Deng Shenzhen, Xu Bingang, Zhao Jingxin, Kan Chi Wai, Liu Xinlong
Nanotechnology Center, School of Fashion and Textiles, The Hong Kong Polytechnic University, Hung Hom, Kowloon, 999077, Hong Kong.
Angew Chem Int Ed Engl. 2024 Apr 22;63(17):e202401996. doi: 10.1002/anie.202401996. Epub 2024 Mar 20.
Metal-organic frameworks (MOFs) show wide application as the cathode of aqueous zinc-ion batteries (AZIBs) in the future owning to their high porosity, diverse structures, abundant species, and controllable morphology. However, the low energy density and poor cycling stability hinder the feasibility in practical application. Herein, an innovative strategy of organic/inorganic double electroactive sites is proposed and demonstrated to obtain extra capacity and enhance the energy density in a manganese-based metal-organic framework (Mn-MOF-74). Simultaneously, its energy storage mechanism is systematically investigated. Moreover, profiting from the coordination effect, the Mn-MOF-74 features with stable structure in ZnSO electrolyte. Therefore, the Zn/Mn-MOF-74 batteries exhibit a high energy density and superior cycling stability. This work aids in the future development of MOFs in AZIBs.
金属有机框架材料(MOFs)因其高孔隙率、多样的结构、丰富的种类和可控的形态,在未来作为水系锌离子电池(AZIBs)的阴极具有广泛的应用前景。然而,低能量密度和较差的循环稳定性阻碍了其在实际应用中的可行性。在此,我们提出并证明了一种有机/无机双电活性位点的创新策略,以在锰基金属有机框架(Mn-MOF-74)中获得额外的容量并提高能量密度。同时,系统地研究了其储能机制。此外,得益于配位效应,Mn-MOF-74在ZnSO电解质中具有稳定的结构。因此,Zn/Mn-MOF-74电池表现出高能量密度和优异的循环稳定性。这项工作有助于MOFs在AZIBs中的未来发展。