A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Interactions between Rigid Polyelectrolytes Mediated by Ordering and Orientation of Multivalent Nonspherical Ions in Salt Solutions
Tekijät: Vahid, Hossein; Scacchi, Alberto; Sammalkorpi, Maria; Ala-Nissila, Tapio
Kustantaja: AMER PHYSICAL SOC
Kustannuspaikka: COLLEGE PK
Julkaisuvuosi: 2023
Journal: Physical Review Letters
Tietokannassa oleva lehden nimi: PHYSICAL REVIEW LETTERS
Lehden akronyymi: PHYS REV LETT
Artikkelin numero: 158202
Vuosikerta: 130
Numero: 15
Sivujen määrä: 6
ISSN: 0031-9007
eISSN: 1079-7114
DOI: https://doi.org/10.1103/PhysRevLett.130.158202
Tiivistelmä
Multivalent ions in solutions with polyelectrolytes (PEs) induce electrostatic correlations that can drastically change ion distributions around the PEs and their mutual interactions. Using coarse-grained molecular dynamics simulations, we show how in addition to valency, ion shape and concentration can be harnessed as tools to control rigid like-charged PE-PE interactions. We demonstrate a correlation between the orientational ordering of aspherical ions and how they mediate the effective PE-PE attraction induced by multivalency. The interaction type, strength, and range can thus be externally controlled in ionic solutions. Our results can be used as generic guidelines to tune the self-assembly of like-charged polyelectrolytes by variation of the characteristics of the ions.
Multivalent ions in solutions with polyelectrolytes (PEs) induce electrostatic correlations that can drastically change ion distributions around the PEs and their mutual interactions. Using coarse-grained molecular dynamics simulations, we show how in addition to valency, ion shape and concentration can be harnessed as tools to control rigid like-charged PE-PE interactions. We demonstrate a correlation between the orientational ordering of aspherical ions and how they mediate the effective PE-PE attraction induced by multivalency. The interaction type, strength, and range can thus be externally controlled in ionic solutions. Our results can be used as generic guidelines to tune the self-assembly of like-charged polyelectrolytes by variation of the characteristics of the ions.
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