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Sulfurized Two-Dimensional Conductive Metal-Organic Framework as a High-Performance Cathode Material for Rechargeable Mg Batteries
被引:9
|作者:
Mu, Yu
[1
]
Nyakuchena, James
[2
]
Wang, Yang
[1
]
Wilkes, James R.
[1
]
Luo, Tongtong
[1
]
Goldstein, Michael
[1
]
Elander, Brooke
[1
]
Mohanty, Udayan
[1
]
Bao, Junwei Lucas
[1
]
Huang, Jier
[1
,2
]
Wang, Dunwei
[1
]
机构:
[1] Boston Coll, Merkert Chem Ctr, Dept Chem, Chestnut Hill, MA 02467 USA
[2] Marquette Univ, Dept Chem, Milwaukee, WI 53201 USA
基金:
美国国家科学基金会;
关键词:
magnesium;
battery;
sulfurization;
MOF;
2D material;
REACTIVITY;
CHEMISTRY;
MECHANISM;
STORAGE;
D O I:
10.1002/anie.202409286
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Rechargeable Mg batteries are a promising energy storage technology to overcome the limitations inherent to Li ion batteries. A critical challenge in advancing Mg batteries is the lack of suitable cathode materials. In this work, we report a cathode design that incorporates S functionality into two-dimensional metal-organic-frameworks (2D-MOFs). This new cathode material enables good Mg2+ storage capacity and outstanding cyclability. It was found that upon the initial Mg2+ insertion and disinsertion, there is an apparent structural transformation that crumbles the layered 2D framework, leading to amorphization. The resulting material serves as the active material to host Mg2+ through reduction and/or oxidation of S and, to a limited extent, O. The reversible nature of S and O redox chemistry was confirmed by spectroscopic characterizations and validated by density functional calculations. Importantly, during the Mg2+ insertion and disinsertion process, the 2D nature of the framework was maintained, which plays a key role in enabling the high reversibility of the MOF cathode. Sulfurized two-dimensional metal-organic framework (2D-MOF) promises high capacity Mg2+ storage. On the one hand, the 2D nature of the material enables fast and reversible Mg2+ diffusion. On the other hand, the S functional groups serve as reversible redox centers to host Mg2+. image
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页数:6
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