Highly reversible zinc metal anode enabled by strong Bronsted acid and hydrophobic interfacial chemistry

被引:29
|
作者
Nian, Qingshun [1 ]
Luo, Xuan [1 ]
Ruan, Digen [1 ]
Li, Yecheng [1 ]
Xiong, Bing-Qing [1 ]
Cui, Zhuangzhuang [1 ]
Wang, Zihong [1 ]
Dong, Qi [1 ]
Fan, Jiajia [1 ]
Jiang, Jinyu [1 ]
Ma, Jun [1 ]
Ma, Zhihao [1 ]
Wang, Dazhuang [1 ]
Ren, Xiaodi [1 ]
机构
[1] Univ Sci & Technol China, Hefei Natl Res Ctr Phys Sci Microscale, Dept Mat Sci & Engn, CAS Key Lab Mat Energy Convers, Hefei 230026, Anhui, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
D O I
10.1038/s41467-024-48444-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Uncontrollable zinc (Zn) plating and hydrogen evolution greatly undermine Zn anode reversibility. Previous electrolyte designs focus on suppressing H2O reactivity, however, the accumulation of alkaline byproducts during battery calendar aging and cycling still deteriorates the battery performance. Here, we present a direct strategy to tackle such problems using a strong Br & oslash;nsted acid, bis(trifluoromethanesulfonyl)imide (HTFSI), as the electrolyte additive. This approach reformulates battery interfacial chemistry on both electrodes, suppresses continuous corrosion reactions and promotes uniform Zn deposition. The enrichment of hydrophobic TFSI- anions at the Zn|electrolyte interface creates an H2O-deficient micro-environment, thus inhibiting Zn corrosion reactions and inducing a ZnS-rich interphase. This highly acidic electrolyte demonstrates high Zn plating/stripping Coulombic efficiency up to 99.7% at 1 mA cm(-2) ( > 99.8% under higher current density and areal capacity). Additionally, Zn | |ZnV6O9 full cells exhibit a high capacity retention of 76.8% after 2000 cycles.
引用
收藏
页数:12
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