Published July 29, 2016 | Version v1
Journal article

Ordered and disordered evolution of the pore mesostructure in hybrid silica anti-reflective films obtained by one-pot self-assembly method

Description

Hybrid mesoporous silica films were prepared in acid-catalysed medium using a one-pot self-assembly method. A gradual content of methyl groups was introduced into the inorganic framework by co-condensation of tetraethyl orthosilicate and methyltriethoxysilane. To better understand how the ordered and disordered transition occurs in mesoporous hybrid organosilica sytem as function of the MTES molar ratio in the starting solution, textural, chemical and optical properties of the films were studied by transmission electronic microscopy (TEM), grazing-incident small angle X-ray scattering (GISAXS), transmission Fourier transformed infrared (FTIR) and UV–visible spectroscopy. Increasing the loading of the incorporated organic groups (up to 40% in the starting solution) led simultaneously to a disorganization of the pore mesostructure and a reduction in the pore diameter. Concomitantly, a disordered domain of the silica rings in the walls was observed, which created bond strains in the silica wall contributing also to the disorganization of the pore mesostructure. Furthermore, an optimal MTES content was identified in order to obtain antireflection coatings, exhibiting low reflection in the visible range. - Highlights: • Mesoporous hybrid silica films where prepared by one-pot co-condensation of MTES and TEOS. • Ordered and disordered mesostructures were studied as function as variable MTES molar ratio. • A rearrangement of the silica cyclic species occurred as the molar ratio of MTES increases. • Transmittance of the silica coatings is affected by the MTES molar ratio.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.tsf.2016.05.018

Additional details

Identifiers

DOI
10.1016/j.tsf.2016.05.018;
PII
S0040-6090(16)30167-5;

Publishing Information

Journal Title
Thin Solid Films
Journal Volume
611
Journal Page Range
p. 117-124
ISSN
0040-6090
CODEN
THSFAP

Optional Information

Copyright
Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.