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Table · dataset · 2026

Role of Frustrated Lewis Pairs in α‑MnO<sub>2</sub> for Low-Temperature Toluene Oxidation with Ozone

Listed in ZivaHub and Deakin Research Online and DMU Figshare — shown once because both records carry DOI 10.1021/acs.iecr.6c02799.s001

The catalytic performance of α-MnO<sub>2</sub> in the ozonation of volatile organic compounds (VOCs) is highly synthesis-dependent, which determines surface defects, redox properties, and active site distribution.

Description

To investigate this, we prepared three α-MnO<sub>2</sub> catalysts through precipitation (MnO<sub>2</sub>–P), hydrothermal synthesis (MnO<sub>2</sub>–H), and the crystal transformation approach (MnO<sub>2</sub>–C).

The superior performance of MnO<sub>2</sub>–C is attributed to its abundant oxygen vacancies and favorable Mn<sup>3+</sup>/Mn<sup>4+</sup> ratio, whereas the efficiency of MnO<sub>2</sub>–P and MnO<sub>2</sub>–H is limited by their coordination-saturated Mn sites and insufficient oxygen vacancies, leading to poor O<sub>3</sub> activation. In contrast, the crystal transformation approach induces structural defects in MnO<sub>2</sub>–C, creating abundant oxygen vacancy clusters and an optimized Mn<sup>3+</sup>/Mn<sup>4+</sup> ratio.

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This unique configuration forms frustrated Lewis pairs (FLPs) between Mn cations (LA) and oxygen anions (LB), synergistically activating O<sub>3</sub> to generate reactive oxygen species. As a result, MnO<sub>2</sub>–C achieves 100% toluene conversion with 85% CO<sub>2</sub> selectivity at 30 °C, far surpassing MnO<sub>2</sub>–P and MnO<sub>2</sub>–H. This work demonstrates that defect engineering via crystal transformation is an effective strategy for designing highly active catalysts for VOC removal.

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ZivaHuboai:figshare.com:article/3404437012 d agoJSON v1
Deakin Research Onlineoai:figshare.com:article/3404437012 d agoJSON v1
DMU Figshareoai:figshare.com:article/3404437012 d agoJSON v1
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