Cobalt Nanoparticles Embedded in Nitrogen-Doped Carbon for the Hydrogen Evolution Reaction

被引:171
|
作者
Fei, Huilong [1 ]
Yang, Yang [1 ,2 ]
Peng, Zhiwei [1 ]
Ruan, Gedeng [1 ]
Zhong, Qifeng [1 ]
Li, Lei [1 ]
Samuel, Errol L. G. [1 ]
Tour, James M. [1 ,2 ,3 ]
机构
[1] Rice Univ, Dept Chem, Houston, TX 77005 USA
[2] Rice Univ, Smalley Inst Nanoscale Sci & Technol, Houston, TX 77005 USA
[3] Rice Univ, Dept Mat Sci & NanoEngn, Houston, TX 77005 USA
关键词
electrocatalytic hydrogen evolution; nitrogen doping graphene; cobalt nanoparticles; synergistic effects; OXYGEN REDUCTION REACTION; CARBIDE NANOPARTICLES; NANOWIRE ARRAYS; ION BATTERIES; ELECTROCATALYST; NANOTUBES; CATALYSTS; GRAPHENE; EFFICIENT; MOS2;
D O I
10.1021/acsami.5b00652
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
There is great interest in renewable and sustainable energy research to develop low-cost, highly efficient, and stable electrocatalysts as alternatives to replace Pt-based catalysts for the hydrogen evolution reaction (HER). Though nanoparticles encapsulated in carbon shells have been widely used to improve the electrode performances in energy storage devices (e.g., lithium ion batteries), they have attracted less attention in energy-related electrocatalysis. Here we report the synthesis of nitrogen-enriched core shell structured cobalt carbon nanoparticles dispersed on graphene sheets and we investigate their HER performances in both acidic and basic media. These catalysts exhibit excellent durability and HER activities with onset over-potentials as low as similar to 70 mV in both acidic (0.5 M H2SO4) and alkaline (0.1 M NaOH) electrolytes, and the overpotentials needed to deliver 10 mA cm(-2) are determined to be 265 mV in acid and 337 mV in base, further demonstrating their potential to replace Pt-based catalysts. Control experiments reveal that the active sites for HER might come from the synergistic effects between the cobalt nanoparticles and nitrogen-doped carbon.
引用
收藏
页码:8083 / 8087
页数:5
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