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Role of Surface States in Photocatalytic Oxygen Evolution with CuWO4 Particles

Journal Article · · Journal of the Electrochemical Society
DOI:https://doi.org/10.1149/2.0021905jes· OSTI ID:1481806
CuWO4 is a medium bandgap (2.3 eV) n-type semiconductor capable of photoelectrochemical water oxidation under applied electrical bias. Here, we show for the first time that suspended microcrystals CuWO4 evolve oxygen photocatalytically under visible illumination from solutions of 0.05 M AgNO3 (10.8 μmol/hour; AQE of 0.56% at 400 nm) and 0.0002 M FeCl3 (1.5 μmol/hour). No oxygen is detected with 0.002 M [Fe(CN)6]3- as sacrificial agent. The activity dependence on the redox potential of the acceptors is due to the presence of Cu2+ based electron trap states in CuWO4. According to surface photovoltage spectroscopy and electrochemistry, these states are located on the particle surface, 1.8 eV above the valence band edge of the material. Controlling the chemistry of these states will be key to uses of CuWO4 particles in tandem catalysts for overall water splitting.
Research Organization:
Univ. of California, Davis, CA (United States)
Sponsoring Organization:
Australian Research Council (ARC); USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22)
Grant/Contract Number:
SC0015329
OSTI ID:
1481806
Alternate ID(s):
OSTI ID: 1612276
Journal Information:
Journal of the Electrochemical Society, Journal Name: Journal of the Electrochemical Society Journal Issue: 5 Vol. 166; ISSN 0013-4651
Publisher:
IOP Publishing - The Electrochemical SocietyCopyright Statement
Country of Publication:
United States
Language:
English

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