DFT Modeling of CO₂ Adsorption and HCOO^• Group Conversion in Anatase Au-TiO₂-Based Photocatalysis

Due to the merits of carbon circulation and hydrocarbon production, solar-assisted photocatalysis has been regarded as an ideal option for securing a sustainable future of energy and environment. In the photocatalytic carbon cycle process, surface reactions including the adsorption of CO₂ and the conversion of CO₂ into CH₄, CH₃OH, etc. are crucial to be examined ascribed to their significant influence on the performance of the photocatalysis. Because the conversion reaction starts from the formation of HCOO^•, the density functional theory (DFT) model was established in this study to investigate the micromechanism of CO₂ adsorption and the conversion of CO₂ to HCOO^• group in the anatase Au-TiO₂ photocatalytic system. The CO₂ adsorption bonding in six configurations was simulated, on which basis the effects of the proportion of water molecules and the lattice temperature increase due to the local surface plasmon resonance (LSPR) on the photocatalytic CO₂ adsorption and conversion were specifically analyzed. The results show that the experimental conditions that water molecules are released before CO₂ are favorable for the formation of the adsorption configuration in which HCOO^• tends to be produced without the need of reaction activation energy. This is reasonable since the intermediate C atoms do not participate in bonding under these conditions. Moreover, Au clusters have an insignificant influence on the adsorption behaviors of CO₂ including the adsorption sites and configurations on TiO₂ surfaces. As a result, the reaction rate is reduced due to the temperature increase caused by the LSPR effect. Nevertheless, the reaction maintains a very high rate. Interestingly, configurations that require activation energy are also possible to be resulted, which exerts a positive influence of temperature on the conversion rate of CO₂. It is found that the rate of the reaction can be improved by approximately 1-10 times with a temperature rise of 50 K above the ambient.