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负载于多层石墨烯上的单分散多金属氧酸盐簇作为高效锂硫电池的双功能电催化剂

Single-dispersed polyoxometalate clusters embedded on multilayer graphene as a bifunctional electrocatalyst for efficient Li-S batteries.

作者信息

Lei Jie, Fan Xiao-Xiang, Liu Ting, Xu Pan, Hou Qing, Li Ke, Yuan Ru-Ming, Zheng Ming-Sen, Dong Quan-Feng, Chen Jia-Jia

机构信息

State Key Laboratory for Physical Chemistry of Solid Surfaces, Department of Chemistry, College of Chemistry and Chemical Engineering, iChem (Collaborative Innovation Center of Chemistry for Energy Materials), Innovation Laboratory for Sciences and Technologies of Energy Materials of Fujian Province (IKKEM), Xiamen University, Xiamen, Fujian, 361005, China.

出版信息

Nat Commun. 2022 Jan 11;13(1):202. doi: 10.1038/s41467-021-27866-5.

DOI:10.1038/s41467-021-27866-5
PMID:35017484
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8752791/
Abstract

The redox reactions occurring in the Li-S battery positive electrode conceal various and critical electrocatalytic processes, which strongly influence the performances of this electrochemical energy storage system. Here, we report the development of a single-dispersed molecular cluster catalyst composite comprising of a polyoxometalate framework ([Co(PWO)]) and multilayer reduced graphene oxide. Due to the interfacial charge transfer and exposure of unsaturated cobalt sites, the composite demonstrates efficient polysulfides adsorption and reduced activation energy for polysulfides conversion, thus serving as a bifunctional electrocatalyst. When tested in full Li-S coin cell configuration, the composite allows for a long-term Li-S battery cycling with a capacity fading of 0.015% per cycle after 1000 cycles at 2 C (i.e., 3.36 A g). An areal capacity of 4.55 mAh cm is also achieved with a sulfur loading of 5.6 mg cm and E/S ratio of 4.5 μL mg. Moreover, Li-S single-electrode pouch cells tested with the bifunctional electrocatalyst demonstrate a specific capacity of about 800 mAh g at a sulfur loading of 3.6 mg cm for 100 cycles at 0.2 C (i.e., 336 mA g) with E/S ratio of 5 μL mg.

摘要

锂硫电池正极中发生的氧化还原反应隐藏着各种关键的电催化过程,这些过程强烈影响着这种电化学储能系统的性能。在此,我们报道了一种由多金属氧酸盐骨架([Co(PWO)])和多层还原氧化石墨烯组成的单分散分子簇催化剂复合材料的开发。由于界面电荷转移和不饱和钴位点的暴露,该复合材料表现出高效的多硫化物吸附和降低的多硫化物转化活化能,从而作为一种双功能电催化剂。在全锂硫硬币电池配置中进行测试时,该复合材料可实现长期的锂硫电池循环,在2C(即3.36A g)下1000次循环后,容量衰减为每循环0.015%。在硫负载量为5.6mg cm且E/S比为4.5μL mg的情况下,还实现了4.55mAh cm的面积容量。此外,用双功能电催化剂测试的锂硫单电极软包电池在硫负载量为3.6mg cm、E/S比为5μL mg、0.2C(即336mA g)下进行100次循环时,比容量约为800mAh g。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09e8/8752791/fd244d7048ee/41467_2021_27866_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09e8/8752791/9655c5831b16/41467_2021_27866_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09e8/8752791/880018113596/41467_2021_27866_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09e8/8752791/c0aa65fb9a68/41467_2021_27866_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09e8/8752791/68ce6687091b/41467_2021_27866_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09e8/8752791/fd244d7048ee/41467_2021_27866_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09e8/8752791/9655c5831b16/41467_2021_27866_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09e8/8752791/880018113596/41467_2021_27866_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09e8/8752791/c0aa65fb9a68/41467_2021_27866_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09e8/8752791/68ce6687091b/41467_2021_27866_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09e8/8752791/fd244d7048ee/41467_2021_27866_Fig5_HTML.jpg

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