Fast Surface Crystal Growth on Molecular Glasses and Its Termination by the Onset of Fluidity

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• 作者：Mariko Hasebe ; Daniele Musumeci ; C. Travis Powell ; Ting Cai ; Erica Gunn ; Lei Zhu ; Lian Yu
• 刊名：Journal of Physical Chemistry B
• 出版年：2014
• 出版时间：July 10, 2014
• 年：2014
• 卷：118
• 期：27
• 页码：7638-7646
• 全文大小：545K
• ISSN：1520-5207

文摘

Organic glasses can grow crystals much faster on the free surface than in the interior, a phenomenon important for fabricating stable amorphous materials. This surface process differs from and is faster than the glass-to-crystal (GC) growth mode existing in the bulk of molecular glasses. We report that similar to GC growth, surface crystal growth terminates if glasses are heated to gain fluidity. In their steady growth below the glass transition temperature T_g, surface crystals rise above the amorphous surface while spreading laterally and are surrounded by depressed grooves. Above T_g, the growth becomes slower, sometimes unstable. This damage is stronger on segregated needles (伪 indomethacin, nifedipine, and o-terphenyl) than on crystals growing in compact domains (纬 indomethacin). This effect arises because the onset of liquid flow causes the wetting and embedding of upward-growing surface crystals. Segregated needles are at greater risk because their slow-growing flanks appear stationary relative to liquid flow at a low temperature. The disruption of surface crystal growth by fluidity supports the view that the process occurs by surface diffusion, not viscous flow. Compared to the bulk GC mode, surface crystal growth is disrupted less abruptly by fluidity. Nevertheless, to the extent that fluidity damages them, both processes are solid-state phenomena terminated in the liquid state.