Interplay between electronic structure and catalytic activity in transition metal oxide model system

• Main Author: Suntivich, Jin
• Other Authors: Yang Shao-Horn.
• Format: Others
• Language: English
• Published: Massachusetts Institute of Technology 2013
• Subjects: Materials Science and Engineering.
• Online Access: http://hdl.handle.net/1721.1/76134

Thesis (Sc. D.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2012. === Cataloged from PDF version of thesis. === Includes bibliographical references (p. 109-125). === The efficiency of many energy storage and conversion technologies, such as hydrogen fuel cells, rechargeable metal-air batteries, and hydrogen production from water splitting, is limited by the slow kinetics of the oxygen electrochemical reactions. Transition-metal oxides can exhibit high catalytic activity for oxygen electrochemical reactions, which can be used to improve efficiency and cost of these devices. Identifying a catalyst "design principle" that links material properties to the catalytic activity can accelerate the development of highly active, abundant transition metal oxide catalysts fore more efficient, cost-effective energy storage and conversion system. In this thesis, we demonstrate that the oxygen electrocatalytic activity for perovskite transition metal oxide catalysts primarily correlates to the a* orbital ("eg") occupation. We further find that the extent of B-site transition metal-oxygen covalency can serve as a secondary activity descriptor. We hypothesize that this correlation reflects the critical influences of the a* orbital and transition metal-oxygen covalency on the ability of the surface to displace and stabilize oxygen-species on surface transition metals. We further propose that this ability to stabilize oxygen-species reflect as the rate-limiting steps of the oxygen electrochemical reactions on the perovskite oxide surfaces, and thus highlight the importance of electronic structure in controlling the oxide catalytic activity. === by Jin Suntivich. === Sc.D.