Radiation spectrum of hot excitons in Si nanocrystals

2016 ◽  
Vol 55 (4) ◽  
Author(s):  
Anton V. Gert ◽  
Irina N. Yassievich

The self-trapped exciton state (STE) is very important for the dynamics of hot excitons in photoexcited silicon nanocrystals embedded in a SiO2 matrix. This fact has been recently confirmed by the experimental data obtained by the femtosecond pump– probe spectroscopy technique in Amsterdam University. In this work we have studied the energy exchange between the exciton localized in the STE state and the hot exciton in the core of silicon nanocrystals and have shown that it determines the dynamics of the energy distribution of the hot excitons. Using the Monte-Carlo we have simulated the energy distribution of excitons in the time interval 10–100 ps after excitation. Thus the model of formation of the distribution of hot excitons in silicon nanocrystals is developed and the fast formation of the wide energy distribution is demonstrated. The form of the photoluminescence spectrum almost directly corresponds to the energy distribution of excitons in a silicon nanocrystal at a given moment. In the result we have found the relaxation times of hot excitons equal to 100 ps and the inner quantum efficiency of the ultrafast photoluminescence of about 0.1%. These values are close to the experimentally observed ones.

2008 ◽  
Vol 1081 ◽  
Author(s):  
Jahan M. Dawlaty ◽  
Shriram Shivaraman ◽  
Mvs Chandrashekhar ◽  
Michael G. Spencer ◽  
Farhan Rana

ABSTRACTUsing ultrafast optical pump-probe spectroscopy, we have measured carrier relaxation times in epitaxial graphene layers grown on SiC wafers. We find two distinct time scales associated with the relaxation of nonequilibrium photogenerated carriers. An initial fast relaxation transient in the 70-120 fs range is followed by a slower relaxation process in the 0.4-1.7 ps range. The slower relaxation time is found to be inversely proportional to the degree of crystalline disorder in the graphene layers as measured by Raman spectroscopy. We relate the measured fast and slow time constants to carrier-carrier and carrier-phonon intraband and interband scattering processes in graphene.


2003 ◽  
Vol 770 ◽  
Author(s):  
Nathanael Smith ◽  
Max J. Lederer ◽  
Marek Samoc ◽  
Barry Luther-Davies ◽  
Robert G. Elliman

AbstractOptical pump-probe measurements were performed on planar slab waveguides containing silicon nanocrystals in an attempt to measure optical gain from photo-excited silicon nanocrystals. Two experiments were performed, one with a continuous-wave probe beam and a pulsed pump beam, giving a time resolution of approximately 25 ns, and the other with a pulsed pump and probe beam, giving a time resolution of approximately 10 ps. In both cases the intensity of the probe beam was found to be attenuated by the pump beam, with the attenuation increasing monotonically with increasing pump power. Time-resolved measurements using the first experimental arrangement showed that the probe signal recovered its initial intensity on a time scale of 45-70 μs, a value comparable to the exciton lifetime in Si nanocrystals. These data are shown to be consistent with an induced absorption process such as confined carrier absorption. No evidence for optical gain was observed.


Processes ◽  
2021 ◽  
Vol 9 (2) ◽  
pp. 312
Author(s):  
Yusuf Tutel ◽  
Gökhan Sevinç ◽  
Betül Küçüköz ◽  
Elif Akhuseyin Yildiz ◽  
Ahmet Karatay ◽  
...  

Meso-substituted borondipyrromethene (BODIPY)-porphyrin compounds that include free base porphyrin with two different numbers of BODIPY groups (BDP-TTP and 3BDP-TTP) were designed and synthesized to analyze intramolecular energy transfer mechanisms of meso-substituted BODIPY-porphyrin dyads and the effect of the different numbers of BODIPY groups connected to free-base porphyrin on the energy transfer mechanism. Absorption spectra of BODIPY-porphyrin conjugates showed wide absorption features in the visible region, and that is highly valuable to increase light-harvesting efficiency. Fluorescence spectra of the studied compounds proved that BODIPY emission intensity decreased upon the photoexcitation of the BODIPY core, due to the energy transfer from BODIPY unit to porphyrin. In addition, ultrafast pump-probe spectroscopy measurements indicated that the energy transfer of the 3BDP-TTP compound (about 3 ps) is faster than the BDP-TTP compound (about 22 ps). Since the BODIPY core directly binds to the porphyrin unit, rapid energy transfer was seen for both compounds. Thus, the energy transfer rate increased with an increasing number of BODIPY moiety connected to free-base porphyrin.


Author(s):  
H.S. Mavi ◽  
S. Rath ◽  
Arun Shukla

Laser-induced etching of silicon is used to generate silicon nanocrystals. The pore structure depends on the substrate type and etching laser wavelength. Porous silicon (PS) samples prepared by Nd:YAG laser (1.16 eV) etching of n-type substrate showed a fairly uniform and highly interconnected network of nearly circular pores separated by thin columnar boundaries, while no circular pits were produced by argon- ion laser (2.41 eV) etching under similar conditions. The size and size distribution of the nanocrystals are investigated by Raman and photoluminescence spectroscopies and analyzed within the framework of quantum confinement models.


1994 ◽  
Vol 61 (1-3) ◽  
pp. 153-165 ◽  
Author(s):  
Robert M. Whitnell ◽  
Kent R. Wilson ◽  
YiJing Yan ◽  
Ahmed H. Zewail

2013 ◽  
Vol 88 (6) ◽  
pp. 065404 ◽  
Author(s):  
Niharika Singh ◽  
Ayan Ray ◽  
R D'Souza ◽  
Q V Lawande ◽  
B N Jagatap

1996 ◽  
Vol 452 ◽  
Author(s):  
Gildardo R. Delgado ◽  
Howard W.H. Lee ◽  
Susan M. Kauzlarich ◽  
Richard A. Bley

AbstractWe studied the optical and electronic properties of silicon nanocrystals derived from two distinct fabrication procedures. One technique uses a controlled chemical reaction. In the other case, silicon nanocrystals are produced by ultrasonic fracturing of porous silicon layers. We report on the photoluminescence, photoluminescence excitation, and absorption spectroscopy of various size distributions derived from these techniques. We compare the different optical properties of silicon nanocrystals made this way and contrast them with that observed in porous silicon. Our results emphasize the dominant role of surface states in these systems as manifested by the different surface passivation layers present in these different fabrication techniques. Experimental absorption measurements are compared to theoretical calculations with good agreement. Our results provide compelling evidence for quantum confinement in both types of Si nanocrystals. Our results also indicate that the blue emission from very small Si nanocrystals corresponds to the bandedge emission, while the red emission arises from traps.


Biochemistry ◽  
1993 ◽  
Vol 32 (29) ◽  
pp. 7512-7518 ◽  
Author(s):  
Sergei Savikhin ◽  
Todd Wells ◽  
Pill Soon Song ◽  
Walter S. Struve

1989 ◽  
Vol 93 (25) ◽  
pp. 8149-8162 ◽  
Author(s):  
Yi Jing Yan ◽  
Laurence E. Fried ◽  
Shaul Mukamel

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