Couturier Alexander A, Roth Connie B
Department of Physics, Emory University, Atlanta, Georgia 30322, United States.
ACS Macro Lett. 2025 Sep 16;14(9):1256-1262. doi: 10.1021/acsmacrolett.5c00404. Epub 2025 Aug 18.
The depth-dependent profile in local glass transition temperature () was measured by pyrene fluorescence within 75 nm thick glassy polystyrene (PS) domains either capped by 600 nm thick poly(-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 () 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 () reduction of ≈30 K, spanning ≈30 nm before bulk 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.
通过芘荧光测量了75纳米厚的玻璃态聚苯乙烯(PS)区域内与深度相关的局部玻璃化转变温度()分布,这些区域要么被600纳米厚的聚甲基丙烯酸丁酯(PnBMA)层覆盖,要么暴露于自由表面。在这两种体系中,PS区域的总尺寸都受到“中性”无扰二氧化硅基底的限制。值得注意的是,对于这种受限的PnBMA/PS双层体系,我们发现6 - 7纳米厚的PnBMA/PS界面的扰动影响与自由表面施加的影响基本相当,这与之前报道的半无限区域之间无约束的玻璃态 - 橡胶态界面高达约250纳米的长程()扰动形成鲜明对比。对于75纳米厚的PS区域,PnBMA界面和自由表面都会使局部()降低约30 K,在恢复本体()之前跨越约30纳米,这表明即使由无扰界面界定,总区域尺寸也会强烈改变动力学梯度的大小和范围。