2D single-faceted IrO2(101) monolayer enabling high-performing proton exchange membrane water electrolysis beyond 8,000 h stability at 1.5 A cm-2 DOI Creative Commons
Jianguo Liu,

Deren Yang,

Shouwei Zuo

и другие.

Research Square (Research Square), Год журнала: 2024, Номер unknown

Опубликована: Окт. 24, 2024

Abstract Both commercially available and laboratory-synthesized IrO2 catalysts typically possess rutile-type structures diverse facet orientations. According to the theoretical results from density functional theory calculations, distinct facets will result in divergent electrocatalytic properties, among which (101) crystal is theoretically predicted as most energetically favorable for oxygen evolution reaction (OER) owing its lowest energy barrier. Maintaining a single-unit-cell thickness while exposing desired of 2D presents significant opportunity challenge development high-performance OER anode catalysts. Herein, we develop an ammonia-induced engineering oriented modulation ultimate limit monolayer thickness, successfully synthesize unique facet. At current 10 mA cm-2geo, ultralow overpotential 230 mV has been achieved on highly activated three-electrode system. More importantly, proton exchange membrane (PEM) electrolyzer, reaches low voltage 1.74 V at industrial-level 2 A much lower than that all commercial electrocatalysts. Though primarily contributes modulating intrinsic activity rather stability, as-prepared IrO2(101) performs over 8,000 hours PEM water electrolysis (PEMWE) stability constant 1.5 with negligible decay rate 4.0 kh-1. Furthermore, even long-term PEMWE test 1000 h using electrode assembly (MEA) ultra-low Ir loading 0.2 mgIr cm-2geo under fluctuating operating conditions performed, ECell remains electrochemically stable time without any signs catalyst degradation. This work proposes could represent novel approach selectively expose facet, thereby enabling facet-dependent performance ultrahigh industrial-scale electrolysis, fluctuations generated by solar wind power.

Язык: Английский

Unravelling the pH-depended mechanism of ferroelectric polarization on different dynamic pathways of photoelectrochemical water oxidation DOI Creative Commons
Xing Ji, Zhouhao Zhu, Ming Zhou

и другие.

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

0

Research progress of Ce-based electrocatalysts in hydrogen evolution reaction DOI
D. Cao,

Meiwen Tie,

Guangrui Zhang

и другие.

Journal of Rare Earths, Год журнала: 2025, Номер unknown

Опубликована: Янв. 1, 2025

Язык: Английский

Процитировано

0

Positively Charged P-Assisted Ru–Zn Dual Active Sites Promote Oxygen Radical Coupling Mechanism for Acidic Water Oxidation DOI
Guolin Zhang, Zijian Li, Haeseong Jang

и другие.

ACS Sustainable Chemistry & Engineering, Год журнала: 2025, Номер unknown

Опубликована: Март 6, 2025

Язык: Английский

Процитировано

0

Triggering the oxide path mechanism of oxygen evolution reaction: Introducing compressive strain on NiFe-LDH by partial replacement using Ba cations DOI

Zhaoyan Li,

Duo Wang, Jidong Li

и другие.

Journal of Colloid and Interface Science, Год журнала: 2025, Номер unknown, С. 137329 - 137329

Опубликована: Март 1, 2025

Язык: Английский

Процитировано

0

Tuning Surface Oxygen Vacancies of Fe-Doped CeVO4 to Promote Direct Hydroxylation of Benzene to Phenol DOI

Yangzhou Deng,

K. Wei,

Yuqi Zhang

и другие.

The Journal of Physical Chemistry C, Год журнала: 2025, Номер unknown

Опубликована: Март 21, 2025

Язык: Английский

Процитировано

0

Ir/Mn Co‐Mixing and Oxide‐Support Interaction Modulation Through Plasma Promoted Asymmetric Oxygen Coupling for Stable Acidic Oxygen Evolution DOI Open Access
Kefeng Zhou, Yongjie Wang, Zhongqing Jiang

и другие.

Advanced 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

0

Precise Substitution of Octahedral Sites in Compression-Strained Co3O4 Nanorods for Enhanced Acidic Oxygen Evolution DOI
Chenyu Yang, Hui Zhang, Wanlin Zhou

и другие.

Nano Energy, Год журнала: 2025, Номер unknown, С. 111143 - 111143

Опубликована: Май 1, 2025

Язык: Английский

Процитировано

0

Phase Engineering of Nanomaterials: Metal Nanomaterials DOI
Ye Chen, Jiawei Liu, Qinbai Yun

и другие.

Chemical Research in Chinese Universities, Год журнала: 2025, Номер unknown

Опубликована: Май 20, 2025

Язык: Английский

Процитировано

0

Modifying Mn3O4 by CeO2 for enhanced electrocatalytic water oxidation DOI
Sisi Li, Shujiao Yang, Xiaohan Liu

и другие.

Chemical 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

0

Constrained Minimal Interface on Iridium Oxide Surfaces for Acidic Water Oxidation with Low Iridium Loading DOI
Fangyi Li,

Renxing Huang,

Jingwen Jiang

и другие.

Inorganic 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