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Honeycomb-Inspired Heterogeneous Bimetallic Co-Mo Oxide Nanoarchitectures for High-Rate Electrochemical Lithium Storage
被引:42
作者:
Mei, Jun
[1
]
Liao, Ting
[1
]
Sprott, Henry
[2
]
Ayoko, Godwin A.
[1
]
Zhao, X. S.
[3
]
Sun, Ziqi
[1
]
机构:
[1] Queensland Univ Technol, Sch Chem Phys & Mech Engn, Brisbane, Qld 4001, Australia
[2] Queensland Univ Technol, Inst Future Environm, Brisbane, Qld 4001, Australia
[3] Univ Queensland, Sch Chem Engn, St Lucia Campus, Brisbane, Qld 4074, Australia
基金:
澳大利亚研究理事会;
关键词:
bioinspired;
cobalt oxide;
honeycombs;
lithium ion batteries;
rate capability;
ELECTRODE MATERIALS;
ENERGY-STORAGE;
BATTERY;
ARRAYS;
D O I:
10.1002/smtd.201900055
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:
Nanostructure engineering has been proved to be an efficient approach for improving electrochemical properties for energy storage by accommodating volume changes, facilitating rapid mass transport paths, and enlarging ion storage sites and interfaces. The well-designed fine nanostructures, unfortunately, are usually destroyed during long-term cycles and ultimately lose their structural advantages. Herein, stimulated by the extraordinary structural stability, robust mechanical properties, and salient ventilation capacity of natural honeycomb species, bioinspired heterogeneous bimetallic Co-Mo oxide (CoMoOx) nanoarchitectures assembled from 2D nanounits are successfully fabricated via a molybdenum-mediated self-assembly strategy for improving the rate capability of electrochemical lithium storage devices. Owing to the robust structural stability and the ultrathin 2D wall structure, CoMoOx nanostructures present well-maintained honeycomb-like structure, rapid capacitive insertion-desertion behaviors, and thus significantly enhanced lithium ion storage performance at high rates (5.0 A g(-1)). It is also revealed that the reversible transition of cobalt and molybdenum phases closely associated with the ultrathin 2D wall structures greatly contribute to the outstanding electrochemical lithium storage performances. This attractive integration of structural and functional advantages achieved by learning from nature offers new insights into the design of cost-effective electrode materials for high-performance energy devices.
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