2006
DOI: 10.1063/1.2402793
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The dynamics of amplified spontaneous emission in CdSe∕ZnSe quantum dots

Abstract: We have used the variable stripe technique and pump-probe spectroscopy to investigate both gain and the dynamics of amplified spontaneous emission from CdSe quantum dot structures. We have found modal gain coefficients of 75 and 32 cm −1 for asymmetric and symmetric waveguide structures, respectively. Amplified spontaneous emission decay times of 150 and 300 ps and carrier capture times of 15 and 40 ps were measured for the structures with high and low material gains respectively. The difference in the capture… Show more

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Cited by 4 publications
(5 citation statements)
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“…The rise time is determined by fitting the rising process with the Boltzmann sigmoidal function where B 1 is the initial value, B 2 is the final value, t s indicates the time center, and τ R represents the time constant for the rising process. The rise time (τ R ) for FX obtained from the fitting is 101 ± 5 ps (results shown in Figure a), which value is larger than that in CdSe QDs (20–40 ps). , The decay curve of the QD samples can be well-fitted by a double-exponential function where I b represents the noise. The fitting results are plotted as solid lines in Figure a.…”
Section: Results and Discussionmentioning
confidence: 87%
See 1 more Smart Citation
“…The rise time is determined by fitting the rising process with the Boltzmann sigmoidal function where B 1 is the initial value, B 2 is the final value, t s indicates the time center, and τ R represents the time constant for the rising process. The rise time (τ R ) for FX obtained from the fitting is 101 ± 5 ps (results shown in Figure a), which value is larger than that in CdSe QDs (20–40 ps). , The decay curve of the QD samples can be well-fitted by a double-exponential function where I b represents the noise. The fitting results are plotted as solid lines in Figure a.…”
Section: Results and Discussionmentioning
confidence: 87%
“…The rise time (τ R ) for FX obtained from the fitting is 101 ± 5 ps (results shown in Figure 4a), 39 which value is larger than that in CdSe QDs (20−40 ps). 40,41 The decay curve of the QD samples can be well-fitted by a double-exponential function 38…”
Section: E E Ementioning
confidence: 99%
“…The emission color of CdSe NCs can be covered in the whole visible range depending on size variations. With these interesting properties, CdSe NCs can become an ideal candidate for optoelectronics such as light-emitting diodes, laser, and bio-sensors [8][9][10][11][12][13][14][15]. In particular, CdSe NCs obtained a higher density of electronic states near the edges of valence and conduction bands compared to bulk semiconductors.…”
Section: Introductionmentioning
confidence: 99%
“…16 Since ASE is an effective indicator to compare the material capability for optical gain, the ASE behaviors of different types of colloidal nanocrystals have been investigated. 19,30–33 Such laterally oriented self-assembly of CQWs has paved the way for the development of ultrathin optical gain media with tunable thickness, thanks to the excellent uniformity and close-packed nature of their films. 16…”
Section: Introductionmentioning
confidence: 99%
“…16 Since ASE is an effective indicator to compare the material capability for optical gain, the ASE behaviors of different types of colloidal nanocrystals have been investigated. 19,[30][31][32][33] Such laterally oriented self-assembly of CQWs has paved the way for the development of ultrathin optical gain media with tunable thickness, thanks to the excellent uniformity and close-packed nature of their films. 16 Herein, different from our previous work, we propose and demonstrate vertically oriented self-assembled monolayer (SAM) film formation of CdSe/CdZnS CQWs by controlling the hydrophilicity/lipophilicity balance of their subphase by using a binary subphase.…”
Section: Introductionmentioning
confidence: 99%