Proton exchange membrane water electrolysis is a promising technology for large-scale green hydrogen production due to its high efficiency, compact design, and rapid dynamic response. However, its commercialization is strictly limited by high material costs, durability issues, and complex multiphysics coupling within the membrane electrode assembly. This work provides a comprehensive and critical review of key physicochemical processes and advanced predictive modeling approaches for PEMWEs. To capture recent paradigm shifts, we introduce an innovative multi-dimensional classification framework—incorporating spatial resolution, temporal dynamics, and methodological paradigms—to critically evaluate lumped-parameter, continuum, microscale, and multiscale models, explicitly defining their applicability bounds and inherent limitations. The fundamental mechanisms governing electrode kinetics, membrane water transport, and gas–liquid two-phase flow are analyzed, establishing state-of-the-art quantitative benchmarks for microstructural parameters and advanced 3D flow field topologies under high-current-density and high-pressure regimes. Furthermore, we systematically examine model validation rigor, typical prediction errors, and the critical failure of static models in capturing dynamic property shifts during extreme bubble breakthrough. Recent breakthroughs integrating in situ diagnostics, pore-scale simulations, density functional theory, and Physics-Informed Neural Networks are extensively discussed. Future efforts must prioritize mechanical–electrochemical–thermal coupling, transient degradation prognostics, and machine learning-driven predictive digital twin technologies to overcome current empirical limitations and accelerate the gigawatt-scale deployment of PEMWE systems.
Yu et al. (2026) studied this question.