Sulfurized Two-Dimensional Conductive Metal-Organic Framework as a High-Performance Cathode Material for Rechargeable Mg Batteries

被引:11
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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