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Metal-organic framework derived hollow porous CuO-CuCo2O4 dodecahedrons as a cathode catalyst for Li-O2 batteries
被引:29
|作者:
Zhen, Shu-ying
[1
]
Wu, Hai-tao
[2
]
Wang, Yan
[2
]
Li, Na
[1
]
Chen, Hao-sen
[1
]
Song, Wei-li
[1
]
Wang, Zhen-hua
[2
]
Sun, Wang
[2
]
Sun, Ke-ning
[2
]
机构:
[1] Beijing Inst Technol, Inst Adv Struct Technol, Beijing 100081, Peoples R China
[2] Beijing Inst Technol, Sch Chem & Chem Engn, Beijing Key Lab Chem Power Source & Green Catalys, Beijing 100081, Peoples R China
来源:
基金:
中国博士后科学基金;
中国国家自然科学基金;
关键词:
LONG-LIFE;
LITHIUM;
CUCO2O4;
ELECTROCATALYST;
ELECTRODE;
D O I:
10.1039/c9ra02860a
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Herein, hollow porous CuO-CuCo2O4 dodecahedrons are synthesized by using a simple self-sacrificial metal-organic framework (MOF) template, which resulted in dodecahedron morphology with hierarchically porous architecture. When evaluated as a cathodic electrocatalyst in lithium-oxygen batteries, the CuO-CuCo2O4 composite exhibits a significantly enhanced electrochemical performance, delivering an initial capacity of 6844 mA h g(-1) with a remarkably decreased discharge/charge overpotential to 1.15 V (vs. Li/Li+) at a current density of 100 mA g(-1) and showing excellent cyclic stability up to 111 charge/discharge cycles under a cut-off capacity of 1000 mA h g (-1) at 400 mA g (-1). The outstanding electrochemical performance of CuO-CuCo2O4 composite can be owing to the intrinsic catalytic activity, unique porous structure and the presence of substantial electrocatalytic sites. The ex situ XRD and SEM are also carried out to reveal the charge/discharge behavior and demonstrate the excellent reversibility of the CuO-CuCo2O4 based electrode.
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页码:16288 / 16295
页数:8
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