Affiliation:
1. State Key Laboratory of Rare Earth Materials Chemistry and Applications College of Chemistry and Molecular Engineering Peking University Beijing 100871 P. R. China
2. State Key Laboratory of New Ceramics and Fine Processing School of Materials Science and Engineering Tsinghua University Beijing 100084 China
3. State Key Laboratory of High Performance Ceramics and Superfine Microstructures Shanghai Institute of Ceramics Chinese Academy of Sciences Shanghai 200050 P. R. China
Abstract
AbstractThe growing consumption of lithium‐ion batteries calls for recycling of electrode materials. Conventional direct recycling mainly consists of cathode‐to‐cathode and anode‐to‐anode strategies. In this work, a cathode‐to‐anode approach is proposed using a LiCoO2 model system and extending to Co‐lean/Co‐free cathodes (LiNi0.8Co0.1Mn0.1O2, LiMn2O4, and LiFePO4). Commercial cathodes are featured with single‐crystalline or secondary‐particle polycrystalline morphology, thus exhibiting higher tap density than anodes (LiCoO2 2.7 g cm−3 vs Si 0.25 g cm−3). By means of an intuitively direct conversion, the anodes are bestowed with well‐assembled morphology and high tap density from cathodes. During discharging, a dual conductive network is formed to facilitate lithium storage, where the binder‐derived carbon functions as electronic‐conductive and LiF/Li2O as ionic‐conductive motifs. Recycled cathodes exhibit an outstanding rate volumetric capacity (883 mAh cm−3, 5 A g−1, LiCoO2) and cyclic performance (1286 mAh cm−3, 1000 cycles, 2 A g−1, LiMn2O4). The morphologically inherited cathode‐to‐anode strategy proves to be a universal method for battery recycling toward high volumetric energy density.
Funder
National Natural Science Foundation of China
Subject
General Materials Science,Renewable Energy, Sustainability and the Environment
Cited by
14 articles.
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