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Plasmonic Diamond Membranes for Ultrafast Silicon Vacancy Emission.
Boyce, Andrew M; Li, Hengming; Wilson, Nathaniel C; Acil, Deniz; Shams-Ansari, Amirhassan; Chakravarthi, Srivatsa; Pederson, Christian; Shen, Qixin; Yama, Nicholas; Fu, Kai-Mei C; Loncar, Marko; Mikkelsen, Maiken H.
Afiliación
  • Boyce AM; Department of Electrical and Computer Engineering, Duke University, Durham, North Carolina 27708, United States.
  • Li H; Department of Electrical and Computer Engineering, Duke University, Durham, North Carolina 27708, United States.
  • Wilson NC; Department of Physics, Duke University, Durham, North Carolina 27708, United States.
  • Acil D; Department of Electrical and Computer Engineering, Duke University, Durham, North Carolina 27708, United States.
  • Shams-Ansari A; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts 02138, United States.
  • Chakravarthi S; Department of Physics, University of Washington, Seattle, Washington 98195, United States.
  • Pederson C; Department of Physics, University of Washington, Seattle, Washington 98195, United States.
  • Shen Q; Department of Physics, Duke University, Durham, North Carolina 27708, United States.
  • Yama N; Department of Electrical and Computer Engineering, University of Washington, Seattle, Washington 98195, United States.
  • Fu KC; Department of Physics, University of Washington, Seattle, Washington 98195, United States.
  • Loncar M; Department of Electrical and Computer Engineering, University of Washington, Seattle, Washington 98195, United States.
  • Mikkelsen MH; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts 02138, United States.
Nano Lett ; 24(12): 3575-3580, 2024 Mar 27.
Article en En | MEDLINE | ID: mdl-38478720
ABSTRACT
Silicon vacancy centers (SiVs) in diamond have emerged as a promising platform for quantum sciences due to their excellent photostability, minimal spectral diffusion, and substantial zero-phonon line emission. However, enhancing their slow nanosecond excited-state lifetime by coupling to optical cavities remains an outstanding challenge, as current demonstrations are limited to ∼10-fold. Here, we couple negatively charged SiVs to sub-diffraction-limited plasmonic cavities and achieve an instrument-limited ≤8 ps lifetime, corresponding to a 135-fold spontaneous emission rate enhancement and a 19-fold photoluminescence enhancement. Nanoparticles are printed on ultrathin diamond membranes on gold films which create arrays of plasmonic nanogap cavities with ultrasmall volumes. SiVs implanted at 5 and 10 nm depths are examined to elucidate surface effects on their lifetime and brightness. The interplay between cavity, implantation depth, and ultrathin diamond membranes provides insights into generating ultrafast, bright SiV emission for next-generation diamond devices.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Nano Lett Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Nano Lett Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos