Loading…
Engineering High‐Energy Interfacial Structures for High‐Performance Oxygen‐Involving Electrocatalysis
Engineering high‐energy interfacial structures for high‐performance electrocatalysis is achieved by chemical coupling of active CoO nanoclusters and high‐index facet Mn3O4 nano‐octahedrons (hi‐Mn3O4). A thorough characterization, including synchrotron‐based near edge X‐ray absorption fine structure,...
Saved in:
Published in: | Angewandte Chemie International Edition 2017-07, Vol.56 (29), p.8539-8543 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Engineering high‐energy interfacial structures for high‐performance electrocatalysis is achieved by chemical coupling of active CoO nanoclusters and high‐index facet Mn3O4 nano‐octahedrons (hi‐Mn3O4). A thorough characterization, including synchrotron‐based near edge X‐ray absorption fine structure, reveals that strong interactions between both components promote the formation of high‐energy interfacial Mn‐O‐Co species and high oxidation state CoO, from which electrons are drawn by MnIII‐O present in hi‐Mn3O4. The CoO/hi‐Mn3O4 demonstrates an excellent catalytic performance over the conventional metal oxide‐based electrocatalysts, which is reflected by 1.2 times higher oxygen evolution reaction (OER) activity than that of Ru/C and a comparable oxygen reduction reaction (ORR) activity to that of Pt/C as well as a better stability than that of Ru/C (95 % vs. 81 % retained OER activity) and Pt/C (92 % vs. 78 % retained ORR activity after 10 h running) in alkaline electrolyte.
Nanocatalysis: Engineering high‐energy interfacial structures is achieved by chemical coupling of active CoO nanoclusters with high‐index facet Mn3O4 nano‐octahedrons. The structures display synergistic effects enhancing their electrocatalytic performance and stability as compared to conventional electrocatalysts for bifunctional oxygen‐involving reactions. |
---|---|
ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.201701531 |