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Probing three-dimensional sodiation-desodiation equilibrium in sodium-ion batteries by in situ hard X-ray nanotomography.


ABSTRACT: Materials degradation-the main limiting factor for widespread application of alloy anodes in battery systems-was assumed to be worse in sodium alloys than in lithium analogues due to the larger sodium-ion radius. Efforts to relieve this problem are reliant on the understanding of electrochemical and structural degradation. Here we track three-dimensional structural and chemical evolution of tin anodes in sodium-ion batteries with in situ synchrotron hard X-ray nanotomography. We find an unusual (de)sodiation equilibrium during multi-electrochemical cycles. The superior structural reversibility during 10 electrochemical cycles and the significantly different morphological change features from comparable lithium-ion systems suggest untapped potential in sodium-ion batteries. These findings differ from the conventional thought that sodium ions always lead to more severe fractures in the electrode than lithium ions, which could have impact in advancing development of sodium-ion batteries.

SUBMITTER: Wang J 

PROVIDER: S-EPMC4491187 | biostudies-literature | 2015 Jun

REPOSITORIES: biostudies-literature

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Probing three-dimensional sodiation-desodiation equilibrium in sodium-ion batteries by in situ hard X-ray nanotomography.

Wang Jiajun J   Eng Christopher C   Chen-Wiegart Yu-Chen Karen YC   Wang Jun J  

Nature communications 20150626


Materials degradation-the main limiting factor for widespread application of alloy anodes in battery systems-was assumed to be worse in sodium alloys than in lithium analogues due to the larger sodium-ion radius. Efforts to relieve this problem are reliant on the understanding of electrochemical and structural degradation. Here we track three-dimensional structural and chemical evolution of tin anodes in sodium-ion batteries with in situ synchrotron hard X-ray nanotomography. We find an unusual  ...[more]

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