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Multiphoton Ionisation of Lithium from an optical Dipole Trap

Moritz Weegen

Published Jun 1, 2018• 0 citations
OpenAlex

Abstract

For this Master thesis, multiphoton ionisation processes of Lithium-6 atoms from an optical dipole trap have been investigated and the momentum distributions of the resulting ions over the whole solid angle in a Reaction Microscope have been obtained for the first time. The atoms have first been trapped in a magneto-optical trap, before being transferred into the purely optical dipole trap. Measurements for five different peak intensities in the range of 6:5 x 1013 W=cm2 to 6:5 x 1014 W=cm2 have been carried out, where a femtosecond laser has been used as the projectile beam. The experimentally obtained momentum distributions are consistent with formerly executed comparable experiments and offer a basis for future experiments.

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Reaction microscopes enable kinematically complete measurements of atomic and molecular fragmentation. An ultracold atomic target is usually provided by a supersonic gas jet. The apparatus developed in the course of this thesis for the first time combines the principle of the reaction microscope with a magneto-optical trap. This allows for the preparation of lithium atoms in the sub-mK range. Being a three-electron system, its simple atomic structure makes lithium a model system of great topical interest for all kinds of ionization reactions. In order not to deteriorate the determination of the momenta of the charged fragments by the magnetic field of the trap, a pulsed mode of operation is adopted, creating field-free conditions during data acquisition and making efficient use of the stored target. The novel apparatus provides a versatile target for investigations on fragmentation of lithium by electron, ion and photon impact. For the first time, momentum-resolved measurements on multiphoton ionization in intense laser fields with pulse durations of 25~fs and peak intensities in the range between 10$^{11}$~W/cm$^2$ and 10$^{16}$~W/cm$^2$ were performed. The acquired photoelectron spectra exhibit unexpected structures such as a preferred emission in the direction perpendicular to the laser polarization axis, which are not fully understood yet. Presently, corresponding calculations are being done in several theory groups.

•Jan 1, 2007•3 citations

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In this work, a reaction microscope with a magneto-optical trap for 6Li atoms, was extended by an optical dipole trap in order to be able to investigate in detail laser-induced atomic and molecular ionization dynamics in a cold quantum gas. \nThe optical dipole trap was operated at a full trap depth of 2.3 mK for 6Li atoms and about \n1% of the atoms in the MOT could be transferred into the dipole trap, with 1/e storage times \nexceeding 5 s. The optically trapped ensemble of 6Li atoms was used as a target for ionisation with intensive and broadband femtosecond laser pulses (λ = 750−820 nm, P = 10^11−10^14 W/cm2, Δt = 30 fs) and allowed to perform kinematically complete experiments, in which 6Li+ ions \nas well as photoelectrons were measured coincidentically. \nAs a first application, in this work, a series of association- and ionization mechanisms, which \nled to production of molecular 6Li2+ ions, were investigated with trapped lithium atoms. \nIn photoassociative ionization, two atoms collide, which were previously lifted into the asymptotic 2p − 3s potential energy curve by ladder excitation. During the collision the atoms autoionize into the 12Σg+(6Li2+) groundstate of the molecular ion, since these two potential energy curves exhibit an avoided crossing. This process was observed when magneto-optically trapped atoms were illuminated with the femtosecond laser. \nIn the dipole trap, using single-color photoassociation, excited state molecules were produced \nin high-lying vibrational states 11Σg+(ν = 65) and 13Σg+(v = 57) and spectroscopically investigated. A fraction of the excited state molecules decay via fluorescence into the molecular ground state. The 11Σg+(ν = 38)(6Li2) ground state molecules created via the singlet res- \nonance 11Σu+(ν = 65)(Li∗2) were detected via direct 3 photon ionisation. The momentum spectra show very low kinetic energies for the photo electrons of below 100 meV. Therefore \nin the molecular ion only vibrational states of Li2+ are getting populated, which are directly below the 3-photon transition energy. \nFinally, a stepwise ionization mechanism was identified, which leads into the continuum via \nan intermediate molecular state of 6Li2∗ after photoassociation. The starting point is a pho- \ntoassociated excited state molecule 11Σu+(ν = 65)(6Li∗2), which absorbs two photons of the dipole trap laser (λ = 1070 nm ± 2 nm). This happens via an intermediate molecular state \n31Σg+(2s + 3s), after which it leads into the 12Σg+(6Li2+) potential.

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Coincident detection of recoil ions and photoelectrons after multiphoton-ionisation of cold 6Li atoms trapped in a dipole trap

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Synopsis We report on performing high resolution recoil ion momentum spectroscopy in a reaction microscope (ReMi) on a target of dipole-force trapped cold 6Li atoms in a non-interacting |1〉-|2〉 spin mixture and coincident detection of recoil ions and photoelectrons. Photo-ionization occurs from the electronic ground state of the 6Li atoms and IR photons significantly contribute to the ion yield via 3-photon resonances. High resolution time-of-flight spectra are obtained by modulating the trap depth synced with the arrival of the fs laser pulses.

Journal of Physics Conference Series•Jan 1, 2020•0 citations

Reaction microscope for investigating ionization dynamics of weakly bound alkali dimers

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We report on the implementation of a far-off-resonant, optical dipole force trap in a reaction microscope combined with a magneto-optical trap. Kinematically complete multi-photon ionization experiments were performed on optically trapped 6Li atoms and photo-associated 6Li2 molecules in their highest vibrational state. The apparatus allows us to distinguish different ionization mechanisms related to the presence of the IR field of the optical dipole trap that can occur during ionization of 6Li and 6Li2 in strong fields. In a series of proof-of-principle experiments, we detect weakly bound dimers via three-photon ionization with femtosecond pulses (τ = 30 fs) at a central wavelength of 780 nm and measure directly the momenta of the photoelectrons in coincidence with recoil ions.

Review of Scientific Instruments•Dec 1, 2021•4 citations
For this Master thesis, multiphoton ionisation processes of Lithium-6 atoms from an optical dipole trap have been investigated and the momentum distributions of the resulting ions over the whole solid angle in a Reaction Microscope have been obtained for the first time. The atoms have first been trapped in a magneto-optical trap, before being transferred into the purely optical dipole trap. Measurements for five different peak intensities in the range of 6:5 x 1013 W=cm2 to 6:5 x 1014 W=cm2 have been carried out, where a femtosecond laser has been used as the projectile beam. The experimentally obtained momentum distributions are consistent with formerly executed comparable experiments and offer a basis for future experiments.
Reaction microscopes enable kinematically complete measurements of atomic and molecular fragmentation. An ultracold atomic target is usually provided by a supersonic gas jet. The apparatus developed in the course of this thesis for the first time combines the principle of the reaction microscope with a magneto-optical trap. This allows for the preparation of lithium atoms in the sub-mK range. Being a three-electron system, its simple atomic structure makes lithium a model system of great topical interest for all kinds of ionization reactions. In order not to deteriorate the determination of the momenta of the charged fragments by the magnetic field of the trap, a pulsed mode of operation is adopted, creating field-free conditions during data acquisition and making efficient use of the stored target. The novel apparatus provides a versatile target for investigations on fragmentation of lithium by electron, ion and photon impact. For the first time, momentum-resolved measurements on multiphoton ionization in intense laser fields with pulse durations of 25~fs and peak intensities in the range between 1011^{11}11~W/cm2^22 and 1016^{16}16~W/cm2^22 were performed. The acquired photoelectron spectra exhibit unexpected structures such as a preferred emission in the direction perpendicular to the laser polarization axis, which are not fully understood yet. Presently, corresponding calculations are being done in several theory groups.
In this work, a reaction microscope with a magneto-optical trap for 6Li atoms, was extended by an optical dipole trap in order to be able to investigate in detail laser-induced atomic and molecular ionization dynamics in a cold quantum gas. \nThe optical dipole trap was operated at a full trap depth of 2.3 mK for 6Li atoms and about \n1% of the atoms in the MOT could be transferred into the dipole trap, with 1/e storage times \nexceeding 5 s. The optically trapped ensemble of 6Li atoms was used as a target for ionisation with intensive and broadband femtosecond laser pulses (λ = 750−820 nm, P = 10^11−10^14 W/cm2, Δt = 30 fs) and allowed to perform kinematically complete experiments, in which 6Li+ ions \nas well as photoelectrons were measured coincidentically. \nAs a first application, in this work, a series of association- and ionization mechanisms, which \nled to production of molecular 6Li2+ ions, were investigated with trapped lithium atoms. \nIn photoassociative ionization, two atoms collide, which were previously lifted into the asymptotic 2p − 3s potential energy curve by ladder excitation. During the collision the atoms autoionize into the 12Σg+(6Li2+) groundstate of the molecular ion, since these two potential energy curves exhibit an avoided crossing. This process was observed when magneto-optically trapped atoms were illuminated with the femtosecond laser. \nIn the dipole trap, using single-color photoassociation, excited state molecules were produced \nin high-lying vibrational states 11Σg+(ν = 65) and 13Σg+(v = 57) and spectroscopically investigated. A fraction of the excited state molecules decay via fluorescence into the molecular ground state. The 11Σg+(ν = 38)(6Li2) ground state molecules created via the singlet res- \nonance 11Σu+(ν = 65)(Li∗2) were detected via direct 3 photon ionisation. The momentum spectra show very low kinetic energies for the photo electrons of below 100 meV. Therefore \nin the molecular ion only vibrational states of Li2+ are getting populated, which are directly below the 3-photon transition energy. \nFinally, a stepwise ionization mechanism was identified, which leads into the continuum via \nan intermediate molecular state of 6Li2∗ after photoassociation. The starting point is a pho- \ntoassociated excited state molecule 11Σu+(ν = 65)(6Li∗2), which absorbs two photons of the dipole trap laser (λ = 1070 nm ± 2 nm). This happens via an intermediate molecular state \n31Σg+(2s + 3s), after which it leads into the 12Σg+(6Li2+) potential.
In the course of this work dynamics in ionization processes of lithium by photon and electron impact were studied. Due to its electronic structure, lithium is an ideal candidate to examine electronic correlation effects and collision dynamics of simple few-body systems. The lithium target is cooled in a magneto-optical trap (MOT) down to the sub-millikelvin regime, which in combination with a reaction microscope (ReMi) allows for the determination of the momentum information of all collision products with unprecedented resolution. An electron gun serving as a new projectile source was implemented in the MOTReMi experiment. From first measurements, which showed that the developed setup is principally operational, time-of-flight and position spectra were analyzed, determining the ratio of Li2+=Li+ ion creation. In a second series of experiments, photoionization of laser-excited lithium has been investigated and fully differential cross sections (FDCS) were examined. As the target and also the laser beam were polarized, orientational effects could be studied. In some cases the electron emission characteristics could directly be deduced from dipole selection rules.
A reaction microscope (ReMi) has been combined with a magneto-optical trap (MOT) for the kinematically complete investigation of atomic break-up processes. With the novel MOTReMi apparatus, the momentum vectors of the fragments of laser-cooled and state-prepared lithium atoms are measured in coincidence and over the full solid angle. The first successful implementation of a MOTReMi could be realized due to an optimized design of the present setup, a nonstandard operation of the MOT, and by employing a switching cycle with alternating measuring and trapping periods. The very low target temperature in the MOT (∼2 mK) allows for an excellent momentum resolution. Optical preparation of the target atoms in the excited Li 2(2)P3/2 state was demonstrated providing an atomic polarization of close to 100%. While first experimental results were reported earlier, in this work, we focus on the technical description of the setup and its performance in commissioning experiments involving target ionization in 266 nm laser pulses and in collisions with projectile ions.
Synopsis We report on performing high resolution recoil ion momentum spectroscopy in a reaction microscope (ReMi) on a target of dipole-force trapped cold 6Li atoms in a non-interacting |1〉-|2〉 spin mixture and coincident detection of recoil ions and photoelectrons. Photo-ionization occurs from the electronic ground state of the 6Li atoms and IR photons significantly contribute to the ion yield via 3-photon resonances. High resolution time-of-flight spectra are obtained by modulating the trap depth synced with the arrival of the fs laser pulses.
We report on the implementation of a far-off-resonant, optical dipole force trap in a reaction microscope combined with a magneto-optical trap. Kinematically complete multi-photon ionization experiments were performed on optically trapped 6Li atoms and photo-associated 6Li2 molecules in their highest vibrational state. The apparatus allows us to distinguish different ionization mechanisms related to the presence of the IR field of the optical dipole trap that can occur during ionization of 6Li and 6Li2 in strong fields. In a series of proof-of-principle experiments, we detect weakly bound dimers via three-photon ionization with femtosecond pulses (τ = 30 fs) at a central wavelength of 780 nm and measure directly the momenta of the photoelectrons in coincidence with recoil ions.