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Direct Observation of Oxygen Dissociation on Non‐Stoichiometric Metal Oxide Catalysts
Author(s) -
Huang YiLin,
Pellegrinelli Chistopher,
Wachsman Eric D.
Publication year - 2016
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201607700
Subject(s) - oxygen , dissociation (chemistry) , chemistry , oxide , stoichiometry , catalysis , metal , inorganic chemistry , limiting , organic chemistry , mechanical engineering , engineering
Oxygen dissociation on metal oxides is a key reaction step, limiting the efficiency of numerous technologies. The complexity of the multi‐step oxygen reduction reaction (ORR) makes it difficult to investigate the oxygen dissociation step independently. Direct observation of the oxygen dissociation process is described, quantitatively, on perovskites La 0.6 Sr 0.4 Co 0.2 Fe 0.8 O 3‐δ and (La 0.8 Sr 0.2 ) 0.95 MnO 3±δ , using gas‐phase isotope‐exchange with a 1:1 16 O 2 : 18 O 2 ratio. Oxygen transport mechanisms between gas–surface reactions and surface–bulk exchange are deconvoluted. Our findings show that regardless of participation of lattice oxygen, La 0.6 Sr 0.4 Co 0.2 Fe 0.8 O 3‐δ is better at oxygen dissociation than (La 0.8 Sr 0.2 ) 0.95 MnO 3±δ . Heteroexchange, involving lattice oxygen, dominates on La 0.6 Sr 0.4 Co 0.2 Fe 0.8 O 3‐δ . In contrast, (La 0.8 Sr 0.2 ) 0.95 MnO 3±δ shows both homoexchange and heteroexchange, with the latter only happening above 600 °C. Using a 1:1 isotope mixture, a simple method is presented for separation of the oxygen dissociation step from the overall ORR.