Fan Chenming, Dou Shixue, Zhan Xiaoqiang, Li Shenggang, Wang Qiang, Li Bing
School of Mechanical and Power Engineering, East China University of Science and Technology, Shanghai 200237, People's Republic of China.
Institute of Energy Materials Science, University of Shanghai for Science and Technology, Shanghai 200093, People's Republic of China.
Nano Lett. 2024 Jun 12;24(23):6957-6964. doi: 10.1021/acs.nanolett.4c01226. Epub 2024 May 28.
Highly active and robust Pt-based electrocatalysts for an oxygen reduction reaction (ORR) are of crucial significance for the development of proton exchange membrane fuel cells (PEMFCs). Herein, the high-loading and well-dispersive Pt clusters on graphitic carbon-supported CeO with abundant oxygen vacancies (Pt/CeO-O@GC) were successfully fabricated by a molten-salt electrochemical-assisted method. The bonding of Pt with the highly electronegative O induces charge redistribution through the Pt-O-Ce structure, thus reducing the adsorption energies of oxygen-containing species. Such a Pt/CeO-O@GC electrocatalyst exhibits a greatly enhanced ORR performance with a mass activity of 0.41 ± 0.02 A·mg at 0.9 V versus a reversible hydrogen electrode, which is 2.7 times the value of a commercial Pt/C catalyst and shows negligible activity decay after 20000 cycles of accelerated degradation tests. It is anticipated that this work will provide enlightening guidance on the controllable synthesis and rational design of high-performance Pt-based electrocatalysts for PEMFCs.
用于氧还原反应(ORR)的高活性和稳健的铂基电催化剂对于质子交换膜燃料电池(PEMFC)的发展至关重要。在此,通过熔盐电化学辅助方法成功制备了具有丰富氧空位的石墨碳负载CeO上的高负载且分散良好的铂簇(Pt/CeO-O@GC)。Pt与高电负性O的键合通过Pt-O-Ce结构诱导电荷重新分布,从而降低含氧化合物的吸附能。这种Pt/CeO-O@GC电催化剂在相对于可逆氢电极0.9 V时表现出大大增强的ORR性能,质量活性为0.41±0.02 A·mg,是商业Pt/C催化剂值的2.7倍,并且在20000次加速降解测试后活性衰减可忽略不计。预计这项工作将为PEMFC高性能铂基电催化剂的可控合成和合理设计提供启发性指导。