Nonlinear Mechanisms in Carbon-Black Suspension in a Limiting Geometry

1997 ◽  
Vol 479 ◽  
Author(s):  
Francois Fougeanet ◽  
Jean-Claude Fabre

AbstractAlthough Carbon-Black suspensions (CBS) have been studied extensively for optical limiting applications, the microscopic mechanisms responsible for their limiting behavior still remain unclear. To study the mechanisms leading to the nonlinearity, we have performed a pump-probe experiment coupled with plasma emission measurements. Time resolved probe transmission have permitted to differentiate bubbles from plasma effects in the case of Carbon-Black in CS2. Other effects are discussed in terms of limiting performance.

1999 ◽  
Vol 597 ◽  
Author(s):  
X. Sun ◽  
Y. N. Xiong ◽  
P. Chen ◽  
J. Y. Lin ◽  
W. Ji ◽  
...  

AbstractWe report an investigation into the mechanism responsible for the optical limiting behavior in multiwalled carbon nanotubes. We conducted energy-dependent transmission measurements, picosecond time-resolved pump-probe, and nonlinear scattering experiments at 532-nm wavelength on multiwalled carbon nanotube suspension. For comparison, C60-toluene solution and carbon black suspension were also studied in the same experiments. The similarities that we observed between the multiwalled carbon nanotubes and carbon black suspension suggest that nonlinear scattering, which is known to be responsible for the limiting action in carbon black suspension, should play an important role in the limiting effect in multiwalled carbon nanotubes.


Science ◽  
2021 ◽  
pp. eabf3286
Author(s):  
R. Wallauer ◽  
M. Raths ◽  
K. Stallberg ◽  
L. Münster ◽  
D. Brandstetter ◽  
...  

Frontier orbitals determine fundamental molecular properties such as chemical reactivities. Although electron distributions of occupied orbitals can be imaged in momentum space by photoemission tomography, it has so far been impossible to follow the momentum-space dynamics of a molecular orbital in time, for example through an excitation or a chemical reaction. Here, we combined time-resolved photoemission using high laser harmonics and a momentum microscope to establish a tomographic, femtosecond pump-probe experiment of unoccupied molecular orbitals. We measured the full momentum-space distribution of transiently excited electrons, connecting their excited-state dynamics to real-space excitation pathways. Because in molecules this distribution is closely linked to orbital shapes, our experiment may in the future offer the possibility to observe ultrafast electron motion in time and space.


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.


2014 ◽  
Vol 70 (a1) ◽  
pp. C1750-C1750
Author(s):  
Pascal Parois ◽  
Richard Cooper

Approaches to determining the influence of individual measurements on the precision of crystallographic least squares parameters have been known for a long while.[1] Situations in which the precision of a single parameter (or linear combination of parameters) is critical can include: determination of novel bond lengths; refinement of site occupancies in mixed metal or mixed oxidation state systems; determination of the fraction of excited state molecules in a time-resolved pump-probe experiment. Such calculations are easily applicable to point-detector instruments, where individual influential reflections could be remeasured one-by-one. However, on a modern area detector instrument many reflections are measured on one frame and therefore some consideration of the appropriate strategy of reciprocal space scans is permitted to allow a more efficient use of the instrument. The highly influential partial data collection is then feed into an appropriate refinement model. Occupancies in mixed-metal or mixed-oxidation state systems and fractions and positions of excited state molecules during a time-resolved pump-probe experiment can be determined using direct refinement of the perturbation of the structure from the ground state. Re-factoring to modern Fortran of the Crystals software is in progress to allow the implementation of new algorithms such as a difference refinement.[2] We present an analysis of diffractometer strategy selection to prioritize scans which give the best improvement in specific least-squares parameters and a novel algorithm for the refinement of the partial data using crystals.


1999 ◽  
Vol 68 (4) ◽  
pp. 689-692 ◽  
Author(s):  
B. Bousquet ◽  
L. Canioni ◽  
J. Plantard ◽  
L. Sarger

2015 ◽  
Vol 91 (4) ◽  
Author(s):  
Philipp Cörlin ◽  
Andreas Fischer ◽  
Michael Schönwald ◽  
Alexander Sperl ◽  
Tomoya Mizuno ◽  
...  

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