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A review of size engineering-enabled electrocatalysts for Li–S chemistry

Li–S batteries (LSBs) have received extensive attention owing to their remarkable theoretical capacity (1672 mA h g(−1)) and high energy density (2600 W h kg(−1)), which are far beyond those of the state-of-the-art Li-ion batteries (LIBs). However, the retarded sulfur reaction kinetics and fatal shu...

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Detalles Bibliográficos
Autores principales: Zhang, Xi, Zhang, Yaping, Wei, Xijun, Wei, Chaohui, Song, Yingze
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9418464/
https://www.ncbi.nlm.nih.gov/pubmed/36132671
http://dx.doi.org/10.1039/d1na00522g
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author Zhang, Xi
Zhang, Yaping
Wei, Xijun
Wei, Chaohui
Song, Yingze
author_facet Zhang, Xi
Zhang, Yaping
Wei, Xijun
Wei, Chaohui
Song, Yingze
author_sort Zhang, Xi
collection PubMed
description Li–S batteries (LSBs) have received extensive attention owing to their remarkable theoretical capacity (1672 mA h g(−1)) and high energy density (2600 W h kg(−1)), which are far beyond those of the state-of-the-art Li-ion batteries (LIBs). However, the retarded sulfur reaction kinetics and fatal shuttle effect have hindered the practical implementations of LSBs. In response, constructing electrocatalysts for Li–S systems has been considered an effective strategy to date. Particularly, size engineering-enabled electrocatalysts show high activity in the sulfur redox reaction, considerably contributing to the latest advances in Li–S system research. In this tutorial review, we provide a systematic summary of nano- to atomic-scale electrocatalysts employed in Li–S chemistry, aiming at figuring out the working mechanism of size engineering-enabled electrocatalysts in the sulfur redox reaction and guiding the rational construction of advanced LSBs toward practically viable applications.
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spelling pubmed-94184642022-09-20 A review of size engineering-enabled electrocatalysts for Li–S chemistry Zhang, Xi Zhang, Yaping Wei, Xijun Wei, Chaohui Song, Yingze Nanoscale Adv Chemistry Li–S batteries (LSBs) have received extensive attention owing to their remarkable theoretical capacity (1672 mA h g(−1)) and high energy density (2600 W h kg(−1)), which are far beyond those of the state-of-the-art Li-ion batteries (LIBs). However, the retarded sulfur reaction kinetics and fatal shuttle effect have hindered the practical implementations of LSBs. In response, constructing electrocatalysts for Li–S systems has been considered an effective strategy to date. Particularly, size engineering-enabled electrocatalysts show high activity in the sulfur redox reaction, considerably contributing to the latest advances in Li–S system research. In this tutorial review, we provide a systematic summary of nano- to atomic-scale electrocatalysts employed in Li–S chemistry, aiming at figuring out the working mechanism of size engineering-enabled electrocatalysts in the sulfur redox reaction and guiding the rational construction of advanced LSBs toward practically viable applications. RSC 2021-08-10 /pmc/articles/PMC9418464/ /pubmed/36132671 http://dx.doi.org/10.1039/d1na00522g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Zhang, Xi
Zhang, Yaping
Wei, Xijun
Wei, Chaohui
Song, Yingze
A review of size engineering-enabled electrocatalysts for Li–S chemistry
title A review of size engineering-enabled electrocatalysts for Li–S chemistry
title_full A review of size engineering-enabled electrocatalysts for Li–S chemistry
title_fullStr A review of size engineering-enabled electrocatalysts for Li–S chemistry
title_full_unstemmed A review of size engineering-enabled electrocatalysts for Li–S chemistry
title_short A review of size engineering-enabled electrocatalysts for Li–S chemistry
title_sort review of size engineering-enabled electrocatalysts for li–s chemistry
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9418464/
https://www.ncbi.nlm.nih.gov/pubmed/36132671
http://dx.doi.org/10.1039/d1na00522g
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