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Hollow Hafnium Oxide (HfO2) Fibers: Using an Effective Combination of Sol-Gel, Electrospinning, and Thermal Degradation Pathway.
Huang, Meng-Ru; Chen, Yi-Fan; Gautam, Bhaskarchand; Hsu, Yen-Shen; Ho, Jhih-Hao; Hsu, Hsun-Hao; Chen, Jiun-Tai.
Afiliación
  • Huang MR; Department of Applied Chemistry, National Yang Ming Chiao Tung University, Taiwan 300093.
  • Chen YF; Department of Applied Chemistry, National Yang Ming Chiao Tung University, Taiwan 300093.
  • Gautam B; Department of Applied Chemistry, National Yang Ming Chiao Tung University, Taiwan 300093.
  • Hsu YS; Department of Applied Chemistry, National Yang Ming Chiao Tung University, Taiwan 300093.
  • Ho JH; Department of Applied Chemistry, National Yang Ming Chiao Tung University, Taiwan 300093.
  • Hsu HH; Department of Applied Chemistry, National Yang Ming Chiao Tung University, Taiwan 300093.
  • Chen JT; Department of Applied Chemistry, National Yang Ming Chiao Tung University, Taiwan 300093.
Langmuir ; 40(9): 4732-4738, 2024 Mar 05.
Article en En | MEDLINE | ID: mdl-38374656
ABSTRACT
In recent years, hafnium oxide (HfO2) has gained increasing interest because of its high dielectric constant, excellent thermal stability, and high band gap. Although HfO2 bulk and film materials have been prepared and well-studied, HfO2 fibers, especially hollow fibers, have been less investigated. In this study, we present a facile preparation method for HfO2 hollow fibers through a unique integration of the sol-gel process and electrospinning technique. Initially, polystyrene (PS) fibers are fabricated by using electrospinning, followed by dipping in a HfO2 precursor solution, resulting in HfO2-coated PS fibers. Subsequent thermal treatment at 800 °C ensures the selective pyrolysis of the PS fibers and complete condensation of the HfO2 precursors, forming HfO2 hollow fibers. Scanning electron microscopy (SEM) characterizations reveal HfO2 hollow fibers with rough surfaces and diminished diameters, a transformation attributed to the removal of the PS fibers and the condensation of the HfO2 precursors. Our study also delves into the influence of precursor solution molar ratios, showcasing the ability to achieve smaller HfO2 fiber diameters with reduced precursor quantities. Validation of the material composition is achieved through thermogravimetric analysis (TGA) and energy-dispersive spectroscopy (EDS) mapping. Additionally, X-ray diffraction (XRD) analysis provides insights into the crystallinity of the HfO2 hollow fibers, highlighting a higher crystallinity in fibers annealed at 800 °C compared with those treated at 400 °C. Notably, the HfO2 hollow fibers demonstrate a water contact angle (WCA) of 38.70 ± 5.24°, underscoring the transformation from hydrophobic to hydrophilic properties after the removal of the PS fibers. Looking forward, this work paves the way for extensive research on the surface properties and potential applications of HfO2 hollow fibers in areas such as filtration, energy storage, and memory devices.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Langmuir Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Langmuir Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article