阳极
材料科学
电解质
法拉第效率
锂(药物)
密度泛函理论
工作职能
化学工程
吸收(声学)
工作(物理)
分子
碳纤维
纳米技术
离子
电极
物理化学
计算化学
复合材料
图层(电子)
有机化学
热力学
化学
医学
内分泌学
工程类
复合数
物理
作者
Naiqing Ren,Lifeng Wang,Xiaodong He,Li-ming Zhang,Jiemin Dong,Fei Chen,Jingchao Xiao,Bicai Pan,Chunhua Chen
标识
DOI:10.1021/acsami.1c14935
摘要
Hard carbons (HC) derived from biomass material are most promising anodes for lithium-ion batteries (LIBs) because of their cost effectiveness and environmental friendliness. However, the low initial Coulombic efficiency (ICE) of HC anodes reduces the energy density of full cells, which seriously impedes their practical applications. Herein, we demonstrate that the ICE of HC anodes can be significantly improved by modulating the work function of a model HC derived from cotton and deliberately treated to form C–Cl bonds on its surface. By X-ray absorption near-edge structure and density functional theory (DFT) calculation studies, it is verified that the introduction of the C–Cl bond leads to the electron transfer from C to Cl and enhances the work function of the system. In addition, this Cl-doped HC anode can inhibit the reduction of solvent molecules in the electrolyte and reduce the formation of a solid electrolyte interface (SEI) film. Consequently, the ICE is improved from 64.8 to 78.1%. This study provides an effective route to reduce the formation of the SEI film and improve the ICE of hard carbon anodes for LIBs.
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