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首页> 外文期刊>Journal of Physics. Condensed Matter >Temperature dependence of low-lying phonon dephasing by ultrafast spectroscopy (optical Kerr effect) in Ag beta-alumina and Tl beta-alumina
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Temperature dependence of low-lying phonon dephasing by ultrafast spectroscopy (optical Kerr effect) in Ag beta-alumina and Tl beta-alumina

机译:超快速光谱法在Agβ-氧化铝和Tlβ-氧化铝中通过低速声子去相的温度依赖性(光学克尔效应)

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摘要

Dephasing processes for low-lying phonons of Ag+ and Tl+ ss-alumina were observed in the time domain using the femtosecond pulse laser in the temperature range of 15-350 K. The dephasing dynamics associated with the time evolution of the vibrational coherence state can be directly identified with the phonon decay in the femtosecond transient. In this study, the temperature dependence of the dephasing property was decomposed into three terms in order to understand the correlation between vibration and diffusion: ( i) a static structural disorder, (ii) an anharmonic coupling and (iii) an ionic diffusion. The dephasing property of the low-lying phonon in Ag ss-alumina as a superionic conductor was compared with that of the isomorphous Tl ss-alumina, whose ionic conductivity was about 10(3) times less than Ag ss-alumina. The magnitude of static disorder shows a large value (h Gamma(0) =0.49 meV) in Ag ss-alumina, which is twice that of Tl ss-alumina (h Gamma(0) = 0.22 meV) with the same structure and the same number of excess cations by nonstoichiometry. The coefficient of phonon lifetimes originating from the cubic anharmonicity of a potential well is about five times larger in Ag ss-alumina than Tl ss-alumina. A strongly temperature dependent decay component is only seen in the superionic conductor Ag ss-alumina above 200 K, and is not observed in Tl ss-alumina. This is attributed to the phonon dephasing caused by the jump motion of the Ag+ ions. The estimated activation energy and pre-exponential factor are Ea = 71 meV and _ h/ tau 0 = 2.86 meV in Ag ss-alumina, respectively, for the correlation time tau(c) = tau(0) exp( E-a/ k(B)T). The value of _ h/ t0 = 2.86 meV, which can be regarded as an attempt frequency for the jump, coincides with the lowlying phonon frequency _ h omega(0) = 2.7 meV, but the E-a = 71 meV is different from that of the dc conductivity (E-a = 173 meV). These results, which are strongly coupled with the elementary excitation from oscillation to ionic diffusion in the picosecond time domain, would be of prime importance for the superionic conduction mechanism.
机译:在15-350 K的温度范围内,使用飞秒脉冲激光在时域中观察到了Ag +和Tl + ss-氧化铝低层声子的相移过程。与振动相干态的时间演化相关的相移动力学可以是直接用飞秒瞬态中的声子衰减来识别。在这项研究中,将移相特性的温度依赖性分解为三个术语,以了解振动和扩散之间的相关性:(i)静态结构无序,(ii)非谐波耦合和(iii)离子扩散。比较了Ag ss-氧化铝中超低声子作为超离子导体的相移性能与同形的Ts ss-氧化铝的相移性,后者的离子电导率比Ag ss-氧化铝小10(3)倍。在相同结构下,Ag ss-氧化铝的静态无序量级显示出较大的值(h Gamma(0)= 0.49 meV),是Tl ss-氧化铝的两倍(h Gamma(0)= 0.22 meV)。非化学计量法可得到相同数量的过量阳离子。源于势阱立方非谐性的声子寿命系数在Ag ss-氧化铝中约为Tl ss-氧化铝的五倍。仅在高于200 K的超离子导体Ag ss-氧化铝中观察到强烈的温度相关衰减成分,而在Tl ss-氧化铝中未观察到。这归因于由Ag +离子的跳跃运动引起的声子移相。对于相关时间tau(c)= tau(0)exp(Ea / k(),在Ag ss-氧化铝中,估计的活化能和前指数因子分别为Ea = 71 meV和_ h / tau 0 = 2.86 meV。 B)T)。 _ h / t0 = 2.86 meV的值(可以视为跳跃的尝试频率)与较低的声子频率_ h omega(0)= 2.7 meV一致,但是Ea = 71 meV与直流电导率(Ea = 173 meV)。这些结果与皮秒时域中从振荡到离子扩散的基本激发紧密相关,对于超离子传导机制至关重要。

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