scholarly journals Noise reduction in X-ray photon correlation spectroscopy with convolutional neural networks encoder–decoder models

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Tatiana Konstantinova ◽  
Lutz Wiegart ◽  
Maksim Rakitin ◽  
Anthony M. DeGennaro ◽  
Andi M. Barbour

AbstractLike other experimental techniques, X-ray photon correlation spectroscopy is subject to various kinds of noise. Random and correlated fluctuations and heterogeneities can be present in a two-time correlation function and obscure the information about the intrinsic dynamics of a sample. Simultaneously addressing the disparate origins of noise in the experimental data is challenging. We propose a computational approach for improving the signal-to-noise ratio in two-time correlation functions that is based on convolutional neural network encoder–decoder (CNN-ED) models. Such models extract features from an image via convolutional layers, project them to a low dimensional space and then reconstruct a clean image from this reduced representation via transposed convolutional layers. Not only are ED models a general tool for random noise removal, but their application to low signal-to-noise data can enhance the data’s quantitative usage since they are able to learn the functional form of the signal. We demonstrate that the CNN-ED models trained on real-world experimental data help to effectively extract equilibrium dynamics’ parameters from two-time correlation functions, containing statistical noise and dynamic heterogeneities. Strategies for optimizing the models’ performance and their applicability limits are discussed.

2017 ◽  
Vol 50 (2) ◽  
pp. 357-368 ◽  
Author(s):  
Oier Bikondoa

Multi-time correlation functions are especially well suited to study non-equilibrium processes. In particular, two-time correlation functions are widely used in X-ray photon correlation experiments on systems out of equilibrium. One-time correlations are often extracted from two-time correlation functions at different sample ages. However, this way of analysing two-time correlation functions is not unique. Here, two methods to analyse two-time correlation functions are scrutinized, and three illustrative examples are used to discuss the implications for the evaluation of the correlation times and functional shape of the correlations.


2006 ◽  
Vol 39 (25) ◽  
pp. 8822-8831 ◽  
Author(s):  
Megan L. Ruegg ◽  
Amish J. Patel ◽  
Suresh Narayanan ◽  
Alec R. Sandy ◽  
Simon G. J. Mochrie ◽  
...  

2015 ◽  
Vol 1754 ◽  
pp. 141-146
Author(s):  
Michael Widera ◽  
Uwe Klemradt

ABSTRACTThrough undulator sources at 3rd generation synchrotrons, highly coherent X-rays with sufficient flux are nowadays routinely available, which allow carrying over photon correlation spectroscopy (PCS) from visible light to the X-ray regime. X-ray photon correlation spectroscopy (XPCS) is based on the auto-correlation of X-ray speckle patterns during the temporal evolution of a material and provides access both to equilibrium and non-equilibrium properties of materials at the Angstrom scale. Owing to technical limitations (detector readout), XPCS has typically been used for the detection of slow dynamics on the scale of seconds. The variety of scattering geometries employed in conventional X-ray analysis can be combined with XPCS. In this work, we report on bulk diffraction (XRD) used to study the prototypical shape memory alloy Ni63Al37 undergoing a structural, diffusionless (martensitic) transformation. Two-time correlation functions reveal non-equilibrium dynamics superimposed with microstructural avalanches.


Crystals ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1109
Author(s):  
Yue Cao ◽  
Dina Sheyfer ◽  
Zhang Jiang ◽  
Siddharth Maddali ◽  
Hoydoo You ◽  
...  

How materials evolve at thermal equilibrium and under external excitations at small length and time scales is crucial to the understanding and control of material properties. X-ray photon correlation spectroscopy (XPCS) at X-ray free electron laser (XFEL) facilities can in principle capture dynamics of materials that are substantially faster than a millisecond. However, the analysis and interpretation of XPCS data is hindered by the strongly fluctuating X-ray intensity from XFELs. Here we examine the impact of pulse-to-pulse intensity fluctuations on sequential XPCS analysis. We show that the conventional XPCS analysis can still faithfully capture the characteristic time scales, but with substantial decrease in the signal-to-noise ratio of the g2 function and increase in the uncertainties of the extracted time constants. We also demonstrate protocols for improving the signal-to-noise ratio and reducing the uncertainties.


2014 ◽  
Vol 70 (a1) ◽  
pp. C1331-C1331
Author(s):  
Naoko Yamamoto ◽  
Yuya Shinohara ◽  
Hiroyuki Kishimoto ◽  
Norihiro Matsumoto ◽  
Yoshiyuki Amemiya

Addition of nanoparticles into rubber is indispensable process for production of rubbery materials, as it improves the viscoelastic and mechanical properties of rubber (reinforcement effect). However, the understanding of reinforcement effect is far from satisfactory in spite of many studies. Further microscopic-scale investigation is required for controlling and improving the properties of rubbery materials. Aiming to construct a microscopic model of filled rubber under elongation, we have investigated nanoparticle dynamics in uniaxially stretched rubber using heterodyne X-ray photon correlation spectroscopy (heterodyne XPCS)[1] at BL03XU, SPring-8, Japan. In heterodyne XPCS, information on the fluctuating and dissipative dynamics of nanoparticles and that on their advective motion are separately extracted from the time correlation of X-ray scattering intensity. The results of heterodyne XPCS experiments showed that the direction of nanoparticles' advective motion corresponds to the macroscopic deformation of the sample in stress relaxation process. Furthermore, we found that chemical bond between nanoparticle and rubber polymer influences the dynamics of nanoparticles. In this presentation, we will show detailed analysis of the heterodyne XPCS results and discuss a microscopic description of filled rubber under elongation. This study was conducted under the approval of the SPring-8 Proposal Advisory Committee (2013A7210, 2013B7259).


2021 ◽  
Vol 11 (13) ◽  
pp. 6179
Author(s):  
Felix Lehmkühler ◽  
Wojciech Roseker ◽  
Gerhard Grübel

X-ray photon correlation spectroscopy (XPCS) enables the study of sample dynamics between micrometer and atomic length scales. As a coherent scattering technique, it benefits from the increased brilliance of the next-generation synchrotron radiation and Free-Electron Laser (FEL) sources. In this article, we will introduce the XPCS concepts and review the latest developments of XPCS with special attention on the extension of accessible time scales to sub-μs and the application of XPCS at FELs. Furthermore, we will discuss future opportunities of XPCS and the related technique X-ray speckle visibility spectroscopy (XSVS) at new X-ray sources. Due to its particular signal-to-noise ratio, the time scales accessible by XPCS scale with the square of the coherent flux, allowing to dramatically extend its applications. This will soon enable studies over more than 18 orders of magnitude in time by XPCS and XSVS.


2020 ◽  
Vol 53 (19) ◽  
pp. 8233-8243
Author(s):  
Ronald M. Lewis ◽  
Grayson L. Jackson ◽  
Michael J. Maher ◽  
Kyungtae Kim ◽  
Suresh Narayanan ◽  
...  

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