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Light scattering study on the glass former o-terphenyl

机译:玻璃原邻三联苯的光散射研究

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摘要

Combining double monochromator, tandem Fabry-?rot interferometry (TFPI), and photon correlation spectroscopy (PCS), the full range of the dynamic susceptibility of the glass former o-terphenyl is covered (240-440 K). A time resolution of 6 ns is reached by the PCS setup, and the measuring gap between PCS and TFPI has significantly shrunk. Combined time domain data are presented, which cover 0.01 ps-100 s. Regarding the primary α -process, no recognizable change in shape and amplitude is observed, i.e., frequency-temperature superposition holds over the entire temperature range investigated. The only change in the susceptibility is the emergence of the excess wing contribution, leading to a flattening of the susceptibility minimum close to T_g. Separating relaxation contribution from fast and slow dynamics, we determine the relaxation strength 1- frel (T) of the fast dynamics, which shows a cusplike temperature dependence with a crossover temperature T_c =316±10 K. Due to relative small changes of 1- frel (T) the effect is difficult to identify in frel (T) itself. The crossover temperature is larger than previously reported as no extrapolation scheme is applied.
机译:结合使用了双单色仪,串联法布里-罗特干涉仪(TFPI)和光子相关光谱仪(PCS),可以覆盖整个玻璃前邻苯三酚的动态磁化率范围(240-440 K)。 PCS设置可以达到6 ns的时间分辨率,并且PCS和TFPI之间的测量间隙已大大缩小。给出了组合的时域数据,涵盖0.01 ps-100 s。关于初级α过程,未观察到形状和幅度的可识别变化,即,在所研究的整个温度范围内保持频率-温度叠加。磁化率的唯一变化是出现过多的机翼,导致磁化率最小值的最小值趋近于T_g。从快速和慢速动力学中分离弛豫贡献,我们确定了快速动力学的弛豫强度1- frel(T),这显示了点状温度依赖性,交叉温度T_c = 316±10K。由于1-的相对较小变化感觉(T)的效果很难在感觉(T)本身中识别。由于未应用外推方案,因此交叉温度比以前报道的要大。

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