Molybdenum Carbide-Decorated Metallic Cobalt@Nitrogen-Doped Carbon Polyhedrons for Enhanced Electrocatalytic Hydrogen Evolution

被引:164
作者
Wu, Can [1 ,2 ]
Liu, Dan [1 ]
Li, Hui [1 ]
Li, Jinghong [1 ]
机构
[1] Tsinghua Univ, Dept Chem, Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China
[2] Hubei Univ, Fac Mat Sci & Engn, Wuhan 430062, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
carbon polyhedrons; cobalt nanoparticles; electrocatalysis; hydrogen evolution reaction; molybdenum carbide; EFFICIENT BIFUNCTIONAL ELECTROCATALYST; HIGHLY-ACTIVE ELECTROCATALYSTS; OXYGEN REDUCTION REACTION; HIGH-PERFORMANCE; RATIONAL DESIGN; MOS2; NANOSHEETS; WATER OXIDATION; N-C; CATALYSTS; NANOPARTICLES;
D O I
10.1002/smll.201704227
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrocatalytic hydrogen evolution reaction (HER) based on water splitting holds great promise for clean energy technologies, in which the key issue is exploring cost-effective materials to replace noble metal catalysts. Here, a sequential chemical etching and pyrolysis strategy are developed to prepare molybdenum carbide-decorated metallic cobalt@nitrogen-doped porous carbon polyhedrons (denoted as Mo/Co@N-C) hybrids for enhanced electrocatalytic hydrogen evolution. The obtained metallic Co nanoparticles are coated by N-doped carbon thin layers while the formed molybdenum carbide nanoparticles are well-dispersed in the whole Co@N-C frames. Benefiting from the additionally implanted molybdenum carbide active sites, the HER performance of Mo/Co@N-C hybrids is significantly promoted compared with the single Co@N-C that is derived from the pristine ZIF-67 both in alkaline and acidic media. As a result, the as-synthesized Mo/Co@N-C hybrids exhibit superior HER electrocatalytic activity, and only very low overpotentials of 157 and 187 mV are needed at 10 mA cm(-2) in 1 M KOH and 0.5 M H2SO4, respectively, opening a door for rational design and fabrication of novel low-cost electrocatalysts with hierarchical structures toward electrochemical energy storage and conversion.
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页数:10
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