
Research Square (Research Square), Год журнала: 2024, Номер unknown
Опубликована: Окт. 24, 2024
Язык: Английский
Research Square (Research Square), Год журнала: 2024, Номер unknown
Опубликована: Окт. 24, 2024
Язык: Английский
Chemical Science, Год журнала: 2025, Номер unknown
Опубликована: Янв. 1, 2025
Free energy, together with the coverage of intermediate states, can scale effect ferroelectric polarization on photoelectrocatalytic performance during different dynamic pathways oxygen evolution reaction.
Язык: Английский
Процитировано
0Journal of Rare Earths, Год журнала: 2025, Номер unknown
Опубликована: Янв. 1, 2025
Язык: Английский
Процитировано
0ACS Sustainable Chemistry & Engineering, Год журнала: 2025, Номер unknown
Опубликована: Март 6, 2025
Язык: Английский
Процитировано
0Journal of Colloid and Interface Science, Год журнала: 2025, Номер unknown, С. 137329 - 137329
Опубликована: Март 1, 2025
Язык: Английский
Процитировано
0The Journal of Physical Chemistry C, Год журнала: 2025, Номер unknown
Опубликована: Март 21, 2025
Язык: Английский
Процитировано
0Advanced Materials, Год журнала: 2025, Номер unknown
Опубликована: Март 23, 2025
Abstract Developing efficient and stable catalysts that facilitate the oxygen‐evolution reaction (OER) through an oxide‐path mechanism (OPM) is of considerable interest. However, it remains a significant challenge due to stringent structural requirements these catalysts. This work reports using strategy integrates Ir/Mn co‐mixing strong oxide‐support interaction (SOSI) modulation, Ir‐based follow OPM for acidic OER can be developed. The mainly relies on optimizing distance oxygeneous intermediate adsorption sites by modulating SOSI plasma defect engineering trigger pathway with lower energy barrier. density‐functional‐theory (DFT) calculations reveal electronic coupling between Ir Mn via Ir─O─Mn bond ready adsorbed site those site, leading asymmetric oxygen OER. developed catalyst merely requires overpotential 240 mV drive 10 mA cm −2 mass‐activity > 75 times higher than IrO 2 . When used in proton‐exchange‐membrane water‐electrolyzers, shows high performance excellent stability at industrial‐level current density 1.0 A
Язык: Английский
Процитировано
0Nano Energy, Год журнала: 2025, Номер unknown, С. 111143 - 111143
Опубликована: Май 1, 2025
Язык: Английский
Процитировано
0Chemical Research in Chinese Universities, Год журнала: 2025, Номер unknown
Опубликована: Май 20, 2025
Язык: Английский
Процитировано
0Chemical Communications, Год журнала: 2025, Номер unknown
Опубликована: Янв. 1, 2025
The introduction of CeO 2 facilitates effective electron transfer from Mn 3 O 4 to , thereby modulating the redox properties and enhancing its intrinsic activity water oxidation.
Язык: Английский
Процитировано
0Inorganic Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Май 26, 2025
Iridium-based oxides are the best commercial catalysts for acidic oxygen evolution reaction (OER) because of their relatively excellent stability. However, high price and low OER activity have greatly impeded commercialization. Doping IrO2 with transition metals significantly enhances its activity; however, instability in kinetic processes can result substantial metal dissolution ion exchange. Herein, we report a metastable amorphous Fe:IrO2 catalyst, which provided structural flexibility, enhancing catalyst's performance minimal Ir loading. Their constrained interface structure ensures stability, as shown by Fe ions after chronopotentiometry tests. In situ FTIR DEMS analyses reveal that catalyst utilizes an *O-*O radical coupling mechanism to generate O2. These findings illustrate important role establishing optimal catalytic pathway stable electrochemical properties.
Язык: Английский
Процитировано
0