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Poly(vinylpyrrolidone)-stabilized silver nanoparticles for strained-silicon surface enhanced Raman spectroscopy

Authors

  • Stuart J. Corr,

    Corresponding author
    1. Nanomaterials Processing Laboratory, (The RINCE Institute), Dublin City University, Dublin 9, Ireland
    2. The Richard E. Smalley Institute for Nanoscale Science and Technology, Rice University, Houston, TX 77005, USA
    Current affiliation:
    1. Rice University, Department of Chemistry, MS-60, 6100 Main Street, Houston, TX 77005-1892.
    • Nanomaterials Processing Laboratory, (The RINCE Institute), Dublin City University, Dublin 9, Ireland.
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  • Lisa O'Reilly,

    1. Nanomaterials Processing Laboratory, (The RINCE Institute), Dublin City University, Dublin 9, Ireland
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  • Eoghan P. Dillon,

    1. The Richard E. Smalley Institute for Nanoscale Science and Technology, Rice University, Houston, TX 77005, USA
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  • Andrew R. Barron,

    1. The Richard E. Smalley Institute for Nanoscale Science and Technology, Rice University, Houston, TX 77005, USA
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  • Patrick J. McNally

    1. Nanomaterials Processing Laboratory, (The RINCE Institute), Dublin City University, Dublin 9, Ireland
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Abstract

Poly(vinylpyrrolidone)-stabilized silver nanoparticles deposited onto strained-silicon layers grown on graded Si1−xGex virtual substrates are utilized for selective amplification of the Si–Si vibration mode of strained silicon via surface-enhanced Raman scattering spectroscopy. This solution-based technique allows rapid, highly sensitive and accurate characterization of strained silicon whose Raman signal would usually be overshadowed by the underlying bulk SiGe Raman spectra. The analysis was performed on strained silicon samples of thickness 9, 17.5 and 42 nm using a 488 nm Ar+ micro-Raman excitation source. The quantitative determination of strained-silicon enhancement factors was also made. Copyright © 2011 John Wiley & Sons, Ltd.

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