Stable solar-driven oxidation of water by semiconducting photoanodes protected by transparent catalytic nickel oxide films
Saadi, Fadl H.
Lichterman, Michael F.
Hale, William G.
Plymale, Noah T.
Omelchenko, Stefan T.
Papadantonakis, Kimberly M.
Brunschwig, Bruce S.
Lewis, Nathan S.
KAUST DepartmentComputer, Electrical and Mathematical Sciences and Engineering (CEMSE) Division
Electrical Engineering Program
KAUST Solar Center (KSC)
Nano Energy Lab
Online Publication Date2015-03-11
Print Publication Date2015-03-24
Permanent link to this recordhttp://hdl.handle.net/10754/564102
MetadataShow full item record
AbstractReactively 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.
CitationSun, 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.1423034112
SponsorsThis 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 Central IDPMC4378389
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