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Electrocatalytic hydrogenation (ECH) of quinoline provides an eco-friendly and prospective route to achieve the highly value-added generation of 1,2,3,4-tetrahydroquinoline (THQ). Co element has been proven to be the efficient catalytic site for ECH of quinoline, but the rational regulation of the electronic structure of active Co site to improve the activity is still a challenge. Herein, the hierarchical core-shell structure consisting of NiCo-MOF nanosheets encapsulated Cu(OH) nanorods (Cu(OH)@CoNi-MOF) is constructed. The heterojunction promotes the transfer of interfacial charge and optimizes the electronic structure of the Co site. The introduction of Ni significantly increases the binding between Co and Cu, preventing the exfoliation of Co sites from Cu(OH) core, and reducing the reaction energy barrier of rate-determining step, thus resulting in superior reactivity and durability. Besides, electrochemical reconstruction further modulates the electronic structure of Co by forming the multi-metallic compound with a low valence state (NiCoCu), achieving an optimal performance with a conversion of 99.5% and THQ selectivity of 100%. A flow-cell system is assembled, demonstrating the prospect for industrial application.
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http://dx.doi.org/10.1002/smll.202412626 | DOI Listing |
Adv Sci (Weinh)
September 2025
Guangxi Key Laboratory of Clean Pulp & Papermaking and Pollution Control, School of Light Industry and Food Engineering, Guangxi University, Nanning, 530004, China.
Carbonized wood has great potential as a self-supported electrode for energy storage/conversion applications. However, developing efficient and economical bifunctional electrodes by customizing the surface structure remains a challenge. This study proposes a novel multifunctional electrode design strategy, using N/P co-doped carbonized wood (NPCW) as carriers and in situ grows copper nanoparticles (Cu NPs) as nucleation centers to induce vertical growth of CuCo-layered double hydroxid (LDH) nanosheets along the substrate.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Leibniz-Institut für Katalyse e.V. (LIKAT), Albert-Einstein-Str. 29a, Rostock 18059, Germany.
Metal-organic frameworks (MOFs) are transformative platforms for heterogeneous catalysis, but distinguishing atomically dispersed metal sites from subnanometric clusters remains a major challenge. This often demands the integration of multiple characterization techniques, many of which either lack the resolving power to distinguish active sites from their surrounding environments (e.g.
View Article and Find Full Text PDFChem Commun (Camb)
September 2025
Key Laboratory of Catalysis and Energy Materials Chemistry of Ministry of Education & Hubei Key Laboratory of Catalysis and Materials Science, South-Central Minzu University, Wuhan 430074, China.
In this study, we unveil a critical function of anions in tailoring the interfacial water coordination environment and electronic structure at the Zn-electrolyte interface. These features thermodynamically hinder water-induced parasitic reactions, enabling highly reversible Zn plating/stripping. And the optimal electrolyte supports high-mass-loading applications in Zn-MnO batteries.
View Article and Find Full Text PDFNan Fang Yi Ke Da Xue Xue Bao
August 2025
Institute of Biomedical and Health Engineering, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.
Objectives: To synthesize a temperature-responsive multimodal motion microrobot (MMMR) using temperature and magnetic field-assisted microfluidic droplet technology to achieve targeted drug delivery and controlled drug release.
Methods: Microfluidic droplet technology was utilized to synthesize the MMMR by mixing gelatin with magnetic microparticles. The microrobot possessed a magnetic anisotropy structure to allow its navigation and targeted drug release by controlling the temperature field and magnetic field.
Angew Chem Int Ed Engl
September 2025
College of Environmental Science and Engineering, Yangzhou University, Yangzhou, 225000, P.R. China.
Despite growing interest in single-atom catalysts (SACs) for Fenton-like reactions, zinc (Zn)-based SACs remain unexplored due to the inherent inertness of Zn, whose fully occupied 3d electronic configuration limits redox activity. Here, we overcome this limitation by introducing boron (B) atoms to reconfigure the electronic structure of Zn-N coordination sites, yielding an activated catalyst denoted as Zn-NBC. This electronic modulation transforms inert Zn-N sites into catalytically active centers (Zn-NB ), enabling significantly enhanced Fenton-like activity.
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