Solid State Sciences, Год журнала: 2025, Номер unknown, С. 107941 - 107941
Опубликована: Апрель 1, 2025
Язык: Английский
Solid State Sciences, Год журнала: 2025, Номер unknown, С. 107941 - 107941
Опубликована: Апрель 1, 2025
Язык: Английский
Journal of Power Sources, Год журнала: 2025, Номер 631, С. 236233 - 236233
Опубликована: Янв. 18, 2025
Язык: Английский
Процитировано
0ACS Applied Energy Materials, Год журнала: 2025, Номер unknown
Опубликована: Янв. 29, 2025
Язык: Английский
Процитировано
0Chemical Engineering Journal, Год журнала: 2025, Номер unknown, С. 160369 - 160369
Опубликована: Фев. 1, 2025
Язык: Английский
Процитировано
0Journal of Colloid and Interface Science, Год журнала: 2025, Номер 687, С. 851 - 859
Опубликована: Фев. 14, 2025
Язык: Английский
Процитировано
0Catalysts, Год журнала: 2025, Номер 15(3), С. 211 - 211
Опубликована: Фев. 22, 2025
Designing efficient and cost-effective electrocatalysts is crucial for the large-scale development of sustainable hydrogen energy. Amorphous catalysts hold great promise application due to their structural flexibility high exposure active sites. We report a novel method in situ growth amorphous CoNiRuOx nanoparticle structures (CoNiRuOx/NF) on nickel foam substrate. In 1 m KOH, CoNiRuOx/NF achieves current density 10 mA/cm2 with evolution reaction (HER) overpotential only 43 mV remains stable over 100 h at mA/cm2. An alkaline electrolyzer assembled as cathode delivers 2.97 times higher than that an IrO2||Pt/C electrode pair potential 2 V exhibits excellent long-term durability exceeding h. Experimental results reveal combined replacement corrosion reactions facilitate formation structure. This work provides valuable insights developing scalable catalysts.
Язык: Английский
Процитировано
0Chemical Engineering Journal, Год журнала: 2025, Номер 509, С. 161003 - 161003
Опубликована: Фев. 25, 2025
Язык: Английский
Процитировано
0Chemical Engineering Journal, Год журнала: 2025, Номер unknown, С. 160997 - 160997
Опубликована: Фев. 1, 2025
Язык: Английский
Процитировано
0Journal of Colloid and Interface Science, Год журнала: 2025, Номер unknown
Опубликована: Март 1, 2025
Язык: Английский
Процитировано
0Electrochimica Acta, Год журнала: 2025, Номер unknown, С. 146025 - 146025
Опубликована: Март 1, 2025
Язык: Английский
Процитировано
0Advanced Functional Materials, Год журнала: 2025, Номер unknown
Опубликована: Март 5, 2025
Abstract Electrocatalytic nitrate reduction (NO3RR) to valued ammonia is an ideal supplementary route the Haber–Bosch method and a strategy for removal utilization of pollutants. However, due fact that NO3RR goes through complicated multi‐electron/proton transfer, catalysts with monovalent metal sites are difficult tackle multitasking it involves, leading unsatisfactory conversion efficiency selectivity. Herein, heterovalent Fe(OH) 2 /Fe pair supported onto carbon nanotubes (Fe(OH) /Fe@CNTs) presented via electrochemical reconstruction CNTs‐supporting FeS/Fe C heterostructure. /Fe@CNTs exhibits high NH 3 yield rate 0.67 mmol h −1 cm −2 FE 95.1% at −0.4 V versus RHE, which mainly attributed regulated electronic structure cooperation iron sites. Meanwhile, adsorption nitrogen‐containing species adjusted * H enhanced. Moreover, balanced content Fe creates “buffering effect” maintain its activity stability. Theoretical calculations combined in situ FTIR Raman spectra reveal novel multiple reaction pathway on sites, entirely different from single or . Clearly, this study offers creative design advanced multivalent
Язык: Английский
Процитировано
0