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Promoting Ge Alloying Reaction via Heterostructure Engineering for High Efficient and Ultra‐Stable Sodium‐Ion Storage

Germanium (Ge)‐based materials have been considered as potential anode materials for sodium‐ion batteries owing to their high theoretical specific capacity. However, the poor conductivity and Na(+) diffusivity of Ge‐based materials result in retardant ion/electron transportation and insufficient sod...

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Autores principales: Shang, Chaoqun, Hu, Le, Luo, Dan, Kempa, Krzysztof, Zhang, Yongguang, Zhou, Guofu, Wang, Xin, Chen, Zhongwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7675052/
https://www.ncbi.nlm.nih.gov/pubmed/33240776
http://dx.doi.org/10.1002/advs.202002358
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author Shang, Chaoqun
Hu, Le
Luo, Dan
Kempa, Krzysztof
Zhang, Yongguang
Zhou, Guofu
Wang, Xin
Chen, Zhongwei
author_facet Shang, Chaoqun
Hu, Le
Luo, Dan
Kempa, Krzysztof
Zhang, Yongguang
Zhou, Guofu
Wang, Xin
Chen, Zhongwei
author_sort Shang, Chaoqun
collection PubMed
description Germanium (Ge)‐based materials have been considered as potential anode materials for sodium‐ion batteries owing to their high theoretical specific capacity. However, the poor conductivity and Na(+) diffusivity of Ge‐based materials result in retardant ion/electron transportation and insufficient sodium storage efficiency, leading to sluggish reaction kinetics. To intrinsically maximize the sodium storage capability of Ge, the nitrogen doped carbon‐coated Cu(3)Ge/Ge heterostructure material (Cu(3)Ge/Ge@N‐C) is developed for enhanced sodium storage. The pod‐like structure of Cu(3)Ge/Ge@N‐C exposes numerous active surface to shorten ion transportation pathway while the uniform encapsulation of carbon shell improves the electron transportation, leading to enhanced reaction kinetics. Theoretical calculation reveals that Cu(3)Ge/Ge heterostructure can offer decent electron conduction and lower the Na(+) diffusion barrier, which further promotes Ge alloying reaction and improves its sodium storage capability close to its theoretical value. In addition, the uniform encapsulation of nitrogen‐doped carbon on Cu(3)Ge/Ge heterostructure material efficiently alleviates its volume expansion and prevents its decomposition, further ensuring its structural integrity upon cycling. Attributed to these unique superiorities, the as‐prepared Cu(3)Ge/Ge@N‐C electrode demonstrates admirable discharge capacity, outstanding rate capability and prolonged cycle lifespan (178 mAh g(−1) at 4.0 A g(−1) after 4000 cycles).
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spelling pubmed-76750522020-11-24 Promoting Ge Alloying Reaction via Heterostructure Engineering for High Efficient and Ultra‐Stable Sodium‐Ion Storage Shang, Chaoqun Hu, Le Luo, Dan Kempa, Krzysztof Zhang, Yongguang Zhou, Guofu Wang, Xin Chen, Zhongwei Adv Sci (Weinh) Communications Germanium (Ge)‐based materials have been considered as potential anode materials for sodium‐ion batteries owing to their high theoretical specific capacity. However, the poor conductivity and Na(+) diffusivity of Ge‐based materials result in retardant ion/electron transportation and insufficient sodium storage efficiency, leading to sluggish reaction kinetics. To intrinsically maximize the sodium storage capability of Ge, the nitrogen doped carbon‐coated Cu(3)Ge/Ge heterostructure material (Cu(3)Ge/Ge@N‐C) is developed for enhanced sodium storage. The pod‐like structure of Cu(3)Ge/Ge@N‐C exposes numerous active surface to shorten ion transportation pathway while the uniform encapsulation of carbon shell improves the electron transportation, leading to enhanced reaction kinetics. Theoretical calculation reveals that Cu(3)Ge/Ge heterostructure can offer decent electron conduction and lower the Na(+) diffusion barrier, which further promotes Ge alloying reaction and improves its sodium storage capability close to its theoretical value. In addition, the uniform encapsulation of nitrogen‐doped carbon on Cu(3)Ge/Ge heterostructure material efficiently alleviates its volume expansion and prevents its decomposition, further ensuring its structural integrity upon cycling. Attributed to these unique superiorities, the as‐prepared Cu(3)Ge/Ge@N‐C electrode demonstrates admirable discharge capacity, outstanding rate capability and prolonged cycle lifespan (178 mAh g(−1) at 4.0 A g(−1) after 4000 cycles). John Wiley and Sons Inc. 2020-10-08 /pmc/articles/PMC7675052/ /pubmed/33240776 http://dx.doi.org/10.1002/advs.202002358 Text en © 2020 The Authors. Published by Wiley‐VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Shang, Chaoqun
Hu, Le
Luo, Dan
Kempa, Krzysztof
Zhang, Yongguang
Zhou, Guofu
Wang, Xin
Chen, Zhongwei
Promoting Ge Alloying Reaction via Heterostructure Engineering for High Efficient and Ultra‐Stable Sodium‐Ion Storage
title Promoting Ge Alloying Reaction via Heterostructure Engineering for High Efficient and Ultra‐Stable Sodium‐Ion Storage
title_full Promoting Ge Alloying Reaction via Heterostructure Engineering for High Efficient and Ultra‐Stable Sodium‐Ion Storage
title_fullStr Promoting Ge Alloying Reaction via Heterostructure Engineering for High Efficient and Ultra‐Stable Sodium‐Ion Storage
title_full_unstemmed Promoting Ge Alloying Reaction via Heterostructure Engineering for High Efficient and Ultra‐Stable Sodium‐Ion Storage
title_short Promoting Ge Alloying Reaction via Heterostructure Engineering for High Efficient and Ultra‐Stable Sodium‐Ion Storage
title_sort promoting ge alloying reaction via heterostructure engineering for high efficient and ultra‐stable sodium‐ion storage
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7675052/
https://www.ncbi.nlm.nih.gov/pubmed/33240776
http://dx.doi.org/10.1002/advs.202002358
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