阴极
材料科学
插层(化学)
电池(电)
镁
化学工程
氧化还原
锂(药物)
离子
动力学
储能
纳米技术
无机化学
化学
物理化学
热力学
冶金
工程类
内分泌学
物理
功率(物理)
有机化学
医学
量子力学
作者
Ze Chen,Qi Yang,Donghong Wang,Ao Chen,Xinliang Li,Zhaodong Huang,Guojin Liang,Ying Wang,Chunyi Zhi
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-03-31
卷期号:16 (4): 5349-5357
被引量:45
标识
DOI:10.1021/acsnano.1c07939
摘要
Magnesium ion batteries (MIBs), due to the low redox potential of Mg, high theoretical capacity, dendrite-free magnesiation, and safe nature, have been recognized as a post-lithium energy storage system. However, an ongoing challenge, sluggish Mg2+ kinetics in the small number of available cathode materials of MIBs, restricts its further development. The existing cathodes mostly deliver unsatisfactory capacity with poor cycling life based on the traditional ion-intercalation mechanism. Herein, we fabricated a conversion-type Mg∥Te battery based on a reversible two-step conversion reaction (Te to MgTe2 to MgTe). High discharge capacities (387 mAh g-1) and rate capability (165 mAh g-1 at 5 A g-1) can be achieved. The diffusivity of Mg2+ can reach 3.54 × 10-8 cm2 s-1, enabled by the high electrical conductivity of Te and increased surface conversion sites. Subsequently, ab initio molecular dynamics simulation was also carried out to further confirm the conversion mechanism and fast Mg2+ transportation kinetics.
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