(1 1 0)-Bridged nanoblocks self-assembled VS4 hollow microspheres as sodium-ion battery anode with superior rate capability and long cycling life

阳极 材料科学 电池(电) 化学工程 电化学 钠离子电池 纳米技术 电极 化学 法拉第效率 工程类 功率(物理) 量子力学 物理 物理化学
作者
Wenbin Li,Jianfeng Huang,Ruizi Li,Liyun Cao,Xifei Li,Liangliang Feng,Shaoyi Chen
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:384: 123385-123385 被引量:41
标识
DOI:10.1016/j.cej.2019.123385
摘要

Development of three-dimensional self-assembled hollow nanoarchitectures combining functional shells and inner voids is an important approach for realizing high-rate and long-life battery electrodes. As a potential high-performance anode for sodium-ion batteries (SIBs), (1 1 0)-bridged nanoblocks self-assembled VS4 hollow microspheres (PNBH-VS4) are controllably synthesized by a facile one-step hydrothermal method. The (1 1 0)-bridged structure constructs the Na+ conducting channels and e− transfer paths among nano-grains and nanoblocks, and the self-assembled hollow structure presents the double space physical entrapment effect for the excessive volume change of nanoblocks, which synergistically improve the Na+ storage kinetics and structure stability. When employed as an anode for SIBs, PNBH-VS4 electrode exhibits the superior rate capability and long cycling life, outperforming those of the ever-reported VS4-based anode materials. At 0.2, 0.5, 1.0 and 2.0 A g−1, the capacity can reach 629, 564, 428 and 400 mAh g−1 after 250, 200, 350 and 700 cycles, respectively. Even at 5.0 A g−1, the capacity can still stabilize at 309 mAh g−1 after 1000 long cycles. In addition, it is revealed that PNBH-VS4 electrode undertakes the insertion and conversion reaction in the potential range of 0.50–3.00 and 0.05–0.50 V, respectively, where the main capacity contribution originates from the insertion reaction. Meanwhile, PNBH-VS4 electrode exhibits better insertion reversibility at lower current densities and conversion reversibility at higher current densities during cycling, respectively.
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