Sequence disorder-induced first order phase transition in confined polyelectrolytes

被引:0
|
作者
Stepanyan, V. [1 ]
Badasyan, A. [2 ]
Morozov, V. [3 ]
Mamasakhlisov, Y. [1 ,3 ]
Podgornik, R. [4 ,5 ,6 ,7 ,8 ]
机构
[1] Yerevan State Univ, Yerevan, Armenia
[2] Univ Nova Gorica, Nova Gorica, Slovenia
[3] Inst Appl Problems Phys, Yerevan, Armenia
[4] Univ Chinese Acad Sci, Sch Phys Sci, Beijing 100049, Peoples R China
[5] Chinese Acad Sci, Inst Phys, CAS Key Lab Soft Matter Phys, Beijing 100190, Peoples R China
[6] Univ Chinese Acad Sci, Kavli Inst Theoret Sci, Beijing 100049, Peoples R China
[7] Univ Chinese Acad Sci, Wenzhou Inst, Wenzhou 325011, Zhejiang, Peoples R China
[8] Univ Ljubljana, Fac Math & Phys, Dept Phys, Jadranska 19, Ljubljana 1000, Slovenia
来源
JOURNAL OF CHEMICAL PHYSICS | 2024年 / 161卷 / 13期
基金
中国国家自然科学基金;
关键词
ADSORPTION; POLYMERS; FORCES;
D O I
10.1063/5.0228162
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We consider a statistical mechanical model of a generic flexible polyelectrolyte, comprised of identically charged monomers with long-range electrostatic interactions and short-range interactions quantified by a disorder field along the polymer contour sequence, which is randomly quenched. The free energy and the monomer density profile of the system for no electrolyte screening are calculated in the case of a system composed of two infinite planar bounding surfaces with an intervening oppositely charged polyelectrolyte chain. We show that the effect of the contour sequence disorder, mediated by short-range interactions, leads to an enhanced localization of the polyelectrolyte chain and a first order phase transition at a critical value of the inter-surface spacing. This phase transition results in an abrupt change of the pressure from negative to positive values, effectively eliminating polyelectrolyte mediated bridging attraction.
引用
收藏
页数:11
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