Phosphorus-modified cobalt single-atom catalysts loaded on crosslinked carbon nanosheets for efficient alkaline hydrogen evolution reaction

被引:67
作者
Huang, Yucong [1 ,2 ]
Hu, Zhiyun [1 ]
Huang, Liang-ai [1 ]
Wang, Zongpeng [1 ]
Lin, Zhiping [1 ]
Shen, Shijie [1 ]
Zhong, Wenwu [1 ]
Pan, Jiaqi [2 ]
机构
[1] Taizhou Univ, Sch Mat Sci & Engn, Zhejiang 318000, Peoples R China
[2] Zhejiang Sci Tech Univ, Dept Phys, Key Lab Opt Field Manipulat Zhejiang Prov, Key Lab ATMMT Minist Educ, Zhejiang 310000, Peoples R China
基金
中国国家自然科学基金;
关键词
ELECTROCATALYST; SITE; GRAPHENE;
D O I
10.1039/d2nr07066a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Efficient and low-cost transition metal single-atom catalysts (TMSACs) for hydrogen evolution reaction (HER) have been recognized as research hotspots recently with advances in delivering good catalytic activity without noble metals. However, the high-cost complex preparation of TMSACs and insufficient stability limited their practical applications. Herein, a simple top-down pyrolysis approach to obtain P-modified Co SACs loaded on the crosslinked defect-rich carbon nanosheets was introduced for alkaline hydrogen evolution, where Co atoms are locally confined before pyrolysis to prevent aggregation. Thereby, the abundant defects and the unsaturated coordination formed during the pyrolysis significantly improved the stability of the monatomic structure and reduced the reaction barrier. Furthermore, the synergy between cobalt atoms and phosphorus atoms was established to optimize the decomposition process of water molecules, which delivers the key to promoting the slow reaction kinetics of alkaline HER. As the result, the cobalt SAC exhibited excellent catalytic activity and stability for alkaline HER, with overpotentials of 70 mV and 192 mV at current densities of -10 mA cm(-2) and -100 mA cm(-2), respectively.
引用
收藏
页码:3550 / 3559
页数:10
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