Sun Hanxue, Wang Juanjuan, Li Mengxue, Jiao Rui, Zhu Zhaoqi, Li An
Department of Chemical Engineering, College of Petrochemical Engineering, Lanzhou University of Technology, Lanzhou 730050, PR China.
Department of Chemical Engineering, College of Petrochemical Engineering, Lanzhou University of Technology, Lanzhou 730050, PR China.
J Colloid Interface Sci. 2024 Nov;673:354-364. doi: 10.1016/j.jcis.2024.06.068. Epub 2024 Jun 8.
Porous iron-nitrogen-doped carbons (FeNC) offer a great platform for construction of cathodic oxygen reduction reaction (ORR) catalysts in fuel cells. However, challenges still remain regarding with the collapse of carbon-skeleton during pyrolysis, uneven distribution of active sites and aggregation of metal atoms. In this work, we synthesized Fe, N co-doped conjugated microporous polymer (FeN-CMP) through a facile bottom-up strategy using 1,3,5-triethynylbenzene and iron-chelated 3,8-dibromo-1,10-phenanthroline as monomers, ensuring the uniform coordination of N with Fe element in network. Then, the resulting FeN-CMP was treated by pyrolysis without structural collapse to obtain porous FeNC electrocatalyst for ORR. The most active catalyst was fabricated under 900 °C, which exhibits remarkable ORR activity in alkaline medium with half-wave potential of 0.796 V (18 mV and 105 mV positive deviation from the commercial Pt/C catalyst and post-doping catalyst), high selectivity with nearly 4e transfer process and excellent methanol tolerance. Our study first developed porous FeNC electrocatalysts derived from Fe, N-anchoring CMPs based on pre-functionalization of monomers, which exhibits great potential as an alternative to commercial Pt/C catalyst for ORR, and provides a feasible strategy of developing multi-atoms doping catalysts for energy storage and conversion as well as heterogeneous catalysis.
多孔铁氮掺杂碳(FeNC)为燃料电池中阴极氧还原反应(ORR)催化剂的构建提供了一个很好的平台。然而,在热解过程中碳骨架的坍塌、活性位点分布不均以及金属原子的聚集等问题仍然存在。在这项工作中,我们采用一种简便的自下而上策略,以1,3,5-三乙炔基苯和铁螯合的3,8-二溴-1,10-菲咯啉为单体,合成了铁、氮共掺杂的共轭微孔聚合物(FeN-CMP),确保了氮与铁元素在网络中的均匀配位。然后,对所得的FeN-CMP进行热解处理而不发生结构坍塌,以获得用于ORR的多孔FeNC电催化剂。最具活性的催化剂是在900℃下制备的,它在碱性介质中表现出显著的ORR活性,半波电位为0.796 V(比商业Pt/C催化剂和后掺杂催化剂正偏移18 mV和105 mV),具有近4e转移过程的高选择性和优异的甲醇耐受性。我们的研究首次基于单体的预功能化开发了源自铁、氮锚定CMPs的多孔FeNC电催化剂,它作为ORR商业Pt/C催化剂替代品具有巨大潜力,并为开发用于能量存储和转换以及多相催化的多原子掺杂催化剂提供了一种可行策略。