CeF3-MnOx-CC复合催化剂的制备及电场辅助室温催化降解甲醛

    Preparation of CeF3-MnOx-CC Composite Catalyst and Electric Field Assisted Catalytic Degradation of Formaldehyde at Room Temperature

    • 摘要: 过渡金属氧化物MnOx在室温下催化降解甲醛(HCHO)污染方面显示出巨大的潜力, 但催化过程中中间产物的积累容易导致催化性能的降低。通过水热电沉积法制备了以碳纤维布(carbon cloth, CC)为衬底的CeF3纳米颗粒锚定的MnOx纳米棒复合催化剂(CeF3/MnOx-CC), 并提出了一种电场辅助催化氧化策略。结果表明, 在HCHO动态性能测试中, 与无电场辅助相比, 电场辅助CeF3/MnOx-CC的HCHO转化率从65.8%提高至76.6%, 且在72 h内没有明显衰减。该复合催化剂利用F的高电负性和电场的辅助作用, 促进催化剂表面晶格氧释放和活性氧物种O*的形成, 加速中间产物的分解, 从而提升HCHO的催化效率和寿命。该电场辅助催化策略为室温下气态污染物的高效、长期降解提供了新的途径。

       

      Abstract: Transition metal oxide MnOx has shown great potential in catalyzing the degradation of formaldehyde (HCHO) pollution at room temperature, however, the accumulation of intermediate products during the catalytic process can easily lead to a decrease in catalytic performance. Hereon, a MnOx nanorod composite catalyst anchored by CeF3 nanoparticles on carbon cloth (CC) substrate was prepared using a hydrothermal deposition method, and an electric field assisted catalytic oxidation strategy was proposed. Results show that in the dynamic performance test of HCHO, compared with no electric field assistance, the HCHO conversion rate of CeF3/MnOx-CC with electric field assistance increases from 65.8% to 76.6%, and there is no significant attenuation within 72 hours. This composite catalyst utilizes the high electronegativity of fluorine and the auxiliary effect of electric field to promote the release of lattice oxygen on the catalyst surface and the formation of active oxygen species O*, accelerate the decomposition of intermediate products, and thus improve the catalytic efficiency and lifespan of HCHO. The electric field assisted catalytic strategy proposed in this article provides a new approach for the efficient and long-term degradation of gaseous pollutants at room temperature.

       

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