International Journal of Hydrogen Energy, Journal Year: 2024, Volume and Issue: 110, P. 83 - 89
Published: March 1, 2024
Language: Английский
International Journal of Hydrogen Energy, Journal Year: 2024, Volume and Issue: 110, P. 83 - 89
Published: March 1, 2024
Language: Английский
Journal of environmental chemical engineering, Journal Year: 2025, Volume and Issue: unknown, P. 115284 - 115284
Published: Jan. 1, 2025
Language: Английский
Citations
2International Journal of Hydrogen Energy, Journal Year: 2024, Volume and Issue: 80, P. 907 - 915
Published: July 18, 2024
Language: Английский
Citations
5Applied Catalysis B Environment and Energy, Journal Year: 2024, Volume and Issue: 359, P. 124469 - 124469
Published: Aug. 6, 2024
Language: Английский
Citations
4Chemical Engineering Journal, Journal Year: 2025, Volume and Issue: 508, P. 161229 - 161229
Published: March 1, 2025
Language: Английский
Citations
0Fuel, Journal Year: 2025, Volume and Issue: 392, P. 134955 - 134955
Published: March 5, 2025
Language: Английский
Citations
0Journal of Materials Chemistry A, Journal Year: 2024, Volume and Issue: 12(36), P. 24005 - 24040
Published: Jan. 1, 2024
Material modifications and magnetic field play a significant role in enhancing the performance of electrocatalyst.
Language: Английский
Citations
3Advanced Functional Materials, Journal Year: 2024, Volume and Issue: unknown
Published: Sept. 18, 2024
Abstract The rational construction of interfacial nanostructures metal/semiconductor (MS) contacted electrocatalysts has a significant impact on improving their intrinsic activities. However, MS contacts are often plagued by strong Fermi‐level pinning effect, resulting in the formation Schottky barrier that affects adsorption hydrogen/oxygen intermediates. Herein, an Ohmic contact between metallic Ni 3 S 2 and semiconducting NiMoN is well‐designed, which effectively reduces electron conduction barriers. as‐obtained NiMoN/Ni remarkable bifunctional water electrolysis performance. At 10 mA·cm −2 , overpotential hydrogen evolution oxygen reaction 70 154 mV, respectively. Impressively, hydroxide during surface reconstruction can avoid chlorine catalyst surface. industrial process temperature 85 °C, it takes only 340 mV for overall seawater splitting 500 . UPS UV‐VIS diffuse spectra combined with theoretical calculation results confirm self‐driven directed transfer derived from induce local enrichment at interface region, thus promoting *O to *OOH. This study provides important insights into coordinated modulation built‐in electric fields preparation efficient multifunctional catalysts high abundance active sites.
Language: Английский
Citations
3Advanced Science, Journal Year: 2024, Volume and Issue: 11(39)
Published: Aug. 13, 2024
Abstract Designing high‐entropy oxyhydroxides (HEOs) electrocatalysts with controlled nanostructures is vital for efficient and stable water‐splitting electrocatalysts. Herein, a novel HEOs material (FeCoNiWCuOOH@Cu) containing five non‐noble metal elements derived by electrodeposition on 3D double‐continuous porous Cu support created. This support, prepared via the liquid dealloying method, offers high specific surface area rapid mass/charge transfer channels. The resulting FeCoNiWCuOOH nanosheets provide dense distribution of active sites. heterostructure between skeletons enhances mass transfer, electronic structure coupling, overall structural stability, leading to excellent activities in oxygen evolution reaction (OER), hydrogen (HER), water splitting reaction. At 10 mA cm −2 , overpotentials OER, HER, 1.0 m KOH solution are 200, 18, 1.40 V, respectively, outperforming most current catalytic performance remains even after operating at 300 100, over 1000 h, correspondingly. has potential applications integrated energy systems. More importantly, density functional theory (DFT) calculations demonstrate synergy enhancing activity. work valuable insights designing industrial electrolysis
Language: Английский
Citations
2Dalton Transactions, Journal Year: 2023, Volume and Issue: 53(1), P. 245 - 250
Published: Nov. 23, 2023
The electrochemical CO2 reduction reaction (CO2RR) gives an ideal approach for producing valuable chemicals, offering dual benefits in terms of environmental preservation and carbon recycling. In this work, a strong synergistic effect is constructed by adopting electron-rich graphdiyne (GDY) as the supporting matrix, which significantly stabilizes Au active sites boosts CO2RR process. as-prepared GDY-supported nanoparticles (Au/GDY) exhibit excellent performance, with extremely high faradaic efficiency 94.6% CO well good stability continuous electrolysis 36 hours. superior activity Au/GDY catalyst can be attributed to electronic interaction between GDY substrate, resulting enhanced electron transfer rates stable network catalytically that ultimately promote CO2RR.
Language: Английский
Citations
5Chem Catalysis, Journal Year: 2024, Volume and Issue: 4(6), P. 101011 - 101011
Published: June 1, 2024
Language: Английский
Citations
1