Hydrogen generated by proton exchange membrane (PEM) electrolyzer holds a promising potential to complement the traditional energy structure and achieve the global target of carbon neutrality for its efficient, clean, and sustainable nature. The acidic oxygen evolution reaction (OER), owing to its sluggish kinetic process, remains a bottleneck that dominates the efficiency of overall water splitting. Over the past few decades, tremendous efforts have been devoted to exploring OER activity, whereas most show unsatisfying stability to meet the demand for industrial application of PEM electrolyzer. In this review, systematic considerations of the origin and strategies based on OER stability challenges are focused on. Intrinsic deactivation of the material and the extrinsic balance of plant-induced destabilization are summarized. Accordingly, rational strategies for catalyst design including doping and leaching, support effect, coordination effect, strain engineering, phase and facet engineering are discussed for their contribution to the promoted OER stability. Moreover, advanced in situ/operando characterization techniques are put forward to shed light on the OER pathways as well as the structural evolution of the OER catalyst, giving insight into the deactivation mechanisms. Finally, outlooks toward future efforts on the development of long-term and practical electrocatalysts for the PEM electrolyzer are provided.
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http://dx.doi.org/10.1002/smtd.202201130 | DOI Listing |
Small Methods
January 2025
Forschungszentrum Juelich GmbH, Institute of Energy Technologies, IET-4, Electrochemical Process Engineering, 52425, Juelich, Germany.
Understanding the sheet resistance of porous electrodes is essential for improving the performance of polymer electrolyte membrane (PEM) water electrolyzers and related technologies. Despite its importance, existing methods often fail to provide reliable and comprehensive data, especially for porous materials with complex morphologies and non-uniform thicknesses. This study introduces a robust and straightforward method for determining the sheet resistance of porous electrodes using a novel probe concept based on industrial printed circuit board (PCB) technology.
View Article and Find Full Text PDFChemSusChem
January 2025
Department of Chemical Engineering, MESA+ Institute for Nanotechnology, Faculty of Science and Technology, University of Twente, Drienerlolaan 5, 7522 NB, Enschede, The, Netherlands.
A niobium (Nb) mesh electrode was coated with boron-doped diamond (BDD) using chemical vapor deposition in a custom-built hot-filament reactor. The BDD-functionalized mesh was tested in a zero-gap electrolysis configuration and evaluated for the anodic formation of HO by selective oxidation of water, including the analysis of the effects on Faradaic efficiency towards HO (FEH2O2) induced by pulsed electrolysis. A low electrolyte flow rate (V⋅) was found to result in a relatively high concentration of HO in single-pass electrolysis experiments.
View Article and Find Full Text PDFNanomaterials (Basel)
January 2025
Département de Génie Électrique, École de Technologie Supérieure, 1100 Notre-Dame Street West, Montreal, QC H3C 1K3, Canada.
This study explored the influence of graphene oxide (GO) on morphological and mechanical properties of Nafion 115 membranes with the objective of enhancing the mechanical properties of the most widely employed membrane in Proton Exchange Membrane Water Electrolyzers (PEMWE) applications. The membrane surface was modified by ultrasonically spraying a GO solution and different annealing temperatures were tested. Scanning Electron Microscopy (SEM) cross-sectional images revealed that annealing the composite membranes was sufficient to favor an interaction between the graphene oxide and the surface of the Nafion membranes.
View Article and Find Full Text PDFMaterials (Basel)
December 2024
Department of Material Science and Engineering, Universidad Carlos III de Madrid, IAAB, 28911 Leganés, Madrid, Spain.
The production of green hydrogen through proton exchange membrane water electrolysis (PEMWE) is a promising technology for industry decarbonization, outperforming alkaline water electrolysis (AWE). However, PEMWE requires significant investment, which can be mitigated through material and design advancements. Components like bipolar porous plates (BPPs) and porous transport films (PTFs) contribute substantially to costs and performance.
View Article and Find Full Text PDFNat Commun
January 2025
School of Materials Science and Engineering, Peking University, Beijing, China.
Using metal oxides to disperse iridium (Ir) in the anode layer proves effective for lowering Ir loading in proton exchange membrane water electrolyzers (PEMWE). However, the reported low-Ir-based catalysts still suffer from unsatisfying electrolytic efficiency and durability under practical industrial working conditions, mainly due to insufficient catalytic activity and mass transport in the catalyst layer. Herein we report a class of porous heterogeneous nanosheet catalyst with abundant Ir-O-Mn bonds, achieving a notable mass activity of 4 A mg for oxygen evolution reaction at an overpotential of 300 mV, which is 150.
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