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Synthesis of layered silicon-graphene hetero-structures by wet jet milling for high capacity anodes in Li-ion batteries

材料科学 阳极 电极 法拉第效率 石墨烯 锂(药物) 扫描电子显微镜 化学工程 电解质 纳米技术 电化学 光电子学 复合材料 化学 医学 工程类 内分泌学 物理化学
作者
Romeo Malik,Qianye Huang,Laura Silvestri,Danqing Liu,Vittorio Pellegrini,Luigi Marasco,Eleonora Venezia,Sara Abouali,Francesco Bonaccorso,Michael Lain,David Greenwood,Geoff West,Paul R. Shearing,Melanie Loveridge
出处
期刊:2D materials [IOP Publishing]
卷期号:8 (1): 015012-015012 被引量:18
标识
DOI:10.1088/2053-1583/aba5ca
摘要

Abstract While silicon-based negative electrode materials have been extensively studied, to develop high capacity lithium-ion batteries (LIBs), implementing a large-scale production method that can be easily transferred to industry, has been a crucial challenge. Here, a scalable wet-jet milling method was developed to prepare a silicon-graphene hybrid material to be used as negative electrode in LIBs. This synthesized composite, when used as an anode in lithium cells, demonstrated high Li ion storage capacity, long cycling stability and high-rate capability. In particular, the electrode exhibited a reversible discharge capacity exceeding 1763 mAh g −1 after 450 cycles with a capacity retention of 98% and a coulombic efficiency of 99.85% (with a current density of 358 mA g −1 ). This significantly supersedes the performance of a Si-dominant electrode structures. The capacity fade rate after 450 cycles was only 0.005% per cycle in the 0.05–1 V range. This superior electrochemical performance is ascribed to the highly layered, silicon-graphene porous structure, as investigated via focused ion beam in conjunction with scanning electron microscopy tomography. The hybrid electrode could retain 89% of its porosity (under a current density of 358 mA g −1 ) after 200 cycles compared with only 35% in a Si-dominant electrode. Moreover, this morphology can not only accommodate the large volume strains from active silicon particles, but also maintains robust electrical connectivity. This confers faster transportation of electrons and ions with significant permeation of electrolyte within the electrode. Physicochemical characterisations were performed to further correlate the electrochemical performance with the microstructural dynamics. The excellent performance of the hybrid material along with the scalability of the synthesizing process is a step forward to realize high capacity/energy density LIBs for multiple device applications.
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