FTIR STUDY OF THE CHANGES IN ORIENTATION AND CHEMISTRY OF LANGMUIR-BLODGETT-FILMS OF CADMIUM ARACHIDATE DURING THE FORMATION OF Q-STATE CDSPARTICLES

Citation
Rs. Urquhart et al., FTIR STUDY OF THE CHANGES IN ORIENTATION AND CHEMISTRY OF LANGMUIR-BLODGETT-FILMS OF CADMIUM ARACHIDATE DURING THE FORMATION OF Q-STATE CDSPARTICLES, Journal of physical chemistry, 99(43), 1995, pp. 15987-15992
Citations number
32
Categorie Soggetti
Chemistry Physical
ISSN journal
00223654
Volume
99
Issue
43
Year of publication
1995
Pages
15987 - 15992
Database
ISI
SICI code
0022-3654(1995)99:43<15987:FSOTCI>2.0.ZU;2-#
Abstract
The formation and growth of Q-state CdS particles during exposure of L angmuir-Blodgett films of cadmium arachidate (CdAr) to hydrogen sulfid e have been studied using grazing angle Fourier transform infrared (FT IR) spectroscopy. Films were studied after prolonged exposure to H2S ( 1 h) and after being subjected to repeated cycles of H2S exposure (1 h ) and subsequent immersion in an aqueous solution containing cadmium c hloride (1.5 h). During each H2S exposure, the CdAr molecules in the f ilm were converted to arachidic acid (ArH). A small proportion of the film, however, was present in the form of the cadmium salt after prolo nged exposure to H2S. Immersion of the film in CdCl2 solution resulted in reconversion of ArH molecules into their cadmium salt. An increase in the average angle of tilt of the surfactant molecules with respect to the gold substrate occurred in conjunction with Q-state particle f ormation. The degree of tilt increased with increasing numbers of gass ing and immersion treatments. Processes such as the conversion of CdAr to ArH as well as breakup of the film into microdomains appear to be responsible for an increase in tilt of the alkyl chains. The ionized a rachidic acid molecules which were found to be present in the films af ter prolonged exposure to H2S appear to form a capping layer around th e CdS particles. The presence of a layer of ionized arachidic acid mol ecules around the particles may also be responsible for an increase in the average angle of tilt of the alkyl chains.