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Автор Uwe Micka
Автор Kurt Kremer
Дата выпуска 1996-11-18
dc.description We present simulations of the basic model of weakly charged polyelectrolyte chains of variable intrinsic stiffness within the Debye - Hückel approximation. For intrinsically flexible chains the persistence length shows a sublinear dependence on the screening length in strong contrast to all known analytical approaches which propose an effective exponent of either y = 2 or y = 1. The observed exponent y varies as a function of the system parameters. With increasing intrinsic stiffness the corresponding effective exponent y crosses over to values of up to 2 when the intrinsic persistence length exceeds the electrostatic one . We find a pronounced minimum of with increasing intrinsic stiffness due to a reduction of entropy. The concept of a unique persistence length is not applicable for these systems.
Формат application.pdf
Издатель Institute of Physics Publishing
Название The persistence length of polyelectrolyte chains
Тип paper
DOI 10.1088/0953-8984/8/47/046
Electronic ISSN 1361-648X
Print ISSN 0953-8984
Журнал Journal of Physics: Condensed Matter
Том 8
Первая страница 9463
Последняя страница 9470
Аффилиация Uwe Micka; Max-Planck-Institut für Polymerforschung, Postfach 3184, D-55021 Mainz, Germany
Аффилиация Kurt Kremer; Max-Planck-Institut für Polymerforschung, Postfach 3184, D-55021 Mainz, Germany
Выпуск 47

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