Charge-Carrier Dynamics at the CuWO4/Electrocatalyst Interface for Photoelectrochemical Water Oxidation

被引:11
|
作者
Shadabipour, Parisa [1 ]
Raithel, Austin L. [1 ]
Hamann, Thomas W. [1 ]
机构
[1] Michigan State Univ, Dept Chem, E Lansing, MI 48824 USA
关键词
water splitting; photoelectrochemical; CuWO4; nickel-iron oxide; shunting; dual-working electrode (photo)electrochemistry;
D O I
10.1021/acsami.0c14705
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Unraveling the charge-carrier dynamics at electrocatalyst/electrode interfaces is critical for the development of efficient photoelectrochemical (PEC) water oxidation. Unlike the majority of photoanodes investigated for PEC water oxidation, the integration of electrocatalysts with CuWO4 electrodes generally results in comparable or worse performance compared to the bare electrode. This is despite the fact that the surface state recombination limits the water oxidation efficiency with CuWO4 electrodes, and an electrocatalyst ought to bypass this reaction and improve performance. Here, we present results that deepen the understanding of the energetics and electron-transfer processes at the CuWO4/electrocatalyst interface, which controls the performance of such systems. Ni(0.75)Fe(0.25)Oy (denoted as Ni75) was chosen as a model electrocatalyst, and through dual-working electrode experiments, we have been able to provide significant insight into the role of the electrocatalyst on the charge-transfer process at the CuWO4/Ni75 interface. We have shown a lack of performance improvement for CuWO4/Ni75 relative to the bare electrode to water oxidation. We attribute this surprising result to water oxidation on the CuWO4 surface kinetically outcompeting hole transfer to the Ni-75 electrocatalyst interface.
引用
收藏
页码:50592 / 50599
页数:8
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