Bio-Inspired Polyanionic Electrolytes for Highly Stable Zinc-Ion Batteries

被引:114
作者
Dong, Haobo [1 ,2 ]
Hu, Xueying [1 ,2 ]
Liu, Ruirui [3 ]
Ouyang, Mengzheng [4 ]
He, Hongzhen
Wang, Tianlei [2 ]
Gao, Xuan [2 ,3 ]
Dai, Yuhang [1 ]
Zhang, Wei [2 ]
Liu, Yiyang [1 ]
Zhou, Yongquan
Brett, Dan J. L. [1 ]
Parkin, Ivan P. [2 ]
Shearing, Paul R. [1 ]
He, Guanjie [1 ]
机构
[1] UCL, Dept Chem Engn, Electrochem Innovat Lab, Torrington Pl, London WC1E 7JE, England
[2] UCL, Dept Chem, Christopher Ingold Labs, 20 Gordon St, London WC1H 0AJ, England
[3] Chinese Acad Sci, Key Lab Comprehens & Highly Efficient Util, Lab Salt Lake Resources Chem Qinghai Prov, Xining 810008, Qinghai, Peoples R China
[4] Imperial Coll, Dept Earth Sci & Engn, London SW7 2AZ, England
基金
英国工程与自然科学研究理事会; 英国科学技术设施理事会; 英国科研创新办公室;
关键词
Bio-Inspired Electrolyte; Interface Engineering; Zinc-Ion Batteries; in situ SEI; ALGINATE; ANODES;
D O I
10.1002/anie.202311268
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
For zinc-ion batteries (ZIBs), the non-uniform Zn plating/stripping results in a high polarization and low Coulombic efficiency (CE), hindering the large-scale application of ZIBs. Here, inspired by biomass seaweed plants, an anionic polyelectrolyte alginate acid (SA) was used to initiate the in situ formation of the high-performance solid electrolyte interphase (SEI) layer on the Zn anode. Attribute to the anionic groups of -COO-, the affinity of Zn2+ ions to alginate acid induces a well-aligned accelerating channel for uniform plating. This SEI regulates the desolvation structure of Zn2+ and facilitates the formation of compact Zn (002) crystal planes. Even under high depth of discharge conditions (DOD), the SA-coated Zn anode still maintains a stable Zn stripping/plating behavior with a low potential difference (0.114 V). According to the classical nucleation theory, the nucleation energy for SA-coated Zn is 97 % less than that of bare Zn, resulting in a faster nucleation rate. The Zn||Cu cell assembled with the SA-coated electrode exhibits an outstanding average CE of 99.8 % over 1,400 cycles. The design is successfully demonstrated in pouch cells, where the SA-coated Zn exhibits capacity retention of 96.9 % compared to 59.1 % for bare Zn anode, even under the high cathode mass loading (>10 mg/cm(2)).
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页数:10
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