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Updated: Mar 7, 2026

Tuning Oxide Properties by Oxygen Vacancy Control During Growth and Annealing
Published on: June 9, 2023
Decoupling Structural Stability and Oxygen Mobility in Perovskites via A-Site Cation Engineering
Tao Long1,2,3,4, Guanghuan Li4, Da Song5,6
1College of Materials Science and Engineering, Guilin University of Technology, Guilin 541004, China.
Abstract:
The rational design of perovskite oxygen carriers for chemical looping is fundamentally constrained by the structural stability and high oxygen mobility. Decoupling these properties requires moving beyond compositional tuning to uncover their atomic-scale structural origin. Herein, by employing AMnO3 (A = Ca, Sr, Ba) as a model system, we directly unveil that the A-site cation orchestrates the connectivity of MnO6 octahedra, providing a powerful structural descriptor to reveal the intrinsic nature of the material. Atomic-resolution AC-HAADF-STEM imaging provides direct atomic-scale evidence: CaMnO3 retains a robust, three-dimensional network of corner-shared octahedra, while SrMnO3 and BaMnO3 form less stable face-sharing configurations, inducing destabilizing Mn4+-Mn4+ electrostatic repulsion. This structural divergence dictates redox reversibility; only corner-shared CaMnO3 undergoes fully reversible phase transitions during cycling. The corner-sharing structure endows CaMnO3 with the largest specific free volume (SFV) for fast oxygen transport and an O 2p-band center closest to the Fermi level, a signature of weak Mn-O bonds that enables facile lattice oxygen release and moderate oxygen vacancy formation energy for lattice oxygen with mild activity inhibiting excessive oxidation of ethane. Furthermore, strong Mn-O covalency leads to electron localization upon oxygen vacancy formation, generating (Mn3+-Vo••-Mn3+) complexes that function as unified active sites for both O2 chemisorption and CO2 activation, evidenced by congruent O2-TPD and CO2-TPD profiles. Consequently, CaMnO3 achieves outstanding and stable ethane oxidative dehydrogenation performance with 85% C2H4 selectivity, 46% C2H4 yield over 20 redox cycles. This work establishes "corner-sharing for stability" as a central design principle, shifting from conventional activity screening to octahedral connectivity engineering for developing next-generation, high-durability oxygen carriers.
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