Homogeneously Distributed Heterostructure Energizes and Replenishes Oxygen Species for Boosting Toluene Oxidation on Perovskite Oxide Catalysts

Enriching oxygen species in perovskite catalysts provides more active sites for the catalytic oxidation of air pollutants, but its further application in environmental chemical engineering is still constrained by the inherent lack of oxygen species reactivity and the difficulty of replenishing depleted oxygen species. Herein, we present a scalable one-pot strategy for the in situ fabrication of a homogeneously distributed heterostructure, which brings La<sub>2</sub>CuO<sub>4</sub> perovskite a 58-fold activity enhancement and robust antisintering/water/coke in toluene oxidation, higher than currently reported perovskite catalysts. Superior to the single "oxygen enrichment" effect of conventional surface-aggregated heterostructures, the homogeneously distributed heterostructures induce the reactivity enhancement of adsorbed oxygen and the backfilling/replenishment of depleted lattice oxygen, which break through the rate-determining steps of the low-temperature Langmuir-Hinshelwood and the high-temperature Mars-van Krevelen mechanisms, respectively. The scalability has been demonstrated in broader perovskite systems and for oxygen evolution reaction, offering a more dependable oxygen supply for environmental catalysis.

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Publication Details

Journal
Environmental Science & Technology
Published
2025-03-07
DOI
https://doi.org/10.1021/acs.est.4c09900
Citations
17
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
8.80

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article

Homogeneously Distributed Heterostructure Energizes and Replenishes Oxygen Species for Boosting Toluene Oxidation on Perovskite Oxide Catalysts

Yanjie Liang, Dong Wang, Qiaowan Chang, Yue Peng et al.
17 citations
Environmental Science & Technology
Catalytic Processes in Materials Science
8.80
article

Homogeneously Distributed Heterostructure Energizes and Replenishes Oxygen Species for Boosting Toluene Oxidation on Perovskite Oxide Catalysts

Yanjie Liang, Dong Wang, Qiaowan Chang, Yue Peng, Tao Luan, Yue Xuan, Bin Wang, Shuai Meng, Wenjie Fan, Junhua Li
article en
17 citations

Abstract

Enriching oxygen species in perovskite catalysts provides more active sites for the catalytic oxidation of air pollutants, but its further application in environmental chemical engineering is still constrained by the inherent lack of oxygen species reactivity and the difficulty of replenishing depleted oxygen species. Herein, we present a scalable one-pot strategy for the in situ fabrication of a homogeneously distributed heterostructure, which brings La<sub>2</sub>CuO<sub>4</sub> perovskite a 58-fold activity enhancement and robust antisintering/water/coke in toluene oxidation, higher than currently reported perovskite catalysts. Superior to the single "oxygen enrichment" effect of conventional surface-aggregated heterostructures, the homogeneously distributed heterostructures induce the reactivity enhancement of adsorbed oxygen and the backfilling/replenishment of depleted lattice oxygen, which break through the rate-determining steps of the low-temperature Langmuir-Hinshelwood and the high-temperature Mars-van Krevelen mechanisms, respectively. The scalability has been demonstrated in broader perovskite systems and for oxygen evolution reaction, offering a more dependable oxygen supply for environmental catalysis.

Environmental Science & TechnologyVol. 59(10)
Shandong University (CN), Washington State University (US), Tsinghua University (CN)
Department of Education of Shandong Province, National Natural Science Foundation of China, Natural Science Foundation of Shandong Province, Taishan Scholar Project of Shandong Province, National Key Research and Development Program of China
Openalex Percentile: Top 2%
Catalytic Processes in Materials Science
8.80
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