151. One-pot hydrothermal preparation of Ni and I co-doped brookite-anatase TiO2 nanoparticles with remarkably enhanced photoreduction activity of CO2 to CH4.
- Author
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Shi, Weina, Zhang, Ran, Wang, Ji-Chao, Li, Wei, Guo, Xiaowei, Guo, Jiao, Li, Renlong, Hou, Yuxia, Zhang, Wanqing, and Gao, Hui-Ling
- Subjects
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DOPING agents (Chemistry) , *CARBON dioxide , *RUTILE , *METHANE , *TITANIUM dioxide , *PHOTOCATALYSTS , *ARSENIC removal (Water purification) , *PHOTOREDUCTION - Abstract
[Display omitted] • Ni and I substitutionally codoped TiO 2 phase junction was synthesized. • The photocalcatalysis for CO 2 reduction in water vapor was accomplished. • The selectivity of CH 4 product reached above 98%. • The electron transfer was enhanced by Ni(III)/Ni(II) pair. • The CO 2 adsorption mode was changed by the doping Ni/I. Ni and I co-doped TiO 2 nanoparticles with mixed anatase-brookite phase (Ni/I-TiO 2) were synthesized by the hydrothermal-calcination method for photocatalytic CO 2 reduction with H 2 O vapor. The I and Ni co-doping, anatase-brookite phase junction, as well as the presence of Ti(III) and Ni(III) endowed the catalyst with promoted visible light absorption, increased reduction ability of photogenerated electrons, facilitated charge separation and migration along with modulated CO 2 adsorption mode and capacity, ultimately resulting in boosted photocatalytic activity and product selectivity as compared with those of pure TiO 2. The CO, CH 4 and O 2 yields of the optimized Ni/I-TiO 2 reached 3.49, 158.25 and 246.30 μmol/g cat after 15 h of light illumination, which decreased slightly after 9 cycles, and the product selectivity was above 98 % for photocatalytic reduction of CO 2 to CH 4 with Ni and I co-doping. The in-situ FTIR results with the observation of CH 3 O and CH 3 intermediates confirmed CH 4 formation, and the possible mechanism of photocatalytic CO 2 reduction over Ni/I-TiO 2 was elucidated. This work provides new insights to pursue efficient catalysts for the selective photocatalytic CO 2 reduction to CH 4. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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