Journal of Colloid and Interface Science, Год журнала: 2024, Номер 677, С. 140 - 149
Опубликована: Июль 22, 2024
Язык: Английский
Journal of Colloid and Interface Science, Год журнала: 2024, Номер 677, С. 140 - 149
Опубликована: Июль 22, 2024
Язык: Английский
Nano Energy, Год журнала: 2024, Номер unknown, С. 110564 - 110564
Опубликована: Дек. 1, 2024
Язык: Английский
Процитировано
39International Journal of Hydrogen Energy, Год журнала: 2025, Номер 101, С. 1044 - 1053
Опубликована: Янв. 6, 2025
Язык: Английский
Процитировано
6Inorganic Chemistry Frontiers, Год журнала: 2025, Номер unknown
Опубликована: Янв. 1, 2025
The heterostructure catalyst Fe-Ni 3 S 2 /NiS exhibits excellent activity and stability. doped Fe acts as a sacrificial agent in the oxygen evolution reaction (OER), maintaining high of Ni, preventing Ni–S bond degradation.
Язык: Английский
Процитировано
4Advanced Sustainable Systems, Год журнала: 2025, Номер unknown
Опубликована: Янв. 22, 2025
Abstract There is an imperative need for highly efficient electrocatalysts cost‐effective hydrogen production. Herein, a self‐supported, hybrid composite as bifunctional electrocatalyst introduced. This achieved by in situ growth of MoS 2 ‐Ni 3 S on nickel foam (NF), designated /NF, synthesized facile one‐step hydrothermal synthesis method. /NF exhibits low overpotentials only 187 and 146 mV OER HER, respectively, to achieve current density 10 mA cm −2 1 M KOH. The practical application the designed verified constructing || symmetrical membrane electrode assembly (MEA) 4 working area anion exchange water electrolyzer. system shows continuous electrolysis monitored 48 h duration. For OER, optimum d‐band center −1.66 eV heterostructure calculated from Density Functional Theory (DFT) studies. factors like unique structure electrocatalyst, enhanced hydrophilicity, improved electrochemically accessible number sites (ECASs), center, are expected be primary contributors system's performance. Thus, present finding unveils straightforward approach creating stable advancing commercial realm renewable electrochemical energy conversion.
Язык: Английский
Процитировано
2Journal of Colloid and Interface Science, Год журнала: 2025, Номер 690, С. 137336 - 137336
Опубликована: Март 14, 2025
Язык: Английский
Процитировано
1Journal of Solid State Chemistry, Год журнала: 2025, Номер unknown, С. 125356 - 125356
Опубликована: Апрель 1, 2025
Язык: Английский
Процитировано
1Applied Catalysis B Environment and Energy, Год журнала: 2024, Номер 365, С. 124925 - 124925
Опубликована: Дек. 10, 2024
Язык: Английский
Процитировано
8Advanced Functional Materials, Год журнала: 2024, Номер unknown
Опубликована: Авг. 2, 2024
Abstract Aiming to efficiently expedite alkaline overall water splitting (OWS) by addressing challenges such as sluggish kinetics and limited stability, a hollow Fe‐doped Ni(OH) 2 ‐NiS@Ni(OH) nanorod array with surface nanosheets is devised, featuring high‐index (101)‐NiS(211) heterostructural interface an upshifted d ‐band center. This nanoarchitecture intensifies the adsorption interaction of H O OH − reactants on electrocatalyst surface, suitably bonds * intermediate in hydrogen evolution reaction (HER) accelerates electron movement H, minimizes energy requirement rate‐limiting phase ( → O) oxygen (OER) facilitating O─H cleavage optimally adsorbs O, amplifies exposure surface‐active centers, ultimately reduces apparent activation energy. Consequently, overpotentials are low 66.4 mV 254.9 at 10 mA cm −2 , alongside high turnover frequencies 142 s −1 (H ) 279 (O 100 300 mV, respectively, markedly outperforming direct‐electrodeposited analogues. When functioning bifunctional electrode OWS, this material merely requires 1.57 V sustains operation for 168 h, approaching Pt/C||RuO benchmark.
Язык: Английский
Процитировано
5Journal of Alloys and Compounds, Год журнала: 2024, Номер 1010, С. 177480 - 177480
Опубликована: Ноя. 10, 2024
Язык: Английский
Процитировано
5International Journal of Hydrogen Energy, Год журнала: 2024, Номер 83, С. 107 - 114
Опубликована: Авг. 10, 2024
Язык: Английский
Процитировано
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