REAL-TIME DETERMINATION OF MOLECULAR-ORIENTATION IN LANGMUIR-BLODGETT MONOLAYERS ON INTEGRATED-OPTICAL STRUCTURES

被引:10
作者
HUGHES, KD
LABUDA, MJ
BOHN, PW
机构
[1] UNIV ILLINOIS,DEPT CHEM,URBANA,IL 61801
[2] UNIV ILLINOIS,BECKMAN INST,URBANA,IL 61801
来源
APPLIED OPTICS | 1991年 / 30卷 / 30期
关键词
D O I
10.1364/AO.30.004406
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Waveguide linear-dichroism measurements were used in determining the molecular orientation of N-(sulfopropyl)-4-(p-dioctylaminostyryl) pyridinium in Langmuir-Blodgett monolayers upon 150-mu-m-thick glass (Ti:Zn) substrates in real time. Acquisition of complete spatial-decay curves in t - 1 s with P(laser) = 100-mu-W was made possible by combining propagation in integrated-optical structures with direct imaging of monolayer or glass fluorescence onto the active area of a charge-coupled device camera. Multichannel detection permitted measurement of optical waveguide loss coefficients and ultimately of molecular orientations in approximately 10(-3) of the amount of time required by previous methodology. The effects of sample preparation and materials processing on the accuracy and precision of dichroic ratios are discussed. Observed dichroic ratios for a hemicyanine dye revealed no measurable change in the orientation of the electronic transition-dipole moment when Langmuir-Blodgett films were deposited at different surface pressures. These results are in good agreement with the results from singly resonant second-harmonic generation experiments.
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页码:4406 / 4411
页数:6
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