Oxygen defect engineering endows Co3O4 nanosheets with advanced aluminum ion storage

被引:7
|
作者
Zheng, Jiening [1 ]
Xu, Tian [1 ]
Xia, Guanglin [1 ]
Yu, Xuebin [1 ]
机构
[1] Fudan Univ, Dept Mat Sci, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
TOTAL-ENERGY CALCULATIONS; CATHODE MATERIAL; ANODE MATERIAL; HIGH-CAPACITY; NANOTUBES; BATTERIES; INTERCALATION; POLYHEDRON; MECHANISM; GROWTH;
D O I
10.1039/d2ta04165k
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
Atomic-level structure modulation is an effective way to boost ionic diffusion kinetics and improve the cycling stability. To relieve the strong coulombic ion-lattice interactions originating from trivalent Al3+ ions, herein oxygen-deficient Co3O4-x porous nanosheets are fabricated via a facile NaBH4 reduction strategy using a metal-organic framework template. Electrochemical kinetics analysis and theoretical calculation results reveal good pseudocapacitive property, appropriate diffusion capability and Al3+ formation energy, corroborating fast Al3+ ion storage/release kinetics and high Al3+ storage capacity. Specifically, Co3O4-x porous nanosheets exhibit a high reversible capacity of 442.3 mA h g(-1) at 1.0 A g(-1) and retain 104.2 mA h g(-1) after 1800 cycles, remarkably higher than those of the previously reported Co3O4-based cathode materials. Furthermore, ex situ analyses reveal the conversion reaction mechanism of the Co3O4-x cathode, followed by its high structural stability upon extended cycling.
引用
收藏
页码:18322 / 18332
页数:11
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