TiO2/graphene/NiFe-layered double hydroxide nanorod array photoanodes for efficient photoelectrochemical water splitting

被引:482
作者
Ning, Fanyu [1 ]
Shao, Mingfei [1 ]
Xu, Simin [1 ]
Fu, Yi [1 ]
Zhang, Ruikang [1 ]
Wei, Min [1 ]
Evans, David G. [1 ]
Duan, Xue [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
OXYGEN EVOLUTION REACTION; TIO2 NANOWIRE ARRAYS; ENHANCED PHOTOCATALYTIC ACTIVITY; LAYERED DOUBLE HYDROXIDE; NITROGEN-DOPED GRAPHENE; SENSITIZED SOLAR-CELLS; CHARGE SEPARATION; H-2; PRODUCTION; OXIDATION; OXIDE;
D O I
10.1039/c6ee01092j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The ever-increasing demand for renewable and clean power sources has triggered the development of novel materials for photoelectrochemical (PEC) water splitting, but how to improve the solar conversion efficiency remains a big challenge. In this work, we report a conceptual strategy in a ternary material system to simultaneously enhance the charge separation and water oxidation efficiency of photoanodes by introducing reduced graphite oxide (rGO) and NiFe-layered double hydroxide (LDH) on TiO2 nanorod arrays (NAs). An experimental-computational combination study reveals that rGO with a high work function and superior electron mobility accepts photogenerated electrons from TiO2 and enables fast electron transportation; while NiFe-LDH acts as a cocatalyst which accelerates the surface water oxidation reaction. This synergistic effect in this ternary TiO2/rGO/NiFe-LDH photoanode gives rise to a largely enhanced photoconversion efficiency (0.58% at 0.13 V) and photocurrent density (1.74 mA cm(-2) at 0.6 V). It is worth mentioning that the photocurrent density of TiO2/rGO/NiFe-LDH, to the best of our knowledge, is superior to previously reported TiO2-based photoanodes in benign and neutral media. In addition, the method presented here can be extended to the preparation of other efficient photoanodes (WO3/rGO/NiFe-LDH and alpha-Fe2O3/rGO/NiFe-LDH) toward high level PEC performance.
引用
收藏
页码:2633 / 2643
页数:11
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