Multi-Site High-Entropy Immobilizer for All-Iodine Species Fixation in High-Performance Zinc-Iodine Batteries

被引:0
|
作者
Li, Yanxin [1 ]
Jia, Hongfeng [1 ]
Hao, Yuehan [1 ]
Ali, Usman [1 ]
Liu, Bingqiu [1 ]
Zhang, Lingyu [1 ]
Li, Lu [1 ]
Lian, Ruqian [2 ]
Wang, Chungang [1 ]
机构
[1] Northeast Normal Univ, Dept Chem, Changchun 130024, Peoples R China
[2] Hebei Univ, Sch Phys Sci & Technol Sci & Engn, Baoding 071002, Peoples R China
基金
中国国家自然科学基金;
关键词
all-iodine species; catalysis; chemical anchoring; high-entropy; zinc-iodine battery; CATALYSTS;
D O I
10.1002/adfm.202419821
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Zinc-iodine (Zn-I2) batteries are of great interest thanks to their high energy density, low cost, and inherent safety. However, the dissolution of I- and the generated polyiodides exacerbated by the dissolved I- severely reduces the utilization of the active substance, resulting in poor coulombic efficiency and a drastic decrease in performance. In this regard, chemical immobilization of iodine species with high-entropy material is developed. Benefiting from the remarkable catalytic and anchoring activity of the high-entropy material, accelerated catalytic conversion and chemisorption of polyiodides are realized. Meanwhile, the distribution characteristics of the multi-active adsorption centers on the high-entropy material enable the abundant active sites to anchor the highly soluble and hard-to-mobilize I- in a chemical bonding manner. Such a unique bonding mode allows all iodine species (I2/I-/I3-) to be firmly immobilized on the electrode, which enhances the effectiveness and utilization of rechargeable Zn-I2 batteries. High-entropy material with the ability to immobilize all species of iodine provides a novel/effective strategy for realizing high-performance Zn-I2 batteries.
引用
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页数:11
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