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负载于MXene上的钴纳米颗粒用于锂硫电池:锚定多硫化物并加速氧化还原反应

Cobalt Nanoparticles Loaded on MXene for Li-S Batteries: Anchoring Polysulfides and Accelerating Redox Reactions.

作者信息

Gu Qinhua, Qi Yujie, Chen Junnan, Lu Ming, Zhang Bingsen

机构信息

Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, Shenyang, 110016, China.

School of Materials Science and Engineering, University of Science and Technology of China, Shenyang, 110016, China.

出版信息

Small. 2022 Oct;18(41):e2204005. doi: 10.1002/smll.202204005. Epub 2022 Sep 12.

Abstract

Catalysis is regarded as an effective strategy to fundamentally increase sulfur utilization, accelerating the kinetics of the transformation between lithium polysulfides (LiPSs) and lithium sulfide (Li S) on a substrate. However, the intermodulation of catalysts and sulfur species is elusive, which is limited to the comprehensive analysis of electrochemical performance in the dynamic reaction process. Herein, cobalt nanoparticles loaded on MXene nanosheets (Co/Ti C) are selected as sulfur hosts and the representative catalyst. By combining ex situ electrochemical results and interfacial structural chemical monitoring, the catalysis process of Co/Ti C toward LiPSs conversion is revealed, and the outstanding performance originates from the optimization of chemical adsorption, catalytic activity, and lithium-ion transfer behaviors, which is based on electronic/ion modulation and sufficient interfaces among catalysts and electrolyte. This work can guide the construction of electronic modulation at triple-phase interface catalysis to overcome the shuttle effect and facilitate sulfur redox kinetics in Li-S batteries.

摘要

催化被视为从根本上提高硫利用率的有效策略,可加速多硫化锂(LiPSs)与硫化锂(Li₂S)在基底上转化的动力学。然而,催化剂与硫物种之间的相互调节难以捉摸,这仅限于对动态反应过程中电化学性能的综合分析。在此,负载在MXene纳米片上的钴纳米颗粒(Co/Ti₃C₂)被选为硫宿主和代表性催化剂。通过结合非原位电化学结果和界面结构化学监测,揭示了Co/Ti₃C₂对LiPSs转化的催化过程,其优异性能源于化学吸附、催化活性和锂离子转移行为的优化,这基于电子/离子调制以及催化剂与电解质之间充足的界面。这项工作可以指导三相界面催化中电子调制的构建,以克服穿梭效应并促进锂硫电池中的硫氧化还原动力学。

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