using a semiconductor, we employed a ferroelectric material, Pb(Zr,Ti)O3 (PZT). By depositing gold nanoparticle arrays and PZT films on ITO substrates, and studying the photocurrent as well as the femtosecond transient absorbance in different configurations, we demonstrate an effective charge transfer between the nanoparticle array and PZT. Most importantly, we show that the photocurrent can be tuned by nearly an order of magnitude when changing the ferroelectric polarization in PZT, demonstrating a versatile and tunable system for energy harvesting.

  7. Photoelectrochemical water splitting enhanced by self-assembled metal nanopillars embedded in an oxide semiconductor photoelectrode

    PubMed Central

    Kawasaki, Seiji; Takahashi, Ryota; Yamamoto, Takahisa; Kobayashi, Masaki; Kumigashira, Hiroshi; Yoshinobu, Jun; Komori, Fumio; Kudo, Akihiko; Lippmaa, Mikk

    2016-01-01

    Production of chemical fuels by direct solar energy conversion in a photoelectrochemical cell is of great practical interest for developing a sustainable energy system. Various nanoscale designs such as nanowires, nanotubes, heterostructures and nanocomposites have been explored to increase the energy conversion efficiency of photoelectrochemical water splitting. Here we demonstrate a self-organized nanocomposite material concept for enhancing the efficiency of photocarrier separation and electrochemical energy conversion. Mechanically robust photoelectrodes are formed by embedding self-assembled metal nanopillars in a semiconductor thin film, forming tubular Schottky junctions around each pillar. The photocarrier transport efficiency is strongly enhanced in the Schottky space charge regions while the pillars provide an efficient charge extraction path. Ir-doped SrTiO3 with embedded iridium metal nanopillars shows good operational stability in a water oxidation reaction and achieves over 80% utilization of photogenerated carriers under visible light in the 400- to 600-nm wavelength range. PMID:27255209

  8. Photoelectrochemical water splitting enhanced by self-assembled metal nanopillars embedded in an oxide semiconductor photoelectrode

    NASA Astrophysics Data System (ADS)

    Kawasaki, Seiji; Takahashi, Ryota; Yamamoto, Takahisa; Kobayashi, Masaki; Kumigashira, Hiroshi; Yoshinobu, Jun; Komori, Fumio; Kudo, Akihiko; Lippmaa, Mikk

    2016-06-01

    Production of chemical fuels by direct solar energy conversion in a photoelectrochemical cell is of great practical interest for developing a sustainable energy system. Various nanoscale designs such as nanowires, nanotubes, heterostructures and nanocomposites have been explored to increase the energy conversion efficiency of photoelectrochemical water splitting. Here we demonstrate a self-organized nanocomposite material concept for enhancing the efficiency of photocarrier separation and electrochemical energy conversion. Mechanically robust photoelectrodes are formed by embedding self-assembled metal nanopillars in a semiconductor thin film, forming tubular Schottky junctions around each pillar. The photocarrier transport efficiency is strongly enhanced in the Schottky space charge regions while the pillars provide an efficient charge extraction path. Ir-doped SrTiO3 with embedded iridium metal nanopillars shows good operational stability in a water oxidation reaction and achieves over 80% utilization of photogenerated carriers under visible light in the 400- to 600-nm wavelength range.

  9. Vertically oriented Ti-Pd mixed oxynitride nanotube arrays for enhanced photoelectrochemical water splitting.

    PubMed

    Allam, Nageh K; Poncheri, Adam J; El-Sayed, Mostafa A

    2011-06-28

    In recent years, considerable efforts have been made to design and discover photoactive nanostructured materials that can be used as anodes in water photoelectrolysis cells. Herein, we report on the growth of a novel photoanode material composed of self-ordered, vertically oriented nanotube arrays of titanium-palladium mixed oxynitride films via anodization of Ti-Pd alloy in an electrolyte solution of formamide containing NH(4)F at room temperature, followed by annealing in an ammonia atmosphere. The nanostructure topology was found to depend on both the anodization time and the applied voltage. Our results demonstrate the ability to grow mixed oxynitride nanotube array films that are several micrometers thick. The Ti-Pd oxynitride nanotube array films were utilized in solar-spectrum water photoelectrolysis, demonstrating a photocurrent density of 1.9 mA/cm(2) and a ∼5-fold increase in the photoconversion efficiency under AM 1.5 illumination (100 mW/cm(2), 1.0 M KOH) compared to pure TiO(2) nanotubes fabricated and tested under the same conditions. The obtained efficiency is among the highest reported values for a TiO(2) nanotube-based photoelectrochemical cell. This enhancement in the photoconversion efficiency is related to the synergistic effects of Pd alloying, nitrogen doping, and the unique structural properties of the fabricated nanotube arrays.

  10. Band-offsets at BaTiO3/Cu2O heterojunction and enhanced photoelectrochemical response: theory and experiment(Conference Presentation)

    NASA Astrophysics Data System (ADS)

    Sharma, Dipika; Satsangi, Vibha R.; Dass Kaura, Sahab; Shrivastav, Rohit; Waghmare, Umesh V.

    2016-10-01

    Band-offsets at BaTiO3/Cu2O heterojunction and enhanced photoelectrochemical response: theory and experiment Dipika Sharmaa, Vibha R. Satsangib, Rohit Shrivastava, Umesh V. Waghmarec, Sahab Dassa aDepartment of Chemistry, Dayalbagh Educational Institute, Agra-282 110 (India) bDepartment of Physics and Computer Sciences, Dayalbagh Educational Institute, Agra-282 110 (India) cTheoretical Sciences Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur, Bangalore-560 064 (India) * Phone: +91-9219695960. Fax: +91-562-2801226. E-mail: drsahabdas@gmail.com. Study on photoelectrochemical activity of pristine BaTiO3, Cu2O and BaTiO3/Cu2O heterojunction has been carried out using DFT based band offsets and charge carriers effective mass calculations and their experimental verification. The results of DFT calculations show that BaTiO3 and Cu2O have staggered type band alignment after the heterojunction formation and high mobility of electrons in Cu2O as compared to the electrons in BaTiO3. Staggered type band edges alignment and high mobility of electrons and holes improved the separation of photo-generated charge carriers in BaTiO3/Cu2O heterojunction. To validate the theoretical results experiments were carried out on pristine BaTiO3, Cu2O and BaTiO3/Cu2O heterojunction with varying thickness of Cu2O. All samples were characterized by X- Ray Diffractometer, SEM and UV-Vis spectrometry. Nanostructured thin films of pristine BaTiO3, Cu2O and BaTiO3/Cu2O heterojunction were used as photoelectrode in the photoelectrochemical cell for water splitting reaction. Maximum photocurrent density of 1.44 mA/cm2 at 0.90 V/SCE was exhibited by 442 nm thick BaTiO3/Cu2O heterojunction photoelectrode Increased photocurrent density and enhanced photoconversion efficiency, exhibited by the heterojunction may be attributed to improved conductivity and enhanced separation of the photogenerated carriers at the BaTiO3/Cu2O interface. The experimental results and first

  11. A review of photoelectrochemical methods for the utilization of solar energy

    NASA Astrophysics Data System (ADS)

    Peraldo Bicelli, L.

    1983-12-01

    A photoelectrochemical cell is defined as a cell in which the irradiation of an electrode in contact with a suitable electrolyte produces a change in the electrode potential with respect to a reference electrode (open-circuit conditions) or produces a change in the current flowing in the galvanic cell containing the electrode (closed-circuit conditions). Such cells can be divided into photovoltaic electrochemical cells and photoelectrosynthetic cells. The latter cells can be subdivided again into photoelectrolytic cells and photocatalytic cells. The theory regarding the considered cells is discussed, taking into account the semiconductor-electrolyte junction, the operating principles of the cells, and photocorrosion and photostability. Design, performance, and problems concerning the cells are illustrated with the aid of examples. Attention is given to studies regarding regenerative cells, polycrystalline and thin film electrodes, water photoelectrolysis, other processes for producing hydrogen, the use of semiconductor materials, organic semiconductor cells, and photogalvanic cells.

  12. Photoelectrochemical Carbon Dioxide Reduction Using a Nanoporous Ag Cathode.

    PubMed

    Zhang, Yan; Luc, Wesley; Hutchings, Gregory S; Jiao, Feng

    2016-09-21

    Solar fuel production from abundant sources using photoelectrochemical (PEC) systems is an attractive approach to address the challenges associated with the intermittence of solar energy. In comparison to electrochemical systems, PEC cells directly utilize solar energy as the energy input, and if necessary, then an additional external bias can be applied to drive the desired reaction. In this work, a PEC cell composing of a Ni-coated Si photoanode and a nanoporous Ag cathode was developed for CO2 conversion to CO. The thin Ni layer not only protected the Si wafer from photocorrosion but also served as the oxygen evolution catalyst. At an external bias of 2.0 V, the PEC cell delivered a current density of 10 mA cm(-2) with a CO Faradaic efficiency of ∼70%. More importantly, a stable performance up to 3 h was achieved under photoelectrolysis conditions, which is among the best literature-reported performances for PEC CO2 reduction cells. The photovoltage of the PEC cell was estimated to be ∼0.4 V, which corresponded to a 17% energy saving by solar energy utilization. Postreaction structural analysis showed the corrosion of the Ni layer at the Si photoanode/catalyst interface, which caused performance degradation under prolonged operations. A stable oxygen evolution catalyst with a robust interface is crucial to the long-term stability of PEC CO2 reduction cells.

  13. Investigation of Cadmium Selenide Photoelectrochemical Cells.

    DTIC Science & Technology

    1980-01-01

    with a Perkin-Elmer model 356 spectrophotometer equipped with 1 millimeter path length cuvettes. The Lambert - Beer absorption law was then applied to...calculate an absorbance spectrum for the following path lengths: 0.5, 2, 5 and 10 m. (The Lambert - Beer law states that ab- , sorbance is directly...UNCLASSIFIED UNCLASSIFIED 5 The basic light sources which were used in the PEC evaluation were as follows: (1) Source No. 1 was the single 250 W quartz-halogen

  14. Self bleaching photoelectrochemical-electrochromic device

    DOEpatents

    Bechinger, Clemens S.; Gregg, Brian A.

    2002-04-09

    A photoelectrochemical-electrochromic device comprising a first transparent electrode and a second transparent electrode in parallel, spaced relation to each other. The first transparent electrode is electrically connected to the second transparent electrode. An electrochromic material is applied to the first transparent electrode and a nanoporous semiconductor film having a dye adsorbed therein is applied to the second transparent electrode. An electrolyte layer contacts the electrochromic material and the nanoporous semiconductor film. The electrolyte layer has a redox couple whereby upon application of light, the nanoporous semiconductor layer dye absorbs the light and the redox couple oxidizes producing an electric field across the device modulating the effective light transmittance through the device.

  15. Microcontact-printing-assisted access of graphitic carbon nitride films with favorable textures toward photoelectrochemical application.

    PubMed

    Liu, Jian; Wang, Hongqiang; Chen, Zu Peng; Moehwald, Helmuth; Fiechter, Sebastian; van de Krol, Roel; Wen, Liping; Jiang, Lei; Antonietti, Markus

    2015-01-27

    An "ink" (cyanamide) infiltrated anodic aluminum oxide (AAO) stamp is found capable of printing carbon nitride films featuring regular microstructures of the stamp onto the substrates via in situ "chemical vapor deposition". A photocurrent density of 30.2 μA cm(-2 --) at 1.23 VRHE is achieved for a film on a conductive substrate, which is so far the highest value for pure carbon nitride based photoelectrochemical devices.

  16. Electrochemical and photoelectrochemical properties of condensed layers of cyanine dyes: Dye layers on platinum

    SciTech Connect

    Sviridov, D.V.; Kulak, A.I.

    1987-12-01

    The authors discuss the electrochemical and photoelectrochemical properties of pigment electrodes based on a number of carbocyanine dyes: the pyridinium slat of 3,3'-di-..gamma..-sulfopropyl-9-ethyl-4,5,4',5'-dibenzothiacarbocyanine betaine, 3,3',9-triethyl-4,5,4',5'-dibenzothiacarbocyanine bromide, 3,3'9-trimethyl-4,5,4',5'-dibenzothiacarbocyanine chloride, and 1,1',3,3'-tetraethyl-5,6,5',6'-tetrachloroimidacarbocyanine iodide.

  17. Enhanced Photoelectrochemical Immunosensing Platform Based on CdSeTe@CdS:Mn Core-Shell Quantum Dots-Sensitized TiO2 Amplified by CuS Nanocrystals Conjugated Signal Antibodies.

    PubMed

    Fan, Gao-Chao; Zhu, Hua; Du, Dan; Zhang, Jian-Rong; Zhu, Jun-Jie; Lin, Yuehe

    2016-03-15

    A new, ultrasensitive photoelectrochemical immunosensing platform was established on the basis of CdSeTe@CdS:Mn core-shell quantum dots-sensitized TiO2 coupled with signal amplification of CuS nanocrystals conjugated signal antibodies. In this proposal, carcinoembryonic antigen (CEA, Ag) was selected as an example of target analyte to show the analytical performances of the platform. Specifically, TiO2-modified electrode was first assembled with CdSeTe alloyed quantum dots (AQDs) via electrostatic adsorption assisted by oppositely charged polyelectrolyte, and then further deposited with CdS:Mn shells on the surface of CdSeTe AQDs via successive ionic layer adsorption and reaction strategy, forming TiO2/CdSeTe@CdS:Mn sensitization structure, which was used as photoelectrochemical matrix to immobilize capture CEA antibodies (Ab1); signal CEA antibodies (Ab2) were labeled with CuS nanocrystals (NCs) to form Ab2-CuS conjugates, which were employed as signal amplification elements when specific immunoreaction occurred. The ultrahigh sensitivity of this immunoassay resulted from the following two aspects. Before detection of target Ag, the TiO2/CdSeTe@CdS:Mn sensitization structure could adequately harvest the exciting light with different bands, evidently expedite the electron transfer, and effectively depress the charge recombination, resulting in noticeably increased photocurrent. When target Ag existed, the Ab2-CuS conjugates could dramatically decrease the photocurrent due to competitive absorption of exciting light and consumption of electron donor for CuS NCs coupled with steric hindrance of Ab2 molecules. The fabricated photoelectrochemical immunosensor showed a low limit of detection of 0.16 pg/mL and a wide linear range from 0.5 pg/mL to 100 ng/mL for CEA detection, and it also exhibited good specificity, reproducibility, and stability.

  18. Au@CdS Core–Shell Nanoparticles‐Modified ZnO Nanowires Photoanode for Efficient Photoelectrochemical Water Splitting

    PubMed Central

    Guo, Chun Xian; Xie, Jiale; Yang, Hongbin

    2015-01-01

    Hydrogen production from water splitting using solar energy based on photoelectrochemical (PEC) cells has attracted increasing attention because it leaves less of a carbon footprint and has economic superiority of solar and hydrogen energy. Oxide semiconductors such as ZnO possessing high stability against photocorrosion in hole scavenger systems have been widely used to build photoanodes of PEC cells but under visible light their conversion efficiencies with respect to incident‐photon‐to‐current conversion efficiency (IPCE) measured without external bias are still not satisfied. An innovative way is presented here to significantly improve the conversion efficiency of PEC cells by constructing a core–shell structure‐based photoanode comprising Au@CdS core–shell nanoparticles on ZnO nanowires (Au@CdS‐ZnO). The Au core offers strong electronic interactions with both CdS and ZnO resulting in a unique nanojunction to facilitate charge transfer. The Au@CdS‐ZnO PEC cell under 400 nm light irradiation without any applied bias provides an IPCE of 14.8%. Under AM1.5 light illumination with a bias of 0.4 V, the Au@CdS‐ZnO PEC cell produces H2 at a constant rate of 11.5 μmol h−1 as long as 10 h. This work provides a fundamental insight to improve the conversion efficiency for visible light in water splitting. PMID:27980921

  19. Photo-electrochemical studies of chemically deposited nanocrystalline meso-porous n-type TiO2 thin films for dye-sensitized solar cell (DSSC) using simple synthesized azo dye

    NASA Astrophysics Data System (ADS)

    Ezema, C. G.; Nwanya, A. C.; Ezema, B. E.; Patil, B. H.; Bulakhe, R. N.; Ukoha, P. O.; Lokhande, C. D.; Maaza, Malik; Ezema, Fabian I.

    2016-04-01

    Nanocrystalline titanium dioxide (TiO2) thin films were deposited by successive ionic layer adsorption and reaction method onto fluorine doped tin oxide coated glass substrate at room temperature (300 K). Titanium trichloride and sodium hydroxide were used as cationic and anionic sources, respectively. The as-deposited and annealed films were characterized for structural, morphological, optical, electrical and wettability properties. The photoelectrochemical study of TiO2 sensitized with a laboratory synthesized organic dye (azo) was evaluated in the polyiodide electrolyte at 40 mW cm-2 light illumination intensity. The photovoltaic characteristics show a fill factor of 0.24 and solar conversion efficiency value of 0.032 % for a TiO2 thickness of 0.96 µm as compared to efficiency of 0.014 % for rose Bengal of the same thickness.

  20. Spectral sensitization of nanocrystalline solar cells

    DOEpatents

    Spitler, Mark T.; Ehret, Anne; Stuhl, Louis S.

    2002-01-01

    This invention relates to dye sensitized polycrystalline photoelectrochemical solar cells for use in energy transduction from light to electricity. It concerns the utility of highly absorbing organic chromophores as sensitizers in such cells and the degree to which they may be utilized alone and in combination to produce an efficient photoelectrochemical cell, e.g., a regenerative solar cell.

  1. Development & Optimization of Materials and Processes for a Cost Effective Photoelectrochemical Hydrogen Production System. Final report

    SciTech Connect

    McFarland, Eric W

    2011-01-17

    The overall project objective was to apply high throughput experimentation and combinatorial methods together with novel syntheses to discover and optimize efficient, practical, and economically sustainable materials for photoelectrochemical production of bulk hydrogen from water. Automated electrochemical synthesis and photoelectrochemical screening systems were designed and constructed and used to study a variety of new photoelectrocatalytic materials. We evaluated photocatalytic performance in the dark and under illumination with or without applied bias in a high-throughput manner and did detailed evaluation on many materials. Significant attention was given to -Fe2O3 based semiconductor materials and thin films with different dopants were synthesized by co-electrodeposition techniques. Approximately 30 dopants including Al, Zn, Cu, Ni, Co, Cr, Mo, Ti, Pt, etc. were investigated. Hematite thin films doped with Al, Ti, Pt, Cr, and Mo exhibited significant improvements in efficiency for photoelectrochemical water splitting compared with undoped hematite. In several cases we collaborated with theorists who used density functional theory to help explain performance trends and suggest new materials. The best materials were investigated in detail by X-ray diffraction (XRD), scanning electron microscopy (SEM), ultraviolet-visual spectroscopy (UV-Vis), X-ray photoelectron spectroscopy (XPS). The photoelectrocatalytic performance of the thin films was evaluated and their incident photon

  2. Graphene oxide modified TiO2 nanotube arrays: enhanced visible light photoelectrochemical properties

    NASA Astrophysics Data System (ADS)

    Song, Peng; Zhang, Xiaoyan; Sun, Mingxuan; Cui, Xiaoli; Lin, Yuehe

    2012-02-01

    Novel nanocomposite films, based on graphene oxide (GO) and TiO2 nanotube arrays, were synthesized by assembling GO on the surface of self-organized TiO2 nanotube arrays through a simple impregnation method. The composite films were characterized with field emission scanning electron microscopy, X-ray diffraction, Raman spectroscopy and UV-vis diffuse reflectance spectroscopy. The photoelectrochemical properties of the composite nanotube arrays were investigated under visible light illumination. Remarkably enhanced visible light photoelectrochemical response was observed for the GO decorated TiO2 nanotube composite electrode compared with pristine TiO2 nanotube arrays. The sensitizing effect of GO on the photoelectrochemical response of the TiO2 nanotube arrays was demonstrated and about 15 times enhanced maximum photoconversion efficiency was obtained with the presence of GO. An enhanced photocatalytic activity of the TiO2 nanotube arrays towards the degradation of methyl blue was also demonstrated after modification with GO. The results presented here demonstrate GO to be efficient for the improved utilization of visible light for TiO2 nanotube arrays.

  3. Graphene oxide modified TiO2 nanotube arrays: enhanced visible light photoelectrochemical properties.

    PubMed

    Song, Peng; Zhang, Xiaoyan; Sun, Mingxuan; Cui, Xiaoli; Lin, Yuehe

    2012-03-07

    Novel nanocomposite films, based on graphene oxide (GO) and TiO(2) nanotube arrays, were synthesized by assembling GO on the surface of self-organized TiO(2) nanotube arrays through a simple impregnation method. The composite films were characterized with field emission scanning electron microscopy, X-ray diffraction, Raman spectroscopy and UV-vis diffuse reflectance spectroscopy. The photoelectrochemical properties of the composite nanotube arrays were investigated under visible light illumination. Remarkably enhanced visible light photoelectrochemical response was observed for the GO decorated TiO(2) nanotube composite electrode compared with pristine TiO(2) nanotube arrays. The sensitizing effect of GO on the photoelectrochemical response of the TiO(2) nanotube arrays was demonstrated and about 15 times enhanced maximum photoconversion efficiency was obtained with the presence of GO. An enhanced photocatalytic activity of the TiO(2) nanotube arrays towards the degradation of methyl blue was also demonstrated after modification with GO. The results presented here demonstrate GO to be efficient for the improved utilization of visible light for TiO(2) nanotube arrays.

  4. Photoelectrochemical decomposition of pollutants with energy recovery

    SciTech Connect

    Rusling, J.F.; Mbindyo, J.

    1995-12-31

    Catalytic photo-oxidation using titanium dioxide converts most organic pollutants to carbon dioxide, water, and inorganic ions. This process was explored by using laboratory scale photoelectrochemical reactors with nanoparticulate titanium dioxide anodes and cathodes capable of producing hydrogen gas by the reduction of water. Using chlorophenols as test pollutants, quantitative mineralization of milligram quantities of 4-chlorophenol in water to CO{sub 2}, H{sub 2}O and HO was demonstrated using simulated sunlight to illuminate the anode. Hydrogen generation was achieved simultaneously with 65% coulombic efficiency when using acidic catholyte and basic anolyte solutions. Alternatively, the reactor can be used to produce electricity. Results suggest the feasibility of a photoreactor which decomposes pollutants with sunlight, and recovers some of the energy input as hydrogen or electricity.

  5. Wiring of Photosystem II to Hydrogenase for Photoelectrochemical Water Splitting.

    PubMed

    Mersch, Dirk; Lee, Chong-Yong; Zhang, Jenny Zhenqi; Brinkert, Katharina; Fontecilla-Camps, Juan C; Rutherford, A William; Reisner, Erwin

    2015-07-08

    In natural photosynthesis, light is used for the production of chemical energy carriers to fuel biological activity. The re-engineering of natural photosynthetic pathways can provide inspiration for sustainable fuel production and insights for understanding the process itself. Here, we employ a semiartificial approach to study photobiological water splitting via a pathway unavailable to nature: the direct coupling of the water oxidation enzyme, photosystem II, to the H2 evolving enzyme, hydrogenase. Essential to this approach is the integration of the isolated enzymes into the artificial circuit of a photoelectrochemical cell. We therefore developed a tailor-made hierarchically structured indium-tin oxide electrode that gives rise to the excellent integration of both photosystem II and hydrogenase for performing the anodic and cathodic half-reactions, respectively. When connected together with the aid of an applied bias, the semiartificial cell demonstrated quantitative electron flow from photosystem II to the hydrogenase with the production of H2 and O2 being in the expected two-to-one ratio and a light-to-hydrogen conversion efficiency of 5.4% under low-intensity red-light irradiation. We thereby demonstrate efficient light-driven water splitting using a pathway inaccessible to biology and report on a widely applicable in vitro platform for the controlled coupling of enzymatic redox processes to meaningfully study photocatalytic reactions.

  6. Biofuel from biomass via photo-electrochemical reactions: An overview

    NASA Astrophysics Data System (ADS)

    Ibrahim, N.; Kamarudin, S. K.; Minggu, L. J.

    2014-08-01

    Biomass is attracting a great deal of attention as a renewable energy resource to reduce carbon dioxide (CO2) emissions. Converting biomass from municipal, agricultural and livestock into biofuel and electrical power has significant environmental and economic advantages. The conversion of biomass into practical energy requires elegant designs and further investigation. Thus, biomass is a promising renewable energy source due to its low production cost and simple manufacturing processes. Biofuel (hydrogen and methanol) from biomass will be possible to be used for transportation with near-zero air pollution, involves efficient uses of land and major contribution to reduce dependence on insecure source of petroleum. Photoelectrochemical (PEC) reactions study has potential pathway for producing fuel from biomass and bio-related compound in the near future. This review highlights recent work related to the PEC conversion of biomass and bio-related compounds into useful biofuels and electricity. This review covers different types of photochemical reaction cells utilizing various types of organic and inorganic waste. It also presents recent developments in photoelectrodes, photocatalysts and electrolytes as well as the production of different types of fuel from PEC cells and highlights current developments and problems in PEC reactions.

  7. Highly active oxide photocathode for photoelectrochemical water reduction.

    PubMed

    Paracchino, Adriana; Laporte, Vincent; Sivula, Kevin; Grätzel, Michael; Thimsen, Elijah

    2011-06-01

    A clean and efficient way to overcome the limited supply of fossil fuels and the greenhouse effect is the production of hydrogen fuel from sunlight and water through the semiconductor/water junction of a photoelectrochemical cell, where energy collection and water electrolysis are combined into a single semiconductor electrode. We present a highly active photocathode for solar H(2) production, consisting of electrodeposited cuprous oxide, which was protected against photocathodic decomposition in water by nanolayers of Al-doped zinc oxide and titanium oxide and activated for hydrogen evolution with electrodeposited Pt nanoparticles. The roles of the different surface protection components were investigated, and in the best case electrodes showed photocurrents of up to -7.6 mA cm(-2) at a potential of 0 V versus the reversible hydrogen electrode at mild pH. The electrodes remained active after 1 h of testing, cuprous oxide was found to be stable during the water reduction reaction and the Faradaic efficiency was estimated to be close to 100%.

  8. Highly active oxide photocathode for photoelectrochemical water reduction

    NASA Astrophysics Data System (ADS)

    Paracchino, Adriana; Laporte, Vincent; Sivula, Kevin; Grätzel, Michael; Thimsen, Elijah

    2011-06-01

    A clean and efficient way to overcome the limited supply of fossil fuels and the greenhouse effect is the production of hydrogen fuel from sunlight and water through the semiconductor/water junction of a photoelectrochemical cell, where energy collection and water electrolysis are combined into a single semiconductor electrode. We present a highly active photocathode for solar H2 production, consisting of electrodeposited cuprous oxide, which was protected against photocathodic decomposition in water by nanolayers of Al-doped zinc oxide and titanium oxide and activated for hydrogen evolution with electrodeposited Pt nanoparticles. The roles of the different surface protection components were investigated, and in the best case electrodes showed photocurrents of up to -7.6 mA cm-2 at a potential of 0 V versus the reversible hydrogen electrode at mild pH. The electrodes remained active after 1 h of testing, cuprous oxide was found to be stable during the water reduction reaction and the Faradaic efficiency was estimated to be close to 100%.

  9. Vertically aligned Ta3N5 nanorod arrays for solar-driven photoelectrochemical water splitting.

    PubMed

    Li, Yanbo; Takata, Tsuyoshi; Cha, Dongkyu; Takanabe, Kazuhiro; Minegishi, Tsutomu; Kubota, Jun; Domen, Kazunari

    2013-01-04

    A vertically aligned Ta(3)N(5) nanorod photoelectrode is fabricated by through-mask anodization and nitridation for water splitting. The Ta(3)N(5) nanorods, working as photoanodes of a photoelectrochemical cell, yield a high photocurrent density of 3.8 mA cm(-2) at 1.23 V versus a reversible hydrogen electrode under AM 1.5G simulated sunlight and an incident photon-to-current conversion efficiency of 41.3% at 440 nm, one of the highest activities reported for photoanodes so far.

  10. Highly stable chemisorption of dyes with pyridyl anchors over TiO2: application in dye-sensitized photoelectrochemical water reduction in aqueous media.

    PubMed

    Takijiri, Kohei; Morita, Kohei; Nakazono, Takashi; Sakai, Ken; Ozawa, Hironobu

    2017-03-09

    A polypyridyl ruthenium sensitizer possessing pyridyl anchors (Ru-py) forms much stronger chemical linkages to TiO2 surfaces compared to the conventional carboxylate and phosphonate ones. A highly stable dye-sensitized photoelectrochemical cell for water reduction is successfully demonstrated using this technique.

  11. [Cell based therapy for COPD].

    PubMed

    Kubo, Hiroshi

    2007-04-01

    To develop a new cell based therapy for chronic obstructive pulmonary disease (COPD), we need to understand 1) the role of tissue-specific and bone marrow-derived stem cells, 2) extracellular matrix, and 3) growth factors. Recently, bronchioalveolar stem cells were identified in murine distal lungs. Impairment of these stem cells may cause improper lung repair after inflammation, resulting in pulmonary emphysema. Bone marrow-derived cells are necessary to repair injured lungs. However, the long term role of these cells is not understood yet. Although we need more careful analysis and additional experiments, growth factors, such as hepatocyte growth factor, are good candidates for the new cell based therapy for COPD. Lung was believed as a non-regenerative organ. Based on these recent reports about lung regeneration and stem cells, however, new strategies to treat COPD and a new point of view to understand the pathophysiology of COPD are rising.

  12. Photocatalysis and photoelectrochemical properties of tungsten trioxide nanostructured films.

    PubMed

    Lai, Chin Wei

    2014-01-01

    Tungsten trioxide (WO₃) possesses a small band gap energy of 2.4-2.8 eV and is responsive to both ultraviolet and visible light irradiation including strong absorption of the solar spectrum and stable physicochemical properties. Thus, controlled growth of one-dimensional (1D) WO₃ nanotubular structures with desired length, diameter, and wall thickness has gained significant interest. In the present study, 1D WO₃ nanotubes were successfully synthesized via electrochemical anodization of tungsten (W) foil in an electrolyte composed of 1 M of sodium sulphate (Na₂SO₄) and ammonium fluoride (NH₄F). The influence of NH₄F content on the formation mechanism of anodic WO₃ nanotubular structure was investigated in detail. An optimization of fluoride ions played a critical role in controlling the chemical dissolution reaction in the interface of W/WO₃. Based on the results obtained, a minimum of 0.7 wt% of NH₄F content was required for completing transformation from W foil to WO₃ nanotubular structure with an average diameter of 85 nm and length of 250 nm within 15 min of anodization time. In this case, high aspect ratio of WO₃ nanotubular structure is preferred because larger active surface area will be provided for better photocatalytic and photoelectrochemical (PEC) reactions.

  13. Photoelectrochemical fabrication of spectroscopic diffraction gratings, phase 2

    NASA Technical Reports Server (NTRS)

    Rauh, R. David; Carrabba, Michael M.; Li, Jianguo; Cartland, Robert F.; Hachey, John P.; Mathew, Sam

    1990-01-01

    This program was directed toward the production of Echelle diffraction gratings by a light-driven, electrochemical etching technique (photoelectrochemical etching). Etching is carried out in single crystal materials, and the differential rate of etching of the different crystallographic planes used to define the groove profiles. Etching of V-groove profiles was first discovered by us during the first phase of this project, which was initially conceived as a general exploration of photoelectrochemical etching techniques for grating fabrication. This highly controllable V-groove etching process was considered to be of high significance for producing low pitch Echelles, and provided the basis for a more extensive Phase 2 investigation.

  14. Applications of Metal Oxide Materials in Dye Sensitized Photoelectrosynthesis Cells for Making Solar Fuels: Let the Molecules do the Work

    SciTech Connect

    Alibabaei, Leila; Luo, Hanlin; House, Ralph L.; Hoertz, Paul G.; Lopez, Rene; Meyer, Thomas J.

    2013-01-01

    Solar fuels hold great promise as a permanent, environmentally friendly, long-term renewable energy source, that would be readily available across the globe. In this account, an approach to solar fuels is described based on Dye Sensitized Photoelectrosynthesis Cells (DSPEC) that mimic the configuration used in Dye Sensitized Solar Cells (DSSC), but with the goal of producing oxygen and a high energy solar fuel in the separate compartments of a photoelectrochemical cell rather than a photopotential and photocurrent.

  15. Wire-shaped quantum dots-sensitized solar cells based on nanosheets and nanowires.

    PubMed

    Chen, Haining; Zhu, Liqun; Wang, Meng; Liu, Huicong; Li, Weiping

    2011-11-25

    Wire-shaped quantum dots-sensitized solar cells (WS-QDSCs) based on nanosheets and nanowires were fabricated and investigated for this paper. The nanosheets grown on stainless steel (SS) wire by electrodeposition were mainly composed of Zn₅(OH)₈Cl₂·H₂O and most of the Zn₅(OH)₈Cl₂·H₂O was converted to ZnO by post-treatment, and ZnO nanowires were directly grown on SS wire by the hydrothermal method. CdS QDs were deposited on nanosheets and nanowires by successive ionic layer adsorption and reaction method. The results of photoelectrochemical performance indicated that WS-QDSCs showed a similar conversion efficiency in polysulfide and Na₂SO₄ electrolytes, while the WS-QDSCs based on the Cu2S counter electrode achieved much higher performance than those based on SS and Cu counter electrodes. By optimizing electrodeposition duration, the WS-QDSCs based on nanosheets presented the highest conversion efficiency of 0.60% for the duration of 20 min. Performance comparison indicated that the WS-QDSC based on nanosheets showed very superior performance to that based on the nanowires with similar film thickness.

  16. Formation of single-walled carbon nanotube thin films enriched with semiconducting nanotubes and their application in photoelectrochemical devices.

    PubMed

    Wei, Li; Tezuka, Noriyasu; Umeyama, Tomokazu; Imahori, Hiroshi; Chen, Yuan

    2011-04-01

    Single-walled carbon nanotube (SWCNT) thin films, containing a high-density of semiconducting nanotubes, were obtained by a gel-centrifugation method. The agarose gel concentration and centrifugation force were optimized to achieve high semiconducting and metallic nanotube separation efficiency at 0.1 wt% agarose gel and 18,000g. The thickness of SWCNT films can be precisely controlled from 65 to 260 nm with adjustable transparency. These SWCNT films were applied in photoelectrochemical devices. Photocurrents generated by semiconducting SWCNT enriched films are 15-35% higher than those by unsorted SWCNT films. This is because of reducing exciton recombination channels as a result of the removal of metallic nanotubes. Thinner films generate higher photocurrents because charge carriers have less chances going in metallic nanotubes for recombination, before they can reach electrodes. Developing more scalable and selective methods for high purity semiconducting SWCNTs is important to further improve the photocurrent generation efficiency by using SWCNT-based photoelectrochemical devices.

  17. The effect of silver nanoparticles/graphene-coupled TiO2 beads photocatalyst on the photoconversion efficiency of photoelectrochemical hydrogen production.

    PubMed

    Ke, Chun-Ren; Guo, Jyun-Sheng; Su, Yen-Hsun; Ting, Jyh-Ming

    2016-10-28

    In this work, a novel configuration of the photoelectrochemical hydrogen production device is demonstrated. It is based on TiO2 beads as the primary photoanode material with the addition of a heterostructure of silver nanoparticles/graphene. The heterostructure not only caters to a great improvement in light harvesting efficiency (LHE) but also enhances the charge collection efficiency. For LHE, the optimized cell based on TiO2 beads/Ag/graphene shows a 47% gain as compared to the cell having a photoanode of commercial P25 TiO2 powders. For the charge collection efficiency, there is a pronounced improvement of an impressive value of 856%. The reason for the improvement in light absorption is attributed to either the light scattering of TiO2 beads or the surface plasmonic resonance on the Ag nanoparticles/graphene. The photoconversion efficiency (PCE) of the resulting cells is also presented and discussed. The PCE of the TiO2 beads/Ag/graphene cell is approximately 2.5 times than that of pure P25 cell.

  18. CuInSe/sub 2/-based photoelectrochemical cells: their use in characterization of thin CuInSe/sub 2/ films, and as photovoltaic cells per se

    SciTech Connect

    Cahen, D; Chen, Y W; Ireland, P J; Noufi, R; Turner, J A; Rincon, C; Bachmann, K J

    1984-05-01

    Photoelectrochemistry has been employed to characterize the p-CuInSe/sub 2/ component of the CdS/CuInSe/sub 2/ on-metal and a nonaqueous electrolyte containing a redox couple not specifically adsorbed onto the semiconductor, we can test the films for photovoltaic activity and obtain effective electronic properties of them, before CdS deposition, in a nondestructive manner. Electrochemical decomposition of CuInSe/sub 2/ was investigated in acetonitrile solutions to determine the mechanism of decomposition (n and p) in the dark and under illumination. Electrochemical, solution chemical and surface analyses confirmed at the light-assisted decomposition of CuInSe/sub 2/ resulted in metal ions and elemental chalcogen. On the basis of the results from the electrochemical decomposition, and studies on the solid state chemistry of the (Cu/sub 2/Se)/sub x/(In/sub 2/Se/sub 3/)/sub 1-x/ system and surface analyses, the CuInSe/sub 2//polyiodide interface was stabilized and up to 11.7% conversion efficiencies were obtained.

  19. Cell memory-based therapy

    PubMed Central

    Anjamrooz, Seyed Hadi

    2015-01-01

    Current cell therapies, despite all of the progress in this field, still faces major ethical, technical and regulatory hurdles. Because these issues possibly stem from the current, restricted, stereotypical view of cell ultrastructure and function, we must think radically about the nature of the cell. In this regard, the author's theory of the cell memory disc offers ‘memory-based therapy’, which, with the help of immune system rejuvenation, nervous system control and microparticle-based biodrugs, may have substantial therapeutic potential. In addition to its potential value in the study and prevention of premature cell aging, age-related diseases and cell death, memory therapy may improve the treatment of diseases that are currently limited by genetic disorders, risk of tumour formation and the availability and immunocompatibility of tissue transplants. PMID:26256679

  20. Graphite-based photovoltaic cells

    DOEpatents

    Lagally, Max; Liu, Feng

    2010-12-28

    The present invention uses lithographically patterned graphite stacks as the basic building elements of an efficient and economical photovoltaic cell. The basic design of the graphite-based photovoltaic cells includes a plurality of spatially separated graphite stacks, each comprising a plurality of vertically stacked, semiconducting graphene sheets (carbon nanoribbons) bridging electrically conductive contacts.

  1. High-Potential Porphyrins Supported on SnO 2 and TiO 2 Surfaces for Photoelectrochemical Applications

    DOE PAGES

    Jiang, Jianbing; Swierk, John R.; Materna, Kelly L.; ...

    2016-12-03

    Here, we report CF3-substituted porphyrins and evaluate their use as photosensitizers in water-splitting dye-sensitized photoelectrochemical cells (WS-DSPECs) by characterizing interfacial electron transfer on metal oxide surfaces. Furthermore, by using (CF3)2C6H3 instead of C6F5 substituents at the meso positions, we obtain the desired high potentials while avoiding the sensitivity of C6F5 substituents to nucleophilic substitution, a process that limits the types of synthetic reactions that can be used. Both the number of CF3 groups and the central metal tune the ground and excited-state potentials. A pair of porphyrins bearing carboxylic acids as anchoring groups were deposited on SnO2 and TiO2 surfacesmore » and the interfacial charge-injection and charge-recombination kinetics were characterized by using a combination of computational modeling, terahertz measurements, and transient absorption spectroscopy. We also found that both free-base and metallated porphyrins inject into SnO2, and that recombination is slower for the latter case. Our findings demonstrate that (CF3)2C6H3-substituted porphyrins are promising photosensitizers for use in WS-DSPECs.« less

  2. Synthesis and characterization of Ag2S x Se1-x nanocrystals and their photoelectrochemical property.

    PubMed

    Ji, Changyin; Zhang, Yu; Zhang, Xiaoyu; Wang, Peng; Shen, Hongzhi; Gao, Wenzhu; Wang, Yiding; Yu, William W

    2017-02-10

    I-VI chalcogenide low-toxicity semiconductors and their near-infrared optical property are of great importance for solar cell and biological probe applications. Here, we report the synthesis of Ag2S x Se1-x (x = 0-1) ternary nanocrystals (NCs) and their photoelectrochemical properties, using a refined simple hot-injection reaction recipe. The ICP-MS results show the change of non-metallic composition in products and precursors, which can be well fitted with Vegard's equation. Ternary alloying broadens the absorption spectrum region of Ag2S NCs. It can also balance the transfer of photo-excited electrons through the interfaces of TiO2/Ag2S x Se1-x and Ag2S x Se1-x /electrolyte by minimizing electron-hole recombination. By tuning the compositions, an increase in power conversion efficiency (PCE) was observed with the increase of S composition and the size of the NCs. The photoelectrochemical results reveal that Ag2S x Se1-x ternary NCs exhibit higher conversion efficiency than pure binary NCs. The drop in PCE of the binary NCs is mainly attributed to the decreases of the charge separation following exciton transition.

  3. Synthesis and characterization of Ag2S x Se1-x nanocrystals and their photoelectrochemical property

    NASA Astrophysics Data System (ADS)

    Ji, Changyin; Zhang, Yu; Zhang, Xiaoyu; Wang, Peng; Shen, Hongzhi; Gao, Wenzhu; Wang, Yiding; Yu, William W.

    2017-02-01

    I-VI chalcogenide low-toxicity semiconductors and their near-infrared optical property are of great importance for solar cell and biological probe applications. Here, we report the synthesis of Ag2S x Se1-x (x = 0-1) ternary nanocrystals (NCs) and their photoelectrochemical properties, using a refined simple hot-injection reaction recipe. The ICP-MS results show the change of non-metallic composition in products and precursors, which can be well fitted with Vegard’s equation. Ternary alloying broadens the absorption spectrum region of Ag2S NCs. It can also balance the transfer of photo-excited electrons through the interfaces of TiO2/Ag2S x Se1-x and Ag2S x Se1-x /electrolyte by minimizing electron-hole recombination. By tuning the compositions, an increase in power conversion efficiency (PCE) was observed with the increase of S composition and the size of the NCs. The photoelectrochemical results reveal that Ag2S x Se1-x ternary NCs exhibit higher conversion efficiency than pure binary NCs. The drop in PCE of the binary NCs is mainly attributed to the decreases of the charge separation following exciton transition.

  4. CuO-Functionalized Silicon Photoanodes for Photoelectrochemical Water Splitting Devices.

    PubMed

    Shi, Yuanyuan; Gimbert-Suriñach, Carolina; Han, Tingting; Berardi, Serena; Lanza, Mario; Llobet, Antoni

    2016-01-13

    One main difficulty for the technological development of photoelectrochemical (PEC) water splitting (WS) devices is the fabrication of active, stable and cost-effective photoelectrodes that ensure high performance. Here, we report the development of a CuO/Silicon based photoanode, which shows an onset potential for the water oxidation of 0.53 V vs SCE at pH 9, that is, an overpotential of 75 mV, and high stability above 10 h. These values account for a photovoltage of 420 mV due to the absorbed photons by silicon, as proven by comparing with analogous CuO/FTO electrodes that are not photoactive. The photoanodes have been fabricated by sputtering a thin film of Cu(0) on commercially available n-type Si wafers, followed by a photoelectrochemical treatment in basic pH conditions. The resulting CuO/Cu layer acts as (1) protective layer to avoid the corrosion of nSi, (2) p-type hole conducting layer for efficient charge separation and transportation, and (3) electrocatalyst to reduce the overpotential of the water oxidation reaction. The low cost, low toxicity, and good performance of CuO-based coatings can be an attractive solution to functionalize unstable materials for solar energy conversion.

  5. Photovoltaic and photoelectrochemical conversion of solar energy.

    PubMed

    Grätzel, Michael

    2007-04-15

    The Sun provides approximately 100,000 terawatts to the Earth which is about 10000 times more than the present rate of the world's present energy consumption. Photovoltaic cells are being increasingly used to tap into this huge resource and will play a key role in future sustainable energy systems. So far, solid-state junction devices, usually made of silicon, crystalline or amorphous, and profiting from the experience and material availability resulting from the semiconductor industry, have dominated photovoltaic solar energy converters. These systems have by now attained a mature state serving a rapidly growing market, expected to rise to 300 GW by 2030. However, the cost of photovoltaic electricity production is still too high to be competitive with nuclear or fossil energy. Thin film photovoltaic cells made of CuInSe or CdTe are being increasingly employed along with amorphous silicon. The recently discovered cells based on mesoscopic inorganic or organic semiconductors commonly referred to as 'bulk' junctions due to their three-dimensional structure are very attractive alternatives which offer the prospect of very low cost fabrication. The prototype of this family of devices is the dye-sensitized solar cell (DSC), which accomplishes the optical absorption and the charge separation processes by the association of a sensitizer as light-absorbing material with a wide band gap semiconductor of mesoporous or nanocrystalline morphology. Research is booming also in the area of third generation photovoltaic cells where multi-junction devices and a recent breakthrough concerning multiple carrier generation in quantum dot absorbers offer promising perspectives.

  6. A new approach to light up the application of semiconductor nanomaterials for photoelectrochemical biosensors: using self-operating photocathode as a highly selective enzyme sensor.

    PubMed

    Wang, Guang-Li; Liu, Kang-Li; Dong, Yu-Ming; Wu, Xiu-Ming; Li, Zai-Jun; Zhang, Chi

    2014-12-15

    Due to the intrinsic hole oxidation reaction occurred on the photoanode surface, currently developed photoelectrochemical biosensors suffer from the interference from coexisting reductive species (acting as electron donor) and a novel design strategy of photoelectrode for photoelectrochemical detection is urgently required. In this paper, a self-operating photocathode based on CdS quantum dots sensitized three-dimensional (3D) nanoporous NiO was designed and created, which showed highly selective and reversible response to dissolved oxygen (acting as electron acceptor) in the electrolyte solution. Using glucose oxidase (GOD) as a biocatalyst, a novel photoelectrochemical sensor for glucose was developed. The commonly encountered interferents such as H2O2, ascorbic acid (AA), cysteine (Cys), dopamine (DA), etc., almost had no effect for the cathodic photocurrent of the 3D NiO/CdS electrode, though these substances were proved to greatly influence the photocurrent of photoanodes, which indicated greatly improved selectivity of the method. The method was applied to detect glucose in real samples including serum and glucose injections with satisfactory results. This study could provide a new train of thought on designing of self-operating photocathode in photoelectrochemical sensing, promoting the application of semiconductor nanomaterials in photoelectrochemistry.

  7. Photoelectrochemical determination of tert-butylhydroquinone in edible oil samples employing CdSe/ZnS quantum dots and LiTCNE.

    PubMed

    Monteiro, Thatyara Oliveira; Tanaka, Auro Atsushi; Damos, Flávio Santos; Luz, Rita de Cássia Silva

    2017-07-15

    A novel photoelectrochemical sensor was developed for determination of tert-butyl-hydroquinone (TBHQ) in edible vegetable oils, based on CdSe/ZnS core-shell quantum dots sensitized with lithium tetracyanoethylenide (LiTCNE). The CdSe/ZnS/LiTCNE photoelectrochemical sensor presented a TBHQ photocurrent about 13-fold higher and a charge transfer resistance 62-fold lower than observed for a CdSe/ZnS sensor. The photoelectrochemical sensor showed selectivity to TBHQ, with a high photocurrent for this antioxidant compared to the photocurrent responses for other phenolic antioxidants. The CdSe/ZnS/LiTCNE photoelectrochemical sensor presented a linear range from 0.6 to 250μmolL(-1), sensitivity of 0.012μALμmol(-1), and a limit of detection of 0.21μmolL(-1) for TBHQ, under optimized experimental conditions. The sensor was successfully employed in the analysis of edible oil samples, with recoveries of between 98.25% and 99.83% achieved.

  8. Different strategies for the detection of bioagents using electrochemical and photoelectrochemical genosensors

    NASA Astrophysics Data System (ADS)

    Voccia, Diego; Bettazi, Francesca; Palchetti, Ilaria

    2015-10-01

    In recent years various kinds of biosensors for the detection of pathogens have been developed. A genosensor consists in the immobilization, onto the surface of a chosen transducer, of an oligonucleotide with a specific base sequence called capture probe. The complementary sequence (the analytical target, i.e. a specific sequence of the DNA/RNA of the pathogen) present in the sample is recognized and captured by the probe through the hybridization reaction. The evaluation of the extent of the hybridization allows one to confirm whether the sample contains the complementary sequence of the probe or not. Electrochemical transducers have received considerable attention in connection with the detection of DNA hybridization. Moreover, recently, with the emergence of novel photoelectrochemically active species and new detection schemes, photoelectrochemistry has resulted in substantial progress in its analytical performance for biosensing applications. In this paper, some examples of electrochemical genosensors for multiplexed pathogen detection are shown. Moreover, the preliminary experiments towards the development of a photoelectrochemical genosensor using a TiO2 - nanocrystal-modified ITO electrode are discussed.

  9. Size-selected TiO₂ nanocluster catalysts for efficient photoelectrochemical water splitting.

    PubMed

    Srivastava, Saurabh; Thomas, Joseph Palathinkal; Rahman, Md Anisur; Abd-Ellah, Marwa; Mohapatra, Mamata; Pradhan, Debabrata; Heinig, Nina F; Leung, Kam Tong

    2014-11-25

    Nanoclusters (NCs) are of great interest because they provide the link between the distinct behavior of atoms and nanoparticles and that of bulk materials. Here, we report precisely controlled deposition of size-selected TiO2 NCs produced by gas-phase aggregation in a special magnetron sputtering system. Carefully optimized aggregation length and Ar gas flow are used to control the size distribution, while a quadrupole mass filter provides precise in situ size selection (from 2 to 15 nm). Transmission electron microscopy studies reveal that NCs larger than a critical size (∼8 nm) have a crystalline core with an amorphous shell, while those smaller than the critical size are all amorphous. The TiO2 NCs so produced exhibit remarkable photoelectrochemical water splitting performance in spite of a small amount of material loading. NCs of three different sizes (4, 6, and 8 nm) deposited on H-terminated Si(100) substrates are tested for the photoelectrochemical catalytic performance, and significant enhancement in photocurrent density (0.8 mA/cm(2)) with decreasing NC size is observed with a low saturation voltage of -0.22 V vs Ag/AgCl (0.78 V vs RHE). The enhanced photoconductivity could be attributed to the increase in the specific surface area and increase in the number of active (defect) sites in the amorphous NCs. The unique advantages of the present technique will be further exploited to develop applications based on tunable, size-selected NCs.

  10. ZnO-Au-SnO2 Z-scheme photoanodes for remarkable photoelectrochemical water splitting.

    PubMed

    Li, Jing-Mei; Cheng, Hao-Yun; Chiu, Yi-Hsuan; Hsu, Yung-Jung

    2016-08-25

    For the first time a ZnO nanorod-based Z-scheme heterostructure system was proposed and realized for efficient photoelectrochemical water splitting. The samples were prepared by depositing a thin layer of SnO2 on the Au surface of Au particle-decorated ZnO nanorods. For ZnO-Au-SnO2 nanorods, the embedded Au can mediate interfacial charge transfer by promoting electron transfer from the conduction band of SnO2 to the valence band of ZnO. This vectorial charge transfer resulted in the situation that the photoexcited electrons accumulated at ZnO while the photogenerated holes concentrated at SnO2, giving ZnO-Au-SnO2 substantially high redox powers. Time-resolved photoluminescence spectra suggested that the interfacial charge transfer across the ZnO/Au/SnO2 interface was significantly improved as a result of the Z-scheme charge transfer mechanism. With the substantially high redox powers and significantly improved interfacial charge transfer, ZnO-Au-SnO2 nanorods performed much better as a photoanode in photoelectrochemical water splitting than pristine ZnO, plasmonic Au-decorated ZnO and type-II SnO2-coated ZnO nanorods did. The present study has provided a viable approach to exploit Z-scheme photoanodes in the design of efficient artificial photosynthesis systems for solar energy conversion.

  11. Plasmonic layer enhanced photoelectrochemical response of Fe2O3 photoanodes

    NASA Astrophysics Data System (ADS)

    Verma, Anuradha; Srivastav, Anupam; Banerjee, Anamika; Sharma, Dipika; Sharma, Shailja; Singh, Udai Bhan; Satsangi, Vibha Rani; Shrivastav, Rohit; Avasthi, Devesh Kumar; Dass, Sahab

    2016-05-01

    Present experimental study focuses on the influence of plasmonic layer in Zr-doped Fe2O3 (Z-F) thin film based photoanodes deposited in different configurations for photo splitting of water. The Au nanoparticles (plasmonic layer) as bottom layer and surface (top) layer are incorporated in the spray pyrolytically deposited Z-F thin layer. In addition to this, fabrication of Z-F sandwiched between two plasmonic Au layers (Au/Z-F/Au) as well as plasmonic Au layer sandwiched between two Z-F layers (Z-F/Au/Z-F) are also undertaken. All configurations using plasmonic layer show enhanced photoresponse in comparison to the pristine Z-F samples. The Z-F sandwiched between two plasmonic layers shows the most significant increase in photocurrent density at 0.8 V/SCE (Saturated Calomel Electrode) and also improved optical absorption due to the presence of two palsmonic layers which promote charge transfer and inhibit charge recombination. The obtained results are supported by characterization techniques viz. X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Energy Dispersive X-ray Analysis (EDAX), UV-Visible absorption spectroscopy, Photoelectrochemical properties, Mott-Schottky analysis and efficiency measurements of photoelectrochemical (PEC) sytstem.

  12. Interplay of light transmission and catalytic exchange current in photoelectrochemical systems

    SciTech Connect

    Fountaine, Katherine T.; Lewerenz, Hans J.; Atwater, Harry A.

    2014-10-27

    We develop an analytic current-voltage expression for a variable junction photoelectrochemical (PEC) cell and use it to investigate and illustrate the influence of the optical and electrical properties of catalysts on the optoelectronic performance of PEC devices. Specifically, the model enables a simple, yet accurate accounting of nanostructured catalyst optical and electrical properties through incorporation of an optical transmission factor and active catalytic area factor. We demonstrate the utility of this model via the output power characteristics of an exemplary dual tandem solar cell with indium gallium phosphide and indium gallium arsenide absorbers with varying rhodium catalyst nanoparticle loading. The approach highlights the importance of considering interactions between independently optimized components for optimal PEC device design.

  13. Phthalocyanine based Schottky solar cells

    NASA Astrophysics Data System (ADS)

    Kwong, Chung Yin; Djurisic, Aleksandra B.; Lam, Lillian S. M.; Chan, Wai Kin

    2003-02-01

    Phthalocyanine (Pc) materials are commonly used in organic solar cells. Four different phthalocyanines, nickel phthalocyanine (NiPc), copper phthalocyanine (CuPc), iron phthalocyanine (FePc), and cobalt phthalocyanine (CoPc) have been investigated for organic solar cell applications. The devices consisted of indium tin oxide (ITO) coated lass substrate, Pc layer, and aluminum (al) electrode. It has been found that ITO/CuPc/Al Schottky cell exhibits the best performance. To investigate the influence of the active layer thickness on the cell performance, cells with several different thicknesses were fabricated and optimal value was found. Schottky cell exhibits optimal performance with one ohmic and one barrier contact. However, it is suspected that ITO/CuPc contact is not ohmic. Therefore, we have investigated various ITO surface treatments for improving the performance of CuPc based Schottky solar cell. We have found that cell on ITO treated with HCl and UV-ozone exhibits the best performance. AM1 power conversion efficiency can be improved by 30% compared to cell made with untreated ITO substrate. To improve power conversion efficiency, double or multiplayer structure are required, and it is expected that suitable ITO treatments for those devices will further improve their performance by improving the contact between ITO and phthalocyanine layer.

  14. Efficient water-splitting device based on a bismuth vanadate photoanode and thin-film silicon solar cells.

    PubMed

    Han, Lihao; Abdi, Fatwa F; van de Krol, Roel; Liu, Rui; Huang, Zhuangqun; Lewerenz, Hans-Joachim; Dam, Bernard; Zeman, Miro; Smets, Arno H M

    2014-10-01

    A hybrid photovoltaic/photoelectrochemical (PV/PEC) water-splitting device with a benchmark solar-to-hydrogen conversion efficiency of 5.2% under simulated air mass (AM) 1.5 illumination is reported. This cell consists of a gradient-doped tungsten-bismuth vanadate (W:BiVO4 ) photoanode and a thin-film silicon solar cell. The improvement with respect to an earlier cell that also used gradient-doped W:BiVO4 has been achieved by simultaneously introducing a textured substrate to enhance light trapping in the BiVO4 photoanode and further optimization of the W gradient doping profile in the photoanode. Various PV cells have been studied in combination with this BiVO4 photoanode, such as an amorphous silicon (a-Si:H) single junction, an a-Si:H/a-Si:H double junction, and an a-Si:H/nanocrystalline silicon (nc-Si:H) micromorph junction. The highest conversion efficiency, which is also the record efficiency for metal oxide based water-splitting devices, is reached for a tandem system consisting of the optimized W:BiVO4 photoanode and the micromorph (a-Si:H/nc-Si:H) cell. This record efficiency is attributed to the increased performance of the BiVO4 photoanode, which is the limiting factor in this hybrid PEC/PV device, as well as better spectral matching between BiVO4 and the nc-Si:H cell.

  15. Quantum-size-controlled photoelectrochemical etching of semiconductor nanostructures

    DOEpatents

    Fischer, Arthur J.; Tsao, Jeffrey Y.; Wierer, Jr., Jonathan J.; Xiao, Xiaoyin; Wang, George T.

    2016-03-01

    Quantum-size-controlled photoelectrochemical (QSC-PEC) etching provides a new route to the precision fabrication of epitaxial semiconductor nanostructures in the sub-10-nm size regime. For example, quantum dots (QDs) can be QSC-PEC-etched from epitaxial InGaN thin films using narrowband laser photoexcitation, and the QD sizes (and hence bandgaps and photoluminescence wavelengths) are determined by the photoexcitation wavelength.

  16. The growth mechanism of ordered mesoporous electrodes in view of their response in dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Mohan, Devendra; Jyoti, Divya; Dhar, Rakesh; Singh, Amrik

    2013-06-01

    The effect of morphology of photoelectrode films on photoelectrochemical properties of solar cells has been studied. Crack free mesoporous anatase and rutile films of thickness˜16μm have been synthesized and characterized in concern with their use in dye-sensitized solar cells (DSSC). Surface morphologies have been studied with the help of scanning electron microscopy (SEM). The open-circuit photovoltage for mesoporous anatase and rutile based cells is approximately same but short-circuit photocurrent of mesoporous rutile based cell is lower than that of the mesoporous anatase based cell.

  17. Enhanced Photoelectrochemical Performance from Rationally Designed Anatase/Rutile TiO2 Heterostructures.

    PubMed

    Cao, Fengren; Xiong, Jie; Wu, Fangli; Liu, Qiong; Shi, Zhiwei; Yu, Yanhao; Wang, Xudong; Li, Liang

    2016-05-18

    In a photoelectrochemical (PEC) cell for water splitting, the critical issue is charge separation and transport, which is usually completed by designing semiconductor heterojunctions. TiO2 anatase-rutile mixed junctions could largely improve photocatalytic properties, but impairs PEC water splitting performance. We designed and prepared two types of TiO2 heterostructures with the anatase thin film and rutile nanowire phases organized in different sequences. The two types of heterostructures were used as PEC photoanodes for water splitting and demonstrated completely opposite results. Rutile nanowires on anatase film demonstrated enhanced photocurrent density and onset potential, whereas strong negative performance was obtained from anatase film on rutile nanowire structures. The mechanism was investigated by photoresponse, light absorption and reflectance, and electrochemical impedance spectra. This work revealed the significant role of phase sequence in performance gain of anatase-rutile TiO2 heterostructured PEC photoanodes.

  18. Electrochemical Infilling of CuInSe2 within TiO2 Nanotube Layers and Subsequent Photoelectrochemical Studies

    PubMed Central

    Das, Sayantan; Sopha, Hanna; Krbal, Milos; Zazpe, Raul; Podzemna, Veronika; Prikryl, Jan

    2017-01-01

    Abstract Anodic self‐organized TiO2 nanotube layers (with different aspect ratios) were electrochemically infilled with CuInSe2 nanocrystals with the aim to prepare heterostructures with a photoelectrochemical response in the visible light. The resulting heterostructure assembly was confirmed by field‐emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), and X‐ray diffraction (XRD). High incident photon‐to‐electron conversion efficiency values exceeding 55% were obtained in the visible‐light region. The resulting heterostructures show promise as a candidate for solid‐state solar cells. PMID:28392991

  19. Quantum-dot-sensitized TiO2 inverse opals for photoelectrochemical hydrogen generation.

    PubMed

    Cheng, Chuanwei; Karuturi, Siva Krishna; Liu, Lijun; Liu, Jinping; Li, Hongxing; Su, Liap Tat; Tok, Alfred Iing Yoong; Fan, Hong Jin

    2012-01-09

    A new nanoarchitecture photoelectrode design comprising CdS quantum-dot-sensitized, optically and electrically active TiO(2) inverse opals is developed for photoelectrochemical water splitting. The photoelectrochemical performance shows high photocurrent density (4.84 mA cm(-2) at 0 V vs. Ag/AgCl) under simulated solar-light illumination.

  20. A three-dimensional interconnected hierarchical FeOOH/TiO2/ZnO nanostructural photoanode for enhancing the performance of photoelectrochemical water oxidation

    NASA Astrophysics Data System (ADS)

    Li, Zhenhu; Feng, Shuanglong; Liu, Shuangyi; Li, Xin; Wang, Liang; Lu, Wenqiang

    2015-11-01

    A novel ZnO/TiO2/FeOOH hierarchical nanostructure has been synthesized by a low temperature chemical bath deposition method. The integrated three-dimensional (3D) nanostructure consists of one-dimensional (1D) ZnO/TiO2 core-shell nanowire arrays and two-dimensional (2D) interconnected FeOOH nanosheets. By applying such a hierarchical nanostructure as a photoanode for photoelectrochemical water reaction, higher photostability and photocurrent density are gained compared with the reported ZnO based nanostructures. It is concluded that the giant enhancement of the properties is because, in the process of photoelectrochemical reaction, electron-hole separation and transfer are enhanced efficiently through the ZnO/TiO2 heterojunction, and in the meanwhile, terminal interconnected FeOOH nanosheets play both the roles of a surface catalyst and a protective layer effectively to accelerate water splitting reaction and enhance photostability. Based on such an environmentally friendly hierarchical nanostructure, photoelectrochemical water splitting and other similar reactions could be performed effectively and economically.A novel ZnO/TiO2/FeOOH hierarchical nanostructure has been synthesized by a low temperature chemical bath deposition method. The integrated three-dimensional (3D) nanostructure consists of one-dimensional (1D) ZnO/TiO2 core-shell nanowire arrays and two-dimensional (2D) interconnected FeOOH nanosheets. By applying such a hierarchical nanostructure as a photoanode for photoelectrochemical water reaction, higher photostability and photocurrent density are gained compared with the reported ZnO based nanostructures. It is concluded that the giant enhancement of the properties is because, in the process of photoelectrochemical reaction, electron-hole separation and transfer are enhanced efficiently through the ZnO/TiO2 heterojunction, and in the meanwhile, terminal interconnected FeOOH nanosheets play both the roles of a surface catalyst and a protective layer

  1. Human Neural Cell-Based Biosensor

    DTIC Science & Technology

    2011-06-11

    astrocytes using defined medium conditions, (3) cell-based methods to detect botulinum toxin, and (4) HTS amenable assays for proliferation...progenitors into dopaminergic neurons, motoneurons and astrocytes using defined medium conditions, (3) cell-based methods to detect botulinum toxin...cell line developed for potential commercial distribution. (3) Development of cell based methods to detect botulinum toxin There has been

  2. Standing surface acoustic wave based cell coculture.

    PubMed

    Li, Sixing; Guo, Feng; Chen, Yuchao; Ding, Xiaoyun; Li, Peng; Wang, Lin; Cameron, Craig E; Huang, Tony Jun

    2014-10-07

    Precise reconstruction of heterotypic cell-cell interactions in vitro requires the coculture of different cell types in a highly controlled manner. In this article, we report a standing surface acoustic wave (SSAW)-based cell coculture platform. In our approach, different types of cells are patterned sequentially in the SSAW field to form an organized cell coculture. To validate our platform, we demonstrate a coculture of epithelial cancer cells and endothelial cells. Real-time monitoring of cell migration dynamics reveals increased cancer cell mobility when cancer cells are cocultured with endothelial cells. Our SSAW-based cell coculture platform has the advantages of contactless cell manipulation, high biocompatibility, high controllability, simplicity, and minimal interference of the cellular microenvironment. The SSAW technique demonstrated here can be a valuable analytical tool for various biological studies involving heterotypic cell-cell interactions.

  3. Facile solution deposition of Cu2ZnSnS4 (CZTS) nano-worm films on FTO substrates and its photoelectrochemical property

    NASA Astrophysics Data System (ADS)

    Huang, Yaohan; Li, Guangli; Fan, Qingfei; Zhang, Meili; Lan, Qi; Fan, Ximei; Zhou, Zuowan; Zhang, Chaoliang

    2016-02-01

    In this work, Cu2ZnSnS4 (CZTS) nanoworm films have been directly deposited on fluorine-doped tin oxide (FTO) conductive glass substrates by a solvothermal method using polyethylene glycol 400 (PEG-400) as the solvent and structure-directing agent. The as-obtained CZTS thin films were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Raman spectroscopy, X-ray photoelectron spectrum (XPS), UV-vis spectra and photoelectrochemical measurement. The synthetic conditions, such as reaction temperature, reaction time, solvents, were investigated to know the formation of CZTS thin films. The results showed that PEG-400 plays a key role in the formation of the nanoworms by affecting the crystal growth process. The p-type CZTS nanoworm film with the band gap of 1.62 eV was synthesized at 180 °C for 22 h and the photovoltaic performance was studied by forming a photoelectrochemical cell.

  4. Mapping Photoelectrochemical Current Distribution at Nanoscale Dimensions on Morphologically Controlled BiVO4.

    PubMed

    Chakthranont, Pongkarn; Seitz, Linsey C; Jaramillo, Thomas F

    2015-09-17

    We develop a method that can be used to qualitatively map photocurrent on photoelectrode surfaces, and show its utility for morphologically controlled W-doped BiVO4. The method is based on the deliberate photoinduced sintering of Au NPs, a photon-driven process that indicates oxidation with nanoscale-resolution. This strategy allows us to identify the active regions on W-doped BiVO4 photoelectrodes, and we observe a strong dependence of photoactivity on the electrode morphology, controlled by varying the relative humidity during the sol-gel fabrication process. We find that photoelectrode morphologies that exhibit the most evenly distributed Au sintering are those that yield the highest photoelectrochemical (PEC) activity. Understanding the correlation between electrode morphology and PEC activity is essential for designing structured semiconductors for PEC water splitting.

  5. Spectroelectrochemical analysis of the mechanism of (photo)electrochemical hydrogen evolution at a catalytic interface

    NASA Astrophysics Data System (ADS)

    Pastor, Ernest; Le Formal, Florian; Mayer, Matthew T.; Tilley, S. David; Francàs, Laia; Mesa, Camilo A.; Grätzel, Michael; Durrant, James R.

    2017-02-01

    Multi-electron heterogeneous catalysis is a pivotal element in the (photo)electrochemical generation of solar fuels. However, mechanistic studies of these systems are difficult to elucidate by means of electrochemical methods alone. Here we report a spectroelectrochemical analysis of hydrogen evolution on ruthenium oxide employed as an electrocatalyst and as part of a cuprous oxide-based photocathode. We use optical absorbance spectroscopy to quantify the densities of reduced ruthenium oxide species, and correlate these with current densities resulting from proton reduction. This enables us to compare directly the catalytic function of dark and light electrodes. We find that hydrogen evolution is second order in the density of active, doubly reduced species independent of whether these are generated by applied potential or light irradiation. Our observation of a second order rate law allows us to distinguish between the most common reaction paths and propose a mechanism involving the homolytic reductive elimination of hydrogen.

  6. Spectroelectrochemical analysis of the mechanism of (photo)electrochemical hydrogen evolution at a catalytic interface

    PubMed Central

    Pastor, Ernest; Le Formal, Florian; Mayer, Matthew T.; Tilley, S. David; Francàs, Laia; Mesa, Camilo A.; Grätzel, Michael; Durrant, James R.

    2017-01-01

    Multi-electron heterogeneous catalysis is a pivotal element in the (photo)electrochemical generation of solar fuels. However, mechanistic studies of these systems are difficult to elucidate by means of electrochemical methods alone. Here we report a spectroelectrochemical analysis of hydrogen evolution on ruthenium oxide employed as an electrocatalyst and as part of a cuprous oxide-based photocathode. We use optical absorbance spectroscopy to quantify the densities of reduced ruthenium oxide species, and correlate these with current densities resulting from proton reduction. This enables us to compare directly the catalytic function of dark and light electrodes. We find that hydrogen evolution is second order in the density of active, doubly reduced species independent of whether these are generated by applied potential or light irradiation. Our observation of a second order rate law allows us to distinguish between the most common reaction paths and propose a mechanism involving the homolytic reductive elimination of hydrogen. PMID:28233785

  7. Thin films of TiO2:N for photo-electrochemical applications.

    PubMed

    Trenczek-Zajac, A; Pamula, E; Radecka, M; Kowalski, K; Reszka, A; Brudnik, A; Kusior, E; Zakrzewska, K

    2012-06-01

    Dc-pulsed magnetron sputtering from Ti target in reactive Ar+O2+N2 atmosphere was used to grow stoichiometric TiO2:N and non-stoichiometric TiO2-x:N thin films. X-ray diffraction at glancing incidence, atomic force microscopy AFM, scanning electron microscopy SEM, X-ray photoelectron spectroscopy XPS, and optical spectrophotometry were applied for sample characterization. Measurements of photocurrent versus voltage and wavelength over the ultraviolet uv and visible vis ranges of the light spectrum were performed in order to assess the performance of nitrogen-doped titanium dioxide thin films as photoanodes for hydrogen generation in photoelectrochemical cells, PEC. Undoped TiO2 and TiO2-x films were found to be composed of anatase and rutile mixture with larger anatase crystallites (25-35 nm) while the growth of smaller rutile crystallites (6-10 nm) predominated at higher nitrogen flow rates etaN2 as measured in standard cubic centimeters, sccm. Nitrogen-to-titanium ratio increased from N/Ti = 0.05 at etaN2 = 0.8 sccm for stoichiometric TiO2:N to N/Ti = 0.11 at etaN2 = 0.8 sccm for nonstoichiometric TiO2-x:N thin films. A red-shift in the optical absorbance was observed with an increase in etaN2. Doping with nitrogen improved photoelectrochemical properties over the visible range of the light spectrum in the case of nonstoichiometric samples.

  8. Human Neural Cell-Based Biosensor

    DTIC Science & Technology

    2011-03-11

    neurons, motoneurons and astrocytes using defined medium conditions, (3) cell-based methods to detect botulinum toxin, and (4) fluorescence based assays...medium conditions, (3) cell-based methods to detect botulinum toxin, and (4) fluorescence based assays for proliferation, cell migration, mitochondrial...line will begin shortly. (3) Development of cell based methods to detect botulinum toxin There has been substantial progress in the development

  9. Carbon-based Fuel Cell

    SciTech Connect

    Steven S. C. Chuang

    2005-08-31

    The direct use of coal in the solid oxide fuel cell to generate electricity is an innovative concept for power generation. The C-fuel cell (carbon-based fuel cell) could offer significant advantages: (1) minimization of NOx emissions due to its operating temperature range of 700-1000 C, (2) high overall efficiency because of the direct conversion of coal to CO{sub 2}, and (3) the production of a nearly pure CO{sub 2} exhaust stream for the direct CO{sub 2} sequestration. The objective of this project is to determine the technical feasibility of using a highly active anode catalyst in a solid oxide fuel for the direct electrochemical oxidation of coal to produce electricity. Results of this study showed that the electric power generation from Ohio No 5 coal (Lower Kittanning) Seam, Mahoning County, is higher than those of coal gas and pure methane on a solid oxide fuel cell assembly with a promoted metal anode catalyst at 950 C. Further study is needed to test the long term activity, selectivity, and stability of anode catalysts.

  10. Unbiased photoelectrochemical water splitting in Z-scheme device using W/Mo-doped BiVO4 and Zn(x)Cd(1-x)Se.

    PubMed

    Park, Hyun S; Lee, Heung Chan; Leonard, Kevin C; Liu, Guanjie; Bard, Allen J

    2013-07-22

    Photoelectrochemical water splitting to generate H2 and O2 using only photon energy (with no added electrical energy) has been demonstrated with dual n-type-semiconductor (or Z-scheme) systems. Here we investigated two different Z-scheme systems; one is comprised of two cells with the same metal-oxide semiconductor (W- and Mo-doped bismuth vanadate), that is, Pt-W/Mo-BiVO4, and the other is comprised of the metal oxide and a chalcogenide semiconductor, that is, Pt-W/Mo-BiVO4 and Zn(0.2)Cd(0.8)Se. The redox couples utilized in these Z-scheme configurations were I(-)/IO3(-) or S(2-)/S(n)(2-), respectively. An electrochemical analysis of the system in terms of cell components is shown to illustrate the behavior of the complete photoelectrochemical Z-scheme water-splitting system. H2 gas from the unbiased photolysis of water was detected using gas chromatography-mass spectroscopy and using a membrane-electrode assembly. The electrode configuration to achieve the maximum conversion efficiency from solar energy to chemical energy with the given materials and the Z-scheme is discussed. Here, the possibilities and challenges of Z-scheme unbiased photoelectrochemical water-splitting devices and the materials to achieve practical solar-fuel generation are discussed.

  11. Synthesis and characterization of transition metal oxide nanotubes for photoelectrochemical hydrogen generation

    NASA Astrophysics Data System (ADS)

    Rangaraju, Raghu Raj

    Two different configurations of photo anodes based on anodic iron oxide were investigated for photo electrochemical water oxidation. Self ordered and vertically oriented array of iron oxide nanotubes was obtained by anodization of pure iron substrate in ethylene glycol based electrolyte containing 0.1 M NH4F + 3 vol% water (EGWF solution) at 50 V for 15 minutes. Annealing of the oxide nanotubes in hydrogen environment at 500 °C for 1 h resulted in predominantly hematite phase. The second type of photo anode was obtained by a two-step anodization procedure. This process resulted in a two- layered oxide structure, a top layer of nano-dendrite morphology and a bottom layer of nanoporous morphology. This electrode configuration combined the better photo catalytic properties of the nano-dendritic iron oxide and better electron transportation behavior of vertically oriented nano-channels. Annealing of these double anodized samples in acetylene environment at 550 °C for 10 minutes resulted in a mixture of maghemite and hematite phases. Photo current densities of 0.74 mA/cm2 at 0.2 VAg/AgCl and 1.8 mA/cm 2 at 0.5 VAg/AgCl were obtained under AM 1.5 illumination in 1 M KOH solution. The double anodized samples showed high photo conductivity and more negative flat band potential (-0.8 VAg/AgCl), which are the properties required for promising photo anode materials. Apart from the above work, mild steel which is 10 times less the cost of Ti is also being tested for its photoelectrochemical properties. TiO2 nanotubes synthesized and annealed in different conditions are compared for their quantum efficiency is also carried out in this work. Quantum efficiency measurements gives more reliable and photocurrent data towards photoelectrochemical applications.

  12. Standalone anion- and co-doped titanium dioxide nanotubes for photocatalytic and photoelectrochemical solar-to-fuel conversion.

    PubMed

    Ding, Yuchen; Nagpal, Prashant

    2016-10-14

    Several strategies are currently being investigated for conversion of incident sunlight into renewable sources of energy, and photocatalytic or photoelectrochemical production of solar fuels can provide an important alternative. Titanium dioxide (TiO2) has been heavily investigated as a material of choice due to its excellent optoelectronic properties and stability, and anion-doping proposed as a pathway to improve light absorption as well as improving the efficiency of oxygen production. While several studies have used morphological tuning, elemental doping, and surface engineering in TiO2 to extend its absorption, there is a need to optimize simultaneously charge transport and improve interfacial chemical reaction kinetics. Here we show anion-doped (nitrogen, carbon) standalone TiO2 nanotube membranes that absorb visible light for the water-splitting reaction, using both wireless (photocatalysis) and wired (photoelectrochemical) solar-to-fuel conversion (STFC) cells. Using simulated solar radiation, we show generation of hydrogen as a solar fuel using visible light photocatalysis. Furthermore, using a model we elucidate detailed photophysics and photoelectrochemical properties of these nanotubes, and explain the kinetics of photogenerated charge carriers following light absorption. We show that while visible light induces a superlinear photoresponse for catalytic reduction and may benefit from higher incident light intensity, ultraviolet light shows a linear photoresponse and saturation with higher light flux due to trapping of photogenerated charges (mainly electrons). These results can have important implications for design of other metal-oxide membranes for solar fuel generation, and appropriate design of dopants and induced energy levels in these photocatalysts.

  13. Photochemical solar cells based on dye-sensitization of nanocrystalline TiO{sub 2}

    SciTech Connect

    Deb, S.K.; Ellingson, R.; Ferrere, S.; Frank, A.J.; Gregg, B.A.; Nozik, A.J.; Park, N.; Schlichthoerl, G.

    1998-09-01

    A photoelectrochemical solar cell that is based on the dye-sensitization of thin nanocrystalline films of TiO{sub 2} (anatase) nanoparticles in contact with a non-aqueous liquid electrolyte is described. The cell, fabricated at NREL, shows a conversion efficiency of {approximately} 9.2% at AM1.5, which approaches the best reported value of 10--11% by Graetzel at EPFL in Lausanne, Switzerland. The femtosecond (fs) pump-probe spectroscopy has been used to time resolve the injection of electrons into the conduction band of nanocrystalline TiO{sub 2} films under ambient conditions following photoexcitation of the adsorbed Ru(II)-complex dye. The measurement indicates an instrument-limited {minus}50 fs upper limit on the electron injection time. The authors also report the sensitization of nanocrystalline TiO{sub 2} by a novel iron-based dye, CIS-[Fe{sup II}(2,2{prime}-bipyridine-4,4,{prime}-dicarboxylic acid){sub 2}(CN){sub 2}], a chromophore with an extremely short-lived, nonemissive excited state. The dye also exhibits a unique band selective sensitization through one of its two absorption bands. The operational principle of the device has been studied through the measurement of electric field distribution within the device structure and studies on the pH dependence of dye-redox potential. The incorporation of WO{sub 3}-based electrochromic layer into this device has led to a novel photoelectrochromic device structure for smart window application.

  14. High-throughput synthesis and screening of photon absorbers and photocatalysts for solar fuel cells

    NASA Astrophysics Data System (ADS)

    Mitrovic, Slobodan; Marcin, Martin; Lin, Sean; Jin, Jian

    2012-02-01

    Joint Center for Artificial Photosynthesis is a D.O.E. Energy Innovation Hub conceived to develop solar fuel cell technologies by bringing together the critical mass of scientist and engineers nationwide. The High-Throughput Experimentation group at JCAP is developing pipelines for accelerated discovery of new materials - photon absorbers, photoelectrochemical and electrochemical catalysts - using combinatorial approaches (ink-jet, sol-gel, physical vapor deposition). Thin films of semiconducting metal-oxides, sulfides, nitrides and phosphides are synthesized and screened in high-throughput according to their optical and photoelectrochemical properties, as well as structure and phase. Vast libraries of materials and data are generated and made available to inside and outside research groups. Here we present data on binary, ternary and quaternary metal-oxide systems prepared by the ink-jet technology. The systems include tungsten-based photo-absorbers and nickel-iron-based catalysts for water splitting.

  15. Standing Surface Acoustic Wave Based Cell Coculture

    PubMed Central

    2015-01-01

    Precise reconstruction of heterotypic cell–cell interactions in vitro requires the coculture of different cell types in a highly controlled manner. In this article, we report a standing surface acoustic wave (SSAW)-based cell coculture platform. In our approach, different types of cells are patterned sequentially in the SSAW field to form an organized cell coculture. To validate our platform, we demonstrate a coculture of epithelial cancer cells and endothelial cells. Real-time monitoring of cell migration dynamics reveals increased cancer cell mobility when cancer cells are cocultured with endothelial cells. Our SSAW-based cell coculture platform has the advantages of contactless cell manipulation, high biocompatibility, high controllability, simplicity, and minimal interference of the cellular microenvironment. The SSAW technique demonstrated here can be a valuable analytical tool for various biological studies involving heterotypic cell–cell interactions. PMID:25232648

  16. A series of BCN nanosheets with enhanced photoelectrochemical performances

    NASA Astrophysics Data System (ADS)

    Li, Junqi; Lei, Nan; Hao, Hongjuan; Zhou, Jian

    2017-03-01

    A series of flake-like BCN compounds were produced by calcination at different reaction temperatures via thermal substitution of C atoms with B atoms of boric acid substructures in graphitic carbon nitrides (g-C3N4). The structural and optical properties of the samples were characterized by XRD, TEM, HRTEM, XPS and UV-vis absorption. The photoelectrochemical (PEC) performance of all samples were characterized through photocurrent and electrochemical impedance spectroscopy (EIS) measurement. The test results demonstrated that BCN nanosheets exhibited higher PEC performance with increasing substituted amount of boron.

  17. Efficiency of luminous-energy conversion in semiconducting photoelectrochemical converters

    SciTech Connect

    Kireev, V.B.; Trukhan, E.M.; Filimonov, D.A.

    1981-03-01

    Factors characterizing the conversion efficiency of luminous into chemical energy in semiconducting photoelectrochemical converters are examined. An expression for /gamma/sub //O is discussed in particular; /gamma/sub //O is the quantum yield of photocurrent of the minority carriers sustaining the reaction during which chemical energy is accumulated. The expression for /gamma/sub //O allows, both for the finite rate of electrode surface processes and for recombination in the semiconductor's space-charge layer. It is shown that over a wide range of converter parameters, recombination in the space-charge layer is one of the most important factors for the size of /gamma/sub //O. 17 refs.

  18. Interpretation of quantum yields exceeding unity in photoelectrochemical systems

    SciTech Connect

    Szklarczyk, M.; Allen, R.E.

    1986-10-20

    In photoelectrochemical systems involving light shining on a semiconductor interfaced with an electrolyte, the quantum yield as a function of photon frequency ..nu.. is observed to exhibit a peak at h..nu..roughly-equal2E/sub g/, where E/sub g/ is the band gap of the semiconductor. The maximum in this peak is sometimes found to exceed unity. We provide an interpretation involving surface states and inelastic electron-electron scattering. The theory indicates that the effect should be observable for p-type semiconductors, but not n-type.

  19. Enhanced photoelectrochemical hydrogen production from silicon nanowire array photocathode.

    PubMed

    Oh, Ilwhan; Kye, Joohong; Hwang, Seongpil

    2012-01-11

    Herein we report that silicon nanowires (SiNWs) fabricated via metal-catalyzed electroless etching yielded a photoelectrochemical hydrogen generation performance superior to that of a planar Si, which is attributed to a lower kinetic overpotential due to a higher surface roughness, favorable shift in the flat-band potential, and light-trapping effects of the SiNW surface. The SiNW photocathode yielded a photovoltage of 0.42 V, one of the highest values ever reported for hydrogen generation on p-type Si/electrolyte interfaces.

  20. Effects of anodizing potential and temperature on the growth of anodic TiO2 and its photoelectrochemical properties

    NASA Astrophysics Data System (ADS)

    Kapusta-Kołodziej, Joanna; Syrek, Karolina; Pawlik, Anna; Jarosz, Magdalena; Tynkevych, Olena; Sulka, Grzegorz D.

    2017-02-01

    Although nanoporous/nanotubular anodic TiO2 has been broadly investigated, there is still much to be learned about the fabrication, morphological characterization and applications of anodic TiO2 formed in the glycerol-based electrolyte. Nanoporous anodic titanium oxide (ATO) layers on Ti were prepared via a three-step anodization in a glycerol solution containing NH4F (0.38 wt%) and H2O (1.79 wt%). The effects of anodizing potential (30-70 V) and temperature (10-40 °C) on the growth and morphology of ATO layers were investigated in detail. The structural and morphological characterizations of received ATO layers were performed for the studied potentials and temperatures. Moreover, photoelectrochemical properties of formed TiO2 were studied as well. It has been shown, that the morphology of fabricated nanoporous ATO layers are strongly altered by anodizing temperature and potential. Particularly, an interesting finding is that the growth rate gradually increases up to 50 V independently of anodizing temperature and then decreases when anodizing potential increases to 70 V. Moreover, for all investigated anodizing temperatures, the structural features of ATO layers, such as the cell size, inner layer pore diameter, outer layer pore diameter, increase with increasing anodizing potential. The annealing of ATO samples synthesized at 20 °C revealed that the anatase grain size increases with increasing anodizing potential. It is noteworthy to mention that the highest photoconversion efficiency values were observed for samples synthesized at the anodizing temperature of 20 °C and 40 V.

  1. 3D Bi2S3/TiO2 cross-linked heterostructure: An efficient strategy to improve charge transport and separation for high photoelectrochemical performance

    NASA Astrophysics Data System (ADS)

    Han, Minmin; Jia, Junhong

    2016-10-01

    A novel 3D cross-linked heterostructure of TiO2 nanorods connecting with each other via ultrathin Bi2S3 nanosheets is constructed by a facile and effective strategy. The growth mechanism has been investigated and proposed based on the evolution of microstructure by changing the reaction parameters. Benefiting from the unique cross-linked heterostructure, the as-prepared Bi2S3 nanosheets modified TiO2 nanorods arrays could achieve a high energy conversion efficiency of 3.29% which is the highest value to date for Bi2S3-only sensitized solar cells as the reported highest value is 2.23% and other reported values are less than 1%. Furthermore, the photoelectrochemical studies clearly reveal that the novel cross-linked heterostructure exhibits much better activity than 0D nanoparticles decorated TiO2 nanorods under visible light irradiation, which may be primarily ascribed to the efficient electron transfer from 2D ultrathin Bi2S3 nanosheets to 1D TiO2 nanorod arrays. The promising results in this work confirm the advantages of cross-linked heterostructure and also undoubtedly offer an attractive synthesis strategy to fabricate other nanorod-based hierarchical architecture as well as nano-devices for solar energy conversion.

  2. α-Fe2O3/TiO2 3D hierarchical nanostructures for enhanced photoelectrochemical water splitting.

    PubMed

    Han, Hyungkyu; Riboni, Francesca; Karlicky, Frantisek; Kment, Stepan; Goswami, Anandarup; Sudhagar, Pitchaimuthu; Yoo, Jeongeun; Wang, Lei; Tomanec, Ondrej; Petr, Martin; Haderka, Ondrej; Terashima, Chiaki; Fujishima, Akira; Schmuki, Patrik; Zboril, Radek

    2017-01-07

    We report the fabrication of 3D hierarchical hetero-nanostructures composed of thin α-Fe2O3 nanoflakes branched on TiO2 nanotubes. The novel α-Fe2O3/TiO2 hierarchical nanostructures, synthesized on FTO through a multi-step hydrothermal process, exhibit enhanced performances in photo-electrochemical water splitting and in the photocatalytic degradation of an organic dye, with respect to pure TiO2 nanotubes. An enhanced separation of photogenerated charge carriers is here proposed as the main factor for the observed photo-activities: electrons photogenerated in TiO2 are efficiently collected at FTO, while holes are transferred to the α-Fe2O3 nanobranches that serve as charge mediators to the electrolyte. The morphology of α-Fe2O3 that varies from ultrathin nanoflakes to nanorod/nanofiber structures depending on the Fe precursor concentration was shown to have a significant impact on the photo-induced activity of the α-Fe2O3/TiO2 composites. In particular, it is shown that for an optimized photo-electrochemical structure, a combination of critical factors should be achieved such as (i) TiO2 light absorption and photo-activation vs.α-Fe2O3-induced shadowing effect and (ii) the availability of free TiO2 surface vs.α-Fe2O3-coated surface. Finally, theoretical analysis, based on DFT calculations, confirmed the optical properties experimentally determined for the α-Fe2O3/TiO2 hierarchical nanostructures. We anticipate that this new multi-step hydrothermal process can be a blueprint for the design and development of other hierarchical heterogeneous metal oxide electrodes suitable for photo-electrochemical applications.

  3. Morphological and photoelectrochemical characterization of core-shell nanoparticle films for dye-sensitized solar cells: Zn-O type shell on SnO2 and TiO2 cores.

    PubMed

    Park, N G; Kang, M G; Kim, K M; Ryu, K S; Chang, S H; Kim, D K; van de Lagemaat, J; Benkstein, K D; Frank, A J

    2004-05-11

    Core-shell type nanoparticles with SnO2 and TiO2 cores and zinc oxide shells were prepared and characterized by surface sensitive techniques. The influence of the structure of the ZnO shell and the morphology ofnanoparticle films on the performance was evaluated. X-ray absorption near-edge structure and extended X-ray absorption fine structure studies show the presence of thin ZnO-like shells around the nanoparticles at low Zn levels. In the case of SnO2 cores, ZnO nanocrystals are formed at high Zn/Sn ratios (ca. 0.5). Scanning electron microscopy studies show that Zn modification of SnO2 nanoparticles changes the film morphology from a compact mesoporous structure to a less dense macroporous structure. In contrast, Zn modification of TiO2 nanoparticles has no apparent influence on film morphology. For SnO2 cores, adding ZnO improves the solar cell efficiency by increasing light scattering and dye uptake and decreasing recombination. In contrast, adding a ZnO shell to the TiO2 core decreases the cell efficiency, largely owing to a loss of photocurrent resulting from slow electron transport associated with the buildup of the ZnO surface layer.

  4. Band structure engineering of TiO2 nanowires by n-p codoping for enhanced visible-light photoelectrochemical water-splitting.

    PubMed

    Zhang, Daoyu; Yang, Minnan

    2013-11-14

    The advantages of one-dimensional nanostructures, such as excellent charge separation and charge transport, low charge carrier recombination losses and so on, render them the photocatalysts of choice for many applications that exploit solar energy. In this work, based on very recently synthesized ultrathin anatase TiO2 nanowires, we explore the possibility of these wires as photocatalysts for photoelectrochemical water-splitting via the mono-doping (C, N, V, and Cr) and n-p codoping (C&V, C&Cr, N&V, and N&Cr) schemes. Our first-principles calculations predict that the C&Cr and C&V codoped ANWs may be strong candidates for photoelectrochemical water-splitting, because they have a substantially reduced band gap of 2.49 eV, appropriate band edge positions, no carrier recombination centers, and enhanced optical absorption in the visible light region.

  5. Biomolecule-assisted synthesis of carbon nitride and sulfur-doped carbon nitride heterojunction nanosheets: An efficient heterojunction photocatalyst for photoelectrochemical applications.

    PubMed

    Tao, Hua Bing; Yang, Hong Bin; Chen, Jiazang; Miao, Jianwei; Liu, Bin

    2014-01-01

    A biomolecule-assisted pyrolysis method has been developed to synthesize sulfur-doped graphitic carbon nitride (CNS) nanosheets. During the synthesis, sulfur could be introduced as a dopant into the lattice of carbon nitride (CN). Sulfur doping changed the texture as well as relative band positions of CN. By growing CN on preformed sulfur-doped CN nanosheets, composite CN/CNS heterojunction nanosheets were constructed, which significantly enhanced the photoelectrochemical performance as compared with various control counterparts including CN, CNS and physically mixed CN and CNS (CN+CNS). The enhanced photoelectrochemical performance of CN/CNS heterojunction nanosheets could be ascribed to the efficient separation of photoexcited charge carriers across the heterojunction interface. The strategy of designing and preparing CN/CNS heterojunction photocatalysts in this work can open up new directions for the construction of all CN-based heterojunction photocatalysts.

  6. Feasibility study of photoelectrochemical degradation of methylene blue with three-dimensional electrode-photocatalytic reactor.

    PubMed

    An, Tai-Cheng; Zhu, Xi-Hai; Xiong, Ya

    2002-02-01

    The photoelectrochemical degradation of methylene blue in aqueous solution was investigated with three-dimensional electrode-photocatalytic reactor. It was found that the methylene blue could be degraded more efficiently by photoelectrochemical process than by photocatalytic oxidation or electrochemical oxidation alone. The decolorization efficiency and COD reduction were 95% and 87% for a photoelectrochemical process, respectively, while they were only 78% and 68% for a single electrochemical process and 89% and 71% for a single photochemical process. The TOC reduction of the former also reached as high as about 81% within a reaction time of 30.0 min. And these degradation reactions conformed to pseudo-first-order kinetics.

  7. Degradation in photoelectrochemical devices: review with an illustrative case study

    NASA Astrophysics Data System (ADS)

    Nandjou, Fredy; Haussener, Sophia

    2017-03-01

    The durability, reliability, and robustness of photoelectrochemical (PEC) devices are key factors for advancing the practical large-scale implementation of cost-competitive solar fuel production. We review the known degradation mechanisms occurring in water-splitting photoelectrochemical devices. The degradation of single components is discussed in detail, and the parameters and conditions which influence it are presented. Device short-term durability depends on the semiconductor material and its interface with the electrolyte. Catalyst and electrolyte degradations are considerable challenges for long-term durability. We highlight how PEC device design choices can affect the salience of alternative degradation mechanisms. The PEC device architecture and the initial operating design point are crucial for observed device performance loss. Device degradation behavior is further impacted by irradiation intensity and concentration, and by current density and concentration. Enhancing a physical understanding of degradation phenomena and investigating their effect on component properties is of utmost importance for predicting performance loss and tackling the durability challenge of PEC devices.

  8. Photoelectrochemical Hydrogen Production Using New Combinatorial Chemistry Derived Materials

    SciTech Connect

    Jaramillo, Thomas F.; Baeck, Sung-Hyeon; Kleiman-Shwarsctein, Alan; Stucky, Galen D.; McFarland, Eric W.

    2004-10-25

    Solar photoelectrochemical water-splitting has long been viewed as one of the “holy grails” of chemistry because of its potential impact as a clean, renewable method of fuel production. Several known photocatalytic semiconductors can be used; however, the fundamental mechanisms of the process remain poorly understood and no known material has the required properties for cost effective hydrogen production. In order to investigate morphological and compositional variations in metal oxides as they relate to opto-electrochemical properties, we have employed a combinatorial methodology using automated, high-throughput, electrochemical synthesis and screening together with conventional solid-state methods. This report discusses a number of novel, high-throughput instruments developed during this project for the expeditious discovery of improved materials for photoelectrochemical hydrogen production. Also described within this report are results from a variety of materials (primarily tungsten oxide, zinc oxide, molybdenum oxide, copper oxide and titanium dioxide) whose properties were modified and improved by either layering, inter-mixing, or doping with one or more transition metals. Furthermore, the morphologies of certain materials were also modified through the use of structure directing agents (SDA) during synthesis to create mesostructures (features 2-50 nm) that increased surface area and improved rates of hydrogen production.

  9. Evolution of ZnO architecture on a nanoporous TiO2 film by a hydrothermal method and the photoelectrochemical performance

    NASA Astrophysics Data System (ADS)

    Yinhua, Jiang; Xiaoli, Wu; Wenli, Zhang; Liang, Ni; Yueming, Sun

    2011-03-01

    The synthesis of ZnO architecture on a fluorine-doped SnO2 (FTO) conducting glass pre-coated with nanoporous TiO2 film has been achieved by a one-step hydrothermal method at a temperature of 70°C. The effect of the reaction time on the morphology of the ZnO architecture has been investigated, and a possible growth mechanism for the formation of the ZnO architecture is discussed in detail. The morphology and phase structures of the as-obtained composite films have been investigated by field-emission scanning electron microscopy (FESEM) and X-ray diffraction (XRD). The results show that the growth time greatly affects the morphology of the obtained ZnO architecture. The photoelectrochemical performances of as-prepared composite films are measured by assembling them into dye sensitized solar cells (DSSCs). The DSSC based on the as-prepared composite film (2 h) has obtained the best power conversion efficiency of 1.845%.

  10. High-Potential Porphyrins Supported on SnO 2 and TiO 2 Surfaces for Photoelectrochemical Applications

    SciTech Connect

    Jiang, Jianbing; Swierk, John R.; Materna, Kelly L.; Hedström, Svante; Lee, Shin Hee; Crabtree, Robert H.; Schmuttenmaer, Charles A.; Batista, Victor S.; Brudvig, Gary W.

    2016-12-03

    Here, we report CF3-substituted porphyrins and evaluate their use as photosensitizers in water-splitting dye-sensitized photoelectrochemical cells (WS-DSPECs) by characterizing interfacial electron transfer on metal oxide surfaces. Furthermore, by using (CF3)2C6H3 instead of C6F5 substituents at the meso positions, we obtain the desired high potentials while avoiding the sensitivity of C6F5 substituents to nucleophilic substitution, a process that limits the types of synthetic reactions that can be used. Both the number of CF3 groups and the central metal tune the ground and excited-state potentials. A pair of porphyrins bearing carboxylic acids as anchoring groups were deposited on SnO2 and TiO2 surfaces and the interfacial charge-injection and charge-recombination kinetics were characterized by using a combination of computational modeling, terahertz measurements, and transient absorption spectroscopy. We also found that both free-base and metallated porphyrins inject into SnO2, and that recombination is slower for the latter case. Our findings demonstrate that (CF3)2C6H3-substituted porphyrins are promising photosensitizers for use in WS-DSPECs.

  11. Infra-red photoresponse of mesoscopic NiO-based solar cells sensitized with PbS quantum dot

    NASA Astrophysics Data System (ADS)

    Raissi, Mahfoudh; Pellegrin, Yann; Jobic, Stéphane; Boujtita, Mohammed; Odobel, Fabrice

    2016-04-01

    Sensitized NiO based photocathode is a new field of investigation with increasing scientific interest in relation with the development of tandem dye-sensitized solar cells (photovoltaic) and dye-sensitized photoelectrosynthetic cells (solar fuel). We demonstrate herein that PbS quantum dots (QDs) represent promising inorganic sensitizers for NiO-based quantum dot-sensitized solar cells (QDSSCs). The solar cell sensitized with PbS quantum dot exhibits significantly higher photoconversion efficiency than solar cells sensitized with a classical and efficient molecular sensitizer (P1 dye = 4-(Bis-{4-[5-(2,2-dicyano-vinyl)-thiophene-2-yl]-phenyl}-amino)-benzoic acid). Furthermore, the system features an IPCE (Incident Photon-to-Current Efficiency) spectrum that spreads into the infra-red region, reaching operating wavelengths of 950 nm. The QDSSC photoelectrochemical device works with the complexes tris(4,4‧-ditert-butyl-2,2‧-bipyridine)cobalt(III/II) redox mediators, underscoring the formation of a long-lived charge-separated state. The electrochemical impedance spectrocopy measurements are consistent with a high packing of the QDs upon the NiO surface, the high density of which limits the access of the electrolyte and results in favorable light absorption cross-sections and a significant hole lifetime. These notable results highlight the potential of NiO-based photocathodes sensitized with quantum dots for accessing and exploiting the low-energy part of the solar spectrum in photovoltaic and photocatalysis applications.

  12. Infra-red photoresponse of mesoscopic NiO-based solar cells sensitized with PbS quantum dot.

    PubMed

    Raissi, Mahfoudh; Pellegrin, Yann; Jobic, Stéphane; Boujtita, Mohammed; Odobel, Fabrice

    2016-04-29

    Sensitized NiO based photocathode is a new field of investigation with increasing scientific interest in relation with the development of tandem dye-sensitized solar cells (photovoltaic) and dye-sensitized photoelectrosynthetic cells (solar fuel). We demonstrate herein that PbS quantum dots (QDs) represent promising inorganic sensitizers for NiO-based quantum dot-sensitized solar cells (QDSSCs). The solar cell sensitized with PbS quantum dot exhibits significantly higher photoconversion efficiency than solar cells sensitized with a classical and efficient molecular sensitizer (P1 dye = 4-(Bis-{4-[5-(2,2-dicyano-vinyl)-thiophene-2-yl]-phenyl}-amino)-benzoic acid). Furthermore, the system features an IPCE (Incident Photon-to-Current Efficiency) spectrum that spreads into the infra-red region, reaching operating wavelengths of 950 nm. The QDSSC photoelectrochemical device works with the complexes tris(4,4'-ditert-butyl-2,2'-bipyridine)cobalt(III/II) redox mediators, underscoring the formation of a long-lived charge-separated state. The electrochemical impedance spectrocopy measurements are consistent with a high packing of the QDs upon the NiO surface, the high density of which limits the access of the electrolyte and results in favorable light absorption cross-sections and a significant hole lifetime. These notable results highlight the potential of NiO-based photocathodes sensitized with quantum dots for accessing and exploiting the low-energy part of the solar spectrum in photovoltaic and photocatalysis applications.

  13. Infra-red photoresponse of mesoscopic NiO-based solar cells sensitized with PbS quantum dot

    PubMed Central

    Raissi, Mahfoudh; Pellegrin, Yann; Jobic, Stéphane; Boujtita, Mohammed; Odobel, Fabrice

    2016-01-01

    Sensitized NiO based photocathode is a new field of investigation with increasing scientific interest in relation with the development of tandem dye-sensitized solar cells (photovoltaic) and dye-sensitized photoelectrosynthetic cells (solar fuel). We demonstrate herein that PbS quantum dots (QDs) represent promising inorganic sensitizers for NiO-based quantum dot-sensitized solar cells (QDSSCs). The solar cell sensitized with PbS quantum dot exhibits significantly higher photoconversion efficiency than solar cells sensitized with a classical and efficient molecular sensitizer (P1 dye = 4-(Bis-{4-[5-(2,2-dicyano-vinyl)-thiophene-2-yl]-phenyl}-amino)-benzoic acid). Furthermore, the system features an IPCE (Incident Photon-to-Current Efficiency) spectrum that spreads into the infra-red region, reaching operating wavelengths of 950 nm. The QDSSC photoelectrochemical device works with the complexes tris(4,4′-ditert-butyl-2,2′-bipyridine)cobalt(III/II) redox mediators, underscoring the formation of a long-lived charge-separated state. The electrochemical impedance spectrocopy measurements are consistent with a high packing of the QDs upon the NiO surface, the high density of which limits the access of the electrolyte and results in favorable light absorption cross-sections and a significant hole lifetime. These notable results highlight the potential of NiO-based photocathodes sensitized with quantum dots for accessing and exploiting the low-energy part of the solar spectrum in photovoltaic and photocatalysis applications. PMID:27125454

  14. Highly stable tandem solar cell monolithically integrating dye-sensitized and CIGS solar cells

    NASA Astrophysics Data System (ADS)

    Chae, Sang Youn; Park, Se Jin; Joo, Oh-Shim; Jun, Yongseok; Min, Byoung Koun; Hwang, Yun Jeong

    2016-08-01

    A highly stable monolithic tandem solar cell was developed by combining the heterogeneous photovoltaic technologies of dye-sensitized solar cell (DSSC) and solution-processed CuInxGa1-xSeyS1-y (CIGS) thin film solar cells. The durability of the tandem cell was dramatically enhanced by replacing the redox couple from to [Co(bpy)3]2+ /[Co(bpy)3]3+), accompanied by a well-matched counter electrode (PEDOT:PSS) and sensitizer (Y123). A 1000 h durability test of the DSSC/CIGS tandem solar cell in ambient conditions resulted in only a 5% decrease in solar cell efficiency. Based on electrochemical impedance spectroscopy and photoelectrochemical cell measurement, the enhanced stability of the tandem cell is attributed to minimal corrosion by the cobalt-based polypyridine complex redox couple.

  15. Highly stable tandem solar cell monolithically integrating dye-sensitized and CIGS solar cells

    PubMed Central

    Chae, Sang Youn; Park, Se Jin; Joo, Oh-Shim; Jun, Yongseok; Min, Byoung Koun; Hwang, Yun Jeong

    2016-01-01

    A highly stable monolithic tandem solar cell was developed by combining the heterogeneous photovoltaic technologies of dye-sensitized solar cell (DSSC) and solution-processed CuInxGa1-xSeyS1-y (CIGS) thin film solar cells. The durability of the tandem cell was dramatically enhanced by replacing the redox couple from to [Co(bpy)3]2+ /[Co(bpy)3]3+), accompanied by a well-matched counter electrode (PEDOT:PSS) and sensitizer (Y123). A 1000 h durability test of the DSSC/CIGS tandem solar cell in ambient conditions resulted in only a 5% decrease in solar cell efficiency. Based on electrochemical impedance spectroscopy and photoelectrochemical cell measurement, the enhanced stability of the tandem cell is attributed to minimal corrosion by the cobalt-based polypyridine complex redox couple. PMID:27489138

  16. Geological and technological evaluation of gold-bearing mineral material after photo-electrochemical activation leaching

    NASA Astrophysics Data System (ADS)

    Manzyrev, DV

    2017-02-01

    The paper reports the lab test results on simulation of heap leaching of unoxidized rebellious ore extracted from deep levels of Pogromnoe open pit mine, with different flowsheets and photo-electrochemically activated solutions. It has been found that pre-treatment of rebellious ore particles –10 mm in size by photo-electrochemically activated solutions at the stage preceding agglomeration with the use of rich cyanide solutions enhances gold recovery by 6%.

  17. Nanoparticle-based monitoring of cell therapy

    NASA Astrophysics Data System (ADS)

    Xu, Chenjie; Mu, Luye; Roes, Isaac; Miranda-Nieves, David; Nahrendorf, Matthias; Ankrum, James A.; Zhao, Weian; Karp, Jeffrey M.

    2011-12-01

    Exogenous cell therapy aims to replace/repair diseased or dysfunctional cells and promises to revolutionize medicine by restoring tissue and organ function. To develop effective cell therapy, the location, distribution and long-term persistence of transplanted cells must be evaluated. Nanoparticle (NP) based imaging technologies have the potential to track transplanted cells non-invasively. Here we summarize the most recent advances in NP-based cell tracking with emphasis on (1) the design criteria for cell tracking NPs, (2) protocols for cell labeling, (3) a comparison of available imaging modalities and their corresponding contrast agents, (4) a summary of preclinical studies on NP-based cell tracking and finally (5) perspectives and future directions.

  18. Construction of dentate bonded TiO2-CdSe heterostructures with enhanced photoelectrochemical properties: versatile labels toward photoelectrochemical and electrochemical sensing.

    PubMed

    Gao, Picheng; Ma, Hongmin; Yan, Tao; Wu, Dan; Ren, Xiang; Yang, Jiaojiao; Du, Bin; Wei, Qin

    2015-01-14

    A facile synthetic route for TiO2-CdSe heterostructures was proposed based on dentate binding of TiO2 to carboxyl. Carboxyl functionalized CdSe quantum dots (CF-CdSe QDs) were successfully bonded onto TiO2 nanoparticles (NPs), which could significantly improve the photoelectrochemical (PEC) properties of TiO2 NPs. This is ascribed to the fact that CdSe QDs with a narrow band gap could be stimulated under visible light irradiation, and the energy levels of TiO2 NPs and CF-CdSe QDs are aligned with an electrolyte solution. High resolution transmission electron microscopy images revealed the heterostructures of the TiO2-CdSe composites. Ultraviolet visible spectroscopy, photoluminescence emission spectroscopy and electrochemical impedance spectroscopy analysis exhibited that the prepared TiO2-CdSe heterostructures have improved light absorption, charge separation efficiency and electron transfer ability in the visible light region. TiO2-CdSe heterostructures were used as versatile labels for fabrication of PEC and electrochemical immunosensors, and human immune globulin G (HIgG) was used as a model analyte. The immunosensor showed high sensitivity, a low detection limit and a wide linear range, which could be applied in practical serum sample analysis. The constructed TiO2-CdSe heterostructures would have potential applications in photocatalysis, aptasensors, cytosensors and other areas of nanotechnology.

  19. Preparation and surface modification of hierarchical nanosheets-based ZnO microstructures for dye-sensitized solar cells

    SciTech Connect

    Meng, Yongming; Lin, Yu Lin, Yibing; Yang, Jiyuan

    2014-02-15

    This paper reports a simple one-step hydrothermal route for the preparation of hierarchical nanosheets-based ZnO microstructures and their application to dye-sensitized solar cells. The morphologies of the products were controlled by the dosage of the reactants. Their physical characteristics were detected by X-ray diffraction, a field-emission scanning electron microscope and a surface analyzer. It is proved that the sample of ZnO microspheres with larger surface area and stronger light-trapping capacity since the superiority of their entirely spherical structures exhibits better photoelectrochemical properties than the mixtures of ZnO microspheres and ZnO microflowers. A dye-sensitized solar cell assembled by the ZnO microspheres as photoanode shows an energy conversion efficiency of 2.94% after surface modification by tetrabutyl titanate solution at 90 {sup °}C. This result is over 1.6 times higher than the non-modified cell fabricated by the ZnO microspheres on the basis of the external improvement and the stability enhancement for the dye-sensitized ZnO photoanode. - Graphical abstract: Influences on energy conversion efficiency of the dye-sensitized solar cells assembled by decorating hierarchical nanosheets-based ZnO microstructures with tetrabutyl titanate solution at different temperatures. Display Omitted - Highlights: • Hierarchical nanosheets-based ZnO microstructures were controllably synthesized. • The ZnO microspheres show good optical and electrochemical properties. • The ZnO microspheres were modified by C{sub 16}H{sub 36}O{sub 4}Ti solution. • Remarkable increase of conversion efficiency is observed after surface modification.

  20. Cell or Cell Membrane-Based Drug Delivery Systems

    PubMed Central

    Tan, Songwei; Wu, Tingting; Zhang, Dan; Zhang, Zhiping

    2015-01-01

    Natural cells have been explored as drug carriers for a long period. They have received growing interest as a promising drug delivery system (DDS) until recently along with the development of biology and medical science. The synthetic materials, either organic or inorganic, are found to be with more or less immunogenicity and/or toxicity. The cells and extracellular vesicles (EVs), are endogenous and thought to be much safer and friendlier. Furthermore, in view of their host attributes, they may achieve different biological effects and/or targeting specificity, which can meet the needs of personalized medicine as the next generation of DDS. In this review, we summarized the recent progress in cell or cell membrane-based DDS and their fabrication processes, unique properties and applications, including the whole cells, EVs and cell membrane coated nanoparticles. We expect the continuing development of this cell or cell membrane-based DDS will promote their clinic applications. PMID:26000058

  1. Design and synthesis of novel organometallic dyes for NiO sensitization and photo-electrochemical applications.

    PubMed

    Massin, Julien; Lyu, Siliu; Pavone, Michele; Muñoz-García, Ana B; Kauffmann, Brice; Toupance, Thierry; Chavarot-Kerlidou, Murielle; Artero, Vincent; Olivier, Céline

    2016-08-02

    Two metallo-organic dyes were synthesized and used for NiO sensitization in view of their photoelectrochemical applications. The new dyes present an original π-conjugated structure containing the [Ru(dppe)2] metal fragment with a highly delocalized allenylidene ligand on one side and a σ-alkynyl ligand bearing an electron-rich group, i.e. a thiophene or triphenylamine unit, and one or two anchoring functions on the other side. The optoelectronic, electrochemical and photoelectrochemical properties of the dyes were systematically investigated. A broad photoresponse was observed with the absorption maximum at 600 nm. The X-ray crystal structure of one precursor was obtained to elucidate the structural conformation of the organometallic complexes and theoretical calculations were performed in order to address the photophysical properties of the new dyes. These photosensitizers were further implemented in NiO-based photocathodes and tested as photocurrent generators under pertinent aqueous conditions in association with [Co(NH3)5Cl]Cl2 as an irreversible electron acceptor. The dye-sensitized photocathodes provided good photocurrent densities (40 to 60 μA cm(-2)) at neutral pH in phosphate buffer and a high stability was observed for the two dyes.

  2. Effect of charge compensation on the photoelectrochemical properties of Ho-doped SrTiO{sub 3} films

    SciTech Connect

    Zhao, Long; Fang, Liang; Dong, Wen; Zheng, Fengang; Shen, Mingrong; Wu, Tom

    2013-03-25

    When Ho{sup 3+} ions are substituted at Sr{sup 2+} sites in SrTiO{sub 3} (STO), the excess positive charges are compensated via three complementary routes: (1) strontium vacancies, (2) titanium vacancies, and (3) conduction electrons. In this study, we show that the photoelectrochemical properties of Ho-doped STO films are dependent on the charge compensation mechanisms. The compensation mechanism via the titanium vacancies exhibits the highest photocurrent density, which is 1.7 times higher than that of the pure STO sample. Based on the measured dielectric properties and electrochemical impedance spectroscopy data, we propose that the enhanced dielectric constant of the films can enlarge the width of the space charge region at the film/liquid interface, which eventually leads to the increase of the photocurrent density. Further enhancement of photocurrent density is obtained in the samples decorated with appropriate amounts of Pt nanoparticles, showing the advantage of composites for achieving the efficient photoelectrochemical property.

  3. Gradient doping - a case study with Ti-Fe2O3 towards an improved photoelectrochemical response.

    PubMed

    Srivastav, Anupam; Verma, Anuradha; Banerjee, Anamika; Khan, Saif A; Gupta, Mukul; Satsangi, Vibha Rani; Shrivastav, Rohit; Dass, Sahab

    2016-12-07

    The present study investigates the effect of gradient doping on modifying the photoelectrochemical response of Ti-doped Fe2O3 photoanodes for their use in sunlight based water splitting for hydrogen evolution. The deposition of a thin film over the ITO (tin doped indium oxide) substrate was carried out using a spray pyrolysis method. The concentration of dopant was varied from 0.5-8.0 at% and two sets of samples were also prepared with low to high (0.5-8%) and high to low (8-0.5%) dopant concentrations in the direction towards the substrate. The prepared thin films were characterized using X-ray Diffractometry (XRD), Scanning Electron Microscopy (SEM), Energy Dispersive X-ray (EDX) Spectroscopy, Secondary Ion Mass Spectroscopy (SIMS), X-ray Photoelectron Spectroscopy (XPS) and UV-visible Spectroscopy. The photoelectrochemical studies revealed that the deposition of dopant layers with a low to high concentration towards the substrate exhibited a highly improved photoresponse (200 times) in comparison to the pristine sample and a two fold enhancement in comparison to 2% Ti-doped Fe2O3. The improvement in the photoresponse has been attributed to the values of a high flat band potential, low resistance, high open circuit voltage, carrier separation efficiency, applied bias photon-to-current conversion efficiency (ABPE), and incident photon-to-current conversion efficiency (IPCE). A reduced charge transfer resistance has been demonstrated with Nyquist plots.

  4. Photoelectrochemical hydrogen production from biomass derivatives and water.

    PubMed

    Lu, Xihong; Xie, Shilei; Yang, Hao; Tong, Yexiang; Ji, Hongbing

    2014-11-21

    Hydrogen, a clean energy carrier with high energy capacity, is a very promising candidate as a primary energy source for the future. Photoelectrochemical (PEC) hydrogen production from renewable biomass derivatives and water is one of the most promising approaches to producing green chemical fuel. Compared to water splitting, hydrogen production from renewable biomass derivatives and water through a PEC process is more efficient from the viewpoint of thermodynamics. Additionally, the carbon dioxide formed can be re-transformed into carbohydrates via photosynthesis in plants. In this review, we focus on the development of photoanodes and systems for PEC hydrogen production from water and renewable biomass derivatives, such as methanol, ethanol, glycerol and sugars. We also discuss the future challenges and opportunities for the design of the state-of-the-art photoanodes and PEC systems for hydrogen production from biomass derivatives and water.

  5. Photocatalytic and photoelectrochemical hydrogen production on strontium titanate single crystals

    SciTech Connect

    Wagner, F.T.; Somorjai, G.A.

    1980-01-01

    Sustained photogeneration of hydrogen was observed on metal-free as well as on platinized SrTiO/sub 3/ single crystals illuminated in aqueous alkaline electrolytes or in the presence of electrolyte films. Hydrogen evolution rates increased with electrolyte hydroxide concentration, most strongly at hydroxide concentrations above 5 N. Both stoichiometric and prereduced metal-free crystals were active for hydrogen photoproduction. No activity was observed from crystals in neutral or acidic solutions or in water vapor in the absence of a crust of a basic deliquescent compounds. Metal-free crystals appear to evolve hydrogen via a photocatalytic mechanism in which all chemistry occurs at the illuminated surface. The results allow direct comparison of the photocatalytic and photoelectrochemical processes and have implications for the development of heterogeneous photocatalysis at the gas-solid interface.

  6. Improved photoelectrochemical performance of GaN nanopillar photoanodes.

    PubMed

    Narangari, Parvathala Reddy; Karuturi, Siva Krishna; Lysevych, Mykhaylo; Hoe Tan, Hark; Jagadish, Chennupati

    2017-04-18

    In this work, we report on the photoelectrochemical (PEC) investigation of n-GaN nanopillar (NP) photoanodes fabricated using metal organic chemical vapour deposition and the top-down approach. Substantial improvement in photocurrents is observed for GaN NP photoanodes compared to their planar counterparts. The role of carrier concentration and NP dimensions on the PEC performance of NP photoanodes is further elucidated. Photocurrent density is almost doubled for doped NP photoanodes whereas no improvement is noticed for undoped NP photoanodes. While the diameter of GaN NP is found to influence the onset potential, carrier concentration is found to affect both the onset and overpotential of the electrodes. Optical and electrochemical impedance spectroscopy characterisations are utilised to further explain the PEC results of NP photoanodes. Finally, improvement in the photostability of NP photoanodes with the addition of NiO as a co-catalyst is investigated.

  7. Semiconductor nanowires for photovoltaic and photoelectrochemical energy conversion

    SciTech Connect

    Dasgupta, Neil; Yang, Peidong

    2013-01-23

    Semiconductor nanowires (NW) possess several beneficial properties for efficient conversion of solar energy into electricity and chemical energy. Due to their efficient absorption of light, short distances for minority carriers to travel, high surface-to-volume ratios, and the availability of scalable synthesis methods, they provide a pathway to address the low cost-to-power requirements for wide-scale adaptation of solar energy conversion technologies. Here we highlight recent progress in our group towards implementation of NW components as photovoltaic and photoelectrochemical energy conversion devices. An emphasis is placed on the unique properties of these one-dimensional (1D) structures, which enable the use of abundant, low-cost materials and improved energy conversion efficiency compared to bulk devices.

  8. Photoelectrochemical response of some layered chalcogenophosphate compounds /MPX3/

    NASA Technical Reports Server (NTRS)

    Byvik, C. E.; Reichman, B.; Coleman, D. W.

    1982-01-01

    New photoelectrochemical results for the layered chalcogenophosphate compounds MPX3, FePS3, NiPS3, and SnPS3 are presented. The compounds were grown by iodine vapor transport in quartz ampules from a stoichiometric amount of the elements. Crystals of the layered type up to 10 mm x 10 mm x 0.1 mm were grown. The results of the layered compounds from the MPX3 series show good stability in acid solutions under photoelectrolysis condition. The relatively slow increase in the photocurrent with increasing electrode potential suggests high recombination rates for the photogenerated carriers in these layered materials. It is noted that improvements may be possible by, for example, optimizing the preparation of the crystals and the electrode surfaces.

  9. Improved photoelectrochemical performance of GaN nanopillar photoanodes

    NASA Astrophysics Data System (ADS)

    Reddy Narangari, Parvathala; Krishna Karuturi, Siva; Lysevych, Mykhaylo; Tan, Hark Hoe; Jagadish, Chennupati

    2017-04-01

    In this work, we report on the photoelectrochemical (PEC) investigation of n-GaN nanopillar (NP) photoanodes fabricated using metal organic chemical vapour deposition and the top-down approach. Substantial improvement in photocurrents is observed for GaN NP photoanodes compared to their planar counterparts. The role of carrier concentration and NP dimensions on the PEC performance of NP photoanodes is further elucidated. Photocurrent density is almost doubled for doped NP photoanodes whereas no improvement is noticed for undoped NP photoanodes. While the diameter of GaN NP is found to influence the onset potential, carrier concentration is found to affect both the onset and overpotential of the electrodes. Optical and electrochemical impedance spectroscopy characterisations are utilised to further explain the PEC results of NP photoanodes. Finally, improvement in the photostability of NP photoanodes with the addition of NiO as a co-catalyst is investigated.

  10. Efficient Photoelectrochemical Energy Conversion using Spinach Photosystem II (PSII) in Lipid Multilayer Films

    PubMed Central

    Zhang, Yun; Magdaong, Nikki M; Shen, Min; Frank, Harry A; Rusling, James F

    2015-01-01

    The need for clean, renewable energy has fostered research into photovoltaic alternatives to silicon solar cells. Pigment–protein complexes in green plants convert light energy into chemical potential using redox processes that produce molecular oxygen. Here, we report the first use of spinach protein photosystem II (PSII) core complex in lipid films in photoelectrochemical devices. Photocurrents were generated from PSII in a ∼2 μm biomimetic dimyristoylphosphatidylcholine (DMPC) film on a pyrolytic graphite (PG) anode with PSII embedded in multiple lipid bilayers. The photocurrent was ∼20 μA cm−2 under light intensity 40 mW cm−2. The PSII–DMPC anode was used in a photobiofuel cell with a platinum black mesh cathode in perchloric acid solution to give an output voltage of 0.6 V and a maximum output power of 14 μW cm−2. Part of this large output is related to a five-unit anode–cathode pH gradient. With catholytes at higher pH or no perchlorate, or using an MnO2 oxygen-reduction cathode, the power output was smaller. The results described raise the possibility of using PSII–DMPC films in small portable power conversion devices. PMID:25969807

  11. Efficient Photoelectrochemical Energy Conversion using Spinach Photosystem II (PSII) in Lipid Multilayer Films.

    PubMed

    Zhang, Yun; Magdaong, Nikki M; Shen, Min; Frank, Harry A; Rusling, James F

    2015-04-01

    The need for clean, renewable energy has fostered research into photovoltaic alternatives to silicon solar cells. Pigment-protein complexes in green plants convert light energy into chemical potential using redox processes that produce molecular oxygen. Here, we report the first use of spinach protein photosystem II (PSII) core complex in lipid films in photoelectrochemical devices. Photocurrents were generated from PSII in a ∼2 μm biomimetic dimyristoylphosphatidylcholine (DMPC) film on a pyrolytic graphite (PG) anode with PSII embedded in multiple lipid bilayers. The photocurrent was ∼20 μA cm(-2) under light intensity 40 mW cm(-2). The PSII-DMPC anode was used in a photobiofuel cell with a platinum black mesh cathode in perchloric acid solution to give an output voltage of 0.6 V and a maximum output power of 14 μW cm(-2). Part of this large output is related to a five-unit anode-cathode pH gradient. With catholytes at higher pH or no perchlorate, or using an MnO2 oxygen-reduction cathode, the power output was smaller. The results described raise the possibility of using PSII-DMPC films in small portable power conversion devices.

  12. Growth and Photoelectrochemical Energy Conversion of Wurtzite Indium Phosphide Nanowire Arrays.

    PubMed

    Kornienko, Nikolay; Gibson, Natalie A; Zhang, Hao; Eaton, Samuel W; Yu, Yi; Aloni, Shaul; Leone, Stephen R; Yang, Peidong

    2016-05-24

    Photoelectrochemical (PEC) water splitting into hydrogen and oxygen is a promising strategy to absorb solar energy and directly convert it into a dense storage medium in the form of chemical bonds. The continual development and improvement of individual components of PEC systems is critical toward increasing the solar to fuel efficiency of prototype devices. Within this context, we describe a study on the growth of wurtzite indium phosphide (InP) nanowire (NW) arrays on silicon substrates and their subsequent implementation as light-absorbing photocathodes in PEC cells. The high onset potential (0.6 V vs the reversible hydrogen electrode) and photocurrent (18 mA/cm(2)) of the InP photocathodes render them as promising building blocks for high performance PEC cells. As a proof of concept for overall system integration, InP photocathodes were combined with a nanoporous bismuth vanadate (BiVO4) photoanode to generate an unassisted solar water splitting efficiency of 0.5%.

  13. Photoelectrochemical properties of spray deposited n-CdSe thin films

    SciTech Connect

    Yadav, A.A.; Barote, M.A.; Masumdar, E.U.

    2010-05-15

    Polycrystalline cadmium selenide (CdSe) thin films have been prepared by spraying a mixture of an equimolar aqueous solutions of cadmium chloride and selenourea on preheated fluorine doped tin oxide (FTO) coated glass substrates at different substrate temperatures. The cell configuration n-CdSe/1 M (NaOH + Na{sub 2}S + S)/C is used for studying the capacitance-voltage (C-V) characteristics in dark, current-voltage (I-V) characteristics in dark and under illumination, photovoltaic power output and spectral response characteristics of the as deposited films. Photoelectrochemical study shows that as deposited CdSe thin films exhibits n-type of conductivity. The spectral response characteristics of the films at room temperature show a prominent sharp peak at 725 nm. The measured values of efficiency ({eta}) and fill factor (FF) are found to be 0.50% and 0.44 respectively for film deposited at 300 C. Electrochemical impedance spectroscopy studies show that the CdSe film deposited at 300 C shows better performance in PEC cell. (author)

  14. Photochemical and photoelectrochemical quenching of chlorophyll fluorescence in photosystem II.

    PubMed

    Vredenberg, Wim; Durchan, Milan; Prásil, Ondrej

    2009-12-01

    This paper deals with kinetics and properties of variable fluorescence in leaves and thylakoids upon excitation with low intensity multi-turnover actinic light pulses corresponding with an excitation rate of about 10 Hz. These show a relatively small and amply documented rise in the sub-s time range towards the plateau level F(pl) followed by a delayed and S-shaped rise towards a steady state level F(m) which is between three and four fold the initial dark fluorescence level F(o). Properties of this retarded slow rise are i) rate of dark recovery is (1-6 s)(-1), ii) suppression by low concentration of protonophores, iii) responsiveness to complementary single turnover flash excitation with transient amplitude towards a level F(m) which is between five and six fold the initial dark fluorescence level F(o) and iv) in harmony with and quantitatively interpretable in terms of a release of photoelectrochemical quenching controlled by the trans-thylakoid proton pump powered by the light-driven Q cycle. Data show evidence for a sizeable fluorescence increase upon release of (photo) electrochemical quenching, defined as qPE. Release of qPE occurs independent of photochemical quenching defined here as qPP even under conditions at which qPP = 1. The term photochemical quenching, hitherto symbolized by qP, will require a new definition, because it incorporates in its present form a sizeable photoelectrochemical component. The same is likely to be true for definition and use of qN as an indicator of non photochemical quenching.

  15. Improving Cell-Based Therapies by Nanomodification

    PubMed Central

    Chen, Wei; Fu, Liwu; Chen, Xiaoyuan

    2015-01-01

    Cell-based therapies are emerging as a promising approach for various diseases. Their therapeutic efficacy depends on rational control and regulation of the functions and behaviors of cells during their treatment. Different from conventional regulatory strategy by chemical adjuvant or genetic engineering, which is restricted by limited synergistic regulatory efficiency or uncertain safety problems, a novel approach based on nanoscale artificial materials can be applied to modify living cells to endow them with novel functions and unique properties. Inspired by the natural “nano shell” and “nano compass” structures, cell nanomodification can be developed through both external and internal pathways. In this review, some novel cell surface engineering and intracellular nanoconjugation strategies are summarized. Their potential applications are also discussed, including cell protection, cell labeling, targeted delivery and in situ regulation. It is believed that these novel cell-material complexes can have great potentials for biomedical applications. PMID:26423238

  16. Human Neural Cell-Based Biosensor

    DTIC Science & Technology

    2010-12-10

    botulinum toxin, and (4) development of fluorescence based assays for proliferation, mitochondrial function and reactive oxygen species generation as sensor...dopaminergic neurons, motoneurons and astrocytes using defined medium conditions, (3) development of cell-based methods to detect botulinum toxin, and...neurons are the target cell type for botulinum toxin and would be a useful cell type for the detection of this potential bioterrorism agent. Astrocytes

  17. Silicon/Organic Heterojunction for Photoelectrochemical Energy Conversion Photoanode with a Record Photovoltage.

    PubMed

    Cui, Wei; Wu, Shan; Chen, Fengjiao; Xia, Zhouhui; Li, Yanguang; Zhang, Xiao-Hong; Song, Tao; Lee, Shuit-Tong; Sun, Baoquan

    2016-09-20

    Silicon (Si) is a good photon absorption material for photoelectrochemical (PEC) conversion. Recently, the relatively low photovoltage of Si-based PEC anode is one of the most significant factors limiting its performance. To achieve a high photovoltage in PEC electrode, both a large barrier height and high-quality surface passivation of Si are indispensable. However, it is still challenging to induce a large band bending and passivate Si surface simultaneously in Si-based PEC photoanodes so far, which hinders their performance. Here, we develop a simple Si/poly(3,4-ethylenedioxythiophene):polystyrenesulfonate (PEDOT:PSS) heterojunction with large band banding and excellent surface passiviation for efficient PEC conversion. A chemically modified PEDOT:PSS film acts as both a surface passiviation layer and an effective catalyst simultaneously without sacrificing band bending level. A record photovoltage for Si-based PEC photoanodes as high as 657 mV is achieved via optimizing the PEDOT:PSS film fabrication process. The density of electron state (DOS) measurement is utilized to probe the passivation quality of the organic/inorganic heterojunction, and a low DOS is found in the Si/PEDOT:PSS heterojunction, which is in accordance with the photovoltage results. The low-temperature solution-processed Si/organic heterojunction photoanode provides a high photovoltage, exhibiting the potential to be the next-generation economical photoanode in PEC applications.

  18. Transparent-conducting-oxide nanowire arrays for efficient photoelectrochemical energy conversion

    NASA Astrophysics Data System (ADS)

    Lee, Sangwook; Park, Sangbaek; Han, Gill Sang; Kim, Dong Hoe; Noh, Jun Hong; Cho, In Sun; Jung, Hyun Suk; Hong, Kug Sun

    2014-07-01

    We report one dimensional (1-D) transparent-conducting-oxide arrays coated with light-absorbing semiconductors to simultaneously maximize light harvesting and charge collection in a photoelectrochemical (PEC) system. Tin-doped indium oxide (ITO) nanowire (NW) arrays are prepared on ITO thin-film substrates as the transparent-conducting-oxide, and TiO2 or CdSe/CdS/TiO2 thin layers were coated on the ITO NW arrays as the solar light-absorbing layers. The optimal PEC performance, 0.85% under 100 mW cm-2 of light illumination, is obtained from ~30 μm-long ITO NW, which is covered with ~20 nm-thick TiO2 nanoshell. We finally demonstrate that the ITO NW-based photoelectrode is also compatible with one of the most efficient visible-light sensitizers, the CdS/CdSe quantum dot. Our approach using the transparent conducting 1-D array has wide potential to improve the PEC performances of conventional semiconducting materials through liberation from the poor charge transport.We report one dimensional (1-D) transparent-conducting-oxide arrays coated with light-absorbing semiconductors to simultaneously maximize light harvesting and charge collection in a photoelectrochemical (PEC) system. Tin-doped indium oxide (ITO) nanowire (NW) arrays are prepared on ITO thin-film substrates as the transparent-conducting-oxide, and TiO2 or CdSe/CdS/TiO2 thin layers were coated on the ITO NW arrays as the solar light-absorbing layers. The optimal PEC performance, 0.85% under 100 mW cm-2 of light illumination, is obtained from ~30 μm-long ITO NW, which is covered with ~20 nm-thick TiO2 nanoshell. We finally demonstrate that the ITO NW-based photoelectrode is also compatible with one of the most efficient visible-light sensitizers, the CdS/CdSe quantum dot. Our approach using the transparent conducting 1-D array has wide potential to improve the PEC performances of conventional semiconducting materials through liberation from the poor charge transport. Electronic supplementary information

  19. Large-scale patterned ZnO nanorod arrays for efficient photoelectrochemical water splitting

    NASA Astrophysics Data System (ADS)

    Hu, Yaping; Yan, Xiaoqin; Gu, Yousong; Chen, Xiang; Bai, Zhiming; Kang, Zhuo; Long, Fei; Zhang, Yue

    2015-06-01

    Nowadays, the fabrication of photoanodes with high light-harvesting capability and charge transfer efficiency is a key challenge for photoelectrochemical (PEC) water splitting. In this paper, large-scale patterned ZnO nanorod arrays (NRAs) were designed and fabricated via two-beam laser interference lithography and hydrothermal synthesis, which were further applied as PEC photoanodes for the first time. By adopting the ZnO NRA photoanodes with square pattern, the PEC cells achieved a maximum efficiency of 0.18%, which was improved 135% compared to the control group with no patterned ZnO NRAs. The large-scale highly ordered ZnO NRAs have enhanced light-harvesting ability due to the light-scattering effect. In addition, the enlarged surface area of the patterned ZnO NRAs accelerated the charge transfer at the photoanode/electrolyte interface. This research demonstrates an effective mean to realize the efficient solar water splitting, and the results suggest that large-scale highly ordered nanostructures are promising candidates in the field of energy harvesting.

  20. Photoelectrochemical water splitting on nanoporous GaN thin films for energy conversion under visible light

    NASA Astrophysics Data System (ADS)

    Cao, Dezhong; Xiao, Hongdi; Fang, Jiacheng; Liu, Jianqiang; Gao, Qingxue; Liu, Xiangdong; Ma, Jin

    2017-01-01

    Nanoporous (NP) GaN thin films, which were fabricated by an electrochemical etching method at different voltages, were used as photoelectrodes during photoelectrochemical (PEC) water splitting in 1 M oxalic acid solution. Upon illumination at a power density of 100 mW cm‑2 (AM 1.5), water splitting is observed in NP GaN thin films, presumably resulting from the valence band edge which is more positive than the redox potential of the oxidizing species. In comparison with NP GaN film fabricated at 8 V, NP GaN obtained at 18 V shows nearly twofold enhancement in photocurrent with the maximum photo-to-hydrogen conversion efficiency of 1.05% at ~0 V (versus Ag/AgCl). This enhancement could be explained with (i) the increase of surface area and surface states, and (ii) the decrease of resistances and carrier concentration in the NP GaN thin films. High stability of the NP GaN thin films during the PEC water splitting further confirms that the NP GaN thin film could be applied to the design of efficient solar cells and solar fuel devices.

  1. Microwave assisted novel MoBi2S5 nanoflowers: Synthesis, characterization, photoelectrochemical performance

    NASA Astrophysics Data System (ADS)

    Pawar, Nita B.; Mali, Sawanta S.; Kharade, Suvarta D.; Kondalkar, Vijay V.; Ghanwat, Vishvanath B.; Khot, Kishorkumar V.; Patil, Pramod S.; Bhosale, Popatrao N.

    2016-11-01

    In the present article, we have studied the effect of post annealing treatment on microstructural, optical and photoelectrochemical (PEC) properties of MoBi2S5 thin films synthesized by microwave assisted technique. The synthesized thin films are vacuum annealed for 4 h at 473 K temperature. The X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS), scanning electron microscopy (SEM) and UV-Vis-NIR spectrophotometer techniques were used for characterization of the as deposited and annealed MoBi2S5 thin films. The XRD patterns confirm the synthesized and annealed thin films have nanocrystalline nature with rhombohedral-orthorhombic crystal structure. SEM micrographs indicate that, nanoflowers exhibit sharper end after annealing. The optical absorption study illustrates that the optical band gap energy has been decrease from 2.0 eV to 1.75 eV with annealing. Finally, applicability of synthesized thin films has been checked for PEC property. The J-V curves revealed that synthesized thin film photoanodes are suitable for PEC cell application. As well, used simple, economical method has great potential for synthesis of various thin film materials.

  2. Plasmon-enhanced nanoporous BiVO4 photoanodes for efficient photoelectrochemical water oxidation

    NASA Astrophysics Data System (ADS)

    Gan, Jiayong; Bangalore Rajeeva, Bharath; Wu, Zilong; Penley, Daniel; Liang, Chaolun; Tong, Yexiang; Zheng, Yuebing

    2016-06-01

    Conversion of solar irradiation into chemical fuels such as hydrogen with the use of a photoelectrochemical (PEC) cell is an attractive strategy for green energy. The promising technique of incorporating metal nanoparticles (NPs) in the photoelectrodes is being explored to enhance the performance of the photoelectrodes. In this work, we developed Au-NPs-functionalized nanoporous BiVO4 photoanodes, and utilized the plasmonic effects of Au NPs to enhance the photoresponse. The plasmonic enhancement leads to an AM 1.5 photocurrent of 5.1 ± 0.1 mA cm-2 at 1.23 V versus a reverse hydrogen electrode. We observed an enhancement of five times with respect to pristine BiVO4 in the photocurrent with long-term stability and high energy-conversion efficiency. The overall performance enhancement is attributed to the synergy between the nanoporous architecture of BiVO4 and the plasmonic effects of Au NPs. Our further study reveals that the commendable photoactivity arises from the different plasmonic effects and co-catalyst effects of Au NPs.

  3. Performance and stability of low-cost dye-sensitized solar cell based crude and pre-concentrated anthocyanins: Combined experimental and DFT/TDDFT study

    NASA Astrophysics Data System (ADS)

    Chaiamornnugool, Phrompak; Tontapha, Sarawut; Phatchana, Ratchanee; Ratchapolthavisin, Nattawat; Kanokmedhakul, Somdej; Sang-aroon, Wichien; Amornkitbamrung, Vittaya

    2017-01-01

    The low cost DSSCs utilized by crude and pre-concentrated anthocyanins extracted from six anthocyanin-rich samples including mangosteen pericarp, roselle, red cabbage, Thai berry, black rice and blue pea were fabricated. Their photo-to-current conversion efficiencies and stability were examined. Pre-concentrated extracts were obtained by solid phase extraction (SPE) using C18 cartridge. The results obviously showed that all pre-concentrated extracts performed on photovoltaic performances in DSSCs better than crude extracts except for mangosteen pericarp. The DSSC sensitized by pre-concentrated anthocyanin from roselle and red cabbage showed maximum current efficiency η = 0.71% while DSSC sensitized by crude anthocyanin from mangosteen pericarp reached maximum efficiency η = 0.97%. In addition, pre-concentrated extract based cells possess more stability than those of crude extract based cells. This indicates that pre-concentration of anthocyanin via SPE method is very effective for DSSCs based on good photovoltaic performance and stability. The DFT/TDDFT calculations of electronic and photoelectrochemical properties of the major anthocyanins found in the samples are employed to support the experimental results.

  4. Upscaling of integrated photoelectrochemical water-splitting devices to large areas

    PubMed Central

    Turan, Bugra; Becker, Jan-Philipp; Urbain, Félix; Finger, Friedhelm; Rau, Uwe; Haas, Stefan

    2016-01-01

    Photoelectrochemical water splitting promises both sustainable energy generation and energy storage in the form of hydrogen. However, the realization of this vision requires laboratory experiments to be engineered into a large-scale technology. Up to now only few concepts for scalable devices have been proposed or realized. Here we introduce and realize a concept which, by design, is scalable to large areas and is compatible with multiple thin-film photovoltaic technologies. The scalability is achieved by continuous repetition of a base unit created by laser processing. The concept allows for independent optimization of photovoltaic and electrochemical part. We demonstrate a fully integrated, wireless device with stable and bias-free operation for 40 h. Furthermore, the concept is scaled to a device area of 64 cm2 comprising 13 base units exhibiting a solar-to-hydrogen efficiency of 3.9%. The concept and its successful realization may be an important contribution towards the large-scale application of artificial photosynthesis. PMID:27601181

  5. Amorphous cobalt potassium phosphate microclusters as efficient photoelectrochemical water oxidation catalyst

    NASA Astrophysics Data System (ADS)

    Zhang, Ye; Zhao, Chunsong; Dai, Xuezeng; Lin, Hong; Cui, Bai; Li, Jianbao

    2013-12-01

    A novel amorphous cobalt potassium phosphate hydrate compound (KCoPO4·H2O) is identified to be active photocatalyst for oxygen evolution reaction (OER) to facilitate hydrogen generation from water photolysis. It has been synthesized through a facile and cost-effective solution-based precipitation method using earth-abundant materials. Its highly porous structure and large surface areas are found to be responsible for the excellent electrochemical performance featuring a low OER onset at ˜550 mVSCE and high current density in alkaline condition. Unlike traditional cobalt-based spinel oxides (Co3O4, NiCo2O4) and phosphate (Co-Pi, Co(PO3)2) electrocatalysts, with proper energy band alignment for light-assisted water oxidation, cobalt potassium phosphate hydrate also exhibits robust visible-light response, generating a photocurrent density of ˜200 μA cm-2 at 0.7 VSCE. This catalyst could thus be considered as a promising candidate to perform photoelectrochemical water splitting.

  6. Upscaling of integrated photoelectrochemical water-splitting devices to large areas

    NASA Astrophysics Data System (ADS)

    Turan, Bugra; Becker, Jan-Philipp; Urbain, Félix; Finger, Friedhelm; Rau, Uwe; Haas, Stefan

    2016-09-01

    Photoelectrochemical water splitting promises both sustainable energy generation and energy storage in the form of hydrogen. However, the realization of this vision requires laboratory experiments to be engineered into a large-scale technology. Up to now only few concepts for scalable devices have been proposed or realized. Here we introduce and realize a concept which, by design, is scalable to large areas and is compatible with multiple thin-film photovoltaic technologies. The scalability is achieved by continuous repetition of a base unit created by laser processing. The concept allows for independent optimization of photovoltaic and electrochemical part. We demonstrate a fully integrated, wireless device with stable and bias-free operation for 40 h. Furthermore, the concept is scaled to a device area of 64 cm2 comprising 13 base units exhibiting a solar-to-hydrogen efficiency of 3.9%. The concept and its successful realization may be an important contribution towards the large-scale application of artificial photosynthesis.

  7. Surface Passivation of GaN Nanowires for Enhanced Photoelectrochemical Water-Splitting.

    PubMed

    Varadhan, Purushothaman; Fu, Hui-Chun; Priante, Davide; Retamal, Jose Ramon Duran; Zhao, Chao; Ebaid, Mohamed; Ng, Tien Khee; Ajia, Idirs; Mitra, Somak; Roqan, Iman S; Ooi, Boon S; He, Jr-Hau

    2017-03-08

    Hydrogen production via photoelectrochemical water-splitting is a key source of clean and sustainable energy. The use of one-dimensional nanostructures as photoelectrodes is desirable for photoelectrochemical water-splitting applications due to the ultralarge surface areas, lateral carrier extraction schemes, and superior light-harvesting capabilities. However, the unavoidable surface states of nanostructured materials create additional charge carrier trapping centers and energy barriers at the semiconductor-electrolyte interface, which severely reduce the solar-to-hydrogen conversion efficiency. In this work, we address the issue of surface states in GaN nanowire photoelectrodes by employing a simple and low-cost surface treatment method, which utilizes an organic thiol compound (i.e., 1,2-ethanedithiol). The surface-treated photocathode showed an enhanced photocurrent density of -31 mA/cm(2) at -0.2 V versus RHE with an incident photon-to-current conversion efficiency of 18.3%, whereas untreated nanowires yielded only 8.1% efficiency. Furthermore, the surface passivation provides enhanced photoelectrochemical stability as surface-treated nanowires retained ∼80% of their initial photocurrent value and produced 8000 μmol of gas molecules over 55 h at acidic conditions (pH ∼ 0), whereas the untreated nanowires demonstrated only <4 h of photoelectrochemical stability. These findings shed new light on the importance of surface passivation of nanostructured photoelectrodes for photoelectrochemical applications.

  8. Mammalian Cell-Based Sensor System

    NASA Astrophysics Data System (ADS)

    Banerjee, Pratik; Franz, Briana; Bhunia, Arun K.

    Use of living cells or cellular components in biosensors is receiving increased attention and opens a whole new area of functional diagnostics. The term "mammalian cell-based biosensor" is designated to biosensors utilizing mammalian cells as the biorecognition element. Cell-based assays, such as high-throughput screening (HTS) or cytotoxicity testing, have already emerged as dependable and promising approaches to measure the functionality or toxicity of a compound (in case of HTS); or to probe the presence of pathogenic or toxigenic entities in clinical, environmental, or food samples. External stimuli or changes in cellular microenvironment sometimes perturb the "normal" physiological activities of mammalian cells, thus allowing CBBs to screen, monitor, and measure the analyte-induced changes. The advantage of CBBs is that they can report the presence or absence of active components, such as live pathogens or active toxins. In some cases, mammalian cells or plasma membranes are used as electrical capacitors and cell-cell and cell-substrate contact is measured via conductivity or electrical impedance. In addition, cytopathogenicity or cytotoxicity induced by pathogens or toxins resulting in apoptosis or necrosis could be measured via optical devices using fluorescence or luminescence. This chapter focuses mainly on the type and applications of different mammalian cell-based sensor systems.

  9. A magnetic cell-based sensor.

    PubMed

    Wang, Hua; Mahdavi, Alborz; Tirrell, David A; Hajimiri, Ali

    2012-11-07

    Cell-based sensing represents a new paradigm for performing direct and accurate detection of cell- or tissue-specific responses by incorporating living cells or tissues as an integral part of a sensor. Here we report a new magnetic cell-based sensing platform by combining magnetic sensors implemented in the complementary metal-oxide-semiconductor (CMOS) integrated microelectronics process with cardiac progenitor cells that are differentiated directly on-chip. We show that the pulsatile movements of on-chip cardiac progenitor cells can be monitored in a real-time manner. Our work provides a new low-cost approach to enable high-throughput screening systems as used in drug development and hand-held devices for point-of-care (PoC) biomedical diagnostic applications.

  10. Interface induce growth of intermediate layer for bandgap engineering insights into photoelectrochemical water splitting

    PubMed Central

    Zhang, Jian; Zhang, Qiaoxia; Wang, Lianhui; Li, Xing’ao; Huang, Wei

    2016-01-01

    A model of interface induction for interlayer growing is proposed for bandgap engineering insights into photocatalysis. In the interface of CdS/ZnS core/shell nanorods, a lamellar solid solution intermediate with uniform thickness and high crystallinity was formed under interface induction process. Merged the novel charge carrier transfer layer, the photocurrent of the core/shell/shell nanorod (css-NR) array was significantly improved to 14.0 mA cm−2 at 0.0 V vs. SCE, nearly 8 times higher than that of the perfect CdS counterpart and incident photon to electron conversion efficiency (IPCE) values above 50% under AM 1.5G irradiation. In addition, this array photoelectrode showed excellent photocatalytic stability over 6000 s. These results suggest that the CdS/Zn1−xCdxS/ZnS css-NR array photoelectrode provides a scalable charge carrier transfer channel, as well as durability, and therefore is promising to be a large-area nanostructured CdS-based photoanodes in photoelectrochemical (PEC) water splitting system. PMID:27250648

  11. Photoelectrochemical performance of birnessite films and photoelectrocatalytic activity toward oxidation of phenol.

    PubMed

    Zhang, Huiqin; Ding, Hongrui; Wang, Xin; Zeng, Cuiping; Lu, Anhuai; Li, Yan; Wang, Changqiu

    2017-02-01

    Birnessite films on fluorine-doped tin oxide (FTO) coated glass were prepared by cathodic reduction of aqueous KMnO4. The deposited birnessite films were characterized with X-ray diffraction, Raman spectroscopy, scanning electron microscopy and atomic force microscopy. The photoelectrochemical activity of birnessite films was investigated and a remarkable photocurrent in response to visible light was observed in the presence of phenol, resulting from localized manganese d-d transitions. Based on this result, the photoelectrocatalytic oxidation of phenol was investigated. Compared with phenol degradation by the electrochemical oxidation process or photocatalysis separately, a synergetic photoelectrocatalytic degradation effect was observed in the presence of the birnessite film coated FTO electrode. Photoelectrocatalytic degradation ratios were influenced by film thickness and initial phenol concentrations. Phenol degradation with the thinnest birnessite film and initial phenol concentration of 10mg/L showed the highest efficiency of 91.4% after 8hr. Meanwhile, the kinetics of phenol removal was fit well by the pseudofirst-order kinetic model.

  12. Cobalt-phosphate-assisted photoelectrochemical water oxidation by arrays of molybdenum-doped zinc oxide nanorods.

    PubMed

    Lin, Yan-Gu; Hsu, Yu-Kuei; Chen, Ying-Chu; Lee, Bing-Wei; Hwang, Jih-Shang; Chen, Li-Chyong; Chen, Kuei-Hsien

    2014-09-01

    We report the first demonstration of cobalt phosphate (Co-Pi)-assisted molybdenum-doped zinc oxide nanorods (Zn(1-x)Mo(x)O NRs) as visible-light-sensitive photofunctional electrodes to fundamentally improve the performance of ZnO NRs for photoelectrochemical (PEC) water splitting. A maximum photoconversion efficiency as high as 1.05% was achieved, at a photocurrent density of 1.4 mA cm(-2). More importantly, in addition to achieve the maximum incident photon to current conversion efficiency (IPCE) value of 86%, it could be noted that the IPCE of Zn(1-x)Mo(x)O photoanodes under monochromatic illumination (450 nm) is up to 12%. Our PEC performances are comparable to those of many oxide-based photoanodes in recent reports. The improvement in photoactivity of PEC water splitting may be attributed to the enhanced visible-light absorption, increased charge-carrier densities, and improved interfacial charge-transfer kinetics due to the combined effect of molybdenum incorporation and Co-Pi modification, contributing to photocatalysis. The new design of constructing highly photoactive Co-Pi-assisted Zn(1-x)Mo(x)O photoanodes enriches knowledge on doping and advances the development of high-efficiency photoelectrodes in the solar-hydrogen field.

  13. Graphitic carbon nitride/BiOCl composites for sensitive photoelectrochemical detection of ciprofloxacin.

    PubMed

    Xu, Li; Li, Henan; Yan, Pengcheng; Xia, Jiexiang; Qiu, Jingxia; Xu, Qian; Zhang, Shanqing; Li, Huaming; Yuan, Shouqi

    2016-12-01

    Ciprofloxacin, as a second generation of fluoroquinolone antibiotics, has been proved to cause environmental harm and exhibits toxic effects on the wastewater and surface water even at low concentrations due to their continuous input and persistence. Despite tremendous efforts, developing ciprofloxacin detection method with accuracy and sensitivity at low-cost remains a great challenge. Herein, graphitic carbon nitride/BiOCl composite (g-CN/BiOCl) has been designed for a facile and sensitive photoelectrochemical (PEC) monitoring platform of ciprofloxacin at first time. BiOCl can be modified with the g-CN nanosheets which are obtained via solvothermal process at low-temperature conditions. The use of g-CN is shown to strongly enhance the PEC response of BiOCl due to the formation of heterojunctions. The photocurrent generated at the g-CN/BiOCl-modified ITO (with 13wt%g-CN content) is much higher and more stable than that of a BiOCl-modified ITO. Based on these findings, the g-CN/BiOCl-modified ITO was used to design a PEC assay for the antibiotic ciprofloxacin. Furthermore, the limit of detection of the ciprofloxacin PEC sensor has been significantly lowered to 0.2ngmL(-1). In addition, the PEC sensor can detect ciprofloxacin in the wide range of 0.5-1840ngmL(-1).

  14. Interface induce growth of intermediate layer for bandgap engineering insights into photoelectrochemical water splitting

    NASA Astrophysics Data System (ADS)

    Zhang, Jian; Zhang, Qiaoxia; Wang, Lianhui; Li, Xing’Ao; Huang, Wei

    2016-06-01

    A model of interface induction for interlayer growing is proposed for bandgap engineering insights into photocatalysis. In the interface of CdS/ZnS core/shell nanorods, a lamellar solid solution intermediate with uniform thickness and high crystallinity was formed under interface induction process. Merged the novel charge carrier transfer layer, the photocurrent of the core/shell/shell nanorod (css-NR) array was significantly improved to 14.0 mA cm‑2 at 0.0 V vs. SCE, nearly 8 times higher than that of the perfect CdS counterpart and incident photon to electron conversion efficiency (IPCE) values above 50% under AM 1.5G irradiation. In addition, this array photoelectrode showed excellent photocatalytic stability over 6000 s. These results suggest that the CdS/Zn1‑xCdxS/ZnS css-NR array photoelectrode provides a scalable charge carrier transfer channel, as well as durability, and therefore is promising to be a large-area nanostructured CdS-based photoanodes in photoelectrochemical (PEC) water splitting system.

  15. Tandem Core-Shell Si-Ta3N5 Photoanodes for Photoelectrochemical Water Splitting.

    PubMed

    Narkeviciute, Ieva; Chakthranont, Pongkarn; Mackus, Adriaan J M; Hahn, Christopher; Pinaud, Blaise A; Bent, Stacey F; Jaramillo, Thomas F

    2016-12-14

    Nanostructured core-shell Si-Ta3N5 photoanodes were designed and synthesized to overcome charge transport limitations of Ta3N5 for photoelectrochemical water splitting. The core-shell devices were fabricated by atomic layer deposition of amorphous Ta2O5 onto nanostructured Si and subsequent nitridation to crystalline Ta3N5. Nanostructuring with a thin shell of Ta3N5 results in a 10-fold improvement in photocurrent compared to a planar device of the same thickness. In examining thickness dependence of the Ta3N5 shell from 10 to 70 nm, superior photocurrent and absorbed-photon-to-current efficiencies are obtained from the thinner Ta3N5 shells, indicating minority carrier diffusion lengths on the order of tens of nanometers. The fabrication of a heterostructure based on a semiconducting, n-type Si core produced a tandem photoanode with a photocurrent onset shifted to lower potentials by 200 mV. CoTiOx and NiOx water oxidation cocatalysts were deposited onto the Si-Ta3N5 to yield active photoanodes that with NiOx retained 50-60% of their maximum photocurrent after 24 h chronoamperometry experiments and are thus among the most stable Ta3N5 photoanodes reported to date.

  16. Natural killer T cell based Immunotherapy

    PubMed Central

    Subrahmanyam, Priyanka B.; Sun, Wenji; East, James E.; Li, Junxin; Webb, Tonya J.

    2013-01-01

    Natural killer T (NKT) cells play an important immunoregulatory role and are thought to bridge the innate and adaptive immune responses. Following activation through cognate interactions with lipid antigen presented in the context of CD1d molecules, NKT cells rapidly produce a plethora of cytokines and can also mediate cytotoxicity. Due to their potent effector functions, extensive research has been performed to increase our understanding on how to effectively modulate these cells. In fact, NKT cell agonists have been used as vaccine adjuvants to enhance antigen specific T and B cell responses to infections and malignancy. In this review, we will focus on recent advances in NKT cell-based vaccination strategies. Given the role that NKT cells play in autoimmune disease, infectious diseases, cancer, transplant immunology and dermatology, it is important to understand how to effectively guide their effector functions in order to develop novel immunotherapeutic strategies. PMID:24089657

  17. Graphene based enzymatic bioelectrodes and biofuel cells.

    PubMed

    Karimi, Anahita; Othman, Ali; Uzunoglu, Aytekin; Stanciu, Lia; Andreescu, Silvana

    2015-04-28

    The excellent electrical conductivity and ease of functionalization make graphene a promising material for use in enzymatic bioelectrodes and biofuel cells. Enzyme based biofuel cells have attracted substantial interest due to their potential to harvest energy from organic materials. This review provides an overview of the functional properties and applications of graphene in the construction of biofuel cells as alternative power sources. The review covers the current state-of-the-art research in graphene based nanomaterials (physicochemical properties and surface functionalities), the role of these parameters in enhancing electron transfer, the stability and activity of immobilized enzymes, and how enhanced power density can be achieved. Specific examples of enzyme immobilization methods, enzyme loading, stability and function on graphene, functionalized graphene and graphene based nanocomposite materials are discussed along with their advantages and limitations. Finally, a critical evaluation of the performance of graphene based enzymatic biofuel cells, the current status, challenges and future research needs are provided.

  18. Graphene based enzymatic bioelectrodes and biofuel cells

    NASA Astrophysics Data System (ADS)

    Karimi, Anahita; Othman, Ali; Uzunoglu, Aytekin; Stanciu, Lia; Andreescu, Silvana

    2015-04-01

    The excellent electrical conductivity and ease of functionalization make graphene a promising material for use in enzymatic bioelectrodes and biofuel cells. Enzyme based biofuel cells have attracted substantial interest due to their potential to harvest energy from organic materials. This review provides an overview of the functional properties and applications of graphene in the construction of biofuel cells as alternative power sources. The review covers the current state-of-the-art research in graphene based nanomaterials (physicochemical properties and surface functionalities), the role of these parameters in enhancing electron transfer, the stability and activity of immobilized enzymes, and how enhanced power density can be achieved. Specific examples of enzyme immobilization methods, enzyme loading, stability and function on graphene, functionalized graphene and graphene based nanocomposite materials are discussed along with their advantages and limitations. Finally, a critical evaluation of the performance of graphene based enzymatic biofuel cells, the current status, challenges and future research needs are provided.

  19. Raman Spectroscopy Cell-based Biosensors

    PubMed Central

    Notingher, Ioan

    2007-01-01

    One of the main challenges faced by biodetection systems is the ability to detect and identify a large range of toxins at low concentrations and in short times. Cell-based biosensors rely on detecting changes in cell behaviour, metabolism, or induction of cell death following exposure of live cells to toxic agents. Raman spectroscopy is a powerful technique for studying cellular biochemistry. Different toxic chemicals have different effects on living cells and induce different time-dependent biochemical changes related to cell death mechanisms. Cellular changes start with membrane receptor signalling leading to cytoplasmic shrinkage and nuclear fragmentation. The potential advantage of Raman spectroscopy cell-based systems is that they are not engineered to respond specifically to a single toxic agent but are free to react to many biologically active compounds. Raman spectroscopy biosensors can also provide additional information from the time-dependent changes of cellular biochemistry. Since no cell labelling or staining is required, the specific time dependent biochemical changes in the living cells can be used for the identification and quantification of the toxic agents. Thus, detection of biochemical changes of cells by Raman spectroscopy could overcome the limitations of other biosensor techniques, with respect to detection and discrimination of a large range of toxic agents. Further developments of this technique may also include integration of cellular microarrays for high throughput in vitro toxicological testing of pharmaceuticals and in situ monitoring of the growth of engineered tissues.

  20. Enhancement of photoelectrochemical activity for water splitting by controlling hydrodynamic conditions on titanium anodization

    NASA Astrophysics Data System (ADS)

    Sánchez-Tovar, R.; Fernández-Domene, R. M.; García-García, D. M.; García-Antón, J.

    2015-07-01

    This work studies the electrochemical and photoelectrochemical properties of a new type of TiO2 nanostructure (nanosponge) obtained by means of anodization in a glycerol/water/NH4F electrolyte under controlled hydrodynamic conditions. For this purpose different techniques such as Scanning Electronic Microscopy (SEM), Raman Spectroscopy, Electrochemical Impedance Spectroscopy (EIS) measurements, Mott-Schottky (M-S) analysis and photoelectrochemical water splitting tests under standard AM 1.5 conditions are carried out. The obtained results show that electron-hole separation is facilitated in the TiO2 nanosponge if compared with highly ordered TiO2 nanotube arrays. As a result, nanosponges enhance the photoelectrochemical activity for water splitting.

  1. Enhanced photoelectrochemical activity of vertically aligned ZnO-coated TiO{sub 2} nanotubes

    SciTech Connect

    Cai, Hua; Yang, Qin; You, Qinghu; Sun, Jian; Xu, Ning; Wu, Jiada; Hu, Zhigao; Duan, Zhihua

    2014-02-03

    Vertically aligned ZnO-TiO{sub 2} hetero-nanostructures constructed of anatase TiO{sub 2} nanotubes (NTs) and wurtzite ZnO coatings are fabricated by atomic layer deposition of ZnO coatings on electrochemical anodization formed TiO{sub 2} NTs, and their photoelectrochemical activities are studied through photoelectrochemical and electrochemical characterization. Compared with bare TiO{sub 2} NTs, the transient photocurrent increases to over 1.5-fold for the annealed ZnO-coated TiO{sub 2} NTs under visible illumination. The ZnO-coated TiO{sub 2} NTs also show a longer electron lifetime, a lower charge-transfer resistance and a more negative flat-band potential than the bare TiO{sub 2} NTs, confirming the improved photoelectrochemical activity due to the enhanced charge separation.

  2. Photoelectrochemical etching of gallium nitride surface by complexation dissolution mechanism

    NASA Astrophysics Data System (ADS)

    Zhang, Miao-Rong; Hou, Fei; Wang, Zu-Gang; Zhang, Shao-Hui; Pan, Ge-Bo

    2017-07-01

    Gallium nitride (GaN) surface was etched by 0.3 M ethylenediamine tetraacetic acid disodium (EDTA-2Na) via photoelectrochemical etching technique. SEM images reveal the etched GaN surface becomes rough and irregular. The pore density is up to 1.9 × 109 per square centimeter after simple acid post-treatment. The difference of XPS spectra of Ga 3d, N 1s and O 1s between the non-etched and freshly etched GaN surfaces can be attributed to the formation of Ga-EDTA complex at the etching interface between GaN and EDTA-2Na. The proposed complexation dissolution mechanism can be broadly applicable to almost all neutral etchants under the prerequisite of strong light and electric field. From the point of view of environment, safety and energy, EDTA-2Na has obvious advantages over conventionally corrosive etchants. Moreover, as the further and deeper study of such nearly neutral etchants, GaN etching technology has better application prospect in photoelectric micro-device fabrication.

  3. Morphologically different WO3 nanocrystals in photoelectrochemical water oxidation

    NASA Astrophysics Data System (ADS)

    Biswas, Soumya Kanti; Baeg, Jin-Ook; Moon, Sang-Jin; Kong, Ki-jeong; So, Won-Wook

    2012-01-01

    Different morphologies of WO3 nanocrystals such as nanorods and nanoplates have been obtained under hydrothermal conditions using ammonium metatungstate as the precursor in presence of different organic acids such as citric, oxalic, and tartaric acid in the reaction medium. Detailed characterization of the crystal structure, particle morphology, and optical band gap of the synthesized powders have been done by X-ray diffraction, transmission electron microscopy, scanning electron microscopy and solid-state UV-visible spectroscopy study. The as-synthesized materials are WO3 hydrates with orthorhombic phase which transform to the hexagonal WO3 through dehydration upon heating at 350 °C. The resultant products are crystalline with nanoscale dimensions. Finally, the photoactivity of the synthesized materials annealed at 500 °C has been compared employing in photoelectrochemical water oxidation under the illumination of AM 1.5G simulated solar light (100 mWcm-2). The photocurrent measurements upon irradiation of light exhibit obvious photocatalytic activity with a photocurrent of about 0.77, 0.61, and 0.65 mAcm-2 for the WO3 film derived with the oxalic acid, tartaric, and citric acid assisting agents, respectively, at 1.8 V versus Ag/AgCl electrode.

  4. Oxidatively Stable Nanoporous Silicon Photocathodes for Photoelectrochemical Hydrogen Evolution

    SciTech Connect

    Neale, Nathan R.; Zhao, Yixin; Zhu, Kai; Oh, Jihun; van de Lagemaat, Jao; Yuan, Hao-Chih; Branz, Howard M.

    2014-06-02

    Stable and high-performance nanoporous 'black silicon' photoelectrodes with electrolessly deposited Pt nanoparticle (NP) catalysts are made with two metal-assisted etching steps. Doubly etched samples exhibit >20 mA/cm2 photocurrent density at +0.2 V vs. reversible hydrogen electrode (RHE) for photoelectrochemical hydrogen evolution under 1 sun illumination. We find that the photocurrent onset voltage of black Si photocathodes prepared from single-crystal planar Si wafers increases in oxidative environments (e.g., aqueous electrolyte) owing to a positive flat-band potential shift caused by surface oxidation. However, this beneficial oxide layer becomes a kinetic barrier to proton reduction that inhibits hydrogen production after just 24 h. To mitigate this problem, we developed a novel second Pt-assisted etch process that buries the Pt NPs deeper into the nanoporous Si surface. This second etch shifts the onset voltage positively, from +0.25 V to +0.4 V vs. RHE, and reduces the charge-transfer resistance with no performance decrease seen for at least two months.

  5. Phosphorus Cation Doping: A New Strategy for Boosting Photoelectrochemical Performance on TiO2 Nanotube Photonic Crystals.

    PubMed

    Li, Zhenzhen; Xin, Yanmei; Wu, Wenlong; Fu, Baihe; Zhang, Zhonghai

    2016-11-16

    Photoelectrochemical (PEC) water splitting is a promising technique for sustainable hydrogen generation. However, PEC performance on current semiconductors needs further improvement. Herein, a phosphorus cation doping strategy is proposed to fundamentally boost PEC performance on TiO2 nanotube photonic crystal (TiO2 NTPC) photoelectrodes in both the visible-light region and full solar-light illumination. The self-supported P-TiO2 NTPC photoelectrodes are fabricated by a facile two-step electrochemical anodization method and subsequent phosphidation treatment. The Ti(4+) is partially replaced by P cations (P(5+)) from the crystal lattice, which narrows the band gap of TiO2 and induces charge imbalance by the formation of Ti-O-P bonds. We believe the combination of unique photonic nanostructures of TiO2 NTPCs and P cation doping strategy will open up a new opportunity for enhancing PEC performance of TiO2-based photoelectrodes.

  6. Enhanced photoelectrochemical property of ZnO nanorods array synthesized on reduced graphene oxide for self-powered biosensing application.

    PubMed

    Kang, Zhuo; Gu, Yousong; Yan, Xiaoqin; Bai, Zhiming; Liu, Yichong; Liu, Shuo; Zhang, Xiaohui; Zhang, Zheng; Zhang, Xueji; Zhang, Yue

    2015-02-15

    We have realized the direct synthesis of ZnO nanorods (ZnO NRs) array on reduced graphene layer (rGO), and demonstrated the enhanced photoelectrochemical (PEC) property of the rGO/ZnO based photoanode under UV irradiation compared with the pristine ZnO NRs array. The introduction of the rGO layer resulted in a favorable energy band structure for electron migration, which finally led to the efficient photoinduced charge separation. Such nanostructure was subsequently employed for self-powered PEC biosensing of glutathione in the condition of 0 V bias, with a linear range from 10 to 200 µM, a detection limit of 2.17 µM, as well as excellent selectivity, reproducibility and stability. The results indicated the rGO/ZnO nanostructure is a competitive candidate in the PEC biosensing field.

  7. Current stem cell based therapies in diabetes

    PubMed Central

    Lilly, Meredith A; Davis, Meghan F; Fabie, Josh E; Terhune, Elizabeth B; Gallicano, G Ian

    2016-01-01

    Diabetes is a disease with wide-ranging personal and societal impacts that has been managed medicinally for over half a century. Since the discovery of stem cells, pancreatic islet regeneration has become a central target for clinical application that has the potential to decrease or eliminate the need for insulin administration and adjunctive medications. The discovery of alternative routes to pluripotency that bypass the ethical implications of embryonic stem cells has significantly expanded the horizons of stem cell based therapy. Engraftment of mature insulin producing cells derived from induced pluripotent stem cells may represent the most promising treatment strategy for diabetic patients with impaired β-cell function. These cells are easily accessible and have been shown to closely mimic endogenous β-cell function in vivo. While the risks of oncogenesis and transplant rejection are still of great concern, large strides have been made on both fronts with the application of integration free induction strategies and the ongoing development of microcapsules that cloak implanted cells from an autoimmune response. This review will focus on the progress and remaining obstacles in diabetes related stem cell research, and will specifically discuss approaches using embryonic, induced pluripotent, germline and mesenchymal derived stem cells. PMID:27853630

  8. Cell-based therapy in ischemic stroke

    PubMed Central

    2009-01-01

    Cell-based therapy for stroke represents a third wave of therapeutics for stroke and one focused on restorative processes with a longer time window of opportunity than neuroprotective therapies. An early time window, within the first week after stroke, is an opportunity for intravenously delivered bone-marrow and perinatally-derived cells that can home to areas of tissue injury and target brain remodeling. Allogeneic cells will likely be the most scalable and commercially viable product. Later time windows, months after stroke, may be opportunities for intracerebral transplantation of neuronally-differentiated cell types. An integrated approach of cell-based therapy with early phase clinical trials and continued pre-clinical work with focus on mechanisms of action is needed. PMID:18671663

  9. Oxygen-deficient metal oxide nanostructures for photoelectrochemical water oxidation and other applications.

    PubMed

    Wang, Gongming; Ling, Yichuan; Li, Yat

    2012-11-07

    This review presents highlights of the latest results of studies directed at developing oxygen-deficient metal oxides, including TiO(2), WO(3), and α-Fe(2)O(3), nanostructures as electrode materials, which show significantly enhanced performance in applications for photoelectrochemical water oxidation. The enhanced photoelectrochemical performance is attributed to improved electrical conductivities by controlled incorporation of oxygen vacancies as shallow donors for metal oxides. We also discuss the potential of these oxygen-deficient metal oxides for other energy conversion and storage applications, such as photocatalytic reactions and charge storage.

  10. Improved photoelectrochemical performance of bismuth vanadate by partial O/F-substitution

    NASA Astrophysics Data System (ADS)

    Anke, B.; Rohloff, M.; Willinger, M. G.; Hetaba, W.; Fischer, A.; Lerch, M.

    2017-01-01

    Fluorine-containing bismuth vanadate (F:BiVO4) powder was synthesized using a new, clean, and simple solid-vapor reaction. Incorporation of fluorine mainly leads to the formation of cation vacancies. Electrodes were fabricated from the pre-synthesized powder samples by electrophoretic deposition onto fluorine-doped tin oxide coated glass slides and subsequent calcination. The photoelectrochemical performance concerning the water oxidation reaction was investigated and compared to pristine BiVO4 revealing strongly enhanced photoelectrochemical behavior for the F-containing BiVO4.

  11. Nanowire-based single-cell endoscopy

    NASA Astrophysics Data System (ADS)

    Yan, Ruoxue; Park, Ji-Ho; Choi, Yeonho; Heo, Chul-Joon; Yang, Seung-Man; Lee, Luke P.; Yang, Peidong

    2012-03-01

    One-dimensional smart probes based on nanowires and nanotubes that can safely penetrate the plasma membrane and enter biological cells are potentially useful in high-resolution and high-throughput gene and drug delivery, biosensing and single-cell electrophysiology. However, using such probes for optical communication across the cellular membrane at the subwavelength level remains limited. Here, we show that a nanowire waveguide attached to the tapered tip of an optical fibre can guide visible light into intracellular compartments of a living mammalian cell, and can also detect optical signals from subcellular regions with high spatial resolution. Furthermore, we show that through light-activated mechanisms the endoscope can deliver payloads into cells with spatial and temporal specificity. Moreover, insertion of the endoscope into cells and illumination of the guided laser did not induce any significant toxicity in the cells.

  12. Theoretical Verification of Photoelectrochemical Water Oxidation Using Nanocrystalline TiO2 Electrodes.

    PubMed

    Yanagida, Shozo; Yanagisawa, Susumu; Yamashita, Koichi; Jono, Ryota; Segawa, Hiroshi

    2015-05-27

    Mesoscopic anatase nanocrystalline TiO2 (nc-TiO2) electrodes play effective and efficient catalytic roles in photoelectrochemical (PEC) H2O oxidation under short circuit energy gap excitation conditions. Interfacial molecular orbital structures of (H2O)3 &OH(TiO2)9H as a stationary model under neutral conditions and the radical-cation model of [(H2O)3&OH(TiO2)9H]+ as a working nc-TiO2 model are simulated employing a cluster model OH(TiO2)9H (Yamashita/Jono's model) and a H2O cluster model of (H2O)3 to examine excellent H2O oxidation on nc-TiO2 electrodes in PEC cells. The stationary model, (H2O)3&OH(TiO2)9H reveals that the model surface provides catalytic H2O binding sites through hydrogen bonding, van der Waals and Coulombic interactions. The working model, [(H2O)3&OH(TiO2)9H]+ discloses to have a very narrow energy gap (0.3 eV) between HOMO and LUMO potentials, proving that PEC nc-TiO2 electrodes become conductive at photo-irradiated working conditions. DFT-simulation of stepwise oxidation of a hydroxide ion cluster model of OH-(H2O)3, proves that successive two-electron oxidation leads to hydroxyl radical clusters, which should give hydrogen peroxide as a precursor of oxygen molecules. Under working bias conditions of PEC cells, nc-TiO2 electrodes are now verified to become conductive by energy gap photo-excitation and the electrode surface provides powerful oxidizing sites for successive H2O oxidation to oxygen via hydrogen peroxide.

  13. Cell-Based Genotoxicity Testing

    NASA Astrophysics Data System (ADS)

    Reifferscheid, Georg; Buchinger, Sebastian

    Genotoxicity test systems that are based on bacteria display an important role in the detection and assessment of DNA damaging chemicals. They belong to the basic line of test systems due to their easy realization, rapidness, broad applicability, high sensitivity and good reproducibility. Since the development of the Salmonella microsomal mutagenicity assay by Ames and coworkers in the early 1970s, significant development in bacterial genotoxicity assays was achieved and is still a subject matter of research. The basic principle of the mutagenicity assay is a reversion of a growth inhibited bacterial strain, e.g., due to auxotrophy, back to a fast growing phenotype (regain of prototrophy). Deeper knowledge of the ­mutation events allows a mechanistic understanding of the induced DNA-damage by the utilization of base specific tester strains. Collections of such specific tester strains were extended by genetic engineering. Beside the reversion assays, test systems utilizing the bacterial SOS-response were invented. These methods are based on the fusion of various SOS-responsive promoters with a broad variety of reporter genes facilitating numerous methods of signal detection. A very important aspect of genotoxicity testing is the bioactivation of ­xenobiotics to DNA-damaging compounds. Most widely used is the extracellular metabolic activation by making use of rodent liver homogenates. Again, genetic engineering allows the construction of highly sophisticated bacterial tester strains with significantly enhanced sensitivity due to overexpression of enzymes that are involved in the metabolism of xenobiotics. This provides mechanistic insights into the toxification and detoxification pathways of xenobiotics and helps explaining the chemical nature of hazardous substances in unknown mixtures. In summary, beginning with "natural" tester strains the rational design of bacteria led to highly specific and sensitive tools for a rapid, reliable and cost effective

  14. Enhanced Photoelectrochemical Method for Sensitive Detection of Protein Kinase A Activity Using TiO2/g-C3N4, PAMAM Dendrimer, and Alkaline Phosphatase.

    PubMed

    Li, Xue; Zhu, Lusheng; Zhou, Yunlei; Yin, Huanshun; Ai, Shiyun

    2017-02-21

    A novel photoelectrochemical (PEC) assay is developed for sensitive detection of protein kinase A (PKA) activity based on PKA-catalyzed phosphorylation reaction in solution and signal amplification strategy triggered by PAMAM dendrimer and alkaline phosphatase (ALP). In this strategy, it is noteworthy at this point that PKA phosphorylation was achieved in solution instead of on the surface of the electrode, which has advantages of the good contact in reactants and simple experimental procedure. For immobilizing the phosphorylated peptide (P-peptide) on electrode surface, graphite-like carbon nitride (g-C3N4) and titanium dioxide (TiO2) complex is synthesized and characterized, which plays a significant role for TiO2 conjugating phosphate groups and g-C3N4 providing PEC signal. Subsequently, PAMAM dendrimer and ALP can be captured on P-peptide and TiO2/g-C3N4 modified ITO electrode via interaction between the -COOH groups on the surface of PAMAM dendrimer and the -NH2 groups of peptide and ALP, which can lead to the increase of ALP amount on the modified electrode surface assisted with the PAMAM dendrimer. As a result, the amount of ALP catalyzes of L-ascorbic acid 2-phosphate trisodium salt (AAP) to produce electron donor of ascorbic acid (AA), resulting in an increased photocurrent. The proposed detection assay displays high selectivity and low detection limit of 0.048 U/mL (S/N = 3) for PKA activity. This biosensor can also be applied for the evaluation of PKA inhibition and PKA activity assay in cell samples. Therefore, the fabricated PEC biosensor is potentionally well in PKA activity detection and inhibitor screening.

  15. Solid polymer MEMS-based fuel cells

    DOEpatents

    Jankowski, Alan F.; Morse, Jeffrey D.

    2008-04-22

    A micro-electro-mechanical systems (MEMS) based thin-film fuel cells for electrical power applications. The MEMS-based fuel cell may be of a solid oxide type (SOFC), a solid polymer type (SPFC), or a proton exchange membrane type (PEMFC), and each fuel cell basically consists of an anode and a cathode separated by an electrolyte layer. The electrolyte layer can consist of either a solid oxide or solid polymer material, or proton exchange membrane electrolyte materials may be used. Additionally catalyst layers can also separate the electrodes (cathode and anode) from the electrolyte. Gas manifolds are utilized to transport the fuel and oxidant to each cell and provide a path for exhaust gases. The electrical current generated from each cell is drawn away with an interconnect and support structure integrated with the gas manifold. The fuel cells utilize integrated resistive heaters for efficient heating of the materials. By combining MEMS technology with thin-film deposition technology, thin-film fuel cells having microflow channels and full-integrated circuitry can be produced that will lower the operating temperature an will yield an order of magnitude greater power density than the currently known fuel cells.

  16. Solid oxide MEMS-based fuel cells

    DOEpatents

    Jankowksi, Alan F.; Morse, Jeffrey D.

    2007-03-13

    A micro-electro-mechanical systems (MEMS) based thin-film fuel cells for electrical power applications. The MEMS-based fuel cell may be of a solid oxide type (SOFC), a solid polymer type (SPFC), or a proton exchange membrane type (PEMFC), and each fuel cell basically consists of an anode and a cathode separated by an electrolyte layer. The electrolyte layer can consist of either a solid oxide or solid polymer material, or proton exchange membrane electrolyte materials may be used. Additionally catalyst layers can also separate the electrodes (cathode and anode) from the electrolyte. Gas manifolds are utilized to transport the fuel and oxidant to each cell and provide a path for exhaust gases. The electrical current generated from each cell is drawn away with an interconnect and support structure integrated with the gas manifold. The fuel cells utilize integrated resistive heaters for efficient heating of the materials. By combining MEMS technology with thin-film deposition technology, thin-film fuel cells having microflow channels and full-integrated circuitry can be produced that will lower the operating temperature an will yield an order of magnitude greater power density than the currently known fuel cells.

  17. Micro-/nanofluidics based cell electroporation

    PubMed Central

    Wang, Shengnian; Lee, L. James

    2013-01-01

    Non-viral gene delivery has been extensively explored as the replacement for viral systems. Among various non-viral approaches, electroporation has gained increasing attention because of its easy operation and no restrictions on probe or cell type. Several effective systems are now available on the market with reasonably good gene delivery performance. To facilitate broader biological and medical applications, micro-/nanofluidics based technologies were introduced in cell electroporation during the past two decades and their advances are summarized in this perspective. Compared to the commercially available bulk electroporation systems, they offer several advantages, namely, (1) sufficiently high pulse strength generated by a very low potential difference, (2) conveniently concentrating, trapping, and regulating the position and concentration of cells and probes, (3) real-time monitoring the intracellular trafficking at single cell level, and (4) flexibility on cells to be transfected (from single cell to large scale cell population). Some of the micro-devices focus on cell lysis or fusion as well as the analysis of cellular properties or intracellular contents, while others are designed for gene transfection. The uptake of small molecules (e.g., dyes), DNA plasmids, interfering RNAs, and nanoparticles has been broadly examined on different types of mammalian cells, yeast, and bacteria. A great deal of progress has been made with a variety of new micro-/nanofluidic designs to address challenges such as electrochemical reactions including water electrolysis, gas bubble formation, waste of expensive reagents, poor cell viability, low transfection efficacy, higher throughput, and control of transfection dosage and uniformity. Future research needs required to advance micro-/nanofluidics based cell electroporation for broad life science and medical applications are discussed. PMID:23405056

  18. Photoelectrochemical properties of Cu(In0.75Ga0.25)3Se5 ordered vacancy compound

    NASA Astrophysics Data System (ADS)

    Djellal, L.; Doulache, M.; Trari, M.

    2011-08-01

    Ordered vacancy compound Cu(In0.75Ga0.25)3Se5 was synthesized by the fusion technique. The starting elements were sealed in evacuated silica tube and submitted to programmed thermal treatment. The x-ray diffraction confirmed the formation of the phase which crystallizes in the chalcopyrite structure. The elemental composition (Cu = 13.45 at.%, In = 22.14 at.%, Ga = 8.42 at.%, Se = 56.0 at.%) was determined by the energy dispersive spectroscopy. The optical gap (Eg) was obtained from the diffuse reflectance spectrum through the Kubelka-Munk equation. The dependence of the absorption coefficient (α) on the photon energy (hν) near the band edge is characteristic of directly allowed optical transition with Eg value of 1.27 eV. The high temperature conductivity data were fitted to a small lattice type polaron hopping based on the strong electron-lattice interaction with an effective mass of 0.76 mo. The material exhibits an excellent chemical stability in basic solution with a corrosion rate of 0.87 µmol per month. The photoelectrochemical characterization was done in KOH (0.5 M) electrolyte and the n-type conductivity was confirmed by the anodic photocurrent. The flat band potential (-0.78 VSCE) and the donor's density (2.73 × 1019 cm-3) were derived respectively from the slope and intercept with the potential axis of the Mott-Schottky plot. The results showed the potentiality of Cu(In0.75Ga0.25)3Se5 for the photoelectrochemical hydrogen evolution.

  19. Cell-based bioassays in microfluidic systems

    NASA Astrophysics Data System (ADS)

    Itle, Laura J.; Zguris, Jeanna C.; Pishko, Michael V.

    2004-12-01

    The development of cell-based bioassays for high throughput drug screening or the sensing of biotoxins is contingent on the development of whole cell sensors for specific changes in intracellular conditions and the integration of those systems into sample delivery devices. Here we show the feasibility of using a 5-(and-6)-carboxy SNARF-1, acetoxymethyl ester, acetate, a fluorescent dye capable of responding to changes in intracellular pH, as a detection method for the bacterial endotoxin, lipopolysaccharide. We used photolithography to entrap cells with this dye within poly(ethylene) glyocol diacrylate hydrogels in microfluidic channels. After 18 hours of exposure to lipopolysaccharide, we were able to see visible changes in the fluorescent pattern. This work shows the feasibility of using whole cell based biosensors within microfluidic networks to detect cellular changes in response to exogenous agents.

  20. Status of photoelectrochemical production of hydrogen and electrical energy

    NASA Technical Reports Server (NTRS)

    Byvik, C. E.; Walker, G. H.

    1976-01-01

    The efficiency for conversion of electromagnetic energy to chemical and electrical energy utilizing semiconductor single crystals as photoanodes in electrochemical cells was investigated. Efficiencies as high as 20 percent were achieved for the conversion of 330 nm radiation to chemical energy in the form of hydrogen by the photoelectrolysis of water in a SrTiO3 based cell. The SrTiO3 photoanodes were shown to be stable in 9.5 M NaOH solutions for periods up to 48 hours. Efficiencies of 9 percent were measured for the conversion of broadband visible radiation to hydrogen using n-type GaAs crystals as photoanodes. Crystals of GaAs coated with 500 nm of gold, silver, or tin for surface passivation show no significant change in efficiency. By suppressing the production of hydrogen in a CdSe-based photogalvanic cell, an efficiency of 9 percent was obtained in conversion of 633 nm light to electrical energy. A CdS-based photogalvanic cell produced a conversion efficiency of 5 percent for 500 nm radiation.

  1. Sn-doped hematite nanostructures for photoelectrochemical water splitting.

    PubMed

    Ling, Yichuan; Wang, Gongming; Wheeler, Damon A; Zhang, Jin Z; Li, Yat

    2011-05-11

    We report on the synthesis and characterization of Sn-doped hematite nanowires and nanocorals as well as their implementation as photoanodes for photoelectrochemical water splitting. The hematite nanowires were prepared on a fluorine-doped tin oxide (FTO) substrate by a hydrothermal method, followed by high temperature sintering in air to incorporate Sn, diffused from the FTO substrate, as a dopant. Sn-doped hematite nanocorals were prepared by the same method, by adding tin(IV) chloride as the Sn precursor. X-ray photoelectron spectroscopy analysis confirms Sn(4+) substitution at Fe(3+) sites in hematite, and Sn-dopant levels increase with sintering temperature. Sn dopant serves as an electron donor and increases the carrier density of hematite nanostructures. The hematite nanowires sintered at 800 °C yielded a pronounced photocurrent density of 1.24 mA/cm(2) at 1.23 V vs RHE, which is the highest value observed for hematite nanowires. In comparison to nanowires, Sn-doped hematite nanocorals exhibit smaller feature sizes and increased surface areas. Significantly, they showed a remarkable photocurrent density of 1.86 mA/cm(2) at 1.23 V vs RHE, which is approximately 1.5 times higher than that of the nanowires. Ultrafast spectroscopy studies revealed that there is significant electron-hole recombination within the first few picoseconds, while Sn doping and the change of surface morphology have no major effect on the ultrafast dynamics of the charge carriers on the picosecond time scales. The enhanced photoactivity in Sn-doped hematite nanostructures should be due to the improved electrical conductivity and increased surface area.

  2. Nanowire-based All Oxide Solar Cells

    SciTech Connect

    Yang*, Benjamin D. Yuhas and Peidong; Yang, Peidong

    2008-12-07

    We present an all-oxide solar cell fabricated from vertically oriented zinc oxide nanowires and cuprous oxide nanoparticles. Our solar cell consists of vertically oriented n-type zinc oxide nanowires, surrounded by a film constructed from p-type cuprous oxide nanoparticles. Our solution-based synthesis of inexpensive and environmentally benign oxide materials in a solar cell would allow for the facile production of large-scale photovoltaic devices. We found that the solar cell performance is enhanced with the addition of an intermediate oxide insulating layer between the nanowires and the nanoparticles. This observation of the important dependence of the shunt resistance on the photovoltaic performance is widely applicable to any nanowire solar cell constructed with the nanowire array in direct contact with one electrode.

  3. LTCC based bioreactors for cell cultivation

    NASA Astrophysics Data System (ADS)

    Bartsch, H.; Welker, T.; Welker, K.; Witte, H.; Müller, J.

    2016-01-01

    LTCC multilayers offer a wide range of structural options and flexibility of connections not available in standard thin film technology. Therefore they are considered as material base for cell culture reactors. The integration of microfluidic handling systems and features for optical and electrical capturing of indicators for cell culture growth offers the platform for an open system concept. The present paper assesses different approaches for the creation of microfluidic channels in LTCC multilayers. Basic functions required for the fluid management in bioreactors include temperature and flow control. Both features can be realized with integrated heaters and temperature sensors in LTCC multilayers. Technological conditions for the integration of such elements into bioreactors are analysed. The temperature regulation for the system makes use of NTC thermistor sensors which serve as real value input for the control of the heater. It allows the adjustment of the fluid temperature with an accuracy of 0.2 K. The tempered fluid flows through the cell culture chamber. Inside of this chamber a thick film electrode array monitors the impedance as an indicator for the growth process of 3-dimensional cell cultures. At the system output a flow sensor is arranged to monitor the continual flow. For this purpose a calorimetric sensor is implemented, and its crucial design parameters are discussed. Thus, the work presented gives an overview on the current status of LTCC based fluid management for cell culture reactors, which provides a promising base for the automation of cell culture processes.

  4. Biotoxin Detection Using Cell-Based Sensors

    PubMed Central

    Banerjee, Pratik; Kintzios, Spyridon; Prabhakarpandian, Balabhaskar

    2013-01-01

    Cell-based biosensors (CBBs) utilize the principles of cell-based assays (CBAs) by employing living cells for detection of different analytes from environment, food, clinical, or other sources. For toxin detection, CBBs are emerging as unique alternatives to other analytical methods. The main advantage of using CBBs for probing biotoxins and toxic agents is that CBBs respond to the toxic exposures in the manner related to actual physiologic responses of the vulnerable subjects. The results obtained from CBBs are based on the toxin-cell interactions, and therefore, reveal functional information (such as mode of action, toxic potency, bioavailability, target tissue or organ, etc.) about the toxin. CBBs incorporate both prokaryotic (bacteria) and eukaryotic (yeast, invertebrate and vertebrate) cells. To create CBB devices, living cells are directly integrated onto the biosensor platform. The sensors report the cellular responses upon exposures to toxins and the resulting cellular signals are transduced by secondary transducers generating optical or electrical signals outputs followed by appropriate read-outs. Examples of the layout and operation of cellular biosensors for detection of selected biotoxins are summarized. PMID:24335754

  5. Sensitive-cell-based fish chromatophore biosensor

    NASA Astrophysics Data System (ADS)

    Plant, Thomas K.; Chaplen, Frank W.; Jovanovic, Goran; Kolodziej, Wojtek; Trempy, Janine E.; Willard, Corwin; Liburdy, James A.; Pence, Deborah V.; Paul, Brian K.

    2004-07-01

    A sensitive biosensor (cytosensor) has been developed based on color changes in the toxin-sensitive colored living cells of fish. These chromatophores are highly sensitive to the presence of many known and unknown toxins produced by microbial pathogens and undergo visible color changes in a dose-dependent manner. The chromatophores are immobilized and maintained in a viable state while potential pathogens multiply and fish cell-microbe interactions are monitored. Low power LED lighting is used to illuminate the chromatophores which are magnified using standard optical lenses and imaged onto a CCD array. Reaction to toxins is detected by observing changes is the total area of color in the cells. These fish chromatophores are quite sensitive to cholera toxin, Staphococcus alpha toxin, and Bordatella pertussis toxin. Numerous other toxic chemical and biological agents besides bacterial toxins also cause readily detectable color effects in chromatophores. The ability of the chromatophore cell-based biosensor to distinguish between different bacterial pathogens was examined. Toxin producing strains of Salmonella enteritis, Vibrio parahaemolyticus, and Bacillus cereus induced movement of pigmented organelles in the chromatophore cells and this movement was measured by changes in the optical density over time. Each bacterial pathogen elicited this measurable response in a distinctive and signature fashion. These results suggest a chromatophore cell-based biosensor assay may be applicable for the detection and identification of virulence activities associated with certain air-, food-, and water-borne bacterial pathogens.

  6. An Integrated Device View on Photo-Electrochemical Solar-Hydrogen Generation.

    PubMed

    Modestino, Miguel A; Haussener, Sophia

    2015-01-01

    Devices that directly capture and store solar energy have the potential to significantly increase the share of energy from intermittent renewable sources. Photo-electrochemical solar-hydrogen generators could become an important contributor, as these devices can convert solar energy into fuels that can be used throughout all sectors of energy. Rather than focusing on scientific achievement on the component level, this article reviews aspects of overall component integration in photo-electrochemical water-splitting devices that ultimately can lead to deployable devices. Throughout the article, three generalized categories of devices are considered with different levels of integration and spanning the range of complete integration by one-material photo-electrochemical approaches to complete decoupling by photovoltaics and electrolyzer devices. By using this generalized framework, we describe the physical aspects, device requirements, and practical implications involved with developing practical photo-electrochemical water-splitting devices. Aspects reviewed include macroscopic coupled multiphysics device models, physical device demonstrations, and economic and life cycle assessments, providing the grounds to draw conclusions on the overall technological outlook.

  7. Nanopillar based electrochemical biosensor for monitoring microfluidic based cell culture

    NASA Astrophysics Data System (ADS)

    Gangadharan, Rajan

    In-vitro assays using cultured cells have been widely performed for studying many aspects of cell biology and cell physiology. These assays also form the basis of cell based sensing. Presently, analysis procedures on cell cultures are done using techniques that are not integrated with the cell culture system. This approach makes continuous and real-time in-vitro measurements difficult. It is well known that the availability of continuous online measurements for extended periods of time will help provide a better understanding and will give better insight into cell physiological events. With this motivation we developed a highly sensitive, selective and stable microfluidic electrochemical glucose biosensor to make continuous glucose measurements in cell culture media. The performance of the microfluidic biosensor was enhanced by adding 3D nanopillars to the electrode surfaces. The microfluidic glucose biosensor consisted of three electrodes---Enzyme electrode, Working electrode, and Counter electrode. All these electrodes were enhanced with nanopillars and were optimized in their respective own ways to obtain an effective and stable biosensing device in cell culture media. For example, the 'Enzyme electrode' was optimized for enzyme immobilization via either a polypyrrole-based or a self-assembled-monolayer-based immobilization method, and the 'Working electrode' was modified with Prussian Blue or electropolymerized Neutral Red to reduce the working potential and also the interference from other interacting electro-active species. The complete microfluidic biosensor was tested for its ability to monitor glucose concentration changes in cell culture media. The significance of this work is multifold. First, the developed device may find applications in continuous and real-time measurements of glucose concentrations in in-vitro cell cultures. Second, the development of a microfluidic biosensor will bring technical know-how toward constructing continuous glucose

  8. Influence of substrates on photoelectrochemical performance of sprayed n-CdIn{sub 2}S{sub 4} electrodes

    SciTech Connect

    Sawant, R.R.; Shinde, S.S.; Bhosale, C.H.; Rajpure, K.Y.

    2010-07-15

    Cadmium indium sulphide (CdIn{sub 2}S{sub 4}) electrodes have been prepared onto the preheated fluorine doped tin oxide (FTO) coated glass and stainless steel (SS) substrates at optimized deposition conditions by using spray pyrolysis. Influence of substrates on the photoelectrochemical (PEC) performance has been carried out using cell configuration n-CdIn{sub 2}S{sub 4}/1 M (NaOH + Na{sub 2}S + S)/C for studying the current-voltage (I-V), photovoltaic output, photovoltaic rise and decay, photo and spectral responses and capacitance-voltage (C-V) characteristics. The junction ideality factor in dark (n{sub D}) and light (n{sub L}), series and shunt resistances (R{sub s} and R{sub sh}), fill factor (FF) and efficiency ({eta}) for the cell have been estimated. The measured fill factor (FF) and cell efficiency ({eta}) of the cells are found to be 0.47%, 0.38%, and 1.06%, 0.38% for FTO and SS substrates respectively. The Energy band diagram of band bending has been constructed using the physical parameters estimated from Mott-Schottky plots. Mott-Schottky plots shows the flat-band potential (V{sub fb}) of CdIn{sub 2}S{sub 4} films to be -1.15 V/SCE and -0.90 V/SCE on FTO and SS substrates respectively. (author)

  9. Atomic Force Microscopy Based Cell Shape Index

    NASA Astrophysics Data System (ADS)

    Adia-Nimuwa, Usienemfon; Mujdat Tiryaki, Volkan; Hartz, Steven; Xie, Kan; Ayres, Virginia

    2013-03-01

    Stellation is a measure of cell physiology and pathology for several cell groups including neural, liver and pancreatic cells. In the present work, we compare the results of a conventional two-dimensional shape index study of both atomic force microscopy (AFM) and fluorescent microscopy images with the results obtained using a new three-dimensional AFM-based shape index similar to sphericity index. The stellation of astrocytes is investigated on nanofibrillar scaffolds composed of electrospun polyamide nanofibers that has demonstrated promise for central nervous system (CNS) repair. Recent work by our group has given us the ability to clearly segment the cells from nanofibrillar scaffolds in AFM images. The clear-featured AFM images indicated that the astrocyte processes were longer than previously identified at 24h. It was furthermore shown that cell spreading could vary significantly as a function of environmental parameters, and that AFM images could record these variations. The new three-dimensional AFM-based shape index incorporates the new information: longer stellate processes and cell spreading. The support of NSF PHY-095776 is acknowledged.

  10. Novel Fuel Cells for Coal Based Systems

    SciTech Connect

    Thomas Tao

    2011-12-31

    The goal of this project was to acquire experimental data required to assess the feasibility of a Direct Coal power plant based upon an Electrochemical Looping (ECL) of Liquid Tin Anode Solid Oxide Fuel Cell (LTA-SOFC). The objective of Phase 1 was to experimentally characterize the interaction between the tin anode, coal fuel and cell component electrolyte, the fate of coal contaminants in a molten tin reactor (via chemistry) and their impact upon the YSZ electrolyte (via electrochemistry). The results of this work will provided the basis for further study in Phase 2. The objective of Phase 2 was to extend the study of coal impurities impact on fuel cell components other than electrolyte, more specifically to the anode current collector which is made of an electrically conducting ceramic jacket and broad based coal tin reduction. This work provided a basic proof-of-concept feasibility demonstration of the direct coal concept.

  11. Photoelectrochemical Conversion from Graphitic C3N4 Quantum Dot Decorated Semiconductor Nanowires.

    PubMed

    An, Tiance; Tang, Jing; Zhang, Yueyu; Quan, Yingzhou; Gong, Xingao; Al-Enizi, Abdullah M; Elzatahry, Ahmed A; Zhang, Lijuan; Zheng, Gengfeng

    2016-05-25

    Despite the recent progress of developing graphitic carbon nitride (g-C3N4) as a metal-free photocatalyst, the synthesis of nanostructured g-C3N4 has still remained a complicated and time-consuming approach from its bulk powder, which substantially limits its photoelectrochemical (PEC) applications as well as the potential to form composites with other semiconductors. Different from the labor-intensive methods used before, such as exfoliation or assistant templates, herein, we developed a facile method to synthesize graphitic C3N4 quantum dots (g-CNQDs) directly grown on TiO2 nanowire arrays via a one-step quasi-chemical vapor deposition (CVD) process in a homemade system. The as-synthesized g-CNQDs uniformly covered over the surface of TiO2 nanowires and exhibited attractive photoluminescence (PL) properties. In addition, compared to pristine TiO2, the heterojunction of g-CNQD-decorated TiO2 nanowires showed a substantially enhanced PEC photocurrent density of 3.40 mA/cm(2) at 0 V of applied potential vs Ag/AgCl under simulated solar light (300 mW/cm(2)) and excellent stability with ∼82% of the photocurrent retained after over 10 h of continuous testing, attributed to the quantum and sensitization effects of g-CNQDs. Density functional theory calculations were further carried out to illustrate the synergistic effect of TiO2 and g-CNQD. Our method suggests that a variety of g-CNQD-based composites with other semiconductor nanowires can be synthesized for energy applications.

  12. Polyaniline hybridized surface defective ZnO nanorods with long-term stable photoelectrochemical activity

    NASA Astrophysics Data System (ADS)

    Bera, Susanta; Khan, Hasmat; Biswas, Indranil; Jana, Sunirmal

    2016-10-01

    We report surfactant/template free precursor solution based synthesis of polyaniline (PANI) hybridized surface defective ZnO nanorods by a two-step process. Initially, ZnO nanorods have been prepared at 95 °C, followed by hybridization (coating) of PANI onto the ZnO via in situ polymerization of aniline monomer, forming ZnO-PANI nanohybrid (ZP). The structural properties of ZP have been analyzed by X-ray diffraction (XRD) and transmission electron microscopic (TEM) studies. The presence of surface defects especially the oxygen vacancies in ZnO has been characterized by photoluminescence emission, high resolution TEM, X-ray photoelectron spectroscopy (XPS) and micro-Raman spectral measurements. The chemical interaction of PANI with ZnO has been examined by Fourier transform infrared (FTIR) and XPS analyses. A significant enhancement in visible absorption of ZP sample is found as evidenced from UV-vis diffused reflectance spectral study. BET nitrogen adsorption-desorption isotherm shows an improved textural property (pore size, pore volume) of ZP. Moreover, a long-term stable photoelectrochemical activity (PEC) of ZP is found compare to pristine ZnO. The synergic effect of PANI hybridization and the presence of surface defects in ZnO NRs can enhance the PEC by prolonging the recombination rate of photogenerated charge carriers. The effect can also provide large number of active sites to make electrolyte diffusion and mass transportation easier in the nanohybrid. This simple synthesis strategy can be adopted for PANI hybridization with different metal oxide semiconductors towards enhancing PEC activity of the hybrid materials.

  13. Fiber and fabric solar cells by directly weaving carbon nanotube yarns with CdSe nanowire-based electrodes.

    PubMed

    Zhang, Luhui; Shi, Enzheng; Ji, Chunyan; Li, Zhen; Li, Peixu; Shang, Yuanyuan; Li, Yibin; Wei, Jinquan; Wang, Kunlin; Zhu, Hongwei; Wu, Dehai; Cao, Anyuan

    2012-08-21

    Electrode materials are key components for fiber solar cells, and when combined with active layers (for light absorption and charge generation) in appropriate ways, they enable design and fabrication of efficient and innovative device structures. Here, we apply carbon nanotube yarns as counter electrodes in combination with CdSe nanowire-grafted primary electrodes (Ti wire) for making fiber and fabric-shaped photoelectrochemical cells with power conversion efficiencies in the range 1% to 2.9%. The spun-twist long nanotube yarns possess both good electrical conductivity and mechanical flexibility compared to conventional metal wires or carbon fibers, which facilitate fabrication of solar cells with versatile configurations. A unique feature of our process is that instead of making individual fiber cells, we directly weave single or multiple nanotube yarns with primary electrodes into a functional fabric. Our results demonstrate promising applications of semiconducting nanowires and carbon nanotubes in woven photovoltaics.

  14. Fiber and fabric solar cells by directly weaving carbon nanotube yarns with CdSe nanowire-based electrodes

    NASA Astrophysics Data System (ADS)

    Zhang, Luhui; Shi, Enzheng; Ji, Chunyan; Li, Zhen; Li, Peixu; Shang, Yuanyuan; Li, Yibin; Wei, Jinquan; Wang, Kunlin; Zhu, Hongwei; Wu, Dehai; Cao, Anyuan

    2012-07-01

    Electrode materials are key components for fiber solar cells, and when combined with active layers (for light absorption and charge generation) in appropriate ways, they enable design and fabrication of efficient and innovative device structures. Here, we apply carbon nanotube yarns as counter electrodes in combination with CdSe nanowire-grafted primary electrodes (Ti wire) for making fiber and fabric-shaped photoelectrochemical cells with power conversion efficiencies in the range 1% to 2.9%. The spun-twist long nanotube yarns possess both good electrical conductivity and mechanical flexibility compared to conventional metal wires or carbon fibers, which facilitate fabrication of solar cells with versatile configurations. A unique feature of our process is that instead of making individual fiber cells, we directly weave single or multiple nanotube yarns with primary electrodes into a functional fabric. Our results demonstrate promising applications of semiconducting nanowires and carbon nanotubes in woven photovoltaics.Electrode materials are key components for fiber solar cells, and when combined with active layers (for light absorption and charge generation) in appropriate ways, they enable design and fabrication of efficient and innovative device structures. Here, we apply carbon nanotube yarns as counter electrodes in combination with CdSe nanowire-grafted primary electrodes (Ti wire) for making fiber and fabric-shaped photoelectrochemical cells with power conversion efficiencies in the range 1% to 2.9%. The spun-twist long nanotube yarns possess both good electrical conductivity and mechanical flexibility compared to conventional metal wires or carbon fibers, which facilitate fabrication of solar cells with versatile configurations. A unique feature of our process is that instead of making individual fiber cells, we directly weave single or multiple nanotube yarns with primary electrodes into a functional fabric. Our results demonstrate promising applications

  15. DNA Based Electrochromic and Photovoltaic Cells

    DTIC Science & Technology

    2012-01-01

    SUBJECT TERMS 16. SECURITY CLASSIFICATION OF: 17. LIMITATION OF ABSTRACT 18. NUMBER OF PAGES 19a. NAME OF RESPONSIBLE PERSON a. REPORT...9550-09-1-0647 final 01-09-2009 ; 30-11-2011 DNA Based Electrochromic and Photovoltaic Cells FA 9550-09-1-0647 Pawlicka, Agnieszka, J. Instituto de...as well as DNA-CTMA and DNA-DODA were also obtained and characterized. High ionic conductivity results combined with transparency and adhesion to the

  16. Human Neural Cell-Based Biosensor

    DTIC Science & Technology

    2011-10-11

    types have potential for being physiologically relevant in vitro models for botulinum toxin detection and neuron-glia interactions, respectively...unknown neurotoxicants. (5) We developed an immunoblot based method for detecting botulinum toxin using the mixed neuronal hN2™ cell line, thus creating...a first generation human cellular model for botulinum toxin detection – standard of comparison for existing and future models.neurotoxicity

  17. Ontology for cell-based geographic information

    NASA Astrophysics Data System (ADS)

    Zheng, Bin; Huang, Lina; Lu, Xinhai

    2009-10-01

    Inter-operability is a key notion in geographic information science (GIS) for the sharing of geographic information (GI). That requires a seamless translation among different information sources. Ontology is enrolled in GI discovery to settle the semantic conflicts for its natural language appearance and logical hierarchy structure, which are considered to be able to provide better context for both human understanding and machine cognition in describing the location and relationships in the geographic world. However, for the current, most studies on field ontology are deduced from philosophical theme and not applicable for the raster expression in GIS-which is a kind of field-like phenomenon but does not physically coincide to the general concept of philosophical field (mostly comes from the physics concepts). That's why we specifically discuss the cell-based GI ontology in this paper. The discussion starts at the investigation of the physical characteristics of cell-based raster GI. Then, a unified cell-based GI ontology framework for the recognition of the raster objects is introduced, from which a conceptual interface for the connection of the human epistemology and the computer world so called "endurant-occurrant window" is developed for the better raster GI discovery and sharing.

  18. Template synthesis and photoelectrochemical properties of Bi{sub 2}S{sub 3} microflowers

    SciTech Connect

    Cao, Feng; Wang, Jianmin; Tu, Wanhong; Lv, Xin; Li, Song; Qin, Gaowu

    2015-08-15

    Highlights: • Bi{sub 2}S{sub 3} microflowers were fabricated by using a sacrificial-template method. • The effect of the specific experimental parameters was examined. • Photoelectrochemical measurements were characterized. - Abstract: Uniform hierarchical Bi{sub 2}S{sub 3} nanostructures were fabricated by using Bi{sub 2}O{sub 2}CO{sub 3} nanoflowers as a sacrificial template through a hydrothermal reaction with an aqueous L-cysteine solution. Multiple techniques, such as X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Mott–Schottky (M–S) plot and electrochemical impedance spectroscopy (EIS) were applied to investigate the structure, morphology and photoelectrochemical properties of the as-prepared samples. This work demonstrated a simple and cost-effective strategy for the design and fabrication of well-defined complex hierarchical nanomaterials, which can be potentially used in energy storage and conversion devices.

  19. Platinum monolayer electrocatalyst on gold nanostructures on silicon for photoelectrochemical hydrogen evolution.

    PubMed

    Kye, Joohong; Shin, Muncheol; Lim, Bora; Jang, Jae-Won; Oh, Ilwhan; Hwang, Seongpil

    2013-07-23

    Pt monolayer decorated gold nanostructured film on planar p-type silicon is utilized for photoelectrochemical H2 generation in this work. First, gold nanostructured film on silicon was spontaneously produced by galvanic displacement of the reduction of gold ion and the oxidation of silicon in the presence of fluoride anion. Second, underpotential deposition (UPD) of copper under illumination produced Cu monolayer on gold nanostructured film followed by galvanic exchange of less-noble Cu monolayer with more-noble PtCl6(2-). Pt(shell)/Au(core) on p-type silicon showed the similar activity with platinum nanoparticle on silicon for photoelectrochemical hydrogen evolution reaction in spite of low platinum loading. From Tafel analysis, Pt(shell)/Au(core) electrocatalyst shows the higher area-specific activity than platinum nanoparticle on silicon demonstrating the significant role of underlying gold for charge transfer reaction from silicon to H(+) through platinum catalyst.

  20. Electrodeposited cobalt-sulfide catalyst for electrochemical and photoelectrochemical hydrogen generation from water.

    PubMed

    Sun, Yujie; Liu, Chong; Grauer, David C; Yano, Junko; Long, Jeffrey R; Yang, Peidong; Chang, Christopher J

    2013-11-27

    A cobalt-sulfide (Co-S) film prepared via electrochemical deposition on conductive substrates is shown to behave as an efficient and robust catalyst for electrochemical and photoelectrochemical hydrogen generation from neutral pH water. Electrochemical experiments demonstrate that the film exhibits a low catalytic onset overpotential (η) of 43 mV, a Tafel slope of 93 mV/dec, and near 100% Faradaic efficiency in pH 7 phosphate buffer. Catalytic current densities can approach 50 mA/cm(2) and activity is maintained for at least 40 h. The catalyst can also be electrochemically coated on silicon, rendering a water-compatible photoelectrochemical system for hydrogen production under simulated 1 sun illumination. The facile preparation of this Co-S film, along with its low overpotential, high activity, and long-term aqueous stability, offer promising features for potential use in solar energy applications.

  1. Surface aspects of sol-gel derived hematite films for the photoelectrochemical oxidation of water.

    PubMed

    Herrmann-Geppert, Iris; Bogdanoff, Peter; Radnik, Jörg; Fengler, Steffen; Dittrich, Thomas; Fiechter, Sebastian

    2013-02-07

    α-Fe(2)O(3) (hematite) photoanodes for the oxygen evolution reaction (OER) were prepared by a cost-efficient sol-gel procedure. Due to low active photoelectrochemical properties observed, it is assumed that the sol-gel procedure leads to hematite films with defects and surface states on which generated charge carriers are recombined or immobilized in trap processes. Electrochemical activation was proven to diminish unfavourable surface groups to some extent. More efficiently, a plasma treatment improves significantly the photoelectrochemical properties of the OER. X-ray photoelectron spectroscopy (XPS) analysis reveals an oxygen enriched surface layer with new oxygen species which may be responsible for the improved electrochemical activity. Due to surface photovoltage an increased fraction of transferred charge carriers from these newly produced surface defects are identified.

  2. Influence of polyaniline on photoelectrochemical characterization of TiO2-PANI layers

    NASA Astrophysics Data System (ADS)

    Tot Pham, Thi; Duyen Nguyen, The; Xuan, Thi Mai; Thanh Thuy Mai, Thi; Yen Tran, Hai; Binh Phan, Thi

    2015-01-01

    TiO2-polyaniline (PANI) composites were prepared by thermal oxidation of titanium substrate combined with chemical polymerization of aniline. Their chemical structures were determined by infrared (IR) spectroscopy and x-ray analysis. Their morphological structures were characterized by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Their electro- and photoelectrochmical properties were examined by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) analysis. The results showed that their photoelectrochemical behavior was better than that of TiO2 electrode; among them the more PANI existed in composite the higher was the anodic photoelectrochemical current. It was also found that the composite has structure in the range of nanosize. Report at 2nd International Workshop on Nanomaterials for Energy Conversion, 17-19 November 2014, Ho Chi Minh City, Vietnam.

  3. Photoelectric processes in CdSe thin film solar cells

    SciTech Connect

    Rickus, E.

    1984-05-01

    Efficiencies exceeding 7 percent have been achieved with CdSe/ZnSe/Au thin film solar cells. The collection efficiency of carriers in highly oriented CdSe films is near unity, resulting in short circuit current densities comparable to values observed on single crystalline cells. Recombination of carriers at the CdSe/ZnSe interface plays a minor role. CdSe /SUB x/ Te /SUB 1-x/ cells show the potential of enhanced short circuit current densities. Crystallographic and chemical inhomogeneities have a major influence on their performance. The comparison of photoelectrochemical cells based on CdSe single crystals and on polycrystalline layers demonstrates the photovoltaic quality of our CdSe films.

  4. [Dendritic cell-based therapeutic cancer vaccines].

    PubMed

    Rizzo, Manglio; Alaniz, Laura; Mazzolini, Guillermo D

    2016-01-01

    In recent years immunotherapy has revolutionized the treatment of patients with advanced cancer. The increased knowledge in the tumor immune-biology has allowed developing rational treatments by manipulation of the immune system with significant clinical impact. This rapid development has significantly changed the prognosis of many tumors without treatment options up to date. Other strategies have explored the use of therapeutic vaccines based on dendritic cells (DC) by inducing antitumor immunity. DC are cells of hematopoietic origin, constitutively expressing molecules capable to present antigens, that are functionally the most potent inducers of the activation and proliferation of antigen specific T lymphocytes. The CD8+ T cells proliferate and acquire cytotoxic capacity after recognizing their specific antigen presented on the surface of DC, although only some types of DC can present antigens internalized from outside the cell to precursors of cytotoxic T lymphocytes (this function is called cross-presentation) requiring translocation mechanisms of complex antigens. The induction of an effective adaptive immune response is considered a good option given its specificity, and prolonged duration of response. The DC, thanks to its particular ability of antigen presentation and lymphocyte stimulation, are able to reverse the poor antitumor immune response experienced by patients with cancer. The DC can be obtained from various sources, using different protocols to generate differentiation and maturation, and are administered by various routes such as subcutaneous, intravenous or intranodal. The wide variety of protocols resulted in heterogeneous clinical responses.

  5. Si/PEDOT hybrid core/shell nanowire arrays as photoelectrodes for photoelectrochemical water-splitting

    NASA Astrophysics Data System (ADS)

    Li, Xiaojuan; Lu, Wenhui; Dong, Weiling; Chen, Qi; Wu, Dan; Zhou, Wenzheng; Chen, Liwei

    2013-05-01

    Si/poly(3,4-ethylenedioxythiophene) (PEDOT) core/shell nanowire arrays have been prepared by chemical etching of Si nanowires followed by vapor-phase polymerization of PEDOT as hybrid photoanodes for photoelectrochemical water-splitting. The PEDOT layer is employed as a multi-functional coating to prevent photocorrosion of Si nanowires, collect photogenerated holes and catalyze the water oxidation reaction. The amino silane modified Si nanowire surface improves PEDOT layer adhesion, and the resulting photoanode exhibits better photoresponse and improved stability. By tuning the length of the nanowires, we identify that the competition between the carrier recombination and catalytic water oxidation reaction is the primary factor determining the photoelectrocatalytic activity of the hybrid photoanode.Si/poly(3,4-ethylenedioxythiophene) (PEDOT) core/shell nanowire arrays have been prepared by chemical etching of Si nanowires followed by vapor-phase polymerization of PEDOT as hybrid photoanodes for photoelectrochemical water-splitting. The PEDOT layer is employed as a multi-functional coating to prevent photocorrosion of Si nanowires, collect photogenerated holes and catalyze the water oxidation reaction. The amino silane modified Si nanowire surface improves PEDOT layer adhesion, and the resulting photoanode exhibits better photoresponse and improved stability. By tuning the length of the nanowires, we identify that the competition between the carrier recombination and catalytic water oxidation reaction is the primary factor determining the photoelectrocatalytic activity of the hybrid photoanode. Electronic supplementary information (ESI) available: The schematic setup of photoelectrochemical performance tests, and the SEM images of different photoanodes before and after photoelectrochemical tests. See DOI: 10.1039/c3nr00867c

  6. A novel quaternary solid solution photo-absorber material for photoelectrochemical hydrogen generation.

    PubMed

    Hong, Tiantian; Liu, Zhifeng; Yan, Weiguo; Wang, Bo; Zhang, Xueqi; Liu, Junqi; Wang, Junkai; Han, Jianhua

    2015-09-14

    We report a novel quaternary solid solution (Ag-Cu-Sb-S or ACSS) serving as a photo-absorber material in the photoelectrochemical field for the first time, and ZnO/ACSS nanoarrays exhibited a photocurrent density of 4.45 mA cm(-2). The research indicates that ZnO/ACSS composite structures have enormous potential in PEC hydrogen generation systems.

  7. Photoelectrochemical characterization of dual-layered anodic TiO2 nanotubes with honeycomb morphology

    NASA Astrophysics Data System (ADS)

    Sitler, S. J.; Raja, K. S.; Karmiol, Z.; Chidambaram, D.

    2017-01-01

    Titanium dioxide (TiO2) nanotubes having a novel honeycomb like morphology were synthesized by a two-step anodization process and characterized for photoelectrochemical behavior. The titania nanotubes with honeycomb morphology showed at least 32% higher photocurrent density than the regular vertically oriented titania nanotubes at any given bias potential. The enhanced photoactivity of the honeycomb morphology was attributed to the better charge transport properties and the presence of a hemispherical surface morphology that enhanced the light harvesting behavior.

  8. Boron-doped diamond semiconductor electrodes: Efficient photoelectrochemical CO2 reduction through surface modification

    NASA Astrophysics Data System (ADS)

    Roy, Nitish; Hirano, Yuiri; Kuriyama, Haruo; Sudhagar, Pitchaimuthu; Suzuki, Norihiro; Katsumata, Ken-Ichi; Nakata, Kazuya; Kondo, Takeshi; Yuasa, Makoto; Serizawa, Izumi; Takayama, Tomoaki; Kudo, Akihiko; Fujishima, Akira; Terashima, Chiaki

    2016-11-01

    Competitive hydrogen evolution and multiple proton-coupled electron transfer reactions limit photoelectrochemical CO2 reduction in aqueous electrolyte. Here, oxygen-terminated lightly boron-doped diamond (BDDL) thin films were synthesized as a semiconductor electron source to accelerate CO2 reduction. However, BDDL alone could not stabilize the intermediates of CO2 reduction, yielding a negligible amount of reduction products. Silver nanoparticles were then deposited on BDDL because of their selective electrochemical CO2 reduction ability. Excellent selectivity (estimated CO:H2 mass ratio of 318:1) and recyclability (stable for five cycles of 3 h each) for photoelectrochemical CO2 reduction were obtained for the optimum silver nanoparticle-modified BDDL electrode at ‑1.1 V vs. RHE under 222-nm irradiation. The high efficiency and stability of this catalyst are ascribed to the in situ photoactivation of the BDDL surface during the photoelectrochemical reaction. The present work reveals the potential of BDDL as a high-energy electron source for use with co-catalysts in photochemical conversion.

  9. Controlled fabrication of Sn/TiO2 nanorods for photoelectrochemical water splitting

    PubMed Central

    2013-01-01

    In this work, we investigate the controlled fabrication of Sn-doped TiO2 nanorods (Sn/TiO2 NRs) for photoelectrochemical water splitting. Sn is incorporated into the rutile TiO2 nanorods with Sn/Ti molar ratios ranging from 0% to 3% by a simple solvothermal synthesis method. The obtained Sn/TiO2 NRs are single crystalline with a rutile structure. The concentration of Sn in the final nanorods can be well controlled by adjusting the molar ratio of the precursors. Photoelectrochemical experiments are conducted to explore the photocatalytic activity of Sn/TiO2 NRs with different doping levels. Under the illumination of solar simulator with the light intensity of 100 mW/cm2, our measurements reveal that the photocurrent increases with increasing doping level and reaches the maximum value of 1.01 mA/cm2 at −0.4 V versus Ag/AgCl, which corresponds to up to about 50% enhancement compared with the pristine TiO2 NRs. The Mott-Schottky plots indicate that incorporation of Sn into TiO2 nanorod can significantly increase the charge carrier density, leading to enhanced conductivity of the nanorod. Furthermore, we demonstrate that Sn/TiO2 NRs can be a promising candidate for photoanode in photoelectrochemical water splitting because of their excellent chemical stability. PMID:24191909

  10. Boron-doped diamond semiconductor electrodes: Efficient photoelectrochemical CO2 reduction through surface modification

    PubMed Central

    Roy, Nitish; Hirano, Yuiri; Kuriyama, Haruo; Sudhagar, Pitchaimuthu; Suzuki, Norihiro; Katsumata, Ken-ichi; Nakata, Kazuya; Kondo, Takeshi; Yuasa, Makoto; Serizawa, Izumi; Takayama, Tomoaki; Kudo, Akihiko; Fujishima, Akira; Terashima, Chiaki

    2016-01-01

    Competitive hydrogen evolution and multiple proton-coupled electron transfer reactions limit photoelectrochemical CO2 reduction in aqueous electrolyte. Here, oxygen-terminated lightly boron-doped diamond (BDDL) thin films were synthesized as a semiconductor electron source to accelerate CO2 reduction. However, BDDL alone could not stabilize the intermediates of CO2 reduction, yielding a negligible amount of reduction products. Silver nanoparticles were then deposited on BDDL because of their selective electrochemical CO2 reduction ability. Excellent selectivity (estimated CO:H2 mass ratio of 318:1) and recyclability (stable for five cycles of 3 h each) for photoelectrochemical CO2 reduction were obtained for the optimum silver nanoparticle-modified BDDL electrode at −1.1 V vs. RHE under 222-nm irradiation. The high efficiency and stability of this catalyst are ascribed to the in situ photoactivation of the BDDL surface during the photoelectrochemical reaction. The present work reveals the potential of BDDL as a high-energy electron source for use with co-catalysts in photochemical conversion. PMID:27892544

  11. Photoelectrochemical reduction of CO{sub 2} using silicate rock powder

    SciTech Connect

    Ohta, Kiyohisa; Ohguchi, Youko; Kaneco, Satochi

    1996-12-31

    Until now, numerous investigators have reported chemical fixation of carbon dioxide, such as electrochemical, photochemical and photoelectrochemical reductions. In these methods, relatively, a few studies on the photoelectrochemical conversion of CO{sub 2} have been reported. We have recently presented a photochemical reduction of carbon dioxide and hydrogen formation by using andesite sands as a photocatalyst under sunlight irradiation. At ambient temperature and atmospheric pressure, 6.5 {times} 10{sup -2} ml g{sup -1} methane and 7.0 {times} 10{sup -2} ml g{sup -1} of hydrogen were formed from carbon dioxide and water on the andesite. This report presents the photoelectrochemical reduction of CO{sub 2} using silicate rock (andesite) powder suspended in water. Carbon dioxide is the end product to complete combustion of all fossil fuels. The generation of carbon dioxide is the primary cause for the greenhouse effect. However, carbon dioxide is a potential carbon source. To utilize such a plentiful carbon source, it has been considered carbon dioxide as a feedstock for organic synthesis of carbonyl- and carboxyl-containing compounds or as an oxidant for oxidative synthesis of more valuable organics.

  12. Photoelectrochemical power, chemical energy and catalytic activity for organic evolution on natural pyrite interfaces.

    PubMed

    Tributsch, H; Fiechter, S; Jokisch, D; Rojas-Chapana, J; Ellmer, K

    2003-04-01

    Natural pyrite (FeS2) has frequently been discussed as a material involved in CO2 fixation in presence of H2S and as a possible catalyst for the origin of life. A straightforward chemical fixation of carbon dioxide as proposed by Wächtershauser could not be verified from thermo-chemical equilibrium calculations by minimizing Gibb's Free Energy in the system C, O, H, S, Fe and appears unlikely due to the experimentally encountered large overpotentials involved in CO2 fixation. However, the hypothesis, by W. R. Edwards, that pyrite in shallow coastal waters may have been involved, can be sustained. In this case, daily available photoelectrochemical power from FeS2/Fe2+/3+ interfaces could have made the difference in combination with electrochemical processes, such as hydrogen insertion, and the solubilization of pyrite by the amino acid cysteine to yield dissolved chemical energy. Periodical changes in energy supply could also have entrained primitive self-organization processes for organic-biological evolution. Natural samples from thirteen ore deposits have been investigated photoelectrochemically. Efficient light-induced current generation has been found with several of these samples so that photoelectrochemical processes generated by pyrite have to be considered as naturally occurring phenomena, which could have been even more pronounced in oxygen deficient environments. Pyrite from the Murgul mine in Turkey of suboceanic volcanic origin was closer examined as a model system to understand the morphology and chemistry of pyrite photoactivity.

  13. Controlled fabrication of Sn/TiO2 nanorods for photoelectrochemical water splitting

    NASA Astrophysics Data System (ADS)

    Sun, Bo; Shi, Tielin; Peng, Zhengchun; Sheng, Wenjun; Jiang, Ting; Liao, Guanglan

    2013-11-01

    In this work, we investigate the controlled fabrication of Sn-doped TiO2 nanorods (Sn/TiO2 NRs) for photoelectrochemical water splitting. Sn is incorporated into the rutile TiO2 nanorods with Sn/Ti molar ratios ranging from 0% to 3% by a simple solvothermal synthesis method. The obtained Sn/TiO2 NRs are single crystalline with a rutile structure. The concentration of Sn in the final nanorods can be well controlled by adjusting the molar ratio of the precursors. Photoelectrochemical experiments are conducted to explore the photocatalytic activity of Sn/TiO2 NRs with different doping levels. Under the illumination of solar simulator with the light intensity of 100 mW/cm2, our measurements reveal that the photocurrent increases with increasing doping level and reaches the maximum value of 1.01 mA/cm2 at -0.4 V versus Ag/AgCl, which corresponds to up to about 50% enhancement compared with the pristine TiO2 NRs. The Mott-Schottky plots indicate that incorporation of Sn into TiO2 nanorod can significantly increase the charge carrier density, leading to enhanced conductivity of the nanorod. Furthermore, we demonstrate that Sn/TiO2 NRs can be a promising candidate for photoanode in photoelectrochemical water splitting because of their excellent chemical stability.

  14. Cell-Based Therapy for Silicosis

    PubMed Central

    Lopes-Pacheco, Miquéias; Bandeira, Elga; Morales, Marcelo M.

    2016-01-01

    Silicosis is the most common pneumoconiosis globally, with higher prevalence and incidence in developing countries. To date, there is no effective treatment to halt or reverse the disease progression caused by silica-induced lung injury. Significant advances have to be made in order to reduce morbidity and mortality related to silicosis. In this review, we have highlighted the main mechanisms of action that cause lung damage by silica particles and summarized the data concerning the therapeutic promise of cell-based therapy for silicosis. PMID:27066079

  15. Optimizing mesenchymal stem cell-based therapeutics.

    PubMed

    Wagner, Joseph; Kean, Thomas; Young, Randell; Dennis, James E; Caplan, Arnold I

    2009-10-01

    Mesenchymal stem cell (MSC)-based therapeutics are showing significant benefit in multiple clinical trials conducted by both academic and commercial organizations, but obstacles remain for their large-scale commercial implementation. Recent studies have attempted to optimize MSC-based therapeutics by either enhancing their potency or increasing their delivery to target tissues. Overexpression of trophic factors or in vitro exposure to potency-enhancing factors are two approaches that are demonstrating success in preclinical animal models. Delivery enhancement strategies involving tissue-specific cytokine pathways or binding sites are also showing promise. Each of these strategies has its own set of distinct advantages and disadvantages when viewed with a mindset of ultimate commercialization and clinical utility.

  16. Photoelectrochemical etching of silicon carbide (SiC) and its characterization

    NASA Technical Reports Server (NTRS)

    Collins, D. M.; Harris, G. L.; Wongchotigul, K.

    1995-01-01

    Silicon carbide (SiC) is an attractive semiconductor material for high speed, high density, and high temperature device applications due to its wide bandgap (2.2-3.2 eV), high thermal conductivity, and high breakdown electric field (4 x 10(exp 6) V/cm). An instrumental process in the fabrication of semiconductor devices is the ability to etch in a highly controlled and selective manner for direct patterning techniques. A novel technique in etching using electrochemistry is described. This procedure involves the ultraviolet (UV) lamp-assisted photoelectrochemical etching of n-type 3C- and 6H-SiC to enhance the processing capability of device structures in SiC. While under UV illumination, the samples are anodically biased in an HF based aqueous solution since SiC has photoconductive properties. In order for this method to be effective, the UV light must be able to enhance the production of holes in the SiC during the etching process thus providing larger currents with light from the photocurrents generated than those currents with no light. Otherwise dark methods would be used as in the case of p-type 3C-SiC. Experiments have shown that the I/V characteristics of the SiC-electrolyte interface reveal a minimum etch voltage of 3 V and 4 V for n- and p-type 3C-SiC, respectively. Hence it is possible for etch-stops to occur. Etch rates calculated have been as high as 0.67 micrometer/min for p-type, 1.4 micrometer/min for n-type, and 1.1 micrometer/min for pn layer. On n-type 3C- SiC, an oxide formation is present where after etching a yellowish layer corresponds to a low Si/C ratio and a white layer corresponds to a high Si/C ratio. P-type 3C-SiC shows a grayish layer. Additionally, n-type 6H-SiC shows a brown layer with a minimum etch voltage of 3 V.

  17. Inorganic-organic solar cells based on quaternary sulfide as absorber materials.

    PubMed

    Hong, Tiantian; Liu, Zhifeng; Yan, Weiguo; Liu, Junqi; Zhang, Xueqi

    2015-12-14

    We report a novel promising quaternary sulfide (CuAgInS) to serve as a semiconductor sensitizer material in the photoelectrochemical field. In this study, CuAgInS (CAIS) sulfide sensitized ZnO nanorods were fabricated on ITO substrates through a facile and low-cost hydrothermal chemical method and applied on photoanodes for solar cells for the first time. The component and stoichiometry were key factors in determining the photoelectric performance of CAIS sulfide, which were controlled by modulating their reaction time. ZnO/Cu0.7Ag0.3InS2 nanoarrays exhibit an enhanced optical and photoelectric performance and the power conversion efficiency of ITO/ZnO/Cu0.7Ag0.3InS2/P3HT/Pt solid-state solar cell was up to 1.80%. The remarkable performance stems from improved electron transfer, a higher efficiency of light-harvesting and appropriate band gap alignment at the interface of the ZnO/Cu0.7Ag0.3InS2 NTs. The research indicates that CAIS as an absorbing material has enormous potential in solar cell systems.

  18. High Performance InGaN-Based Solar Cells

    DTIC Science & Technology

    2012-05-12

    quantum efficiency (EQE) for our solar cells ; increasing the total absorption in our solar ...in Fig. 1.2(a), which shows a typical plot of the dependence of external quantum efficiency (EQE) on wavelength for an InGaN-based solar cell . Aside... solar cells are examined in Section 8. Section 9 then discusses how to best integrate InGaN-based solar cells with GaAs -based multijunction solar

  19. Enhanced photoelectrochemical biosensing performances for graphene (2D) - Titanium dioxide nanowire (1D) heterojunction polymer conductive nanosponges.

    PubMed

    Muthuchamy, N; Lee, K-P; Gopalan, A-I

    2017-03-15

    In this work, an efficient photoelectrochemical (PEC) biosensing platform has been designed and developed based on graphene (G) through modifying it into an electroconductive polymer nanosponge (EPNS) and with the incorporation of titanium dioxide nanowires (TiO2 NW) (designated as TiO2 (G) NW@EPNS). Functioning as an efficient immobilization matrix for immobilization of the enzyme Cytochrome C (Cyt C), TiO2 (G) NW@EPNS delivers features for an efficient PEC biosensor, such as fast kinetics of direct electron transfer (DET) to the electrode and effective separation of photogenerated holes and electrons. TiO2 (G) NW@EPNS exhibited DET to the electrode with a highly heterogeneous electron transfer rate constant of 6.29±0.002s(-1). The existence of TiO2, G and EPNS in conjunction facilitates DET between the electrode surface and the protein. The fabricated PEC nitrite ion (NO2(-)) biosensor showed superior analytical performances such as wide linear range (0.5-9000µM), lowest detection limit (0.225mM) and excellent specificity for NO2(-) in the presence other interferences at a very low bias potential (-0.11V). This study opens up the feasibility of fabricating a PEC biosensor for any analyte using a matrix comprising of G and a photoactive material and EPNS, because these components synergistically contribute to effective immobilization of on enzyme, DET to the electrode and simple read-out under the light.

  20. A sensitive and label-free photoelectrochemical aptasensor using Co-doped ZnO diluted magnetic semiconductor nanoparticles.

    PubMed

    Li, Hongbo; Qiao, Yunfei; Li, Jing; Fang, Hailin; Fan, Dahe; Wang, Wei

    2016-03-15

    Co-doped ZnO diluted magnetic semiconductor as a novel photoelectric beacon was first constructed for photoelectrochemical (PEC) aptasensor of acetamiprid. The fabricated PEC sensing is based on the specific binding of acetamiprid and its aptamer, which induces the decreasement of enhanced photocurrent produced by the electron donor of quercetin. Co(2+) doping has a beneficial effect in extending the band width of light absorption of ZnO into the visible region and to promote the separation of the photoinduced carriers due to the sp-d exchange interactions existing between the band electrons and the localized d electrons of Co(2+). The fabricated aptasensor was linear with the concentration of acetamiprid in the range of 0.5-800 nmolL(-1) with the detection limit of 0.18 nmolL(-1). The presence of same concentration of other conventional pesticides did not interfere in the detection of acetamiprid and the recovery is between 96.2% and 103.7%. This novel PEC aptasensor has good performances with high sensitivity, good selectivity, low cost and portable features. The strategy of Co-doped ZnO diluted magnetic semiconductor paves a new way to improve the performances of PEC aptasensor.

  1. Cl-doped ZnO nanowires with metallic conductivity and their application for high-performance photoelectrochemical electrodes.

    PubMed

    Wang, Fei; Seo, Jung-Hun; Li, Zhaodong; Kvit, Alexander V; Ma, Zhenqiang; Wang, Xudong

    2014-01-22

    Doping semiconductor nanowires (NWs) for altering their electrical and optical properties is a critical strategy for tailoring the performance of nanodevices. ZnO NWs grown by hydrothermal method are pervasively used in optoelectronic, photovoltaic, and piezoelectric energy-harvesting devices. We synthesized in situ Cl-doped ZnO NWs with metallic conductivity that would fit seamlessly with these devices and improve their performance. Possible Cl doping mechanisms were discussed. UV-visible absorption spectroscopy confirmed the visible light transparency of Cl-doped ZnO NWs. Cl-doped ZnO NW/TiO2 core/shell-structured photoelectrochemical (PEC) anode was fabricated to demonstrate the application potential of highly conductive ZnO NWs. Higher photocurrent density and overall PEC efficiency compared with the undoped ZnO NW-based device were achieved. The successful doping and low resistivity of ZnO could unlock the potential of ZnO NWs for applications in low-cost flexible transparent electrodes.

  2. Cu2O/CuO Bilayered Composite as a High-Efficiency Photocathode for Photoelectrochemical Hydrogen Evolution Reaction

    PubMed Central

    Yang, Yang; Xu, Di; Wu, Qingyong; Diao, Peng

    2016-01-01

    Solar powered hydrogen evolution reaction (HER) is one of the key reactions in solar-to-chemical energy conversion. It is desirable to develop photocathodic materials that exhibit high activity toward photoelectrochemical (PEC) HER at more positive potentials because a higher potential means a lower overpotential for HER. In this work, the Cu2O/CuO bilayered composites were prepared by a facile method that involved an electrodeposition and a subsequent thermal oxidation. The resulting Cu2O/CuO bilayered composites exhibited a surprisingly high activity and good stability toward PEC HER, expecially at high potentials in alkaline solution. The photocurrent density for HER was 3.15 mA·cm−2 at the potential of 0.40 V vs. RHE, which was one of the two highest reported at the same potential on copper-oxide-based photocathode. The high photoactivity of the bilayered composite was ascribed to the following three advantages of the Cu2O/CuO heterojunction: (1) the broadened light absorption band that made more efficient use of solar energy, (2) the large space-charge-region potential that enabled a high efficiency for electron-hole separation, and (3) the high majority carrier density that ensured a faster charge transportation rate. This work reveals the potential of the Cu2O/CuO bilayered composite as a promising photocathodic material for solar water splitting. PMID:27748380

  3. Cu2O/CuO Bilayered Composite as a High-Efficiency Photocathode for Photoelectrochemical Hydrogen Evolution Reaction

    NASA Astrophysics Data System (ADS)

    Yang, Yang; Xu, Di; Wu, Qingyong; Diao, Peng

    2016-10-01

    Solar powered hydrogen evolution reaction (HER) is one of the key reactions in solar-to-chemical energy conversion. It is desirable to develop photocathodic materials that exhibit high activity toward photoelectrochemical (PEC) HER at more positive potentials because a higher potential means a lower overpotential for HER. In this work, the Cu2O/CuO bilayered composites were prepared by a facile method that involved an electrodeposition and a subsequent thermal oxidation. The resulting Cu2O/CuO bilayered composites exhibited a surprisingly high activity and good stability toward PEC HER, expecially at high potentials in alkaline solution. The photocurrent density for HER was 3.15 mA·cm‑2 at the potential of 0.40 V vs. RHE, which was one of the two highest reported at the same potential on copper-oxide-based photocathode. The high photoactivity of the bilayered composite was ascribed to the following three advantages of the Cu2O/CuO heterojunction: (1) the broadened light absorption band that made more efficient use of solar energy, (2) the large space-charge-region potential that enabled a high efficiency for electron-hole separation, and (3) the high majority carrier density that ensured a faster charge transportation rate. This work reveals the potential of the Cu2O/CuO bilayered composite as a promising photocathodic material for solar water splitting.

  4. Efficient Electrochemical and Photoelectrochemical H2 Production from Water by a Cobalt Dithiolene One-Dimensional Metal-Organic Surface.

    PubMed

    Downes, Courtney A; Marinescu, Smaranda C

    2015-11-04

    Solar-driven hydrogen evolution from water has emerged as an important methodology for the storage of renewable energy in chemical bonds. Efficient and practical clean-energy devices for electrochemical or photoelectrochemical splitting of water require the immobilization of stable and active hydrogen-evolving catalysts onto electrode or photocathode materials, which remains a significant challenge. Here we show that cobalt(II) reacts with benzene-1,2,4,5-tetrathiol in the presence of base to form a cobalt dithiolene polymer 1. The generated polymer is immobilized onto glassy carbon electrodes (GCE) to generate a metal-organic surface (MOS 1|GCE), which displays efficient H2-evolving activity and stability in acidic aqueous solutions. Moreover, the generated polymer is integrated with planar p-type Si to generate very efficient photocathode materials (MOS 1|Si) for solar-driven hydrogen production from water. Photocurrents up to 3.8 mA/cm(2) at 0 V vs RHE were achieved under simulated 1 Sun illumination. MOS 1|Si photocathodes operate at potentials 550 mV more positive than MOS 1|GCE cathodes to reach the same activity for H2 evolution from water (1 mA/cm(2)).

  5. Visible photocatalytic and photoelectrochemical activities of TiO2 nanobelts modified by In2O3 nanoparticles.

    PubMed

    Yang, Hongru; Tian, Jian; Bo, Yanyan; Zhou, Yanli; Wang, Xinzhen; Cui, Hongzhi

    2017-02-01

    Novel In2O3 nanoparticle/TiO2 nanobelt heterostructures with enhanced visible-light photocatalytic and photoelectrochemical (PEC) performance were successfully prepared via a facile hydrothermal method. Well-dispersed In2O3 nanoparticles with small sizes are uniformly attached on the surface of TiO2 nanobelts to form In2O3 nanoparticle/TiO2 nanobelt heterostructures. The TiO2 nanobelts as backbones restrict the aggregation of In2O3 nanoparticles, resulting in the formation of smaller In2O3 nanoparticles with more interaction sites for pollutants. The visible photocatalytic activity of as-prepared heterostructures for degradation of methyl blue (MB) is higher than those of TiO2 nanobelts and In2O3 nanoparticles alone. Moreover, the In2O3 nanoparticle/TiO2 nanobelt heterostructure shows an enhanced PEC performance under irradiation of visible light. The enhanced photocatalytic and PEC activities are mainly ascribed to the synergic effect of efficient charge separation of heterostructure, visible-light harvesting ability of In2O3, and the formation of preferential adsorption sites by the small size of In2O3 nanoparticles. Finally, based on the experimental results of Mott-Schottky, UV-vis DRS, photocurrent and open-circuit voltage response, a possible photocatalytic mechanism over the In2O3 nanoparticle/TiO2 nanobelt heterostructure is proposed.

  6. Stem cells engineering for cell-based therapy.

    PubMed

    Taupin, Philippe

    2007-09-01

    Stem cells carry the promise to cure a broad range of diseases and injuries, from diabetes, heart and muscular diseases, to neurological diseases, disorders and injuries. Significant progresses have been made in stem cell research over the past decade; the derivation of embryonic stem cells (ESCs) from human tissues, the development of cloning technology by somatic cell nuclear transfer (SCNT) and the confirmation that neurogenesis occurs in the adult mammalian brain and that neural stem cells (NSCs) reside in the adult central nervous system (CNS), including that of humans. Despite these advances, there may be decades before stem cell research will translate into therapy. Stem cell research is also subject to ethical and political debates, controversies and legislation, which slow its progress. Cell engineering has proven successful in bringing genetic research to therapy. In this review, I will review, in two examples, how investigators are applying cell engineering to stem cell biology to circumvent stem cells' ethical and political constraints and bolster stem cell research and therapy.

  7. TOPICAL REVIEW: Stem cells engineering for cell-based therapy

    NASA Astrophysics Data System (ADS)

    Taupin, Philippe

    2007-09-01

    Stem cells carry the promise to cure a broad range of diseases and injuries, from diabetes, heart and muscular diseases, to neurological diseases, disorders and injuries. Significant progresses have been made in stem cell research over the past decade; the derivation of embryonic stem cells (ESCs) from human tissues, the development of cloning technology by somatic cell nuclear transfer (SCNT) and the confirmation that neurogenesis occurs in the adult mammalian brain and that neural stem cells (NSCs) reside in the adult central nervous system (CNS), including that of humans. Despite these advances, there may be decades before stem cell research will translate into therapy. Stem cell research is also subject to ethical and political debates, controversies and legislation, which slow its progress. Cell engineering has proven successful in bringing genetic research to therapy. In this review, I will review, in two examples, how investigators are applying cell engineering to stem cell biology to circumvent stem cells' ethical and political constraints and bolster stem cell research and therapy.

  8. Using silver nanocluster/graphene nanocomposite to enhance photoelectrochemical activity of CdS:Mn/TiO2 for highly sensitive signal-on immunoassay.

    PubMed

    Song, Jie; Wang, Jiamian; Wang, Xiuyun; Zhao, Wei; Zhao, Yanqiu; Wu, Shuo; Gao, Zhanming; Yuan, Jingli; Meng, Changgong

    2016-06-15

    A highly sensitive signal-on photoelectrochemical (PEC) immunosensor was fabricated here using CdS:Mn/TiO2 as photoelectrochemical sensing platform, and silver nanoclusters and graphene naocomposites (AgNCs-GR) as signal amplification tags. The immunosensor was constructed based on the specific sandwich immunoreaction, and the photo-to-current conversion efficiency of the isolated protein modified CdS:Mn/TiO2 matrix was improved based on the synergistic effect of AgNCs-GR. Under irradiation, the photogenerated electrons from the AgNCs at a higher conduction band edge level could be transport to the CdS:Mn/TiO2 matrix with the assistance of highly conductive graphene nanosheets, as well as recycle the trapped excitons in the defects-rich CdS:Mn/TiO2 interface. The electron transport and exciton recycle reduced the possibility of electron-hole recombination and greatly improved the photo-to-current conversion efficiency of the sensing matrix. Based on the signal enhancement, a signal-on PEC immunosensors was fabricated for the detection of carcinoembryonic antigen (CEA), a model analyte related to many malignant diseases. Under optimal conditions, the as-prepared immunosensor showed excellent analytical performance, with a wide linear range from 1.0 pg/mL to 100 ng/mL and a low limit of detection of 1.0 pg/mL. The signal-on mode provided 2.48 times higher sensitivity compared with signal-off mode. This strategy demonstrated good accuracy and high selectivity for practical sample analysis, thus may have great application prospective in the prediction and early diagnosis of diseases.

  9. Semiconductor nanostructure-based photovoltaic solar cells.

    PubMed

    Zhang, Genqiang; Finefrock, Scott; Liang, Daxin; Yadav, Gautam G; Yang, Haoran; Fang, Haiyu; Wu, Yue

    2011-06-01

    Substantial efforts have been devoted to design, synthesize, and integrate various semiconductor nanostructures for photovoltaic (PV) solar cells. In this article, we will review the recent progress in this exciting area and cover the material chemistry and physics related to all-inorganic nanostructure solar cells, hybrid inorganic nanostructure-conductive polymer composite solar cells, and dye-sensitized solar cells.

  10. Semiconductor nanostructure-based photovoltaic solar cells

    NASA Astrophysics Data System (ADS)

    Zhang, Genqiang; Finefrock, Scott; Liang, Daxin; Yadav, Gautam G.; Yang, Haoran; Fang, Haiyu; Wu, Yue

    2011-06-01

    Substantial efforts have been devoted to design, synthesize, and integrate various semiconductor nanostructures for photovoltaic (PV) solar cells. In this article, we will review the recent progress in this exciting area and cover the material chemistry and physics related to all-inorganic nanostructure solar cells, hybrid inorganic nanostructure-conductive polymer composite solar cells, and dye-sensitized solar cells.

  11. An in situ photoelectrochemical determination of hydrogen sulfide through generation of CdS nanoclusters onto TiO2 nanotubes.

    PubMed

    Li, Hong; Tian, Yang; Deng, Zifeng; Liang, Yan

    2012-10-07

    A novel and facile photoelectrochemical method has been developed to detect H(2)S in water samples with high sensitivity and selectivity. The protocol is based on the photocurrent generated by CdS nanoclusters which are deposited onto TiO(2) nanotubes exposing in CdSO(4) solution with the gradual addition of Na(2)S, with low-cost, environment-friendly, theoretical and technical simplicity. The developed method shows a very broad linear range from 10(-8) M to 10(-3) M and a low detection limit of 0.31 nM (9.92 ppt), far lower than the ceiling value in drinking water provided by WHO. Furthermore, the present method has been applied for determination of H(2)S in water samples. The concentrations of H(2)S in water samples determined by the present method are in a good agreement with those monitored by traditional spectrophotometry.

  12. Influence of pH on the quantum-size-controlled photoelectrochemical etching of epitaxial InGaN quantum dots

    SciTech Connect

    Xiao, Xiaoyin; Lu, Ping; Fischer, Arthur J.; Coltrin, Michael E.; Wang, George T.; Koleske, Daniel D.; Tsao, Jeffrey Y.

    2015-11-18

    Illumination by a narrow-band laser has been shown to enable photoelectrochemical (PEC) etching of InGaN thin films into quantum dots with sizes controlled by the laser wavelength. Here, we investigate and elucidate the influence of solution pH on such quantum-size-controlled PEC etch process. We find that although a pH above 5 is often used for PEC etching of GaN-based materials, oxides (In2O3 and/or Ga2O3) form which interfere with quantum dot formation. Furthermore, at pH below 3, however, oxide-free QDs with self-terminated sizes can be successfully realized.

  13. Influence of pH on the quantum-size-controlled photoelectrochemical etching of epitaxial InGaN quantum dots

    DOE PAGES

    Xiao, Xiaoyin; Lu, Ping; Fischer, Arthur J.; ...

    2015-11-18

    Illumination by a narrow-band laser has been shown to enable photoelectrochemical (PEC) etching of InGaN thin films into quantum dots with sizes controlled by the laser wavelength. Here, we investigate and elucidate the influence of solution pH on such quantum-size-controlled PEC etch process. We find that although a pH above 5 is often used for PEC etching of GaN-based materials, oxides (In2O3 and/or Ga2O3) form which interfere with quantum dot formation. Furthermore, at pH below 3, however, oxide-free QDs with self-terminated sizes can be successfully realized.

  14. Photo-electrochemical Bioanalysis of Guanosine Monophosphate Using Coupled Enzymatic Reactions at a CdS/ZnS Quantum Dot Electrode.

    PubMed

    Sabir, Nadeem; Khan, Nazimuddin; Völkner, Johannes; Widdascheck, Felix; del Pino, Pablo; Witte, Gregor; Riedel, Marc; Lisdat, Fred; Konrad, Manfred; Parak, Wolfgang J

    2015-11-18

    A photo-electrochemical sensor for the specific detection of guanosine monophosphate (GMP) is demonstrated, based on three enzymes combined in a coupled reaction assay. The first reaction involves the adenosine triphosphate (ATP)-dependent conversion of GMP to guanosine diphosphate (GDP) by guanylate kinase, which warrants substrate specificity. The reaction products ADP and GDPare co-substrates for the enzymatic conversion of phosphoenolpyruvate to pyruvate in a second reaction mediated by pyruvate kinase. Pyruvate in turn is the co-substrate for lactate dehydrogenase that generates lactate via oxidation of nicotinamide adenine dinucleotide (reduced form) NADH to NAD(+). This third enzymatic reaction is electrochemically detected. For this purpose a CdS/ZnS quantum dot (QD) electrode is illuminated and the photocurrent response under fixed potential conditions is evaluated. The sequential enzyme reactions are first evaluated in solution. Subsequently, a sensor for GMP is constructed using polyelectrolytes for enzyme immobilization.

  15. Advancing the Chemistry of CuWO4 for Photoelectrochemical Water Oxidation.

    PubMed

    Lhermitte, Charles R; Bartlett, Bart M

    2016-06-21

    Photoelectrochemical (PEC) cells are an ongoing area of exploration that provide a means of converting solar energy into a storable chemical form (molecular bonds). In particular, using PEC cells to drive the water splitting reaction to obtain H2 could provide a clean and sustainable route to convert solar energy into chemical fuels. Since the discovery of catalytic water splitting on TiO2 photoelectrodes by Fujishima and Honda, significant efforts have been directed toward developing high efficiency metal oxides to use as photocatalysts for this reaction. Improving the efficiency of PEC cells requires developing chemically stable, and highly catalytic anodes for the oxygen-evolution reaction (OER). This water oxidation half reaction requires four protons and four electrons coupling in two bond making steps to form O2, which limits the rate. Our group has accelerated efforts in CuWO4 as a candidate for PEC OER chemistry. Its small band gap of 2.3 eV allows for using visible light to drive OER, and the reaction proceeds with a high degree of chemoselectivity, even in the presence of more kinetically accessible anions such as chloride, which is common to seawater. Furthermore, CuWO4 is a chemically robust material when subjected to the highly oxidizing conditions of PEC OER. The next steps for accelerating research using this (and other), ternary phase oxides, is to move beyond reporting the basic PEC measurements to understanding fundamental chemical reaction mechanisms operative during OER on semiconductor surfaces. In this Account, we outline the process for PEC OER on CuWO4 thin films with emphasis on the chemistry of this reaction, the reaction rate and selectivity (determined by controlled-potential coulometry and oxygen-detection experiments). We discuss key challenges with CuWO4 such as slow kinetics and the presence of an OER-mediating mid-gap state, probed by electrochemical impedance spectroscopy. We propose that this mid-gap state imparts the observed

  16. Research Update: Photoelectrochemical water splitting and photocatalytic hydrogen production using ferrites (MFe2O4) under visible light irradiation

    NASA Astrophysics Data System (ADS)

    Dillert, Ralf; Taffa, Dereje H.; Wark, Michael; Bredow, Thomas; Bahnemann, Detlef W.

    2015-10-01

    The utilization of solar light for the photoelectrochemical and photocatalytic production of molecular hydrogen from water is a scientific and technical challenge. Semiconductors with suitable properties to promote solar-driven water splitting are a desideratum. A hitherto rarely investigated group of semiconductors are ferrites with the empirical formula MFe2O4 and related compounds. This contribution summarizes the published results of the experimental investigations on the photoelectrochemical and photocatalytic properties of these compounds. It will be shown that the potential of this group of compounds in regard to the production of solar hydrogen has not been fully explored yet.

  17. Enhanced photoelectrochemical detection of bioaffinity reactions by vertically oriented au nanobranches complexed with a biotinylated polythiophene derivative.

    PubMed

    Zhou, Huiqiong; Tang, Yanli; Zhai, Jin; Wang, Shu; Tang, Zhiyong; Jiang, Lei

    2009-01-01

    Four nanostructured Au electrodes were prepared by a simple and templateless electrochemical deposition technique. After complexing with a biotinylated polythiophene derivative (PTBL), photocurrent generation and performance of PTBL/Au-nanostructured electrodes as photoelectrochemical biosensors were investigated. Among these four nanostructured Au electrodes, vertically oriented nanobranches on the electrode significantly improved the photoelectric conversion, because the vertically oriented nanostructures not only benefit light harvesting but also the transfer of the photogenerated charge carriers. Owing to this advantaged nanostructure, the PTBL/Au-nanobranch electrode showed higher sensitivity and faster response times in the photoelectrochemical detection of a streptavidin-biotin affinity reaction compared to a PTBL/Au-nanoparticle electrode.

  18. Synergetic Effect of Ti(3+) and Oxygen Doping on Enhancing Photoelectrochemical and Photocatalytic Properties of TiO2/g-C3N4 Heterojunctions.

    PubMed

    Li, Kai; Huang, Zhenyu; Zeng, Xiaoqiao; Huang, Baibiao; Gao, Shanmin; Lu, Jun

    2017-04-05

    To improve the utilization of visible light and reduce photogenerated electron/hole recombination, Ti(3+) self-doped TiO2/oxygen-doped graphitic carbon nitride (Ti(3+)-TiO2/O-g-C3N4) heterojunctions were prepared via hydrothermal treatment of a mixture of g-C3N4 and titanium oxohydride sol obtained from the reaction of TiH2 with H2O2. In this way, exfoliated O-g-C3N4 and Ti(3+)-TiO2 nanoparticles were obtained. Simultaneously, strong bonding was formed between Ti(3+)-TiO2 nanoparticles and exfoliated O-g-C3N4 during the hydrothermal process. Charge transfer and recombination processes were characterized by transient photocurrent responses, electrochemical impedance test, and photoluminescence spectroscopy. The photocatalytic performances were investigated through rhodamine B degradation test under an irradiation source based on 30 W cold visible-light-emitting diode. The highest visible-light photoelectrochemical and photocatalytic activities were observed from the heterojunction with 1:2 mass ratio of Ti(3+)-TiO2 to O-g-C3N4. The photodegradation reaction rate constant based on this heterojuction is 0.0356 min(-1), which is 3.87 and 4.56 times higher than those of pristine Ti(3+)-TiO2 and pure g-C3N4, respectively. The remarkably high photoelectrochemical and photocatalytic performances of the heterojunctions are mainly attributed to the synergetic effect of efficient photogenerated electron-hole separation, decreased electron transfer resistance from interfacial chemical hydroxy residue bonds, and oxidizing groups originating from Ti(3+)-TiO2 and O-g-C3N4.

  19. Laser-based direct-write techniques for cell printing.

    PubMed

    Schiele, Nathan R; Corr, David T; Huang, Yong; Raof, Nurazhani Abdul; Xie, Yubing; Chrisey, Douglas B

    2010-09-01

    Fabrication of cellular constructs with spatial control of cell location (+/-5 microm) is essential to the advancement of a wide range of applications including tissue engineering, stem cell and cancer research. Precise cell placement, especially of multiple cell types in co- or multi-cultures and in three dimensions, can enable research possibilities otherwise impossible, such as the cell-by-cell assembly of complex cellular constructs. Laser-based direct writing, a printing technique first utilized in electronics applications, has been adapted to transfer living cells and other biological materials (e.g., enzymes, proteins and bioceramics). Many different cell types have been printed using laser-based direct writing, and this technique offers significant improvements when compared to conventional cell patterning techniques. The predominance of work to date has not been in application of the technique, but rather focused on demonstrating the ability of direct writing to pattern living cells, in a spatially precise manner, while maintaining cellular viability. This paper reviews laser-based additive direct-write techniques for cell printing, and the various cell types successfully laser direct-written that have applications in tissue engineering, stem cell and cancer research are highlighted. A particular focus is paid to process dynamics modeling and process-induced cell injury during laser-based cell direct writing.

  20. Laser-based direct-write techniques for cell printing

    PubMed Central

    Schiele, Nathan R; Corr, David T; Huang, Yong; Raof, Nurazhani Abdul; Xie, Yubing; Chrisey, Douglas B

    2016-01-01

    Fabrication of cellular constructs with spatial control of cell location (±5 μm) is essential to the advancement of a wide range of applications including tissue engineering, stem cell and cancer research. Precise cell placement, especially of multiple cell types in co- or multi-cultures and in three dimensions, can enable research possibilities otherwise impossible, such as the cell-by-cell assembly of complex cellular constructs. Laser-based direct writing, a printing technique first utilized in electronics applications, has been adapted to transfer living cells and other biological materials (e.g., enzymes, proteins and bioceramics). Many different cell types have been printed using laser-based direct writing, and this technique offers significant improvements when compared to conventional cell patterning techniques. The predominance of work to date has not been in application of the technique, but rather focused on demonstrating the ability of direct writing to pattern living cells, in a spatially precise manner, while maintaining cellular viability. This paper reviews laser-based additive direct-write techniques for cell printing, and the various cell types successfully laser direct-written that have applications in tissue engineering, stem cell and cancer research are highlighted. A particular focus is paid to process dynamics modeling and process-induced cell injury during laser-based cell direct writing. PMID:20814088

  1. Cartesian-cell based grid generation and adaptive mesh refinement

    NASA Technical Reports Server (NTRS)

    Coirier, William J.; Powell, Kenneth G.

    1993-01-01

    Viewgraphs on Cartesian-cell based grid generation and adaptive mesh refinement are presented. Topics covered include: grid generation; cell cutting; data structures; flow solver formulation; adaptive mesh refinement; and viscous flow.

  2. Bioorthogonal Click Chemistry-Based Synthetic Cell Glue.

    PubMed

    Koo, Heebeom; Choi, Myunghwan; Kim, Eunha; Hahn, Sei Kwang; Weissleder, Ralph; Yun, Seok Hyun

    2015-12-22

    Artificial methods of cell adhesion can be effective in building functional cell complexes in vitro, but methods for in vivo use are currently lacking. Here, a chemical cell glue based on bioorthogonal click chemistry with high stability and robustness is introduced. Tetrazine (Tz) and trans-cyclooctene (TCO) conjugated to the cell surface form covalent bonds between cells within 10 min in aqueous conditions. Glued, homogeneous, or heterogeneous cell pairs remain viable and stably attached in a microfluidic flow channel at a shear stress of 20 dyn cm(-2) . Upon intravenous injection of assembled Jurkat T cells into live mice, fluorescence microscopy shows the trafficking of cell pairs in circulation and their infiltration into lung tissues. These results demonstrate the promising potential of chemically glued cell pairs for various applications ranging from delivering therapeutic cells to studying cell-cell interactions in vivo.

  3. Visible-light-activated photoelectrochemical biosensor for the study of acetylcholinesterase inhibition induced by endogenous neurotoxins.

    PubMed

    Huang, Qilin; Chen, Hua; Xu, Lili; Lu, Danqin; Tang, Linlin; Jin, Litong; Xu, Zhiai; Zhang, Wen

    2013-07-15

    In this report, a novel visible-light-activated photoelectrochemical biosensor was fabricated to study the inhibition of acetylcholinesterase (AChE) activity induced by two endogenous neurotoxins, 1(R)-methyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline [(R)-Sal] and 1(R),2(N)-dimethyl-6,7-dihydroxy-1,2,3,4-tetra-hydroisoquinoline [(R)-NMSal], which have drawn much attention in the study of the pathogenesis of neurodegenerative diseases such as Parkinson's disease. The photoelectrode was prepared by three steps, as follows. At first, nitrogen and fluorine co-doped TiO2 nanotubes (TNs) were obtained by anodic oxidation of a Ti sheet. Secondly, silver nanoparticles (AgNPs) were deposited onto the TNs through a microwave-assisted heating polyol (MAHP) process. At last, AChE was immobilized on the obtained photoelectrode and the biosensor was marked as AChE/Ag/NFTNs. Due to the nitrogen and fluorine co-doping, the photoelectrochemical biosensors can produce high photocurrent under visible light irradiation. Moreover, the presence of AgNPs greatly increased the photocurrent response of the biosensor. AChE/Ag/NFTNs hybrid system was used to study AChE inhibition induced by (R)-Sal and (R)-NMSal. The result proved that both (R)-Sal and (R)-NMSal exhibited mixed and reversible inhibition against AChE. This strategy is of great significance for the development of novel photoelectrochemical biosensors in the future.

  4. Silicon nanostructures-induced photoelectrochemical solar water splitting for energy applications

    NASA Astrophysics Data System (ADS)

    Dadwal, U.; Ranjan, Neha; Singh, R.

    2016-05-01

    We study the photoelectrochemical (PEC) solar water splitting assisted with synthesized nanostructures. Si nanowires decorated with silver dendrite nanostructures have been synthesized using metal assisted wet chemical etching of (100) Si wafer. Etching has been carried out in an aqueous solution consisting of 5M HF and 0.02M AgNO3. Investigations showed that such type of semiconductor nanostructures act as efficient working electrodes for the splitting of normal water in PEC method. An enhancement in the photon-to-current conversion efficiency and solar-to-hydrogen evolution was observed for obtaining a practical source of clean and renewable fuel.

  5. Photoelectrochemical behavior of Nb-doped TiO2 electrodes.

    PubMed

    Emeline, Alexei V; Furubayashi, Yutaka; Zhang, Xintong; Jin, Ming; Murakami, Taketoshi; Fujishima, Akira

    2005-12-29

    The photoelectrochemical behavior of degenerate Nb-doped TiO2 (Ti(1-x)Nb(x)O2: x = 0, 0.01, 0.03, 0.06, 0.1) electrodes prepared by pulsed laser deposition on LaAlO3 (LAO) and SrTiO3 (STO) was examined, revealing that an increase in Nb concentration causes a significant decay of titania photoactivity. One reason for such behavior may be a Burstein-Moss effect, which leads to a blue shift of the spectral limit of photoactivity. Another reason typical for metal-doped photocatalysts is the increase of the efficiency of charge carrier recombination.

  6. Photocatalytic and photoelectrochemical oxidation mechanisms of methanol on TiO2 in aqueous solution

    NASA Astrophysics Data System (ADS)

    Ahmed, Amira Y.; Kandiel, Tarek A.; Ivanova, Irina; Bahnemann, Detlef

    2014-11-01

    Methanol is an available, small, and colorless molecule, which can be used for the photocatalytic activity evaluation without the sensitization problem associated with most dye molecules. Thus, TiO2 suspended in aqueous methanol solutions is commonly employed as a model test for the photocatalytic degradation of organic pollutants in aerobic system or for photocatalytic hydrogen production in absence of molecular oxygen. It is, hence, important to explore the mechanism of its photocatalytic and photoelectrochemical oxidation on TiO2 in aqueous solution. In this mini-review, the possible mechanisms for water and methanol oxidation on TiO2 will therefore be presented and discussed.

  7. Photoelectrochemical protection of stainless alloys from the stress-corrosion cracking in BWR primary coolant environment

    SciTech Connect

    Akashi, Masatsune; Iso-o, Hiroyuki; Kubota, Nobuhiko; Fukuda, Takanori; Ayabe, Muneo; Hirano, Kenji

    1995-12-31

    The feasibility of counteracting or preventing the stress-corrosion cracking in the BWR core internals by the photoelectrochemical method has been examined. For the purpose TiO{sub 2} semiconductor is noted for its capability of photo electrochemically inducing the water-oxidizing anodic reaction in low enough potential domain if supplied with a light of a wavelength shorter than 410 nm. This paper offers an empirical proof by showing that Type 304 stainless steel and Alloy 600 stainless alloy that have been plasma-spray coated with TiO{sub 2} film will do quite well in environments of BWR primary coolant.

  8. Quantum-dot-based cell motility assay.

    PubMed

    Gu, Weiwei; Pellegrino, Teresa; Parak, Wolfgang J; Boudreau, Rosanne; Le Gros, Mark A; Gerion, Daniele; Alivisatos, A Paul; Larabell, Carolyn A

    2005-06-28

    Because of their favorable physical and photochemical properties, colloidal CdSe/ZnS-semiconductor nanocrystals (commonly known as quantum dots) have enormous potential for use in biological imaging. In this report, we present an assay that uses quantum dots as markers to quantify cell motility. Cells that are seeded onto a homogeneous layer of quantum dots engulf and absorb the nanocrystals and, as a consequence, leave behind a fluorescence-free trail. By subsequently determining the ratio of cell area to fluorescence-free track area, we show that it is possible to differentiate between invasive and noninvasive cancer cells. Because this assay uses simple fluorescence detection, requires no significant data processing, and can be used in live-cell studies, it has the potential to be a powerful new tool for discriminating between invasive and noninvasive cancer cell lines or for studying cell signaling events involved in migration.

  9. Silicon based microfluidic cell for terahertz frequencies

    NASA Astrophysics Data System (ADS)

    Baragwanath, A. J.; Swift, G. P.; Dai, D.; Gallant, A. J.; Chamberlain, J. M.

    2010-07-01

    We present a detailed analysis of the design, fabrication and testing of a silicon based, microfluidic cell, for transmission terahertz time-domain spectroscopy. The sensitivity of the device is tested through a range of experiments involving primary alcohol/water mixtures. The dielectric properties of these solutions are subsequently extracted using a Nelder-Mead search algorithm, and are in good agreement with literature values obtained via alternative techniques. Quantities in the order of 2 μmol can be easily distinguished for primary alcohols in solution, even with the subwavelength optical path lengths used. A further display of the device sensitivity is shown through the analysis of commercial whiskeys, where there are clear, detectable differences between samples. Slight absorption variations were identified between samples of the same commercial brand, owing to a 2.5% difference in their alcoholic content. Results from data taken on subsequent days after system realignment are also presented, confirming the robustness of the technique, and the data extraction algorithm used. One final experiment, showing the possible use of this device to analyze aqueous biological samples is detailed; where biotin, a molecule known for its specific terahertz absorptions, is analyzed in solution. The device sensitivity is once again displayed, where quantities of 3 nmol can be clearly detected between samples.

  10. Cellular Silica Encapsulation for Development of Robust Cell Based Biosensors

    NASA Astrophysics Data System (ADS)

    Johnston, Robert; Rogelj, Snezna; Harper, Jason; Tartis, Michaelann

    2014-03-01

    In order to detect chemical and biological threats both on the battlefield and in civilian life, development of portable, robust detection systems capable of real-time identification of the chemical and biological agents are needed. Living cell-based sensors have proven effective as sensitive, specific, near real-time detectors; however, living cell-based sensors require frequent cell replenishment due to cell sensitivity to the ex-vivo environment, which limits sensor stability. Incorporation of living cells within a biocompatible matrix that provides mechanical protection and maintains access to the external environment may facilitate the development of long-term stable cell-based biosensors. We are exploring the use of a novel Chemical Vapor into Liquid (CViL) deposition process for whole cell encapsulation in silica. In CViL, the high vapor pressure of common silica alkoxides is utilized to deliver silica into an aqueous medium, creating a silica sol. Mixing of cells with the resulting silica sol facilitates encapsulation of cells in silica while minimizing cell contact with the cytotoxic products of silica generating reactions. Using fluorescence microscopy analysis with multiple silica specific markers, encapsulation of multiple eukaryotic cell types (Saccharomyces cerevisiae, Jurkat, HeLa, and U87 cells) with CViL generated silica is shown, providing a foundation for development of long -term stable cell-based biosensors with diverse sensing capabilities.

  11. Cell-based therapies for regenerating bone

    PubMed Central

    GOODMAN, S. B.

    2013-01-01

    Cellular therapies to replenish bone lost due to acquired conditions such as trauma, infection, tumor, periprosthetic osteolysis and other etiologies have become widespread. Traditional, open, surgical bone grafting techniques have given way to newer cellular therapies that are potentially less invasive and have a lower complication rate and faster recovery time. These new technologies include bone marrow harvesting with concentration of osteoprogenitor cells with/without cell culture, scaffolds which are both osteoconductive and osteoinductive, attempts to facilitate mesenchymal stem cell and osteoprogenitor cell homing both locally and systemically, genetic engineering of specialized stem cells, and the use of potentially immune-privileged fetal and other types of stem cells. Some of these techniques have already been introduced into the orthopaedic clinic, whereas others are still in the pre-clinical testing phase. Given the limited supply of autologous graft, these new techniques will have a dramatic impact on bone regeneration in the future. PMID:24436510

  12. Engineering anatase hierarchically cactus-like TiO2 arrays for photoelectrochemical and visualized sensing platform.

    PubMed

    Gao, Chaomin; Wang, Yanhu; Yuan, Shuai; Xue, Jie; Cao, Bingqiang; Yu, Jinghua

    2017-04-15

    This work described that one-step synthesis three dimensional anatase hierarchically cactus-like TiO2 arrays (AHCT) and their application in constructing a novel photoelectrochemical (PEC) and visualized sensing platform based on molecular imprinting technique, which reports its result with the prussian blue (PB) electrode served as the electrochromic indicator for the detection of glycoprotein (RNase B). The AHCT arrays were perpendicularly grown on FTO substrate with tunable sizes, offering many advantages, such as large contact area, rapid charge electron separation and transport. A possible formation process of the interesting AHCT arrays has been investigated based on time-dependent experiment. In addition, the PEC and visualized sensing platform was constructed based on the molecularly imprinted polymer modified AHCT arrays. Specifically, in the proposed system, the more RNase B being, the more insulating layer was formed on the surface of AHCT arrays that impeded the harvesting of light and electron transfer, resulting in the reduction of photocurrent. When upon light illumination, the photogenerated electrons flow through an external circuit to PB, leading to the reduction of PB to prussian white (PW), which is transparent. The rate of decolourization of PB is proportional to the concentration of RNase B. In this way, a visualized PEC sensing platform that gives its quantitative information could be performed by monitoring the change of color intensity. Under optimal conditions, the protocol possessed a detection range of 0.5pM to 2μM (r=0.997) and the limit of detection was 0.12 pM toward RNase B. Our method eliminates the need for sophisticated instruments and high detection expenses, making it possible to be a reliable alternative in resource-constrained regions.

  13. Novel Flexible Plastic-Based Solar Cells

    DTIC Science & Technology

    2012-10-19

    Fabrication of newly designed hybrid solar cells that are composed of a electron transport layer ( TiO2 ), a light sensitizing layer (NCs), and a hole...coating and spraying techniques, to produce broad-band light harvesting hybrid solar cells with bulk and layered heterojunction of inorganic...fabrication of hybrid bulk heterojunction photovoltaic cell using a blend film of polymer-inorganic NCs, 2) Fabrication of newly designed hybrid solar

  14. MoS2 nanodot decorated In2S3 nanoplates: a novel heterojunction with enhanced photoelectrochemical performance.

    PubMed

    Liu, Fangyang; Jiang, Yan; Yang, Jia; Hao, Mengmeng; Tong, Zhengfu; Jiang, Liangxing; Wu, Zhuangzhi

    2016-01-31

    MoS2 nanodot decorated In2S3 nanoplates were successfully synthesized via a modified one-pot method. The In2S3/MoS2 heterojunction nanocomposite exhibits superior optical and photoelectrochemical performance to the bare ones, owing to the synergistic effect.

  15. An agarose-gel based method for transporting cell lines.

    PubMed

    Yang, Lingzhi; Li, Chufang; Chen, Ling; Li, Zhiyuan

    2009-12-16

    Cryopreserved cells stored in dry ice or liquid nitrogen is the classical method for transporting cells between research laboratories in different cities around the world in order to maintain cell viability. An alternative method is to ship the live cells in flasks filled with cell culture medium. Both methods have limitations of either a requirement on special shipping container or short times for the cells to survive on the shipping process. We have recently developed an agarose gel based method for directly transporting the live adherent cells in cell culture plates or dishes in ambient temperature. This convenient method simplifies the transportation of live cells in long distance that can maintain cells in good viability for several days.

  16. [Targeted molecular therapy based on advanced cancer stem cell model].

    PubMed

    Hirao, Atsushi

    2015-08-01

    Improvement of cell purification and transplantation techniques have contributed to the identification of cell populations known as tumor-initiating cells (TICs). Although it was hypothesized that tumors are organized as hierarchies of tumor cells that are sustained by rare TICs, like normal tissue stem cells, there are several controversies towards such cancer stem cell model, e.g. reversible change of stem cell like population based on epigenetic changes, clonal genetic evolution and problems in xenotransplantation system. Despite complexity in cancer stem cell models, studies in cancer stem cell field have revealed that there are close relationship between cancer malignancy and stem cell properties, called "stemness". Understanding molecular mechanisms for controlling stemness would contribute to establishment of novel diagnostics or therapeutics for cancer.

  17. Silicon Micropore based Electromechanical Transducer to Differentiate Tumor Cells

    NASA Astrophysics Data System (ADS)

    Ali, Waqas; Raza, Muhammad U.; Khanzada, Raja R.; Kim, Young-Tae; Iqbal, Samir M.

    2015-03-01

    Solid-state micropores have been used before to differentiate cancer cells from normal cells using size-based filtering. Tumor cells differ from normal ones not only in size but also in physical properties like elasticity, shape, motility etc. Tumor cells show different physical attributes depending on the stage and type of cancer. We report a micropore based electromechanical transducer that differentiated cancer cells based on their mechanophysical properties. The device was interfaced with a high-speed patch-clamp measurement system that biased the ionic solution across the silicon-based membrane. The bias resulted in the flow of ionic current. Electrical pulses were generated when cells passed through. Different cells depicted characteristic pulses. Translocation profiles of cells that were either small or were more elastic and flexible caused electrical pulses shorter in widths and amplitudes whereas cells with larger size or lesser elasticity/flexibility showed deeper and wider pulses. Three non-small cell lung cancer (NSCLC) cell lines NCI-H1155, A549 and NCI-H460 were successfully differentiated. NCI-H1155, due to their comparatively smaller size, were found quickest in translocating through. The solid-sate micropore based electromechanical transducer could process the whole blood sample of cancer patient without any pre-processing requirements and is ideal for point-of-care applications. Support Acknowledged from NSF through ECCS-1201878.

  18. All solid-state solar cells based on CH3NH3PbI3-sensitized TiO2 nanotube arrays

    NASA Astrophysics Data System (ADS)

    Yang, Xiuchun; Liu, Wei; Ren, Peng

    2016-09-01

    TiO2 nanotube arrays (TiO2 NTAs) were firstly used as photoanode in methylammonium lead iodide (CH3NH3PbI3) perovskite/TiO2 NTAs heterojunction solar cell, where CH3NH3PbI3 functions as both light absorber and hole conductor. The composition, structure and photoelectrochemical properties of the as-prepared samples were characterized by x-ray diffractometer (XRD), field-emission scanning electron microscope (FE-SEM), ultraviolet-visible (UV-vis) spectrophotometer and electrochemical workstation. The results indicate that the as-prepared CH3NH3PbI3 belongs to the cubic crystal system, and TiO2 NTAs sensitized by 0.3 M CH3NH3I and PbI2 exhibit the best photoelectrochemical properties with an open-circuit voltage of 0.422 V and a short-circuit current density of 173.4 μA cm-2. The EIS result shows that the extremely large resistance at CH3NH3PbI3/FTO interface contributes to the low current density of the perovskite solar cell.

  19. Fabrication and photoelectrochemical properties of silicon nanowires/g-C3N4 core/shell arrays

    NASA Astrophysics Data System (ADS)

    Chen, Zhen; Ma, Ge; Chen, Zhihong; Zhang, Yongguang; Zhang, Zhe; Gao, Jinwei; Meng, Qingguo; Yuan, Mingzhe; Wang, Xin; Liu, Jun-ming; Zhou, Guofu

    2017-02-01

    A photoelectrochemical (PEC) cell made of metal-free carbon nitride (g-C3N4) @siliconnanowire(Si NW) arrays (denoted as Si NWs/g-C3N4) is presented in this work. The as-prepared photoelectrodes with different mass contents of g-C3N4 have been synthesized via a metal-catalyzed electroless etching (MCEE), liquid atomic layer deposition (LALD) and annealing methods. The amount of g-C3N4 on the Si NW arrays can be controlled by tuning the concentration of the cyanamide solution used in the LALD procedure. The dense and vertically aligned Si NWs/g-C3N4 core/shell nanostructures were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffraction (XRD). In comparison with FTO/g-C3N4 and Si NW samples, the Si NWs/g-C3N4 samples showed significantly enhanced photocurrents over the entire potential sweep range. Electrochemical impedance spectroscopy (EIS) was conducted to investigate the properties of the charge transfer process, and the results indicated that the enhanced PEC performance may be due to the increased photo-generated interfacial charge transfer between the Si NWs and g-C3N4. The photocurrent density reached 45 μA/cm2 under 100 mW/cm2 (AM 1.5 G) illumination at 0 V (vs. Pt) in neutral Na2SO4 solution (pH ∼ 7.62). Finally, a systematical PEC mechanism of the Si NWs/g-C3N4 was proposed.

  20. Non-genetic engineering of cells for drug delivery and cell-based therapy.

    PubMed

    Wang, Qun; Cheng, Hao; Peng, Haisheng; Zhou, Hao; Li, Peter Y; Langer, Robert

    2015-08-30

    Cell-based therapy is a promising modality to address many unmet medical needs. In addition to genetic engineering, material-based, biochemical, and physical science-based approaches have emerged as novel approaches to modify cells. Non-genetic engineering of cells has been applied in delivering therapeutics to tissues, homing of cells to the bone marrow or inflammatory tissues, cancer imaging, immunotherapy, and remotely controlling cellular functions. This new strategy has unique advantages in disease therapy and is complementary to existing gene-based cell engineering approaches. A better understanding of cellular systems and different engineering methods will allow us to better exploit engineered cells in biomedicine. Here, we review non-genetic cell engineering techniques and applications of engineered cells, discuss the pros and cons of different methods, and provide our perspectives on future research directions.