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Journal ArticleDOI

Peroxo complexes of titanium

01 Nov 1970-Inorganic Chemistry (American Chemical Society)-Vol. 9, Iss: 11, pp 2381-2390
About: This article is published in Inorganic Chemistry.The article was published on 1970-11-01. It has received 228 citations till now. The article focuses on the topics: Titanium.
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TL;DR: In this paper, the preparation of a colloidal colloidal by un procede sol gel is described, and a procedure for determination des proprietes electriques et electrochimiques is described.

2,040 citations

Journal ArticleDOI
TL;DR: In this article, a method was developed to determine the concentration of titanium dioxide in poultry digesta samples, obtained from the lower half of the small intestine of three-week-old male broiler chickens.

900 citations

Journal ArticleDOI
TL;DR: In this paper, the most common chemical additives used in the sol-gel process are explained in terms of chemical reactivity, and the most important parameters appear to be the reactivity of the new ligand towards hydrolysis, the charge distribution in the new molecular precursor and the coordination numbers of the metal atom.
Abstract: The chemical reactivity of metal alkoxides offers a broad range of possibilities for chemical modification of these molecular precursors. The whole hydrolysis-condensation process may then be completely different leading to new products. An analysis is presented concerning some of the most common chemical additives used in the sol-gel process. Their role is explained in terms of chemical reactivity. The most important parameters appear to be the reactivity of the new ligand towards hydrolysis, the charge distribution in the new molecular precursor and the coordination numbers of the metal atom.

760 citations

Journal ArticleDOI
TL;DR: The results give strong support to the previously proposed mechanism that the oxygen photoevolution is initiated by a nucleophilic attack of a H2O molecule on a photogenerated hole at a surface lattice O site, not by oxidation of surface OH group by the hole.
Abstract: Primary intermediates of oxygen photoevolution (water photooxidation) reaction at the TiO2 (rutile)/aqueous solution interface were investigated by in situ multiple internal reflection infrared (MIRIR) absorption and photoluminescence (PL) measurements. UV irradiation of TiO2 in the presence of 10 mM Fe3+ in the solution caused the appearance of a new peak at 838 cm-1 and a shoulder at 812 cm-1. Detailed investigations of the effects of solution pH, the presence of methanol as a hole scavenger, and isotope exchange in water (H216O→H218O) on the spectra have shown that the 838- and 812-cm-1 bands can be assigned to the O−O stretching mode of surface TiOOH and TiOOTi, respectively, produced as primary intermediates of the oxygen photoevolution reaction. The results give strong support to our previously proposed mechanism that the oxygen photoevolution is initiated by a nucleophilic attack of a H2O molecule on a photogenerated hole at a surface lattice O site, not by oxidation of surface OH group by the hole...

445 citations

Journal ArticleDOI
TL;DR: To harness solar energy efficiently, a new water-splitting photocatalyst that is active over a wider range of the visible spectrum has been developed, and two effective strategies for overall water splitting were developed.
Abstract: One of the simplest methods for splitting water into H2 and O2 with solar energy entails the use of a particulate-type semiconductor photocatalyst. To harness solar energy efficiently, a new water-splitting photocatalyst that is active over a wider range of the visible spectrum has been developed. In particular, a complex perovskite-type oxynitride, LaMgxTa1−xO1+3xN2−3x (x≥1/3), can be employed for overall water splitting at wavelengths of up to 600 nm. Two effective strategies for overall water splitting were developed. The first entails the compositional fine-tuning of a photocatalyst to adjust the bandgap energy and position by forming a series of LaMgxTa1−xO1+3xN2−3x solid solutions. The second method is based on the surface coating of the photocatalyst with a layer of amorphous oxyhydroxide to control the surface redox reactions. By combining these two strategies, the degradation of the photocatalyst and the reverse reaction could be prevented, resulting in successful overall water splitting.

362 citations