4.7 Article

Investigation of Cu/TiO2 synthesis methods and conditions for CO2 photocatalytic reduction via conversion of bicarbonate/carbonate to formate

Journal

JOURNAL OF CO2 UTILIZATION
Volume 70, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.jcou.2023.102428

Keywords

Titania; Band offset; CO2 reduction; Photocatalysis; Copper-doping

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This work aimed to enhance the photocatalytic activity of TiO2 in CO2 reduction. TiO2 and Cu/TiO2 at 5 wt% copper bulk loading were synthesized using the sol-gel method. Cu was also doped into the commercial TiO2 samples via the incipient wetness method. Low pH and copper inhibited the transformation of anatase to rutile. Copper existed in Cu(I) and Cu(II) states, and the Cu(I) to Cu(II) ratio was closely related to the anatase to rutile ratio. The study demonstrated the synergistic effect of the anatase-rutile mixture, reaction pH, and copper dopant in improving the photocatalytic activity of TiO2.
This work is aimed at improving the photocatalytic activity of TiO2 in the reduction of CO2. TiO2 and Cu/TiO2 at 5 wt% copper bulk loading were synthesised using the sol-gel method at a pH of 0.4 and 1.5. The synthesised pure TiO2 samples, alongside the commercial TiO2 (Degussa (R) P25), were also doped with copper via the incipient wetness method. The low pH and the presence of copper inhibited the anatase-rutile transformation. Copper existed in Cu(I) and Cu(II) states in all the doped samples, with the Cu(I) to Cu(II) ratio intimately linked with the anatase to rutile ratio. The UPS data have shown the type II band offset between TiO2 and CuO. The performance of the samples prepared was tested through the reduction of sodium bicarbonate-carbonate buffered at pH > 8. Commercial TiO2 impregnated with Cu demonstrated the highest formate production rate of 173 mu mol center dot g(-1)center dot h(-1) at pH 11. This study demonstrated the synergetic effect of the anatase-rutile mixture of phases, the reaction pH, and the copper dopant in improving the photocatalytic activity of TiO2.

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