Metal-Ligand Cooperative Proton Transfer/Electron Transfer and Acid-Assisted Protonation Mechanism for Mo-Catalyzed...

Density functional theory (DFT) study of Mo-catalyzed photoreduction of H⁺ and CO₂ reveals a metal-ligand cooperative proton transfer/electron transfer (PT/ET) process and an intermolecular acid-assisted protonation mechanism. The key metal-hydride complex ²3 pt-H is generated via two-electron-two-proton reduction of the initial catalyst Mo-2Hqpdt, where the redox noninnocent dithiolene ligand plays a crucial role in accepting and transferring electrons. In the generation of ²3 pt-H, the one-electron reduction of ¹2 pt to ²3 pt has a Gibbs energy barrier of 17.8 kcal/mol (¹4 → TS_ET2) and constitutes the overall rate-determining step for both H₂ and HCOOH formation. The Mo-H moiety in ²3 pt-H tends to be protonated by a carbonate molecule for the formation of H₂, which presents a Gibbs energy barrier of 8.7 kcal/mol (²13 → ²TS5). Alternatively, the Mo-H could also nucleophilically attack CO₂ to form HCOOH, with a Gibbs energy barrier of 11.1 kcal/mol (²3 pt-H → ²TS6'). Such a barrier difference of 2.4 kcal/mol could explain why H₂ is the favored product in the experiments. The rate-determining step for CO formation is C-O cleavage with a total Gibbs energy barrier of 28.8 kcal/mol (¹4 → ²TS9), which is 11.0 kcal/mol higher than that of H₂ and HCOOH; therefore, CO is a byproduct in the experiment. Moreover, intermolecular protonation rather than intramolecular protonation in ²3 pt-H is confirmed as the pathway for H₂ generation, which underscores the indispensable role of a small acid and provides valuable information for suppressing undesired hydrogen evolution.