| Literature DB >> 27323284 |
Zhishan Luo1, Erdem Irtem1, Maria Ibáñez1, Raquel Nafria1, Sara Martı́-Sánchez2, Aziz Genç2, Maria de la Mata2, Yu Liu1, Doris Cadavid1, Jordi Llorca3, Jordi Arbiol2,4, Teresa Andreu1, Joan Ramon Morante1,5, Andreu Cabot1,4.
Abstract
Mn3O4@CoMn2O4 nanoparticles (NPs) were produced at low temperature and ambient atmosphere using a one-pot two-step synthesis protocol involving the cation exchange of Mn by Co in preformed Mn3O4 NPs. Selecting the proper cobalt precursor, the nucleation of CoxOy crystallites at the Mn3O4@CoMn2O4 surface could be simultaneously promoted to form Mn3O4@CoMn2O4-CoxOy NPs. Such heterostructured NPs were investigated for oxygen reduction and evolution reactions (ORR, OER) in alkaline solution. Mn3O4@CoMn2O4-CoxOy NPs with [Co]/[Mn] = 1 showed low overpotentials of 0.31 V at -3 mA·cm(-2) and a small Tafel slope of 52 mV·dec(-1) for ORR, and overpotentials of 0.31 V at 10 mA·cm(-2) and a Tafel slope of 81 mV·dec(-1) for OER, thus outperforming commercial Pt-, IrO2-based and previously reported transition metal oxides. This cation-exchange-based synthesis protocol opens up a new approach to design novel heterostructured NPs as efficient nonprecious metal bifunctional oxygen catalysts.Entities:
Keywords: OER; ORR; cation exchange; cobalt oxide; colloidal; electrocatalysis; manganese oxide; nanoparticle
Year: 2016 PMID: 27323284 DOI: 10.1021/acsami.6b02786
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229