arXiv subjects

Aaron Gilad Kusne

Publications and source records attributed to Aaron Gilad Kusne.

5 recordsLinked to original sources

arXiv2026

Autonomous epitaxial atomic-layer synthesis via real-time computer vision of electron diffraction

Autonomous science platforms which make decisions on the fly are fundamentally changing the outlook for materials development. AI-driven schemes can effectively reduce the total number of iterations needed to arrive at the best stoichiometry for desired properties or optimum synthesis parameters by significant margins. Here, we demonstrate real-time closed-loop autonomous navigation of a multi-dimensional synthesis parameter space for fabricating phase-pure epitaxial films of a metastable functional oxide phase using pulsed laser deposition. Sequential growth iterations in search of the optimized recipe to stabilize the desired crystal phase were performed using frame-by-frame quantitative computer vision of electron diffraction images at the unit-cell level. Our scheme regularly resulted in > 30-fold reduction in the number of experiments compared to comprehensive parameter-space mapping. The real-time workflow developed here can be readily extended to other thin film synthesis platforms opening the door for self-driving atomic-level materials design as well as autonomous semiconductor manufacturing.

cond-mat.mtrl-sci↗

arXiv2021

Graph Neural Network Predictions of Metal Organic Framework CO2 Adsorption Properties

The increasing CO2 level is a critical concern and suitable materials are needed to capture such gases from the environment. While experimental and conventional computational methods are useful in finding such materials, they are usually slow and there is a need to expedite such processes. We use Atomistic Line Graph Neural Network (ALIGNN) method to predict CO2 adsorption in metal organic frameworks (MOF), which are known for their high functional tunability. We train ALIGNN models for hypothetical MOF (hMOF) database with 137953 MOFs with grand canonical Monte Carlo (GCMC) based CO2 adsorption isotherms. We develop high accuracy and fast models for pre-screening applications. We apply the trained model on CoREMOF database and computationally rank them for experimental synthesis. In addition to the CO2 adsorption isotherm, we also train models for electronic bandgaps, surface area, void fraction, lowest cavity diameter, and pore limiting diameter, and illustrate the strength and limitation of such graph neural network models. For a few candidate MOFs we carry out GCMC calculations to evaluate the deep-learning (DL) predictions.

cond-mat.mtrl-sci↗

arXiv2019

Fast and interpretable classification of small X-ray diffraction datasets using data augmentation and deep neural networks

X-ray diffraction (XRD) data acquisition and analysis is among the most time-consuming steps in the development cycle of novel thin-film materials. We propose a machine-learning-enabled approach to predict crystallographic dimensionality and space group from a limited number of thin-film XRD patterns. We overcome the scarce-data problem intrinsic to novel materials development by coupling a supervised machine learning approach with a model agnostic, physics-informed data augmentation strategy using simulated data from the Inorganic Crystal Structure Database (ICSD) and experimental data. As a test case, 115 thin-film metal halides spanning 3 dimensionalities and 7 space-groups are synthesized and classified. After testing various algorithms, we develop and implement an all convolutional neural network, with cross validated accuracies for dimensionality and space-group classification of 93% and 89%, respectively. We propose average class activation maps, computed from a global average pooling layer, to allow high model interpretability by human experimentalists, elucidating the root causes of misclassification. Finally, we systematically evaluate the maximum XRD pattern step size (data acquisition rate) before loss of predictive accuracy occurs, and determine it to be 0.16°, which enables an XRD pattern to be obtained and classified in 5.5 minutes or less.

physics.data-an↗

arXiv2018

Accelerating Photovoltaic Materials Development via High-Throughput Experiments and Machine-Learning-Assisted Diagnosis

Accelerating the experimental cycle for new materials development is vital for addressing the grand energy challenges of the 21st century. We fabricate and characterize 75 unique halide perovskite-inspired solution-based thin-film materials within a two-month period, with 87% exhibiting band gaps between 1.2 eV and 2.4 eV that are of interest for energy-harvesting applications. This increased throughput is enabled by streamlining experimental workflows, developing a set of precursors amenable to high-throughput synthesis, and developing machine-learning assisted diagnosis. We utilize a deep neural network to classify compounds based on experimental X-ray diffraction data into 0D, 2D, and 3D structures more than 10 times faster than human analysis and with 90% accuracy. We validate our methods using lead-halide perovskites and extend the application to novel lead-free compositions. The wider synthesis window and faster cycle of learning enables three noteworthy scientific findings: (1) we realize four inorganic layered perovskites, A3B2Br9 (A = Cs, Rb; B = Bi, Sb) in thin-film form via one-step liquid deposition; (2) we report a multi-site lead-free alloy series that was not previously described in literature, Cs3(Bi1-xSbx)2(I1-xBrx)9; and (3) we reveal the effect on bandgap (reduction to <2 eV) and structure upon simultaneous alloying on the B-site and X-site of Cs3Bi2I9 with Sb and Br. This study demonstrates that combining an accelerated experimental cycle of learning and machine-learning based diagnosis represents an important step toward realizing fully-automated laboratories for materials discovery and development.

physics.app-ph↗

arXiv2018

Machine-learning guided discovery of a high-performance spin-driven thermoelectric material

Thermoelectric conversion using Seebeck effect for generation of electricity is becoming an indispensable technology for energy harvesting and smart thermal management. Recently, the spin-driven thermoelectric effects (STEs), which employ emerging phenomena such as the spin-Seebeck effect (SSE) and the anomalous Nernst effect (ANE), have garnered much attention as a promising path towards low cost and versatile thermoelectric technology with easily scalable manufacturing. However, progress in development of STE devices is hindered by the lack of understanding of the mechanism and materials parameters that govern the STEs. To address this problem, we enlist machine learning modeling to establish the key physical parameters controlling SSE. Guided by these models, we have carried out a high-throughput experiment which led to the identification of a novel STE material with a thermopower an order of magnitude larger than that of the current generation STE devices.

cond-mat.mtrl-sci↗