4.6 Article

Synthesis of Nickel Nanoparticles Supported on Nanoporous Silicon Oxycarbide (SiCO) Sheath-Core Fibers

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 114, Issue 27, Pages 11776-11782

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jp104605b

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Funding

  1. U.S. National Science Foundation [CMMI 0700272]
  2. National Textile Center [M02-CD05]
  3. University of California, Davis

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Nickel (Ni) nanoparticles with average diameters less than 5 nm were successfully synthesized on nanoporous silicon oxycarbide (SiCO) sheath-core fibers by incipient wetness impregnation of Ni acetylacetonate precursor followed by reduction at temperatures above 250 degrees C. The SiCO fibers were fabricated by pyrolyzing electrospun 5/15 PUS/PMMA composite fibers at temperatures from 250 to 1000 degrees C to contain nanoporous cores and striated sheaths. The SiCO fibers pyrolyzed up to 600 degrees C were superhydrophobic and became superhydrophilic when pyrolyzed at 800 degrees C and above. Such a drastic switch from superhydrophobicity to superhydrophilicity coincided with the disappearance of aliphatic methyl and methylene groups. The SiCO ceramic fibers pyrolyzed at 1000 degrees C were highly porous with BET surface area 95.7 m(2)/g, pore volume 0.352 cm(3)/g, and average pore size 26 nm. They were thermally and chemically stable enough to support the Ni acetylaeetonate precursor to be reduced to Ni nanoparticles at 250, 500, and 900 degrees C. SEM observation and EDS elemental mappings showed the reduced Ni nanoparticles to be homogeneously distributed in the fibrous structures without any aggregation. The Ni nanoparticles were monodispersed as confirmed by TEM and in a face-centered-cubic crystalline structure as evidenced by SAED and XRD.

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