Mechanistic exploration in controlling the product selectivity via metals in TiO2 for photocatalytic carbon dioxide reduction

Abstract

Harnessing the power of the sun, the photocatalytic CO2 reduction process emerges as a pivotal sustainable solution, utilizing solar energy a premier, clean energy source known for its efficiency and economic viability in the current energy paradigm. This study investigates the impact of metals (Cu, Ag, Au) on enhancing the photocatalytic CO2 reduction capabilities of TiO2. In-depth mechanistic analysis conducted using in-situ DRIFTS for identifying the key reaction intermediates, highlights that the catalytic performance, both in terms of activity and product selectivity, is tightly linked to the underlying reaction mechanisms route, optoelectronic properties, and substrate's (CO2 and H2O) affinities to the catalyst surface. Enhanced light absorption and reduced charge recombination (lifetime enhancement from 0.21 ns to ∼1.2 ns) in case of metal incorporated resulted in enhanced overall photocatalytic performance. With Au as dopant, demonstrated highest electron selectivity for H2 (>97%) compared to Ag and Cu, which showed relatively higher CO2 reduction electron selectivity (∼20% for Cu). The study reveals the crucial interplay of intermediate stabilization, demonstrating its critical role in governing the reaction pathways i.e., carbene or formaldehyde routes as observed in case of Ag and Cu respectively and thus the specific final products. For enhancing the selectivity of CO, engineering the catalyst surface to favour weak CO adsorption is vital. Observations in the CO-TPD measurements demonstrated that Ag sites were effective in promoting the weaker CO* stabilization thus displayed more selectivity towards CO as compared to Cu. While higher CH3OH formation rates in case of Cu, were found to be related to the augmented reactive M=O species stabilization which promotes the oxidation of CH4 to CH3OH. Additionally, in case of Cu, the CH3O* intermediates stabilized effectively, which contributed to more Methanol selectivity through favoured formaldehyde route. While in case of Ag, the CH2* stabilization suggests more probability of the carbene pathway in comparison to the formaldehyde route (as in case of Cu) for producing the CH4 as the final hydrogenated C1 product. These insights guide the strategic design of catalysts for controlling the reaction pathways and thus selective C1 product production in photocatalytic CO2 reduction, offering insights for advanced catalyst design. © 2024