• DocumentCode
    1531211
  • Title

    Alkylamine-effected formation of PVB-capped silver nanoparticles in alcohol solution at room temperature

  • Author

    Zhina Jin ; Guoqing Wang ; Wenge Li ; Hong Wang

  • Author_Institution
    Key Lab. for Green Chem. Technol., Tianjin Univ., Tianjin, China
  • Volume
    7
  • Issue
    5
  • fYear
    2012
  • fDate
    5/1/2012 12:00:00 AM
  • Firstpage
    496
  • Lastpage
    500
  • Abstract
    Silver nanoparticles were first generated by reduction of silver-amine complex with isobutyraldehyde in the presence of polyvinyl butyral in alcohol solution at room temperature. The fully organic phase is composed of silver acetate (SA) as a silver precursor, alkylamine as a ligand dissolving SA and alkaline-regulating agent accelerating the reaction. 1H NMR and Fourier transformation infrared spectra were performed to analyse the formation of silver-amine complex. The products were characterised by X-ray powder diffraction, UV-vis absorption spectroscopy, transmission electron microscopy and scanning electron microscopy, proving that nearly monodispersed silver nanospheres were obtained.
  • Keywords
    Fourier transform spectra; X-ray diffraction; infrared spectra; nanofabrication; nanoparticles; proton magnetic resonance; reduction (chemical); scanning electron microscopy; silver; transmission electron microscopy; ultraviolet spectra; visible spectra; 1H NMR spectra; Ag; Fourier transformation infrared spectra; PVB-capped silver nanoparticles; UV-vis absorption spectroscopy; X-ray powder diffraction; alcohol solution; alkaline-regulating agent; alkylamine ligand; alkylamine-effected formation; dissolution; fully organic phase; isobutyraldehyde; monodispersed nanospheres; polyvinyl butyral; reduction; scanning electron microscopy; silver acetate; silver precursor; silver-amine complex; structural characterisation; temperature 293 K to 298 K; transmission electron microscopy;
  • fLanguage
    English
  • Journal_Title
    Micro & Nano Letters, IET
  • Publisher
    iet
  • ISSN
    1750-0443
  • Type

    jour

  • DOI
    10.1049/mnl.2012.0276
  • Filename
    6210987