Accelerated Reaction Exploration across Scales: A Hybrid Operando and Modeling Study of Oxidation Kinetics in Monolayer Tungsten Disulfide

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Authors: Jad Jaafar, Ye Fan, Maryam Kazemzadeh-Atoufi, Ryo Mizuta, Jinfeng Yang, Jack E. N. Swallow, E. Jones, Matthijs A. van Spronsen, Georg Held, Robert S. Weatherup, Peter Voorhees, David J. Wales
+2 more Gabor Csanyi, Stephan Hofmann
Cited by: 1
References: 69

Abstract

High Resolution Image Download MS PowerPoint Slide The commercialization of emerging materials is hindered by the empirical nature of process development, with the underpinning solid-state reaction kinetics remaining elusive due to their inherent multistep and multiscale character and the vast configurational and parameter space. We combine high-throughput operando scanning electron microscopy (OSEM) with extended classical continuum and phase-field simulations and atomistic machine-learned interatomic potential (MLIP) surrogate models to demonstrate effective foundational reaction exploration, using thermal oxidation of chemical-vapor-deposited monolayer WS 2 across a temperature range of 450–680 °C as our benchmark reaction. OSEM provides statistically relevant reaction data sets of spatiotemporal basal plane nucleation kinetics and propagation of tens of thousands of individual 1D reaction facets, revealing time-dependent rates. By extending Avrami theory and employing a calibrated phase-field model, we extract an apparent nucleation barrier of 1.1 eV and show that the complex rate behavior arises from mixed reaction–diffusion control. Atomistic reaction exploration via MLIPs guided by these experimental data reveals that oxidative reaction chains leading to W volatilization and etch pit formation are driven not by the most common sulfur or substitutional oxygen point defects but by more complex defects such as W vacancies. MLIP diffusion barrier screening identifies the role of chemisorbed hydroxyl species for this reaction scenario, while systematic screening of 1D edge configurations and their terminations uncovers the structural origins of the pronounced in-plane reaction anisotropies. We discuss the potential of our synergistic approach to effectively bring experimental and computational approaches closer together and accelerate critically required process discovery for advanced materials.

Fields of Study & Subjects

2D Materials and Applications Catalysis and Oxidation Reactions Electrocatalysts for Energy Conversion

Publication details

Journal / source
Journal of the American Chemical Society
Publisher
American Chemical Society (ACS)
Volume
148
Issue
21
Pages
21996–22007
Publication date
20 May 2026
Language
EN