阳极
离子
硅
材料科学
锂(药物)
电池(电)
离子运输机
电子
锂离子电池
钾离子电池
化学工程
无机化学
光电子学
化学
磷酸钒锂电池
工程类
电极
功率(物理)
有机化学
物理
物理化学
医学
量子力学
内分泌学
作者
Kanghou Ma,NULL AUTHOR_ID,Xinyue Zhao,Sunfa Wang,NULL AUTHOR_ID,NULL AUTHOR_ID,Fangshuo Zhou,Wei Shi,NULL AUTHOR_ID
标识
DOI:10.1016/j.cej.2024.153846
摘要
Silicon (Si) stands as a promising candidate for high-capacity anode materials in the next-generation lithium-ion batteries (LIBs) due to extremely high specific capacity. However, silicon application is hindered by its inherently poor electron and ion conductivities, as well as structural instability during the repeated charging/discharging. To address these challenges, a novel functional surface modification agent, diethylenetriaminepenta(methylenephosphonic) acid (DTPMP), was decorated on the surface of silicon particles for the first time. The experimental results demonstrate that the DTPMP effectively enhances the cohesion between nano Si particles. This study combines experimental observations with theoretical calculations to analyze the nucleophilic and electrophilic sites of DTPMP and carboxymethyl cellulose (CMC), elucidating the existence state of DTPMP on the nano Si surface. Furthermore, by examining the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO), along with the electrostatic potential (ESP) of DTPMP and solvent molecules in conjunction with Li+, the impact of the phosphate group on the diffusion of Li+ and electrons at the nano Si surface was studied. The electron density difference (EDD) maps for DTPMP and CMC reveal that DTPMP exhibits a more pronounced response in the presence of an electric field, suggesting its enhanced role in facilitating Li+ diffusion. This research offers a novel perspective on enhancing the electrochemical performance of nano Si surfaces, paving the way for the development of advanced LIBs with improved energy storage capabilities.
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