# Optimizing the Catalytic Performance of Ba1−xCexMnO3 and Ba1−xLaxCu0.3Mn0.7O3 Perovskites for Soot Oxidation in Simulated GDI Exhaust Conditions

**Authors:** Nawel Ghezali, Álvaro Díaz-Verde, María José Illán-Gómez

PMC · DOI: 10.3390/molecules29133190 · Molecules · 2024-07-04

## TL;DR

This study investigates how substituting elements in perovskite materials affects their ability to catalyze soot oxidation under simulated gasoline engine exhaust conditions.

## Contribution

The novel contribution is identifying optimal substitution levels of Ce and La in perovskites for soot oxidation under varying oxygen conditions.

## Key findings

- BMC-La0.1 is the best catalyst in the absence of oxygen due to copper's catalytic effect.
- BM-Ce0.1 is most active in the presence of oxygen due to higher Mn(IV) content.
- Higher substitution levels than x = 0.1 do not improve catalytic performance.

## Abstract

Ba1−xCexMnO3 (BM-Cex) and Ba1−xLaxMn0.7Cu0.3O3 (BMC-Lax) perovskite-type mixed oxides were synthesized using the sol–gel method adapted for aqueous media with different values of x (0, 0.1, 0.3, 0.6) to estimate the effect of the degree of the partial substitution of Ba by Ce or La on the structure and properties that are relevant for their use as catalysts for gasoline direct injection (GDI) soot oxidation. The samples were deeply characterized by ICP-OES, XRD, XPS, N2 adsorption, H2-TPR, and O2-TPD, and their potential as catalysts for soot oxidation has been analyzed in various scenarios that replicate the exhaust conditions of a GDI engine. By comparing the catalytic performance for soot oxidation of the two tested series (BM-Cex and BMC-Lax) and in the two conditions used (100% He and 1% O2 in He), it could be concluded that (i) in the absence of oxygen in the reaction atmosphere (100% He), BMC-La0.1 is the best catalyst, as copper is also able to catalyze the soot oxidation; and (ii) if oxygen is present in the reaction atmosphere (1% O2/He), BM-Ce0.1 is the most-active catalyst as it presents a higher proportion of Mn(IV) than BMC-La0.1. Thus, it seems that the addition of an amount of Ce or La higher than that corresponding to x = 0.1 in Ba1−xCexMnO3 and Ba1−xLaxCu0.3Mn0.7O3 does not allow us to improve the catalytic performance of BM-Ce0.1 and BMC-La0.1 for soot oxidation in the tested conditions.

## Linked entities

- **Chemicals:** Ce (PubChem CID 23974), La (PubChem CID 23926), Mn(IV) (PubChem CID 23930), Cu (PubChem CID 23978), He (PubChem CID 23987), O2 (PubChem CID 977)

## Full-text entities

- **Chemicals:** Ce (MESH:D002563), La (MESH:D007811), He (MESH:D006371), N2 (MESH:D009584), BM-Ce0.1 (-), copper (MESH:D003300), O2 (MESH:D010100), Ba (MESH:D001464), Mn (MESH:D008345)

## Full text

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## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11243024/full.md

## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC11243024/full.md

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Source: https://tomesphere.com/paper/PMC11243024