Zhou Qingyan, Cai Jiajun, Zhang Zhen, Gao Rui, Chen Bo, Wen Guobin, Zhao Lei, Deng Yaping, Dou Haozhen, Gong Xiaofei, Zhang Yunlong, Hu Yongfeng, Yu Aiping, Sui Xulei, Wang Zhenbo, Chen Zhongwei
MIIT Key Laboratory of Critical Materials Technology for New Energy Conversion and Storage, State Key Lab of Urban Water Resource and Environment, School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin, 150001, P. R. China.
Department of Chemical Engineering, Waterloo Institute for Nanotechnology, Waterloo Institute for Sustainable Energy, University of Waterloo, Waterloo, Ontario, N2L 3G1, Canada.
Small Methods. 2021 Jun;5(6):e2100024. doi: 10.1002/smtd.202100024. Epub 2021 Apr 22.
Mn and N codoped carbon materials are proposed as one of the most promising catalysts for the oxygen reduction reaction (ORR) but still confront a lot of challenges to replace Pt. Herein, a novel gas-phase migration strategy is developed for the scale synthesis of atomically dispersed Mn and N codoped carbon materials (g-SA-Mn) as highly effective ORR catalysts. Porous zeolitic imidazolate frameworks serve as the appropriate support for the trapping and anchoring of Mn-containing gaseous species and the synchronous high-temperature pyrolysis process results in the generation of atomically dispersed Mn-N active sites. Compared to the traditional liquid phase synthesis method, this unique strategy significantly increases the Mn loading and enables homogeneous dispersion of Mn atoms to promote the exposure of Mn-N active sites. The developed g-SA-Mn-900 catalyst exhibits excellent ORR performance in the alkaline media, including a high half-wave potential (0.90 V vs reversible hydrogen electrode), satisfactory durability, and good catalytic selectivity. In the practical application, the Zn-air battery assembled with g-SA-Mn-900 catalysts shows high power density and prominent durability during the discharge process, outperforming the commercial Pt/C benchmark. Such a gas-phase synthetic methodology offers an appealing and instructive guide for the logical synthesis of atomically dispersed catalysts.
锰和氮共掺杂的碳材料被认为是氧还原反应(ORR)最有前景的催化剂之一,但在取代铂方面仍面临诸多挑战。在此,开发了一种新颖的气相迁移策略,用于规模化合成原子分散的锰和氮共掺杂碳材料(g-SA-Mn)作为高效的ORR催化剂。多孔沸石咪唑框架作为捕获和锚定含锰气态物种的合适载体,同步高温热解过程导致生成原子分散的Mn-N活性位点。与传统的液相合成方法相比,这种独特的策略显著提高了锰负载量,并使锰原子均匀分散,促进了Mn-N活性位点的暴露。所开发的g-SA-Mn-900催化剂在碱性介质中表现出优异的ORR性能,包括高半波电位(相对于可逆氢电极0.90 V)、令人满意的耐久性和良好的催化选择性。在实际应用中,用g-SA-Mn-900催化剂组装的锌空气电池在放电过程中显示出高功率密度和突出的耐久性,优于商业Pt/C基准。这种气相合成方法为原子分散催化剂的合理合成提供了有吸引力和启发性的指导。