• Title/Summary/Keyword: Multiphoton ionization

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Numerical Analysis of Optical Damage in Dielectrics Irradiated by Ultra-Short Pulsed Lasers (극초단 펄스 레이저에 의한 절연체의 광학 손상 해석)

  • Lee, Seong-Hyuk;Kang, Kwang-Gu;Lee, Joon-Sik;Choi, Young-Ki;Park, Seung-Ho;Ryou, Hong-Sun
    • Proceedings of the KSME Conference
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    • 2004.11a
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    • pp.1213-1218
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    • 2004
  • The present article reports extensive numerical results on the non-local characteristics of ultra-short pulsed laser-induced breakdowns of fused silica ($SiO_{2}$) by using the multivariate Fokker-Planck equation. The nonlocal type of multivariate Fokker-Planck equation is modeled on the basis of the Boltzmann transport formalism to describe the ultra-short pulsed laser-induced damage phenomena in the energy-position space, together with avalanche ionization, three-body recombination, and multiphoton ionization. Effects of electron avalanche, recombination, and multiphoton ionization on the electronic transport are examined. From the results, it is observed that the recombination becomes prominent and contributes to reduce substantially the rate of increase in electron number density when the electron density exceeds a certain threshold. With very intense laser irradiation, a strong absorption of laser energy takes place and an initially transparent solid is converted to a metallic state, well known as laser-induced breakdown. It is also found that full ionization is provided at intensities above threshold, all further laser energy is deposited within a thin skin depth.

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Stabilization of ionization in an intense laser field (초강력 레이저에 의한 원자의 이온화의 안정화)

  • 권덕희;이해웅;이용주
    • Proceedings of the Optical Society of Korea Conference
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    • 2002.07a
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    • pp.10-11
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    • 2002
  • 최근 수년간 원자의 쿨롱(Coulomb) 인력을 능가하는 전기장을 발생하는 강력한 레이저(I>$10^{16}$ W/$\textrm{cm}^2$)와 상호작용하는 원자계에서 보여지는 많은 흥미로운 비선형 현상들, 예를 들면 다중광자 이온화(multiphoton ionization), 임계 이상의 이온화(above-threshold ionization), 고차조화파 발생(high-harmonic generation)등에 대한 연구가 활발히 진행되어왔다. 또 하나의 비선형 현상으로 원자의 이온화의 안정화(stabilization)가 있고, 이 현상은 레이저의 세기가 증가하면서 이온화율이 포화되거나 감소하는 것을 의미한다. (중략)

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Rapid Detection of Trace 1,4-Dichlorobenzene Using Laser Mass Spectrometry

  • Ding, Lei;Ma, Jing;Zheng, Haiyang;Fang, Li;Zhang, Weijun;Kim, Duk-Hyeon;Cha, Hyung-Ki
    • Bulletin of the Korean Chemical Society
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    • v.27 no.9
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    • pp.1393-1396
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    • 2006
  • The 1+1 two-photon Resonant Enhanced Multiphoton Ionization (REMPI) spectra of 1,4-dichlorobenzene was obtained from 240 nm through to 250 nm on a laser mass spectrometer. Special care was taken to build up a heatable sample inlet system suitable for detecting a trace semi-volatile organic compound and reducing the memory effort on the inner wall of the inlet system. The detection limits of 1,4-dichlorobenzene in ppbV/V concentration range at certain wavelengths are presented.

Suppression of the Methyl Radical Loss from Acetone Cation within (CH3COCH3)n{CH3COCH3}+ Clusters

  • Lee, Yong-Hoon;Oh, Myoung-Kyu;Choi, Sung-Chul;Ko, Do-Kyeong;Lee, Jong-Min
    • Bulletin of the Korean Chemical Society
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    • v.29 no.8
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    • pp.1519-1524
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    • 2008
  • We have investigated the photophysics of the acetone radical cation in the vacuum ultraviolet energy region by multiphoton ionization combined with time-of-flight mass spectrometry in a cluster beam. We have found that the loss of methyl radical from the acetone radical cations is remarkably suppressed at 10.5 eV when they are solvated by a few neutral acetone molecules. The cluster ion mass spectra obtained by nanosecond and picosecond laser pulses reveal that there are intermolecular processes, occurring in several tens of picoseconds, which are responsible for the survival of the acetone cations in clusters. This remarkable solvation effect on the yield of the methyl radical loss from the acetone cation can be rationalized by the intracluster vibrational energy redistribution and the self-catalyzed enolization which compete with the methyl radical loss process.

Photoelectron Imaging Spectroscopy for (2+1) Resonance-Enhanced Multiphoton Ionization of Atomic Bromine

  • Kim, Yong-Shin;Jung, Young-Jae;Kang, Wee-Kyung;Jung, Kyung-Hoon
    • Bulletin of the Korean Chemical Society
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    • v.23 no.2
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    • pp.189-194
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    • 2002
  • Two-photon resonant third photon ionization of atomic bromine $(4p^5\;^2P_{3/2}\;and\;^2P_{1/2})$ has been studied using a photoelectron imaging spectroscopy in the wavelength region 250 - 278 nm. The technique has yielded simultaneously both relative branching ratios to the three levels of $Br^+(^3P_2,\;^3P_{0.1}\;and^1D_2)$ with $4p^4$ configuration and the angular distributions of outgoing photoelectrons. The product branching ratios reveal a strong propensity to populate particular levels in many cases. Several pathways have been documented for selective formation of $Br^+(^3P_2)$ and $Br^+(^3P_{0.1})$ ions. In general, the final ion level distributions are dominated by the preservation of the ion core configuration of a resonant excited state. Some deviations from this simple picture are discussed in terms of the configuration interaction of resonant states and the autoionization in the continuum. The photoelectron angular distributions are qualitatively similar for all transitions, with a positive $A_2$ anisotropy coefficient of 1.0-2.0 and negligible $A_4$ in most cases, which suggests that the angular distribution is mainly determined by the single-photon ionization process of a resonant excited state induced from the third photon absorption.

Laser Intensity Dependence in Resonant Multiphoton Ionization of Hg Atoms (수은 원자에서의 공명 다광자 이온화 과정의 레이저 강도 의존성)

  • 한재민;정도영;차형기;김철중;이종민
    • Korean Journal of Optics and Photonics
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    • v.1 no.1
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    • pp.7-11
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    • 1990
  • Resonant multi photon ionization (RMPD of Hg atoms is studied by focusing a high-power laser into the ionization cell. The intermediate resonant state is taken as $6d^1D_2$ with the 4-photon resonance wavelength of 560.7 nm. The ionization signal is measured as Hg vapor pressure (0.1-3.0 Torr), laser intensity $(10-120GW/\textrm{cm}^2)$, and laser wavelength (559-569 nm) vary. AC Stark shift and line broadening of the resonant state $(6d^1D_2)$ are observed and the shift factor is measured to be $-0.6(cm^{-1}/GW/\textrm{cm}^2$. It is also observed that the ionization signal increases as the Hg vapor pressure increases up to a certain value of pressure, however, if the pressure further increases, the signal decreases. The order of non-linearity, which discribes the laser intensity dependence of ionization rate, is measured to be 3 at the resonance, and compared with the theoretical results.esults.

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N(2D) Product Velocity Mapped Imaging in the VUV Photolysis of Nitrous Oxide at 118.2 nm

  • Cosofret, Bogdan R.;Lambert, H. Mark;Houston, Paul L.
    • Bulletin of the Korean Chemical Society
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    • v.23 no.2
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    • pp.179-183
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    • 2002
  • Resonance-enhanced multiphoton ionization with time-of-flight product imaging of the $N(^2D)$ atoms has been used to study the $N_2O$ photodissociation at 118.2 nm and the two-photon dissociation at 268.9 nm. These imaging experiments allowed the determination of the total kinetic energy distribution of the $NO(X^2{\prod})$ and $N(^2D_{5/2})$ products. The $NO(X^2{\prod})$ fragments resulting from the photodissociation processes are produced in highly vibrationally excited states. The two-photon photodissociation process yields a broad $NO(X^2{\prod})$ vibrational energy distribution, while the 118.2 nm dissociation appears to produce a vibrational distribution sharply peaked at $NO(X^2{\prod},\;{\nu}=14)$.

Femtosecond Photoelectron Imaging of N2 at 410 nm

  • Guo, Wei;Wei, Shanshan;Lu, Xingqiang;Wang, Li
    • Bulletin of the Korean Chemical Society
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    • v.31 no.12
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    • pp.3693-3696
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    • 2010
  • We experimentally measure the kinetic energy and angular distributions of photoelectrons of $N_2$ as a function of 410 nm femtosecond laser intensity by using velocity map imaging technique. The strong-field multiphoton ionization of molecules shares many of the characteristics with those of atoms. Electron kinetic energies are nearly independent of laser intensities. The independence suggests that the electron peaks in the photoelectron spectrum actually result from a two-step process, indicative of the occurrence of real population in the intermediate states. The relative amplitudes of electron peaks indicate that in the two-step process, nonresonant population transfer dominates for low intensities, while resonant population transfer dominates for higher intensities.