Liu Yong, Su Miaojun, Li Dahuan, Li Shenshen, Li Xiying, Zhao Junwei, Liu Fujian
Henan Key Laboratory of Polyoxometalate Chemistry, College of Chemistry and Chemical Engineering, Henan University Kaifeng 475004 P. R. China
National Engineering Research Center of Chemical Fertilizer Catalyst (NERC-CFC), School of Chemical Engineering, Fuzhou University Fuzhou 350002 P. R. China
RSC Adv. 2020 Feb 13;10(12):6763-6771. doi: 10.1039/c9ra07539a.
The development of highly efficient oxygen reduction reaction (ORR) catalysts is of great significance for the large-scale commercialization of fuel cells. In this work, honeycomb-like Fe-N co-doped porous carbon materials (Fe-N-PC) were prepared through a facile one-step pyrolysis strategy using soybean straw biomass as the precursor. The obtained Fe-N-PC catalyst exhibits excellent ORR performance with an onset potential of 0.989 V and a half-wave potential of 0.854 V in alkaline conditions, which positively shift only by 5 mV and 27 mV, respectively than those of the commercial Pt/C catalyst. Furthermore, the onset potential and the half-wave potential of the Fe-N-PC catalysts are up to 0.886 V and 0.754 V, respectively, under acidic conditions, which are superior to those of many other Fe, N-doped electrocatalysts. The ORR process can be regarded as a four-electron transfer process based on RRDE measurements. Moreover, the Fe-N-PC catalyst also shows greater stability and satisfactory methanol tolerance than the Pt/C catalyst. The superior electrocatalytic performance of Fe-N-PC may be attributed to the abundant nanoporous structure, large BET surface area, and Fe-N co-doping, which provide abundant and highly efficient active sites.
高效氧还原反应(ORR)催化剂的开发对于燃料电池的大规模商业化具有重要意义。在这项工作中,以大豆秸秆生物质为前驱体,通过简便的一步热解策略制备了蜂窝状Fe-N共掺杂多孔碳材料(Fe-N-PC)。所制备的Fe-N-PC催化剂在碱性条件下表现出优异的ORR性能,起始电位为0.989 V,半波电位为0.854 V,与商业Pt/C催化剂相比,正向偏移仅分别为5 mV和27 mV。此外,在酸性条件下,Fe-N-PC催化剂的起始电位和半波电位分别高达0.886 V和0.754 V,优于许多其他Fe、N掺杂的电催化剂。基于旋转环盘电极(RRDE)测量,ORR过程可视为四电子转移过程。此外,Fe-N-PC催化剂还表现出比Pt/C催化剂更高的稳定性和令人满意的甲醇耐受性。Fe-N-PC优异的电催化性能可能归因于丰富的纳米多孔结构、大的比表面积以及Fe-N共掺杂,它们提供了丰富且高效的活性位点。