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Metal organic framework-derived transition metal-doped CoSx nanocage for enhanced visible light-assisted methanol electrocatalytic oxidation
被引:4
|作者:
Li, Meng
[1
]
Du, Quan
[1
]
Li, Guanfeng
[1
]
Qian, Lei
[1
]
Zeng, Ying
[1
]
机构:
[1] Chengdu Univ Technol, Coll Mat & Chem & Chem Engn, Chengdu 610059, Sichuan, Peoples R China
基金:
中国国家自然科学基金;
中国博士后科学基金;
关键词:
COBALT SULFIDE;
HYDROGEN EVOLUTION;
FACILE SYNTHESIS;
PERFORMANCE;
WATER;
PHOTOCATALYST;
CATALYST;
CDS;
NANOSTRUCTURES;
FABRICATION;
D O I:
10.1039/d3cp03002d
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Designing noble metal-free anode catalysts for visible light-assisted direct methanol fuel cells still remains a significant challenge. In this study, combining the photocatalytic and electrocatalytic properties of CoSx, a visible light-assisted methanol electrocatalytic oxidation strategy was provided. Doping engineering was employed to adjust the electronic structure of CoSx and improve their photoassisted methanol electrocatalytic oxidation activity. Using ZIF-67 as precursor, transition metal-doped CoSx (M-CoSx, M = Zn, Cu, Ni, and Cd) nanocage was synthesized by cation exchange and l-cysteine-controlled etching. Cd doping not only widens the light adsorption to the visible region but also enhances the separation efficiency of photogenerated electron-hole pairs. The electrochemical and photochemical results indicated that the strong oxidative photogenerated hole, OH center dot , and O-2(center dot- ) are beneficial for methanol electrocatalytic oxidation. The synergistic electrocatalytic and photocatalytic effect will be a practical strategy for improving the methanol electrocatalytic oxidation activity of noble metal-free semiconductor catalysts.
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页码:27331 / 27341
页数:11
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