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To adapt fluctuating renewable energy for water splitting is challenging, since the growth of electrochemically generated nanobubbles at early stage requires high supersaturation during the repeated start-stop cycles, which can accelerate the deactivation of electrodes and cause extra energy consumption. Herein, we propose a "bubble seeding" strategy by introducing nanobubbles (NBs, ~200 nm in diameter) into electrolyte to promote the generation of macroscopic bubbles. The precursive nanobubbles can act as the beforehand nuclei with a certain supersaturation, lower the supersaturation barrier for further growth, and result in reduced overpotential as high as 130 mV for oxygen evolution reaction. The enhancement depends on nanobubble coverage and size, with higher coverage and larger sizes favoring macrobubble growth. The nanobubbles with inert gas species (e.g. N for oxygen evolution reaction) can also work as the seeds, while the interfering or consumable gas species (e.g. O for hydrogen evolution reaction) would hinder the generation of macroscopic bubbles and enlarge the overpotential. The water splitting device working at presence of nanobubbles exhibits stable operation voltage during repeated start-stop cycles in contrast to traditional electrolyte without NBs, indicating great potential of such traceless nanobubble additive strategy for stabilizing gas evolution applications.
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http://dx.doi.org/10.1038/s41467-025-61131-3 | DOI Listing |
ACS 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 PDFAdv Mater
September 2025
Department of Materials Science and Engineering, Yonsei University, Seoul, 03722, Republic of Korea.
Recently, halide perovskite materials have attracted significant research interest in photoelectrochemical cells as promising photoabsorbers due to their superior optoelectronic properties. However, their instability under environmental conditions remains a major obstacle to the development of stable water-splitting devices. This review thoroughly examines the growing array of encapsulation strategies that have accelerated the integration of perovskite materials into water-splitting systems.
View Article and Find Full Text PDFNanoscale Adv
August 2025
School of Electronic Science, Odisha University of Technology and Research Bhubaneswar India.
A novel electrocatalyst, zirconium ferrite nanoparticles (NPs) (ZrFeO NPs), was synthesized through coprecipitation and calcination processes at 300 °C and 500 °C using iron rust. The ZrFeO NPs were used as catalysts for the hydrogen evolution reaction. Furthermore, these NPs in an alkaline medium exhibited superior properties of a fractional order supercapacitor, based on which a prototype device was fabricated to demonstrate its energy storage applications.
View Article and Find Full Text PDFElectrochem Energ Rev
September 2025
Institute of New Energy Materials and Engineering, College of Materials Science and Engineering, Fuzhou University, Fuzhou, 350108 Fujian China.
Unlabelled: Proton exchange membrane water electrolyzers (PEMWEs) are a promising technology for large-scale hydrogen production, yet their industrial deployment is hindered by the harsh acidic conditions and sluggish oxygen evolution reaction (OER) kinetics. This review provides a comprehensive analysis of recent advances in iridium-based electrocatalysts (IBEs), emphasizing novel optimization strategies to enhance both catalytic activity and durability. Specifically, we critically examine the mechanistic insights into OER under acidic conditions, revealing key degradation pathways of Ir species.
View Article and Find Full Text PDFRSC Adv
August 2025
King Abdulaziz City for Science and Technology (KACST), Hydrogen Technologies Institute Saudi Arabia
This study reports the enhanced photoelectrochemical (PEC) performance of TiO/α-FeO heterostructure films fabricated a sequential aerosol-assisted chemical vapour deposition (AACVD) of hematite at 450 °C, followed by atmospheric pressure CVD (APCVD) of anatase TiO with controlled thickness. Structural analyses (XRD, Raman, XPS) confirmed phase purity and oxidation states, while UV-vis spectroscopy revealed a narrowed bandgap and extended visible light absorption for the heterostructures compared to pristine films. The optimized TiO/α-FeO (8 min) photoanode achieved a photocurrent density of 1.
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