Mixed equilibrium/nonequilibrium effects govern surface mobility in polymer glasses

• 成果类型: Article
• 署名作者: Xu, Jianquan; Ghanekarade, Asieh; Li, Li; Zhu, Huifeng; Yuan, Hailin; Yan, Jinsong; Simmons, David S.; Tsui, Ophelia K. C.; Wang, Xinping
• 署名单位: Zhejiang Sci-Tech University; State University System of Florida; University of South Florida; Hong Kong University of Science & Technology; Hong Kong University of Science & Technology
• 刊物名称: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
• ISSN/ISSBN: 0027-13661
• DOI: 10.1073/pnas.2406262121
• 发表日期: 2024-10-03
• 关键词: transition temperature; t-g; DYNAMICS; dependence; EQUIVALENCE; copolymers; nanometer; liquids; films; view

摘要

Using angle-resolved X-ray photoelectron spectroscopy, sum-frequency generation vibrational spectroscopy, contact angle measurements, and molecular dynamics simulations, we verify that the glass transition temperature (T-g) of polymer glass is lower near the free surface. However, the experimental T-g-gradients showed a linear variation with depth (z) from the free surface, while the simulated equilibrium T-g-gradients exhibited a double exponential z-dependence. In typical simulations, T-g is determined based on the relaxation time of the system reaching a prescribed threshold value at equilibrium. Conversely, the experiments determined T-g by observing the unfreezing of molecular mobility during heating from a kinetically arrested, nonequilibrium glassy state. To investigate the impact of nonequilibrium effects on the T-g-gradient, we reduced the thermal annealing time in simulations, allowing the system to fall out of equilibrium. We observe a decrease in the relaxation time and the emergence of a modified z-dependence consistent with a linear T-g-gradient near the free surface. We further validate the impact of nonequilibrium effects by studying the dependence of the T-g on the heating/cooling rate for polymer films of varying thickness (h). Our experimental results reveal significant variations in the T-g-heating/cooling rate dependence with h below the bulk T-g, which are also observed in simulation when the simulated system is not equilibrated. We explain our findings by the reduction in mass density within the inner region of the system under nonequilibrium conditions, as observed in simulation, and recent research indicating a decrease in the local T-g of a polymer when placed next to a softer material.