Fabrication of Hollow CoP/TiOx Heterostructures for Enhanced Oxygen Evolution Reaction

被引:140
|
作者
Liang, Zibin [1 ]
Zhou, Wenyang [1 ]
Gao, Song [1 ]
Zhao, Ruo [1 ]
Zhang, Hao [1 ]
Tang, Yanqun [1 ]
Cheng, Jinqian [1 ]
Qiu, Tianjie [1 ]
Zhu, Bingjun [1 ]
Qu, Chong [1 ]
Guo, Wenhan [1 ]
Wang, Qian [1 ]
Zou, Ruqiang [1 ]
机构
[1] Peking Univ, Coll Engn, Dept Mat Sci & Engn, Beijing Key Lab Theory & Technol Adv Battery Mat, Beijing 100871, Peoples R China
关键词
cobalt phosphide; heterostructures; oxygen evolution reaction; synergistic effect; titanium oxide; COP NANOPARTICLES; EFFICIENT; HYDROGEN; PERFORMANCE; ELECTROCATALYSTS; NANOCRYSTALS; CONVERSION; CATALYSTS; STORAGE; TIO2;
D O I
10.1002/smll.201905075
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition-metal phosphides have flourished as promising candidates for oxygen evolution reaction (OER) electrocatalysts. Herein, it is demonstrated that the electrocatalytic OER performance of CoP can be greatly improved by constructing a hybrid CoP/TiOx heterostructure. The CoP/TiOx heterostructure is fabricated using metal-organic framework nanocrystals as templates, which leads to unique hollow structures and uniformly distributed CoP nanoparticles on TiOx. The strong interactions between CoP and TiOx in the CoP/TiOx heterostructure and the conductive nature of TiOx with Ti3+ sites endow the CoP-TiOx hybrid material with high OER activity comparable to the state-of-the-art IrO2 or RuO2 OER electrocatalysts. In combination with theoretical calculations, this work reveals that the formation of CoP/TiOx heterostructure can generate a pathway for facile electron transport and optimize the water adsorption energy, thus promoting the OER electrocatalysis.
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页数:10
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