Phase evolution of conversion-type electrode for lithium ion batteries
Jing Li,
Sooyeon Hwang,
Fangming Guo,
Shuang Li,
Zhongwei Chen (),
Ronghui Kou,
Ke Sun,
Cheng-Jun Sun,
Hong Gan,
Aiping Yu,
Eric A. Stach,
Hua Zhou () and
Dong Su ()
Additional contact information
Jing Li: Brookhaven National Laboratory
Sooyeon Hwang: Brookhaven National Laboratory
Fangming Guo: Argonne National Laboratory
Shuang Li: Brookhaven National Laboratory
Zhongwei Chen: University of Waterloo
Ronghui Kou: Argonne National Laboratory
Ke Sun: Brookhaven National Laboratory
Cheng-Jun Sun: Argonne National Laboratory
Hong Gan: Brookhaven National Laboratory
Aiping Yu: University of Waterloo
Eric A. Stach: University of Pennsylvania
Hua Zhou: Argonne National Laboratory
Dong Su: Brookhaven National Laboratory
Nature Communications, 2019, vol. 10, issue 1, 1-10
Abstract:
Abstract Batteries with conversion-type electrodes exhibit higher energy storage density but suffer much severer capacity fading than those with the intercalation-type electrodes. The capacity fading has been considered as the result of contact failure between the active material and the current collector, or the breakdown of solid electrolyte interphase layer. Here, using a combination of synchrotron X-ray absorption spectroscopy and in situ transmission electron microscopy, we investigate the capacity fading issue of conversion-type materials by studying phase evolution of iron oxide composited structure during later-stage cycles, which is found completely different from its initial lithiation. The accumulative internal passivation phase and the surface layer over cycling enforce a rate−limiting diffusion barrier for the electron transport, which is responsible for the capacity degradation and poor rate capability. This work directly links the performance with the microscopic phase evolution in cycled electrode materials and provides insights into designing conversion-type electrode materials for applications.
Date: 2019
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-09931-2
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DOI: 10.1038/s41467-019-09931-2
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