Coordination of Atomic Co–Pt Coupling Species at Carbon Defects as Active Sites for Oxygen Reduction Reaction

Longzhou Zhang, Julia Melisande Theresa Agatha Fischer, Yi Jia, Xuecheng Yan, Wei Xu, Xiyang Wang, Jun Chen, Dongjiang Yang, Hongwei Liu, Linzhou Zhuang, Marlies Hankel, Debra J. Searles, Keke Huang, Shouhua Feng, Christopher L. Brown, Xiangdong Yao

Platinum (Pt) is the state-of-the-art catalyst for oxygen reduction reaction (ORR), but its high cost and scarcity limit its large-scale use. However, if the usage of Pt reduces to a sufficiently low level, this critical barrier may be overcome. Atomically dispersed metal catalysts with high activity and high atom efficiency have the possibility to achieve this goal. Herein, we report a locally distributed atomic Pt-Co nitrogen-carbon-based catalyst (denoted as A-CoPt-NC) with high activity and robust durability for ORR (267 times higher than commercial Pt/C in mass activity). The A-CoPt-NC shows a high selectivity for the 4e- pathway in ORR, differing from the reported 2e- pathway characteristic of atomic Pt catalysts. Density functional theory calculations suggest that this high activity originates from the synergistic effect of atomic Pt-Co located on a defected C/N graphene surface. The mechanism is thought to arise from asymmetry in the electron distribution around the Pt/Co metal centers, as well as the metal atoms' coordination with local environments on the carbon surface. This coordination results from N8V4 vacancies (where N8 represents the number of nitrogen atoms and V4 indicates the number of vacant carbon atoms) within the carbon shell, which enhances the oxygen reduction reaction via the so-called synergistic effect.