Additives Capable of Stably Supplying Anions/Cations for Homogeneous Lithium Deposition/Stripping

IF 16 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Shangshu Qian, Xiao Tan, Yutong Zhu, Yun Wang, Hao Chen, Mengting Zheng, Cheng Zhang*, Shanqing Zhang* and Jun Lu*, 
{"title":"Additives Capable of Stably Supplying Anions/Cations for Homogeneous Lithium Deposition/Stripping","authors":"Shangshu Qian,&nbsp;Xiao Tan,&nbsp;Yutong Zhu,&nbsp;Yun Wang,&nbsp;Hao Chen,&nbsp;Mengting Zheng,&nbsp;Cheng Zhang*,&nbsp;Shanqing Zhang* and Jun Lu*,&nbsp;","doi":"10.1021/acsnano.4c1322910.1021/acsnano.4c13229","DOIUrl":null,"url":null,"abstract":"<p >One of the important factors leading to lithium dendrites is a slow lithium-ion mass transport and imbalanced distribution of the Li<sup>+</sup> concentration and nuclei sites on the anode surface. To achieve uniform lithium deposition during the charge and discharge process, we introduce a homemade new copolymer (with the quaternary ammonium group N<sub>3</sub>R<sup>+</sup>I<sup>–</sup> on its side chain as the main functional group), named P35, as a functional electrolyte additive to regulate the lithium deposition. Theoretical calculations show that under the strong coordinating interaction between I<sup>–</sup> and N<sub>3</sub>R<sup>+</sup>, P35 preferentially adsorbs onto the lithium foil surface, effectively countering the adsorption of lithium salt anions such as PF<sub>6</sub><sup>–</sup>. Moreover, the positive charge carried by the quaternary ammonium salt group of P35 could interact with PF<sub>6</sub><sup>–</sup> to limit their mobility. Consequently, the dipole interaction on lithium ions is diminished, leading to an enhancement in the transport rate and a decrease in the concentration gradient of lithium ions. Furthermore, a more efficient SEI was formed due to the dual charges electrostatic shield formed by N<sub>3</sub>R<sup>+</sup>I<sup>–</sup>. Li–Li symmetric cells and Li–LiFePO<sub>4</sub> full cells assembled with electrolytes with P35 exhibit better rate performance, smaller polarization, and smoother deposition morphology in comparison to the cells without the P35 additive.</p>","PeriodicalId":21,"journal":{"name":"ACS Nano","volume":"18 50","pages":"34363–34374 34363–34374"},"PeriodicalIF":16.0000,"publicationDate":"2024-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Nano","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsnano.4c13229","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

One of the important factors leading to lithium dendrites is a slow lithium-ion mass transport and imbalanced distribution of the Li+ concentration and nuclei sites on the anode surface. To achieve uniform lithium deposition during the charge and discharge process, we introduce a homemade new copolymer (with the quaternary ammonium group N3R+I on its side chain as the main functional group), named P35, as a functional electrolyte additive to regulate the lithium deposition. Theoretical calculations show that under the strong coordinating interaction between I and N3R+, P35 preferentially adsorbs onto the lithium foil surface, effectively countering the adsorption of lithium salt anions such as PF6. Moreover, the positive charge carried by the quaternary ammonium salt group of P35 could interact with PF6 to limit their mobility. Consequently, the dipole interaction on lithium ions is diminished, leading to an enhancement in the transport rate and a decrease in the concentration gradient of lithium ions. Furthermore, a more efficient SEI was formed due to the dual charges electrostatic shield formed by N3R+I. Li–Li symmetric cells and Li–LiFePO4 full cells assembled with electrolytes with P35 exhibit better rate performance, smaller polarization, and smoother deposition morphology in comparison to the cells without the P35 additive.

Abstract Image

能为均匀锂沉积/剥离稳定提供阴/阳离子的添加剂
导致锂枝晶的重要因素之一是锂离子质量传输缓慢以及阳极表面的 Li+ 浓度和核位点分布不平衡。为了在充放电过程中实现均匀的锂沉积,我们引入了一种名为 P35 的自制新型共聚物(其侧链上的季铵基团 N3R+I- 为主要官能团),作为调节锂沉积的功能性电解质添加剂。理论计算表明,在 I- 和 N3R+ 的强配位作用下,P35 会优先吸附在锂箔表面,从而有效抵消 PF6- 等锂盐阴离子的吸附。此外,P35 的季铵盐基团所带的正电荷可与 PF6- 相互作用,限制其移动性。因此,锂离子上的偶极相互作用减弱,从而提高了锂离子的传输速率,降低了锂离子的浓度梯度。此外,由于 N3R+I- 形成的双电荷静电屏蔽,形成了更有效的 SEI。与未添加 P35 的电池相比,使用含 P35 的电解质组装的锂-锂对称电池和锂-锂铁PO4 全电池表现出更好的速率性能、更小的极化和更平滑的沉积形态。
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
ACS Nano
ACS Nano 工程技术-材料科学:综合
CiteScore
26.00
自引率
4.10%
发文量
1627
审稿时长
1.7 months
期刊介绍: ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.
×
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