Picosecond Photon-Solid Interaction

1984 ◽  
Vol 35 ◽  
Author(s):  
H. Kurz ◽  
N. Bloembergen

ABSTRACTSome of the fundamental aspects of pulsed laser interactions with semiconductors are reviewed within the frame of recent experimental work with picosecond laser pulses. Main emphasis is placed on data obtained in space-time resolved measurements of transmission and reflectivity of picosecond pulse irradiated silicon at different probing wavelengths. Four distinct interaction regimes can be defined, depending on the fluence of the laser pulse. Special attention is devoted to the phase transition from solid to liquid state at the surface. The optical heating model is found to be valid even on a time scale of picoseconds. Firm data of the electron-hole plasma density and lattice temperature are derived. The thermal nature of the phase transition is confirmed.

1984 ◽  
Vol 35 ◽  
Author(s):  
J.M. Liu ◽  
A.M. Malvezzi ◽  
N. Bloembergen

ABSTRACTDetailed analysis of the second harmonic signals in reflection from crystalline GaAs surfaces reveals that the structural transition associated with surface melting occurs in less than 2 ps. Preliminary results of picosecond time-resolved reflectivity measurements are also presented.


1985 ◽  
Vol 51 ◽  
Author(s):  
J.M. Liu ◽  
A.M. Malvezzi ◽  
N. Bloembergen

ABSTRACTThe interactions of picosecond laser pulses at 532 nm wavelength with GaAs surfaces have been studied with time-resolved reflectivity and transmission measurements at three probe wavelengths. At fluences below the melting threshold, the laser-generated electron-hole plasma is limited to a density below ≈1020cm−3. The high reflectivities of molten GaAs observed at fluences above the tlhreshold have a wavelength dependence inconsistent with a simple Drude model for a metallic GaAs molten layer. At high fluences, the evolution of a laser-induced vapor cloud is observed.


2009 ◽  
Vol 106 (6) ◽  
pp. 063501 ◽  
Author(s):  
Huan Huang ◽  
Fangyuan Zuo ◽  
Fengxiao Zhai ◽  
Yang Wang ◽  
Tianshu Lai ◽  
...  

1981 ◽  
Vol 4 ◽  
Author(s):  
R. Yen ◽  
J. M. Liu ◽  
H. Kurz ◽  
N. Bloembergen

ABSTRACTThe changes in reflectivity of a silicon surface, irradiated by a green picosecond pulse, are probed during and following that pulse with a spatial resolution of 10μm. The data indicate the development of a liquid phase, and a resolidification either into a single crystal or an amorphous phase. The latter has a characteristic ring-type pattern, and occurs only at locations where the incident picosecond laser fluence lies between 0.2 and 0.26 J/cm2. The reflectivity data appear to be in good quantitative agreement with a “simple heating” model, in which the electrons and phonons maintain a local thermodynamic equilibrium on a picosecond time scale.


1989 ◽  
Vol 10 (2) ◽  
pp. 63-72 ◽  
Author(s):  
H. Willwohl ◽  
J. Wolfrum ◽  
R. Gleiter

The photochromism of N-phenyl-rhodaminelactame (3' ,6' -bis-(diethylamino)-2-phenyl-spiro[1H-isoindole-1,9'[9H] Xanthaen]-3-[2H]-one) was investigated in solutions of acetonitrile, dioxane and mixtures of dioxane with H20, methanol and ethanol by laser flash time resolved absorption measurements. The colouring reaction kinetics and the relative quantum yield of the red product were measured using nanosecond excimer laser excitation at 308 nm. In most cases, first order kinetics was.observed. The first order rate constants and the quantum yield were found to be dependent on the solvent and the number of laser pulses that had previously irradiated the solution. The thermal fading reaction occurred on a millisecond timescale and showed large deviations from first order kinetics in all solvents. In addition, picosecond laser pulses at 285 nm were used to measure the fluorescence lifetime of the S1 state of the rhodamine derivative with picosecond resolution. Single exponential decays were observed in all solvents and the lifetime ranged between 3 and 6 nanoseconds. We conclude that the photoreaction does not proceed directly from the S1 state, and propose a mechanism for the photochromic process, in which an intermediate decomposes to rotameric isomers of the coloured product, which are not equilibrated on the millisecond time scale of the reverse reaction.


1999 ◽  
Vol 597 ◽  
Author(s):  
W. L. Tan ◽  
W. Ji ◽  
J. L. Zuo ◽  
J. F. Bai ◽  
X. Z. You ◽  
...  

AbstractWe report an investigation of optical-limiting behavior in two neutral nickel complexes with multi-sulfur 1,2 dithiolene ligands, [Ni(medt)2] I (medt = 5,6-dihydro-6-methyl-1,4-dithiin-2,3- dithiolate) and [Ni(phdt)2] 2 (phdt = 5,6-dihydro-5-phenyl-l,4-dithiin-2,3-dithiolate) in benzene solution. The fluence-dependent transmission of the complexes was observed with nanosecond and picosecond laser pulses at 532-nm wavelength. The limiting thresholds of the complexes were ˜0.3 J/cm2, when measured with the picosecond pulses. Both picosecond time-resolved pump-probe and Z-scan measurement revealed that the limiting effects should originate from excited-state absorption and refraction. The transparency window (400˜900 nm), observed in the linear absorption spectra of the complexes, indicated that their limiting response should cover a wider range than those of fullerenes and phthalocyanines.


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