Functional modified separator with high-entropy material for high performance Zn-I2 batteries

IF 6.1 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Hongfeng Jia, Yanxin Li, Yuehan Hao, Usman Ali, Bingqiu Liu, Lu Li, Lingyu Zhang, Liang Zhao, Hang Sun, Chungang Wang
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引用次数: 0

Abstract

The problems of soluble polyiodide shuttling and slow redox kinetics result in irrational cycling stability and restrict the further development of Zn-I2 batteries. In this paper, self-supporting layers containing high-entropy materials (HEMs) with adsorption-catalytic-conversion integrated functions were applied for the first time for separator modification of Zn-I2 batteries. Benefiting from the multi-elemental composition of HEMs, the widely distributed d-band centers improve the bonding between metals and molecules to realize the reduced adsorption energies to reactants or intermediates, giving the HEMs substantial highly active sites as adsorption and catalytic centers. This allows the polyiodides to be chemically anchored and catalytically converted by the modified layer once they are formed. The entire iodine conversion reaction proceeds efficiently without polyiodide shuttle and dissolution. As a result, satisfactory cycling stability was achieved. HEM is proposed as separator modification materials with adsorption-catalytic-conversion synergies, presenting an effective strategy and new inspiration for realizing high-performance Zn-I2 batteries.
高性能锌- i2电池用高熵材料功能改性隔板
可溶性多碘化物的穿梭和氧化还原动力学缓慢等问题导致循环稳定性不合理,制约了锌- i2电池的进一步发展。本文首次将具有吸附-催化-转化一体化功能的高熵材料(HEMs)自支撑层应用于Zn-I2电池的隔膜改性。得益于HEMs的多元素组成,广泛分布的d带中心改善了金属与分子之间的键合,从而降低了对反应物或中间体的吸附能,使HEMs具有大量的高活性位点作为吸附和催化中心。这使得多碘化物一旦形成,就可以通过修饰层进行化学锚定和催化转化。整个碘转化反应有效进行,没有多碘离子穿梭和溶解。结果,获得了令人满意的循环稳定性。提出了HEM作为具有吸附-催化-转化协同作用的隔膜改性材料,为实现高性能锌- i2电池提供了有效的策略和新的启示。
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来源期刊
Inorganic Chemistry Frontiers
Inorganic Chemistry Frontiers CHEMISTRY, INORGANIC & NUCLEAR-
CiteScore
10.40
自引率
7.10%
发文量
587
审稿时长
1.2 months
期刊介绍: The international, high quality journal for interdisciplinary research between inorganic chemistry and related subjects
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