Progresses and Prospects of Asymmetrically Coordinated Single Atom Catalysts for Lithium−Sulfur Batteries

IF 13 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Energy & Environmental Materials Pub Date : 2024-02-11 DOI:10.1002/eem2.12703
Rong Zhou, Shaonan Gu, Meng Guo, Shuzheng Xu, Guowei Zhou
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Abstract

Lithium–sulfur batteries (LSBs) are widely regarded as promising next-generation batteries due to their high theoretical specific capacity and low material cost. However, the practical applications of LSBs are limited by the shuttle effect of lithium polysulfides (LiPSs), electronic insulation of charge and discharge products, and slow LiPSs conversion reaction kinetics. Accordingly, the introduction of catalysts into LSBs is one of the effective strategy to solve the issues of the sluggished LiPS conversion. Because of their nearly 100% atom utilization and high electrocatalytic activity, single-atom catalysts (SACs) have been widely used as reaction mediators for LSBs' reactions. Excitingly, the SACs with asymmetric coordination structures have exhibited intriguing electronic structures and superior catalytic activities when compared to the traditional M–N4 active sites. In this review, we systematically describe the recent advancements in the installation of asymmetrically coordinated single-atom structure as reactions catalysts in LSBs, including asymmetrically nitrogen coordinated SACs, heteroatom coordinated SACs, support effective asymmetrically coordinated SACs, and bimetallic coordinated SACs. Particularly noteworthy is the discussion of the catalytic conversion mechanism of LiPSs spanning asymmetrically coordinated SACs. Finally, a perspective on the future developments of asymmetrically coordinated SACs in LSB applications is provided.

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用于锂硫电池的不对称配位单原子催化剂的研究进展与前景
锂硫电池(LSB)因其理论比容量高、材料成本低而被广泛认为是有前途的下一代电池。然而,由于多硫化锂(LiPSs)的穿梭效应、充放电产物的电子绝缘以及缓慢的多硫化锂转化反应动力学,LSBs 的实际应用受到了限制。因此,在 LSB 中引入催化剂是解决锂多硫化物转化缓慢问题的有效策略之一。单原子催化剂(SAC)具有近乎 100% 的原子利用率和高电催化活性,因此被广泛用作 LSB 反应的反应介质。令人兴奋的是,与传统的 M-N4 活性位点相比,具有不对称配位结构的 SAC 表现出了奇妙的电子结构和卓越的催化活性。在这篇综述中,我们系统地介绍了将不对称配位单原子结构作为 LSB 反应催化剂的最新进展,包括不对称氮配位 SAC、杂原子配位 SAC、支持有效的不对称配位 SAC 和双金属配位 SAC。尤其值得注意的是对跨越不对称配位 SAC 的 LiPS 催化转换机制的讨论。最后,还展望了不对称配位 SAC 在 LSB 应用中的未来发展。
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来源期刊
Energy & Environmental Materials
Energy & Environmental Materials MATERIALS SCIENCE, MULTIDISCIPLINARY-
CiteScore
17.60
自引率
6.00%
发文量
66
期刊介绍: Energy & Environmental Materials (EEM) is an international journal published by Zhengzhou University in collaboration with John Wiley & Sons, Inc. The journal aims to publish high quality research related to materials for energy harvesting, conversion, storage, and transport, as well as for creating a cleaner environment. EEM welcomes research work of significant general interest that has a high impact on society-relevant technological advances. The scope of the journal is intentionally broad, recognizing the complexity of issues and challenges related to energy and environmental materials. Therefore, interdisciplinary work across basic science and engineering disciplines is particularly encouraged. The areas covered by the journal include, but are not limited to, materials and composites for photovoltaics and photoelectrochemistry, bioprocessing, batteries, fuel cells, supercapacitors, clean air, and devices with multifunctionality. The readership of the journal includes chemical, physical, biological, materials, and environmental scientists and engineers from academia, industry, and policy-making.
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