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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)...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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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 |
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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 |
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