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Sr, Mg co-doped LaGaO3-δ supported Fe2O3 improved the water gas shift reaction with chemical looping.

Authors :
He, Haihua
Jiang, Haojie
Yang, Feiyong
Zhang, Wenxia
Jin, Min
Li, Zhenfang
Source :
International Journal of Hydrogen Energy. Jan2023, Vol. 48 Issue 4, p1263-1276. 14p.
Publication Year :
2023

Abstract

Fe 2 O 3 is prospective for the chemical looping redox cycles but must contain a significant amount of inert supports to ensure high stability. The traditional inert supports (Al 2 O 3 , MgAl 2 O 4 , etc.) have a dilution effect on Fe 2 O 3 , which results in a compromised reactivity. In this work, we propose several Sr, Mg co-doped LaGaO 3-δ to support Fe 2 O 3 for chemical looping water splitting and investigated the synergy for the enhanced performance. Mechanistic study manifests that doping Sr increases the amount of oxygen vacancies, promoting the oxygen release and uptake during the redox reaction. Doping Mg mitigated the interaction between Fe 2 O 3 and the supports, leading to much enhanced stability. Therefore, Fe 2 O 3 /La 0.6 Sr 0.4 Mg 0.4 Ga 0.6 O 3-δ shows both high hydrogen yield (9.75 mmol.g−1) and peak hydrogen production rate (3.7 mmol.g−1.min−1). The performance shows only a slight decrease even after 100 cycles. The observed results can also inspire the selection and development of advanced supports to improve both the reactivity and stability of oxygen carriers. [Display omitted] • Sr improves oxygen vacancy concentration of the oxygen carriers. • High oxygen vacancy concentration improves the oxygen release/uptake rate. • Mg mitigates the reaction between iron and support to ensure reversible phase change. • Fe 2 O 3 /La 0.6 Sr 0.4 Mg 0.4 Ga 0.6 O 3-δ is highly active and stable for chemical looping reaction. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03603199
Volume :
48
Issue :
4
Database :
Academic Search Index
Journal :
International Journal of Hydrogen Energy
Publication Type :
Academic Journal
Accession number :
161015532
Full Text :
https://doi.org/10.1016/j.ijhydene.2022.10.018