Core-shell structured SiO @C with controllable mesopores as anode materials for lithium-ion batteries

材料科学 阳极 介孔材料 乙烯基三乙氧基硅烷 锂(药物) 化学工程 聚苯乙烯 纳米技术 多孔性 聚合物 电极 复合材料 催化作用 硅烷 化学 有机化学 工程类 医学 物理化学 冶金 内分泌学
作者
Zhiyuan Wang,Nan Yang,Li Ren,Xiaomei Wang,Xiaomei Wang
出处
期刊:Microporous and Mesoporous Materials [Elsevier BV]
卷期号:307: 110480-110480 被引量:31
标识
DOI:10.1016/j.micromeso.2020.110480
摘要

The high-capacity silicon oxide (SiOx) is a promising anode candidate for lithium-ion batteries (LIBs), but the huge volume expansion during the cycle severely limits their practical application. Mesoporous SiOx is widely investigated as an effective solution due to the self-buffering inner-space. Nevertheless, both excessive and deficient inner-space have bad impacts on the anode material, so exploring a suitable pore volume is the top priority. In this work, an impressive and novel approach has been developed to prepare SiOx@C core-shell microspheres with different mesopores of SiOx. Vinyl-SiO2 nanoparticles are gestated in the framework of sulfonated polystyrene (SCLPS) microspheres to form the vinyl-SiO2/SCLPS composites by vinyltriethoxysilane as the silicon source and in-suit catalyzed by SCLPS. Afterwards, the vinyl-SiO2/SCLPS are covered by resorcinol/formaldehyde polymer, and then the core-shell microspheres are carbonized to prepare SiOx@C. The inner pore space of SiOx can be controlled by adjusting the cross-linking degrees (CLDs) of the SCLPS microspheres. After comparison, SiOx[email protected] with the most suitable porous structure is selected, which exhibits a large reversible capacity (761 mAh g−1 at 100 mA g−1) and acceptable cycling capacity (534 mAh g−1 after 150 cycles). This work provides novel insights on exploring an appropriate inner-space to overcome the challenge of volume expansion.

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