Department of Chemistry and Biochemistry, University of Colorado Boulder, Boulder, Colorado 80309, United States.
J Am Chem Soc. 2013 Mar 6;135(9):3383-6. doi: 10.1021/ja400178g. Epub 2013 Feb 25.
We describe the charge transfer interactions between photoexcited CdS nanorods and mononuclear water oxidation catalysts derived from the Ru(bpy)(tpy)Cl parent structure. Upon excitation, hole transfer from CdS oxidizes the catalyst (Ru(2+) → Ru(3+)) on a 100 ps to 1 ns timescale. This is followed by 10-100 ns electron transfer (ET) that reduces the Ru(3+) center. The relatively slow ET dynamics may provide opportunities for the accumulation of multiple holes at the catalyst, which is necessary for water oxidation.
我们描述了 CdS 纳米棒与单核水氧化催化剂之间的电荷转移相互作用,该催化剂源自 Ru(bpy)(tpy)Cl 母体结构。在激发后,CdS 的空穴转移在 100 ps 到 1 ns 的时间尺度内将催化剂(Ru(2+) → Ru(3+))氧化。随后是 10-100 ns 的电子转移(ET),还原 Ru(3+)中心。相对较慢的 ET 动力学可能为催化剂中多个空穴的积累提供机会,这对于水氧化是必要的。