High-efficiency metal selenide as an electrocatalyst in a separator for lithium–sulfur batteries†

IF 6.4 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Yujuan Hu, Bo Jin and Hui Liu
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Abstract

The construction of a modified separator with excellent catalytic ability and the ability to adsorb lithium polysulfides (LiPSs) is crucial for properly solving the challenges associated with lithium–sulfur batteries (LSBs). Herein, a metal–organic framework (MOF) substrate with a porous polyhedron structure is initially designed, then a mixture of ZIF-67 and melamine is carbonized into N-doped carbon (NC) covered with cobalt nanoparticles that are surrounded with carbon nanotubes to obtain Co/NCC. Finally, Co/NCC is selenized in situ to form CoSe/NCC which has good adsorption properties and accelerated polysulfide conversion ability. The CoSe/NCC material is coated onto a polypropylene (PP) separator (CoSe/NCC/PP) to inhibit LiPSs passing through the separator. Multi-walled carbon nanotubes (MWCNTs) are fused with sulfur to give MWCNTs/S which is used as the positive electrode. CoSe, derived from a MOF, has sulfurophilic properties and acts synergistically on the separator with the highly conductive NC and carbon nanotubes (CNTs) that originate from the melamine. CoSe/NCC possesses many active sites and uses Lewis acid–base interactions to anchor the LiPSs, thus promoting multi-stage redox reaction kinetics. Electrochemical tests show that the initial discharge capacity of a lithium–sulfur battery with a CoSe/NCC/PP separator and a MWCNTs/S cathode is 1270 mAh g−1 at 0.5 C, and the discharge capacity is still 932 mAh g−1 after 100 cycles, with a capacity retention rate of 73%. In addition, the battery also has good cycling performance under high current densities of 1 and 5 C. This work provides ideas and methods for the application of metal selenides as separator modification materials in LSBs and would be expected to be applied to other rechargeable batteries.

Abstract Image

高效金属硒化物作为锂硫电池分离器电催化剂
构建具有良好催化能力和吸附效果的多硫化锂(LiPSs)隔膜改性剂,是妥善解决锂硫电池(LSBs)难题的关键。本文首先设计了一种具有多孔多面体的金属有机框架(MOF)基底,然后将 ZIF-67 和三聚氰胺的混合物碳化成掺杂 N 的碳(NC),并在碳纳米管中包覆钴纳米颗粒,得到 Co/NCC,最后将其原位硒化,形成具有高吸附效果和加速多硫化物转化能力的 CoSe/NCC。CoSe/NCC 被涂覆在聚丙烯(PP)分离器(CoSe/NCC/PP)上,以抑制锂离子穿梭通过分离器。多壁碳纳米管(MWCNTs)习惯于熔硫作为正极(MWCNTs/S)。具有高导电性和亲硫性的 CoSe/NCC 拥有许多活性位点,可锚定锂离子电池,从而促进多级氧化还原反应动力学。电化学测试表明,采用 CoSe/NCC/PP 隔膜和 MWCNTs/S 正极的锂硫电池在 0.5 C 下的初始放电容量为 1270 mAh g-1,循环 100 次后放电容量保持在 932 mAh g-1,容量保持率为 73%。这项工作为金属硒化物作为隔膜改性材料在 LSB 中的应用提供了思路和方法,有望应用于其他充电电池。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Inorganic Chemistry Frontiers
Inorganic Chemistry Frontiers CHEMISTRY, INORGANIC & NUCLEAR-
CiteScore
10.40
自引率
7.10%
发文量
587
审稿时长
1.2 months
期刊介绍: The international, high quality journal for interdisciplinary research between inorganic chemistry and related subjects
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