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深入了解富含缺陷的硫化钒在调节锂硫电池中多硫化物吸附-催化转化行为方面的催化作用。

Insight into the Catalytic Role of Defect-Enriched Vanadium Sulfide for Regulating the Adsorption-Catalytic Conversion Behavior of Polysulfides in Li-S Batteries.

作者信息

Zeng Peng, Zhou Ziyi, Li Bin, Yu Hao, Zhou Xi, Chen Gairong, Chang Baobao, Chen Manfang, Shu Hongbo, Su Jincang, Wang Xianyou

机构信息

National Base for International Science and Technology Cooperation, National Local Joint Engineering Laboratory for Key Materials of New Energy Storage Battery, Hunan Province Key Laboratory of Electrochemical Energy Storage and Conversion, School of Chemistry, Xiangtan University, Xiangtan 411105, China.

School of Chemistry and Material Engineering, Xinxiang University, Henan 453003, China.

出版信息

ACS Appl Mater Interfaces. 2022 Aug 10;14(31):35833-35843. doi: 10.1021/acsami.2c09791. Epub 2022 Jul 28.

Abstract

The performance promotion of Li-S batteries relies primarily on inhibition of the shuttle effect and improvement of the catalytic-conversion reaction kinetics of polysulfides. Herein, we prepare defect-enriched VS nanosheets (VS) as catalysts for Li-S batteries and further study the catalytic mechanism of VS via ex situ X-ray diffraction and in situ UV-vis spectroscopy. A multifunctional S cathode was also obtained by assembling VS on a C cloth to achieve high S loading for Li-S batteries. It was found that VS catalysts undergo a lithiation process in the work voltage of Li-S batteries, and the triggered LiVS intermediates reciprocate VS with a high catalytic activity so as to enhance the performance of Li-S batteries by promoting the dissociation process of S to S. Consequently, Li-S batteries with a C/VS/S cathode deliver a high reversible capacity (1471 mAh g at 0.1 C) and good cycling performance (low fading rate of 0.064% per cycle after 400 cycles). Meanwhile, the CC@VS/S cathode with a high S areal loading of 5.6 mg cm can render a satisfactory areal capacity of 4.22 mAh cm at 0.2 C and a cycle stability of over 100 cycles. Therefore, the study on the catalysis of LiVS intermediates provides a scientific view for revealing the catalysis mechanism of a sulfide-based electrocatalyst and boosting the development of an electrocatalyst for Li-S batteries.

摘要

锂硫电池性能的提升主要依赖于抑制穿梭效应以及改善多硫化物的催化转化反应动力学。在此,我们制备了富含缺陷的硫化钒纳米片(VS)作为锂硫电池的催化剂,并通过非原位X射线衍射和原位紫外-可见光谱进一步研究了VS的催化机理。通过将VS组装在碳布上,还获得了一种多功能硫正极,以实现锂硫电池的高硫负载量。研究发现,VS催化剂在锂硫电池的工作电压下会经历一个锂化过程,所触发的LiVS中间体以高催化活性与VS相互作用,从而通过促进S到S的离解过程来提升锂硫电池的性能。因此,具有C/VS/S正极的锂硫电池具有高可逆容量(在0.1 C下为1471 mAh g)和良好的循环性能(400次循环后每循环的低衰减率为0.064%)。同时,具有5.6 mg cm高硫面负载量的CC@VS/S正极在0.2 C下可提供4.22 mAh cm的令人满意的面积容量和超过100次循环的循环稳定性。因此,对LiVS中间体催化作用的研究为揭示基于硫化物的电催化剂的催化机理以及推动锂硫电池电催化剂的发展提供了科学视角。

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