Ferrite@TiO2-nanocomposites as Z-scheme photocatalysts for CO2 conversion

Subtitle:insight into the correlation of the Co-Zn metal composition and the catalytic activity

Photocatalytic conversion of CO2 in the gas phase involving Z-scheme mechanism was studied in the presence of CoxZn1-xFe2O@TiO2 (x = 1; 0.2; 0.4; 0.6; 0.8; 0) catalyst nanocomposites. The catalysts were obtained in a two-step approach, consisting of a co-precipitation reaction forming the magnetic Ferrite nanoparticles and a hydrolysis-condensation reaction of the Ti-source forming the titania anatase phase, followed by a calcination procedure. The structural characterization was done by X-ray diffraction, Raman and UV-DR spectroscopy, and physisorption, confirming the presence of both structures in the nanocomposites, with a band gap between 3 and 3.23 eV. In order to determine the CO2 conversion, a photocatalytic gas phase fixed-bed batch reactor in tandem with a GC analyzer were used. The tests were done under UVC light irradiation and CO, CH4 were identified as the main products during photoconversion of CO2. All the samples showed higher conversions compared to the well-known reference material P25 (Degussa). The CO2 conversion was observed to be directly proportional with the Zn/Co metal ratio in the Ferrite structure, achieving for ZnFe2O4@TiO2 similar to 50 mu mol g(cat). (-1) h(-1) CO and similar to 30 mu mol g(cat).(-1) h(-1) CH4. Moreover, for the ZnFe2O4@TiO2 catalyst methanol (CH3OH) formation was observed, while no traces of methanol were detected for the samples containing Co. The electrochemistry analyses clarified the different heterojunctions formed between Ferrites and TiO2. Mott-Schottky plots revealed the formation of a Z-scheme mechanism for ZnFe2O4@TiO2 explaining the best conversion results. On the other hand, the lower activity of CoFe2O4@TiO2 was attributed to the formation of a type I heterojunction system.

Publication year:2020

Keywords:A1 Journal article

BOF-keylabel:yes

BOF-publication weight:6

CSS-citation score:1

Authors from:Government

Accessibility:Closed