Abstract
Solar thermochemical cycles offer a viable option for the production of green synthetic fuels from CO 2 and H 2 O. Two-step cycles using redox materials consist of a high-temperature reduction creating oxygen vacancies, followed by a re-oxidation step with an oxidant gas (CO 2 and/or H 2 O), resulting in CO and/or H 2 production. This study focuses on the thermochemical performance in a solar reactor of a new kind of composite reactive material: reticulated ceria foam with uniform perovskite coating, forming a dual-phase layered heterostructure. La 0.5 Sr 0.5 Mn 0.9 Mg 0.1 O 3 (LSMMg) was selected as perovskite coating due to its high fuel productivity and thermochemical stability upon cycling. The perovskite coating improves the reduction step by increasing the reduction extent reached by the reactive material. The results revealed significant enhancement of oxygen exchange in the dual-phase composite material during reduction compared to individual components. The enhanced reduction extent had a beneficial effect on the oxygen release rate and the total amount of fuel produced by CO 2 and H 2 O splitting, whereas an adverse impact on the peak rate during H 2 /CO evolution was noticed. Decreasing the reduction pressure allowed enhancing the non-stoichiometric oxygen extent, while the re-oxidation extent increased with the inlet oxidant molar fraction. With suitable operating conditions (reduction at 0.100 bar and oxidation in 100% CO 2), the LSMMg-coated ceria foam produced a higher amount of fuel but with lower fuel production rate in comparison with pure ceria foam. This study points out the beneficial effects of composite redox materials consisting of LSMMg-coated ceria foam in enhancing the oxygen exchange capacity of ceria for solar fuel production.