Investigation of High Oxygen Reduction Reaction Catalytic Performance on Mn-Based Mullite SmMn₂O₅


An alternative material SmMn₂O₅ mullite with regard to Pt/C is proposed to catalyze the oxygen reduction reaction (ORR) by combining density functional theory (DFT) calculations and experimental validations. Theoretical calculations are performed to investigate the bulk phase diagram, as well as the stability and electrocatalytic activity of the ORR under alkaline conditions for SmMn₂O₅ (001) surfaces, which are passivated by nitrogen atoms to avoid any spurious interference. The adsorptions of relevant ORR species (O*, OH*, OOH* and OO*) tend to compensate the coordination of manganese atoms to form Mn-centered octahedral or pyramidal crystal fields, and the corresponding binding energies fulfill a linear relationship. An oxygen molecule prefers to be reduced to OH⁻ via a four-electron pathway and this prediction is verified by electrochemical measurements on the as-prepared SmMn₂O₅ catalyst with a nanorod structure. Volcano curves are obtained to describe the trends in theoretical ORR activity as a function of a single parameter, i.e. the oxygen binding energy. An overpotential of 0.43 V is obtained at the O* binding energy around 3.4 eV, which is close to the experimental observation (0.413 V) in this work. SmMn₂O₅ mullite exhibits favorable ORR activity and superior stability with only ~5% decay in activity over 20 000 s of chronoamperometric operation in contrast to ~15% decrease of Pt/C, making it a promising candidate for a cathode catalyst.



Oxides, Manganese oxides, Diesel motor exhaust gas, Oxidation, Electrocatalysts, Chemistry, Materials science, Mullite

National Key Research and Development Program (Grant No. 2016YFB0901600), the National Natural Science Foundation of China (21573117 and 11404172), Tianjin Natural Science Foundation (14JCZDJC37700), and the National Basic Research Program of China (973 Program with No. 2014CB931703).


©2017 The Royal Society of Chemistry. This article may not be further made available or distributed.