A COPOLYMER NEAR A SELECTIVE INTERFACE: VARIATIONAL CHARACTERIZATION OF THE FREE ENERGY
In this paper, we consider a random copolymer near a selective interface separating two solvents. The configurations of the copolymer are directed paths that can make i.i.d. excursions of finite length above and below the interface. The excursion length distribution is assumed to have a tail that is...
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description | In this paper, we consider a random copolymer near a selective interface separating two solvents. The configurations of the copolymer are directed paths that can make i.i.d. excursions of finite length above and below the interface. The excursion length distribution is assumed to have a tail that is logarithmically equivalent to a power law with exponent α ≥ 1. The monomers carry i.i.d. real-valued types whose distribution is assumed to have zero mean, unit variance, and a finite moment generating function. The interaction Hamiltonian rewards matches and penalizes mismatches of the monomer types and the solvents, and depends on two parameters: the interaction strength β ≥ 0 and the interaction bias h ≥ 0. We are interested in the behavior of the copolymer in the limit as its length tends to infinity. The quenched free energy per monomer (β, h) ↦ gque (β, h) has a phase transition along a quenched critical curve $\beta \mapsto h^{\text{que}}_{c} (\beta )$ separating a localized phase, where the copolymer stays close to the interface, from a delocalized phase, where the copolymer wanders away from the interface. We derive variational formulas for both these quantities. We compare these variational formulas with their analogues for the annealed free energy per monomer (β, h) ↦ gann (β, h) and the annealed critical curve $\beta \mapsto h^{\text{ann}}_{c} (\beta )$, both of which are explicitly computable. This comparison leads to: (1) A proof that gque (β, h) < gann (β, h) for all α ≥ 1 and (β, h) in the annealed localized phase. (2) A proof that $h^{\text{ann}}_{c}(\beta / \alpha) \ \textless \ h^{\text{que}}_{c}(\beta) \ \textless \ h^{\text{ann}}_{c} (\beta)$ for all α > 1 and β > 0. (3) A proof that $\text{lim inf} _{\beta\downarrow0}h_{c}^{\mathrm{que}}(\beta)/\beta\geq(1+\alpha)/2\alpha$ for all α ≥ 2. (4) A proof that lim $\text{lim inf}_{\beta\downarrow0}h_{c}^{\mathrm{que}}(\beta)/\beta\geq K_{c}^{*}(\alpha)$ for all 1 < α < 2 with $K_{c}^{*}(\alpha)$ given by an explicit integral criterion. (5) An upper bound on the total number of times the copolymer visits the interface in the interior of the quenched delocalized phase. (6) An identification of the asymptotic frequency at which the copolymer visits the interface in the quenched localized phase. The copolymer model has been studied extensively in the literature. The goal of the present paper is to open up a window with a variational view and to settle a number of open problems. |
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The configurations of the copolymer are directed paths that can make i.i.d. excursions of finite length above and below the interface. The excursion length distribution is assumed to have a tail that is logarithmically equivalent to a power law with exponent α ≥ 1. The monomers carry i.i.d. real-valued types whose distribution is assumed to have zero mean, unit variance, and a finite moment generating function. The interaction Hamiltonian rewards matches and penalizes mismatches of the monomer types and the solvents, and depends on two parameters: the interaction strength β ≥ 0 and the interaction bias h ≥ 0. We are interested in the behavior of the copolymer in the limit as its length tends to infinity. The quenched free energy per monomer (β, h) ↦ gque (β, h) has a phase transition along a quenched critical curve $\beta \mapsto h^{\text{que}}_{c} (\beta )$ separating a localized phase, where the copolymer stays close to the interface, from a delocalized phase, where the copolymer wanders away from the interface. We derive variational formulas for both these quantities. We compare these variational formulas with their analogues for the annealed free energy per monomer (β, h) ↦ gann (β, h) and the annealed critical curve $\beta \mapsto h^{\text{ann}}_{c} (\beta )$, both of which are explicitly computable. This comparison leads to: (1) A proof that gque (β, h) < gann (β, h) for all α ≥ 1 and (β, h) in the annealed localized phase. (2) A proof that $h^{\text{ann}}_{c}(\beta / \alpha) \ \textless \ h^{\text{que}}_{c}(\beta) \ \textless \ h^{\text{ann}}_{c} (\beta)$ for all α > 1 and β > 0. (3) A proof that $\text{lim inf} _{\beta\downarrow0}h_{c}^{\mathrm{que}}(\beta)/\beta\geq(1+\alpha)/2\alpha$ for all α ≥ 2. (4) A proof that lim $\text{lim inf}_{\beta\downarrow0}h_{c}^{\mathrm{que}}(\beta)/\beta\geq K_{c}^{*}(\alpha)$ for all 1 < α < 2 with $K_{c}^{*}(\alpha)$ given by an explicit integral criterion. (5) An upper bound on the total number of times the copolymer visits the interface in the interior of the quenched delocalized phase. (6) An identification of the asymptotic frequency at which the copolymer visits the interface in the quenched localized phase. The copolymer model has been studied extensively in the literature. The goal of the present paper is to open up a window with a variational view and to settle a number of open problems.</description><identifier>ISSN: 0091-1798</identifier><identifier>EISSN: 2168-894X</identifier><identifier>DOI: 10.1214/14-aop880</identifier><language>eng</language><publisher>Hayward: Institute of Mathematical Statistics</publisher><subject>60F10 ; 60K37 ; 82B27 ; 82B44 ; Copolymer ; Copolymers ; critical curve ; free energy ; large deviation principle ; localization vs delocalization ; Mathematical functions ; Mathematical models ; Probability distribution ; selective interface ; Solvents ; specific relative entropy ; Studies ; variational formula</subject><ispartof>The Annals of probability, 2015-03, Vol.43 (2), p.875-933</ispartof><rights>Copyright © 2015 Institute of Mathematical Statistics</rights><rights>Copyright Institute of Mathematical Statistics Mar 2015</rights><rights>Copyright 2015 Institute of Mathematical Statistics</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c437t-c70b8371739effc5e0564c41eef463eb8c1f56f348d25bb8c6767e615a9e74903</citedby><cites>FETCH-LOGICAL-c437t-c70b8371739effc5e0564c41eef463eb8c1f56f348d25bb8c6767e615a9e74903</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/24519160$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/24519160$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,776,780,799,828,881,921,27901,27902,57992,57996,58225,58229</link.rule.ids></links><search><creatorcontrib>Bolthausen, Erwin</creatorcontrib><creatorcontrib>den Hollander, Frank</creatorcontrib><creatorcontrib>Opoku, Alex A.</creatorcontrib><title>A COPOLYMER NEAR A SELECTIVE INTERFACE: VARIATIONAL CHARACTERIZATION OF THE FREE ENERGY</title><title>The Annals of probability</title><description>In this paper, we consider a random copolymer near a selective interface separating two solvents. The configurations of the copolymer are directed paths that can make i.i.d. excursions of finite length above and below the interface. The excursion length distribution is assumed to have a tail that is logarithmically equivalent to a power law with exponent α ≥ 1. The monomers carry i.i.d. real-valued types whose distribution is assumed to have zero mean, unit variance, and a finite moment generating function. The interaction Hamiltonian rewards matches and penalizes mismatches of the monomer types and the solvents, and depends on two parameters: the interaction strength β ≥ 0 and the interaction bias h ≥ 0. We are interested in the behavior of the copolymer in the limit as its length tends to infinity. The quenched free energy per monomer (β, h) ↦ gque (β, h) has a phase transition along a quenched critical curve $\beta \mapsto h^{\text{que}}_{c} (\beta )$ separating a localized phase, where the copolymer stays close to the interface, from a delocalized phase, where the copolymer wanders away from the interface. We derive variational formulas for both these quantities. We compare these variational formulas with their analogues for the annealed free energy per monomer (β, h) ↦ gann (β, h) and the annealed critical curve $\beta \mapsto h^{\text{ann}}_{c} (\beta )$, both of which are explicitly computable. This comparison leads to: (1) A proof that gque (β, h) < gann (β, h) for all α ≥ 1 and (β, h) in the annealed localized phase. (2) A proof that $h^{\text{ann}}_{c}(\beta / \alpha) \ \textless \ h^{\text{que}}_{c}(\beta) \ \textless \ h^{\text{ann}}_{c} (\beta)$ for all α > 1 and β > 0. (3) A proof that $\text{lim inf} _{\beta\downarrow0}h_{c}^{\mathrm{que}}(\beta)/\beta\geq(1+\alpha)/2\alpha$ for all α ≥ 2. (4) A proof that lim $\text{lim inf}_{\beta\downarrow0}h_{c}^{\mathrm{que}}(\beta)/\beta\geq K_{c}^{*}(\alpha)$ for all 1 < α < 2 with $K_{c}^{*}(\alpha)$ given by an explicit integral criterion. (5) An upper bound on the total number of times the copolymer visits the interface in the interior of the quenched delocalized phase. (6) An identification of the asymptotic frequency at which the copolymer visits the interface in the quenched localized phase. The copolymer model has been studied extensively in the literature. The goal of the present paper is to open up a window with a variational view and to settle a number of open problems.</description><subject>60F10</subject><subject>60K37</subject><subject>82B27</subject><subject>82B44</subject><subject>Copolymer</subject><subject>Copolymers</subject><subject>critical curve</subject><subject>free energy</subject><subject>large deviation principle</subject><subject>localization vs delocalization</subject><subject>Mathematical functions</subject><subject>Mathematical models</subject><subject>Probability distribution</subject><subject>selective interface</subject><subject>Solvents</subject><subject>specific relative entropy</subject><subject>Studies</subject><subject>variational formula</subject><issn>0091-1798</issn><issn>2168-894X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNo9kM1Kw0AUhQdRsFYXPoAw4MpFdCbzG1cOw6QNxKTEtFo3IU0n0KCmJunCt3e0pavDPffj3MsB4Bqje-xj-oCpV7ZbKdEJGPmYS08G9O0UjBAKsIdFIM_BRd83CCEuBB2BVwV1Okvj5bPJYGJUBhV8MbHRebQwMEpyk4VKm0e4UFmk8ihNVAz1VGVKu1X0_m_BNIT51MAwMwaaxGST5SU4q8uP3l4ddAzmocn11IvTSaRV7FWUiMGrBFpJIrAgga3rilnEOK0otramnNiVrHDNeE2oXPts5UYuuLAcszKwggaIjMHTPnfbtY2tBrurPjbrYtttPsvup2jLTaHn8cE9iCuowNT3pWRMcBdxe4z43tl-KJp21325rwsspECEIkYddbenqq7t-87WxxsYFX_Vu8hCpTNXvWNv9mzTD213BH3KcIA5Ir_vPXfM</recordid><startdate>20150301</startdate><enddate>20150301</enddate><creator>Bolthausen, Erwin</creator><creator>den Hollander, Frank</creator><creator>Opoku, Alex A.</creator><general>Institute of Mathematical Statistics</general><general>The Institute of Mathematical Statistics</general><scope>AAYXX</scope><scope>CITATION</scope><scope>JQ2</scope></search><sort><creationdate>20150301</creationdate><title>A COPOLYMER NEAR A SELECTIVE INTERFACE: VARIATIONAL CHARACTERIZATION OF THE FREE ENERGY</title><author>Bolthausen, Erwin ; den Hollander, Frank ; Opoku, Alex A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c437t-c70b8371739effc5e0564c41eef463eb8c1f56f348d25bb8c6767e615a9e74903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>60F10</topic><topic>60K37</topic><topic>82B27</topic><topic>82B44</topic><topic>Copolymer</topic><topic>Copolymers</topic><topic>critical curve</topic><topic>free energy</topic><topic>large deviation principle</topic><topic>localization vs delocalization</topic><topic>Mathematical functions</topic><topic>Mathematical models</topic><topic>Probability distribution</topic><topic>selective interface</topic><topic>Solvents</topic><topic>specific relative entropy</topic><topic>Studies</topic><topic>variational formula</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bolthausen, Erwin</creatorcontrib><creatorcontrib>den Hollander, Frank</creatorcontrib><creatorcontrib>Opoku, Alex A.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Computer Science Collection</collection><jtitle>The Annals of probability</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bolthausen, Erwin</au><au>den Hollander, Frank</au><au>Opoku, Alex A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A COPOLYMER NEAR A SELECTIVE INTERFACE: VARIATIONAL CHARACTERIZATION OF THE FREE ENERGY</atitle><jtitle>The Annals of probability</jtitle><date>2015-03-01</date><risdate>2015</risdate><volume>43</volume><issue>2</issue><spage>875</spage><epage>933</epage><pages>875-933</pages><issn>0091-1798</issn><eissn>2168-894X</eissn><abstract>In this paper, we consider a random copolymer near a selective interface separating two solvents. The configurations of the copolymer are directed paths that can make i.i.d. excursions of finite length above and below the interface. The excursion length distribution is assumed to have a tail that is logarithmically equivalent to a power law with exponent α ≥ 1. The monomers carry i.i.d. real-valued types whose distribution is assumed to have zero mean, unit variance, and a finite moment generating function. The interaction Hamiltonian rewards matches and penalizes mismatches of the monomer types and the solvents, and depends on two parameters: the interaction strength β ≥ 0 and the interaction bias h ≥ 0. We are interested in the behavior of the copolymer in the limit as its length tends to infinity. The quenched free energy per monomer (β, h) ↦ gque (β, h) has a phase transition along a quenched critical curve $\beta \mapsto h^{\text{que}}_{c} (\beta )$ separating a localized phase, where the copolymer stays close to the interface, from a delocalized phase, where the copolymer wanders away from the interface. We derive variational formulas for both these quantities. We compare these variational formulas with their analogues for the annealed free energy per monomer (β, h) ↦ gann (β, h) and the annealed critical curve $\beta \mapsto h^{\text{ann}}_{c} (\beta )$, both of which are explicitly computable. This comparison leads to: (1) A proof that gque (β, h) < gann (β, h) for all α ≥ 1 and (β, h) in the annealed localized phase. (2) A proof that $h^{\text{ann}}_{c}(\beta / \alpha) \ \textless \ h^{\text{que}}_{c}(\beta) \ \textless \ h^{\text{ann}}_{c} (\beta)$ for all α > 1 and β > 0. (3) A proof that $\text{lim inf} _{\beta\downarrow0}h_{c}^{\mathrm{que}}(\beta)/\beta\geq(1+\alpha)/2\alpha$ for all α ≥ 2. (4) A proof that lim $\text{lim inf}_{\beta\downarrow0}h_{c}^{\mathrm{que}}(\beta)/\beta\geq K_{c}^{*}(\alpha)$ for all 1 < α < 2 with $K_{c}^{*}(\alpha)$ given by an explicit integral criterion. (5) An upper bound on the total number of times the copolymer visits the interface in the interior of the quenched delocalized phase. (6) An identification of the asymptotic frequency at which the copolymer visits the interface in the quenched localized phase. The copolymer model has been studied extensively in the literature. The goal of the present paper is to open up a window with a variational view and to settle a number of open problems.</abstract><cop>Hayward</cop><pub>Institute of Mathematical Statistics</pub><doi>10.1214/14-aop880</doi><tpages>59</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 60F10 60K37 82B27 82B44 Copolymer Copolymers critical curve free energy large deviation principle localization vs delocalization Mathematical functions Mathematical models Probability distribution selective interface Solvents specific relative entropy Studies variational formula |
title | A COPOLYMER NEAR A SELECTIVE INTERFACE: VARIATIONAL CHARACTERIZATION OF THE FREE ENERGY |
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