{"title":"In Batteria Electrochemical Polymerization to Form a Protective Conducting Layer on Se/C Cathodes for High-Performance Li–Se Batteries","authors":"Seungmin Lee, Haeun Lee, Naram Ha, Jung Tae Lee, Jaehan Jung, KwangSup Eom","doi":"10.1002/adfm.202000028","DOIUrl":null,"url":null,"abstract":"<p>The lithium–selenium (Li–Se) battery is a promising energy storage system for portable devices owing to its high energy density (2528 Wh L<sup>−1</sup>) and electrical conductivity (10<sup>−3</sup> S m<sup>−1</sup>). The main issue with Li–Se batteries is their poor stability originating from the dissolution of Se-containing compounds. Hence, many studies have focused on the immobilization of Se using protective layers prepared via ex situ or in situ approaches. However, these strategies are too complicated and costly for practical use. Herein, a facile in batteria electrochemical treatment to form a protective conductive layer on a Se-based cathode is introduced. Specifically, aniline monomers added to an assembled Li–Se cell are polymerized into electrically conductive polyaniline. The treated Li–Se cell exhibits 40% higher capacity retention compared to untreated one. Moreover, at a high rate (4 C), the treated cell maintains a capacity of 1538 mAh cm<sup>−3</sup>, whereas the untreated cell exhibits no capacity. The enhanced cyclic stability and rate capability are attributed to the electrochemical formation of a uniform, ultrathin (≤10 nm) polyaniline layer, to confine lithium polyselenides with its C−N bonds, and improve ionic conductivity by self-doping with lithium salts to form delocalized polaron lattice in the polyaniline.</p>","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"30 19","pages":""},"PeriodicalIF":19.9000,"publicationDate":"2020-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/adfm.202000028","citationCount":"22","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/adfm.202000028","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: 22
Abstract
The lithium–selenium (Li–Se) battery is a promising energy storage system for portable devices owing to its high energy density (2528 Wh L−1) and electrical conductivity (10−3 S m−1). The main issue with Li–Se batteries is their poor stability originating from the dissolution of Se-containing compounds. Hence, many studies have focused on the immobilization of Se using protective layers prepared via ex situ or in situ approaches. However, these strategies are too complicated and costly for practical use. Herein, a facile in batteria electrochemical treatment to form a protective conductive layer on a Se-based cathode is introduced. Specifically, aniline monomers added to an assembled Li–Se cell are polymerized into electrically conductive polyaniline. The treated Li–Se cell exhibits 40% higher capacity retention compared to untreated one. Moreover, at a high rate (4 C), the treated cell maintains a capacity of 1538 mAh cm−3, whereas the untreated cell exhibits no capacity. The enhanced cyclic stability and rate capability are attributed to the electrochemical formation of a uniform, ultrathin (≤10 nm) polyaniline layer, to confine lithium polyselenides with its C−N bonds, and improve ionic conductivity by self-doping with lithium salts to form delocalized polaron lattice in the polyaniline.
锂硒(Li-Se)电池具有高能量密度(2528 Wh L−1)和电导率(10−3 S m−1)的优点,是一种很有前途的便携式设备储能系统。锂硒电池的主要问题是其稳定性差,这是由于含硒化合物的溶解造成的。因此,许多研究都集中在利用非原位或原位方法制备的保护层来固定硒。然而,这些策略对于实际应用来说过于复杂和昂贵。本文介绍了一种在电池电化学处理中易于在硒基阴极上形成保护性导电层的方法。具体地说,苯胺单体添加到组装好的锂硒电池中聚合成导电聚苯胺。处理后的锂硒电池的容量保持率比未处理的高40%。此外,在高倍率(4℃)下,处理过的电池保持1538 mAh cm−3的容量,而未经处理的电池则没有容量。循环稳定性和速率能力的增强主要归功于电化学形成了均匀的超薄(≤10 nm)聚苯胺层,用其C−N键限制了聚硒化锂,并通过在聚苯胺中自掺杂锂盐形成离域极化子晶格提高了离子电导率。
期刊介绍:
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