Dye-Sensitized Photocatalysis: Hydrogen Evolution and Alcohol-to-Aldehyde Oxidation without Sacrifical Electron Donor

被引:8
作者
Romito, Deborah [1 ]
Govind, Chinju [2 ]
Nikolaou, Vasilis [1 ]
Fernandez-Teran, Ricardo J. [2 ]
Stoumpidi, Aspasia [3 ]
Agapaki, Eleni [3 ]
Charalambidis, Georgios [4 ]
Diring, Stephane [1 ]
Vauthey, Eric [2 ]
Coutsolelos, Athanassios G. [3 ,5 ]
Odobel, Fabrice [1 ]
机构
[1] Nantes Univ, CNRS, CEISAM, UMR 6230, F-44000 Nantes, France
[2] Univ Geneva, Dept Phys Chem, 30 Quai Ernest Ansermet, CH-1211 Geneva, Switzerland
[3] Univ Crete, Dept Chem, Lab Bioinorgan Chem, Voutes Campus, Iraklion 70013, Crete, Greece
[4] Natl Hellen Res Fdn, Theoret & Phys Chem Inst, 48 Vassileos Constantinou Ave, Athens 11635, Greece
[5] Fdn Res & Technol Hellas FORTH, Inst Elect Struct & Laser IESL, GR-70013 Iraklion, Crete, Greece
基金
瑞士国家科学基金会;
关键词
photocatalysis; hydrogen; alcohol oxidation; DSP systems; ANCHORING GROUPS; SOLAR; WATER;
D O I
10.1002/anie.202318868
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
There is a growing interest in developing dye-sensitized photocatalytic systems (DSPs) to produce molecular hydrogen (H2) as alternative energy source. To improve the sustainability of this technology, we replaced the sacrificial electron donor (SED), typically an expensive and polluting chemical, with an alcohol oxidation catalyst. This study demonstrates the firstdye-sensitized system using a diketopyrrolopyrrole dye covalently linked to 2,2,6,6-tetramethyl-1-piperidine-N-oxyl (TEMPO) based catalyst for simultaneous H2 evolution and alcohol-to-aldehyde transformation operating in water with visible irradiation. This study shows that a two-hole oxidation process such as TEMPO catalyzed alcohol oxidation is a viable reaction to couple with reduction reaction to eliminate SED and generate two added-value chemicals in dye-sensitized photocatalytic systems. image
引用
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页数:6
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