Chemical Engineering Journal ( IF 13.3 ) Pub Date : 2021-01-31 , DOI: 10.1016/j.cej.2021.128736 Canlong Wu , Guangyu Zhao , Xianbo Yu , Chao Liu , Pengbo Lyu , Guillaume Maurin , Shiru Le , Kening Sun , Naiqing Zhang
Mg ions exhibit sluggish kinetics when migrating in most of traditional two-dimensional (2D) layered materials, leading to the dissatisfactory Mg-storage capabilities. Lattice engineering can settle this issue by constructing van der Waals’ heterostructures (vdWHs) comprising heterogeneous monolayers, which establish specific ionic diffusion path with lower energy barriers. Herein, MoS2 monolayer and graphene (GR) are alternately overlapped with each other to construct a vdWH with a reduced Mg-diffusion barrier of 0.4 eV, and this brings the diffusion rate 11 orders of magnitude faster than that of pristine MoS2. The facilitated diffusion kinetics delivers a desirable Mg-storage capacity of 210 mAh g−1 at 20 mA g−1, and outstanding rate performance (90 mAh g−1 at 500 mA g−1). Moreover, enhanced structure durability of MoS2/GR allows the chemical reversibility for the repeated intercalation/deintercalation of Mg2+, thus 87% of initial remains after 300 cycles.
中文翻译:
MoS 2 /石墨烯异质结构,具有促进镁扩散动力学的高性能可充电镁电池
在大多数传统的二维(2D)层状材料中迁移时,Mg离子表现出缓慢的动力学,导致Mg储存能力不令人满意。晶格工程可以通过构建包括异质单层的范德华斯异质结构(vdWHs)解决这一问题,该异质单层建立具有较低能垒的特定离子扩散路径。在此,MoS 2单层和石墨烯(GR)彼此交替地重叠以构建具有0.4eV的降低的Mg扩散势垒的vdWH,这使扩散速率比原始MoS 2快11个数量级。促进的扩散动力学在20 mA g -1下提供了210 mAh g -1的理想Mg存储容量和优秀率性能(90毫安克-1以500mA克-1)。此外,MoS 2 / GR的增强的结构耐久性允许Mg 2+的重复嵌入/脱嵌的化学可逆性,因此在300次循环后初始残留量为87%。