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Updated: Aug 26, 2025

Developing Photosensitizer-Cobaloxime Hybrids for Solar-Driven H2 Production in Aqueous Aerobic Conditions
Published on: October 5, 2019
Complexed Semiconductor Cores Activate Hexaniobate Ligands as Nucleophilic Sites for Solar-Light Reduction of CO2 by
Guanyun Zhang1,2, Fei Wang3, Tal Tubul1
1Department of Chemistry and the Ilse Katz Institute for Nanoscale Science & Technology, Ben-Gurion University of the Negev, Beer Sheva, 84105, Israel.
Abstract:
Although pure and functionalized solid-state polyniobates such as layered perovskites and niobate nanosheets are photocatalysts for renewable-energy processes, analogous reactions by molecular polyoxoniobate cluster-anions are nearly absent from the literature. We now report that under simulated solar light, hexaniobate cluster-anion encapsulated 30-NiII -ion "fragments" of surface-protonated cubic-phase-like NiO cores activate the hexaniobate ligands towards CO2 reduction by water. Photoexcitation of the NiO cores promotes charge-transfer reduction of NbV to NbIV , increasing electron density at bridging oxo atoms of Nb-μ-O-Nb linkages that bind and convert CO2 to CO. Photogenerated NiO "holes" simultaneously oxidize water to dioxygen. The findings point to molecular complexation of suitable semiconductor "fragments" as a general method for utilizing electron-dense polyoxoniobate anions as nucleophilic photocatalysts for solar-light driven activation and reduction of small molecules.
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