Cargando…

Riemannian Surface on Carbon Anodes Enables Li-Ion Storage at −35 °C

[Image: see text] Since sluggish Li(+) desolvation leads to severe capacity degradation of carbon anodes at subzero temperatures, it is urgently desired to modulate electron configurations of surface carbon atoms toward high capacity for Li-ion batteries. Herein, a carbon-based anode material (O-DF)...

Descripción completa

Detalles Bibliográficos
Autores principales: Lu, Zongjing, Wang, Jingnan, Cheng, Xuechun, Xie, Weiwei, Gao, Zhiyi, Zhang, Xuejing, Xu, Yong, Yi, Ding, Yang, Yijun, Wang, Xi, Yao, Jiannian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9335919/
https://www.ncbi.nlm.nih.gov/pubmed/35912350
http://dx.doi.org/10.1021/acscentsci.2c00411
_version_ 1784759437481738240
author Lu, Zongjing
Wang, Jingnan
Cheng, Xuechun
Xie, Weiwei
Gao, Zhiyi
Zhang, Xuejing
Xu, Yong
Yi, Ding
Yang, Yijun
Wang, Xi
Yao, Jiannian
author_facet Lu, Zongjing
Wang, Jingnan
Cheng, Xuechun
Xie, Weiwei
Gao, Zhiyi
Zhang, Xuejing
Xu, Yong
Yi, Ding
Yang, Yijun
Wang, Xi
Yao, Jiannian
author_sort Lu, Zongjing
collection PubMed
description [Image: see text] Since sluggish Li(+) desolvation leads to severe capacity degradation of carbon anodes at subzero temperatures, it is urgently desired to modulate electron configurations of surface carbon atoms toward high capacity for Li-ion batteries. Herein, a carbon-based anode material (O-DF) was strategically synthesized to construct the Riemannian surface with a positive curvature, which exhibits a high reversible capacity of 624 mAh g(–1) with an 85.9% capacity retention at 0.1 A g(–1) as the temperature drops to −20 °C. Even if the temperature drops to −35 °C, the reversible capacity is still effectively retained at 160 mAh g(–1) after 200 cycles. Various characterizations and theoretical calculations reveal that the Riemannian surface effectively tunes the low-temperature sluggish Li(+) desolvation of the interfacial chemistry via locally accumulated charges of non-coplanar sp(x) (2 < x < 3) hybridized orbitals to reduce the rate-determining step of the energy barrier for the charge-transfer process. Ex-situ measurements further confirm that the sp(x)-hybridized orbitals of the pentagonal defect sites should denote more negative charges to solvated Li(+) adsorbed on the Riemannian surface to form stronger Li–C coordinate bonds for Li(+) desolvation, which not only enhances Li-adsorption on the curved surface but also results in more Li(+) insertion in an extremely cold environment.
format Online
Article
Text
id pubmed-9335919
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-93359192022-07-30 Riemannian Surface on Carbon Anodes Enables Li-Ion Storage at −35 °C Lu, Zongjing Wang, Jingnan Cheng, Xuechun Xie, Weiwei Gao, Zhiyi Zhang, Xuejing Xu, Yong Yi, Ding Yang, Yijun Wang, Xi Yao, Jiannian ACS Cent Sci [Image: see text] Since sluggish Li(+) desolvation leads to severe capacity degradation of carbon anodes at subzero temperatures, it is urgently desired to modulate electron configurations of surface carbon atoms toward high capacity for Li-ion batteries. Herein, a carbon-based anode material (O-DF) was strategically synthesized to construct the Riemannian surface with a positive curvature, which exhibits a high reversible capacity of 624 mAh g(–1) with an 85.9% capacity retention at 0.1 A g(–1) as the temperature drops to −20 °C. Even if the temperature drops to −35 °C, the reversible capacity is still effectively retained at 160 mAh g(–1) after 200 cycles. Various characterizations and theoretical calculations reveal that the Riemannian surface effectively tunes the low-temperature sluggish Li(+) desolvation of the interfacial chemistry via locally accumulated charges of non-coplanar sp(x) (2 < x < 3) hybridized orbitals to reduce the rate-determining step of the energy barrier for the charge-transfer process. Ex-situ measurements further confirm that the sp(x)-hybridized orbitals of the pentagonal defect sites should denote more negative charges to solvated Li(+) adsorbed on the Riemannian surface to form stronger Li–C coordinate bonds for Li(+) desolvation, which not only enhances Li-adsorption on the curved surface but also results in more Li(+) insertion in an extremely cold environment. American Chemical Society 2022-06-08 2022-07-27 /pmc/articles/PMC9335919/ /pubmed/35912350 http://dx.doi.org/10.1021/acscentsci.2c00411 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Lu, Zongjing
Wang, Jingnan
Cheng, Xuechun
Xie, Weiwei
Gao, Zhiyi
Zhang, Xuejing
Xu, Yong
Yi, Ding
Yang, Yijun
Wang, Xi
Yao, Jiannian
Riemannian Surface on Carbon Anodes Enables Li-Ion Storage at −35 °C
title Riemannian Surface on Carbon Anodes Enables Li-Ion Storage at −35 °C
title_full Riemannian Surface on Carbon Anodes Enables Li-Ion Storage at −35 °C
title_fullStr Riemannian Surface on Carbon Anodes Enables Li-Ion Storage at −35 °C
title_full_unstemmed Riemannian Surface on Carbon Anodes Enables Li-Ion Storage at −35 °C
title_short Riemannian Surface on Carbon Anodes Enables Li-Ion Storage at −35 °C
title_sort riemannian surface on carbon anodes enables li-ion storage at −35 °c
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9335919/
https://www.ncbi.nlm.nih.gov/pubmed/35912350
http://dx.doi.org/10.1021/acscentsci.2c00411
work_keys_str_mv AT luzongjing riemanniansurfaceoncarbonanodesenablesliionstorageat35c
AT wangjingnan riemanniansurfaceoncarbonanodesenablesliionstorageat35c
AT chengxuechun riemanniansurfaceoncarbonanodesenablesliionstorageat35c
AT xieweiwei riemanniansurfaceoncarbonanodesenablesliionstorageat35c
AT gaozhiyi riemanniansurfaceoncarbonanodesenablesliionstorageat35c
AT zhangxuejing riemanniansurfaceoncarbonanodesenablesliionstorageat35c
AT xuyong riemanniansurfaceoncarbonanodesenablesliionstorageat35c
AT yiding riemanniansurfaceoncarbonanodesenablesliionstorageat35c
AT yangyijun riemanniansurfaceoncarbonanodesenablesliionstorageat35c
AT wangxi riemanniansurfaceoncarbonanodesenablesliionstorageat35c
AT yaojiannian riemanniansurfaceoncarbonanodesenablesliionstorageat35c