Multifunctional cu-Cu3P heterojunction embedded in hierarchically porous carbon nanofibers to strengthen adsorption and catalytic effects based on built-in electric field for liS cell

IF 8.9 2区 工程技术 Q1 ENERGY & FUELS
Chunhua Zhu, Yayi Lu, Yanan Li, Hao Wang, Fan Zhang, Yongbing Jin, Bowen Cheng, Nanping Deng, Weimin Kang
{"title":"Multifunctional cu-Cu3P heterojunction embedded in hierarchically porous carbon nanofibers to strengthen adsorption and catalytic effects based on built-in electric field for liS cell","authors":"Chunhua Zhu,&nbsp;Yayi Lu,&nbsp;Yanan Li,&nbsp;Hao Wang,&nbsp;Fan Zhang,&nbsp;Yongbing Jin,&nbsp;Bowen Cheng,&nbsp;Nanping Deng,&nbsp;Weimin Kang","doi":"10.1016/j.est.2024.114638","DOIUrl":null,"url":null,"abstract":"<div><div>Lithium sulfur batteries (LSBs) are considered a highly promising next-generation battery system. However, severe shuttle effect and slow redox kinetics of lithium polysulfides (LiPSs) in LSBs are still the main obstacles hindering their rapid developments. In this study, the multifunctional Cu-Cu<sub>3</sub>P heterojunction nanoparticles embedded in hierarchically porous carbon nanofibers (PCNFs) are designed and prepared for modifying separator of LSBs. The highly conductive metal Cu and PCNFs can synergistically enhance the conductivity of electrons and ions, and physically suppress “shuttle effect” of lithium LiPSs. Meanwhile, based on the spontaneous built-in electric field at the formed heterogeneous interfaces of Cu-Cu<sub>3</sub>P, the heterojunction also can chemically adsorb LiPSs and greatly catalyze conversion of LiPSs, thus further suppressing the “shuttle effect” and excellent reaction kinetics of LiPSs. Based on these merits, the assembled LSBs using the heterojunction Cu-Cu<sub>3</sub>P@PCNFs modified separator show outstanding initial specific discharge capacities up to 1009.2 mAh g<sup>−1</sup> at 1C and 998.5 mAh g<sup>−1</sup> at 2C, and stable cycling with an average capacity decay rate of 0.067 % and 0.084 % at 1C during 800 cycles and at 2C during 580 cycles, respectively. Even at a high sulfur loading of 2.5 mg cm<sup>−2</sup>, an excellent specific discharge capacity of 784.6 mAh g<sup>−1</sup> after 180 cycles 0.5C still can be realized. The work provides a novel perspective on understanding adsorption and catalytic design in energy storage equipment based on heterojunction engineering and built-in electric field.</div></div>","PeriodicalId":15942,"journal":{"name":"Journal of energy storage","volume":"104 ","pages":"Article 114638"},"PeriodicalIF":8.9000,"publicationDate":"2024-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of energy storage","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2352152X24042245","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
引用次数: 0

Abstract

Lithium sulfur batteries (LSBs) are considered a highly promising next-generation battery system. However, severe shuttle effect and slow redox kinetics of lithium polysulfides (LiPSs) in LSBs are still the main obstacles hindering their rapid developments. In this study, the multifunctional Cu-Cu3P heterojunction nanoparticles embedded in hierarchically porous carbon nanofibers (PCNFs) are designed and prepared for modifying separator of LSBs. The highly conductive metal Cu and PCNFs can synergistically enhance the conductivity of electrons and ions, and physically suppress “shuttle effect” of lithium LiPSs. Meanwhile, based on the spontaneous built-in electric field at the formed heterogeneous interfaces of Cu-Cu3P, the heterojunction also can chemically adsorb LiPSs and greatly catalyze conversion of LiPSs, thus further suppressing the “shuttle effect” and excellent reaction kinetics of LiPSs. Based on these merits, the assembled LSBs using the heterojunction Cu-Cu3P@PCNFs modified separator show outstanding initial specific discharge capacities up to 1009.2 mAh g−1 at 1C and 998.5 mAh g−1 at 2C, and stable cycling with an average capacity decay rate of 0.067 % and 0.084 % at 1C during 800 cycles and at 2C during 580 cycles, respectively. Even at a high sulfur loading of 2.5 mg cm−2, an excellent specific discharge capacity of 784.6 mAh g−1 after 180 cycles 0.5C still can be realized. The work provides a novel perspective on understanding adsorption and catalytic design in energy storage equipment based on heterojunction engineering and built-in electric field.
嵌入分层多孔碳纳米纤维的多功能铜铟镓硒异质结,基于内置电场增强 liS 电池的吸附和催化效应
锂硫电池(LSB)被认为是一种极具潜力的下一代电池系统。然而,多硫化锂(LiPSs)在 LSBs 中严重的穿梭效应和缓慢的氧化还原动力学仍然是阻碍其快速发展的主要障碍。本研究设计并制备了嵌入分层多孔碳纳米纤维(PCNFs)的多功能 Cu-Cu3P 异质结纳米粒子,用于改性 LSBs 的隔膜。高导电性金属铜和 PCNFs 能协同增强电子和离子的导电性,从物理上抑制锂离子电池的 "穿梭效应"。同时,基于 Cu-Cu3P 异质界面的自发内置电场,异质结还能化学吸附锂离子,极大地催化锂离子的转化,从而进一步抑制锂离子的 "穿梭效应",并获得优异的反应动力学性能。基于这些优点,使用异质结 Cu-Cu3P@PCNFs 改性隔膜组装的 LSB 在 1C 和 2C 条件下分别表现出了高达 1009.2 mAh g-1 和 998.5 mAh g-1 的初始比放电容量,并且循环稳定,在 1C 条件下 800 次循环的平均容量衰减率为 0.067 %,在 2C 条件下 580 次循环的平均容量衰减率为 0.084 %。即使硫含量高达 2.5 mg cm-2,在 0.5C 循环 180 次后仍能实现 784.6 mAh g-1 的出色比放电容量。这项研究为理解基于异质结工程和内置电场的储能设备中的吸附和催化设计提供了一个新的视角。
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
Journal of energy storage
Journal of energy storage Energy-Renewable Energy, Sustainability and the Environment
CiteScore
11.80
自引率
24.50%
发文量
2262
审稿时长
69 days
期刊介绍: Journal of energy storage focusses on all aspects of energy storage, in particular systems integration, electric grid integration, modelling and analysis, novel energy storage technologies, sizing and management strategies, business models for operation of storage systems and energy storage developments worldwide.
×
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:481959085
Book学术官方微信