Effect of the valence state of Mn in MnO/TiO composites on the catalytic performance for oxygen reduction reaction and oxygen evolution reaction

• Published in: RSC advances 2021-01, Vol.11 (3), p.1524-153
• Main Authors: Bai, Fan, Xu, Lincheng, Wang, Daode, An, Li, Hao, Zhanzhong, Li, Fan
• Format: Article
• ISSN: 2046-2069
• DOI: 10.1039/d0ra08575h

Manganese oxide composites with mixed valence states were prepared through the hydrothermal method by compositing with Ti 4 O 7 and calcining at different temperatures, and their ORR and OER catalytic performance were investigated. The prepared catalysts were characterized by XRD, SEM-EDS, HRTEM-EDS, and XPS methods to analyse their phase constitution, morphology feature, and surface composition. The major phase of manganese oxides was Mn 3 O 4 , which is a one-dimensional structure, and its growth was induced by Ti 4 O 7 . The ORR and OER catalytic activity can be enhanced due to the preferred orientation of manganese oxides. Electrochemical measurements, namely CV, LSV and EIS, were utilized for determining the ORR and OER catalytic activity, whereas CA and ADT were used for studying the durability and stability. A Li-O 2 battery was assembled to test the electrochemical behavior and properties in practical application. MnO x /Ti 4 O 7 calcined at 300 °C exhibited the best catalytic activity of 0.72 V vs. RHE half-wave potential for ORR and 0.67 V vs. RHE overpotential for OER. The proportion of Mn 3+ was also highest in all the MnO x /Ti 4 O 7 composites. The assembled Li-O 2 battery shows high performance with a voltage gap of only 0.85 V. Therefore, it can be affirmed that the inducement of Ti 4 O 7 could strengthen the preferred orientation in manganese oxide growth and Mn 3+ in MnO x /Ti 4 O 7 plays a vital role in catalyzing ORR and OER, with both improving the ORR and OER bifunctional catalytic performance of manganese oxides. Manganese oxide composites with mixed valence states were prepared by compositing with Ti 4 O 7 and calcination temperature could influence their ORR and OER catalytic performance observably.