Scalable, Green Fabrication of Single-Crystal Noble Metal Films and Nanostructures for Low-Loss Nanotechnology Applications. V. Grayli, S., Zhang, X., MacNab, F. C., Kamal, S., Star, D., & Leach, G. W. ACS Nano, American Chemical Society, May, 2020.
Scalable, Green Fabrication of Single-Crystal Noble Metal Films and Nanostructures for Low-Loss Nanotechnology Applications [link]Paper  doi  abstract   bibtex   8 downloads  
The confinement of spatially extended electromagnetic waves to nanometer-scale metal structures can be harnessed for application in information processing, energy harvesting, sensing, and catalysis. Metal nanostructures enable negative refractive index, subwavelength resolution imaging, and patterning through engineered metamaterials and promise technologies that will operate in the quantum plasmonics regime. However, the controlled fabrication of high-definition single-crystal subwavelength metal nanostructures has remained a significant hurdle due to the tendency for polycrystalline metal growth using conventional physical vapor deposition methods and the challenges associated with placing solution-grown nanocrystals in desired orientations and locations on a surface to manufacture functional devices. Here, we introduce a scalable and green wet chemical approach to monocrystalline noble metal thin films and nanostructures. The method enables the fabrication of ultrasmooth, epitaxial, single-crystal films of controllable thickness that are ideal for the subtractive manufacture of nanostructures through ion beam milling and additive crystalline nanostructure via lithographic patterning for large-area, single-crystal metasurfaces and high aspect ratio nanowires. Our single-crystal nanostructures demonstrate improved feature quality, pattern transfer yield, reduced optical and resistive losses, and tailored local fields to yield greater optical response and improved stability compared to those of polycrystalline structures—supporting greater local field enhancements and enabling practical advances at the nanoscale.
@Article{V.Grayli2020,
  author    = {V. Grayli, Sasan and Zhang, Xin and MacNab, Finlay C. and Kamal, Saeid and Star, Dmitry and Leach, Gary W.},
  journal   = {ACS Nano},
  title     = {Scalable, {Green} {Fabrication} of {Single}-{Crystal} {Noble} {Metal} {Films} and {Nanostructures} for {Low}-{Loss} {Nanotechnology} {Applications}},
  year      = {2020},
  issn      = {1936-0851},
  month     = may,
  abstract  = {The confinement of spatially extended electromagnetic waves to nanometer-scale metal structures can be harnessed for application in information processing, energy harvesting, sensing, and catalysis. Metal nanostructures enable negative refractive index, subwavelength resolution imaging, and patterning through engineered metamaterials and promise technologies that will operate in the quantum plasmonics regime. However, the controlled fabrication of high-definition single-crystal subwavelength metal nanostructures has remained a significant hurdle due to the tendency for polycrystalline metal growth using conventional physical vapor deposition methods and the challenges associated with placing solution-grown nanocrystals in desired orientations and locations on a surface to manufacture functional devices. Here, we introduce a scalable and green wet chemical approach to monocrystalline noble metal thin films and nanostructures. The method enables the fabrication of ultrasmooth, epitaxial, single-crystal films of controllable thickness that are ideal for the subtractive manufacture of nanostructures through ion beam milling and additive crystalline nanostructure via lithographic patterning for large-area, single-crystal metasurfaces and high aspect ratio nanowires. Our single-crystal nanostructures demonstrate improved feature quality, pattern transfer yield, reduced optical and resistive losses, and tailored local fields to yield greater optical response and improved stability compared to those of polycrystalline structures—supporting greater local field enhancements and enabling practical advances at the nanoscale.},
  doi       = {10.1021/acsnano.0c03466},
  file      = {Full Text PDF:https\://pubs.acs.org/doi/pdf/10.1021/acsnano.0c03466:application/pdf;ACS Full Text Snapshot:https\://pubs.acs.org/doi/full/10.1021/acsnano.0c03466:text/html},
  publisher = {American Chemical Society},
  url       = {https://doi.org/10.1021/acsnano.0c03466},
  urldate   = {2020-06-19TZ},
}

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