Applied Surface Science, Journal Year: 2025, Volume and Issue: unknown, P. 163087 - 163087
Published: March 1, 2025
Language: Английский
Applied Surface Science, Journal Year: 2025, Volume and Issue: unknown, P. 163087 - 163087
Published: March 1, 2025
Language: Английский
International Journal of Hydrogen Energy, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 1, 2025
Language: Английский
Citations
0Small, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 6, 2025
Hydrogen spillover-based binary (HSBB) system has attracted significant attention in alkaline hydrogen evolution reaction (HER). Accelerating spillover the HSBB is crucial for HER activity. Herein, a highly efficient developed by anchoring nano-Ru on oxygen vacancy (Vo) rich amorphous/crystal ZrO
Language: Английский
Citations
0International Journal of Hydrogen Energy, Journal Year: 2025, Volume and Issue: 102, P. 1084 - 1092
Published: Jan. 14, 2025
Language: Английский
Citations
0Small, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 15, 2025
Abstract Inducing magnetic ordering in a non‐ferrous layered double hydroxides (LDHs) instigates higher spin polarization, which leads to enhanced efficiency during oxygen evolution reaction (OER). In nano‐sized materials, the concept of elongated grains drives domain alignment under application an external field. Hence, near solid electrode interface, modified magnetohydrodynamics (MHD) positively impacts electrocatalytic ability nanocatalysts. Consequently, significant improvement water‐splitting kinetics can be obtained by using even low fields. At 100 Gauss, 20% and 10% decrement overpotential is reported for OER hydrogen (HER), respectively. Density functional theory (DFT) calculations are also presented explain thermodynamics HER/OER processes. It established that Gibbs energy process reduce exchange barrier dopant like cobalt. The additional cobalt metal active site have highest probability adsorption reactive intermediates HER OER, results efficiencies.
Language: Английский
Citations
0Chemical Engineering Journal, Journal Year: 2025, Volume and Issue: unknown, P. 160052 - 160052
Published: Jan. 1, 2025
Language: Английский
Citations
0Published: Jan. 1, 2025
Language: Английский
Citations
0International Journal of Hydrogen Energy, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 1, 2025
Language: Английский
Citations
0Catalysts, Journal Year: 2025, Volume and Issue: 15(3), P. 205 - 205
Published: Feb. 21, 2025
Recent advances in transition metal-based electrocatalysts have significantly enhanced the hydrogen evolution reaction (HER) and oxygen (OER) water electrocatalysis. Self-supported electrodes, where active sites are directly integrated with substrates, offer superior kinetics stability compared to traditional powder-based electrocatalysts. The electrospinning technique is particularly effective for fabricating self-supported high surface areas, porosity, uniform distribution of sites, leading improved catalytic performance. Despite extensive research on electrocatalysts, a comprehensive review focusing those developed via remains scarce. This provides detailed overview process, fundamental principles electrocatalysis, recent progress development fabricated through this approach.
Language: Английский
Citations
0International Journal of Hydrogen Energy, Journal Year: 2025, Volume and Issue: 111, P. 33 - 39
Published: Feb. 24, 2025
Language: Английский
Citations
0Nano-Micro Letters, Journal Year: 2025, Volume and Issue: 17(1)
Published: Feb. 24, 2025
Abstract Electrocatalytic urea wastewater treatment technology has emerged as a promising method for environmental remediation. However, the realization of highly efficient and scalable electrocatalytic (SEUWT) is still an enormous challenge. Herein, through regulating adsorption behavior functional groups, SEUWT coupled hydrogen production realized in anion exchange membrane water electrolyzer (AEMWE). Density theory calculations indicate that self-driven electron transfer at heterogeneous interface (NiO/Co 3 O 4 ) can induce charge redistribution, resulting electron-rich NiO electron-deficient Co , which are superior to adsorbing C=O (electron-withdrawing group) –NH 2 (electron-donating group), respectively, molecule accelerating reaction kinetics oxidation. This viewpoint further verified by temperature-programmed desorption experiments. The AEMWE assembled with NiO/Co (anode) NiCoP (cathode) continuously treat initial current density 600 mA cm −2 average efficiency about 53%. Compared overall splitting, H rate (8.33 mmol s −1 increases approximately 3.5 times. work provides cost-effective strategy purifying urea-rich energy-saving production.
Language: Английский
Citations
0