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Electrochem, Volume 6, Issue 4 (December 2025) – 4 articles

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36 pages, 1413 KB  
Review
Water Management Strategies for Proton Exchange Membrane Fuel Cells: A Comprehensive Review
by Mahfouz Saeed, Mohamed A. El-Hameed, Essa Al-Hajri and Adnan Kabbani
Electrochem 2025, 6(4), 38; https://doi.org/10.3390/electrochem6040038 - 27 Oct 2025
Viewed by 466
Abstract
Proton exchange membrane fuel cells (PEMFCs) are a promising clean energy technology due to their zero gas emissions, low operating temperature, and high efficiency. This review synthesizes research from 2015–2025 on (i) materials-level approaches (advanced/modified PFSA membranes and composite membranes) that improve water [...] Read more.
Proton exchange membrane fuel cells (PEMFCs) are a promising clean energy technology due to their zero gas emissions, low operating temperature, and high efficiency. This review synthesizes research from 2015–2025 on (i) materials-level approaches (advanced/modified PFSA membranes and composite membranes) that improve water retention and ionic conduction, (ii) engineered gas diffusion layers and hydrophobic/hydrophilic gradients (including Janus and asymmetric GDL architectures) that facilitate directional water transport and have been shown to increase peak power density in some reports (e.g., from ≈1.17 to ≈1.89 W·cm−2 with Janus GDL designs), (iii) flow-field design strategies. This review examines the key aspects of water management in PEMFCs, including their impact on cell performance, the underlying causes of related issues, and the mechanisms of water transport within these cells. Additionally, it discusses the methods and materials used to enhance water management, highlighting recent advancements and potential directions for future research. Topics such as water transport, water flooding, and water control strategies in PEMFCs are also addressed. Both excess water (flooding) and water depletion (dehydration) can negatively influence fuel cell performance and lifespan. Particular attention is given to water dehydration, with a detailed discussion of its effects on the cathode, Anode, gas diffusion layer, catalyst layer, and flow channels. Full article
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29 pages, 4970 KB  
Review
Metal–Organic Frameworks for Seawater Electrolysis and Hydrogen Production: A Review
by Ivelina Tsacheva, Mehmet Suha Yazici, Abdul Hanif Mahadi, Aytekin Uzunoglu and Dzhamal Uzun
Electrochem 2025, 6(4), 37; https://doi.org/10.3390/electrochem6040037 - 20 Oct 2025
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Abstract
Electrolysis utilizing renewable electricity is an environmentally friendly, non-polluting, and sustainable method of hydrogen production. Seawater is the most desirable and inexpensive electrolyte for this process to achieve commercial acceptance compared to competing hydrogen production technologies. We reviewed metal–organic frameworks as possible electrocatalysts [...] Read more.
Electrolysis utilizing renewable electricity is an environmentally friendly, non-polluting, and sustainable method of hydrogen production. Seawater is the most desirable and inexpensive electrolyte for this process to achieve commercial acceptance compared to competing hydrogen production technologies. We reviewed metal–organic frameworks as possible electrocatalysts for hydrogen production by seawater electrolysis. Metal–organic frameworks are interesting for seawater electrolysis due to their large surface area, tunable permeability, and ease of functional processing, which makes them extremely suitable for obtaining modifiable electrode structures. Here we discussed the development of metal–organic framework-based electrocatalysts as multifunctional materials with applications for alkaline, PEM, and direct seawater electrolysis for hydrogen production. Their advantages and disadvantages were examined in search of a pathway to a successful and sustainable technology for developing electrode materials to produce hydrogen from seawater. Full article
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23 pages, 2465 KB  
Review
Electrochemical and Redox Strategies for the Synthesis of Catecholamine- and Dihydroxynaphthalene-Based Materials: A Comparative Review
by Chloé Laporte and Vincent Ball
Electrochem 2025, 6(4), 36; https://doi.org/10.3390/electrochem6040036 - 18 Oct 2025
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Abstract
Melanins are multifunctional biopolymers with unique properties, ranging from UV and radiation protection to antioxidant activity and metal chelation, making them highly attractive for biomedical applications. Despite extensive research, the mechanisms underlying melanin formation remain only partially understood, and access to these biopolymers [...] Read more.
Melanins are multifunctional biopolymers with unique properties, ranging from UV and radiation protection to antioxidant activity and metal chelation, making them highly attractive for biomedical applications. Despite extensive research, the mechanisms underlying melanin formation remain only partially understood, and access to these biopolymers therefore relies on suitable molecular precursors. While most studies have focused on catecholamine-derived eumelanins such as 3,4-dihydroxyphenylalanine (L-DOPA) and dihydroxyindole (DHI), nitrogen-free precursors such as 1,8-dihydroxynaphthalene (1,8-DHN) are emerging as promising routes to allomelanins. To date, however, these two precursor classes have largely been investigated separately, limiting a broader understanding of structure–function relationships. This review aims to compare electrochemical and redox-based pathways to catecholamine- and DHN-derived materials, emphasizing both their common principles and distinctive features. By bridging these parallel research streams, we propose a methodological framework for guiding future research on melanin-inspired materials and bioelectrochemical technologies. Full article
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30 pages, 8552 KB  
Article
Analytical–Computational Integration of Equivalent Circuit Modeling, Hybrid Optimization, and Statistical Validation for Electrochemical Impedance Spectroscopy
by Francisco Augusto Nuñez Perez
Electrochem 2025, 6(4), 35; https://doi.org/10.3390/electrochem6040035 - 8 Oct 2025
Viewed by 966
Abstract
Background: Electrochemical impedance spectroscopy (EIS) is indispensable for disentangling charge-transfer, capacitive, and diffusive phenomena, yet reproducible parameter estimation and objective model selection remain unsettled. Methods: We derive closed-form impedances and analytical Jacobians for seven equivalent-circuit models (Randles, constant-phase element (CPE), and Warburg impedance [...] Read more.
Background: Electrochemical impedance spectroscopy (EIS) is indispensable for disentangling charge-transfer, capacitive, and diffusive phenomena, yet reproducible parameter estimation and objective model selection remain unsettled. Methods: We derive closed-form impedances and analytical Jacobians for seven equivalent-circuit models (Randles, constant-phase element (CPE), and Warburg impedance (ZW) variants), enforce physical bounds, and fit synthetic spectra with 2.5% and 5.0% Gaussian noise using hybrid optimization (Differential Evolution (DE) → Levenberg–Marquardt (LM)). Uncertainty is quantified via non-parametric bootstrap; parsimony is assessed with root-mean-square error (RMSE), Akaike Information Criterion (AIC), and Bayesian Information Criterion (BIC); physical consistency is checked by Kramers–Kronig (KK) diagnostics. Results: Solution resistance (Rs) and charge-transfer resistance (Rct) are consistently identifiable across noise levels. CPE parameters (Q,n) and diffusion amplitude (σ) exhibit expected collinearity unless the frequency window excites both processes. Randles suffices for ideal interfaces; Randles+CPE lowers AIC when non-ideality and/or higher noise dominate; adding Warburg reproduces the 45 tail and improves likelihood when diffusion is present. The (Rct+ZW)CPE architecture offers the best trade-off when heterogeneity and diffusion coexist. Conclusions: The framework unifies analytical derivations, hybrid optimization, and rigorous statistics to deliver traceable, reproducible EIS analysis and clear applicability domains, reducing subjective model choice. All code, data, and settings are released to enable exact reproduction. Full article
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