Synergistically Enhanced Oxygen Evolution Reaction Catalysis for Multielement Transition-Metal Oxides
Autor: | Kaisei Asai, Saori I. Kawaguchi, Tasuku Uchimura, Ikuya Yamada, Shunsuke Yagi, T. Shirakawa, Hidekazu Ikeno, Akihiko Takamatsu, Hideo Ohzuku, Hirofumi Tsukasaki, Kouhei Wada, Shigeo Mori |
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Rok vydání: | 2018 |
Předmět: |
Materials science
Inorganic chemistry Oxide Oxygen evolution Energy Engineering and Power Technology 02 engineering and technology Materials design 010402 general chemistry 021001 nanoscience & nanotechnology Electrochemistry 01 natural sciences Transition metal ions 0104 chemical sciences Catalysis chemistry.chemical_compound chemistry Transition metal Materials Chemistry Chemical Engineering (miscellaneous) Electrical and Electronic Engineering 0210 nano-technology Perovskite (structure) |
Zdroj: | ACS Applied Energy Materials. 1:3711-3721 |
ISSN: | 2574-0962 |
DOI: | 10.1021/acsaem.8b00511 |
Popis: | Transition metal oxides have been extensively investigated as novel catalysts for oxygen evolution reaction (OER). Partial elemental substitutions are effective ways to increase catalytic performance and such electronic interactions between multiple elements are known as synergistic effects. However, serious issues such as random atomic arrangement and ambiguous roles of constituent elements humper theoretical investigations for rational materials design. Herein, we describe systematic study on OER activity of AA′3B4O12-type quadruple perovskite oxides, in which multiple transition metal ions are located at distinct crystallographic sites. Electrochemical measurements demonstrate that OER catalytic activities of quadruple perovskite oxide series, CaCu3B4O12 (B = Ti, V, Cr, Mn, Fe, and Co), are all superior to those of simple perovskite counterparts CaBO3. The order of activity of B-site transition metal ions for CaBO3 (Fe4+ > Co4+ ≫ Ti4+, V4+, Cr4+, Mn4+) is retained in CaCu3B4O12, indicating that B-site ... |
Databáze: | OpenAIRE |
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