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◆ Cleaner Engineering and Technology2026-02-03· Nanocomposite

Highly efficient photocatalytic conversion of CO2 to hydrocarbons using visible-active co-doped TiO2/ PDMS nanocomposite

Majed Bahadorian, Farzaneh Arabpour Roghabadi, Vahid Ahmadi, Afsanehsadat Larimi

原始摘要(英文原文)· Original abstract
Considering the rising emission of the carbon dioxide (CO 2 ) and its detrimental effects on the environment, conversion of CO 2 into value-added products has emerged as a critical area of research. In particular, the photocatalytic reduction of CO 2 into fuels using solar energy has recently attracted significant attention. In this study, a nanocomposite of co-doped titanium dioxide (TiO 2 ) nanoparticles with polydimethylsiloxane (PDMS) is utilized for photocatalytic reduction of CO 2 . Photo, chemical, and thermal- stable PDMS serves as a transparent flexible binder for photocatalyst nanoparticles, facilitating their usage and recycling. To make TiO 2 photocatalysts visible-active, reduce the charge recombination rate, and improve the charge transport and lifetime, they are co-doped using nonmetal nitrogen (N) and metal silver (Ag) with different concentrations. Following the optical, morphological, and structural analysis of the photocatalysts, their photocatalytic performance is evaluated in a fixed gas bed photoreactor. The TiO 2 photocatalyst shows the lowest yield for methane (3.2 μmol/g catalyst) and ethane (0.42 μmol/g catalyst). While, the yield for methane and ethane using Ag-N-TiO 2 photocatalyst reaches 34.42 and 1.01 μmol/g catalyst, respectively. Remarkably, when the PDMS-Ag-N-TiO 2 nanocomposite is employed, the highest methane and ethane yield of 122.21 and 10.22 μmol/g catalyst are achieved, respectively. Thus, in the presence of PDMS polymer, instantaneous quadrupolar interactions occur between its siloxane groups and carbon dioxide molecules. This promotes the adsorption of greater amounts of CO 2 , making it more available for the photocatalytic reduction reaction and thereby enhancing hydrocarbon production.
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