Modulating Co-catalyst/Facet Junction for Enhanced Photoelectrochemical Water Splitting

被引:3
作者
An, Yang [3 ]
Hao, Jingxuan [3 ]
Lin, Cheng [2 ]
Zhang, Shaowei [1 ]
Zhang, Kan [2 ]
Min, Yulin [3 ]
机构
[1] Shanghai Spaceflight Control Technol Inst, Shanghai 201109, Peoples R China
[2] Nanjing Univ Sci & Technol, Coll Mat Sci & Engn, MIIT Key Lab Adv Display Mat & Devices, Nanjing 210094, Peoples R China
[3] Shanghai Univ Elect Power, Shanghai Key Lab Mat Protect & Adv Mat Elect Powe, Shanghai 200090, Peoples R China
基金
中国国家自然科学基金;
关键词
TiO2 nanorod arrays; internal electric field; photovoltage generation; water splitting; Fermi pinning effect; TIO2 NANOTUBE ARRAYS; PHOTOCATALYTIC ACTIVITY; NANOWIRE ARRAYS; PHOTOANODE; LAYER; COCATALYSTS; GENERATION; DEPENDENCE; DEPOSITION;
D O I
10.1021/acsami.2c12181
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Rational construction of electric field via assembling appropriate co-catalysts on anisotropic facets is of great significance for improving the photogenerated charge separation efficiency. However, this strategy usually gives rise to Fermi-level pinning which is not contributive to the charge separation but deleterious to the photoelectrochemical performance through consuming the measurable photovoltage. Herein, we demonstrate that manganese dioxide electrodeposited on the (111) facet of titanium dioxide nanorods could tremendously boost the catalytic activity of pristine photoanode via a stronger interface electric field and less photovoltage decay compared with the counterpart grown on the (110) facet. A photocurrent density of 1.65 mA??cm???2 at 1.23 V (vs reversible hydrogen electrode), nearly the theoretical maximum of titanium dioxide, is achieved by the optimum photoanode with an extremely high separation efficiency of 95.15%. This study offers more in-depth insights into the design of carrier separation strategy through loading co-catalysts on different substrate surfaces for more efficient solar energy conversion. <comment>Superscript/Subscript Available</comment
引用
收藏
页码:42134 / 42143
页数:10
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