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A mesoporous carbon-based catalyst derived from cobalt and boron co-doped melamine formaldehyde gel for oxygen reduction reaction

机译:衍生自钴和硼共掺杂三聚氰胺甲醛凝胶的介孔碳基催化剂用于氧还原反应

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摘要

Non-precious metal catalysts are playing an increasingly important role in research on oxygen reduction reaction (ORR) catalysts for fuel cells due to their relatively low cost. In this work, a novel mesoporous catalyst derived from cobalt- and boron-co-doped melamine formaldehyde (MF) gel (Co, B-MF) was successfully synthesized by a facile self-assembly pyrolysis method. It was found that doping of Co and B could provide various active sites and an appropriate pyrolysis temperature was beneficial to increase the number of active sites. As a result, the obtained Co, B-MF-900 catalyst (pyrolyzed at 900 degrees C) exhibited an outstanding ORR performance in 0.1 M KOH solution with a high onset potential of 1.1 V versus reversible hydrogen electrode (vs RHE), which was 0.1 V higher than that of the commercial Johnson Matthey Pt/C. Additionally, Co, B-MF-900 displayed good stability and superior methanol tolerance. The superior ORR performance of Co, B-MF-900 can be attributed to its mesoporous structure, the synergistic effect of active sites, and the excellent conductivity of the carbon carrier. (C) 2019 Elsevier Ltd. All rights reserved.
机译:由于其相对较低的成本,非贵金属催化剂在对燃料电池的氧还原反应(ORR)催化剂的研究中起着越来越重要的作用。在这项工作中,通过容易自组装热解法成功地合成了衍生自钴和硼 - 共掺杂三聚氰胺甲醛(MF)凝胶(CO,B-MF)的新型介孔催化剂。结果发现CO和B的掺杂可以提供各种活性位点,并且适当的热解温有利于增加活性位点的数量。结果,所得CO,B-MF-900催化剂(在900℃下热解)在0.1M KOH溶液中表现出优异的ORR性能,具有1.1V的高发起潜力与可逆氢电极(Vs RHE),这是0.1V高于商业约翰逊Matthey Pt / c的0.1V。另外,CO,B-MF-900显示出良好的稳定性和优异的甲醇耐受性。 CO,B-MF-900的卓越ORR性能可归因于其中孔结构,活性位点的协同效应和碳载体的优异导电性。 (c)2019 Elsevier Ltd.保留所有权利。

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