期刊
ACS APPLIED MATERIALS & INTERFACES
卷 14, 期 46, 页码 51954-51964出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c15355
关键词
silicon; graphite composite; functionally gradient electrode; chemomechanical simulations; multilayer coating approach; lithium-ion batteries
资金
- National Natural Science Foundation of China
- [12172143]
This study proposed a multilayer coating method for the fabrication of functionally gradient Si/graphite composite electrodes, which effectively mitigated the volume change-caused structural degradation and realized high capacity in lithium-ion batteries. The PG-Si/Gr electrode exhibited excellent stability and high reversible capacity, even at high mass loadings. When paired with a commercial NCM532 cathode, the PG-Si/Gr||NCM532 full cell demonstrated a stable areal capacity after cycling.
Silicon (Si) is regarded as one of the most promising anode materials for high-energy-density lithium (Li)-ion batteries (LIBs). However, Li insertion/extraction induced large volume change, which can lead to the fracture of the Si material itself and the delamination/pulverization of electrodes, is the major challenge for the practical application of Si-based anodes. Herein, a facile and scalable multilayer coating approach was proposed for the large-scale fabrication of functionally gradient Si/graphite (Si/ Gr) composite electrodes to simultaneously mitigate the volume change-caused structural degradation and realize high capacity by regulating the spatial distributions of Si and Gr particles in the electrodes. Both our experimental characterizations and chemomechanical simulations indicated that, with a parabolic gradient (PG) distribution of Si through the thickness direction that the two Si-poor surface layers guarantee the major mechanical support and the middle Si-rich layer ensures the high capacity, the as prepared PG-Si/Gr electrode can not only effectively improve the stability of the electrode structure but also efficiently enable high capacity and stable electrochemical reactions. Consequently, the PG-Si/Gr electrode with a mass loading of 3.15 mg cm-2 exhibited a reversible capacity of 579.2 mAh g-1 (1.82 mAh cm-2) after 200 cycles at 0.2C. Even with a mass loading of 8.45 mg cm-2, the PGSi/Gr anodes still delivered a high reversible capacity of 4.04 mAh cm-2 after 100 cycles and maintained excellent cycling stability. Moreover, when paired with a commercial LiNi0.5Mn0.3Co0.2O2 (NCM532) cathode (9.56 mg cm-2), the PG-Si/Gr||NCM532 full cell revealed an initial reversible areal capacity of 1.64 mAh cm-2 and sustained a stable areal capacity of 0.94 mAh cm-2 at 0.2C after 100 cycles.
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