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We study optical field emission from silver nanotips, showing the combined influence of the illumination wavelength and the exact shape of the nanotip on the strong-field response. This is particularly relevant in the case of FIB milled nano tips, where the nanotip fabrication capabilities could become a new ingredient for the study of strong-field physics. The influence of the thermal load on the nanotip and its effect on the emission is studied as well by switching the repetition rate of the laser source from 1 kHz to 62 MHz, showing a clear transition towards the quenching of the strongfield emission.
Bell's inequality violation experiments are becoming increasingly popular in the practical teaching of undergraduate and master's degree students. Bell's parameter S is obtained from 16 polarization correlation measurements performed on entangled photons pairs. We first report here a detailed analysis of the uncertainty u(S) of Bell's parameter taking into account coincidence count statistics and errors in polarizers' orientation. We show using both computational modeling and experimental measurement that the actual sequence of the polarizer settings has an unexpected and strong influence on the error budget. This result may also be relevant to measurements in other settings in which errors in parameters may have non-random effects in the measurement.
We report results of experimental investigation of field electron emission from diamond nanoemitters. The measurements were performed with single crystal diamond needles fixed at tungsten tips. The voltage drop along diamond needles during emission was revealed and measured using electron energy spectroscopy. The observed linear dependence of the voltage drop in diamond on voltage applied to the tungsten tip is explained in the frame of a simple macroscopic electrical model combining Poole–Frenkel conduction along the diamond tip and Fowler–Nordheim tunneling at the diamond-vacuum junction. Experimental evidences of electron emission sensitivity to laser illumination are discussed for possible modification of diamond emitter characteristics and voltage drop.
High-order harmonic generation in polyatomic molecules generally involves multiple channels of ionization. Their relative contribution can be strongly influenced by the presence of resonances, whose assignment remains a major challenge for high-harmonic spectroscopy. Here we present a multi-modal approach for the investigation of unaligned polyatomic molecules, using SF6 as an example. We combine methods from extreme-ultraviolet spectroscopy, above-threshold ionization and attosecond metrology. Fragment-resolved above-threshold ionization measurements reveal that strong-field ionization opens at least three channels. A shape resonance in one of them is found to dominate the signal in the 20–26 eV range. This resonance induces a phase jump in the harmonic emission, a switch in the polarization state and different dynamical responses to molecular vibrations. This study demonstrates a method for extending high-harmonic spectroscopy to polyatomic molecules, where complex attosecond dynamics are expected.
Sujets
Time-resolved photoelectron spectroscopy
Boîte quantique semiconductrice
Chirp modulation rotational states quantum theory energy level crossing laser beams dissociation
Pulse shaping
Acétylène
Atom-photon collisions
ENERGY
Autocorrelation function
Oscillations de Rabi
Photoémission
NO2
Echantillon multidiffusant
ELEMENTAL FRACTIONATION
4265Ky
Interférences de chemins quantiques
Quantum path interferences
Couplage spatio-temporel
XUV
Gauss sums
Champ fort
Adiabatic rapid passage
CYCLIC-N-3
7960Jv
Cold Molecules
Coherent pulse propagation
Génération d'harmoniques d'ordre élevé
Caractérisation spatio-temporelle
Ultraviolet
Femtosecond
Femtoseconde
Passage adiabatique rapide
Extreme ultraviolet
Attoseconde
Rabi oscillations
CHLORINE AZIDE
4230Kq
Femtosecond lasers
Number theory
Femtosecond pulse
CIN3
Anharmonicity
Complete characterization
Mise en forme d'impulsions
Factorisation
Photoemission
Factorization
Transitoires cohérents
Rubidium atom
Cold molecules
Expériences pompe-sonde
7867Pt
ALIGNED MOLECULES
Cold field emission
Femtosecond laser
4225Ja
Bell's inequality
Diamond nanotip
Expérience pompe-sonde
Coherent control
Caractérisation
Emission par champ froid
Diffractive optical element
ClN3
Mise en forme d'impulsion
Dynamique moléculaire
Femtochemistry
Wave packet interferences
Caractérisation complète
Half revival
Excited states sodium
Impulsions à dérive de fréquence
Quantum dots
Femtosecond spectroscopy
Coherent transients
CHARGE-TRANSFER
4265Re
Coherent Transients
Contrôle cohérent
Chlorine azide
Femtosecond pulses
Ultrashort pulses
Pump-probe
Attosecond
Chirped pulses
ATOMS
Velocity map imaging
Contrôle spatio-temporel
Chirped laser pulses
Quantum state measurement
Ultrashort lasers
C2H2
Coherent Transient
Azoture de chlore
Azulene
Optical Parametric Amplifier
AOPDF
Spin-orbit precession
Ultrafast nonlinear optics
Characterisation
Molecular dynamics