Surfactant removal and silica condensation during the photochemical calcination of thin film silica mesophases

被引:40
作者
Dattelbaum, AM
Amweg, ML
Ruiz, JD
Ecke, LE
Shreve, AP
Parikh, AN
机构
[1] Los Alamos Natl Lab, Biosci Div, Los Alamos, NM 87545 USA
[2] Univ Calif Davis, Dept Appl Sci, Davis, CA 95616 USA
关键词
D O I
10.1021/jp051401+
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
The evolution of photochemical surfactant removal and silica condensation from organically templated thin film silica nanocomposites with mesoscopic ordering has been probed using a combined application of Fourier transform infrared (FT-IR) spectroscopy and single wavelength ellipsometry. Thin films of silica nanocomposites were prepared by a previously reported evaporation-induced self-assembly process. Specifically, oxidized silicon and gold substrates were withdrawn at 25 mm/min from a subcritical micelle concentration solution containing an ethylene oxide surfactant as a structure-directing agent and tetraethyl orthosilicate as a silica precursor. Real-time grazing incidence difference FT-IR spectra of the nanocomposite films on gold taken during exposure to short-wavelength ultraviolet light (184-257 nm) show that surfactant removal and silica condensation occur gradually and concomitantly. Surfactant removal and silica reconstructions were found to be nearly complete after 90 min of exposure. Further, a transient feature was observed in the FT-IR spectra around 1713 cm(-1) during the UV exposure process and was assigned to a carbonyl (C=O) stretching mode absorption, reflecting the transient formation of a partially oxidized surfactant intermediate. From these data we propose a stepwise model for surfactant removal from the nanocomposite films. Ellipsometrically determined index of refraction values collected as a function of UV exposure are also shown to support such a stepwise mechanism of surfactant removal from the ordered nanocomposite silica thin film mesophases studied here.
引用
收藏
页码:14551 / 14556
页数:6
相关论文
共 47 条
[11]   Ordered porous materials for emerging applications [J].
Davis, ME .
NATURE, 2002, 417 (6891) :813-821
[12]   Infrared spectra of large H2O clusters:: New understanding of the elusive bending mode of ice [J].
Devlin, JP ;
Sadlej, J ;
Buch, V .
JOURNAL OF PHYSICAL CHEMISTRY A, 2001, 105 (06) :974-983
[13]   Optically, defined multifunctional patterning of photosensitive thin-film silica mesophases [J].
Doshi, DA ;
Huesing, NK ;
Lu, MC ;
Fan, HY ;
Lu, YF ;
Simmons-Potter, K ;
Potter, BG ;
Hurd, AJ ;
Brinker, CJ .
SCIENCE, 2000, 290 (5489) :107-111
[14]   Functionalized monolayers on ordered mesoporous supports [J].
Feng, X ;
Fryxell, GE ;
Wang, LQ ;
Kim, AY ;
Liu, J ;
Kemner, KM .
SCIENCE, 1997, 276 (5314) :923-926
[15]   Characterization of mesoporous materials by vibrational spectroscopic techniques [J].
Geidel, E ;
Lechert, H ;
Döbler, J ;
Jobic, H ;
Calzaferri, G ;
Bauer, F .
MICROPOROUS AND MESOPOROUS MATERIALS, 2003, 65 (01) :31-42
[16]   Low-temperature elimination of organic components from mesostructured organic-inorganic composite films using vacuum ultraviolet light [J].
Hozumi, A ;
Sugimura, H ;
Hiraku, K ;
Kameyama, T ;
Takai, O .
CHEMISTRY OF MATERIALS, 2000, 12 (12) :3842-3847
[17]   Order-disorder transitions and evolution of silica structure in self-assembled mesostructured silica films studied through FTIR spectroscopy [J].
Innocenzi, P ;
Falcaro, P ;
Grosso, D ;
Babonneau, F .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (20) :4711-4717
[18]   Concentration of surface hydroxyl groups on MCM-41 [J].
Jentys, A ;
Kleestorfer, K ;
Vinek, H .
MICROPOROUS AND MESOPOROUS MATERIALS, 1999, 27 (2-3) :321-328
[19]   Ozone treatment for the removal of surfactant to form MCM-41 type materials [J].
Keene, MTJ ;
Denoyel, R ;
Llewellyn, PL .
CHEMICAL COMMUNICATIONS, 1998, (20) :2203-2204
[20]   Calcination of the MCM-41 mesophase: mechanism of surfactant thermal degradation and evolution of the porosity [J].
Keene, MTJ ;
Gougeon, RDM ;
Denoyel, R ;
Harris, RK ;
Rouquerol, J ;
Llewellyn, PL .
JOURNAL OF MATERIALS CHEMISTRY, 1999, 9 (11) :2843-2850