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Single Quantum Dot Optical Spectroscopy
Presented by Rohini Vidya Shankar Amrita Urdhwareshe
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Motivation Discrete atom-like states in 0 D quantum dots
Discrete exciton levels just below the bandgap Quantum confinement effect for excitons Ultra narrow transitions and spectra expected
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Observed quantum dot emission
Optical spectra of 35 Ao CdSe nanocrystals: no discrete lines, even at low T Ref [1]
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Inhomogeneous broadening
Ensemble averaging of optical properties Need to take single dot spectra
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Experimental techniques
Samples of single quantum dots to look at Chemically prepared and spin coated on substrates Usually II-VI semiconductors. E.g. CdSe, PbS, CdS, etc. Particle size ~ Ao Core-shell quantum dots E.g. CdSe coated with ZnS or CdS, etc. Particle size ~ Ao Epitaxially deposited Usually III-V semiconductors. E.g. GaAs, InGaAs, AlGaAs, etc. Particle size ~ nm
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Experimental techniques (contd.)
Optical techniques used Far-field epifluorescence microscopy/spectroscopy Near-field optical spectroscopy
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Far-field epifluorescence spectroscopy
Light focused and collected using the same objective Both images and spectra obtained by switching between a mirror and a diffraction grating Need low areal densities ~ one quantum dot per µm2
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Far field images and spectrum
A) Image of single CdSe 45 Ao nanocrystals at 10 K (Ref [2]) B) Image of the same region as in (A) with narrowed entrance slit C) Spectrally dispersed image of the entrance slit in (B)
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Near field optical spectroscopy
Low temperature nano-probing system based on shear-force distance regulation. Near field excitation of the sample and near-field collection of the luminescence Useful for quantum dot areal densities of the order of 100/µm2
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Near-field imaging Near-field luminescence image of a single In0.4Ga0.6As/Al0.5Ga0.5As QD (T = 5 K) (Ref [3]) Quantum dot emits light in a narrow band centered at a wavelength of 733nm
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Observations Same 35 Ao CdSe spectra (Ref [1]): dotted lines show ensemble measurement. Solid lines: single quantum dot measurement Narrow peakwidth at low T!
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Observations Ensemble vs single CdSe nanocrystal spectra (Ref [2])
Ensemble spectrum: average of many single nanocrystal spectra Shift in energy peaks with average nanocrystal size
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Fluorescence blinking
On/off nature of fluorescence spectra (Ref [4]) Typical on-off timescale ~.5 sec. Not observed for ensembles
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Blinking (contd.) On times: dependent on excitation intensity
Vary inversely as excitation intensity Off times: Independent of excitation intensity Proposed explanation Photo ionization of nanocrystals Also possibly, thermally activated charge trapping
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Spectral diffusion Different lineshapes for different nanocrystals
Excitation intensity and integration time dependent linewidths Spectral diffusion: result of locally changing electric fields Possibly correlated to fluorescence intermittency Ref [2]
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Spectra of capped nanocrystals
Capping materials: higher bandgap semiconductors Highly enhanced quantum yield of spectra (as high as 50%) Red shift of the emission peak Decreases intermittency to a timescale ~several seconds to few minutes
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Polarized photoluminescence studies
Narrower linewidth enables precise measurements of luminescence character Information about the spin-related effects such as Zeeman splittings. Relaxation processes in single GaAs/InAs quantum dots studied using polarized photoluminescence (PL) spectroscopy in an external magnetic field
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Unpolarized and Polarized Spectra
Typical unpolarized photoluminescence spectra from a single GaAs quantum dot ~20nm at various magnetic fields (Ref [5]) Luminescence spectra for all polarization geometries at 8 T (Ref [5])
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Summary Need to observe single quantum dot spectra
Techniques of sample preparation and spectrum acquisition Salient features of the spectra Narrow linewidths Size dependence of emission peaks Blinking/intermittency Spectral diffusion Polarization dependence
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Potential applications
DNA and protein labeling Highly luminescent single quantum dots can overcome the functional limitations encountered with chemical and organic dyes Easily tunable emission wavelength by changing the particle size or composition Optical coherence tomography using quantum dots Quantum-dot-based super-luminescent light-emitting diodes High-bandwidth high-power light sources Spectra of these devices can be largely tuned
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References [1] U. Banin, M. Bruchez, A. P. Alivisatos, T. Ha, S. Weiss and D. S. Chemla, Journal of Chemical Physics 110 No. 2, 1195 – 1201 (1999) [2] Stephen A. Empedocles, Robert Neuhauser, Kentaro Shimizu and Moungi G. Bawendi, Advanced Materials 11, No. 15, (1999) [3] A. Chavez-Pirson, J. Temmyo, H. Kamada, H. Gotoh, and H. Ando, Applied Physics Letters 72, No. 6, (1998) [4] M. Nirmal, B. O. Dabbousi, M. G. Bawendi, J. J. Macklin, J. K. Trautman, T. D. Harris and L. E. Brus, Nature 383, (1996) [5] Y. Toda, S. Shinomori, K. Suzuki and Y. Arakawa, Physical Review B 58 No. 16, R R (1998)
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Thank You!
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