Affiliation:
1. Henan Institute of Advanced Technology Zhengzhou University Zhengzhou 450003 China
2. School of Minerals Processing and Bioengineering Central South University Changsha 410083 China
3. College of Chemistry and Chemical Engineering Central South University Changsha 410083 China
Abstract
AbstractCaptured by relatively low energy consumption and harmful gas‐emission, direct regeneration has captured numerous attention, but still suffers from different particle sizes and diverse doping hetero‐elements, hardly meeting the market demand. Herein, assisted by the crush‐sinter regeneration from element to grain further to particle, homogenized recovery of hetero spent LiCoO2 is successfully carried out. More interestingly, after tailoring Li/Co anti‐sites ratio, the redox activity of Co‐ions is remarkably enhanced, effectively inhibiting the irreversible escape of O‐atoms under high voltage, bringing about the fascinating electrochemical performance and structural stability. As anticipated, the regenerated LiCoO2 delivered a considerable capacity of 175.2 mAh g−1 at 1.0 C, whilst its capacity retention can remain at 88.86% even after 500 cycles at 5.0 C, better than that of commercial materials. Assembling regenerated materials versus. graphite pouch cell, their considerable practical capacity retention can be kept at ≈91.4% even after 500 cycles. Supported by in situ XRD, electronic structure analysis, and detailed DFT calculations, the excellent high voltage stability of optimized samples mainly comes from the alleviating of phase conversion and oxygen redox. This work is expected to shed light on the potential value of homogenized regenerations, and offer effective strategies of upcycling about spent LCO.
Funder
National Natural Science Foundation of China
National Key Research and Development Program of China
State Key Laboratory of Microbial Resources, Chinese Academy of Sciences
Department of Transportation of Hunan Province
Cited by
3 articles.
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