Hui Fu

ORCID: 0000-0003-3314-7466
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About
Contact & Profiles
Research Areas
  • Corrosion Behavior and Inhibition
  • Concrete Corrosion and Durability
  • Hydrogen embrittlement and corrosion behaviors in metals
  • Perovskite Materials and Applications
  • Advanced Photocatalysis Techniques
  • Solid-state spectroscopy and crystallography
  • Luminescence Properties of Advanced Materials
  • Quantum Dots Synthesis And Properties
  • Catalytic C–H Functionalization Methods
  • Water Quality Monitoring and Analysis
  • 2D Materials and Applications
  • Advanced Sensor and Energy Harvesting Materials
  • Hydrogels: synthesis, properties, applications
  • Advanced Polymer Synthesis and Characterization
  • Catalytic Processes in Materials Science
  • biodegradable polymer synthesis and properties
  • Quinazolinone synthesis and applications
  • Covalent Organic Framework Applications
  • Morinda citrifolia extract uses
  • Asymmetric Hydrogenation and Catalysis
  • NMR spectroscopy and applications
  • Catalysis and Oxidation Reactions
  • Polyoxometalates: Synthesis and Applications
  • Conducting polymers and applications
  • Optical properties and cooling technologies in crystalline materials

Ningbo University of Technology
2020-2025

Shandong University
2021-2025

State Key Laboratory of Crystal Materials
2022-2025

Peking University
2005-2024

Beijing National Laboratory for Molecular Sciences
2014-2023

Tianjin University
2023

Ningbo University
2023

Center for Life Sciences
2023

State Key Laboratory of Rare Earth Materials Chemistry and Application
2014-2022

Beijing Institute of Technology
2018-2021

In comparison to the traditional petroleum-based plastics, polylactic acid, most popular biodegradable plastic, can be decomposed into carbon dioxide and water in environment. However, natural degradation of acid requires a substantial period time and, more importantly, it is carbon-emitting process. Therefore, highly desirable develop novel transformation process that upcycle plastic trash value-added products, especially with high chemical selectivity. Here we demonstrate one-pot catalytic...

10.1021/jacs.1c08159 article EN Journal of the American Chemical Society 2021-09-30

Solar-driven photocatalytic water splitting offers a sustainable pathway to produce green hydrogen, yet its practical application encounters several challenges including inefficient photocatalysts, sluggish oxidation, severe reverse reactions and the necessity of separating produced hydrogen oxygen gases. Herein, we design develop system composed two separate reaction parts: evolution cell containing halide perovskite photocatalysts (MoSe2-loaded CH(NH2)2PbBr3-xIx) an NiFe-layered double...

10.1038/s41467-025-56314-x article EN cc-by-nc-nd Nature Communications 2025-01-24

Direct selective oxidation of light alkanes, such as ethane, into value-added chemical products under mild reaction conditions remains a challenge in both industry and academia. Herein, the iridium cluster atomically dispersed catalysts have been successfully fabricated using nanodiamond support. The obtained catalyst shows remarkable performance for ethane oxygen at 100 °C, with an initial activity high 7.5 mol/mol/h selectivity to acetic acid higher than 70% after five situ recycles....

10.1021/jacs.9b06986 article EN Journal of the American Chemical Society 2019-10-24

In recent years, two-dimensional (2D) and quasi-2D Ruddlesden–Popper (RP) perovskite materials have been developed as emerging semiconductor for solar cells due to their structural diversity high power-conversion efficiency, but there are few reports on the photocatalytic applications. Here, 2D/quasi-2D RP BA2MAn–1PbnI3n+1 was fabricated a hydrogen evolution photocatalyst hydrohalic acid splitting. Theoretical experimental surveys show that stress in can significantly influence...

10.1021/acscatal.3c03933 article EN ACS Catalysis 2023-11-01

The oxidative dehydrogenation (ODH) of propane on single-crystal V(2)O(5)(001) is studied by periodic density functional theory (DFT) calculations. energetics and pathways for the to propene conversion are determined. We show that (i) C-H bond can be activated both terminal bridging lattice O atoms surface with similar activation energies. At site radical oxo-insertion likely activation, while only mechanism feasible at site. (ii) Compared site, production from propoxide much easier due...

10.1021/ja0611745 article EN Journal of the American Chemical Society 2006-08-01
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