Tin oxide surfaces. Part 12.—A comparison of the nature of tin(IV) oxide, tin(IV) oxide–silica and tin(IV) oxide–palladium oxide: surface hydroxyl groups and ammonia adsorption

1984 ◽  
Vol 80 (6) ◽  
pp. 1341 ◽  
Author(s):  
Philip G. Harrison ◽  
Barry M. Maunders
Keyword(s):  
Tin Oxide ◽  
Palladium Oxide ◽  
Oxide Surfaces ◽  
Oxide Surface ◽  
Hydroxyl Groups ◽  
Ammonia Adsorption ◽  
Surface Hydroxyl ◽  
Surface Hydroxyl Groups

Self Terminating Reaction of Dipivaloylmethanate Complexes with Hydroxyl Groups on Oxide Surface

1991 ◽  
Vol 222 ◽  
Author(s):  
Rika Sekine ◽  
Maki Kawai ◽  
Kiyotaka Asakura ◽  
Yasuhiro Iwasawa
Keyword(s):  
Fine Structure ◽  
Photoelectron Spectroscopy ◽  
Oxide Surface ◽  
Hydroxyl Groups ◽  
Adsorbed Species ◽  
Oh Groups ◽  
X Ray ◽  
Surface Hydroxyl ◽  
Surface Hydroxyl Groups ◽  
X Ray Absorption

ABSTRACTWe have already reported that copper and calcium dipivaloylmethanates [Cu(DPM)2 and Ca(DPM)2 ] reacts selectively and stoichiometrically with surface hydroxyl groups (OH) on SiO2. In order to clarify the structure of the adsorbed species and the origin of the reaction between M(DPM)2 (M=Cu and Ca) and OH groups, the surface adsorbed species are studied by infrared spectroscopy (IR), X-ray photoelectron spectroscopy (XPS), and the extended X-ray absorption fine structure (EXAFS). As a result, it was found that H from surface OH has moved into M(DPM)2 after the adsorption, where the four oxygen coordinated structure around Cu still exists in the adsorbed Cu(DPM)2. Introducing water vapor at 673 K to this surface results in the removal of ligand DPM from the adsorbed Cu(DPM)2. At 673 K, Cu atoms decomposed from the adsorbates aggregated on the surface. This fact supports that the interaction between the adsorbed Cu(DPM)2 and SiO2 surface is originated from that between the ligands and the surface.

The synthesis and structure of silica-supported bis(h5-cyclopentadienyl)dichlorotitanium(IV) complexes

1986 ◽  
Vol 51 (7) ◽  
pp. 1430-1438 ◽  
Author(s):  
Alena Reissová ◽  
Zdeněk Bastl ◽  
Martin Čapka
Keyword(s):  
Free Surface ◽  
Hydroxyl Groups ◽  
Titanium Complex ◽  
Surface Hydroxyl ◽  
Surface Hydroxyl Groups ◽  
Free Hydroxyl ◽  
Cyclopentadienyl Anion

The title complexes have been obtained by functionalization of silica with cyclopentadienylsilanes of the type Rx(CH3)3 - xSi(CH2)nC5H5 (x = 1-3, n = 0, 1, 3), trimethylsilylation of free surface hydroxyl groups, transformation of the bonded cyclopentadienyl group to the cyclopentadienyl anion, followed by coordination of (h5-cyclopentadienyl)trichlorotitanium. The effects of single steps of the above immobilization on texture of the support, the number of free hydroxyl groups, the coverage of the surface by cyclopentadienyl groups and the degree of their utilization in anchoring the titanium complex have been investigated. ESCA study has shown that the above anchoring leads to formation of the silica-supported bis(h5-cyclopentadienyl)dichlorotitanium(IV) complex.

Controllable synthesis of phosphate-modified BiPO4 nanorods with high photocatalytic activity: surface hydroxyl groups concentrations effects

RSC Advances ◽  
2015 ◽  
Vol 5 (121) ◽  
pp. 99712-99721 ◽  
Author(s):  
Yan Li ◽  
Yawen Wang ◽  
Yu Huang ◽  
Junji Cao ◽  
Wingkei Ho ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Surface Modification ◽  
Photocatalytic Performance ◽  
High Photocatalytic Activity ◽  
Hydroxyl Groups ◽  
Controllable Synthesis ◽  
Surface Hydroxyl ◽  
Methylene Orange ◽  
Surface Hydroxyl Groups

Surface modification by phosphate efficiently improves the photocatalytic performance of BiPO4 for the degradation of methylene orange (MO), by enhancing the concentration of surface hydroxyl groups and improving its hydrophilicity.

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