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Full-Text Articles in Physics

Ultrafast Two-Photon Free Induction Decay, D. Keusters, Peifang Tian, W. Warren Dec 2002

Ultrafast Two-Photon Free Induction Decay, D. Keusters, Peifang Tian, W. Warren

Peifang Tian

No abstract provided.


Ultrafast Measurement Of Two-Photon Absorption By Loss Modulation, Peifang Tian, Warren Warren Aug 2002

Ultrafast Measurement Of Two-Photon Absorption By Loss Modulation, Peifang Tian, Warren Warren

Peifang Tian

We demonstrate a direct and sensitive technique for measuring two-photon absorption (TPA).An intensity- modulated femtosecond laser beam passes through a sample exhibiting TPA.A TPA signal at twice the modulation frequency is then generated and subsequently measured by a lock-in amplifier. The absolute TPA cross section of Rhodamine 6G at 800nm is found to be 15.32.010 -50 cm 4 s / photon and agrees well with previously published results obtained with much higher intensity [J.Chem.Phys. 112, 9201 (2000)]. Our method may be especially useful in measuring nonlinear absorptions of nonfluorescent materials.


Infrared Depletion Spectroscopy Of Aniline-Acetonitrile Cation And Aniline-Acetonitrile-Water Cation Clusters, H. Nagai, Naveed Piracha, T. Nakanaga Aug 2002

Infrared Depletion Spectroscopy Of Aniline-Acetonitrile Cation And Aniline-Acetonitrile-Water Cation Clusters, H. Nagai, Naveed Piracha, T. Nakanaga

Naveed K. Piracha

The vibrational spectra of the aniline-acetonitrile^+ and the aniline-acetonitrile-water^+ cluster cations have been measured by the infrared depletion spectroscopy in the frequency region of NH and OH stretching vibrations. One absorption band was observed at 3437cm^-^1 in the infrared spectrum of the aniline-acetonitrile^+ cluster cation, and was assigned to the NH stretching vibration of free NH of aniline. As for the aniline-water-acetonitrile^+ cluster cation, three absorptions were observed at 3722, 3634 and 3247cm^-^1, which were assigned to the anti-symmetric stretching and symmetric stretching vibrations of OH of water and the stretching vibrations of NH bond interacting with water, respectively. In …


Infrared Spectroscopy Of Aniline–Ne Clusters And The Corresponding Cluster Cations In The Nh2-Stretching Vibration Region, Naveed Piracha, T. Nakanaga Jun 2002

Infrared Spectroscopy Of Aniline–Ne Clusters And The Corresponding Cluster Cations In The Nh2-Stretching Vibration Region, Naveed Piracha, T. Nakanaga

Naveed K. Piracha

The vibrational spectra of the NH2-stretching modes of aniline–Ne and aniline–Ne+ have been measured using infrared depletion spectroscopy and REMPI–TOF mass spectrometry. In the NH2-stretching vibration region of the aniline–Ne clusters, two absorption bands at 3422 and 3508cm−1 were observed. The frequency shifts from the monomer was found to be negligibly small. As for the aniline–Ne+ cluster cations, the observed frequencies of the vibrational modes were 3394 and 3488cm−1. These values agreed with ones observed for aniline–Ar+ cluster within the error limit. This fact suggests that the effect of neon to aniline in forming the cluster is not significant in …


The Evidence Of The Mode Selectivity Of The Infrared Predissociation Reaction Of The Hydrogen Bonds In The Aniline–Water–Pyrrole Cluster Cation, Taisuke Nakanaga, Naveed Piracha, Fumiyuki Ito Oct 2001

The Evidence Of The Mode Selectivity Of The Infrared Predissociation Reaction Of The Hydrogen Bonds In The Aniline–Water–Pyrrole Cluster Cation, Taisuke Nakanaga, Naveed Piracha, Fumiyuki Ito

Naveed K. Piracha

The infrared spectrum of aniline–water–pyrrole cluster cation has been measured in the 3 μm region. Four strong vibrational bands were observed at 3313, 3515, 3637, and 3721cm−1, and the cluster dissociated into fragments in two reaction paths, AWP+→AW++P and AWP+→AP++W (A: aniline, W: water, P: pyrrole) when it absorbed an infrared photon. The branching ratio (AW+/AP+) has been determined to be 0.20±0.02 for the NH stretching vibration of aniline (3313cm−1, hydrogen-bonded to pyrrole) and 0.14±0.03 for the other three bands. This vibrational mode dependence should be due to the fast energy transfer from the NH to the intermolecular vibration through …


Investigation Of The Structure Of T He Ternary Cluster Of Aniline−Water−Tetrahydrofuran And Its Cation By Infrared Depletion Spectroscopy, Taisuke Nakanaga, Naveed Piracha, Fumiyuki Ito May 2001

Investigation Of The Structure Of T He Ternary Cluster Of Aniline−Water−Tetrahydrofuran And Its Cation By Infrared Depletion Spectroscopy, Taisuke Nakanaga, Naveed Piracha, Fumiyuki Ito

Naveed K. Piracha

No abstract provided.


Femtosecond Polarization Detection Using High-Speed Pulse Shaping, D. Keusters, Peifang Tian, W. Warren Dec 2000

Femtosecond Polarization Detection Using High-Speed Pulse Shaping, D. Keusters, Peifang Tian, W. Warren

Peifang Tian

This book presents the latest advances in ultrafast science, including ultrafast laser and measurement technology as well as studies of ultrafast phenomena. Pico- and femtosecond processes relevant in physics, chemistry, biology and engineering are presented. Ultrafast technology has had a profound impact in a wide range of applications, among them imaging, material diagnostics and transformation and high-speed optoelectronics. This book summarizes the results presented at the 12th Ultrafast Phenomena Conference and reviews the state of the art of this important and rapidly advancing field.


Two-Photon Optogalvanic Spectra Of Argon: Odd Parity Rydberg States, Naveed Piracha, M. Baig, S. Khan, B. Suleman Mar 1997

Two-Photon Optogalvanic Spectra Of Argon: Odd Parity Rydberg States, Naveed Piracha, M. Baig, S. Khan, B. Suleman

Naveed K. Piracha

Extensive new data on the odd-parity, single-colour, two-photon optogalvanic spectra of argon in the visible region is reported using an excimer-pumped dye laser in conjunction with an argon discharge cell. The experimental technique enables us to record a pure two-photon spectrum in a region which is dominated by one-photon transitions. A large number of two-photon transitions, originating from the two metastable states [...] and [...] to the excited states of configurations [...] (J=0, 2) and [...] (J = 0 - 4) of argon, has been recorded and arranged into 10 Rydberg series. The interchannel interactions among the [...] and the …