1993Molecular crystals and liquid crystals science technology. Section A, Molecular crystals and liquid crystals/Molecular crystals and liquid crystals science and technology. Section A, Molecular crystals and liquid crystalsRequires access

Copolysiloxanes as Pyroelectric Langmuir-Blodgett Films

T. Richardson, Simon J. Holder, D. Lacey

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Abstract

A series of aliphatic acid side-chain copolysiloxanes based on a poly(hydrogenmethyldimethylsiloxane) backbone have been synthesised and evaluated. The length of the aliphatic acid side-chain of each compound has been varied in order to examine the effect on the Langmuir film properties. The surface pressure - area isotherms have indicated that each copolysiloxane forms a stable monomolecular layer on a pure watersubphase. Alternate layer structures, in which each siloxane copolymer is co-deposited with a monomeric eicosylamine, have been prepared in order to measure their static pyroelectric coefficients. The magnitude of the coefficient increases as the length of the aliphatic acid side-chain is reduced. The thickness dependence of the coefficient has also been characterised for one of the copolysiloxane derivatives and shows that the pyroelectric effect is greatest for a 25 layer sample (13 layers of copolysiloxane 8/12 layers of eicosylamine).

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A series of aliphatic acid side-chain copolysiloxanes based on a poly(hydrogenmethyldimethylsiloxane) backbone have been synthesised and evaluated. The length of the aliphatic acid side-chain of each compound has been varied in order to examine the effect on the Langmuir film properties. The surface pressure - area isotherms have indicated that each copolysiloxane forms a stable monomolecular layer on a pure watersubphase. Alternate layer structures, in which each siloxane copolymer is co-deposited with a monomeric eicosylamine, have been prepared in order to measure their static pyroelectric coefficients. The magnitude of the coefficient increases as the length of the aliphatic acid side-chain is reduced. The thickness dependence of the coefficient has also been characterised for one of the copolysiloxane derivatives and shows that the pyroelectric effect is greatest for a 25 layer sample (13 layers of copolysiloxane 8/12 layers of eicosylamine).

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Available abstract

A series of aliphatic acid side-chain copolysiloxanes based on a poly(hydrogenmethyldimethylsiloxane) backbone have been synthesised and evaluated. The length of the aliphatic acid side-chain of each compound has been varied in order to examine the effect on the Langmuir film properties. The surface pressure - area isotherms have indicated that each copolysiloxane forms a stable monomolecular layer on a pure watersubphase. Alternate layer structures, in which each siloxane copolymer is co-deposited with a monomeric eicosylamine, have been prepared in order to measure their static pyroelectric coefficients. The magnitude of the coefficient increases as the length of the aliphatic acid side-chain is reduced. The thickness dependence of the coefficient has also been characterised for one of the copolysiloxane derivatives and shows that the pyroelectric effect is greatest for a 25 layer sample (13 layers of copolysiloxane 8/12 layers of eicosylamine).

Key concepts: Pyroelectricity, Siloxane, Side chain, Monomer, Layer (electronics), Langmuir, Copolymer, Polymer chemistry

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