Unveiling the Working Mechanism of Graphene Bubble Film/Silicon Composite Anodes in Li-Ion Batteries: From Experiment to Modeling

石墨烯 阳极 材料科学 氧化物 复合数 纳米技术 电解质 气泡 电极 复合材料 光电子学 化学 物理化学 计算机科学 冶金 并行计算
作者
Kimal Chandula Wasalathilake,Sashini N. S. Hapuarachchi,Yinbo Zhao,Joseph F. S. Fernando,Hao Chen,Jawahar Y. Nerkar,Dmitri Golberg,Shanqing Zhang,Cheng Yan
出处
期刊:ACS applied energy materials [American Chemical Society]
卷期号:3 (1): 521-531 被引量:45
标识
DOI:10.1021/acsaem.9b01778
摘要

In spite of the fact that there are plenty of recent studies on Si/graphene composite anodes, the influence of graphene on Li diffusion at the interface and lithiation associated mechanical behavior have not been well-understood. Furthermore, it is still a technical challenge to maintain a high capacity and an ultralong cycle life with high mass loading. Using a simple self-assembly approach, we have developed an all-integrated architecture of Si nanoparticles (SiNPs) encapsulated inside reduced graphene oxide (rGO) bubble films anchored in a 3D rGO macroporous network (encapsulated Si@rGO) as an anode for Li-ion batteries (LIBs). The enhanced electrochemical performance and structural stability of the anode are accomplished by the unique multifunctional rGO bubble film, which smoothly wraps SiNPs with notable void spaces. Its residual functional groups covalently bind with SiNPs, preventing their detachment from the electrode. The bubble wrap together with the outermost 3D framework accommodate the volume change, contributing to a stabilized solid electrolyte interphase (SEI) layer while maintaining ionic and electronic conductive pathways. Density functional theory (DFT) simulations show that the graphene coating boosts the mobility of the Li atoms at the Si–graphene interface. Molecular dynamics (MD) simulations confirm that graphene bubble film can effectively control the stress build-up near the Si surface, maintaining the structural integrity of the anode. The encapsulated Si@rGO anode with a mass loading of 2.6 mg cm–2 demonstrates exceptional cycling stability and superior rate capabilities. The anode demonstrates a high reversible capacity of 1346 mAh g–1 after 200 cycles at 500 mA g–1. Even at a high current density of 2.5 A g–1, a reversible capacity of 998 mAh g–1 is maintained after 1000 cycles with a capacity retention of 97%.
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