Enhanced Adsorption-Catalytic Conversion of Iodine Species by Amorphous CoP@C Host Materials for Zinc Iodine Battery.

Chem & Bio Engineering Pub Date : 2025-03-13 eCollection Date: 2025-06-26 DOI:10.1021/cbe.4c00176
Yang Fu, Lingfeng Zhu, Xiaorui Zheng, Hua Fan, Shiwen Wang, Hui Li, Tianyi Ma
{"title":"Enhanced Adsorption-Catalytic Conversion of Iodine Species by Amorphous CoP@C Host Materials for Zinc Iodine Battery.","authors":"Yang Fu, Lingfeng Zhu, Xiaorui Zheng, Hua Fan, Shiwen Wang, Hui Li, Tianyi Ma","doi":"10.1021/cbe.4c00176","DOIUrl":null,"url":null,"abstract":"<p><p>Extensive applications of aqueous zinc iodine batteries (AZIBs) are hindered by the sluggish iodine redox reaction and shuttling effect of the polyiodides. In this study, amorphous cobalt phosphide grown on activated carbon (ACoP@C) was proposed as an iodine host material to address these issues. Specifically, the ACoP@C can offer numerous iodine anchoring sites and proposed electrocatalytic properties, which significantly reduce shuttling and enhance the conversion kinetics of iodine species. Additionally, the conductive carbon substrate with abundant porous channels facilitates rapid and continuous long-range electron and ion transport. As a result, the ACoP@C/I<sub>2</sub> cathode demonstrated high capacities of 173.7 mA h g<sup>-1</sup> at 0.1 A g<sup>-1</sup> and 99.0 mA h g<sup>-1</sup> at 5.0 A g<sup>-1</sup>, along with a stable long cycle capacity of 80.0 mA h g<sup>-1</sup> over 850 cycles at 1.0 A g<sup>-1</sup>. Moreover, UV spectroscopy and electrochemical measurements revealed enhanced redox mechanisms of the iodine species. This study provides valuable insights for the design and development of efficient amorphous catalyst materials for future AZIBs.</p>","PeriodicalId":100230,"journal":{"name":"Chem & Bio Engineering","volume":"2 6","pages":"341-349"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12207277/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chem & Bio Engineering","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1021/cbe.4c00176","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/26 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Extensive applications of aqueous zinc iodine batteries (AZIBs) are hindered by the sluggish iodine redox reaction and shuttling effect of the polyiodides. In this study, amorphous cobalt phosphide grown on activated carbon (ACoP@C) was proposed as an iodine host material to address these issues. Specifically, the ACoP@C can offer numerous iodine anchoring sites and proposed electrocatalytic properties, which significantly reduce shuttling and enhance the conversion kinetics of iodine species. Additionally, the conductive carbon substrate with abundant porous channels facilitates rapid and continuous long-range electron and ion transport. As a result, the ACoP@C/I2 cathode demonstrated high capacities of 173.7 mA h g-1 at 0.1 A g-1 and 99.0 mA h g-1 at 5.0 A g-1, along with a stable long cycle capacity of 80.0 mA h g-1 over 850 cycles at 1.0 A g-1. Moreover, UV spectroscopy and electrochemical measurements revealed enhanced redox mechanisms of the iodine species. This study provides valuable insights for the design and development of efficient amorphous catalyst materials for future AZIBs.

无定形CoP@C锌碘电池主体材料对碘的吸附催化转化。
水锌碘电池的广泛应用受到碘氧化还原反应迟缓和多碘离子穿梭效应的制约。本研究提出了在活性炭(ACoP@C)上生长的无定形磷化钴作为碘宿主材料来解决这些问题。具体来说,ACoP@C可以提供大量的碘锚定位点和提出的电催化特性,这大大减少了穿梭和提高了碘种的转化动力学。此外,具有丰富多孔通道的导电碳衬底有利于快速和连续的远程电子和离子传输。结果,ACoP@C/I2阴极在0.1 a g-1和5.0 a g-1下的高容量分别为173.7 mA h g-1和99.0 mA h g-1,以及在1.0 a g-1下850次循环的稳定长周期容量为80.0 mA h g-1。此外,紫外光谱和电化学测量揭示了碘的氧化还原机制。该研究为未来azib高效非晶催化剂材料的设计和开发提供了有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信