动力学
扩散
耐久性
离子
材料科学
镁
化学工程
分子
无机化学
化学
复合材料
冶金
热力学
有机化学
物理
工程类
量子力学
作者
Canlong Wu,Li Zhang,Guangyu Zhao,Xianbo Yu,Chao Liu,Junjie He,Kening Sun,Naiqing Zhang
标识
DOI:10.1002/celc.202100879
摘要
Abstract One obstacle that hinders the development of rechargeable magnesium batteries (RMBs) is the limited selection of cathode materials with decent Mg diffusion kinetics due to the highly polarizing nature of divalent Mg 2+ . To promote Mg 2+ diffusion kinetics, water molecules (H 2 O) are incorporated into the gaps of MoS 2 with enlarged interlayer spacing through an electrochemically assisted method. Owing to the charge shielding effect of crystal H 2 O, the electrostatic interaction between Mg 2+ and host frameworks is weakened, thus hydrous MoS 2 (H−MoS 2 ) delivers a Mg diffusion rate three times faster than that of MoS 2 before hydration. The facilitated Mg diffusion kinetics in H−MoS 2 ensure a high capacity of 190.3 mAh g −1 at 20 mA g −1 , accompanied by excellent rate performance (75.1 mAh g −1 retains at 500 mA g −1 ). Additionally, crystal H 2 O plays the role of pillars, endowing that the layered structure of H−MoS 2 retains stable during repetitive Mg intercalation, thus 91.2 % of initial capacity is retained after 300 cycles.
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