期刊
ADVANCED FUNCTIONAL MATERIALS
卷 31, 期 42, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202103214
关键词
graphene; Li; (+); Mg; (2+) co-intercalation; Li; (+); Mg; (2+) hybrid-ion batteries; MoS; (2); van der Waals heterostructure
类别
资金
- National Natural Science Foundation of China [21776052, 22078078]
By constructing van der Waals heterostructures (MoS2/G VH) with graphene monolayers intercalating into MoS2, migration energy barriers of Li+ and Mg2+ were significantly reduced, leading to superior electrochemical performance in Li+/Mg2+ hybrid-ion batteries.
Owing to the low-cost, dendrite-free formation, and high volumetric capacity, rechargeable Li+/Mg2+ hybrid-ion batteries (LMIBs) have attracted great attention and are regarded as promising energy storage devices. However, due to the strong Coulombic interaction of Mg2+ with host materials, the traditional Daniell Type LMIBs with only Li+ intercalation usually cannot ensure a satisfactory energy density. Herein, graphene monolayers are arranged intercalating into MoS2 interlamination to construct van der Waals heterostructures (MoS2/G VH). This operation transforms the construction of ion channels from pristine interlamination of two MoS2 monolayers to the interlamination of MoS2 monolayer with graphene monolayer, thereby greatly reducing ion diffusion energy barriers. Compared with pristine MoS2, the MoS2/G VH can obviously reduce the migration energy barriers of Li+ (from 0.67 to 0.09 eV) and Mg2+ (from 1.01 to 0.21 eV). Moreover, it is also demonstrated that MoS2/G VHs realize Li+/Mg2+ co-intercalation even at a rate current of 1000 mA g(-1). As expected, the MoS2/G VH exhibits superior electrochemical performance with a reversible capacity of 145.8 mAh g(-1) at 1000 mA g(-1) after 2200 cycles, suggesting the feasibility of potential applications for high-performance energy storage devices.
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