超过1 Wh的初级硬币电池由超厚无溶剂加工电极实现

IF 13.1 1区 化学 Q1 Energy
Yifan Li , Dengcheng Liu , Yanyan Lu , Nan Qin , Mingzhe Xue , Cunman Zhang , Zonghai Chen , Jim P. Zheng , Liming Jin
{"title":"超过1 Wh的初级硬币电池由超厚无溶剂加工电极实现","authors":"Yifan Li ,&nbsp;Dengcheng Liu ,&nbsp;Yanyan Lu ,&nbsp;Nan Qin ,&nbsp;Mingzhe Xue ,&nbsp;Cunman Zhang ,&nbsp;Zonghai Chen ,&nbsp;Jim P. Zheng ,&nbsp;Liming Jin","doi":"10.1016/j.jechem.2025.05.033","DOIUrl":null,"url":null,"abstract":"<div><div>The imperative pursuit of elevated energy density in lithium primary coin cells (LPCCs) necessitates strategic architectural optimization to align with evolving market demands. A predominant approach involves the systematic replacement of metallic structural support components (MSSCs) to minimize non-active constituent ratios, contingent upon maintaining robust interfacial contact integrity among electrodes, separators, and battery shells. Herein, we present a novel LPCC configuration employing solvent-free processed ultra-thick fluorinated carbon cathode (UCF<em><sub>x</sub></em>C) to achieve complete MSSCs elimination. The engineered UCF<em><sub>x</sub></em>C demonstrates exceptional areal capacity metrics (249.45 mg cm<sup>−2</sup>, 215.77 mAh cm<sup>−2</sup>), enabling a 27.8% mass reduction compared with conventional laboratory-assembled coin cell while achieving 941.5% energy density enhancement through optimized electrode conductivity. Notably, single-walled carbon nanotube (SWCNT)-modified UCF<em><sub>x</sub></em>C architectures exhibited superior performance with energy exceeding 1.0 Wh at 50 °C. This architectural paradigm provides valuable insights for developing next-generation high-energy-density LPCC systems, with practical implications for advancing miniaturized power source technologies.</div></div>","PeriodicalId":15728,"journal":{"name":"Journal of Energy Chemistry","volume":"109 ","pages":"Pages 138-145"},"PeriodicalIF":13.1000,"publicationDate":"2025-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Beyond 1 Wh primary coin cells enabled by ultrathick solvent-free processing electrodes\",\"authors\":\"Yifan Li ,&nbsp;Dengcheng Liu ,&nbsp;Yanyan Lu ,&nbsp;Nan Qin ,&nbsp;Mingzhe Xue ,&nbsp;Cunman Zhang ,&nbsp;Zonghai Chen ,&nbsp;Jim P. Zheng ,&nbsp;Liming Jin\",\"doi\":\"10.1016/j.jechem.2025.05.033\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The imperative pursuit of elevated energy density in lithium primary coin cells (LPCCs) necessitates strategic architectural optimization to align with evolving market demands. A predominant approach involves the systematic replacement of metallic structural support components (MSSCs) to minimize non-active constituent ratios, contingent upon maintaining robust interfacial contact integrity among electrodes, separators, and battery shells. Herein, we present a novel LPCC configuration employing solvent-free processed ultra-thick fluorinated carbon cathode (UCF<em><sub>x</sub></em>C) to achieve complete MSSCs elimination. The engineered UCF<em><sub>x</sub></em>C demonstrates exceptional areal capacity metrics (249.45 mg cm<sup>−2</sup>, 215.77 mAh cm<sup>−2</sup>), enabling a 27.8% mass reduction compared with conventional laboratory-assembled coin cell while achieving 941.5% energy density enhancement through optimized electrode conductivity. Notably, single-walled carbon nanotube (SWCNT)-modified UCF<em><sub>x</sub></em>C architectures exhibited superior performance with energy exceeding 1.0 Wh at 50 °C. This architectural paradigm provides valuable insights for developing next-generation high-energy-density LPCC systems, with practical implications for advancing miniaturized power source technologies.</div></div>\",\"PeriodicalId\":15728,\"journal\":{\"name\":\"Journal of Energy Chemistry\",\"volume\":\"109 \",\"pages\":\"Pages 138-145\"},\"PeriodicalIF\":13.1000,\"publicationDate\":\"2025-05-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Energy Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2095495625004267\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"Energy\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Energy Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2095495625004267","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Energy","Score":null,"Total":0}
引用次数: 0

摘要

为了提高初级硬币电池(lpcc)的能量密度,必须对战略架构进行优化,以适应不断变化的市场需求。一种主要的方法是系统地更换金属结构支撑部件(mscs),以最大限度地减少非活性成分的比例,这取决于保持电极、分离器和电池壳之间牢固的界面接触完整性。在这里,我们提出了一种新的LPCC结构,采用无溶剂加工的超厚氟化碳阴极(UCFxC)来实现完全消除mscs。设计的UCFxC具有出色的面容量指标(249.45 mg cm - 2, 215.77 mAh cm - 2),与传统实验室组装的硬币电池相比,质量降低了27.8%,同时通过优化电极电导率实现了941.5%的能量密度增强。值得注意的是,单壁碳纳米管(SWCNT)修饰的UCFxC结构在50°C时能量超过1.0 Wh,表现出优异的性能。这种架构范例为开发下一代高能量密度LPCC系统提供了有价值的见解,并对推进小型化电源技术具有实际意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Beyond 1 Wh primary coin cells enabled by ultrathick solvent-free processing electrodes
The imperative pursuit of elevated energy density in lithium primary coin cells (LPCCs) necessitates strategic architectural optimization to align with evolving market demands. A predominant approach involves the systematic replacement of metallic structural support components (MSSCs) to minimize non-active constituent ratios, contingent upon maintaining robust interfacial contact integrity among electrodes, separators, and battery shells. Herein, we present a novel LPCC configuration employing solvent-free processed ultra-thick fluorinated carbon cathode (UCFxC) to achieve complete MSSCs elimination. The engineered UCFxC demonstrates exceptional areal capacity metrics (249.45 mg cm−2, 215.77 mAh cm−2), enabling a 27.8% mass reduction compared with conventional laboratory-assembled coin cell while achieving 941.5% energy density enhancement through optimized electrode conductivity. Notably, single-walled carbon nanotube (SWCNT)-modified UCFxC architectures exhibited superior performance with energy exceeding 1.0 Wh at 50 °C. This architectural paradigm provides valuable insights for developing next-generation high-energy-density LPCC systems, with practical implications for advancing miniaturized power source technologies.
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
Journal of Energy Chemistry
Journal of Energy Chemistry CHEMISTRY, APPLIED-CHEMISTRY, PHYSICAL
CiteScore
19.10
自引率
8.40%
发文量
3631
审稿时长
15 days
期刊介绍: The Journal of Energy Chemistry, the official publication of Science Press and the Dalian Institute of Chemical Physics, Chinese Academy of Sciences, serves as a platform for reporting creative research and innovative applications in energy chemistry. It mainly reports on creative researches and innovative applications of chemical conversions of fossil energy, carbon dioxide, electrochemical energy and hydrogen energy, as well as the conversions of biomass and solar energy related with chemical issues to promote academic exchanges in the field of energy chemistry and to accelerate the exploration, research and development of energy science and technologies. This journal focuses on original research papers covering various topics within energy chemistry worldwide, including: Optimized utilization of fossil energy Hydrogen energy Conversion and storage of electrochemical energy Capture, storage, and chemical conversion of carbon dioxide Materials and nanotechnologies for energy conversion and storage Chemistry in biomass conversion Chemistry in the utilization of solar energy
×
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