Polyelectrolyte spin-assembly

doi:10.1021/la011333s

2001-12-06

114

PRE

DOI：10.1021/la011333s

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摘要

En 中文

Polyelectrolyte thin films composed of alternating layers were spin-assembled by sequentially dropping cationic and anionic aqueous solutions onto a spinning substrate. In this work, we show the applicability of our technique to multiple systems and present two methods for producing linear film growth. The polycations used were PEI (poly(ethylenimine), PDDA (poly(diallyldimethylammonium chloride), PAH (poly(allylamine hydrochloride), and two poly(propylenimine) dendrimers (generations 3.0 and 4.0). The polyanions used were PAZO (poly [1-[4-(3-carboxy-4-hydroxy-phenylazo)benzene sulfonamidol-1,2-ethanediyl, sodium salt]), PSS (poly(styrenesulfonate)), and PAA (poly(acrylic acid)). Layer thicknesses for all systems were determined using single-wavelength ellipsometry. UV-vis spectroscopy was used to measure deposition amounts in films containing the chromophoric polyanions PAZO and PSS. We demonstrate the ability to spin-assemble multilayered thin films up to 50 bilayers with linear increases in deposition amount between bilayers. Additionally, we show that layers of a single polyelectrolyte species can be spin-assembled with multiple deposition cycles in which consistent amounts are deposited in each cycle. In a comparison of films built from two dendrimer generations, films incorporating generation 3.0 dendrimer and PAZO show signs of higher interpenetration between layers and a more collapsed film structure than films assembled from generation 4.0 dendrimer and PAZO. Our results also suggest that a substrate effect influences the packing density of the first few bilayers, eventually dissipating around a film thickness of 50-80 Angstrom.

Keyword:

LIGHT-EMITTING-DIODES

THIN-FILMS

POLYMER-FILMS

SOLVENT

THICKNESS

EVAPORATION

MULTILAYERS

AZOBENZENE

ADSORPTION

DEPOSITION