Affiliation:
1. Graduate School of Engineering Tohoku University 6‐6‐01 Aoba, Aramaki, Aoba‐ku Sendai 980‐8579 Japan
2. Institute of Multidisciplinary Research for Advanced Materials Tohoku University 2‐1‐1, Katahira Aoba‐ku Sendai 980‐8577 Japan
3. Department of Applied Quantum Physics and Nuclear Engineering Kyushu University 744 Motooka, Nishi‐ku Fukuoka 819‐0395 Japan
4. Department of Chemistry Graduate School of Science Tokyo Metropolitan University 1‐1 Minami Osawa, Hachioji Tokyo 192‐0397 Japan
Abstract
AbstractInstead of conventional cation doping strategy, anion doping is a promising new strategy for advances of energy conversion and storage technologies such as batteries, catalysts, electrolysis, and fuel cells. To synthesize mixed‐anion compounds, novel synthesis techniques such as topochemical reaction, high‐pressure reaction, solvothermal reaction have been developed. Despite these excellent synthesis techniques, synthesizable mixed‐anion compounds are still limited. For further expansion of the material exploration of mixed‐anion compounds, herein, an electrochemical anion doping technique is developed, which can flexibly control a species of anion, the doping rate and the degree of anion doping. The concept of the new synthesis technique is verified by F doping to the perovskite oxide La0.5Sr0.5CoO3−δ. Quantitative control of F in the perovskite host material is succeeded by using an electrochemical reactor composed of La0.5Sr0.5CoO3−δ‐BaF2|BaF2|PbF2‐Pb, and phase‐pure F‐doped La0.5Sr0.5CoO3−δ powder is obtained. Moreover, nano‐size crystalline domains with amorphous phase are formed on the particle surface under the high‐rate F doping, suggesting that tuning the anion doping rate enables the control of the formation of metastable phase. As demonstrated, the electrochemical anion doping technique opens up new possibilities for advances of energy materials by utilizing function of anionic species.
Funder
Murata Science Foundation
Subject
Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials
Cited by
2 articles.
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