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Recoil splitting of x-ray-induced optical fluorescence
KTH, Skolan för bioteknologi (BIO), Teoretisk kemi (stängd 20110512).
KTH, Skolan för bioteknologi (BIO), Teoretisk kemi (stängd 20110512).
St Petersburg Universitet.
KTH, Skolan för bioteknologi (BIO), Teoretisk kemi (stängd 20110512).ORCID-id: 0000-0002-1763-9383
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2010 (Engelska)Ingår i: Physical Review A. Atomic, Molecular, and Optical Physics, ISSN 1050-2947, E-ISSN 1094-1622, Vol. 81, nr 3, artikel-id 035401Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

We show that the anisotropy of the recoil velocity distribution of x-ray-ionized atoms or molecules leads to observable splittings in subsequent optical fluorescence or absorption when the polarization vector of the x rays is parallel to the momentum of the fluorescent photons. The order of the magnitude of the recoil-induced splitting is about 10 mu eV, which can be observed using Fourier or laser-absorption spectroscopic techniques.

Ort, förlag, år, upplaga, sidor
2010. Vol. 81, nr 3, artikel-id 035401
Nyckelord [en]
Photoion Rotational Distributions
Nationell ämneskategori
Industriell bioteknik
Identifikatorer
URN: urn:nbn:se:kth:diva-14110DOI: 10.1103/PhysRevA.81.035401ISI: 000276262500238Scopus ID: 2-s2.0-77949744532OAI: oai:DiVA.org:kth-14110DiVA, id: diva2:329814
Forskningsfinansiär
VetenskapsrådetCarl Tryggers stiftelse för vetenskaplig forskning
Anmärkning

QC 20100713

Tillgänglig från: 2010-07-13 Skapad: 2010-07-13 Senast uppdaterad: 2017-12-12Bibliografiskt granskad
Ingår i avhandling
1. Molecular electronic,  vibrational and rotational motion in optical and x-ray fields
Öppna denna publikation i ny flik eller fönster >>Molecular electronic,  vibrational and rotational motion in optical and x-ray fields
2009 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

The subject of this theoretical  study is the role ofelectronic structure as well as of rotational and vibrational motionson interactions between molecules and electromagnetic radiation,ranging from optical to x-ray. The thesis concerns both linear and nonlinear regimes of the light-matter interaction. The first part of the thesis is devoted to propagation of opticalpulses with different time-structure through various nonlinear absorbers.First we explain the double-exponential decay of fluorescence caused by photobleaching of pyrylium  salt irradiated by a train of short (100 fs) optical pulses. The main reason for this effect is the transversal inhomogeneity of the light beam which makes the dynamics of the photobleaching differ in the core of the pulse and on its periphery. We also explore the optical power limitingof C60 fullerene irradiated by either microsecond optical pulses or a picosecond pulse trains. Enhancement of nonlinear absorption is caused by strong triplet-triplet absorption that becomes important due toelongation of the interaction time.Here we show the importance of the repetitionrate for the optical power limiting performance.The second part of the thesis addresses the interaction of optical and x-rayfields with rotational degrees of freedom of molecules. In this part the main attention is paid to the rotational heating caused by the recoil, experienced by molecules due to the ejection of photoelectrons. We have quantitatively explained two qualitatively different experiments with the N2 molecule.We predict the interference modulation of the recoil-induced shift,which is a shift of the photoelectron line caused by the rotational recoil effect, as a function of the photon energy.The developed theory also explains the rotational heating ofmolecules observed in the optical fluorescence induced by x-ray radiation.Based on this explanation, we suggest a new scheme of the optical fluorescence induced by x-rays that allows to detect the recoil effect via the recoil-inducedsplitting of the optical resonance.The last part of the thesis focuses on multi-mode nuclear dynamics of the resonant Auger scattering from the C2H2 molecule, that was the subject of a recent experimental study.Here we develop a theory that explains the observed vibrationalscattering anisotropy. We have found that three qualitatively different mechanisms are responsible for this phenomenon. The first mechanism is the interference of the direct and resonance scattering channels. The second mechanismis the interference of the resonant scattering channels through core excitedstate with the orthogonal orientation of the vibrational modes of core excitedstate. The Young's double slit like interference of the quantum pathways through the double-well potential of the bending motion of core excited state is the third mechanism of the vibrational scattering anisotropy.

Ort, förlag, år, upplaga, sidor
Stockholm: KTH, 2009. s. viii, 67
Serie
Trita-BIO-Report, ISSN 1654-2312 ; 2009:24
Nyckelord
x-ray, nonlinear optics, photobleaching, recoil, anisotropy, Auger
Nationell ämneskategori
Atom- och molekylfysik och optik
Identifikatorer
urn:nbn:se:kth:diva-11386 (URN)978-91-7415-483-2 (ISBN)
Disputation
2009-12-01, FB 53, AlbaNova, Roslagstullsbacken 21, Stockholm, 10:00 (Engelska)
Opponent
Handledare
Anmärkning
QC 20100713Tillgänglig från: 2009-11-10 Skapad: 2009-11-03 Senast uppdaterad: 2011-11-23Bibliografiskt granskad

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Ågren, Hans

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Gavrilyuk, SergeySun, YupingÅgren, HansGelmukhanov, Faris
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Teoretisk kemi (stängd 20110512)
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Physical Review A. Atomic, Molecular, and Optical Physics
Industriell bioteknik

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