Issue 2, 2023

How machine learning can accelerate electrocatalysis discovery and optimization

Abstract

Advances in machine learning (ML) provide the means to bypass bottlenecks in the discovery of new electrocatalysts using traditional approaches. In this review, we highlight the currently achieved work in ML-accelerated discovery and optimization of electrocatalysts via a tight collaboration between computational models and experiments. First, the applicability of available methods for constructing machine-learned potentials (MLPs), which provide accurate energies and forces for atomistic simulations, are discussed. Meanwhile, the current challenges for MLPs in the context of electrocatalysis are highlighted. Then, we review the recent progress in predicting catalytic activities using surrogate models, including microkinetic simulations and more global proxies thereof. Several typical applications of using ML to rationalize thermodynamic proxies and predict the adsorption and activation energies are also discussed. Next, recent developments of ML-assisted experiments for catalyst characterization, synthesis optimization and reaction condition optimization are illustrated. In particular, the applications in ML-enhanced spectra analysis and the use of ML to interpret experimental kinetic data are highlighted. Additionally, we also show how robotics are applied to high-throughput synthesis, characterization and testing of electrocatalysts to accelerate the materials exploration process and how this equipment can be assembled into self-driven laboratories.

Graphical abstract: How machine learning can accelerate electrocatalysis discovery and optimization

Article information

Article type
Review Article
Submitted
15 okt. 2022
Accepted
07 des. 2022
First published
09 des. 2022
This article is Open Access
Creative Commons BY-NC license

Mater. Horiz., 2023,10, 393-406

How machine learning can accelerate electrocatalysis discovery and optimization

S. N. Steinmann, Q. Wang and Z. W. Seh, Mater. Horiz., 2023, 10, 393 DOI: 10.1039/D2MH01279K

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