High-entropy perovskite fluoride ultrasmall nanoparticles embedded in carbon nanofibers enable accelerated redox kinetic for K storage†

IF 32.4 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Jiaying Liao, Caoyang Shao, Jingchen Han, Zeyu Yuan, Qiao Hu, Yichen Du, Shaohua Guo, Xiaosi Zhou and Haoshen Zhou
{"title":"High-entropy perovskite fluoride ultrasmall nanoparticles embedded in carbon nanofibers enable accelerated redox kinetic for K storage†","authors":"Jiaying Liao, Caoyang Shao, Jingchen Han, Zeyu Yuan, Qiao Hu, Yichen Du, Shaohua Guo, Xiaosi Zhou and Haoshen Zhou","doi":"10.1039/D4EE02151G","DOIUrl":null,"url":null,"abstract":"<p >With the development of potassium-ion batteries, perovskite fluorides with three-dimensional framework structures and high theoretical capacities are attracting increasing attention. However, their intrinsically low electronic conductivities and high K<small><sup>+</sup></small> diffusion barriers hinder the release of their potential capabilities. Herein, the embedding of ultrasmall perovskite fluoride nanoparticles (∼10 nm) in carbon nanofibers, along with a high-entropy strategy, is pioneered to strengthen structural stability, enhance electronic conductivity, and lower the K<small><sup>+</sup></small> diffusion barrier. The high-entropy leads to a high reactivity and bonding effect between the fluoride surface and carbon nanofiber matrix that controls the growth of fluoride grains. The obtained high-entropy KMg<small><sub>0.2</sub></small>Mn<small><sub>0.2</sub></small>Fe<small><sub>0.2</sub></small>Co<small><sub>0.2</sub></small>Ni<small><sub>0.2</sub></small>F<small><sub>3</sub></small>-embedded carbon nanofiber cathode delivers a high reversible capacity of 122 mA h g<small><sup>−1</sup></small> at 20 mA g<small><sup>−1</sup></small> and an outstanding cycling life of over 5000 cycles at 500 mA g<small><sup>−1</sup></small>. More importantly, the robust high-entropy structure suppresses the fluoride conversion reaction and exhibits a low-strain intercalation reaction mechanism, which fully exerts the positive effect of high entropy during the entire cycle life.</p>","PeriodicalId":72,"journal":{"name":"Energy & Environmental Science","volume":" 19","pages":" 7362-7371"},"PeriodicalIF":32.4000,"publicationDate":"2024-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy & Environmental Science","FirstCategoryId":"88","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/ee/d4ee02151g","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: 0

Abstract

With the development of potassium-ion batteries, perovskite fluorides with three-dimensional framework structures and high theoretical capacities are attracting increasing attention. However, their intrinsically low electronic conductivities and high K+ diffusion barriers hinder the release of their potential capabilities. Herein, the embedding of ultrasmall perovskite fluoride nanoparticles (∼10 nm) in carbon nanofibers, along with a high-entropy strategy, is pioneered to strengthen structural stability, enhance electronic conductivity, and lower the K+ diffusion barrier. The high-entropy leads to a high reactivity and bonding effect between the fluoride surface and carbon nanofiber matrix that controls the growth of fluoride grains. The obtained high-entropy KMg0.2Mn0.2Fe0.2Co0.2Ni0.2F3-embedded carbon nanofiber cathode delivers a high reversible capacity of 122 mA h g−1 at 20 mA g−1 and an outstanding cycling life of over 5000 cycles at 500 mA g−1. More importantly, the robust high-entropy structure suppresses the fluoride conversion reaction and exhibits a low-strain intercalation reaction mechanism, which fully exerts the positive effect of high entropy during the entire cycle life.

Abstract Image

嵌入碳纳米纤维的高熵过氧化物氟化物超微纳米粒子可加速氧化还原动力学,实现 K 储存
随着钾离子电池的发展,具有三维框架结构和高理论容量的过氧化物氟化物越来越受到关注。然而,它们固有的低电子传导性和高 K+ 扩散阻力阻碍了其潜在能力的释放。在此,我们率先将超小型过晶石氟化物纳米颗粒(约 10 nm)嵌入碳纳米纤维,并采用高熵策略来加强结构稳定性、提高电子电导率并降低 K+ 扩散阻力。高熵导致了氟化物表面与碳纳米纤维基体之间的高反应性和键合效应,从而控制了氟化物晶粒的生长。所获得的高熵 KMg0.2Mn0.2Fe0.2Co0.2Ni0.2F3 嵌入式碳纳米纤维阴极在 20 mA g-1 电流条件下的可逆容量高达 122 mAh g-1,在 500 mA g-1 电流条件下的循环寿命超过 5000 次。更重要的是,坚固的高熵结构抑制了氟化物转化反应,并表现出低应变插层反应机制,在整个循环寿命期间充分发挥了高熵的积极作用。
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
Energy & Environmental Science
Energy & Environmental Science 化学-工程:化工
CiteScore
50.50
自引率
2.20%
发文量
349
审稿时长
2.2 months
期刊介绍: Energy & Environmental Science, a peer-reviewed scientific journal, publishes original research and review articles covering interdisciplinary topics in the (bio)chemical and (bio)physical sciences, as well as chemical engineering disciplines. Published monthly by the Royal Society of Chemistry (RSC), a not-for-profit publisher, Energy & Environmental Science is recognized as a leading journal. It boasts an impressive impact factor of 8.500 as of 2009, ranking 8th among 140 journals in the category "Chemistry, Multidisciplinary," second among 71 journals in "Energy & Fuels," second among 128 journals in "Engineering, Chemical," and first among 181 scientific journals in "Environmental Sciences." Energy & Environmental Science publishes various types of articles, including Research Papers (original scientific work), Review Articles, Perspectives, and Minireviews (feature review-type articles of broad interest), Communications (original scientific work of an urgent nature), Opinions (personal, often speculative viewpoints or hypotheses on current topics), and Analysis Articles (in-depth examination of energy-related issues).
×
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