阳极
锂(药物)
透视图(图形)
钠
钾
碳纤维
离子
材料科学
钾离子电池
无机化学
化学
计算机科学
磷酸钒锂电池
冶金
电极
医学
复合材料
内科学
有机化学
人工智能
物理化学
复合数
作者
Sreehari K. Saju,Shreyasi Chattopadhyay,Jianan Xu,Salma Alhashim,Atin Pramanik,Pulickel M. Ajayan
标识
DOI:10.1016/j.xcrp.2024.101851
摘要
Due to its overall performance, hard carbon (HC) is a promising anode for rechargeable lithium-, sodium-, and potassium-ion batteries (LIBs, NIBs, KIBs). The microcrystalline structure morphology of HCs facilitates the alkali metal -ion uptake and fast ion intercalation and deintercalation throughout the pores with low-potential intercalation properties. However, the large-scale industrial application of HCs is still lagging because of the first-cycle reversible capacity, which results in low initial Coulombic efficiency (ICE) and voltage hysteresis. This review focuses on the fundamental mechanism of HCs as alkali metal-ion batteries, with the current issues being discussed. This includes the formation of solid electrolyte interphase during the first cycle with low ICE, safety concerns, and improved performances, which are vital for practical applicability. The current state-of-the-art of HC anodes is discussed here with recent literature. Furthermore, the challenges and the corresponding effective strategies to overcome the difficulties related to the commercialization of HCs as rechargeable battery anodes are discussed.
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