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The sluggish kinetics of the oxygen evolution reaction (OER) necessitate the use of efficient, non-precious metal catalysts. This work reports the rational design of an indium-doped bimetallic metal-organic framework (MOF-74-CoIn) as a precatalyst, achieved through post-synthetic modification of MOF-74-Co. Structural and spectroscopic analyses confirm that In(III) incorporation induces CoO bond contraction while preserves the overall structural integrity. After the complete electrochemical activation, MOF-74-CoIn-OER exhibits exceptional OER performance in 1.0 M KOH solution, achieving a low overpotential of 308 mV at 10 mA cm, a reduced Tafel slope (58.1 mV dec), and high stability (95.2 % current retention after 120 h). A series of physicochemical characterizations reveal that In(III) doping accelerates the electrochemical reconstruction into an amorphous but active In-doped CoOOH phase, with In stabilizing Co sites and facilitating rapid phase transformation. Furthermore, theoretical calculations confirm that In incorporation effectively lowers the energy barrier of In-O-Co electronic bridge for OER by altering the density of states of CoOOH. This study demonstrates the critical role of indium as an electronic modulator, offering atomic-level insights into dynamic activation of MOF precatalysts for efficient water oxidation.
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http://dx.doi.org/10.1016/j.jcis.2025.138865 | DOI Listing |
Nano Lett
September 2025
State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070, China.
Constructing heterogeneous dual-site catalysts is anticipated for oxygen evolution reaction (OER). However, compared to the adsorbate evolution mechanism (AEM), the triggering oxide pathway mechanism (OPM) for catalysts poses challenges due to elusive structural evolution and low intrinsic activity. Herein, considering the distinct adsorption propensity of heterogeneous Ni-Fe sites toward differential intermediates (OH-O), the PO-induced deep reconstruction triggers a dual-site Ni-Fe discrepant oxide pathway mechanism (DOPM) for R-PO-NiCoFeOOH.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Department of Chemical Engineering, Faculty of Engineering, Chulalongkorn University, Bangkok 10330, Thailand.
The accumulation of nitrate (NO) from agricultural runoff poses a growing threat to ecosystems and public health. Converting nitrate into ammonia (NH) through the electrochemical nitrate reduction reaction (NORR) offers a promising strategy to mitigate environmental contamination while creating a sustainable circular route to fertilizer production. However, achieving high NH production and energy efficiency remains challenging.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Confucius Energy Storage Lab, School of Energy and Environment & Z Energy Storage Center, Southeast University, Nanjing 211189, China.
Developing efficient and durable catalysts for the oxygen evolution reaction (OER) in acidic media is essential for advancing proton exchange membrane water electrolysis (PEMWE). However, catalyst instability caused by lattice oxygen (O) depletion and metal dissolution remains a critical barrier. Here, we propose an oxophilic-site-mediated dynamic oxygen replenishment mechanism (DORM), in which O actively participates in O-O bond formation and is continuously refilled by water-derived species.
View Article and Find Full Text PDFNAR Cancer
September 2025
Institute of Physiology, University of Zürich, Zürich, CH-8057, Switzerland.
Hypoxia-inducible factor (HIF) is a master regulator of cancer cell adaptation to tumor hypoxia and is involved in cancer progression. Single-cell (sc) differences in the HIF response allow for tumor evolution and cause therapy resistance. These sc-differences are usually ascribed to tumor microenvironmental differences and/or clonal (epi)genetic variability.
View Article and Find Full Text PDFElectrochem Energ Rev
September 2025
Institute of New Energy Materials and Engineering, College of Materials Science and Engineering, Fuzhou University, Fuzhou, 350108 Fujian China.
Unlabelled: Proton exchange membrane water electrolyzers (PEMWEs) are a promising technology for large-scale hydrogen production, yet their industrial deployment is hindered by the harsh acidic conditions and sluggish oxygen evolution reaction (OER) kinetics. This review provides a comprehensive analysis of recent advances in iridium-based electrocatalysts (IBEs), emphasizing novel optimization strategies to enhance both catalytic activity and durability. Specifically, we critically examine the mechanistic insights into OER under acidic conditions, revealing key degradation pathways of Ir species.
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