To develop an efficient photocatalytic carbon dioxide (CO) reduction aimed at mitigating CO emissions and greenhouse effects, we propose a straightforward strategy involving hydrogen reduction treatment of PtCu/Ti to create the PtCu/Ti-H catalyst with a distinctive interface structure. Compared with the fresh PtCu/Ti catalyst and the benchmark anatase TiO, the CH production of the PtCu/Ti-H catalyst increased by 2 times and 81.6 times, respectively. Comprehensive characterizations confirmed the formation of Pt-Ov-Ti and Cu-Ov-Ti interface structures on the hydrogen-treated PtCu/Ti-H catalyst, enhancing light absorption and the separation of photogenerated charge carriers. Further investigation into the reaction mechanism revealed that the Pt-Ov-Ti and Cu-Ov-Ti species on PtCu/Ti-H serve as more favorable sites for CO adsorption and activation, promoting an enhanced formaldehyde mechanism. This study not only elucidates the relation between photocatalytic CO reduction activity and the PtCu/Ti interface structure but also offers a novel strategy for designing alloy/oxide-based catalysts for CO photoreduction, overcoming the limitations of previous studies that focused on metal or vacancy systems.
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http://dx.doi.org/10.1016/j.envres.2024.120191 | DOI Listing |
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