Issue 6, 2023

Multiple and nonlocal cation redox in Ca–Ce–Ti–Mn oxide perovskites for solar thermochemical applications

Abstract

Modeling-driven design of redox-active off-stoichiometric oxides for solar thermochemical H2 production (STCH) seldom has resulted in empirical demonstration of competitive materials. We report the theoretical prediction and experimental evidence that the perovskite Ca2/3Ce1/3Ti1/3Mn2/3O3 is synthesizable with high phase purity, stable, and has desirable redox thermodynamics for STCH, with a predicted average neutral oxygen vacancy (VO) formation energy, Ev = 3.30 eV. Flow reactor experiments suggest potentially comparable or greater H2 production capacity than recent promising Sr–La–Mn–Al and Ba–Ce–Mn metal oxide perovskites. Utilizing quantum-based modeling of a solid solution on both A and B sub-lattices, we predict the impact of nearest-neighbor composition on Ev and determine that A-site Ce4+ reduction dominates the redox-activity of Ca2/3Ce1/3Ti1/3Mn2/3O3. X-ray absorption spectroscopy measurements provide evidence that supports these predictions and reversible Ce4+-to-Ce3+ reduction. Our models predict that Ce4+ reduces even when it is not nearest-neighbor to the VO, suggesting that refinement of Ce stoichiometry has the possibility of further enhancing performance.

Graphical abstract: Multiple and nonlocal cation redox in Ca–Ce–Ti–Mn oxide perovskites for solar thermochemical applications

Supplementary files

Article information

Article type
Paper
Submitted
23 Jan 2023
Accepted
03 Apr 2023
First published
03 May 2023

Energy Environ. Sci., 2023,16, 2550-2560

Multiple and nonlocal cation redox in Ca–Ce–Ti–Mn oxide perovskites for solar thermochemical applications

R. B. Wexler, G. Sai Gautam, R. T. Bell, S. Shulda, N. A. Strange, J. A. Trindell, J. D. Sugar, E. Nygren, S. Sainio, A. H. McDaniel, D. Ginley, E. A. Carter and E. B. Stechel, Energy Environ. Sci., 2023, 16, 2550 DOI: 10.1039/D3EE00234A

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