Mathew J. Cherukara

Mathew J. Cherukara

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Mathew J. Cherukara

Advanced Photon Source, Argonne National Laboratory, Lemont, USA

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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21 March 2018 in Nature Communications
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Diana BermanDiana Berman
Diana Berman
BNBadri Narayanan
Badri Narayanan
MCMathew J. Cherukara
Mathew J. Cherukara
SSSubramanian K. R. S. Sankaranarayanan
Subramanian K. R. S. Sankaranarayanan
AEAli Erdemir
Ali Erdemir
ASAnirudha Sumant
Anirudha Sumant
Stress-induced reactions at the sliding interface during relative movement are known to cause structural or chemical modifications in contacting materials. The nature of these modifications at the atomic level and formation of byproducts in an oil-free environment, however, remain poorly understood and pose uncertainties in predicting the tribological performance of the complete tribosystem. Here, we demonstrate that tribochemical reactions occur even in dry conditions when hydrogenated diamond-like carbon (H-DLC) surface is slid against two-dimensional (2D) molybdenum disulfide along with nanodiamonds in dry nitrogen atmosphere. Detailed experimental studies coupled with reactive molecular dynamics simulations reveal that at high contact pressures, diffusion of sulfur from the dissociated molybdenum disulfide led to amorphization of nanodiamond and subsequent transformation to onion-like carbon structures (OLCs). The in situ formation of OLCs at the sliding interface provide reduced contact area as well as incommensurate contact with respect to the H-DLC surface, thus enabling successful demonstration of superlubricity

22 January 2019 in Nature Communications
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HCHenry Chan
Henry Chan
MCMathew J. Cherukara
Mathew J. Cherukara
BNBadri Narayanan
Badri Narayanan
TLTroy D. Loeffler
Troy D. Loeffler
CBChris Benmore
Chris Benmore
SSSubramanian K. R. S. Sankaranarayanan
Subramanian K. R. S. Sankaranarayanan
An accurate and computationally efficient molecular level description of mesoscopic behavior of ice-water systems remains a major challenge. Here, we introduce a set of machine-learned coarse-grained (CG) models (ML-BOP, ML-BOPdih, and ML-mW) that accurately describe the structure and thermodynamic anomalies of both water and ice at mesoscopic scales, all at two orders of magnitude cheaper computational cost than existing atomistic models. In a significant departure from conventional force-field fitting, we use a multilevel evolutionary strategy that trains CG models against not just energetics from first-principles and experiments but also temperature-dependent properties inferred from on-the-fly molecular dynamics (~ 10’s of milliseconds of overall trajectories). Our ML BOP models predict both the correct experimental melting point of ice and the temperature of maximum density of liquid water that remained elusive to-date. Our ML workflow navigates efficiently through the high-dimensional parameter space to even improve upon existing high-quality CG models (e.g. mW model).

3 January 2019 in The Journal of Physical Chemistry C
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HCHenry Chan
Henry Chan
BNBadri Narayanan
Badri Narayanan
MCMathew J. Cherukara
Mathew J. Cherukara
FSFatih G. Sen
Fatih G. Sen
KSKiran Sasikumar
Kiran Sasikumar
SSSubramanian K. R. S. Sankaranarayanan
Subramanian K. R. S. Sankaranarayanan

27 July 2020 in Applied Physics Letters
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MCMathew J. Cherukara
Mathew J. Cherukara
TZTao Zhou
Tao Zhou
YNYoussef Nashed
Youssef Nashed
PEPablo Enfedaque
Pablo Enfedaque
AHAlex Hexemer
Alex Hexemer
MHMartin V. Holt
Martin V. Holt
Ptychographic imaging is a powerful means of imaging beyond the resolution limits of typical x-ray optics. Recovering images from raw ptychographic data, however, requires the solution of an inverse problem, namely, phase retrieval. Phase retrieval algorithms are computationally expensive, which precludes real-time imaging. In this work, we propose PtychoNN, an approach to solve the ptychography data inversion problem based on a deep convolutional neural network. We demonstrate how the proposed method can be used to predict real-space structure and phase at each scan point solely from the corresponding far-field diffraction data. Our results demonstrate the practical application of machine learning to recover high fidelity amplitude and phase contrast images of a real sample hundreds of times faster than current ptychography reconstruction packages. Furthermore, by overcoming the constraints of iterative model-based methods, we can significantly relax sampling constraints on data acquisition while still producing an excellent image of the sample. Besides drastically accelerating acquisition and analysis, this capability has profound implications for the imaging of dose sensitive, dynamic, and extremely voluminous samples.

13 June 2015 in The Journal of Physical Chemistry C
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MWMitchell A. Wood
Mitchell A. Wood
MCMathew J. Cherukara
Mathew J. Cherukara
EKEdward M. Kober
Edward M. Kober
ASAlejandro Strachan
Alejandro Strachan

8 November 2018 in Scientific Reports
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MCMathew J. Cherukara
Mathew J. Cherukara
YNYoussef Nashed
Youssef Nashed
RHRoss J. Harder
Ross J. Harder
Phase retrieval, or the process of recovering phase information in reciprocal space to reconstruct images from measured intensity alone, is the underlying basis to a variety of imaging applications including coherent diffraction imaging (CDI). Typical phase retrieval algorithms are iterative in nature, and hence, are time-consuming and computationally expensive, making real-time imaging a challenge. Furthermore, iterative phase retrieval algorithms struggle to converge to the correct solution especially in the presence of strong phase structures. In this work, we demonstrate the training and testing of CDI NN, a pair of deep deconvolutional networks trained to predict structure and phase in real space of a 2D object from its corresponding far-field diffraction intensities alone. Once trained, CDI NN can invert a diffraction pattern to an image within a few milliseconds of compute time on a standard desktop machine, opening the door to real-time imaging.