In situ characterization of heterogeneous surface wetting in porous materials.

The performance of nano- and micro-porous materials in capturing and releasing fluids, such as during CO2 geo-storage and water/gas removal in fuel cells and electrolyzers, is determined by their wettability in contact with the solid. However, accurately characterizing wettability is challenging due to spatial variations in dynamic forces, chemical heterogeneity, and surface roughness. In situ measurements can potentially measure wettability locally as a contact angle - the angle a denser phase (e.g water) contacts solid in the presence of a second phase (e.g. hydrogen, air, CO2) - but suffer from difficulties in accurately capturing curvatures, contact areas, and contact loops of multiphase fluids. We introduce a novel extended topological method for in situ contact angle measurement and provide a comparative review of current geometric and topological methods, assessing their accuracy on ideal surfaces, porous rocks containing CO2, and water in gas diffusion layers. The new method demonstrates higher accuracy and reliability of in situ measurements for uniformly wetting systems compared to previous topological approaches, while geometric measurements perform best for mixed-wetting domains. This study further provides a comprehensive open-source platform for in situ characterization of wettability in porous materials with implications for gas geo-storage, fuel cells and electrolyzers, filtration, and catalysis.

Large-scale physically accurate modelling of real proton exchange membrane fuel cell with deep learning.

Proton exchange membrane fuel cells, consuming hydrogen and oxygen to generate clean electricity and water, suffer acute liquid water challenges. Accurate liquid water modelling is inherently challenging due to the multi-phase, multi-component, reactive dynamics within multi-scale, multi-layered porous media. In addition, currently inadequate imaging and modelling capabilities are limiting simulations to small areas (<1 mm2) or simplified architectures. Herein, an advancement in water modelling is achieved using X-ray micro-computed tomography, deep learned super-resolution, multi-label segmentation, and direct multi-phase simulation. The resulting image is the most resolved domain (16 mm2 with 700 nm voxel resolution) and the largest direct multi-phase flow simulation of a fuel cell. This generalisable approach unveils multi-scale water clustering and transport mechanisms over large dry and flooded areas in the gas diffusion layer and flow fields, paving the way for next generation proton exchange membrane fuel cells with optimised structures and wettabilities.