34,154 research outputs found
Sideband pump-probe technique resolves nonlinear modulation response of PbS/CdS quantum dots on a silicon nitride waveguide
For possible applications of colloidal nanocrystals in optoelectronics and nanophotonics, it is of high interest to study their response at low excitation intensity with high repetition rates, as switching energies in the pJ/bit to sub-pJ/bit range are targeted. We develop a sensitive pump-probe method to study the carrier dynamics in colloidal PbS/CdS quantum dots deposited on a silicon nitride waveguide after excitation by laser pulses with an average energy of few pJ/pulse. We combine an amplitude modulation of the pump pulse with phase-sensitive heterodyne detection. This approach permits to use co-linearly propagating co-polarized pulses. The method allows resolving transmission changes of the order of 10(-5) and phase changes of arcseconds. We find a modulation on a sub-nanosecond time scale caused by Auger processes and biexciton decay in the quantum dots. With ground state lifetimes exceeding 1 mu s, these processes become important for possible realizations of opto-electronic switching and modulation based on colloidal quantum dots emitting in the telecommunication wavelength regime
On-chip hybrid integration of silicon nitride microdisk with colloidal quantum dots
We report on the fabrication of on-chip freestanding silicon nitride microdisks hybridly integrated with embedded colloidal quantum dots. An efficient coupling of quantum dot emission to resonant disk modes in the visible range is demonstrated
Optical properties of SOI waveguides functionalized with close-packed quantum dot films
It is shown that dipolar coupling between neighboring quantum dots enhances the absorption of light in close packed monolayers of colloidal quantum dots. Based on this concept, the experimentally determined losses in planarized waveguides coated by a quantum dot monolayer can be successfully simulated. These simulations rely on replacing the quantum dot layer by an effective medium with a dielectric function determined by dipolar coupling and use the dielectric constant of the quantum dot host medium as the only adjustable parameter. This leads to a generic approach for the simulation of optical materials including close packed quantum dot layers
Characterizing Quantum-Dot Blinking Using Noise Power Spectra
Fluctuations in the fluorescence from macroscopic ensembles of colloidal
semiconductor quantum dots have the spectral form of 1/f noise. The measured
power spectral density reflects the fluorescence intermittency of individual
dots with power-law distributions of "on" and "off" times, and can thus serve
as a simple method for characterizing such blinking behavior
Gb/s visible light communications with colloidal quantum dot color converters
This paper reports the utilization of colloidal semiconductor
quantum dots as color converters for Gb/s visible light
communications. We briefly review the design and properties of
colloidal quantum dots and discuss them in the context of fast
color conversion of InGaN light sources, in particular in view of
the effects of self-absorption. This is followed by a description of
a CQD/polymer composite format of color converters. We show
samples of such color-converting composite emitting at green, yellow/orange
and red wavelengths, and combine these with a blueemitting
microsize LED to form hybrid sources for wireless visible
light communication links. In this way data rates up to 1 Gb/s over
distances of a few tens of centimeters have been demonstrated. Finally,
we broaden the discussion by considering the possibility for
wavelength division multiplexing as well as the use of alternative
colloidal semiconductor nanocrystals
Ag2ZnSnS4 Nanocrystals Expand the Availability of RoHS Compliant Colloidal Quantum Dots
The demonstration of the quantum confinement effect in colloidal quantum dots (QDs) has been extensively studied and exploited mainly in Pb and Cd chalcogenide systems. There has been an urgent need recently for the development of non(less)-toxic colloidal QDs to warrant compliance with current safety regulations (Restriction of Hazardous Substances (RoHS) Directive 2002/95/EC). Herein, we report Pb/Cd-free, solution processed luminescent Ag2ZnSnS4 (AZTS) colloidal QDs. We present a selective and controlled amine and thiol-free synthesis of air stable luminescent AZTS QDs by the hot injection technique. By controlling the reaction conditions we obtain controlled size variation and demonstrate the quantum confinement effect that is in good agreement with the theoretically calculated values. The band gap of the AZTS QDs is size-tunable in the near-infrared from 740 to 850 nm. Finally, we passivate the surface with Zn-oleate, which yields higher quantum yield (QY), longer lifetime, and better colloidal stability.Peer ReviewedPostprint (published version
Germanium quantum dots: Optical properties and synthesis
Three different size distributions of Ge quantum dots (>~200, 110, and 60 Å) have been synthesized via the ultrasonic mediated reduction of mixtures of chlorogermanes and organochlorogermanes (or organochlorosilanes) by a colloidal sodium/potassium alloy in heptane, followed by annealing in a sealed pressure vessel at 270 °C. The quantum dots are characterized by transmission electron microscopy, x-ray powder diffraction, x-ray photoemission, infrared spectroscopy, and Raman spectroscopy. Colloidal suspensions of these quantum dots were prepared and their extinction spectra are measured with ultraviolet/visible (UV/Vis) and near infrared (IR) spectroscopy, in the regime from 0.6 to 5 eV. The optical spectra are correlated with a Mie theory extinction calculation utilizing bulk optical constants. This leads to an assignment of three optical features to the E(1), E(0'), and E(2) direct band gap transitions. The E(0') transitions exhibit a strong size dependence. The near IR spectra of the largest dots is dominated by E(0) direct gap absorptions. For the smallest dots the near IR spectrum is dominated by the Gamma25-->L indirect transitions
Fluorescence enhancement by dark plasmon modes
We investigate the fluorescence properties of colloidal quantum dots attached
to gold rod nanoantennas. These structures are fabricated by a two step
electron beam lithography process in combination with a chemical linking
method. By varying the nanoantenna length, the plasmon modes of the
nanoantennas are successively tuned through the emission band of the quantum
dots. We observe a pronounced fluorescence enhancement both for short and long
nanoantennas. These findings can be attributed to the coupling of the quantum
dots to bright and dark plasmon modes, respectively
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