Promoting charge carrier utilization by integrating layered double hydroxide nanosheet arrays with porous BiVO4 photoanode for efficient photoelectrochemical water splitting

被引:62
作者
Huang, Yi
Yu, Yifu
Xin, Yani
Meng, Nannan
Yu, Yu
Zhang, Bin [1 ]
机构
[1] Tianjin Univ, Tianjin Key Lab Mol Optoelect Sci, Sch Sci, Dept Chem, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
photoelectrocatalysis; water splitting; synergistic effect; layered double hydroxides; porous photoanode; OXYGEN-EVOLUTION; BISMUTH VANADATE; OXIDATION; ELECTROCATALYST; OXYHYDROXIDE; CATALYSTS; CO2; NI; NANOPARTICLES; PERFORMANCE;
D O I
10.1007/s40843-016-5168-0
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The increasing exploration of renewable and clean power sources have driven the development of highly active materials for photoelectrochemical (PEC) water splitting. However, it is still a great challenge to enhance the charge utilization. Herein, we report a facile method to fabricate composite photoanode with porous BiVO4 film as the photon absorber and layered double hydroxide (LDH) nanosheet arrays as the oxygen-evolution cocatalysts (OECs). The as-prepared BiVO4/NiFe-LDH photoanode shows an excellent performance for PEC water splitting benefitting from the synergistic effect of the superior charge separation efficiency facilitated by porous BiVO4 film and the excellent water oxidation activity resulting from LDH nanosheet arrays. A photocurrent density is 4.02 mA cm(-2) at 1.23 V vs. the reversible hydrogen electrode (RHE). Furthermore, the O-2 evolution rate at the surface of BiVO4/NiFe-LDH photoanode is as high as 29.6 mu mol h(-1) cm(-2) and the high activity for water oxidation is maintained for over 30 h. Impressively, the performance of the as-fabricated composite photoanode for PEC water splitting can be further enhanced through incorporating a certain amount of Co2+ cation into NiFe-LDH as OEC. The photocurrent density is achieved up to 4.45 mA cm(-2) at 1.23 V vs. RHE. This value is the highest yet reported for un-doped BiVO4-based photoanodes so far.
引用
收藏
页码:193 / 207
页数:15
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