Song Kunpeng, Li Guanghui, Yu Junchen, Zheng Tianyue, Wang Jingyu
Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education), Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, 1037 Luoyu Road, Wuhan 430074, China; Chemical Synthesis and Pollution Control Key Laboratory of Sichuan Province, College of Chemistry and Chemical Engineering, China West Normal University, 1 Shida Road, Nanchong 637009, China.
Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education), Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, 1037 Luoyu Road, Wuhan 430074, China.
J Colloid Interface Sci. 2025 Feb;679(Pt B):364-372. doi: 10.1016/j.jcis.2024.10.096. Epub 2024 Oct 19.
Efficient methods for preparing carbon nanotube (CNT)-confined metal catalysts are of great significance for electrocatalysis. Hence, in this study, Fe and Co promoters were added to the precursors of commercial carbon black and melamine to form N-doped CNTs confined bimetallic catalysts (FeCo@N-CNTs) via in situ pyrolysis. The FeCo@N-CNT catalysts exhibited a bamboo-like morphology with FeCo alloy nanoparticles encapsulated in the CNTs and high activity toward the oxygen reduction reaction, with a half-wave potential of 0.864 mV, higher than that of commercial Pt/C (0.827 mV) in alkaline solutions. The catalytic performance is attributable to the synergistic effects between the FeCo alloy and N-doped CNT structure. Moreover, the confinement of the FeCo nanoparticles inside the CNTs imparted the prepared catalysts with resistance to methanol poisoning and long-term stability. This versatile method of synthesizing CNTs directly from carbon black provides a new strategy for preparing high-performance non-precious-metal-based N-doped CNT catalysts for practical fuel cell applications.
制备碳纳米管(CNT)限域金属催化剂的有效方法对电催化具有重要意义。因此,在本研究中,将铁和钴促进剂添加到商用炭黑和三聚氰胺的前驱体中,通过原位热解形成氮掺杂碳纳米管限域双金属催化剂(FeCo@N-CNTs)。FeCo@N-CNT催化剂呈现出竹状形态,FeCo合金纳米颗粒封装在碳纳米管中,并且对氧还原反应具有高活性,在碱性溶液中的半波电位为0.864 mV,高于商用Pt/C(0.827 mV)。催化性能归因于FeCo合金与氮掺杂碳纳米管结构之间的协同效应。此外,碳纳米管内部FeCo纳米颗粒的限域作用使制备的催化剂具有抗甲醇中毒性能和长期稳定性。这种直接从炭黑合成碳纳米管的通用方法为制备用于实际燃料电池应用的高性能非贵金属基氮掺杂碳纳米管催化剂提供了一种新策略。