In-situ X-ray scattering study of continuous silica-surfactant self-assembly during steady-state dip coating

被引:45
作者
Doshi, DA
Gibaud, A
Liu, NG
Sturmayr, D
Malanoski, AP
Dunphy, DR
Chen, HJ
Narayanan, S
MacPhee, A
Wang, J
Reed, ST
Hurd, AJ
van Swol, F
Brinker, CJ
机构
[1] Univ New Mexico, Dept Chem & Nucl Engn, Albuquerque, NM 87131 USA
[2] Univ New Mexico, Ctr Microengn Mat, Albuquerque, NM 87131 USA
[3] Univ Maine, Fac Sci, UMR 6087, CNRS 72085, Le Mans 09, France
[4] Argonne Natl Lab, Adv Photon Source, Argonne, IL 60439 USA
[5] Vienna Univ Technol, Inst Mat Chem, Vienna, Austria
关键词
D O I
10.1021/jp027214i
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Inorganic mesoporous thin-films are important for applications such as membranes, sensors, low-dielectric-constant insulators (so-called low kappa dielectrics), and fluidic devices. Over the past five years, several research groups have demonstrated the efficacy of using evaporation accompanying conventional coating operations such as spin- and dip-coating as an efficient means of driving the self-assembly of homogeneous solutions into highly ordered, oriented, mesostructured films. Understanding such evaporation-induced self-assembly (EISA) processes is of interest for both fundamental and technological reasons. Here, we use spatially resolved 2D grazing incidence X-ray scattering in combination with optical interferometry during steady-state dip-coating of surfactant-templated silica thin-films to structurally and compositionally characterize the EISA process. We report the evolution of a hexagonal (p6 mm) thin-film mesophase from a homogeneous precursor solution and its further structural development during drying and calcination. Monte Carlo simulations of water/ethanol/surfactant bulk phase behavior are used to investigate the role of ethanol in the self-assembly process, and we propose a mechanism to explain the observed dilation in unit cell dimensions during solvent evaporation.
引用
收藏
页码:7683 / 7688
页数:6
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