AI-guided ab initio molecular dynamics study of proton migration in a hydrated MOF for PEMFC applications

Proton exchange membrane fuel cells (PEMFCs) have recently garnered attracted considerable attention due to their low operating temperatures and high energy conversion efficiencies. In this work, we theoretically demonstrate that a novel three-dimensional sodium-based metal-organic framework (MOF UAX-2) exhibits high proton migration conductivity. Sodium-based MOFs are rare, as the coordinated solvent molecules that bind to sodium ions often lead to structural collapse upon activation, as these solvents are removed. Remarkably, MOF UAX-2 retains its structural, thermal, dynamic, and mechanical stability at and above room temperature. The mechanism of proton transport within the MOF was investigated using ab initio molecular dynamics (AIMD) simulations, employing the Verlet integration algorithm as implemented in the SIESTA software package. Simulations were conducted across various temperatures, proton locations, and initial velocities conditions. This study proposes MOF UAX-2 as a promising candidate for use as a proton exchange membrane (PEM) in next-generation fuel cell technologies.