Two-dimensional hexagonal mesoporous silica thin films prepared from black copolymers: Detailed characterization amd formation mechanism

被引:225
作者
Grosso, D
Balkenende, AR
Albouy, PA
Ayral, A
Amenitsch, H
Babonneau, F
机构
[1] Univ Paris 06, Lab Chim & Mat Condensee, F-75252 Paris 05, France
[2] Philips Res Labs, NL-5656 AA Eindhoven, Netherlands
[3] UMII, ENSCM, CNRS, UMR 5635,Lab Mat & Procedes Membranaires, F-34296 Montpellier 5, France
[4] Austrian Acad Sci, Inst Biophys & Xray Struct Res, A-8010 Graz, Austria
关键词
D O I
10.1021/cm001225b
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
Silica thin films with a two-dimensional (2D) hexagonal structure were produced from TEOS and the F127 triblock copolymer PEO106PPO70PEO106 The structure of the films was deduced from transmission electron microscopy (TEM) performed on microtomed sections and from a 2D X-ray scattering technique adapted for film characterization. Both methods are complementary and allow for a detailed characterization of the film structure. The pore channels within the coatings are organized in domains, which spin and curve inside the film, but align with the surface plan at the air/film and film/substrate interfaces. The formation of the film was monitored by in situ time-resolved SAXS experiments to follow the structural evolution during the first minutes after deposition. Cylindrical micelles, which gives rise to a wormlike structure, form first at the air/film interface and extend toward the film/substrate interface via solvent evaporation. When most of the liquid phase is evaporated, the well-aligned domains located at both interfaces are obtained by a self-arrangement of the micelles parallel to the intel faces. This rearrangement occurs when the film is considered to be dry. The atom content profiles in the as-prepared films were obtained by Rutherford backscattering (RBS) and show homogeneous distribution of atoms throughout the film thickness. To stiffen the network and remove the surfactant, various postsynthesis treatments were applied to the coatings, that is, thermal treatment, base-catalyzed condensation, and solvent extraction. Each method induces shrinkage, leading to 2D-centered rectangular films through a contraction of the initial 2D hexagonal structure. As-prepared and treated films exhibit excellent optical transparency and high degree of organization. Ellipsometry measurements and Nz adsorption/desorption isotherms were thus used to estimate the refractive index and the porosity of the films. Refractive index down to 1.2 was obtained in the film that was pretreated under a NH3 atmosphere before solvent extraction of the surfactant. This shows the efficiency of this treatment to minimize the network shrinkage. NP adsorption-desorption measurement performed on films calcined at 350 degreesC gives a surface area of 800 m(2) g(-1) and a porosity of 63%.
引用
收藏
页码:1848 / 1856
页数:9
相关论文
共 27 条
[1]  
Ayral A, 1998, J MATER SCI LETT, V17, P883, DOI 10.1023/A:1026428814961
[2]   Tailored porous materials [J].
Barton, TJ ;
Bull, LM ;
Klemperer, WG ;
Loy, DA ;
McEnaney, B ;
Misono, M ;
Monson, PA ;
Pez, G ;
Scherer, GW ;
Vartuli, JC ;
Yaghi, OM .
CHEMISTRY OF MATERIALS, 1999, 11 (10) :2633-2656
[3]   A NEW FAMILY OF MESOPOROUS MOLECULAR-SIEVES PREPARED WITH LIQUID-CRYSTAL TEMPLATES [J].
BECK, JS ;
VARTULI, JC ;
ROTH, WJ ;
LEONOWICZ, ME ;
KRESGE, CT ;
SCHMITT, KD ;
CHU, CTW ;
OLSON, DH ;
SHEPPARD, EW ;
MCCULLEN, SB ;
HIGGINS, JB ;
SCHLENKER, JL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (27) :10834-10843
[4]   FUNDAMENTALS OF SOL-GEL DIP COATING [J].
BRINKER, CJ ;
FRYE, GC ;
HURD, AJ ;
ASHLEY, CS .
THIN SOLID FILMS, 1991, 201 (01) :97-108
[5]  
Brinker CJ, 1999, ADV MATER, V11, P579, DOI 10.1002/(SICI)1521-4095(199905)11:7<579::AID-ADMA579>3.0.CO
[6]  
2-R
[7]   Ordered mesoporous materials [J].
Ciesla, U ;
Schüth, F .
MICROPOROUS AND MESOPOROUS MATERIALS, 1999, 27 (2-3) :131-149
[8]  
GROSSON D, 2000, IN PRESS MAT RES SOC, P628
[9]   Phase behavior and structure of ternary amphiphilic block copolymer-alkanol-water systems: Comparison of poly(ethylene oxide) poly(propylene oxide) to poly(ethylene oxide) poly(tetrahydrofuran) copolymers [J].
Holmqvist, P ;
Alexandridis, P ;
Lindman, B .
LANGMUIR, 1997, 13 (09) :2471-2479
[10]   In situ luminescence probing of the chemical and structural changes during formation of dip-coated lamellar phase sodium dodecyl sulfate sol-gel thin films [J].
Huang, MH ;
Dunn, BS ;
Zink, JI .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (15) :3739-3745