Orientation and electronic structure of ion exchanged dye molecules on mica: An X-ray absorption study

被引:42
作者
Fischer, D
Caseri, WR
Hahner, G
机构
[1] ETH Zurich, Dept Mat Sci, Surface Sci & Technol Lab, CH-8092 Zurich, Switzerland
[2] ETH Zurich, Dept Mat, Inst Polymers, CH-8092 Zurich, Switzerland
关键词
silicates; muscovite mica; specific surface area; ion exchange; triphenylmethane dyes; crystal violet; malachite green; orientation; X-ray spectroscopy; NEXAFS; XPS;
D O I
10.1006/jcis.1997.5296
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
Dye molecules are frequently used to determine the specific surface area and the ion exchange capacity of high-surface-area materials such as mica. The organic molecules are often considered to be planar and to adsorb in a flat orientation. In the present study we have investigated the orientation and electronic structure of crystal violet (CV) and malachite green (MG) on muscovite mica, prepared by immersing the substrates for extended periods into aqueous solutions of the dyes of various concentrations, The K+ ions of the mica surface are replaced by the organic cations via ion exchange. X-ray photoelectron spectroscopy reveals that only one amino group is involved in the interaction of CV and MG with the muscovite surface, i.e., certain resonance structures are abolished upon adsorption. With near edge X-ray absorption fine structure spectroscopy a significant tilt angle with respect to the surface was found for all investigated species. A flat orientation, as has often been proposed before, can effectively be ruled out. Hence, our results are in marked contrast to the often quoted orientation and suggest that the specific surface areas determined with dyes may, in general, be overestimated. (C) 1998 Academic Press.
引用
收藏
页码:337 / 346
页数:10
相关论文
共 48 条
[21]   Self-assembled layers of substituted poly(p-phenylene)s on gold and copper investigated by soft X-ray spectroscopy [J].
Hahner, G ;
Marti, A ;
Spencer, ND ;
Brunner, S ;
Caseri, WR ;
Suter, UW ;
Rehahn, M .
LANGMUIR, 1996, 12 (03) :719-725
[23]  
HOFMANN U, 1969, CHIMIA, V23, P476
[24]  
HOFMANN U, 1967, GIESSEREI, V54, P97
[25]  
HORSLEY JA, 1985, J CHEM PHYS, V83, P6069
[26]   POLYMER METAL INTERFACES STUDIED BY CARBON NEAR-EDGE X-RAY ABSORPTION FINE-STRUCTURE SPECTROSCOPY [J].
JORDANSWEET, JL ;
KOVAC, CA ;
GOLDBERG, MJ ;
MORAR, JF .
JOURNAL OF CHEMICAL PHYSICS, 1988, 89 (04) :2482-2489
[27]   SOLVENT EFFECTS ON THE VISIBLE ABSORPTION-SPECTRUM OF CRYSTAL VIOLET [J].
KORPPITOMMOLA, J ;
YIP, RW .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1981, 59 (02) :191-194
[28]   THE TEMPERATURE-DEPENDENT RED-SHIFT OF THE VISIBLE ABSORPTION-SPECTRA OF CRYSTAL VIOLET IN ALCOHOL-SOLUTIONS [J].
KORPPITOMMOLA, J ;
KOLEHMAINEN, E ;
SALO, E ;
YIP, RW .
CHEMICAL PHYSICS LETTERS, 1984, 104 (04) :373-377
[29]   INTERCALATION AND EXCHANGE-REACTIONS OF CLAY-MINERALS AND NON-CLAY LAYER COMPOUNDS [J].
LAGALY, G ;
BENEKE, K .
COLLOID AND POLYMER SCIENCE, 1991, 269 (12) :1198-1211
[30]  
Lagaly G ., 1993, TONMINERALE TONE