{"title":"高能锌离子电池中多功能离子液体的动态卤素耦合研究","authors":"Xuanrui Huang, Shunshun Zhao, Sinian Yang, Xinwei Wang, Lili Liu, Shimou Chen","doi":"10.1002/adfm.202519437","DOIUrl":null,"url":null,"abstract":"Aqueous Zn-I<sub>2</sub> batteries are promising for sustainable energy storage, exhibit excellent safety, low cost, and high energy density. However, their practical application is limited by the two-electron I<sup>−</sup>/I⁰ redox reaction and the severe shuttle effect of polyiodide species. Here, a multifunctional ionic liquid, 1-butyl-3-methylimidazolium bromide (BmimBr), is introduced to establish a dynamic interhalogen coupling between iodine and bromine species, which enables a six-electron transfer pathway involving I<sup>−</sup>/I⁰/I⁺ and Br<sup>−</sup>/Br⁰. In situ characterizations and theoretical calculations show that Br<sup>−</sup> acts as a dynamic mediator, forming an [IBr<sub>2</sub>]<sup>−</sup> intermediate with iodine. This significantly lowers the energy barrier for oxidizing I⁰ to I⁺, thereby contributing additional capacity and accelerating kinetics. Simultaneously, Bmim⁺ provides dual interfacial functions: confining polyiodides at the cathode to suppress shuttling, and forming a protective layer on the zinc anode, which reduces interfacial water, inhibits dendrite growth and side reactions. Leveraging this synergistic design, the Zn-I<sub>2</sub> battery achieves a high specific capacity of 511 mAh g<sup>−1</sup> at 1 A g<sup>−1</sup> and retains 90.22% of its capacity after 30 000 cycles at 10 A g<sup>−1</sup>. The dynamic interhalogen coupling strategy offers a novel route to activate multielectron reactions and stabilize electrode interfaces in Zn-I<sub>2</sub> batteries.","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"73 1","pages":""},"PeriodicalIF":19.0000,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dynamic Interhalogen Coupling Engineered by Multifunctional Ionic Liquid for High-Energy Aqueous Zn-I2 Batteries\",\"authors\":\"Xuanrui Huang, Shunshun Zhao, Sinian Yang, Xinwei Wang, Lili Liu, Shimou Chen\",\"doi\":\"10.1002/adfm.202519437\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Aqueous Zn-I<sub>2</sub> batteries are promising for sustainable energy storage, exhibit excellent safety, low cost, and high energy density. However, their practical application is limited by the two-electron I<sup>−</sup>/I⁰ redox reaction and the severe shuttle effect of polyiodide species. Here, a multifunctional ionic liquid, 1-butyl-3-methylimidazolium bromide (BmimBr), is introduced to establish a dynamic interhalogen coupling between iodine and bromine species, which enables a six-electron transfer pathway involving I<sup>−</sup>/I⁰/I⁺ and Br<sup>−</sup>/Br⁰. In situ characterizations and theoretical calculations show that Br<sup>−</sup> acts as a dynamic mediator, forming an [IBr<sub>2</sub>]<sup>−</sup> intermediate with iodine. This significantly lowers the energy barrier for oxidizing I⁰ to I⁺, thereby contributing additional capacity and accelerating kinetics. Simultaneously, Bmim⁺ provides dual interfacial functions: confining polyiodides at the cathode to suppress shuttling, and forming a protective layer on the zinc anode, which reduces interfacial water, inhibits dendrite growth and side reactions. Leveraging this synergistic design, the Zn-I<sub>2</sub> battery achieves a high specific capacity of 511 mAh g<sup>−1</sup> at 1 A g<sup>−1</sup> and retains 90.22% of its capacity after 30 000 cycles at 10 A g<sup>−1</sup>. The dynamic interhalogen coupling strategy offers a novel route to activate multielectron reactions and stabilize electrode interfaces in Zn-I<sub>2</sub> batteries.\",\"PeriodicalId\":112,\"journal\":{\"name\":\"Advanced Functional Materials\",\"volume\":\"73 1\",\"pages\":\"\"},\"PeriodicalIF\":19.0000,\"publicationDate\":\"2025-09-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Functional Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1002/adfm.202519437\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adfm.202519437","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
锌- i2水溶液电池具有良好的安全性、低成本和高能量密度等优点,是一种具有可持续能源存储前景的电池。然而,它们的实际应用受到双电子I - /I⁰氧化还原反应和多碘化物物种严重的穿梭效应的限制。本文引入了一种多功能离子液体,1-丁基-3-甲基咪唑溴(BmimBr),在碘和溴之间建立了动态卤素偶联,从而实现了一个涉及I - /I⁰/I⁺和Br - /Br⁰的六电子转移途径。原位表征和理论计算表明,Br−作为动态介质,与碘形成[IBr2]−中间体。这显著降低了I⁰氧化成I⁺的能垒,从而贡献了额外的容量和加速动力学。同时,Bmim⁺提供了双重界面功能:将多碘化物限制在阴极上抑制穿梭,在锌阳极上形成保护层,减少界面水分,抑制枝晶生长和副反应。利用这种协同设计,锌- i2电池在1ag - 1下实现了511 mAh g - 1的高比容量,并在10ag - 1下循环3万次后保持了90.22%的容量。动态卤素耦合策略为激活Zn-I2电池中的多电子反应和稳定电极界面提供了一条新的途径。
Dynamic Interhalogen Coupling Engineered by Multifunctional Ionic Liquid for High-Energy Aqueous Zn-I2 Batteries
Aqueous Zn-I2 batteries are promising for sustainable energy storage, exhibit excellent safety, low cost, and high energy density. However, their practical application is limited by the two-electron I−/I⁰ redox reaction and the severe shuttle effect of polyiodide species. Here, a multifunctional ionic liquid, 1-butyl-3-methylimidazolium bromide (BmimBr), is introduced to establish a dynamic interhalogen coupling between iodine and bromine species, which enables a six-electron transfer pathway involving I−/I⁰/I⁺ and Br−/Br⁰. In situ characterizations and theoretical calculations show that Br− acts as a dynamic mediator, forming an [IBr2]− intermediate with iodine. This significantly lowers the energy barrier for oxidizing I⁰ to I⁺, thereby contributing additional capacity and accelerating kinetics. Simultaneously, Bmim⁺ provides dual interfacial functions: confining polyiodides at the cathode to suppress shuttling, and forming a protective layer on the zinc anode, which reduces interfacial water, inhibits dendrite growth and side reactions. Leveraging this synergistic design, the Zn-I2 battery achieves a high specific capacity of 511 mAh g−1 at 1 A g−1 and retains 90.22% of its capacity after 30 000 cycles at 10 A g−1. The dynamic interhalogen coupling strategy offers a novel route to activate multielectron reactions and stabilize electrode interfaces in Zn-I2 batteries.
期刊介绍:
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