Yanan Qi, H. Chen, Feng Hong, Xiangbin Cai, Zhehan Ying, Jiangyong Diao, Zhimin Jia, Jiawei Chen, Ning Wang, Shengling Xiang, Xiaowen Chen, Guodong Wen, Bo Sun, Geng Sun, Hongyang Liu
Abstract Single-atom catalysts (SACs) have demonstrated excellent performance in heterogeneous catalytic reactions owing to their maximized atomic efficiency, distinctive geometric, and electronic configurations. However, the efficacy of SACs remains limited for certain reactions requiring simultaneous activation of multiple reactants over metallic active sites. Herein, we report an atomically dispersed Pt 1 Ru 1 dual-atom pair site anchored on nanodiamond@graphene (ND@G) for CO oxidation. The Pt 1 Ru 1 dual-atom catalyst shows an exceptional turnover frequency (TOF) of 17.6 × 10 −2 s −1 at significantly lower temperature (30 °C), achieving a tenfold increase in TOF compared to single-atom Pt 1 /ND@G catalyst (1.5 × 10 −2 s −1 ) and surpassing to previously reported Pt-based catalysts under similar conditions. Moreover, the catalyst demonstrates excellent stability, maintaining its activity for 40 h at 80 °C without significant deactivation. The superior catalytic performance of Pt-Ru dual-atom catalysts is attributed to the synergistic effect between Pt and Ru atoms with enhanced metallicity for improving simultaneous adsorption and activation of CO and O 2 , and the tuning of conventional competitive reactant adsorption into a non-competitive pathway over dual-atom pair sites. The present work manifests the advantages of dual-atom pair sites in heterogeneous catalysis and paves the way for precise design of catalysts at the atomic scale.