Singh Baghendra, Indra Arindam
Department of Chemistry, Indian Institute of Technology (BHU) Varanasi, Uttar Pradesh, 221005, India.
Chem Asian J. 2020 Mar 16;15(6):607-623. doi: 10.1002/asia.201901810. Epub 2020 Feb 21.
To achieve efficient water splitting, it is essential to develop catalysts with high electrochemical performance, enhanced durability and tunable properties. Most of the transition metal-based catalysts employed for the water splitting have been fabricated on the solid-electrode support by using binder, which decreases the activity and durability of the catalyst system. In this respect, self-supported metal organic framework (MOF) derived catalysts have been introduced with enhanced catalytic activity and mechanical stability for the electrochemical water splitting. The self-supported MOF derived catalysts exhibit improved electronic conductivity, high electrochemical surface area, enhanced mechanical stability and strong catalyst-support interaction. Moreover, these catalysts possess highly porous and hollow structure with designed morphology and multi-metallic composition. Recently, a tremendous effort has been provided to explore this newly growing field and new dimensions and directions have been achieved. Looking at this point, we have described here the basic principles of catalyst design from self-supported MOF, structural and interface engineering by controlling the electronic structure of the catalysts to improve the water splitting activity. In addition, the challenges and difficulties associated with this field have been pointed out and addressed for the future progress in this field.
为实现高效的水分解,开发具有高电化学性能、增强的耐久性和可调性能的催化剂至关重要。用于水分解的大多数过渡金属基催化剂是通过使用粘合剂在固体电极载体上制备的,这降低了催化剂体系的活性和耐久性。在这方面,已引入自支撑金属有机框架(MOF)衍生的催化剂,用于电化学水分解,其具有增强的催化活性和机械稳定性。自支撑MOF衍生的催化剂表现出改善的电子导电性、高电化学表面积、增强的机械稳定性和强的催化剂-载体相互作用。此外,这些催化剂具有高度多孔的中空结构,具有设计的形态和多金属组成。最近,人们付出了巨大努力来探索这个新出现的领域,并取得了新的维度和方向。鉴于此,我们在此描述了自支撑MOF催化剂设计的基本原理、通过控制催化剂的电子结构进行结构和界面工程以提高水分解活性。此外,还指出并解决了与该领域相关的挑战和困难,以促进该领域的未来发展。