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Synergetic modulation on ionic association and solvation structure by electron- withdrawing effect for aqueous zinc-ion batteries
被引:68
|作者:
Wang, Rui
[1
]
Yao, Minjie
[1
]
Yang, Min
[1
]
Zhu, Jiacai
[1
]
Chen, Jun
[1
]
Niu, Zhiqiang
[1
]
机构:
[1] Nankai Univ, Coll Chem, Renewable Energy Convers & Storage Ctr, Key Lab Adv Energy Mat Chem,Minist Educ,Haihe Lab, Tianjin 300071, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
low ionic association;
electron-withdrawing effect;
aqueous zinc-ion batteries;
STABILITY;
D O I:
10.1073/pnas.2221980120
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:
Aqueous zinc- ion batteries are emerging as one of the most promising large- scale energy storage systems due to their low cost and high safety. However, Zn anodes often encoun-ter the problems of Zn dendrite growth, hydrogen evolution reaction, and formation of by-products. Herein, we developed the low ionic association electrolytes (LIAEs) by introducing 2, 2, 2-trifluoroethanol (TFE) into 30 m ZnCl2 electrolyte. Owing to the electron-withdrawing effect of - CF3 groups in TFE molecules, in LIAEs, the Zn2+ sol-vation structures convert from larger aggregate clusters into smaller parts and TFE will construct H- bonds with H2O in Zn2+ solvation structure simultaneously. Consequently, ionic migration kinetics are significantly enhanced and the ionization of solvated H2O is effectively suppressed in LIAEs. As a result, Zn anodes in LIAE display a fast plating/ stripping kinetics and high Coulombic efficiency of 99.74%. The corresponding full batteries exhibit an improved comprehensive performance such as high- rate capability and long cycling life.
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