Cobalt-Ruthenium Nanoalloys Parceled in Porous Nitrogen-Doped Graphene as Highly Efficient Difunctional Catalysts for Hydrogen Evolution Reaction and Hydrolysis of Ammonia Borane

被引:98
|
作者
Wei, Zhihong [1 ]
Liu, Yuan [2 ]
Peng, Zhikun [1 ]
Song, Haoqiang [3 ]
Liu, Zhongyi [1 ]
Liu, Baozhong [3 ]
Li, Baojun [1 ]
Yang, Bai [4 ]
Lu, Siyu [1 ]
机构
[1] Zhengzhou Univ, Coll Chem & Mol Engn, 100 Sci Ave, Zhengzhou 450001, Henan, Peoples R China
[2] Zhengzhou Univ, Coll Mat Sci & Engn, 100 Sci Ave, Zhengzhou 450001, Henan, Peoples R China
[3] Henan Polytech Univ, Coll Chem & Chem Engn, 2001 Century Ave, Jiaozuo City 454000, Peoples R China
[4] Jilin Univ, Coll Chem, State Key Lab Supramol Struct & Mat, 2699 Qianjin St, Changchun 130012, Jilin, Peoples R China
来源
基金
中国博士后科学基金;
关键词
Cobalt-ruthenium nanoalloys; Difunctional catalysts; Hydrogen evolution reaction; Hydrolysis of ammonia borane; OXYGEN REDUCTION; CARBON; NANOPARTICLES; WATER; ELECTROCATALYST; DEHYDROGENATION; ENERGY; NANOCATALYST; NANOSHEETS; FRAMEWORK;
D O I
10.1021/acssuschemeng.8b06745
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of clean fuels for hydrogen utilization will benefit from low-cost and active catalysts to produce hydrogen via hydrolytic dehydrogenation by electro-chemical and chemical means. Herein, we designed and synthesized a high-efficiency and stable catalyst with low ruthenium content CoRu alloy nanoparticles supported on porous nitrogen-doped graphene layers (CoRux@N-C) via pyrolysis of small organic metal molecules. The amount of ruthenium in the catalyst that showed the highest activity was only 5.07 wt %. CoRu0.25@N-C can efficiently catalyze the hydrogen evolution reaction (HER) with a wide pH range and low overpotential to drive current densities of 10 mA.cm(-2) of only 27 mV (1.0 M KOH) and 94 mV (0.5 M H2SO4). CoRu0.25@N-C also showed decent durability with negligible degradation after and alkaline solutions. It also has excellent catalytic activity and can easily sustain 1000 cyclic-voltammetry cycles in both acidic ammonia borane hydrolysis with an initial turnover frequency (TOF) of 457.8 mol(H2) min(-1) mol(cat)(-1) under ambient conditions. CoRu0.25@N-C can readily perform both NH3BH3 hydrolytic dehydrogenation and electrochemical hydrogen evolution as a result of its highly specific surface area, carbon layer protection, metal vacancies, and a porous carbon matrix doped with heteroatoms. The creation of a multifunctional composite/hybrid by the use of small metal organic molecules can lead to cost-effective and highly efficient catalysts for energy conversion.
引用
收藏
页码:7014 / 7023
页数:19
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