Ma Yuqi, Sung Ki-Wook, Ahn Hyo-Jin
Department of Materials Science and Engineering, Seoul National University of Science and Technology, Seoul 01811, Republic of Korea.
Nanomaterials (Basel). 2023 Jul 18;13(14):2093. doi: 10.3390/nano13142093.
The oxygen reduction reaction is crucial in the cathode of fuel cells and metal-air batteries. Consequently, designing robust and durable ORR catalysts is vital to developing metal-air batteries and fuel cells. Metal-organic frameworks feature an adjustable structure, a periodic porosity, and a large specific surface area, endowing their derivative materials with a unique structure. In this study, F and N co-doped on the carbon support surface (Co/FN-C) via the pyrolysis of ZIF-67 as a sacrificial template while using Co/FN-C as the non-noble metal catalysts. The Co/FN-C displays excellent long-term durability and electrochemical catalytic performance in acidic solutions. These performance improvements are achieved because the CQDs alleviate the structural collapse during the pyrolysis of ZIF-67, which increases the active sites in the Co nanoparticles. Moreover, F- and N-doping improves the catalytic activity of the carbon support by providing additional electrons and active sites. Furthermore, F anions are redox-stable ligands that exhibit long-term operational stability. Therefore, the well-dispersed Co NPs on the surface of the Co/FN-C are promising as the non-noble metal catalysts for ORR.
氧还原反应在燃料电池和金属空气电池的阴极中至关重要。因此,设计坚固耐用的氧还原反应催化剂对于开发金属空气电池和燃料电池至关重要。金属有机框架具有可调节的结构、周期性的孔隙率和大的比表面积,使其衍生材料具有独特的结构。在本研究中,通过热解作为牺牲模板的ZIF-67,在碳载体表面共掺杂F和N(Co/FN-C),同时将Co/FN-C用作非贵金属催化剂。Co/FN-C在酸性溶液中表现出优异的长期耐久性和电化学催化性能。这些性能的提升是因为碳量子点减轻了ZIF-67热解过程中的结构坍塌,从而增加了钴纳米颗粒中的活性位点。此外,F和N掺杂通过提供额外的电子和活性位点提高了碳载体的催化活性。此外,F阴离子是氧化还原稳定的配体,具有长期的操作稳定性。因此,Co/FN-C表面分散良好的钴纳米颗粒有望作为氧还原反应的非贵金属催化剂。