NiSb/nitrogen-doped carbon derived from Ni-based framework as advanced anode for lithium-ion batteries

被引:47
作者
Su, Mingru [1 ]
Li, Jinlin [1 ]
He, Kuidong [1 ]
Fu, Kai [1 ]
Nui, Penghu [1 ]
Chen, Yichang [1 ]
Zhou, Yu [1 ]
Dou, Aichun [1 ]
Hou, Xiaochuan [2 ]
Liu, Yunjian [1 ]
机构
[1] Jiangsu Univ, Sch Mat Sci & Engn, Zhenjiang 212013, Peoples R China
[2] Zhejiang NewEra Zhongneng Recycling Technol Co Ltd, Shaoxing 312369, Peoples R China
基金
中国国家自然科学基金;
关键词
Lithium-ion batteries; Anode; NiSb alloy; Ni-based framework; Nitrogen-doped carbon; LI-ION; HIGH-CAPACITY; COMPOSITE ANODE; POROUS CARBON; QUANTUM DOTS; PERFORMANCE; SB; NANOPARTICLES; NANOSHEETS; STORAGE;
D O I
10.1016/j.jcis.2022.08.126
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
Antimony anode has attracted much attention owing to its low lithium-embedded platform and high specific capacity. However, the dramatic volume expansion during the insertion and detachment of Li' seriously affects its application in lithium-ion batteries. In this work, NiSb alloy embedded in nitrogen -doped carbon (NiSb/C) derived from a Ni-based framework was synthesized by a simple hydrothermal reaction followed by annealing treatment. NiSb alloy nanoparticles could alleviate significant volume expansion during lithium/delithiation owing to the good buffering action of Ni. Nitrogen-doped carbon provides abundant active sites for Li' and serves as a conductive network to accelerate electron transport. Moreover, the uniformly dispersed NiSb alloy particles and the nitrogen-doped carbon can effectively cooperate to retain the structural completeness of antimony, which promotes the cycling stability and high-rate performance of the NiSb/C anode. At a high density of 2 A g(-1), the prepared NiSb/C anode exhibits a reversible specific capacity of 426 mAh g(-1) after 450 cycles. It can also exhibit a superior rate capability of 387 mAh g(-1) at 5.0 A g(-1), which can provide a possibility for designing new anode materials for rechargeable batteries. (C) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:83 / 91
页数:9
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