中文版 | English
题名

Identification of polypyrrole-encapsulated BiSCl as a viable conversion/alloying anode material for high-performance lithium storage

作者
通讯作者Feng,Jun
发表日期
2024-08-01
DOI
发表期刊
EISSN
2468-6069
卷号44
摘要
Anode materials combining conversion and alloying mechanisms are increasingly valued in advanced rechargeable batteries for their exceptional theoretical capacities and advantageous working voltages. This study showcases BiSCl as a promising conversion/alloying anode material, demonstrating a high specific capacity and enhanced durability through polypyrrole encapsulation. Employing in situ X-ray diffraction, X-ray photoelectron spectroscopy, ex situ transmission electron microscopy, and field emission scanning electron microscopy, we offer a detailed analysis of the lithiation mechanism in BiSCl. The anode exhibits a low average working potential of approximately 0.6 V, supporting a theoretical specific capacity of 784 mAh/g and a volumetric capacity of 4664 mAh/cm. The innovative BiSCl-PPy core-shell composite effectively addresses the challenges of volumetric expansion and polysulfide dissolution. This composite delivers a remarkable reversible capacity of 753 mAh/g at a current rate of 100 mA/g, maintaining 96% of its specific capacity over 400 cycles, and sustains 419 mAh/g at 500 mA/g after 800 cycles, demonstrating more superior performance than that of BiSCl. These findings establish BiSCl as a highly promising conversion/alloying anode material for lithium storage, significantly enhanced in durability by the BiSCl-PPy core-shell composite.
关键词
相关链接[Scopus记录]
收录类别
SCI ; EI
语种
英语
学校署名
第一 ; 通讯
EI入藏号
20242416254862
EI主题词
Chlorine compounds ; Durability ; Field emission microscopes ; High resolution transmission electron microscopy ; Lithium ; Polypyrroles ; Scanning electron microscopy ; Shells (structures) ; Storage (materials) ; X ray photoelectron spectroscopy
EI分类号
Structural Members and Shapes:408.2 ; Lithium and Alloys:542.4 ; Alkali Metals:549.1 ; Storage:694.4 ; Electron Tubes:714.1 ; Optical Devices and Systems:741.3 ; Organic Polymers:815.1.1
Scopus记录号
2-s2.0-85195676887
来源库
Scopus
引用统计
被引频次[WOS]:1
成果类型期刊论文
条目标识符http://sustech.caswiz.com/handle/2SGJ60CL/778626
专题工学院_材料科学与工程系
南方科技大学
量子科学与工程研究院
作者单位
1.Department of Materials Science and Engineering,Southern University of Science and Technology,Shenzhen,Guangdong,518055,China
2.Department of Industrial Systems Engineering,The Hong Kong Polytechnic University,Hong Kong SAR,100872,China
3.Department of Pharmacology,Graduate School of Medicine,Kagawa University,Takamatsu,1750-1,761-0793,Japan
4.Department of Advanced Materials Science,Faculty of Engineering and Design,Kagawa University,Takamatsu,2217-20,761-0396,Japan
5.Guangdong Provincial Key Laboratory of Functional Oxide Materials and Devices,Southern University of Science and Technology,Shenzhen,Guangdong,518055,China
6.Institute for Quantum Science and Engineering,Southern University of Science and Technology,Shenzhen,Guangdong,518055,China
第一作者单位材料科学与工程系
通讯作者单位材料科学与工程系;  南方科技大学;  量子科学与工程研究院
第一作者的第一单位材料科学与工程系
推荐引用方式
GB/T 7714
Li,Sen,Huang,Zhiyuan,Hua,Yingkai,et al. Identification of polypyrrole-encapsulated BiSCl as a viable conversion/alloying anode material for high-performance lithium storage[J]. Materials Today Energy,2024,44.
APA
Li,Sen.,Huang,Zhiyuan.,Hua,Yingkai.,Liu,Xingchen.,Chen,Xi.,...&Feng,Jun.(2024).Identification of polypyrrole-encapsulated BiSCl as a viable conversion/alloying anode material for high-performance lithium storage.Materials Today Energy,44.
MLA
Li,Sen,et al."Identification of polypyrrole-encapsulated BiSCl as a viable conversion/alloying anode material for high-performance lithium storage".Materials Today Energy 44(2024).
条目包含的文件
条目无相关文件。
个性服务
原文链接
推荐该条目
保存到收藏夹
查看访问统计
导出为Endnote文件
导出为Excel格式
导出为Csv格式
Altmetrics Score
谷歌学术
谷歌学术中相似的文章
[Li,Sen]的文章
[Huang,Zhiyuan]的文章
[Hua,Yingkai]的文章
百度学术
百度学术中相似的文章
[Li,Sen]的文章
[Huang,Zhiyuan]的文章
[Hua,Yingkai]的文章
必应学术
必应学术中相似的文章
[Li,Sen]的文章
[Huang,Zhiyuan]的文章
[Hua,Yingkai]的文章
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
[发表评论/异议/意见]
暂无评论

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。