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Статті в журналах з теми "Photo- electrochemical cell"
Chu, Li-Kang, Chun-Wan Yen, and Mostafa A. El-Sayed. "Bacteriorhodopsin-based photo-electrochemical cell." Biosensors and Bioelectronics 26, no. 2 (October 15, 2010): 620–26. http://dx.doi.org/10.1016/j.bios.2010.07.013.
Повний текст джерелаBedoya-Lora, Franky E., Anna Hankin, and Geoff H. Kelsall. "En route to a unified model for photo-electrochemical reactor optimisation. I - Photocurrent and H2 yield predictions." Journal of Materials Chemistry A 5, no. 43 (2017): 22683–96. http://dx.doi.org/10.1039/c7ta05125e.
Повний текст джерелаIfraemov, Raya, Ran Shimoni, Wenhui He, Guiming Peng, and Idan Hod. "A metal–organic framework film with a switchable anodic and cathodic behaviour in a photo-electrochemical cell." Journal of Materials Chemistry A 7, no. 7 (2019): 3046–53. http://dx.doi.org/10.1039/c8ta10483b.
Повний текст джерелаAmiry, C., P. Clechet, and J. R. Martin. "(Photo)electrochemical laminar flow cell with two reference electrodes." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 269, no. 2 (September 1989): 423–33. http://dx.doi.org/10.1016/0022-0728(89)85149-6.
Повний текст джерелаJäker, Philipp, Dino Aegerter, Till Kyburz, Roman Städler, Rea Fonjallaz, Blanka Detlefs, and Dorota Koziej. "Flow cell for operando X-ray photon-in-photon-out studies on photo-electrochemical thin film devices." Open Research Europe 2 (June 7, 2022): 74. http://dx.doi.org/10.12688/openreseurope.14433.1.
Повний текст джерелаJäker, Philipp, Dino Aegerter, Till Kyburz, Roman Städler, Rea Fonjallaz, Blanka Detlefs, and Dorota Koziej. "Flow cell for operando X-ray photon-in-photon-out studies on photo-electrochemical thin film devices." Open Research Europe 2 (December 23, 2022): 74. http://dx.doi.org/10.12688/openreseurope.14433.2.
Повний текст джерелаCardenas-Morcoso, Drialys, Raya Ifraemov, Miguel García-Tecedor, Itamar Liberman, Sixto Gimenez, and Idan Hod. "A metal–organic framework converted catalyst that boosts photo-electrochemical water splitting." Journal of Materials Chemistry A 7, no. 18 (2019): 11143–49. http://dx.doi.org/10.1039/c9ta01559k.
Повний текст джерелаWalch, Gregor, Bernhard Rotter, Georg Christoph Brunauer, Esmaeil Esmaeili, Alexander Karl Opitz, Markus Kubicek, Johann Summhammer, Karl Ponweiser, and Jürgen Fleig. "A solid oxide photoelectrochemical cell with UV light-driven oxygen storage in mixed conducting electrodes." Journal of Materials Chemistry A 5, no. 4 (2017): 1637–49. http://dx.doi.org/10.1039/c6ta08110j.
Повний текст джерелаSmandek, Bernhard, and Heinz Gerischer. "Photo- and electroluminescence on n-TiO2 in an electrochemical cell." Electrochimica Acta 34, no. 10 (October 1989): 1411–15. http://dx.doi.org/10.1016/0013-4686(89)87180-4.
Повний текст джерелаRonaszegi, Krisztian, Eric S. Fraga, Jawwad Darr, Paul R. Shearing, and Dan J. L. Brett. "Application of Photo-Electrochemically Generated Hydrogen with Fuel Cell Based Micro-Combined Heat and Power: A Dynamic System Modelling Study." Molecules 25, no. 1 (December 28, 2019): 123. http://dx.doi.org/10.3390/molecules25010123.
Повний текст джерелаДисертації з теми "Photo- electrochemical cell"
García, García Matías Alejandro. "Photo-anodes based on molybdenum oxides for the hydrolysis of water in a photo-electrochemical cell." Tesis, Universidad de Chile, 2019. http://repositorio.uchile.cl/handle/2250/170678.
Повний текст джерелаLas fuentes de energía limpias y sostenibles deben ser consideradas una base importante para el futuro crecimiento y desarrollo económico de cualquier país. Actualmente, el suministro mundial de energía depende en gran medida de los combustibles fósiles. Esto conlleva a que tecnologías tales como las celdas foto-electroquímicas se vuelvan especialmente atractivas, ya que permiten usar energía solar para producir hidrógeno. El funcionamiento de las celdas foto-electroquímicas se basa en el uso de semiconductores como electrodos, que al ser irradiados generan pares hueco-electrón, los cuales pueden migrar en la superficie del semiconductor y reaccionar con las especies adsorbidas o recombinarse entre sí. El hueco electrónico generado por la migración de un electrón puede oxidar una molécula de agua para producir oxígeno en el ánodo, mientras que los electrones generados viajan hacia el cátodo para reducir los protones presentes en el agua formando hidrógeno El presente trabajo de tesis tuvo como objetivo general la sintesis (a través de los métodos de electrodeposición y de spin-coating) y caracterización del desempeño de foto-ánodos basados en óxidos de molibdeno para la producción de hidrógeno en una celda foto-electroquímica a partir de electrólisis de agua. Películas de óxido de molibdeno dopadas con niquel y sin dopar se electrodepositaron aplicando un potencial de -1,377 V vs Ag / AgCl (KCl 3 M) durante 3 horas en un vidrio de cuarzo cubierto con dióxido de estaño dopado con flúor - FTO - sumergido en soluciones acuosas de molibdato-citrato a pH 9. Por otra parte, se depositaron peliculas de MoOx, WO3 y MoOx dopado con W sobre vidrio de aluminoborosilicato recubierto con óxido de estaño dopado con flúor. Este proceso se realizó mediante spin-coating a 4000 rpm durante 40 segundos. La caracterización de los foto-ánodos fabricados a través de electrodeposición y spin-coating sugiere que presentan propiedades semiconductoras y catalíticas que los hacen atractivos para su uso en una celda foto-electroquímica para la hidrólisis del agua. Sin embargo, aunque los foto-electrodos sintetizados a través de las técnicas mencionadas tienen un intervalo de banda prohibida óptimo para aprovechar eficientemente la luz solar, la caracterización foto-electroquímica mostró que estos electrodos no exhiben una estabilidad en solución acuosa y que son susceptibles a la foto-corrosion, que son factores limitantes para el uso de semiconductores convencionales como foto-electrodos.
Eskandari, Azin. "A preliminary theoretical and experimental study of a photo-electrochemical cell for solar hydrogen production." Thesis, Université Clermont Auvergne (2017-2020), 2019. http://www.theses.fr/2019CLFAC104.
Повний текст джерелаIn order to meet the energy and climate challenge of the coming 21st century, one solution consists of developing processes for producing storable energy carriers by artificial photosynthesis to synthesize solar fuels, in particular hydrogen, in order to valorize the solar resource. The understanding of these processes and the achievement of high kinetic and energetic performances require the development of generic, robust and predictive knowledge models considering radiative transfer as a physical process controlling the process at several scales but also including the various other phenomena involved in the structure or reification of the model.In this PhD work, the photo-reactive process at the heart of the study was the photo-electrochemical cell. More complex than the simple photoreactor, with a photo-anode and a (photo)cathode, the photo-electrochemical cell spatially dissociates the oxidation and reduction steps. Based both on the existing literature (mainly in the field of electrochemistry) and by deploying the tools developed by the research team on radiative transfer and thermokinetic coupling formulation, it was possible to establish performance indicators of photo-electrochemical cells.In parallel to the establishment of this model, an experimental approach was undertaken based first on a commercial Grätzel-type cell (DS-PEC) indicating the general trends of such photon energy converters with in particular a drop in energy efficiency as a function of the incident photon flux density. A modular experimental device (Minucell) has also been developed and validated in order to characterize photo-anodes of different compositions such as chromophore impregnated TiO2 electrodes for operation in Grätzel cells or Fe2O3 hematite electrodes (SC-PEC) where the semiconductor plays both the functions of photon absorption and charge carrier conduction. Above all, the Minucell device allowed to test, characterize and model the behavior of a bio-inspired photo-electrochemical cell for H2 production using at the photo-anode a Ru-RuCat molecular catalyst (developed by ICMMO Orsay/CEA Saclay) and at the cathode a CoTAA catalyst (developed by LCEMCA Brest). Minucell was used to characterize each constituent element of a photo-electrochemical cell and then the cell as a whole confirming the trends and observations obtained on energy efficiencies.This preliminary work opens up a wide range of research prospects, lays common ground between electrochemistry and photo-reactive systems engineering, and provides insights into the design and kinetic and energy optimization of photo-electrochemical cells for the production of hydrogen and solar fuels
Gonzalez, Aravena Arely Carolina. "Strategies to enhance extracellular electron transfer rates in wild-type cyanobacterium Synechococcus elongatus PCC7942 for photo-bioelectricity generation." Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/274353.
Повний текст джерелаZhu, Jianfeng M. Eng Massachusetts Institute of Technology. "An evaluation of the hydrogen economy and metal oxide based photo-electrochemical cells." Thesis, Massachusetts Institute of Technology, 2010. http://hdl.handle.net/1721.1/62684.
Повний текст джерелаCataloged from PDF version of thesis.
Includes bibliographical references (p. 130-142).
Fossil fuels depletion and climate change are driving the need for sustainable development and renewable energy sources globally [1]. Solar being the most abundant and widespread source of renewable energy is resulting in a rapidly growing, with a growth rate more than 35% annually for the past 10 years [4]. Hydrogen is an ideal energy carrier for next generation given its high efficiency, environmental friendliness, wide application as well as several attractive methods for storage and distribution [17]. The hydrogen economy, a proposed system of producing, delivering and employing energy by using hydrogen, is under intensive research and development, and is projected to be realized at the end of this century as one of the leading suppliers [60]. Photo-electrochemical (PEC) cells connect the solar energy and hydrogen economy together by directly converting solar energy into chemical energy in the form of hydrogen gas. The metal oxide based PEC cell has advantages of low cost, high stability and durability and environmental friendliness [14], a good option for commercialization. With the rapid development of nanotechnology in recent years, novel nano-structured metal oxide PEC cells can have higher efficiency and better performance due to the effects of quantization, large surface areas, improved charge transport, etc. In this thesis, the current status and future development of the hydrogen economy in terms of identifying the markets, opportunities and risks of solar-hydrogen has been reviewed and accessed. The technology review of PEC cells in terms of the working mechanism and efficiency determining factors has been studied. The current research efforts on metal oxide based PEC cells for optimizing the performances and processing methods have also been studied. A case study and cost modeling in the context of scenario has been conducted; the analysis showed the cost of PEC cells was still very high mainly due to the high materials and processing costs. Thus, future research development should focus on the technological approaches with low materials and processing costs and high energy conversion efficiency for earlier commercialization of PEC cells. Besides, hydrogen storage, distribution, safety codes and standards, education and training as well as fuel cell technology must also require intensive research and development to insure the realization of solar-hydrogen economy.
by Jianfeng Zhu.
M.Eng.
DESTRO, MATTEO. "Towards Realization of an Innovative Li-Ion Battery: Materials Optimization and System Up-Scalable Solutions." Doctoral thesis, Politecnico di Torino, 2013. http://hdl.handle.net/11583/2506270.
Повний текст джерелаDelices, Annette. "Organized Organic Dye / Hole Transporting Materials for TiO2- and ZnO- based Solid-State Dye-Sensitized Solar Cells (s-DSSCs)." Thesis, Sorbonne Paris Cité, 2017. http://www.theses.fr/2017USPCC066/document.
Повний текст джерелаDue to instability problems of dye sensitized solar cells (DSSCs) in longtime uses, the iodine based liquidelectrolyte has been replaced by several types of solid hole transporting materials (HTM) to perform solidstate DSSCs (s-DSSCs). Among them, the substitution by conducting polymers (CP) has attractedconsiderable attention because of their good stability, high hole-conductivity and simple deposition withinthe mesoporous TiO2 semiconductor. In this thesis work, several s-DSSCs based on CPs used as HTM havebeen developed in order to improve their photovoltaic performances taking into account the following twoobjectives: (i) the optimization of the interfacial charge transfer processes within the solar cell, and (ii) theoptimization of the charge transport within the n-type oxide semiconductor. To reach these goals, eachcomponent that constitutes the device was varied in order to investigate its effect on the device’sperformances. As first attempt, an analytical study is carried out by varying the sensitizer in order todetermine the fragments of the dyes structures, that have an important effect on the in-situ photoelectrochemical polymerization process (PEP) both in organic and in aqueous media and hence on theperformances of the s-DSSCs. Based on these results, a new concept of removing completely the interfacebetween the dye and the HTM is developed. This is achieved by the synthesis of new dyes covalently linkedto an electroactive monomer which is co-polymerized by in-situ PEP. The resulting co-polymer, used asHTM, is covalently linked to the dye. In addition, the nature of the chemical bond linking the triphenylamineresidue TPA to the monomer is also investigated as a key factor in the s-DSSCs performances. Besides, andto optimize the charge transport processes within this type of s-DSSC, the elaboration of novel ZnO baseds-DSSCs has been achieved and investigated
You, Sheng Mu. "Metal organic frameworks as efficient photosensitizer for TiO₂ nanoarray anode and application to water splitting in PEC cells Fe/Ni Bimetallic organic framework deposited on TiO₂ nanotube array for enhancing higher and stable activity of oxygen evolution reaction Novel nano-architectured water splitting photoanodes based on TiO₂-nanorod mats surface sensitized by ZIF-67 coatings Surface sensitization of TiO₂ nanorod mats by electrodeposition of ZIF-67 for water photo-oxidation Electrochemically capacitive deionization of copper (II) using 3D hierarchically reduced graphene oxide architectures." Thesis, université Paris-Saclay, 2020. http://www.theses.fr/2020UPASF015.
Повний текст джерелаThe fossil fuel reserves are dwindling and their unrestricted use has generated profound changes in Earth's surface temperature and climate. Storing solar energy in the form of hydrogen produced by dissociation of water is an ideal way to mitigate global warming. Materials from the “metal organic framework” (MOF) family are starting to be used as photo-electrocatalysts, especially for photo-dissociation of water. Their extremely high porosity and their great versatility, both chemical and structural, designate them as potential candidates to facilitate the absorption of solar radiation and catalyze the dissociation of water in photoelectrochemical cells. By controlling the chemical composition and doping of the linker used in the MOF, it is possible to adjust the band gap energy, to favor the functionalization on very varied substrates or even to adjust their resistance to corrosion in various chemical environments. They are therefore materials of great interest for catalysis, electrocatalysis or photo-electro-catalysis. On the other hand, nano-structured TiO₂, for example in the form of nanotube or nanowire mats, sometimes called TiO₂ nanoarray (TNA), is a material very suitable for the construction of photoanodes for the evolution of oxygen in aqueous medium. It has already been extensively studied and described in the literature. During our thesis, we manufactured composite materials made up of MOFs of transition metals (Ni, Co, Fe) deposited on TNA (network of nanotubes or nanowires). For this we used an electrochemical method of electrodeposition (cyclic voltammetry). This allowed us to deposit metallic nanoparticles on TNA with fixed potential - 1.0 V and then transform them by chemical reaction with organic ligands (1,3,5-benzenetricarboxylic acid, BTC, 1,4-benzenedicarboxylic acid, BDC and imidazole, 2MZ) by thermal-thermal route. The materials obtained exhibit significant electrocatalytic activity and excellent photoelectrochemical durability. These composite materials have been successfully used as an active phase in photo-electrodes for the oxygen release reaction (OER)
Lai, Chien-Ming, and 賴建銘. "Investigation of the Electrochemical Impedance Spectroscopy on the Direct Methanol Fuel Cell and Silicon Photo-electrochemical Etching." Thesis, 2008. http://ndltd.ncl.edu.tw/handle/33638895267346313990.
Повний текст джерела國立中央大學
機械工程研究所
96
The technique of electrochemical impedance spectroscopy (EIS) diagnosis has been used to investigate the electrochemical kinetics in the systems of (1) direct methanol fuel cell (DMFC) and (2) photo-electrochemical etching on silicon. The results and contributions of this work were summarized as follows. 1. EIS was carried out to monitor the performance of DMFC under a variety of current densities. Based on analysis of the EIS data that depend upon the performing conditions, an innovative model including the qualitative sketch and its quantitative description relying on postulated equivalent circuit (EQC) was established to delineate the reaction mechanism of DMFC on the membrane electrode assembly (MEA). This model provides a satisfactory diagnosis in the performance of DMFC in terms of the EQC sets. One EQC sets comprises elements such as the internal resistance (Rs) at the highest frequency, the high-frequency impedance (Rif /Cif) that is a parallel combination of the interfacial resistance (Rif) and interfacial capacitance (Cif) resultant from the interfaces in the cell, the medium-frequency impedance (Rrxn /Crxn) that is a parallel combination of the resistance (Rrxn) and capacitance (Crxn) resultant from electrochemical reactions, and the low-frequency impedance (LCO /RCO) that is a parallel combination of the resistance (RCO) and inductance (LCO) resultant from the adsorption and relaxation of CO. This postulated model provides a useful tool to diagnose the degradation mechanism for a cell subject to a test of accelerating degradation. Through the diagnosing and the evidences supported by the examinations through instruments such as the electron probe microanalyzer (EPMA), transmission electron microscope (TEM) and X-ray photoelectron spectroscope (XPS), the degradation is major attributed to (a) the increase of Rif and Rrxn resultant from catalytic degradation that may arise from a series of processes including the dissolution of Ru from the anodic catalyst Pt-Ru, the migration of Ru ions to be reduced on the membrane nearby the cathode. The Ru-dissolution leads to a decrease of catalytic activity on the anode that could be confirmed by the technique of CO stripping in company with the observation through EPMA and XPS. The particles reduced on the membrane nearby the cathode were verified by the examination through TEM and EPMA. (b) The increase of internal resistance (Rs) is ascribed to the loss of sulfonic-acid group from the graded membrane near the anode. Membrane degradation possibly arisen from the heat accumulation in a severely acidic environment near the anode derived from cell reactions. The loss of sulfonic acid group was verified by EPMA and XPS analyses. 2. The photo-electrochemical etching on Si (100) surface reveals different SEM morphologies depending on whether or not the HF solution contains ethanol. Finer smooth pores (around 4 μm in diameter) were formed in the presence of ethanol but larger rough pores (around 8 μm in diameter) formed in 2 M HF solution alone during silicon etched at 0.250 V (vs. SCE) under 50W-illumination for 3 h. The characteristic potentials and current such as transition potential (Etrans), half-wave potential (Ep/2), and limiting current density (jlimit), resulted from dc anodic polarization, were the major parameters used in EIS to diagnose the etching system. There appears an extra low-frequency inductive loop in the Nyquist plot for the etching system in the presence of ethanol. This loop is attributed to relaxation of the adsorption of ethanol in the pores. The contact angle between the etching solution and the silicon decreases with increasing the ethanol concentration. Accordingly, ethanol plays a wetting role in the etching process thus forming fine smooth pores.
Ding, Jia-Chi, and 丁嘉碁. "Photo-Electrochemical Polymerization and Photovoltaic Properties of Polyaniline Used as a Hole Transport Layer in Solid-State Dye-Sensitized Solar Cell." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/17808308465213967703.
Повний текст джерела國立高雄應用科技大學
化學工程與材料工程系
99
Various morphologies polyaniline (PANI) deposited on the interface betweenTiO2 and Dye (TiO2-Dye/PANI) and ITO counter electrode (PANI-ITO C.E.) were prepared by photo-chemical and electrochemical polymerization method, respectively, where deposited PANI used as the electro hole transport layer material (HTM) in the part of solid state dye-sensitized solar cell (DSSC). The solid state TiO2-Dye/PANI/ITO and TiO2/Dye/PANI-ITO solar cells were further fabricated by using sandwich assembling technique. As a result, in spite of the photo-chemical polymerization method can effectively improve the electric contact between TiO2 and PANI, leading to increase in current density, but the PANI chains may penetrate into the TiO2-Dye layer and growth on the surface of ITO, results in the total photoelectric conversion efficiency () is apparently depressed. As the total charge is 0.3 coulomb, the deposited PANI exhibits the best surface roughness, conjugated degree and electrochemical activity than those of applied coulombs. When 4-tert-Butylpyridine (TBP) added into HTM, the electron-hole recombination between TiO2 and HTM is significantly reduced; the Voc hence increases to 0.52 V. As TBP and LiI added into HTM, LiI acts as the dopant of PANI and the redox couple in the solar cell, leading to the improvement of photovoltaic characteristics. At 0.7M TBP and 0.1 M LiI, the η of TiO2/Dye/PANI-ITO solar cells is 0.643 %.
TAVELLA, FRANCESCO. "Development of Catalytic Electrodes and Cell Design for Solar Fuel Generation." Doctoral thesis, 2018. http://hdl.handle.net/11570/3131224.
Повний текст джерелаЧастини книг з теми "Photo- electrochemical cell"
Alexander, John Callum. "Principles of Photo-Electrochemical Cells." In Springer Theses, 47–92. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-34229-0_3.
Повний текст джерелаFukuzawa, Kenji, Keiichi Yanagisawa, and Hiroki Kuwano. "Photo-Electrochemical Cell Utilizing Bacteriorhodopsin Immobilized onto a Thin-Film Lattice Fabricated by Micromachining Techniques." In Biosensors '94, 340. Elsevier, 1994. http://dx.doi.org/10.1016/b978-1-85617-242-4.50284-6.
Повний текст джерелаChawla, Priyanka, Shivangi Trivedi, and Kumari Pooja. "Investigation on Various Polymer Electrolytes for Development of Dye Sensitized Solar Cell." In Materials Science: A Field of Diverse Industrial Applications, 158–73. BENTHAM SCIENCE PUBLISHERS, 2023. http://dx.doi.org/10.2174/9789815051247123010012.
Повний текст джерелаPutz, Mihai V., Marina A. Tudoran, and Marius C. Mirica. "Bondonic Electrochemistry." In Renewable and Alternative Energy, 277–359. IGI Global, 2017. http://dx.doi.org/10.4018/978-1-5225-1671-2.ch010.
Повний текст джерелаPutz, Mihai V., Marina A. Tudoran, and Marius C. Mirica. "Bondonic Electrochemistry." In Sustainable Nanosystems Development, Properties, and Applications, 328–411. IGI Global, 2017. http://dx.doi.org/10.4018/978-1-5225-0492-4.ch010.
Повний текст джерелаLee, Byunghong, and Robert Bob Chang. "A New Generation of Energy Harvesting Devices." In Solar Cells [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.94291.
Повний текст джерелаP. Khirade, Pankaj, and Anil V. Raut. "Perovskite Structured Materials: Synthesis, Structure, Physical Properties and Applications." In Recent Advances in Perovskite Materials [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.106252.
Повний текст джерелаHaga, Masa-aki. "Surface-Confined Ruthenium Complexes Bearing Benzimidazole Derivatives: Toward Functional Devices." In Ruthenium - an Element Loved by Researchers [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.97071.
Повний текст джерелаТези доповідей конференцій з теми "Photo- electrochemical cell"
Maity, Subhasis, and Nabin Baran Manik. "Safranine T dye based photo electrochemical solar cell: Effect of electrodes on device mechanism." In 2007 International Workshop on Physics of Semiconductor Devices. IEEE, 2007. http://dx.doi.org/10.1109/iwpsd.2007.4472584.
Повний текст джерелаTseng, C. Y., C. H. Wu, H. Y. Shin, and C. T. Lee. "Investigation of Surface Passivation on III-V compound Solar Cell using Photo-electrochemical Oxidation Method." In 2009 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2009. http://dx.doi.org/10.7567/ssdm.2009.p-6-8.
Повний текст джерелаCardenas-Valencia, A. M., D. P. Fries, G. Steimle, H. Broadbent, L. C. Langebrake, and R. F. Benson. "Fabrication of Micro-Actuated Galvanic Cells as Power on Demand for Lab on a Chip Applications by Means of Novel PCB/MEMS Technology." In ASME 2003 1st International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2003. http://dx.doi.org/10.1115/fuelcell2003-1731.
Повний текст джерелаLiu, Xiaolu, Yang Liu, Kai Ren, Paul Lawson, Andrew Moening, Matthew Haubert, Yong X. Gan, et al. "Clean Energy Generation by a Nanostructured Biophotofuel Cell." In ASME 2013 11th International Conference on Fuel Cell Science, Engineering and Technology collocated with the ASME 2013 Heat Transfer Summer Conference and the ASME 2013 7th International Conference on Energy Sustainability. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/fuelcell2013-18261.
Повний текст джерелаLi, Jinwei, and Yong Shi. "Electron Transport and Recombination in TiO2 Nanofiber Dye Sensitized Solar Cell." In ASME 2011 International Mechanical Engineering Congress and Exposition. ASMEDC, 2011. http://dx.doi.org/10.1115/imece2011-64979.
Повний текст джерелаNagayama, Gyoko, Ryuji Ando, Kei Muramatsu, and Takaharu Tsuruta. "Fabrication of Macroporous on No-Mask Silicon Substrate for Application to Microsystems." In 2008 Second International Conference on Integration and Commercialization of Micro and Nanosystems. ASMEDC, 2008. http://dx.doi.org/10.1115/micronano2008-70323.
Повний текст джерелаPaudel, Yamuna, and Matthew Y. Sfeir. "GaAs photo diode for electrochemical process enhancement." In Frontiers in Optics. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/fio.2022.jw4a.48.
Повний текст джерелаSmirnov, Vladimir, and Katharina Welter. "Multijunction Si Solar Cells for Integrated Photo-Electrochemical Devices." In nanoGe Fall Meeting 2018. València: Fundació Scito, 2018. http://dx.doi.org/10.29363/nanoge.fallmeeting.2018.056.
Повний текст джерелаSmirnov, Vladimir, and Katharina Welter. "Multijunction Si Solar Cells for Integrated Photo-Electrochemical Devices." In nanoGe Fall Meeting 2018. València: Fundació Scito, 2018. http://dx.doi.org/10.29363/nanoge.nfm.2018.056.
Повний текст джерелаElsenberg, A., T. Emmler, M. Schieda, F. Gärtner, and T. Klassen. "Aerosol Deposition of BiVO4 Films for Solar Hydrogen Generation." In ITSC2022. DVS Media GmbH, 2022. http://dx.doi.org/10.31399/asm.cp.itsc2022p0056.
Повний текст джерела