通过硫阴极的催化伪 8 电子氧化还原反应补救锂硫电池中的穿梭效应

IF 4.7 3区 工程技术 Q2 ELECTROCHEMISTRY Electrochemistry Communications Pub Date : 2024-08-23 DOI:10.1016/j.elecom.2024.107797
Dantong Qiu, Huainan Qu, Dong Zheng, Xiaoxiao Zhang, Deyang Qu
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引用次数: 0

摘要

通过促进锂硫电池中高阶多硫离子的歧化,实现了硫的催化伪 8 电子氧化还原反应。电化学生成的多硫离子(Sx2-,其中 3 < x < 7)在双功能碳宿主/催化剂的催化下迅速歧化为元素硫(S8)和 Li2S2。硫阴极的整体催化氧化还原反应表现为 S8+8Li++8e⇌4Li2S2。与多硫离子的物理或化学封闭方法不同,这种方法通过将电解液中的可溶性多硫化物迅速转化为阴极基质中的元素硫和不溶性 Li2S2 来消除穿梭效应。因此,溶解的多硫化物与锂阳极之间的不利化学作用得到了缓解。
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Remediation of shuttle effect in a Li-sulfur battery via a catalytic pseudo-8-electron redox reaction at the sulfur cathode

A catalytic pseudo-8-electron redox reaction of sulfur is achieved by facilitating the disproportionation of high-order polysulfide ions in a Li-Sulfur battery. Electrochemically generated polysulfide ions (Sx2-, where 3 < x < 7) undergo rapid disproportionation into elemental sulfur (S8) and Li2S2, catalyzed by a bifunctional carbon host/catalyst. The overall catalytic redox reaction at the sulfur cathode is represented as S8+8Li++8e4Li2S2. In contrast to physical or chemical confinement methods for polysulfide ions, this approach remediates the shuttle effect by swiftly converting soluble polysulfides in the electrolyte to elemental sulfur and insoluble Li2S2 within the cathode matrix. As a result, the adverse chemical interaction between dissolved polysulfides and the Li anode is mitigated.

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来源期刊
Electrochemistry Communications
Electrochemistry Communications 工程技术-电化学
CiteScore
8.50
自引率
3.70%
发文量
160
审稿时长
1.2 months
期刊介绍: Electrochemistry Communications is an open access journal providing fast dissemination of short communications, full communications and mini reviews covering the whole field of electrochemistry which merit urgent publication. Short communications are limited to a maximum of 20,000 characters (including spaces) while full communications and mini reviews are limited to 25,000 characters (including spaces). Supplementary information is permitted for full communications and mini reviews but not for short communications. We aim to be the fastest journal in electrochemistry for these types of papers.
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