A photocatalyst of nanometer TiO2/conjugated polymer complex was successfully synthesized and characterized by spectroscopic methods and photocatalytic experiments. The complex photocatalyst could be activated by abso...A photocatalyst of nanometer TiO2/conjugated polymer complex was successfully synthesized and characterized by spectroscopic methods and photocatalytic experiments. The complex photocatalyst could be activated by absorbing both ultraviolet and visible light (λ = 190-800 nm). Methylene blue (MB) could be degraded more efficiently on the complex photocatalyst than on the TiO2 under natural light. The conjugated polymer played a promoting role in the photocatalytic degradation of MB. The calcination temperature had an important effect in degradation of dye and could be summarized as 260℃ 〉 300 ℃ 〉 340 ℃ 〉 220 ℃ 〉 180 ℃.展开更多
Designing visible light photocatalysts with a metal oxide semiconductor as the starting material could expand a new horizon for the conversion and storage of solar energy.Here,the benchmark photocatalyst TiO_(2) was u...Designing visible light photocatalysts with a metal oxide semiconductor as the starting material could expand a new horizon for the conversion and storage of solar energy.Here,the benchmark photocatalyst TiO_(2) was used to pursue this goal by anchoring aromatic acids.Extending the aromatic acid was strategically deployed to design TiO_(2) complexes with violet light-induced selective aerobic oxidation of sulfide as the probe reaction.With benzoic acid(BA)as the initial molecule,horizontally extending one or two benzene rings furnishes 2-naphthoic acid(2-NA)and 2-anthracene acid(2-AA).Moreover,triethylamine(TEA),an electron transfer mediator,was introduced to maintain the integrity of the anchored aromatic acids.Notably,there was a direct correlation between theπ-conjugation of aromatic acid ligand and the selective aerobic oxidation of sulfides.Among the three aromatic acids,2-AA delivered the best result over TiO_(2) due to the most extensiveπ-conjugated system.Ultimately,violet light-induced selective aerobic oxidation of sulfides into corresponding sulfoxides was conveniently realized by cooperative photocatalysis of 2-AA-TiO_(2) with 10 mol%of TEA.This work affords an extending strategy for designing the next-generation ligands for semiconductors to expand visible light-induced selective reactions.展开更多
文摘A photocatalyst of nanometer TiO2/conjugated polymer complex was successfully synthesized and characterized by spectroscopic methods and photocatalytic experiments. The complex photocatalyst could be activated by absorbing both ultraviolet and visible light (λ = 190-800 nm). Methylene blue (MB) could be degraded more efficiently on the complex photocatalyst than on the TiO2 under natural light. The conjugated polymer played a promoting role in the photocatalytic degradation of MB. The calcination temperature had an important effect in degradation of dye and could be summarized as 260℃ 〉 300 ℃ 〉 340 ℃ 〉 220 ℃ 〉 180 ℃.
基金funded by the National Natural Science Foundation of China(Nos.22072108 and 21773173)。
文摘Designing visible light photocatalysts with a metal oxide semiconductor as the starting material could expand a new horizon for the conversion and storage of solar energy.Here,the benchmark photocatalyst TiO_(2) was used to pursue this goal by anchoring aromatic acids.Extending the aromatic acid was strategically deployed to design TiO_(2) complexes with violet light-induced selective aerobic oxidation of sulfide as the probe reaction.With benzoic acid(BA)as the initial molecule,horizontally extending one or two benzene rings furnishes 2-naphthoic acid(2-NA)and 2-anthracene acid(2-AA).Moreover,triethylamine(TEA),an electron transfer mediator,was introduced to maintain the integrity of the anchored aromatic acids.Notably,there was a direct correlation between theπ-conjugation of aromatic acid ligand and the selective aerobic oxidation of sulfides.Among the three aromatic acids,2-AA delivered the best result over TiO_(2) due to the most extensiveπ-conjugated system.Ultimately,violet light-induced selective aerobic oxidation of sulfides into corresponding sulfoxides was conveniently realized by cooperative photocatalysis of 2-AA-TiO_(2) with 10 mol%of TEA.This work affords an extending strategy for designing the next-generation ligands for semiconductors to expand visible light-induced selective reactions.