Ceramics (Dec 2023)

Oxygen-Bonding State and Oxygen-Reduction Reaction Mechanism of Pr<sub>0.7</sub>Ca<sub>0.3</sub>Mn<sub>1−x</sub>Co<sub>x</sub>O<sub>3−d</sub> (x = 0, 0.1, 0.2, 0.3)

  • Kanghee Jo,
  • Seungjae Lee,
  • Heesoo Lee

DOI
https://doi.org/10.3390/ceramics6040146
Journal volume & issue
Vol. 6, no. 4
pp. 2386 – 2393

Abstract

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We investigated the effects of Co doping on Pr0.7Ca0.3MnO3−d in the perspective of an oxygen-bonding state change. In all compositions, Pr0.7Ca0.3Mn1−xCoxO3−d (PCMCx, x = 0, 0.1, 0.2, 0.3) showed an orthorhombic structure, and the lattice gradually contracted with increasing Co content. The doped Co was mostly present as 2+ and 3+, which decreased the average oxidation value of the B site and created oxygen vacancies for charge compensation. However, as the Co content increased, the proportion of Co3+ increased, and the content of oxygen vacancies gradually decreased. In addition, the ratio of adsorbed oxygen in PCMC0.1 was the highest, and the B-O covalency was enhanced. Accordingly, the electrochemical reaction of oxygen with the cathode material in PCMC0.1 could occur most easily, showing the smallest polarization resistance among the Co-doped Pr0.7Ca0.3MnO3−d. We can confirm the formation of oxygen vacancies via Co doping and the effect of B-O covalency on the oxygen-reduction reaction of Pr0.7Ca0.3MnO3−d.

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