Insights into lithium manganese oxide-water interfaces using machine learning potentials

Unraveling the atomistic and the electronic structure of solid-liquid interfaces is the key to the design of new materials for many important applications, from heterogeneous catalysis to battery technology. Density functional theory (DFT) calculations can, in principle, provide a reliable description of such interfaces, but the high computational costs severely restrict the accessible time and length scales. Here, we report machine learning-driven simulations of various interfaces between water and lithium manganese oxide (LixMn2O4), an important electrode material in lithium ion batteries and a catalyst for the oxygen evolution reaction. We employ a high-dimensional neural network potential to compute the energies and forces several orders of magnitude faster than DFT without loss in accuracy. In addition, a high-dimensional neural network for spin prediction is utilized to analyze the electronic structure of the manganese ions. Combining these methods, a series of interfaces is investigated by large-scale molecular dynamics. The simulations allow us to gain insights into a variety of properties, such as the dissociation of water molecules, proton transfer processes, and hydrogen bonds, as well as the geometric and electronic structure of the solid surfaces, including the manganese oxidation state distribution, Jahn-Teller distortions, and electron hopping. Published under an exclusive license by AIP Publishing.

Automated summary

The atomistic and electronic structure of solid-liquid interfaces are crucial for designing new materials for various applications. Machine learning-driven simulations of water and lithium manganese oxide interfaces provide insights into these structures with high accuracy and efficiency. Through large-scale molecular dynamics simulations, properties such as water molecule dissociation, proton transfer processes, hydrogen bonds, and the geometric and electronic structure of solid surfaces are investigated.