| Literature DB >> 33786969 |
Miaomiao Tong1, Fanfei Sun2,3, Ying Xie4, Ying Wang1, Yuqi Yang2,3, Chungui Tian4, Lei Wang4, Honggang Fu4.
Abstract
Dual-metal single-atom catalysts exhibit superior performance for oxygen reduction reaction (ORR), however, the synergistic catalytic mechanism is not deeply understood. Herein, we report a dual-metal single-atom catalyst consisted of Cu-N4 and Zn-N4 on the N-doped carbon support (Cu/Zn-NC). It exhibits high-efficiency ORR activity with an Eonset of 0.98 V and an E1/2 of 0.83 V, excellent stability (no degradation after 10 000 cycles), surpassing state-of-the-art Pt/C and great mass of Pt-free single atom catalysts. Operando XANES demonstrates that the Cu-N4 as active center experiences the change from atomic dispersion to cluster with the cooperation of Zn-N4 during ORR process, and then turns to single atom state again after reaction. DFT calculation further indicates that the adjustment effect of Zn on the d-orbital electron distribution of Cu could benefit to the stretch and cleavage of O-O on Cu active center, speeding up the process of rate determining step of OOH*.Entities:
Keywords: cooperative catalysis; dual-metal single atom; mechanism; operando XANES; oxygen reduction reaction
Year: 2021 PMID: 33786969 DOI: 10.1002/anie.202102053
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336