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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.
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页码:11167 / 11173
页数:7
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