Luo Jian, Xiao Peng, Li Yangjie, Xiong Jiangzhi, Zhou Peng, Pang Liang, Xie Xilei, Li Yang
Powder Metallurgy Research Institute, Central South University, Changsha 410083, P. R. China.
National Key Laboratory of Science and Technology for National Defence on High-strength Structural Materials, Central South University, Changsha 410083, P. R. China.
Dalton Trans. 2023 Feb 21;52(8):2463-2471. doi: 10.1039/d2dt03775k.
Microscale porous silicon materials have shown great application potential as anodes for next-generation lithium-ion batteries (LIBs); however, they face significant challenges, including mechanical structure instability, low intrinsic conductivity, and uncontrollable processing. In this study, a modified etching strategy combined with a facile sol-gel method is demonstrated to prepare microscale porous Si microspheres encapsulated by an inner amorphous carbon shell (≈10 nm) and an outer rigid anatase titanium oxide (TiO) shell (≈20 nm) (PSi@C@TiO), with the intact porous framework and core-shell-shell spherical structure. The interconnected pores can sufficiently accommodate the expansion of the Si core during lithiation. Moreover, the double shells can not only enhance the kinetic behavior of the PSi@C@TiO microspheres, but can act as a compact fence to force the Si core to expand toward the internal pores during lithiation, ensuring the integrity of the porous spherical structure. As a result, the PSi@C@TiO anodes show greatly superior high specific capacity, excellent rate capability, stable solid-electrolyte interphase (SEI) films and steady mechanical structure. It delivers a high reversible capacity of 1004 mA h g after 250 cycles at 0.5 A g. This study provides a modified method to prepare microscale porous Si anodes with a stable mechanical structure and long cycle life for LIBs.
微尺度多孔硅材料作为下一代锂离子电池(LIBs)的阳极已显示出巨大的应用潜力;然而,它们面临着重大挑战,包括机械结构不稳定、本征电导率低和加工过程不可控。在本研究中,展示了一种改进的蚀刻策略与简便的溶胶 - 凝胶法相结合,以制备由内部非晶碳壳(约10纳米)和外部刚性锐钛矿型二氧化钛(TiO)壳(约20纳米)包覆的微尺度多孔硅微球(PSi@C@TiO),其具有完整的多孔框架和核 - 壳 - 壳球形结构。相互连接的孔隙能够充分容纳锂化过程中硅核的膨胀。此外,双层壳不仅可以增强PSi@C@TiO微球的动力学行为,还可以作为一个致密的屏障,迫使硅核在锂化过程中向内部孔隙膨胀,确保多孔球形结构的完整性。结果,PSi@C@TiO阳极表现出极大的高比容量、优异的倍率性能、稳定的固体电解质界面(SEI)膜和稳定的机械结构。在0.5 A g下循环250次后,其可逆容量高达1004 mA h g。本研究提供了一种改进方法,用于制备具有稳定机械结构和长循环寿命的用于LIBs的微尺度多孔硅阳极。