{"title":"Impact of Domain Size on the Length Scale of Local Glass Transition Perturbations Caused by an Immiscible Glassy–Rubbery Interface","authors":"Alexander A. Couturier, and , Connie B. Roth*, ","doi":"10.1021/acsmacrolett.5c00404","DOIUrl":null,"url":null,"abstract":"<p >The depth-dependent profile in local glass transition temperature <i>T</i><sub>g</sub>(<i>z</i>) was measured by pyrene fluorescence within 75 nm thick glassy polystyrene (PS) domains either capped by 600 nm thick poly(<i>n</i>-butyl methacrylate) (PnBMA) layers or exposed to the free surface. In both systems, the total PS domain size is constrained by a “neutral” nonperturbing silica substrate. Remarkably, for this constrained PnBMA/PS bilayer system, we find the perturbing influence of the 6–7 nm PnBMA/PS interface to be essentially equivalent to that imposed by the free surface, in stark contrast to the previously reported long-range <i>T</i><sub>g</sub>(<i>z</i>) perturbations of up to ≈250 nm for unconstrained glassy–rubbery interfaces between semi-infinite domains. For the 75 nm PS domains, both the PnBMA interface and free surface impart a local <i>T</i><sub>g</sub>(<i>z</i>) reduction of ≈30 K, spanning ≈30 nm before bulk <i>T</i><sub>g</sub> is recovered, demonstrating that the total domain size strongly alters both the magnitude and extent of the dynamical gradient even when bounded by a nonperturbing interface.</p>","PeriodicalId":18,"journal":{"name":"ACS Macro Letters","volume":"14 9","pages":"1256–1262"},"PeriodicalIF":5.2000,"publicationDate":"2025-08-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12444983/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Macro Letters","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsmacrolett.5c00404","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
The depth-dependent profile in local glass transition temperature Tg(z) was measured by pyrene fluorescence within 75 nm thick glassy polystyrene (PS) domains either capped by 600 nm thick poly(n-butyl methacrylate) (PnBMA) layers or exposed to the free surface. In both systems, the total PS domain size is constrained by a “neutral” nonperturbing silica substrate. Remarkably, for this constrained PnBMA/PS bilayer system, we find the perturbing influence of the 6–7 nm PnBMA/PS interface to be essentially equivalent to that imposed by the free surface, in stark contrast to the previously reported long-range Tg(z) perturbations of up to ≈250 nm for unconstrained glassy–rubbery interfaces between semi-infinite domains. For the 75 nm PS domains, both the PnBMA interface and free surface impart a local Tg(z) reduction of ≈30 K, spanning ≈30 nm before bulk Tg is recovered, demonstrating that the total domain size strongly alters both the magnitude and extent of the dynamical gradient even when bounded by a nonperturbing interface.
期刊介绍:
ACS Macro Letters publishes research in all areas of contemporary soft matter science in which macromolecules play a key role, including nanotechnology, self-assembly, supramolecular chemistry, biomaterials, energy generation and storage, and renewable/sustainable materials. Submissions to ACS Macro Letters should justify clearly the rapid disclosure of the key elements of the study. The scope of the journal includes high-impact research of broad interest in all areas of polymer science and engineering, including cross-disciplinary research that interfaces with polymer science.
With the launch of ACS Macro Letters, all Communications that were formerly published in Macromolecules and Biomacromolecules will be published as Letters in ACS Macro Letters.