Find in Library

As a representative sulfur-containing volatile organic compounds (S-VOCs), CH₃SH has attracted widespread attention due to its adverse environmental and health risks. The performance of Mn-based catalysts and the effect of their crystal structure on the CH₃SH catalytic reaction have yet to be systematically investigated. In this paper, two different crystalline phases of tunneled MnO₂ (α-MnO₂ and β-MnO₂) with the similar nanorod morphology were used to remove CH₃SH, and their physicochemical properties were comprehensively studied using high-resolution transmission electron microscope (HRTEM) and electron paramagnetic resonance (EPR), H₂-TPR, O₂-TPD, Raman, and X-ray photoelectron spectroscopy (XPS) analysis. For the first time, we report that the specific reaction rate for α-MnO₂ (0.029 mol g⁻¹ h⁻¹) was approximately 4.1 times higher than that of β-MnO₂ (0.007 mol g⁻¹ h⁻¹). The as-synthesized α-MnO₂ exhibited higher CH₃SH catalytic activity towards CH₃SH than that of β-MnO₂, which can be ascribed to the additional oxygen vacancies, stronger surface oxygen migration ability, and better redox properties from α-MnO₂. The oxygen vacancies on the catalyst surface provided the main active sites for the chemisorption of CH₃SH, and the subsequent electron transfer led to the decomposition of CH₃SH. The lattice oxygen on catalysts could be released during the reaction and thus participated in the further oxidation of sulfur-containing species. CH₃SSCH₃, S⁰, SO₃²⁻, and SO₄²⁻ were identified as the main products of CH₃SH conversion. This work offers a new understanding of the interface interaction mechanism between Mn-based catalysts and S-VOCs.