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自组装多金属氧酸盐纳米点作为锂硫电池中多硫化物/硫化物氧化还原转化的双向簇催化剂

Self-Assembled Polyoxometalate Nanodots as Bidirectional Cluster Catalysts for Polysulfide/Sulfide Redox Conversion in Lithium-Sulfur Batteries.

作者信息

Ni Lubin, Yang Guang, Liu Yi, Wu Zhen, Ma Zhiyuan, Shen Chao, Lv Zengxiang, Wang Qi, Gong Xiangxiang, Xie Ju, Diao Guowang, Wei Yongge

机构信息

School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou, 225002 Jiangsu, P. R. China.

Testing Center, Yangzhou University, Yangzhou, 225002 Jiangsu, P. R. China.

出版信息

ACS Nano. 2021 Jul 27;15(7):12222-12236. doi: 10.1021/acsnano.1c03852. Epub 2021 Jun 22.

Abstract

Polyoxometalates (POMs) are a class of discrete molecular inorganic metal-oxide clusters with reversible multielectron redox capability. Taking advantage of their redox properties, POMs are thus expected to be directly involved in the lithium-sulfur batteries (Li-S, LSBs) system as a bidirectional molecular catalyst. Herein, we design a three-dimensional porous structure of reduced graphene-carbon nanotube skeleton supported POM catalyst as a high-conductive and high-stability host material. Based on various spectroscopic techniques and electrochemical studies together with computational methods, the catalytic mechanism of POM clusters in Li-S battery was systematically clarified at the molecular level. The constructed POM-based sulfur cathode delivers a reversible capacity 1110 mAh g at 1.0 C and cycling stability up to 1000 cycles at 3.0 C. Furthermore, Li-S pouch/beaker batteries with a POM-based cathode were successfully demonstrated. This work provides essential inputs to promote molecular catalyst design and its application in LSBs.

摘要

多金属氧酸盐(POMs)是一类具有可逆多电子氧化还原能力的离散分子无机金属氧化物簇。利用其氧化还原特性,POMs有望作为双向分子催化剂直接参与锂硫电池(Li-S,LSBs)系统。在此,我们设计了一种由还原石墨烯-碳纳米管骨架负载的POM催化剂构成的三维多孔结构,作为高导电性和高稳定性的主体材料。基于各种光谱技术、电化学研究以及计算方法,在分子水平上系统地阐明了POM簇在锂硫电池中的催化机制。构建的基于POM的硫阴极在1.0 C时提供1110 mAh g的可逆容量,在3.0 C时循环稳定性高达1000次循环。此外,成功展示了具有基于POM阴极的锂硫软包/烧杯电池。这项工作为促进分子催化剂设计及其在锂硫电池中的应用提供了重要依据。

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