Department of Mechanical Engineering, University of Wisconsin-Milwaukee, 3200 North Cramer Street, Milwaukee, WI, 53211, USA.
Department of Chemistry and Food Chemistry, Technische Universitaet Dresden, 01062, Dresden, Germany.
Small. 2015 Nov 25;11(44):5940-8. doi: 10.1002/smll.201502297. Epub 2015 Oct 9.
A novel 3D nanoarchitecture comprising in situ-formed N-doped CoNi alloy-encapsulated carbon nanotubes (CoNi-NCNTs) grown on N-doped porous carbon nanosheets (NPCNs) is designed and constructed for both oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). When evaluated as an electrocatalyst for ORR, the hybrid shows efficient catalytic activity, high selectivity, superior durability, and strong tolerance against methanol crossover compared with the commercial Pt/C catalyst. Such good oxygen reduction reaction performance is comparable to most of the previously reported results and the synergistic effect is found to boost the catalytic performance. Moreover, the constructed hybrid exhibits an excellent ORR activity with a current density of 10 mA cm(-2) at 1.59 V and an onset potential of 1.57 V, even beyond the state-of-the-art Ir/C catalyst in alkaline media. The enhancement in electrochemical performance can be attributed to the unique morphology and defect structures, high porosity, good conductive networks, and strongly interacting CoNi-NCNT and NPCN in the hybrid. These results suggest the possibility for the development of effective nanocarbon electrocatalysts to replace commercial noble metal catalysts for direct use in fuel cells and water splitting devices.
一种新颖的 3D 纳米结构由原位形成的氮掺杂 CoNi 合金封装的碳纳米管(CoNi-NCNTs)组成,生长在氮掺杂多孔碳纳米片(NPCNs)上,用于氧还原反应(ORR)和析氧反应(OER)。当作为 ORR 的电催化剂进行评估时,与商业 Pt/C 催化剂相比,该杂化材料表现出高效的催化活性、高选择性、卓越的耐久性和对甲醇交叉的强耐受性。这种良好的氧还原反应性能可与大多数先前报道的结果相媲美,并且发现协同效应可提高催化性能。此外,构建的杂化材料在碱性介质中具有出色的 ORR 活性,在 1.59 V 时的电流密度为 10 mA cm(-2),起始电位为 1.57 V,甚至超过了最先进的 Ir/C 催化剂。电化学性能的增强可归因于独特的形态和缺陷结构、高孔隙率、良好的导电网络以及在杂化材料中强烈相互作用的 CoNi-NCNT 和 NPCN。这些结果表明,有可能开发有效的纳米碳电催化剂来替代商业贵金属催化剂,直接用于燃料电池和水分解装置。