Interface engineering in core-shell Co9S8@MoS2 nanocrystals induces enhanced hydrogen evolution in acidic and alkaline media

被引:5
|
作者
Hao, Jiace [1 ]
Hu, Hongyin [1 ]
Dong, Yuan [1 ]
Hu, Jingwen [1 ]
Sang, Xinxin [1 ]
Duan, Fang [1 ]
Lu, Shuanglong [1 ]
Zhu, Han [1 ]
Du, Mingliang [1 ]
机构
[1] Jiangnan Univ, Sch Chem & Mat Engn, Minist Educ, Key Lab Synthet & Biol Colloids, Wuxi 214122, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
SUPERIOR BIFUNCTIONAL ELECTROCATALYSTS; EFFICIENT OXYGEN EVOLUTION; CARBON NANOFIBERS; HIGHLY EFFICIENT; REDUCTION; NANOPARTICLES; PERFORMANCE; MICROSPHERES; NANOSPHERES; FABRICATION;
D O I
10.1039/d1nj01221e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Core-shell structure electrocatalysts with excellent activity and stability are promising candidates for the hydrogen evolution reaction (HER). Here, carbon nanofiber-supported Co9S8 nanocrystals fully (F-Co9S8@MoS2/CNFs) and semi-wrapped (S-Co9S8@MoS2/CNFs) with interfaces were successfully synthesized. Interface engineering in Co9S8@MoS2 core shell structures leads to the formation of abundant Co-S-Mo nanointerfaces with remarkable charge transfer. Benefiting from the novel semi core-shell structure, S-Co9S8@MoS2/CNFs with exposed Co-S-Mo nanointerfaces display superior HER activity, requiring overpotentials of only 77 mV and 122 mV to achieve current densities of 10 mA cm(-2) in acidic and alkaline media, respectively. Beyond that, S-Co9S8@MoS2/CNFs can afford a high current density of similar to 100 mA cm(-2) for at least 10 h with negligible degradation. The results indicate that the construction of the core-shell structure facilitates charge redistribution between Co9S8 and MoS2, inducing electron transfer from Co to Mo through Co-S-Mo nanointerfaces. This work indicates the vital effect of nanointerfaces for electrocatalytic HER.
引用
收藏
页码:11167 / 11173
页数:7
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