Zhao Tao, Wang Dong, Cheng Chen, Zhong Dazhong, Hao Genyan, Liu Guang, Li Jinping, Zhao Qiang
College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan, 030024, Shanxi, P. R. China.
Shanxi Key Laboratory of Gas Energy Efficient and Clean Utilization, Taiyuan, 030024, Shanxi, P. R. China.
Chem Asian J. 2021 Jan 4;16(1):64-71. doi: 10.1002/asia.202001235. Epub 2020 Nov 30.
Although metal-organic frameworks have proven to be excellent electrocatalytic materials, their application as electrode materials remains limited. The preparation of heterostructures is considered an effective method to improve catalytic activity. Herein, we describe the design and assembly of a dual-MOF heterostructure (CoNi-ZIF-67@Fe-MIL-100, denoted ZIF@MIL). Specifically, we grew a layer of MIL-100 in situ on a bimetallic ZIF-67 surface using a solvothermal method. We demonstrate that the ZIF@MIL has remarkable OER electrocatalytic performance, requiring a low overpotential and showing a small Tafel slope, compared to pure ZIF-67 and MIL-100 in 1.0 m KOH. More importantly, it has excellent operational durability for 50 h at 100 mA cm . The high catalytic activity of ZIF@MIL can be attributed to the heterostructure that can expose more active sites, the synergistic effect between ZIF-67 and MIL-100, and improvement of electron transfer ability. Our work provides a new way to design and prepare dual-MOF crystals with different structures as electrocatalysts.
尽管金属有机框架已被证明是优异的电催化材料,但其作为电极材料的应用仍然有限。制备异质结构被认为是提高催化活性的有效方法。在此,我们描述了一种双金属有机框架异质结构(CoNi-ZIF-67@Fe-MIL-100,记为ZIF@MIL)的设计与组装。具体而言,我们采用溶剂热法在双金属ZIF-67表面原位生长了一层MIL-100。我们证明,与1.0 m KOH中的纯ZIF-67和MIL-100相比,ZIF@MIL具有卓越的析氧反应(OER)电催化性能,所需过电位低且塔菲尔斜率小。更重要的是,它在100 mA cm下具有50 h的优异操作耐久性。ZIF@MIL的高催化活性可归因于能暴露更多活性位点的异质结构、ZIF-67与MIL-100之间的协同效应以及电子转移能力的提高。我们的工作为设计和制备具有不同结构的双金属有机框架晶体作为电催化剂提供了一种新方法。