材料科学
阳极
多孔性
纳米孔
硅
锂(药物)
电极
多孔硅
化学工程
体积膨胀
电化学
复合材料
纳米技术
体积热力学
光电子学
医学
化学
物理
物理化学
量子力学
内分泌学
内科学
工程类
作者
Fang Dai,Ran Yi,Hui Yang,Yuming Zhao,Langli Luo,Mikhail L. Gordin,Hiesang Sohn,Shuru Chen,Chongmin Wang,Sulin Zhang,Donghai Wang
标识
DOI:10.1021/acsami.9b01501
摘要
Silicon (Si) remains one of the most promising anode materials for next-generation lithium-ion batteries (LIBs). The key challenge for Si anodes is the huge volume change during lithiation-delithiation cycles that leads to electrode pulverization and rapid capacity fading. Here, we report a hierarchical porous Si (hp-Si) with a tailored porous structure [tunable primary pores (20-200 nm) and secondary nanopores (∼3-10 nm)] that can effectively minimize the volume expansion. An in situ transmission electron microscopy (TEM) study revealed that the hp-Si material with the same porosity but larger primary pores can more effectively accommodate lithiation-induced volume expansion, giving rise to a much reduced apparent volume expansion on both material and electrode levels. Chemomechanical modeling revealed that because of the different relative stiffnesses of the lithiated and unlithiated Si phases, the primary pore size plays a key role in accommodating the volume expansion of lithiated Si. The higher structural stability of the hp-Si materials with larger primary pores also maintains the fast diffusion channels of the connective pores, giving rise to better power capability and capacity retention upon electrochemical cycling. Our findings point toward an optimized hp-Si material with minimal volume change during electrochemical cycling for next-generation LIBs.
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