Wen Hui, Zhang Shengqi, Yu Tao, Yi Ziyu, Guo Rui
School of Materials Science and Engineering, Northeastern University, Shenyang 110819, China.
Nanoscale. 2021 Jul 28;13(28):12058-12087. doi: 10.1039/d1nr01669e. Epub 2021 Jul 7.
As a new type of crystalline porous material, the imidazole zeolite framework (ZIF) has attracted widespread attention due to its ultra-high surface area, large pore volume, and unique advantage of easy functionalization. Developing different methods to control the shape and composition of ZIF is very important for its practical application as catalyst. In recent years, nano-ZIF has been considered an electrode material with excellent oxygen evolution reaction (OER) performance, which provides a new way to research electrolyzed water. This review focuses on the morphological engineering of the original ZIF-67 and its derivatives (core-shell, hollow, and array structures) through doping (cation doping, anion doping, and co-doping), derivative composition engineering (metal oxide, phosphide, sulfide, selenide, and telluride), and the corresponding single-atom catalysis. Besides, combined with DFT calculations, it emphasizes the in-depth understanding of actual active sites and provides insights into the internal mechanism of enhancing the OER and proposes the challenges and prospects of ZIF-67 based electrocatalysts. We summarize the application of ZIF-67 and its derivatives in the OER for the first time, which has significantly guided research in this field.
作为一种新型的晶体多孔材料,咪唑沸石骨架(ZIF)因其超高的比表面积、大孔容以及易于功能化的独特优势而备受关注。开发不同方法来控制ZIF的形状和组成对于其作为催化剂的实际应用非常重要。近年来,纳米ZIF被认为是一种具有优异析氧反应(OER)性能的电极材料,这为研究电解水提供了新途径。本综述重点介绍了通过掺杂(阳离子掺杂、阴离子掺杂和共掺杂)、衍生物组成工程(金属氧化物、磷化物、硫化物、硒化物和碲化物)以及相应的单原子催化对原始ZIF-67及其衍生物(核壳、中空和阵列结构)进行的形态工程。此外,结合密度泛函理论(DFT)计算,强调了对实际活性位点的深入理解,深入探讨了增强OER的内在机制,并提出了基于ZIF-67的电催化剂面临的挑战和前景。我们首次总结了ZIF-67及其衍生物在OER中的应用,这对该领域的研究具有重要的指导意义。