4.7 Article

Effect of crystal structure on nanofiber morphology and chemical modification; design of CeO2/PVDF membrane

Journal

POLYMER TESTING
Volume 110, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.polymertesting.2022.107568

Keywords

Polyvinylidene fluoride; CeO2; Nanofiber; Structure; Morphology; Molecular simulation

Funding

  1. Ministry of Education, Youth and Sports of the Czech Republic via the SGS -Grant Agency of the V.SB-TUO
  2. Internal Grant Agency of the J. E. Purkyn.e University in Usti nad Labem [SP2020/24, UJEP-SGS-2019-53-0063]
  3. Research Infrastructure NanoEnviCz project [LM2018124, CZ.02.1.01/0.0/0.0/18_046/0015586]
  4. Research Infrastructure ProNanoEnviCz project [LM2018124, CZ.02.1.01/0.0/0.0/18_046/0015586]
  5. project ERDF/ESF UniQSurf -Centre of biointerfaces and hybrid functional materials [CZ.02.1.01/0.0/0.0/17_ 048/0007411]
  6. Doctoral grant competition VSB -Technical University of Ostrava within the Operational Programme Research, Development and Education [DGS/TEAM/2020-007, CZ.02.2.69/0.0/0.0/19_073/0016945]

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Layered crystal structures form flat platelet-like crystallites, and nanofibers with such structures exhibit strip-like morphology. In this study, PVDF nanofibers were prepared with strip-like morphology and longitudinal folding, and surface-modified with CeO2 nanoparticles. Molecular modeling showed that the dominant PVDF(100) plane is suitable for anchoring the CeO2 nanoparticles. Preferred crystallographic orientations of the anchored CeO2 nanoparticles were also revealed. This successful surface modification provides potential applications for the CeO2/PVDF membrane.
Layered crystal structures tend to form flat platelet-like crystallites, and nanofibers having such a structure exhibit strip-like morphology. Crystallographic plane forming the dominant flat surface of the nanofibers can be used for surface modification with catalytically active nanoparticles capable of anchoring to the dominant flat surface. In this study, polyvinylidene fluoride (PVDF) nanofibers exhibiting strip-like morphology and longitudinal folding were prepared using wire electrospinning, and surface modified with CeO2 nanoparticles. Experimental characterization of the CeO2/PVDF membrane using (high-resolution) scanning electron microscopy and X-ray photoelectron spectroscopy was supplemented by a force field-based molecular modeling. The modeling has shown that the dominant PVDF(100) plane is suitable for anchoring the CeO2 nanoparticles. In this respect, the PVDF(100) plane is comparable to the less exposed fluorine-oriented PVDF(010) plane, and both planes show stronger interaction with CeO2 compared to hydrogen-oriented PVDF(010) plane. Molecular modeling also revealed preferred crystallographic orientations of anchored CeO2 nanoparticles: these are the catalytically active planes (100), (110), and (111). The successful surface modification and the finding that CeO2 nanoparticles on the dominant PVDF(100) surface can preferentially exhibit these crystallographic orientations thus provides the possibility of various practical applications of the CeO2/PVDF membrane.

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