硫族元素
离子
纳米技术
材料科学
化学
化学工程
结晶学
工程类
有机化学
作者
Hongqing Li,Jintu Qi,Yongchao Tang,Guigui Liu,Jianping Yan,Zhenfeng Feng,Yue Wei,Qi Yang,Minghui Ye,Yufei Zhang,Zhipeng Wen,Xiaoqing Liu,Cheng Chao Li
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-05-20
卷期号:24 (22): 6465-6473
被引量:8
标识
DOI:10.1021/acs.nanolett.4c00198
摘要
Neutrophilic superhalide-anion-triggered chalcogen conversion-based Zn batteries, despite latent high-energy merit, usually suffer from a short lifespan caused by dendrite growth and shuttle effect. Here, a superhalide-anion-motivator reforming strategy is initiated to simultaneously manipulate the anode interface and Se conversion intermediates, realizing a bipolar regulation toward longevous energy-type Zn batteries. With ZnF2 chaotropic additives, the original large-radii superhalide zincate anion species in ionic liquid (IL) electrolytes are split into small F-containing species, boosting the formation of robust solid electrolyte interphases (SEI) for Zn dendrite inhibition. Simultaneously, ion radius reduced multiple F-containing Se conversion intermediates form, enhancing the interion interaction of charged products to suppress the shuttle effect. Consequently, Zn||Se batteries deliver a ca. 20-fold prolonged lifespan (2000 cycles) at 1 A g–1 and high energy/power density of 416.7 Wh kgSe–1/1.89 kW kgSe–1, outperforming those in F-free counterparts. Pouch cells with distinct plateaus and durable cyclability further substantiate the practicality of this design.
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