{"title":"同时捕获Zn2+的多齿状有机添加剂和稳定锌金属水电池的界面工程","authors":"Honglan Huang, Ying Zhao, Zixiong Zhen, Zhihang Liu, Xing Peng, Yifan Liu, Jinbo Fan, Xuebo Chen, long chen, Pan Xiong, Junwu Zhu","doi":"10.1039/d5ta04634c","DOIUrl":null,"url":null,"abstract":"Aqueous zinc-ion batteries (AZIBs) have recently attracted widespread interest due to their intrinsically high specific capacity and inherent safety. Nevertheless, the application of aqueous electrolytes introduces significant challenges, including zinc dendrite growth, side reactions, and fragile solid electrolyte interphase (SEI) layers. To overcome these challenges, this study proposes a novel multi-dentate electrolyte additive, 2,2'-bipyridine-6,6'-dicarboxylic acid, which features multiple coordination sites, including two carboxyl groups and two pyridinic nitrogen atoms. The multifunctional sites can significantly enhance the coordination effects with Zn2+ ions, while carboxyl ends can robustly anchor onto the zinc anode surface, and effectively stabilizing the SEI layer during the electrochemical process. The electrochemical results indicate that symmetric cells incorporating this additive exhibit remarkably stable overpotentials during cycling and maintain stable galvanostatic plating/stripping performance for over 550 h at a high areal capacity of 5 mAh cm−2 and a current density of 5 mA cm−2. Furthermore, full cells employing the additive demonstrate stable cycling performance for over 1000 cycles with an outstanding Coulombic efficiency of 99.89%. Accordingly, the incorporation of this electrolyte additive is expected to enable the advancement of AZIBs with enhanced stability and electrochemical performance.","PeriodicalId":82,"journal":{"name":"Journal of Materials Chemistry A","volume":"74 1","pages":""},"PeriodicalIF":9.5000,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Multi-dentate organic additives for simultaneous Zn2+ capturing and interfacial engineering toward stable aqueous zinc metal batteries\",\"authors\":\"Honglan Huang, Ying Zhao, Zixiong Zhen, Zhihang Liu, Xing Peng, Yifan Liu, Jinbo Fan, Xuebo Chen, long chen, Pan Xiong, Junwu Zhu\",\"doi\":\"10.1039/d5ta04634c\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Aqueous zinc-ion batteries (AZIBs) have recently attracted widespread interest due to their intrinsically high specific capacity and inherent safety. Nevertheless, the application of aqueous electrolytes introduces significant challenges, including zinc dendrite growth, side reactions, and fragile solid electrolyte interphase (SEI) layers. To overcome these challenges, this study proposes a novel multi-dentate electrolyte additive, 2,2'-bipyridine-6,6'-dicarboxylic acid, which features multiple coordination sites, including two carboxyl groups and two pyridinic nitrogen atoms. The multifunctional sites can significantly enhance the coordination effects with Zn2+ ions, while carboxyl ends can robustly anchor onto the zinc anode surface, and effectively stabilizing the SEI layer during the electrochemical process. The electrochemical results indicate that symmetric cells incorporating this additive exhibit remarkably stable overpotentials during cycling and maintain stable galvanostatic plating/stripping performance for over 550 h at a high areal capacity of 5 mAh cm−2 and a current density of 5 mA cm−2. Furthermore, full cells employing the additive demonstrate stable cycling performance for over 1000 cycles with an outstanding Coulombic efficiency of 99.89%. Accordingly, the incorporation of this electrolyte additive is expected to enable the advancement of AZIBs with enhanced stability and electrochemical performance.\",\"PeriodicalId\":82,\"journal\":{\"name\":\"Journal of Materials Chemistry A\",\"volume\":\"74 1\",\"pages\":\"\"},\"PeriodicalIF\":9.5000,\"publicationDate\":\"2025-09-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Materials Chemistry A\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1039/d5ta04634c\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Chemistry A","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1039/d5ta04634c","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
水锌离子电池(azib)由于其固有的高比容量和固有的安全性,近年来引起了广泛的关注。然而,水电解质的应用带来了重大挑战,包括锌枝晶生长、副反应和脆弱的固体电解质间相(SEI)层。为了克服这些挑战,本研究提出了一种新的多齿电解质添加剂,2,2'-联吡啶-6,6'-二羧酸,它具有多个配位位点,包括两个羧基和两个吡啶氮原子。多功能位点能显著增强与Zn2+离子的配位效应,羧基端能牢固锚定在锌阳极表面,在电化学过程中有效稳定SEI层。电化学结果表明,含有该添加剂的对称电池在循环过程中表现出非常稳定的过电位,并在5mah cm - 2的高面容量和5ma cm - 2的电流密度下保持稳定的恒流镀/剥离性能超过550小时。此外,使用添加剂的全电池具有稳定的循环性能,循环次数超过1000次,库仑效率达到99.89%。因此,该电解质添加剂的加入有望提高azib的稳定性和电化学性能。
Multi-dentate organic additives for simultaneous Zn2+ capturing and interfacial engineering toward stable aqueous zinc metal batteries
Aqueous zinc-ion batteries (AZIBs) have recently attracted widespread interest due to their intrinsically high specific capacity and inherent safety. Nevertheless, the application of aqueous electrolytes introduces significant challenges, including zinc dendrite growth, side reactions, and fragile solid electrolyte interphase (SEI) layers. To overcome these challenges, this study proposes a novel multi-dentate electrolyte additive, 2,2'-bipyridine-6,6'-dicarboxylic acid, which features multiple coordination sites, including two carboxyl groups and two pyridinic nitrogen atoms. The multifunctional sites can significantly enhance the coordination effects with Zn2+ ions, while carboxyl ends can robustly anchor onto the zinc anode surface, and effectively stabilizing the SEI layer during the electrochemical process. The electrochemical results indicate that symmetric cells incorporating this additive exhibit remarkably stable overpotentials during cycling and maintain stable galvanostatic plating/stripping performance for over 550 h at a high areal capacity of 5 mAh cm−2 and a current density of 5 mA cm−2. Furthermore, full cells employing the additive demonstrate stable cycling performance for over 1000 cycles with an outstanding Coulombic efficiency of 99.89%. Accordingly, the incorporation of this electrolyte additive is expected to enable the advancement of AZIBs with enhanced stability and electrochemical performance.
期刊介绍:
The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.