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Asymmetric Growth in Polyelectrolyte Multilayers
Author(s) -
Ramy A. Ghostine,
Marie Z. Markarian,
Joseph B. Schlenoff
Publication year - 2013
Publication title -
journal of the american chemical society
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/ja401318m
Subject(s) - polyelectrolyte , chemistry , counterion , chemical physics , polymer , styrene , diffusion , layer by layer , chemical engineering , surface charge , stoichiometry , layer (electronics) , polymer chemistry , nanotechnology , ion , thermodynamics , organic chemistry , copolymer , materials science , physics , engineering
Radioactive counterions were used to track the ratio of positive to negative polymer repeat units within a polyelectrolyte multilayer made from poly(diallyldimethylammonium chloride), PDADMAC, and poly(styrene sulfonate), PSS. For this widely employed pair of "linearly" assembled polyelectrolytes it was found that the accepted model of charge overcompensation for each layer is incorrect. In fact, overcompensation at the surface occurs only on the addition of the polycation, whereas PSS merely compensates the PDADMAC. After the assembly of about a dozen layers, excess positive sites begin to accrue in the multilayer. Treating the surface as a reaction-diffusion region for pairing of polymer charges, a model profile was constructed. It is shown that different reaction-diffusion ranges of positive and negative polyelectrolyte charge lead to a blanket of glassy, stoichiometric complex growing on top of a layer of rubbery, PDADMAC-rich complex. Though overcompensation and growth was highly asymmetric with respect to the layer number, entirely conventional "linear" assembly of the multilayer was observed. The impact of asymmetric growth on various properties of multilayers is discussed.

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