4.8 Article

Polyvinylpyrrolidone-induced anisotropic growth of gold nanoprisms in plasmon-driven synthesis

Journal

NATURE MATERIALS
Volume 15, Issue 8, Pages 889-+

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/NMAT4683

Keywords

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Funding

  1. Air Force Office of Scientific Research [FA9550-14-1-0304]
  2. National Science Foundation [CHE-1308644]
  3. CCI Center for Nanostructured Electronic Materials [CHE-1038015]
  4. University of Florida (UF) Howard Hughes Medical Institute (HHMI) Intramural Award
  5. UF University Scholars Program
  6. UF's Student Science Training Program
  7. US Department of Energy (DOE), Office of Basic Energy Sciences [DE-SC0012704]
  8. DOE Office of Biological and Environmental Research at the Pacific Northwest National Laboratory (PNNL) (Richland, Washington)
  9. US DOE [DE-AC06-76RLO1930]

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After more than a decade, it is still unknown whether the plasmon-mediated growth of silver nanostructures can be extended to the synthesis of other noble metals, as the molecular mechanisms governing the growth process remain elusive. Herein, we demonstrate the plasmon-driven synthesis of gold nanoprisms and elucidate the details of the photochemical growth mechanism at the single-nanoparticle level. Our investigation reveals that the surfactant polyvinylpyrrolidone preferentially adsorbs along the nanoprism perimeter and serves as a photochemical relay to direct the anisotropic growth of gold nanoprisms. This discovery confers a unique function to polyvinylpyrrolidone that is fundamentally different from its widely accepted role as a crystal-face-blocking ligand. Additionally, we find that nanocrystal twinning exerts a profound influence on the kinetics of this photochemical process by controlling the transport of plasmon-generated hot electrons to polyvinylpyrrolidone. These insights establish a molecular-level description of the underlying mechanisms regulating the plasmon-driven synthesis of gold nanoprisms.

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