Atomically Dispersed Binary Co-Ni Sites in Nitrogen-Doped Hollow Carbon Nanocubes for Reversible Oxygen Reduction and Evolution

© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 31(2019), 49 vom: 22. Dez., Seite e1905622
1. Verfasser: Han, Xiaopeng (VerfasserIn)
Weitere Verfasser: Ling, Xiaofei, Yu, Deshuang, Xie, Dengyu, Li, Linlin, Peng, Shengjie, Zhong, Cheng, Zhao, Naiqin, Deng, Yida, Hu, Wenbin
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2019
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article binary sites metal-air batteries oxygen reduction/evolution single-atom catalysts synergistic effects
Beschreibung
Zusammenfassung:© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
With the inspiration of developing bifunctional electrode materials for reversible oxygen electrocatalysis, one strategy of heteroatom doping is proposed to fabricate dual metal single-atom catalysts. However, the identification and mechanism functions of polynary single-atom structures remain elusive. Atomically dispersed binary Co-Ni sites embedded in N-doped hollow carbon nanocubes (denoted as CoNi-SAs/NC) are synthesized via proposed pyrolysis of dopamine-coated metal-organic frameworks. The atomically isolated bimetallic configuration in CoNi-SAs/NC is identified by combining microscopic and spectroscopic techniques. When employing as oxygen electrocatalysts in alkaline medium, the resultant CoNi-SAs/NC hybrid manifests outstanding catalytic performance for bifunctional oxygen reduction/evolution reactions, boosting the realistic rechargeable zinc-air batteries with high efficiency, low overpotential, and robust reversibility, superior to other counterparts and state-of-the-art precious-metal catalysts. Theoretical computations based on density functional theory demonstrate that the homogenously dispersed single atoms and the synergistic effect of neighboring Co-Ni dual metal center can optimize the adsorption/desorption features and decrease the overall reaction barriers, eventually promoting the reversible oxygen electrocatalysis. This work not only sheds light on the controlled synthesis of atomically isolated advanced materials, but also provides deeper understanding on the structure-performance relationships of nanocatalysts with multiple active sites for various catalytic applications
Beschreibung:Date Completed 09.12.2019
Date Revised 30.09.2020
published: Print-Electronic
Citation Status PubMed-not-MEDLINE
ISSN:1521-4095
DOI:10.1002/adma.201905622