A new copper(I) complex with the ability to bind to TiO(2) was synthesised and successfully employed as a solar cell sensitizer. Furthermore, we demonstrated that the copper(I) dye-sensitised TiO(2)-based photocatalyst exhibits impressive effectiveness for the selective photoreduction of CO(2) to CH(4) under visible light.
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http://dx.doi.org/10.1039/c2dt30865g | DOI Listing |
RSC Adv
January 2023
Department of Chemistry, University of Basel BPR 1096, Mattenstrasse 24a 4058 Basel Switzerland
Metal complexes used as sensitisers in dye-sensitised solar cells (DSCs) are conventionally constructed using a push-pull strategy with electron-releasing and electron-withdrawing (anchoring) ligands. In a new paradigm we have designed new DπA ligands incorporating diarylaminophenyl donor substituents and phosphonic acid anchoring groups. These new ligands function as organic dyes.
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March 2014
School of Chemistry and EaStChem, University of Edinburgh, King's Buildings, Edinburgh, UK.
Heteroleptic neutral copper(I) dipyrrin complexes have been synthesised with the general formula [Cu(4,4'-(R)-6,6'-(CH3)-bipyridine)(dipyrrin)], R = CH3 or CO2Et, and H-dipyrrin is either 1,3,7,9-tetramethyldipyrromethene (HL1), 1,13-diphenyl-6,8-diisoindolemethene (HL2), or 1,13-diphenyl-3,11-di(trifluoromethyl)-6,8-diisoindolemethene (HL3). Improved stability was observed across the series , likely due to better steric constraints between the ligands. Visible light absorption has also been enhanced with a red-shift in absorption from 450 nm to 600 nm.
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August 2012
Eco-Materials and Renewable Energy Research Center, National Laboratory of Solid State Microstructures, Department of Materials Science and Engineering, Nanjing University, Nanjing, Jiangsu 210093, P.R. China.
A new copper(I) complex with the ability to bind to TiO(2) was synthesised and successfully employed as a solar cell sensitizer. Furthermore, we demonstrated that the copper(I) dye-sensitised TiO(2)-based photocatalyst exhibits impressive effectiveness for the selective photoreduction of CO(2) to CH(4) under visible light.
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