A photobleaching method was used to measure the
reorientation of dilute probes in liquid
o-terphenyl near a crystal growth front. Near the glass-transition temperature
Tg, mobility in the supercooled liquid was enhanced within 10 渭m of the crystal growth front, by as much as a factor of 4. This enhanced mobility appears to be caused by tension created in the sample as a result of the density difference between the supercooled liquid and crystal. The maximum observed mobility enhancement corresponds to a tension of about 鈭? MPa, close to the cavitation limit for liquid
o-terphenyl. Whereas the observed mobility near the growing crystal is not large enough to explain the extraordinary fast crystal growth observed near
Tg in
o-terphenyl and some other low-molecular-weight glassformers, these observations suggest that cavitation or
fracture plays a key role in releasing tension and allowing fast crystal growth to occur at a steady rate.
Keywords:
GC crystal; organic glassformers; molecular mobility; rotational diffusion