Researchers enhance CO₂ photoreduction with new metal-organic framework

Photocatalytic conversion of CO₂ into C₂ products is an important process in the quest to address the energy crisis and achieve carbon neutrality. However, generating C₂ products is challenging due to the sluggish multi-electron transfer process and inert C–C coupling processes.

In a study published in Angewandte Chemie International Edition, Prof. Liu Tianfu from Fujian Institute of Research on the Structure of Matter of the Chinese Academy of Sciences and Prof. Wu Xinping from East China University of Science and Technology constructed a metal-organic framework (MOF) with delocalized orbitals and proposed a strategy of direct charge transfer to enhance electron transfer and separation efficiency, thereby boosting photocatalytic reaction performance.

Researchers constructed the MOF compound (PFC-98) featuring delocalized orbitals over the metal cluster and linker in MOF by elaborately regulating the building units. They found that the photocatalytic performance sharply improved in the isoreticular MOF (PFC-98) after simply replacing the 1,4-Di(1H-pyrazol-4-yl)benzene (H2DPB) linker into an electron-deficient linker 2,5-di(1H-pyrazol-4-yl)thiazolo[5,4-d]thiazole (PyTT).

Photocatalytic experiments demonstrated that PFC-98 exhibited exceptional rates of 58.14 μmol g⁻¹ h⁻¹ and 43.14 μmol g⁻¹ h⁻¹ for acetate and ethanol in the CO₂ overall reaction, respectively, exceeding the catalytic performance of most materials reported thus far.

Additionally, the researchers revealed that the lowest unoccupied molecular orbital (LUMO) energy levels of the ligand and cluster in PFC-98 were well-matched to construct delocalized orbitals that facilitate direct electron excitation transfer from the ligand to the metal cluster through theoretical calculations, thereby enhancing electron transfer and separation efficiency.

They verified that a long-lived intermediate charge-separated state appeared upon photoexcitation from spectroscopy characterizations, prolonging the excited state lifetime and improving electron-hole separation efficiency.

Furthermore, the researchers discovered that the electron density on the metal cluster was obviously much higher in PFC-98 than in the isoreticular, thereby promoting the occurrence of C₂ generation from CO₂ photocatalytic reaction.

This study provides a novel approach for the photocatalytic reduction of CO₂ to create C₂ products.