This paper presents the first sympathetic cooling of molecular ions using laser-cooled atomic ions. To this end, we developed a novel combination of sympathetic cooling and in situ mass spectroscopy that allows the use of laser-cooled atomic ions to detect sympathetically-cooled molecular ions non-destructively. We demonstrate this technique by cooling and mass-analysing ions of ultra-high-vacuum residual gas and externally introduced air in situ with less than 80 ions each, confined in a radio-frequency quadrupole (RFQ). This capability to detect and identify sympathetically-cooled molecules with potentially-high sensitivity in situ in an RFQ should be useful for molecular spectroscopy, chemical analysis and study of cold molecules and clusters.
This paper presents the first sympathetic cooling of molecular ions using laser-cooled atomic ions. To this end, we developed a novel combination of sympathetic cooling and in situ mass spectroscopy that allows the use of laser-cooled atomic ions to detect sympathetically-cooled molecular ions non-destructively. We demonstrate this technique by cooling and mass-analysing ions of ultra-high-vacuum residual gas and externally introduced air in situ with less than 80 ions each, confined in a radio-frequency quadrupole (RFQ). This capability to detect and identify sympathetically-cooled molecules with potentially-high sensitivity in situ in an RFQ should be useful for molecular spectroscopy, chemical analysis and study of cold molecules and clusters.
We formulated a model to reproduce the spectral shape of in situ mass spectra of sympathetically cooled molecular ions trapped in a linear radio-frequency-quadrupole. The molecular ions are sympathetically cooled by laser cooled ions. The mass spectrum is obtained by observing fluorescence emitted from the laser-cooled ions as we excite the resonant motion of the sympathetically cooled molecular ions in the trap. The model, which uses a pseudopotential and space-charge approach, reproduces the mass spectra of molecules. The model suggests that the variation of the space-charge density of the laser-cooled ions can produce in-trap kinetic excitation without the loss of the excited ions from the trap.
Trapping molecular ions that have been sympathetically cooled with laser-cooled atomic ions is a useful platform for exploring cold ion chemistry. We designed and characterized a new experimental apparatus for probing chemical reaction dynamics between molecular cations and neutral radicals at temperatures below 1 K. The ions are trapped in a linear quadrupole radio-frequency trap and sympathetically cooled by co-trapped, laser-cooled, atomic ions. The ion trap is coupled to a time-of-flight mass spectrometer to readily identify product ion species and to accurately determine trapped ion numbers. We discuss, and present in detail, the design of this ion trap time-of-flight mass spectrometer and the electronics required for driving the trap and mass spectrometer. Furthermore, we measure the performance of this system, which yields mass resolutions of m/Δm ≥ 1100 over a wide mass range, and discuss its relevance for future measurements in chemical reaction kinetics and dynamics.
One of the current themes in quantum physics is the creation of cold ( 1 K) molecules to study molecule-molecule, molecule-atom, and molecule-radiation interactions under these novel low-temperature conditions. This book highlights the field of cold trapped molecular ions. In particular, the development of a novel, universal cooling method for charged particles, sympathetic cooling using laser-cooled atoms, together with the experimental and computational techniques required are extensively reviewed. The book also reviews first spectacular applications of the cold ion ensembles produced: the study of the properties of cold non-neutral plasmas, the study of ion-neutral chemical reactions and of photodissociation processes, and high-resolution rotational overtone spectroscopy of cold hydrogen molecular ions with unprecedented spectral resolution. The large potential of this field of research and its possible impact to other fields of physics, chemistry, and biology are highlighted. The book summarizes the main lines of research in cold trapped molecular ion physics, thus, making it useful as an introduction for advanced students and experienced researchers.
This work presents various novel results in the field of experimental and theoretical trapped ion studies. All investigations involve laser-cooled 138Ba+ ions confined in a linear quadrupole ion trap, which serve as coolant for complex molecular ions, as target for collisions with neutral atoms, or as model system in theoretical analyses. The special feature of the apparatus used in this work, is a molecular ion source based on electrospray ionization that allows for the production of gas-phase molecular ions of almost arbitrary species with a maximum mass-to-charge ratio of 2,000 Da. Trapped together with laser-cooled 138Ba+ ions, the molecular ions can be cooled down, kept cold and investigated for many minutes and in principle for up to hours in a nearly collisionless environment.
In this work, the sympathetic cooling of complex molecular ions to translational temperatures below 1 K is demonstrated for different types of molecules covering a mass range from 182 to 12,400 Da. Using the example of the protein cytochrome c, with a mass of about 12,400 Da the most massive molecular species sympathetically cooled in an ion trap so far, the methods for detection of successful trapping and cooling, and temperature determination are presented in detail. In one case, multiply protonated molecules of the protein cytochrome c have been cooled to less than 0.75 K. Furthermore, two methods for measuring photodestruction rates of cold, trapped complex molecular ions have been developed that can, for example, be applied in destructive spectroscopy schemes. Both techniques are demonstrated using the example of singly protonated glycyrrhetinic acid molecules (GAH+) dissociated by an ultraviolet (UV) laser. Measurements of the photodestruction rate were performed at different intensities of the UV laser, and rates as low as 0.05 s-1 and less have been determined, which is only possible due to the long ion storage times that can be achieved with this apparatus. For the UV laser wavelength of 266 nm, a destruction cross section of (1.1±0.1)∙10E-17 cm2 for GAH+ has been determined.
In this work, feasibility studies towards internal cooling of trapped complex molecular ions have been performed. Such an additional internal cooling could be realized via collisions with laser-cooled neutral atoms. To test their suitability, neutral atoms of Li, Na, K, Rb, Cs, and Yb have been collided with trapped laser-cooled and not cooled Ba+ ions as well as with complex molecular ions. For all species charge exchange reactions with Ba+ ions have been observed excluding these species for collisional cooling. While K, Rb, and Cs showed charge exchange reactions with ground state and laser-excited Ba+ ions, the charge exchange rates of Yb and Ba+ were found to be state dependent. Collisions of neutral Yb atoms were found to be reactive and lead to the formation of adducts and fragments, in contrast to the alkali metals for which no such reactions have been observed. In addition, the motion of cooled, trapped ions has been studied theoretically via simulations. When the translational energy of a trapped ion ensemble is sufficiently reduced, a first-order phase transition from a liquid to a solid state occurs with the ion ensemble changing from a disordered ion cloud to an ordered ion crystal. As ions in a linear quadrupole trap arrange in shell structures, a free motion in radial direction is disabled, and ions can only move to neighboring shells when their kinetic energy is high enough to overcome a certain potential barrier. The simulations have shown that intershell diffusion rates in the considered ion crystals increase exponentially when the ion temperatures exceed values that well agree with the predictions of other established models. Ion ensembles of different ion numbers (300, 500, and 1000 138Ba+ ions) and symmetries (prolate and spherical) have been investigated showing a clear tendency for the phase transition temperatures: The higher the ion number, the lower is the transition temperature.
Trapped laser-cooled atomic ions are a new tool for understanding cold molecular ions. The atomic ions not only sympathetically cool the molecular ions to millikelvin temperatures, but the bright atomic ion fluorescence can also serve as a detector of both molecular reactions and molecular spectra. We are working towards the detection of single molecular ion spectra by sympathetic heating spectroscopy. Sympathetic heating spectroscopy uses the coupled motion of two trapped ions to measure the spectra of one ion by observing changes in the fluorescence of the other ion. Sympathetic heating spectroscopy is a generalization of quantum logic spectroscopy, but does not require ions in the motional ground state or coherent control of the ion internal states. We have recently demonstrated this technique using two isotopes of Ca+ [Phys. Rev. A, 81, 043428 (2010)]. Limits of the method and potential applications for molecular spectroscopy are discussed.
We report the sympathetic cooling and Coulomb crystallization of molecular ions above the surface of an ion-trap chip. N2+ and CaH+ ions were confined in a surface-electrode radio-frequency (rf) ion trap and cooled by the interaction with laser-cooled Ca+ ions to secular translational temperatures in the millikelvin range. The configuration of trapping potentials generated by the surface electrodes enabled the formation of planar bicomponent Coulomb crystals and the spatial separation of the molecular from the atomic ions on the chip. The structural and thermal properties of the Coulomb crystals were characterized using molecular dynamics simulations. The present study extends chip-based trapping techniques to cold molecular ions with potential applications in mass spectrometry, chemistry, quantum information science, and spectroscopy.