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Kinetic and Mechanistic Investigations of the Light Induced Formation of Gold Nanoparticles on the Surface of TiO 2
Author(s) -
Mohamed Hanan H.,
Dillert Ralf,
Bahnemann Detlef W.
Publication year - 2012
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201102799
Subject(s) - colloidal gold , nanoclusters , nanoparticle , materials science , surface plasmon resonance , metal , absorbance , x ray photoelectron spectroscopy , titanium dioxide , photochemistry , inorganic chemistry , chemistry , chemical engineering , nanotechnology , chromatography , engineering , metallurgy
The kinetics of the formation of gold nanoparticles on the surface of pre‐illuminated TiO 2 have been investigated using stopped‐flow technique and steady state UV/Vis spectroscopy. Excess electrons were loaded on the employed nanosized titanium dioxide particles by UV‐A photolysis in the presence of methanol serving as hole scavenger, stored on them in the absence of oxygen and subsequently used for the reduction of Au III ions. The formation of gold nanoparticles with an average diameter of 5 nm was confirmed after mixing of the TiO 2 nanoparticles loaded with electrons with aqueous solution of tetrachloroaureate (HAuCl 4 ) by their surface plasmon absorbance band at 530 nm, as well as by XRD and HRTEM measurements. The rate of formation of the gold nanoparticles was found to be a function of the concentration of the gold ions and the concentration of the stored electrons, respectively. The effect of PVA as a stabilizer of the gold nanoclusters was also studied. The observed kinetic behavior suggests that the formation of the gold nanoparticles on the TiO 2 surface is an autocatalytic process comprising of two main steps: 1) Reduction of the gold ions by the stored electrons on TiO 2 forming gold atoms that turn into gold nuclei. 2) Growth of the metal nuclei on the surface of TiO 2 forming the gold particles. Interestingly, at higher TiO 2 electron loading the excess electrons are subsequently transferred to the deposited gold metal particles resulting in “bleaching” of their surface plasmon band. This bleaching in the surface plasmon band is explained by the Fermi level equilibration of the Au/TiO 2 nanocomposites. Finally, the reduction of water resulting in the evolution of molecular hydrogen initiated by the excess electrons that have been transferred to the previously formed gold particles has also been observed. The mechanism of the underlying multistep electron‐transfer process has been discussed in detail.