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Anion exchange membrane water electrolyzers (AEMWEs) offer a promising alternative to proton exchange membrane (PEM) electrolyzers, leveraging non-precious-metal catalysts and alkaline electrolytes for cost reduction. However, challenges persist in achieving long-term durability, high current densities, and stable membrane performance. While previous studies have examined AEM development, a comprehensive structural-electrochemical analysis of AEMWE components under prolonged operation remains limited. This study presents a detailed structural and electrochemical characterization of a commercial AEMWE, where its full-cell performance was matched with the intrinsic half-electrode performance through the use of dual reference electrodes. The electrochemical analysis was supported by a thorough tomographic and spectroscopic investigation of each electrode, thereby providing for the first time a complete materials analysis of the commercial NiFeO anode and Raney nickel cathode. Electrochemical characterization using LSV, EIS, and a dual reference electrode setup revealed full-cell performance of 1.0 A cm at 2.2 V (ambient) and 1.1 A cm at 2.0 V (60 °C), with an HHV efficiency of 74.5% at 1.0 A cm. Long-term operation over 1000 h at 1.0 A cm, 60 °C, in 1.0 M KOH resulted in a substantial polarization resistance increase beyond 230 h, despite an unexpected continuous improvement in MEA performance due to membrane degradation. DRT analysis, coupled with reference electrode studies, was critical in isolating losses. Low-frequency peaks (1.5-25 Hz) were linked to bubble formation, while intermediate-frequency (50-2000 Hz) and high-frequency (>2000 Hz) processes corresponded to charge transfer and ionic transport. The NiFeO anode exhibited better charge transfer, whereas the Raney nickel cathode showed higher polarization resistance.
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http://dx.doi.org/10.1021/acs.energyfuels.5c01799 | DOI Listing |
Int J Mass Spectrom
December 2025
Department of Chemistry, Purdue University, 560 Oval Drive, West Lafayette, IN 47907-2084, USA.
An electrostatic linear ion trap (ELIT) is used to trap ions between two ion mirrors with image current detection by central detection electrode. Transformation of the time-domain signal to the frequency-domain via Fourier transform (FT) yields an ion frequency spectrum that can be converted to a mass-to-charge scale. Injection of ions into an ELIT from an external ion source leads to a time-of-flight ion separation that ultimately determines the range of over which ions can be collected from a given ion injection step.
View Article and Find Full Text PDFPLoS One
September 2025
School of Geography and Resources, Guizhou Education University, Guiyang, China.
Antimony (Sb) is extensively utilized in industrial activities, but most of its compounds exhibit human toxicity and are classified as priority-controlled pollutants. Unlike traditional electrochemical methods that remove metallic pollutants via coagulation or precipitation, electrochemical hydride generation technology converts antimony (Sb) in wastewater into stibine gas (SbH3) for efficient removal. Furthermore, the generated SbH₃ can be decomposed thermally to partially recover metallic antimony.
View Article and Find Full Text PDFRev Sci Instrum
September 2025
Department of Physics, University of Michigan, Ann Arbor, Michigan 48109, USA.
Rydberg atoms are widely employed in precision spectroscopy and quantum information science. To minimize atomic decoherence caused by the dc Stark effect, the electric field noise at the Rydberg atom location should be kept below ∼10 mV/cm. Here, we present a simple yet effective electronic circuit, referred to as a clamp switch, that allows one to realize such conditions.
View Article and Find Full Text PDFFront Chem
August 2025
Departamento de Ingeniería en Metalurgia, Universidad de Atacama, Copiapó, Chile.
The growing global demand for clean and sustainable energy has intensified the development of novel technologies capable of harnessing naturally available resources. Among these, blue energy, referring to the power generated from the mixing of waters with different salinities, has emerged as a promising yet underutilized source. This perspective presents a comprehensive synthesis of recent advances in electrochemical harvesting systems, with a particular focus on Mixing Entropy Batteries (MEBs) as efficient, membrane-free devices for salinity gradient energy recovery.
View Article and Find Full Text PDFBrain Res
September 2025
Department of Neurosciences, Faculty of Medicine and Health Sciences, McGill University, Montréal, Canada; Research Center of the Douglas Mental Health University Institute, Montréal, Canada; Department of Psychiatry, Faculty of Medicine and Health Sciences, McGill University, Montréal, Canada. E
Perceiving a stimulus involves the awareness that it is we who are perceiving it. Representations activated by the stimulus are thus automatically bound to representations of the self. Interestingly, previous research has shown that the amplitude of the P2 event-related brain potential (ERP) is larger for stimuli to which participants can refer themselves.
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