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Although a gas diffusion electrode (GDE) has been widely employed in the electrochemical CO reduction reaction (CORR) to effectively mitigate mass transport limitations, knowledge of the active region within the catalyst layer on the GDE remains incomplete. In this work, we employed a thin layer of Bi as a reporter to identify the active region within the Ag catalyst layer by taking advantage of the distinct selectivity of these two metals in the CORR. Through manipulating the position of the Bi layer within the Ag layer, we showed that at 100 mA cm, the active region was located between 150 and 600 nm from the PTFE substrate. Current density, feed gas humidity, and the hydrophobicity of the substrate were found to impact both the location and thickness of the active region. Further, Raman spectroscopy capable of characterizing the cross-section of the catalyst layer was developed to locate the active region inside the catalyst layer.
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http://dx.doi.org/10.1021/jacs.5c03143 | DOI Listing |
ACS Electrochem
September 2025
Department of Material Science and Engineering, The Pennsylvania State University, University Park, Pennsylvania 16802, United States.
Bipolar membranes (BPMs) are increasingly recognized as a promising electrolyte option for water electrolysis, attributable to their distinctive properties derived from the membrane's layered structure, which consists of an anion exchange (AEL) and a cation exchange layer (CEL). This study investigates four different BPMs and the influence they have on the performance of a water electrolysis cell under two different feed configurations: (1) a symmetric deionized water feed to both anode and cathode compartments and (2) an asymmetric feed with a 0.5 mol/L NaCl catholyte feed and a deionized water anolyte feed.
View Article and Find Full Text PDFACS Nano
September 2025
Eastern Institute for Advanced Study, Eastern Institute of Technology, Ningbo, Zhejiang 315200, P. R. China.
Ni-Fe (oxy)hydroxides are among the most active oxygen evolution reaction (OER) catalysts in alkaline media. However, achieving precise control over local asymmetric Fe-O-Ni active sites in Ni-Fe oxyhydroxides for key oxygenated intermediates' adsorption steric configuration regulation of the OER is still challenging. Herein, we report a two-step dealloying strategy to fabricate asymmetric Fe-O-Ni pair sites in the shell of NiOOH@FeOOH/NiOOH heterostructures from NiFe Prussian blue analogue (PBA) nanocubes, involving anion exchange and structure reconstruction.
View Article and Find Full Text PDFNanomicro Lett
September 2025
Department of Mechanical, Aerospace & Biomedical Engineering, University of Tennessee, Knoxville, Knoxville, TN, 37996, USA.
3D printing, as a versatile additive manufacturing technique, offers high design flexibility, rapid prototyping, minimal material waste, and the capability to fabricate complex, customized geometries. These attributes make it particularly well-suited for low-temperature hydrogen electrochemical conversion devices-specifically, proton exchange membrane fuel cells, proton exchange membrane electrolyzer cells, anion exchange membrane electrolyzer cells, and alkaline electrolyzers-which demand finely structured components such as catalyst layers, gas diffusion layers, electrodes, porous transport layers, and bipolar plates. This review provides a focused and critical summary of the current progress in applying 3D printing technologies to these key components.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Surface Science Laboratory, Department of Materials and Geosciences, Technical University of Darmstadt, Peter-Grünberg-Straße 4, 64287 Darmstadt, Germany.
The performance of NiO-based electrocatalysts for the oxygen evolution reaction (OER) is strongly influenced by the interface between the metal support (current collector) and the catalyst layer, which modulates electronic properties and electrochemical activity. This study systematically investigates the solid-solid interface behavior of NiO thin films prepared by reactive magnetron sputtering on Pt, Au, and Ni, followed by electrochemical characterization. Stepwise NiO deposition and X-ray photoelectron spectroscopy reveal distinct band alignment and electronic structure differences at the metal-catalyst interface.
View Article and Find Full Text PDFAdv Sci (Weinh)
September 2025
Guangxi Key Laboratory of Clean Pulp & Papermaking and Pollution Control, School of Light Industry and Food Engineering, Guangxi University, Nanning, 530004, China.
Carbonized wood has great potential as a self-supported electrode for energy storage/conversion applications. However, developing efficient and economical bifunctional electrodes by customizing the surface structure remains a challenge. This study proposes a novel multifunctional electrode design strategy, using N/P co-doped carbonized wood (NPCW) as carriers and in situ grows copper nanoparticles (Cu NPs) as nucleation centers to induce vertical growth of CuCo-layered double hydroxid (LDH) nanosheets along the substrate.
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