Impact of Domain Size on the Length Scale of Local Glass Transition Perturbations Caused by an Immiscible Glassy–Rubbery Interface

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.

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Publication Details

Journal
ACS Macro Letters
Published
2025-08-18
DOI
https://doi.org/10.1021/acsmacrolett.5c00404
Citations
1
Primary Topic
Material Dynamics and Properties
Type
article
Field-Weighted Citation Impact
0.52

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article

Impact of Domain Size on the Length Scale of Local Glass Transition Perturbations Caused by an Immiscible Glassy–Rubbery Interface

Connie B. Roth, Alexander A. Couturier
1 citations
ACS Macro Letters
Material Dynamics and Properties
0.52
article

Impact of Domain Size on the Length Scale of Local Glass Transition Perturbations Caused by an Immiscible Glassy–Rubbery Interface

Connie B. Roth, Alexander A. Couturier
article en
1 citations

Abstract

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.

ACS Macro LettersVol. 14(9)
Emory University (US)
National Science Foundation, Emory University, Division of Materials Research
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Openalex Percentile: Top 34%
Material Dynamics and Properties
0.52
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