International Journal of Hydrogen Energy, Год журнала: 2024, Номер 110, С. 234 - 250
Опубликована: Март 1, 2024
Язык: Английский
International Journal of Hydrogen Energy, Год журнала: 2024, Номер 110, С. 234 - 250
Опубликована: Март 1, 2024
Язык: Английский
Coordination Chemistry Reviews, Год журнала: 2024, Номер 522, С. 216190 - 216190
Опубликована: Сен. 5, 2024
Язык: Английский
Процитировано
11Small, Год журнала: 2024, Номер unknown
Опубликована: Авг. 30, 2024
Avoiding the stacking of active sites in catalyst structural design is a promising route for realizing oxygen evolution reaction (OER). Herein, using CoFe Prussian blue analoge cube with hollow structure (C-CoFe PBA) as derived support, highly effective Ni
Язык: Английский
Процитировано
6JACS Au, Год журнала: 2024, Номер 4(12), С. 4639 - 4654
Опубликована: Ноя. 21, 2024
For the aim of achieving carbon-free energy scenario, green hydrogen (H
Язык: Английский
Процитировано
5Small, Год журнала: 2025, Номер unknown
Опубликована: Фев. 3, 2025
Abstract Pt single‐atoms catalysts have been widely confirmed as ideal electrocatalysts for high‐efficiency hydrogen evolution reaction (HER), but their activity and durability at high current density remain great challenges, especially in alkaline media. Herein, a unique Ohmic contact heterostructure is fabricated by integrating Ni NiO to immobilize (Ni‐NiO‐Pt) via Pt‐O 4 coordination boosting the HER. Owing transient temperature pressure laser ablation process, heterojunctions are constructed interfaces between metal core nanoporous semiconducting shell with adequate oxygen vacancies. The large work function difference triggers electron transfer from Pt‐decorated NiO, which dramatically eliminates conduction impedance regulates charge redistribution. Density functional theory calculation unveils that multiple regulations of energy barrier redistribution on endow Ni‐NiO‐Pt outstanding electrical conductivity favorable binding energy. Consequently, displays superior HER performances an overpotential 23.54 mV 10 mA cm −2 protruding 75 h 500 , drastically outperforming commercial Pt/C most reported electrocatalysts. immobilization opens up avenue toward rational design
Язык: Английский
Процитировано
0Carbon, Год журнала: 2025, Номер 235, С. 120098 - 120098
Опубликована: Фев. 6, 2025
Язык: Английский
Процитировано
0Nano Letters, Год журнала: 2025, Номер unknown
Опубликована: Фев. 7, 2025
Due to the impediments of spatial and temporal resolution, comprehension microdynamic processes still remains limited, which seriously hinders advancement catalyst regulating expansion application. Herein, efficient selective bimetallic atomic electrode interface was cultivated via high-throughput screening, achieving self-adaptive parallel electrochemical reduction Cu(II) As(III). Combined in situ X-ray absorption fine structure (XAFS) spectroscopy coordination field theory verified Ni-Cu specific energy level matching promoted by permitted d-d transition also reproduced microscopic dynamic process. Additionally, it discovered that Fe-As bonding barrier smallest potential-determining step (1.40 eV) were derived from linear shift main s p peaks key arsenic intermediates high-energy orbital. This work offers insights into transient reaction dynamics methods theoretical simulations, broadens design multisite catalysts.
Язык: Английский
Процитировано
0Journal of Colloid and Interface Science, Год журнала: 2025, Номер 688, С. 233 - 240
Опубликована: Фев. 24, 2025
Язык: Английский
Процитировано
0Advanced Materials, Год журнала: 2025, Номер unknown
Опубликована: Март 4, 2025
The unique hydrogen adsorption characteristics of negatively charged platinum play a crucial role in enhancing the electrocatalytic evolution reaction. However, atomically dispersed Pt atoms are typically anchored to support through non-metallic atom bonds, resulting high oxidation state. Here, oxygen-deficient NiFe-LDH. Electron transfer between and NiFe-LDH occurs primarily Pt─Ni bonds rather than conventional Pt─O bonds. Oxygen vacancies promote additional electron from Ni Pt, thereby reducing valence state adsorption. Meanwhile, elevated increases catalyst's hydrophilicity reduces energy barrier for hydrolysis dissociation. This catalyst demonstrates remarkably low overpotentials 4 9 mV at 10 mA cm-2 1 m KOH KPi, respectively. Additionally, its mass activity is 51.5 23.7 times higher that Pt/C, study presents novel strategy performance rational design coordination environments electronic structures supported metal catalysts.
Язык: Английский
Процитировано
0Materials Science in Semiconductor Processing, Год журнала: 2025, Номер 194, С. 109553 - 109553
Опубликована: Апрель 9, 2025
Язык: Английский
Процитировано
0Separation and Purification Technology, Год журнала: 2024, Номер 349, С. 127909 - 127909
Опубликована: Май 10, 2024
Язык: Английский
Процитировано
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