When It's Heavier: Interfacial and Solvation Chemistry of Isotopes in Aqueous Electrolytes for Zn-ion Batteries

被引:23
|
作者
Gao, Xuan [1 ,2 ]
Dai, Yuhang [2 ]
Zhang, Chengyi [3 ]
Zhang, Yixuan [4 ]
Zong, Wei [1 ]
Zhang, Wei [1 ]
Chen, Ruwei [2 ]
Zhu, Jiexin [2 ]
Hu, Xueying [1 ]
Wang, Mingyue [1 ]
Chen, Ruizhe [1 ]
Du, Zijuan [1 ]
Guo, Fei [2 ]
Dong, Haobo [2 ]
Liu, Yiyang [2 ]
He, Hongzhen [2 ]
Zhao, Siyu [2 ]
Zhao, Fangjia [1 ]
Li, Jianwei [2 ]
Parkin, Ivan P. [1 ]
Carmalt, Claire J. [1 ]
He, Guanjie [1 ]
机构
[1] UCL, Dept Chem, Christopher Ingold Lab, 20 Gordon St, London WC1H 0AJ, England
[2] UCL, Dept Chem Engn, London WC1E 7JE, England
[3] Wuhan Univ, Inst Technol Sci, Wuhan 430072, Hubei, Peoples R China
[4] Tech Univ Darmstadt, Inst Mat Sci, D-64287 Darmstadt, Germany
基金
英国工程与自然科学研究理事会;
关键词
Interface; Solvation structure; Isotopes; Zinc-ion Batteries; GEL ELECTROLYTE; H2O;
D O I
10.1002/anie.202300608
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The electrochemical effect of isotope (EEI) of water is introduced in the Zn-ion batteries (ZIBs) electrolyte to deal with the challenge of severe side reactions and massive gas production. Due to the low diffusion and strong coordination of ions in D2O, the possibility of side reactions is decreased, resulting in a broader electrochemically stable potential window, less pH change, and less zinc hydroxide sulfate (ZHS) generation during cycling. Moreover, we demonstrate that D2O eliminates the different ZHS phases generated by the change of bound water during cycling because of the consistently low local ion and molecule concentration, resulting in a stable interface between the electrode and electrolyte. The full cells with D2O-based electrolyte demonstrated more stable cycling performance which displayed similar to 100 % reversible efficiencies after 1,000 cycles with a wide voltage window of 0.8-2.0 V and 3,000 cycles with a normal voltage window of 0.8-1.9 V at a current density of 2 A g(-1).
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页数:11
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