Consecutive Charging of a Perylene Bisimide Dye by Multistep Low-Energy Solar-Light-Induced Electron Transfer Towards H2 Evolution |
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Authors: | Yucheng Xu Jiaxin Zheng Dr Joachim O Lindner Xinbo Wen Dr Nianqiang Jiang Dr Zhicheng Hu Prof Dr Linlin Liu Prof Dr Fei Huang Prof Dr Frank Würthner Prof Dr Zengqi Xie |
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Institution: | 1. Institute of Polymer Optoelectronic Materials and Devices, State Key Laboratory of Luminescent Materials and Devices, South China University of Technology, Guangzhou, 510640 P. R. China;2. Institut für Organische Chemie & Center for Nanosystems Chemistry, Universität Würzburg, Am Hubland, 97074 Würzburg, Germany |
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Abstract: | A photocatalytic system containing a perylene bisimide (PBI) dye as a photosensitizer anchored to titanium dioxide (TiO2) nanoparticles through carboxyl groups was constructed. Under solar-light irradiation in the presence of sacrificial triethanolamine (TEOA) in neutral and basic conditions (pH 8.5), a reaction cascade is initiated in which the PBI molecule first absorbs green light, giving the formation of a stable radical anion (PBI.−), which in a second step absorbs near-infrared light, forming a stable PBI dianion (PBI2−). Finally, the dianion absorbs red light and injects an electron into the TiO2 nanoparticle that is coated with platinum co-catalyst for hydrogen evolution. The hydrogen evolution rates (HERs) are as high as 1216 and 1022 μmol h−1 g−1 with simulated sunlight irradiation in neutral and basic conditions, respectively. |
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Keywords: | electron transfer hydrogen evolution nanoparticles perylene bisimides solar energy |
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