利用电子离域提高全固态薄膜电池异质结构阴极的容量和稳定性

IF 19 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Yongkun Yu, Sheng Cao, Chenxu Dong, Hanxiao Wang, Cheng Zhou, Zhiying Miao, Kaijian Yan, Minjian Gong, Liqiang Mai, Xu Xu
{"title":"利用电子离域提高全固态薄膜电池异质结构阴极的容量和稳定性","authors":"Yongkun Yu, Sheng Cao, Chenxu Dong, Hanxiao Wang, Cheng Zhou, Zhiying Miao, Kaijian Yan, Minjian Gong, Liqiang Mai, Xu Xu","doi":"10.1002/adfm.202423990","DOIUrl":null,"url":null,"abstract":"Due to the maturation of Internet of Things (IoT) technology, all-solid-state thin-film batteries (ATFBs) have become an optimal power source for microelectronic devices by virtue of their exceptional compatibility and ease of integration. Nevertheless, ATFBs face challenges related to the electron and ion transport properties of electrode materials, resulting in a limited specific capacity and comprehensive performance that often falls short of practical application requirements. Herein, a strategy of constructing V<sub>2</sub>O<sub>5</sub>-Cu<sub>2</sub>V<sub>2</sub>O<sub>7</sub> heterostructures is proposed with an electron delocalization interface via introducing copper heteroatom, which effectively improves the lithium storage capacity. Meanwhile, the construction of the built-in electric field and the electron delocalization effect enhance the electron and ion transport kinetics. Consequently, the initial discharge specific capacity of the heterostructured thin-film cathode is up to 76.4 µAh cm<sup>−2</sup> µm<sup>−1</sup> and exhibited ultra-high cycling stability over 4000 cycles in liquid half cells. Finally, benefiting from this high capacity and stable heterostructured cathode, a highly durable and flexible ATFB is further demonstrated. This work provides new ideas to further improve the energy density and cycling stability of thin-film cathodes and is expected to extend the potential applications in microelectronics.","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"208 1","pages":""},"PeriodicalIF":19.0000,"publicationDate":"2025-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Harnessing Electron Delocalization for Enhanced Capacity and Stability in Heterostructured Cathode for All-Solid-State Thin-Film Battery\",\"authors\":\"Yongkun Yu, Sheng Cao, Chenxu Dong, Hanxiao Wang, Cheng Zhou, Zhiying Miao, Kaijian Yan, Minjian Gong, Liqiang Mai, Xu Xu\",\"doi\":\"10.1002/adfm.202423990\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Due to the maturation of Internet of Things (IoT) technology, all-solid-state thin-film batteries (ATFBs) have become an optimal power source for microelectronic devices by virtue of their exceptional compatibility and ease of integration. Nevertheless, ATFBs face challenges related to the electron and ion transport properties of electrode materials, resulting in a limited specific capacity and comprehensive performance that often falls short of practical application requirements. Herein, a strategy of constructing V<sub>2</sub>O<sub>5</sub>-Cu<sub>2</sub>V<sub>2</sub>O<sub>7</sub> heterostructures is proposed with an electron delocalization interface via introducing copper heteroatom, which effectively improves the lithium storage capacity. Meanwhile, the construction of the built-in electric field and the electron delocalization effect enhance the electron and ion transport kinetics. Consequently, the initial discharge specific capacity of the heterostructured thin-film cathode is up to 76.4 µAh cm<sup>−2</sup> µm<sup>−1</sup> and exhibited ultra-high cycling stability over 4000 cycles in liquid half cells. Finally, benefiting from this high capacity and stable heterostructured cathode, a highly durable and flexible ATFB is further demonstrated. This work provides new ideas to further improve the energy density and cycling stability of thin-film cathodes and is expected to extend the potential applications in microelectronics.\",\"PeriodicalId\":112,\"journal\":{\"name\":\"Advanced Functional Materials\",\"volume\":\"208 1\",\"pages\":\"\"},\"PeriodicalIF\":19.0000,\"publicationDate\":\"2025-04-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Functional Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1002/adfm.202423990\",\"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}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adfm.202423990","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

摘要

随着物联网(IoT)技术的成熟,全固态薄膜电池(ATFB)凭借其卓越的兼容性和易于集成的特点,已成为微电子设备的最佳电源。然而,全固态薄膜电池面临着与电极材料的电子和离子传输特性有关的挑战,导致其特定容量和综合性能有限,往往无法满足实际应用要求。本文提出了一种构建 V2O5-Cu2V2O7 异质结构的策略,通过引入铜杂原子形成电子析出界面,有效提高了锂存储容量。同时,内置电场的构建和电子析出效应增强了电子和离子的传输动力学。因此,异质结构薄膜正极的初始放电比容量高达 76.4 µAh cm-2 µm-1,并在液态半电池中实现了 4000 次以上的超高循环稳定性。最后,得益于这种高容量和稳定的异质结构阴极,进一步展示了一种高度耐用和灵活的 ATFB。这项工作为进一步提高薄膜阴极的能量密度和循环稳定性提供了新思路,有望拓展其在微电子领域的潜在应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Harnessing Electron Delocalization for Enhanced Capacity and Stability in Heterostructured Cathode for All-Solid-State Thin-Film Battery

Harnessing Electron Delocalization for Enhanced Capacity and Stability in Heterostructured Cathode for All-Solid-State Thin-Film Battery
Due to the maturation of Internet of Things (IoT) technology, all-solid-state thin-film batteries (ATFBs) have become an optimal power source for microelectronic devices by virtue of their exceptional compatibility and ease of integration. Nevertheless, ATFBs face challenges related to the electron and ion transport properties of electrode materials, resulting in a limited specific capacity and comprehensive performance that often falls short of practical application requirements. Herein, a strategy of constructing V2O5-Cu2V2O7 heterostructures is proposed with an electron delocalization interface via introducing copper heteroatom, which effectively improves the lithium storage capacity. Meanwhile, the construction of the built-in electric field and the electron delocalization effect enhance the electron and ion transport kinetics. Consequently, the initial discharge specific capacity of the heterostructured thin-film cathode is up to 76.4 µAh cm−2 µm−1 and exhibited ultra-high cycling stability over 4000 cycles in liquid half cells. Finally, benefiting from this high capacity and stable heterostructured cathode, a highly durable and flexible ATFB is further demonstrated. This work provides new ideas to further improve the energy density and cycling stability of thin-film cathodes and is expected to extend the potential applications in microelectronics.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Advanced Functional Materials
Advanced Functional Materials 工程技术-材料科学:综合
CiteScore
29.50
自引率
4.20%
发文量
2086
审稿时长
2.1 months
期刊介绍: Firmly established as a top-tier materials science journal, Advanced Functional Materials reports breakthrough research in all aspects of materials science, including nanotechnology, chemistry, physics, and biology every week. Advanced Functional Materials is known for its rapid and fair peer review, quality content, and high impact, making it the first choice of the international materials science community.
×
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