Stable solar-driven oxidation of water by semiconducting photoanodes protected by transparent catalytic nickel oxide films
Type
ArticleAuthors
Sun, KeSaadi, Fadl H.
Lichterman, Michael F.
Hale, William G.
Wang, Hsinping
Zhou, Xinghao
Plymale, Noah T.
Omelchenko, Stefan T.
He, Jr-Hau

Papadantonakis, Kimberly M.
Brunschwig, Bruce S.
Lewis, Nathan S.
KAUST Department
Computer, Electrical and Mathematical Sciences and Engineering (CEMSE) DivisionElectrical Engineering Program
KAUST Solar Center (KSC)
Nano Energy Lab
Date
2015-03-11Online Publication Date
2015-03-11Print Publication Date
2015-03-24Permanent link to this record
http://hdl.handle.net/10754/564102
Metadata
Show full item recordAbstract
Reactively sputtered nickel oxide (NiOx) films provide transparent, antireflective, electrically conductive, chemically stable coatings that also are highly active electrocatalysts for the oxidation of water to O2(g). These NiOx coatings provide protective layers on a variety of technologically important semiconducting photoanodes, including textured crystalline Si passivated by amorphous silicon, crystalline n-type cadmium telluride, and hydrogenated amorphous silicon. Under anodic operation in 1.0 M aqueous potassium hydroxide (pH 14) in the presence of simulated sunlight, the NiOx films stabilized all of these self-passivating, high-efficiency semiconducting photoelectrodes for >100 h of sustained, quantitative solar-driven oxidation of water to O2(g). © 2015, National Academy of Sciences. All rights reserved.Citation
Sun, K., Saadi, F. H., Lichterman, M. F., Hale, W. G., Wang, H.-P., Zhou, X., … Lewis, N. S. (2015). Stable solar-driven oxidation of water by semiconducting photoanodes protected by transparent catalytic nickel oxide films. Proceedings of the National Academy of Sciences, 112(12), 3612–3617. doi:10.1073/pnas.1423034112Sponsors
This material is based on work performed by the Joint Center for Artificial Photosynthesis, a Department of Energy (DOE) Energy Innovation Hub, supported through the Office of Science of the US DOE under Award DE-SC0004993. N.T.P. acknowledges support from the Graduate Research Fellowship Program of the US National Science Foundation. B.S.B. was supported by the Beckman Institute of the California Institute of Technology. This work was also supported by the Gordon and Betty Moore Foundation under Award GBMF1225.PubMed ID
25762067PubMed Central ID
PMC4378389Additional Links
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4378389ae974a485f413a2113503eed53cd6c53
10.1073/pnas.1423034112
Scopus Count
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