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25 March 2005 Single carbon nanotube photonics
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Abstract
The electronic structure of SWNTs was investigated using the complementary techniques of single molecule photoluminescence spectroscopy and ultrafast optical spectroscopy. We found that photoexcited electrons in SWNTs isolated in surfactant micelles decay through many channels, exhibiting a range of decay times (~200 fs to ~ 120 ps). The magnitude of the longest-lived component in the ultrafast signal specifically depends on resonant excitation, thus suggesting that this lifetime corresponds to the band-edge relaxation time. Fluorescence spectra from single SWNTs are well described by a single, Lorentzian lineshape. However, nanotubes with identical structure fluoresce over a distribution of peak positions and line widths not observed in ensemble studies, caused by localized defects and electrostatic perturbations. Unlike for most other single molecules, for SWNTs the photoluminescence unexpectedly does not show any intensity or spectral fluctuations at 300K. This lack of photoluminescence intensity blinking or bleaching demonstrates that SWNTs have the potential to provide a stable, single molecule infrared photon source, allowing for the exciting possibility of single nanotube integrated photonic devices and biophotonic sensors.
© (2005) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Libai Huang, Achim Hartschuh, Hermenegildo N. Pedrosa, Jeffrey Peterson, Mathias Steiner, Lukas Novotny, and Todd D. Krauss "Single carbon nanotube photonics", Proc. SPIE 5732, Quantum Sensing and Nanophotonic Devices II, (25 March 2005); https://doi.org/10.1117/12.582685
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