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

IF 5.2 Q1 POLYMER SCIENCE
Alexander A. Couturier,  and , Connie B. Roth*, 
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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.

Abstract Image

Abstract Image

Abstract Image

非混相玻璃-橡胶界面引起的局部玻璃化跃迁微扰长度尺度的影响。
在75 nm厚的玻璃状聚苯乙烯(PS)结构域内,通过600 nm厚的聚甲基丙烯酸正丁酯(PnBMA)层覆盖或暴露在自由表面,用芘荧光测量了局部玻璃化转变温度Tg(z)的深度依赖剖面。在这两种体系中,总PS畴尺寸受到“中性”无扰动二氧化硅衬底的限制。值得注意的是,对于这种受约束的PnBMA/PS双层体系,我们发现6-7 nm PnBMA/PS界面的扰动影响基本上相当于自由表面施加的扰动影响,这与之前报道的半无限域之间无约束的玻璃-橡胶界面高达≈250 nm的远程Tg(z)扰动形成了明显对比。对于75 nm的PS畴,PnBMA界面和自由表面都使局部Tg(z)降低了约30 K,在大块Tg恢复之前跨度约30 nm,这表明即使在无扰动界面的边界下,总畴尺寸也强烈地改变了动态梯度的大小和范围。
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来源期刊
CiteScore
10.40
自引率
3.40%
发文量
209
审稿时长
1 months
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.
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