A Monodisperse Rh2P-Based Electrocatalyst for Highly Efficient and pH-Universal Hydrogen Evolution Reaction

被引:191
作者
Yang, Fulin [1 ,2 ]
Zhao, Yuanmeng [1 ,2 ]
Du, Yeshuang [1 ,2 ]
Chen, Yongting [1 ,2 ]
Cheng, Gongzhen [1 ,2 ]
Chen, Shengli [1 ,2 ]
Luo, Wei [1 ,2 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Hubei, Peoples R China
[2] Hubei Key Lab Electrochem Power Sources Wuhan, Wuhan 430072, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
DFT; hydrogen evolution reaction; monodisperse Rh2P; pH-universal; transition metal phosphides; BIFUNCTIONAL ELECTROCATALYSTS; NICKEL PHOSPHIDE; LOW-COST; CATALYSTS; DESIGN; CARBON; ENERGY; COPPER; ELECTROLYSIS; MOLYBDENUM;
D O I
10.1002/aenm.201703489
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The search for Pt-free electrocatalysts exceeding pH-universal hydrogen evolution reaction (HER) activities when compared to the state-of-the-art commercial Pt/C is highly desirable for the development of renewable energy conversion systems but still remains a huge challenge. Here a colloidal synthesis of monodisperse Rh2P nanoparticles with an average size of 2.8 nm and their superior catalytic activities for pH-universal HER are reported. Significantly, the Rh2P catalyst displays remarkable HER performance with overpotentials of 14, 30, and 38 mV to achieve 10 mA cm(-2) in 0.5 m H2SO4, 1.0 m KOH, and 1.0 M phosphate-buffered saline, respectively, exceeding almost all the documented electrocatalysts, including the commercial 20 wt% Pt/C. Density functional theory calculations reveal that the introduction of P into Rh can weaken the H adsorption strength of Rh2P to nearly zero, beneficial for boosting HER performance.
引用
收藏
页数:7
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