A Stress Self‐Adaptive Structure to Suppress the Chemo‐mechanical Degradation for High Rate and Ultralong Cycle Life Sodium Ion Batteries

Author:

Liu Yiming1,Wang Jing2,Shi Qinhao1,Yan Mouhui1,Zhao Shengyu1,Feng Wuliang1,Qi Ruijuan3,Xu Jiaqiang1,Luo Jiayan4,Zhang Jiujun1,Zhao Yufeng1ORCID

Affiliation:

1. College of Science & Institute for Sustainable Energy Shanghai University Shanghai 200444 China

2. Hebei Key Laboratory of Heavy Metal Deep-Remediation in Water and Resource Reuse Yanshan University Qinhuangdao 066004 China

3. Key Laboratory of Polar Materials and Devices (MOE) & Department of Electronics East China Normal University Shanghai 200062 China

4. State Key Laboratory of Metal Matrix Composites School of Materials Science and Engineering Shanghai Jiao Tong University Shanghai 200240 China

Abstract

AbstractTransition‐metal phosphides (TMPs) as typical conversion‐type anode materials demonstrate extraordinary theoretical charge storage capacity for sodium ion batteries, but the unavoidable volume expansion and irreversible capacity loss upon cycling represent their long‐standing limitations. Herein we report a stress self‐adaptive structure with ultrafine FeP nanodots embedded in dense carbon microplates skeleton (FeP@CMS) via the spatial confinement of carbon quantum dots (CQDs). Such an architecture delivers a record high specific capacity (778 mAh g−1 at 0.05 A g−1) and ultra‐long cycle stability (87.6 % capacity retention after 10 000 cycles at 20 A g−1), which outperform the state‐of‐the‐art literature. We decode the fundamental reasons for this unprecedented performance, that such an architecture allows the spontaneous stress transfer from FeP nanodots to the surrounding carbon matrix, thus overcomes the intrinsic chemo‐mechanical degradation of metal phosphides.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Shanghai

Publisher

Wiley

Subject

General Medicine

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