Liu Zhonggang, Lu Dongzhen, Wang Wei, Yue Liguo, Zhu Junlu, Zhao Ligong, Zheng He, Wang Jianbo, Li Yunyong
School of Materials and Energy, Guangdong University of Technology, No. 100 Waihuan Xi Road, Guangzhou Higher Education Mega Center, Guangzhou 510006, China.
School of Physics and Technology, Center for Electron Microscopy, MOE Key Laboratory of Artificial Micro- and Nano-structures, and Institute for Advanced Studies, Wuhan University, Wuhan, 430072, China.
ACS Nano. 2022 Mar 22;16(3):4642-4653. doi: 10.1021/acsnano.1c11298. Epub 2022 Mar 7.
High-theoretical-capacity silicon anodes hold promise in lithium-ion batteries (LIBs). Nevertheless, their huge volume expansion (∼300%) and poor conductivity show the need for the simultaneous introduction of low-density conductive carbon and nanosized Si to conquer the above issues, yet they result in low volumetric performance. Herein, we develop an integration strategy of a dually encapsulated Si structure and dense structural engineering to fabricate a three-dimensional (3D) highly dense TiCT MXene and graphene dual-encapsulated Si monolith architecture (HD-Si@TiCT@G). Because of its high density (1.6 g cm), high conductivity (151 S m), and 3D dense dual-encapsulated Si architecture, the resultant HD-Si@TiCT@G monolith anode displays an ultrahigh volumetric capacity of 5206 mAh cm (gravimetric capacity: 2892 mAh g) at 0.1 A g and a superior long lifespan of 800 cycles at 1.0 A g. Notably, the thick and dense monolithic anode presents a large areal capacity of 17.9 mAh cm. TEM and SEM techniques, and systematic kinetics and structural stability analysis during cycling demonstrate that such superior volumetric and areal performances stem from its dual-encapsulated Si architecture by the 3D conductive and elastic networks of MXene and graphene, which can provide fast electron and ion transfer, effective volume buffer, and good electrolyte permeability even with a thick electrode, whereas the dense structure results in a large volumetric performance. This work offers a simple and feasible strategy to greatly improve the volumetric and areal capacity of alloy-based anodes for large-scale applications via integrating a dual-encapsulated strategy and dense-structure engineering.
高理论容量的硅阳极在锂离子电池(LIBs)中具有广阔前景。然而,其巨大的体积膨胀(约300%)和较差的导电性表明,需要同时引入低密度导电碳和纳米尺寸的硅来解决上述问题,但这又导致体积性能较低。在此,我们开发了一种双封装硅结构与致密结构工程的集成策略,以制备三维(3D)高密度TiCT MXene和石墨烯双封装硅整体结构(HD-Si@TiCT@G)。由于其高密度(1.6 g/cm³)、高导电性(151 S/m)以及3D致密双封装硅结构,所得的HD-Si@TiCT@G整体阳极在0.1 A/g电流密度下展现出5206 mAh/cm³的超高体积容量(重量容量:2892 mAh/g),并在1.0 A/g电流密度下具有800次循环的优异长寿命。值得注意的是,这种厚且致密的整体阳极呈现出17.9 mAh/cm²的大面容量。透射电子显微镜(TEM)和扫描电子显微镜(SEM)技术以及循环过程中的系统动力学和结构稳定性分析表明,如此优异的体积和面性能源于其由MXene和石墨烯的3D导电及弹性网络对硅的双封装结构,这即使在电极较厚时也能提供快速的电子和离子传输、有效的体积缓冲以及良好的电解质渗透性,而致密结构则带来了较大的体积性能。这项工作通过整合双封装策略和致密结构工程,提供了一种简单可行的策略,可大幅提高合金基阳极的体积和面容量,以用于大规模应用。