Chen Guangbo, Zhong Haixia, Feng Xinliang
Center for Advancing Electronics Dresden (cfaed) and Faculty of Chemistry and Food Chemistry, Technische Universität Dresden Mommsenstr. 4 01062 Dresden Germany
Department of Synthetic Materials and Functional Devices, Max Planck Institute of Microstructure Physics Weinberg 2 Halle (Saale) D-06120 Germany.
Chem Sci. 2021 Nov 10;12(48):15802-15820. doi: 10.1039/d1sc05867c. eCollection 2021 Dec 15.
The electrocatalytic oxygen reduction reaction (ORR) is the vital process at the cathode of next-generation electrochemical storage and conversion technologies, such as metal-air batteries and fuel cells. Single-metal-atom and nitrogen co-doped carbonaceous electrocatalysts (M-N-C) have emerged as attractive alternatives to noble-metal platinum for catalyzing the kinetically sluggish ORR due to their high electrical conductivity, large surface area, and structural tunability at the atomic level, however, their application is limited by the low intrinsic activity of the metal-nitrogen coordination sites (M-N ) and inferior site density. In this Perspective, we summarize the recent progress and milestones relating to the active site engineering of single atom carbonous electrocatalysts for enhancing the ORR activity. Particular emphasis is placed on the emerging strategies for regulating the electronic structure of the single metal site and populating the site density. In addition, challenges and perspectives are provided regarding the future development of single atom carbonous electrocatalysts for the ORR and their utilization in practical use.
电催化氧还原反应(ORR)是下一代电化学储能和转换技术(如金属空气电池和燃料电池)阴极的关键过程。单金属原子与氮共掺杂的碳质电催化剂(M-N-C)因其高电导率、大表面积以及原子水平上的结构可调性,已成为催化动力学缓慢的ORR的贵金属铂的有吸引力替代品。然而,它们的应用受到金属氮配位位点(M-N)固有活性低和位点密度低的限制。在这篇展望文章中,我们总结了与单原子碳质电催化剂活性位点工程相关的最新进展和里程碑,以提高ORR活性。特别强调了调节单金属位点电子结构和增加位点密度的新兴策略。此外,还提供了关于单原子碳质电催化剂用于ORR的未来发展及其在实际应用中的利用的挑战和展望。