成核
插层(化学)
材料科学
扩散
碳纤维
离子键合
化学工程
涂层
复合数
电极
电导率
动力学
离子电导率
复合材料
无机化学
离子
化学
电解质
热力学
物理化学
有机化学
物理
工程类
量子力学
作者
Anna Iarchuk,Victoria A. Nikitina,Evgeny A. Karpushkin,Vladimir G. Sergeyev,Evgeny V. Antipov,Keith J. Stevenson,Artem M. Abakumov
标识
DOI:10.1002/celc.201901219
摘要
Abstract We report on a comparative study of Li + intercalation kinetics for LiFePO 4 materials with polydopamine‐derived and glucose‐derived carbon coatings. We demonstrate that the uniform polydopamine‐derived carbon coating affects the charge transfer rates and transport properties (electronic conductivity) of composite electrodes only slightly (compared to the inhomogeneous glucose‐derived coatings), whereas much more pronounced effects are observed for the apparent diffusion coefficients and nucleation barriers. Thick and uniform carbon surface layers cause a sharp decrease in the ionic diffusion coefficients, which results in the loss of capacity at higher charge/discharge rates for LiFePO 4 composite electrodes. The new phase nucleation rates are also demonstrated to decrease significantly for the samples with thicker coatings inducing higher potential differences between charge and discharge curves. The analysis of the rate determining factors for the LiFePO 4 electrodes points to the rate limitations induced by the slow nucleation and slow ionic diffusion, whereas the formation of a polydopamine‐derived uniform carbon layer tends to hinder the (de)intercalation reaction and does not provide additional benefits compared to glucose‐derived carbon coatings comprising conductive yet inhomogeneous layers.
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