Pushparaj Robert Ilango, Cakir Deniz, Zhang Xin, Xu Shuai, Mann Michael, Hou Xiaodong
Institute for Energy Studies, University of North Dakota, Grand Forks, North Dakota 58202, United States.
Department of Physics and Astrophysics, University of North Dakota, Grand Forks, North Dakota 58202, United States.
ACS Appl Mater Interfaces. 2021 Dec 22;13(50):59950-59961. doi: 10.1021/acsami.1c18993. Epub 2021 Dec 7.
A novel coal-derived graphene-intercalated MoS heterostructure was prepared with a facile in situ hydrothermal approach followed by high-temperature calcination. XRD, FE-SEM, HR-TEM, HR-Raman, and TOC analytical instruments, combined with first-principles simulations, were employed to explore the structural and electrochemical properties of this heterostructure for use as an electrode material. The XRD measurements and simulations confirmed the formation of the MoS/graphene (MoS-G) heterostructure. The microstructure analysis indicated that a well-defined 3D flower-like structure with tunable interlayer distances was created in the MoS layer. The novel MoS-09% G anode exhibits a remarkable initial discharge capacity of ∼929 mAh/g due to its interlayer expansion from the intercalation of graphene between the MoS layers. This anode maintains a capacity of ∼813 mAh/g with a Coulombic efficiency (CE) of ∼99% after 150 cycles at a constant current density of 100 mA/g. This anode also delivers a high-rate capability of ∼579 mAh/g at a current density of 2000 mA/g, significantly higher than that of other comparable structures. The unique flower-like arrangement, sufficient interlayer spacing for Li-ion diffusion, and the increased conductive matrix created using coal-derived graphene enhance the electrode kinetics during electrochemical reactions. Our first-principles calculations revealed that the diffusion barriers are significantly lower in heterostructures compared to that of bare MoS. This heterostructure design has significant potential as a new type of anode for Li-ion storage in next-generation batteries.
采用简便的原位水热法并结合高温煅烧制备了一种新型的煤基石墨烯插层MoS异质结构。利用XRD、FE-SEM、HR-TEM、HR-Raman和TOC分析仪器,并结合第一性原理模拟,来探究这种异质结构作为电极材料的结构和电化学性能。XRD测量和模拟证实了MoS/石墨烯(MoS-G)异质结构的形成。微观结构分析表明,在MoS层中形成了具有可调节层间距的明确的三维花状结构。新型的MoS-09%G阳极由于石墨烯插入MoS层之间导致层间膨胀,展现出约929 mAh/g的显著初始放电容量。该阳极在100 mA/g的恒定电流密度下循环150次后,保持约813 mAh/g的容量,库仑效率(CE)约为99%。该阳极在2000 mA/g的电流密度下也具有约579 mAh/g的高倍率性能,明显高于其他可比结构。独特的花状排列、足够的层间距用于锂离子扩散以及使用煤基石墨烯形成的导电基体增强了电化学反应过程中的电极动力学。我们的第一性原理计算表明,与裸MoS相比,异质结构中的扩散势垒显著更低。这种异质结构设计作为下一代电池中锂离子存储的新型阳极具有巨大潜力。