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Conventional hydrogen generation mostly depends on steam methane reforming (SMR), thereby contributing to greenhouse gas emissions. Alkaline water electrolysis using KOH is a promising method for green hydrogen production, but faces significant technical challenges such as high energy consumption and lower hydrogen production. Despite extensive research on various electrolyte modifications, a significant gap exists in the application of biodegradable and biocompatible amino acid-based ionic liquids as electrolyte additives. This study used a modified Hofman cell reaction setup for performing water electrolysis experiments. The selected ionic liquid (IL) was synthesized, and its chemical structure and purity were characterized by FT-IR and H NMR spectroscopy. Subsequently, comprehensive electrochemical analyses, including linear sweep voltammetry, electrochemical impedance spectroscopy, Tafel analysis, and chronoamperometry, were conducted to investigate the electrochemical behavior of the system. The electrochemical analyses were conducted using a three-electrode setup in a 1 M KOH solution with 0 to 4 vol % choline proline [Cho]-[Pro] as an additive. Consequently, the decrease in charge transfer resistance ( ) was observed from 36.1 to 20.5 kΩ during electrochemical impedance spectroscopy. Moreover, the incorporation of [Cho]-[Pro] increases hydrogen production by 1.6-fold and reduces power consumption by 1.3-fold compared to pure 1 M KOH. The findings demonstrate that amino acid-based ionic liquids can significantly enhance the efficiency and sustainability of alkaline water electrolysis, thereby promoting the transition to sustainable energy systems and reducing dependence on fossil fuels.
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http://dx.doi.org/10.1021/acsomega.5c03083 | DOI Listing |
Dalton Trans
September 2025
Sun Yat-Sen University, MOE Laboratory of Polymeric Composite and Functional Materials, School of Materials Science and Engineering, Guangzhou 510275, China.
The main bottleneck faced by traditional hydrogen production technology through water electrolysis lies in the high energy consumption of the anodic oxygen evolution reaction (OER). Combining the thermodynamically favorable ethanol oxidation reaction (EOR) with the hydrogen evolution reaction provides a promising route to reduce the energy consumption of hydrogen production and generate high value-added products. In this study, a facile method was developed for nickel oxyhydroxide (NiOOH) fabrication.
View Article and Find Full Text PDFChem Rec
September 2025
School of Chemistry and Chemical Engineering, Southeast University, Nanjing, Jiangsu, 211189, China.
Water electrolysis for hydrogen production has become an industrial focus in the era of green chemistry due to its high purity of hydrogen production and environmentally friendly, efficient process. As the half reaction of water splitting at the anode, the oxygen evolution reaction (OER) features a complex and sluggish process that restricts the efficiency of water splitting. The mechanism of OER varies with different electrolytes.
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 PDFACS Appl Mater Interfaces
September 2025
Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, Advanced Catalysis and Green Manufacturing Collaborative Innovation Center, Changzhou University, Changzhou 213164, P. R. China.
The development of high-performance, cost-effective non-noble metal catalysts for the oxygen evolution reaction (OER) is critical to advancing sustainable hydrogen production via water electrolysis. Herein, we report a facile and mild strategy for synthesizing amorphous bimetallic organic framework materials (NiFe-MOFs) using pyridine-modified threonine (l-PyThr) as an organic ligand. The optimized NiFe-PyThr-4:1 catalyst exhibits remarkable OER activity, requiring low overpotentials of only 162 and 222 mV to achieve current densities of 10 and 100 mA cm, respectively, along with a small Tafel slope of 34.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Confucius Energy Storage Lab, School of Energy and Environment & Z Energy Storage Center, Southeast University, Nanjing 211189, China.
Developing efficient and durable catalysts for the oxygen evolution reaction (OER) in acidic media is essential for advancing proton exchange membrane water electrolysis (PEMWE). However, catalyst instability caused by lattice oxygen (O) depletion and metal dissolution remains a critical barrier. Here, we propose an oxophilic-site-mediated dynamic oxygen replenishment mechanism (DORM), in which O actively participates in O-O bond formation and is continuously refilled by water-derived species.
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