The development of hydrogen energy sources based on electrochemical water splitting is of increasing interest due to its advantages in energy and environmental fields. In this study, CoOwas decorated on carbon cloth (CC) by a hydrothermal method and was used as an electrode for water splitting. The structural and morphological properties of the materials are assessed using a range of reliable techniques such as X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) with EDX mapping, and diffuse reflectance spectroscopy (DRS). Results indicate that the CoO/CC material was synthesized at 140 °C for 9 h and calcined at 350 °C achieving a superior overall water-splitting activity in the direction of hydrogen evolution reaction (HER) reaction than that of the oxygen evolution reaction (OER). In detail, HER characteristics with an overpotential at -0.234 V and a current density at 10 mA cm. In addition, the CoO/CC material also gives overpotential at 0.54 V for OER process. Furthermore, the electrochemical surface area of CoO/CC material is 7.6 times higher than CC electrode. Moreover, the CC fabric is destroyed when the annealing temperature is higher than 350 °C, leading to a significant decrease in the activity of CoO/CC. The as-prepared CoO shows good adhesion and stability based on CC substrate without binder substance or further treatment of CC.
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http://dx.doi.org/10.1007/s11356-023-31188-y | DOI Listing |
Angew Chem Int Ed Engl
January 2025
Chinese Academy of Sciences Qingdao Industrial Energy Storage Technology Institute, Department of Energy Science and Energy Technology, Songling Road, 189, 266101, Qingdao City, CHINA.
Membrane-assisted direct seawater splitting (DSS) technologies are actively studied as a promising route to produce green hydrogen (H2), whereas the indispensable use of supporting electrolytes that help to extract water and provide electrochemically-accelerated reaction media results in a severe energy penalty, consuming up to 12.5% of energy input when using a typical KOH electrolyte. We bypass this issue by designing a zero-gap electrolyzer configuration based on the integration of cation exchange membrane and bipolar membrane assemblies, which protects stable DSS operation against the precipitates and corrosion in the absence of additional supporting electrolytes.
View Article and Find Full Text PDFNat Commun
January 2025
Shanghai Key Lab of Chemical Assessment and Sustainability, School of Chemical Science and Engineering, Tongji University, Shanghai, China.
Photocatalytic overall water splitting is a promising approach for a sustainable hydrogen provision using solar energy. For sufficient solar energy utilization, this reaction ought to be operated based on visible-light-active semiconductors, which is very challenging. In this work, an F-expedited nitridation strategy is applied to modify the wide-bandgap semiconductor SrTiO for visible-light-driven photocatalytic overall water splitting.
View Article and Find Full Text PDFNat Commun
January 2025
Max Planck Institute of Colloids and Interfaces, Colloid Chemistry Department, Am Mühlenberg 1, 14476, Potsdam, Germany.
Covalent semiconductors of the carbon nitride family are among the most promising systems to realize "artificial photosynthesis", that is exploiting synthetic materials which use sunlight as an energy source to split water into its elements or converting CO into added value chemicals. However, the role of surface interactions and electronic properties on the reaction mechanism remain still elusive. Here, we use in-situ spectroscopic techniques that enable monitoring surface interactions in carbon nitride under artificial photosynthetic conditions.
View Article and Find Full Text PDFNanoscale
January 2025
Department of Chemistry, Material Science Lab, Annamalai University, Annamalai Nagar, Tamil Nadu 608002, India.
The urgent need to address escalating environmental pollution and energy management challenges has underscored the importance of developing efficient, cost-effective, and multifunctional electrocatalysts. To address these issues, we developed an eco-friendly, cost-effective, and multifunctional electrocatalyst a solvothermal synthesis approach. Due to the merits of the ideal synthesis procedure, the FeCoHS@NF electrocatalyst exhibited multifunctional activities, like OER, HER, OWS, UOR, OUS, and overall alkaline seawater splitting, with required potentials of 1.
View Article and Find Full Text PDFSmall Methods
January 2025
Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei, 10607, Taiwan.
Electrochemical water splitting is a pivotal process for sustainable hydrogen energy production, relying on efficient hydrogen evolution reaction (HER) catalysts, particularly in acidic environments, where both high activity and durability are crucial. Despite the favorable kinetics of platinum (Pt)-based materials, their performance is hindered under harsh conditions, driving the search for alternatives. Due to their unique structural characteristic, Prussian blue analogs (PBAs) emerge as attractive candidates for designing efficient HER electrocatalysts.
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