Zhang Linlin, Gao Yan, Ding Xin, Yu Ze, Sun Licheng
State Key Laboratory of Fine Chemicals, Institute of Artificial Photosynthesis, DUT-KTH Joint Education and Research Center on Molecular Devices, Dalian University of Technology (DUT), Dalian 116024 (PR China).
ChemSusChem. 2014 Oct;7(10):2801-4. doi: 10.1002/cssc.201402561. Epub 2014 Aug 19.
Two photoanodes based on a binuclear (2) and a mononuclear ruthenium (3) water oxidation catalysts were assembled in combination with a molecular photosensitizer (1) by using a co-adsorption method. The anodes were used in dye-sensitized photoelectrochemical cells (DS-PECs) for visible-light-driven water splitting. A DS-PEC device using TiO2 (1+2) as working electrode (WE) exhibits better performance than TiO2 (1+3) as WE in light-driven water splitting. Detailed photoelectrochemical studies on these DS-PEC devices are discussed.
通过共吸附法,将基于双核(2)和单核钌(3)水氧化催化剂的两个光阳极与分子光敏剂(1)组装在一起。这些阳极被用于染料敏化光电化学电池(DS-PEC)中,以实现可见光驱动的水分解。使用TiO2(1+2)作为工作电极(WE)的DS-PEC装置在光驱动水分解方面比使用TiO2(1+3)作为WE的装置表现出更好的性能。本文讨论了对这些DS-PEC装置的详细光电化学研究。