Polycrystalline CoP/CoP2 Structures for Efficient Full Water Splitting

被引:105
作者
Li, Shanpeng [1 ,2 ]
Zhang, Gong [3 ]
Tu, Xinman [1 ]
Li, Jinghong [2 ]
机构
[1] Nanchang Hangkong Univ, Coll Environm & Chem Engn, Nanchang 330063, Jiangxi, Peoples R China
[2] Tsinghua Univ, Dept Chem, Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China
[3] Tsinghua Univ, Sch Environm, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
CoP; heterostructures; electrocatalysis; water splitting; ELECTROCATALYTIC HYDROGEN EVOLUTION; GRAPHENE OXIDE SHEETS; BIFUNCTIONAL ELECTROCATALYST; CARBON CLOTH; PHOSPHIDE; NANOPARTICLES; COBALT; CATALYSTS; ELECTRODE; CATHODE;
D O I
10.1002/celc.201701112
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Transition-metal phosphides (TMPs) have attracted extensive attention for use in the field of full water splitting. Various methods have been investigated to obtain high catalytic activity, but in these synthetic processes other active materials are inevitably introduced to modify or load onto the surface of the TMP to further improve the catalytic performance. Herein, we describe a novel approach for preparing CoP/CoP2 structures (650 degrees C) by pyrolysis of a complex formed from Co ions crosslinked with phytic acid (PA) using 2-methylimidazole (MeIM). The integration of CoP2 and CoP in the structures can enhance the intrinsic electrical conductivity, and facilitate electron transfer from solution to the electrode. Overpotentials of only 250 and 239 mV were required to support the current densities of 10 and 20 mAcm(-2) for the oxygen evolution reaction and hydrogen evolution reaction, respectively, demonstrating the potential of the novel material for practical overall water splitting.
引用
收藏
页码:701 / 707
页数:7
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