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X 射线光子相关光谱学研究表面和薄膜。

X-ray photon correlation spectroscopy studies of surfaces and thin films.

机构信息

Dept. of Physics, University of California San Diego, 9500 Gilman Drive, La Jolla, CA, 92093-0319, USA.

出版信息

Adv Mater. 2014 Dec 10;26(46):7764-85. doi: 10.1002/adma.201401094. Epub 2014 Sep 18.

Abstract

The technique of X-ray Photon Correlation Spectroscopy (XPCS) is reviewed as a method for studying the relatively slow dynamics of materials on time scales ranging from microseconds to thousands of seconds and length scales ranging from microns down to nanometers. We focus on the application of this technique to study dynamical fluctuations of surfaces, interfaces and thin films. We first discuss instrumental issues such as the effects of partial coherence (or alternatively finite instrumental resolution) and optimization of signal-to-noise ratios in the experiments. We then review what has been learned from recent XPCS studies of capillary wave fluctuations on liquid surfaces and polymer films, of nanoparticles used as probes to study the interior dynamics of polymer films, of liquid crystals and multilamellar surfactant films, and of metal surfaces, and magnetic domain wall fluctuations in antiferromagnets. We then discuss studies of non-equilibrium dynamics described by 2-time correlation functions. Finally, we briefly speculate on possible future XPCS experiments at new synchrotron sources currently under development including studies of dynamics on time scales down to femtoseconds.

摘要

X 射线光子相关光谱学(XPCS)技术综述作为一种研究材料相对缓慢动力学的方法,其时间尺度范围从微秒到数千秒,长度尺度范围从微米到纳米。我们专注于将该技术应用于研究表面、界面和薄膜的动力学波动。我们首先讨论仪器方面的问题,例如部分相干性的影响(或者替代的有限仪器分辨率)以及实验中信噪比的优化。然后,我们回顾了最近在液体表面和聚合物薄膜上的毛细波波动、用作探针研究聚合物薄膜内部动力学的纳米粒子、液晶和多层表面活性剂薄膜以及金属表面的研究中所学到的知识,以及反铁磁体中的磁畴壁波动。然后,我们讨论了由双时间相关函数描述的非平衡动力学研究。最后,我们简要地推测了当前正在开发的新同步辐射源的可能的未来 XPCS 实验,包括研究达到飞秒时间尺度的动力学。

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