Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Improved charge separation and photosensitized H/sub 2/ evolution from water with TiO/sub 2/ particles on colloidal SiO/sub 2/ carriers

Journal Article · · J. Am. Chem. Soc.; (United States)
DOI:https://doi.org/10.1021/ja00246a012· OSTI ID:6135467

Laser flash photolysis and steady-state photolysis studies show that electrostatic interactions have a dramatic influence on the kinetics for charge separation and hydrogen production in aqueous systems (pH 9.8) of 20-nm diameter TiO/sub 2/-modified SiO/sub 2/ colloids in various combinations with an electron relay, a photosensitizer, and a Pt catalyst. Either direct excitation of the semiconductor or the photosensitizer Ru(bpy)/sub 3//sup 2 +/ (bpy = 2,2'-bipyridine), electrostatically adsorbed to the colloid, initiate electron transfer to either the zwitterionic electron relay, N,N'-bis(3-sulfonatopropyl)-4,4'-bipyridinium (PVS/sup 0/), or N,N'-bis(3-sulfonatopropyl)-2,2'-bipyridinium (DQS/sup 0/), or methyl viologen (MV/sup 2 +/). The rates and quantum yields for the formation of the radical PVS/sup -/ anion in both the TiO/sub 2/-SiO/sub 2//PVS/sup 0/ and the TiO/sub 2/-SiO/sub 2//Ru(bpy)/sub 3//sup 2 +//PVS/sup 0/ systems decline with increasing ionic strength. The rate and quantum yields for H/sub 2/ production in both the TiO/sub 2/-SiO/sub 2//DQS/sup 0//Pt and the TiO/sub 2/-SiO/sub 2//Ru(bpy)/sub 3//sup 2 +//DQS/sup 0//Pt systems also show a similar ionic strength dependence.

Research Organization:
Solar Energy Research Institute, Golden, CO
OSTI ID:
6135467
Journal Information:
J. Am. Chem. Soc.; (United States), Journal Name: J. Am. Chem. Soc.; (United States) Vol. 109:12; ISSN JACSA
Country of Publication:
United States
Language:
English