Field theoretic approach for block polymer melts: SCFT and FTS

dc.contributor.authorMatsen, M. W.
dc.date.accessioned2026-10-30T13:03:59Z
dc.date.issued2020-02-17
dc.description.abstractThis Perspective addresses the development of polymer field theory for predicting the equilibrium phase behavior of block polymer melts. The approach is tailored to the high-molecular-weight limit, where universality reduces all systems to the standard Gaussian chain model, an incompressible melt of elastic threads interacting by contact forces. Using mathematical identities, this particle-based version of the model is converted to an equivalent field-based version that depends on fields rather than particle coordinates. The statistical mechanics of the field-based model is typically solved using the saddle-point approximation of self-consistent field theory (SCFT), which equates to mean field theory, but it can also be evaluated using field theoretic simulations (FTS). While SCFT has matured into one of the most successful theories in soft condensed matter, FTS is still in its infancy. The two main obstacles of FTS are the high computational cost and the occurrence of an ultraviolet divergence, but fortunately there has been recent groundbreaking progress on both fronts. As such, FTS is now well poised to become the method of choice for predicting fluctuation corrections to mean field theory.
dc.identifier.urihttps://doi.org/10.1063/1.5145098
dc.identifier.urihttps://hdl.handle.net/10012/24618
dc.language.isoen
dc.publisherAmerican Institute of Physics (AIP)
dc.relation.ispartofseriesJournal of Chemical Physics; 152; 110901
dc.subjectphase transitions
dc.subjectpolymers
dc.subjectmean field theory
dc.subjectultraviolet divergences
dc.subjectstatistical mechanics
dc.subjectLangevin dynamics
dc.subjectfield theory models
dc.titleField theoretic approach for block polymer melts: SCFT and FTS
dc.typeArticle
dcterms.bibliographicCitationMatsen, M. W. (2020). Field theoretic approach for block polymer melts: SCFT and FTS. The Journal of Chemical Physics, 152(11). https://doi.org/10.1063/1.5145098
uws.contributor.affiliation1Faculty of Science
uws.contributor.affiliation2Physics and Astronomy
uws.peerReviewStatusReviewed
uws.scholarLevelFaculty
uws.typeOfResourceTexten

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