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Scalable microchip ion traps and guides for cold molecular ions

Arezoo Mokhberi

Published Jan 1, 2016• 1 citation
Publisher

Abstract

Sympathetic cooling and Coulomb crystallisation of molecular ions above the \nsurface of an ion-trap chip were demonstrated. N2+ and CaH+ ions were confined \nin a surface-electrode radiofrequency ion trap and cooled by the interaction \nwith laser-cooled Ca+ ions to secular translational temperatures in the \nmilliKelvin range. The configuration of trapping potentials generated by the surface \nelectrodes enabled the formation of planar bicomponent Coulomb crystals \nand the spatial separation of the molecular from the atomic ions. The structural \nand thermal properties of the crystals were characterized using molecular \ndynamics simulations. The effects of trap anharmoncities on the shape and \nenergy of bicomponent crystals were theoretically investigated. It was shown \nthat the trapping potentials can also deliberately be engineered to spatially \nseparate ion species in bicomponent crystals. Furthermore, a multi-functional \nsurface-electrode radiofrequency ion-trap chip has been developed to enable experiments \nwith cold molecular ions using a monolithic device. The chip was \ndesigned to combine various tasks such as loading and preparation of ions, mass \nspectrometry, spectroscopy, reaction studies, and manipulation of ion crystals \nin a miniaturised device. This chip features carefully engineered ion channel \nintersections that enable transporting sympathetically cooled molecular ions in \nthe form of bicomponent crystals. A detailed description of the fabrication and \nsimulation of the two chips are presented. The present study extends chipbased \ntrapping techniques to Coulomb-crystallised molecular ions with potential \napplications in mass spectrometry, cold chemistry, quantum technology, and \nspectroscopy.

DOI
10.5451/unibas-006656237

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•Jan 1, 2015•0 citations
Sympathetic cooling and Coulomb crystallisation of molecular ions above the \nsurface of an ion-trap chip were demonstrated. N2+ and CaH+ ions were confined \nin a surface-electrode radiofrequency ion trap and cooled by the interaction \nwith laser-cooled Ca+ ions to secular translational temperatures in the \nmilliKelvin range. The configuration of trapping potentials generated by the surface \nelectrodes enabled the formation of planar bicomponent Coulomb crystals \nand the spatial separation of the molecular from the atomic ions. The structural \nand thermal properties of the crystals were characterized using molecular \ndynamics simulations. The effects of trap anharmoncities on the shape and \nenergy of bicomponent crystals were theoretically investigated. It was shown \nthat the trapping potentials can also deliberately be engineered to spatially \nseparate ion species in bicomponent crystals. Furthermore, a multi-functional \nsurface-electrode radiofrequency ion-trap chip has been developed to enable experiments \nwith cold molecular ions using a monolithic device. The chip was \ndesigned to combine various tasks such as loading and preparation of ions, mass \nspectrometry, spectroscopy, reaction studies, and manipulation of ion crystals \nin a miniaturised device. This chip features carefully engineered ion channel \nintersections that enable transporting sympathetically cooled molecular ions in \nthe form of bicomponent crystals. A detailed description of the fabrication and \nsimulation of the two chips are presented. The present study extends chipbased \ntrapping techniques to Coulomb-crystallised molecular ions with potential \napplications in mass spectrometry, cold chemistry, quantum technology, and \nspectroscopy.
We report the sympathetic cooling and Coulomb crystallization of molecular ions above the surface of an ion-trap chip. N2+{\mathrm{N}}_{2}^{+}N2+​ and CaH+{\mathrm{CaH}}^{+}CaH+ ions were confined in a surface-electrode radio-frequency (rf) ion trap and cooled by the interaction with laser-cooled Ca+{\mathrm{Ca}}^{+}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.
Cold molecular ions are of great interest for applications in cold collision studies, chemistry, precision spectroscopy and quantum technologies. In this context, sympathetic cooling of molecular ions by the interaction with laser-cooled atomic ions is a powerful method to cool their translational motion and achieve translational temperatures in the millikelvin range. Recently, we implemented this method in a surface-electrode ion trap. The flexibility in shaping the trapping potentials offered by the surface-electrode structure enabled us to generate planar bicomponent Coulomb crystals and spatially separate the molecular from the atomic ions. Here, we present a detailed description of the fabrication and simulation of the trap as well as a theoretical and experimental investigation of the structural and energetic properties of the Coulomb crystals obtained in the device. We discuss in more detail the separation of different ion species using static electric fields and explore the effects of trap anharmoncities on the shape of bicomponent crystals.
We discuss the design and optimisation of two types of junctions between surface-electrode radiofrequency ion-trap arrays that enable the integration of experiments with sympathetically cooled molecular ions on a monolithic chip device. A detailed description of a multi-objective optimisation procedure applicable to an arbitrary planar junction is presented, and the results for a cross junction between four quadrupoles as well as a quadrupole-to-octupole junction are discussed. Based on these optimised functional elements, we propose a multi-functional ion-trap chip for experiments with translationally cold molecular ions at temperatures in the millikelvin range. This study extends complex chip-based trapping techniques to Coulomb-crystallised molecular ions with potential applications in mass spectrometry, spectroscopy, controlled chemistry and quantum technology.
Translationally cold, spatially localised molecular ions prepared by sympathetic cooling with laser-cooled atomic ions in ion traps have recently found a wide range of applications in both chemistry and physics. The very low temperatures of the ions (down to millikelvins), their tight localisation in the trap and the ability to control and manipulate single isolated molecules on the quantum level offer intriguing possibilities for new experiments in the realms of cold chemistry, precision molecular spectroscopy, mass spectrometry and quantum technology. The present article gives an overview of the basic experimental methods, current topics and recent developments in this field.
Ensembles of cold atomic and molecular ions in ion traps prepared at millikelvin temperatures by laser and sympathetic cooling have recently found considerable interest in both physics and chemistry. At very low temperatures the ions form ordered structures in the trap also known as "Coulomb crystals". Ion Coulomb crystals exhibit a range of intriguing properties which render them attractive systems for novel experiments in chemical dynamics, ultrahigh-resolution spectroscopy and quantum-information processing. In this article we review the methods used to prepare atomic and molecular ion Coulomb crystals and discuss some recent studies in mass spectrometry, low-temperature chemistry and precision spectroscopy to illustrate their scientific potential for chemical applications. Finally, we conclude with an outlook on outstanding challenges and prospective further developments in the field.
A promising new approach for studying cold ion-molecule chemical reactions is the combination of laser- or sympathetically-cooled trapped ions and slow-moving molecules from a cold molecule source, such as a quadrupole velocity selector or a Stark decelerator. Previous reaction studies using trapped atomic ions and slow molecules from a quadrupole velocity selector were able to reach average collision energies as low as 1 K. However, the guided molecules had an approximately room temperature rotational energy distribution, so the reactions studied were not truly cold. Thus, a new molecular source for producing translationally and rotationally cold molecules utilizing buffer gas cooling and quadrupole velocity selection was constructed by K. Twyman and characterized for use in cold reaction studies. This new source of cold molecules is referred to as the buffer gas guide. A new ion trap has been designed and built for use with the existing buffer gas guide. The new ion trap apparatus is compact and mechanically compatible with this new guide. It uses a linear Paul ion trap with cylindrical electrodes to trap ions. Two optical axes (one axial and one radial) enable efficient cooling of small ion crystals. A field-free time-of-flight tube and ion detection assembly are also incorporated into the apparatus. A new technique for determining the mass and quantity of trapped ions has also been developed, termed digital ion trap mass spectrometry. The new technique uses a digital RF waveform to trap ions before ejecting the ions radially from the trap using an ejection pulse applied to the trap electrodes. The ions are then detected after free flight along a time-of-flight tube. This technique was characterized by ejecting crystals of various sizes and compositions: Ca+ only, Ca+/CaF +, Ca+/CaOH +/CaOD+, and Ca+/NH +3 /NH +4 /H3O+. A linear relationship between the number of ions ejected (determined by comparing experimental and simulated crystal images) and the integral of the time-of-flight peak was observed for Ca+ and Ca+/CaF +. All mass peaks were resolved. Simulations of the trapped ions and their trajectories through the time-of-flight tube were also performed, and excellent agreement between the simulated and experimental mass resolution was observed. Progress towards combining the buffer gas guide with the previously independent ion trap is also presented. It is anticipated that the combined buffer gas guide ion trap apparatus will enable the study of ion-molecule reactions at low temperatures with translationally and rotationally cold molecules. It is anticipated that the new digital ion trap mass spectrometry technique will simplify the study of reactions when multiple product ions whose masses are separated by only 1 AMU are formed. A new ion trap has been designed and built for use with the existing buffer gas guide. The new ion trap apparatus is compact and mechanically compatible with this new guide. It uses a linear Paul ion trap with cylindrical electrodes to trap ions. Two optical axes (one axial and one radial) enable efficient cooling of small ion crystals. A field-free time-of-flight tube and ion detection assembly are also incorporated into the apparatus. A new technique for determining the mass and quantity of trapped ions has also been developed, termed digital ion trap mass spectrometry. The new technique uses a digital RF waveform to trap ions before ejecting the ions radially from the trap using an ejection pulse applied to the trap electrodes. The ions are then detected after free flight along a time-of-flight tube. This technique was characterized by ejecting crystals of various sizes and compositions: Ca+ only, Ca+/CaF+, Ca+/CaOH+/CaOD+, and Ca+/NH+3/NH+4/H3O+. A linear relationship between the number of ions ejected (determined by comparing experimental and simulated crystal images) and the integral of the time-of-flight peak was observed for Ca+ and Ca+/CaF+. All mass peaks were resolved. Simulations of the trapped ions and their trajectories through the time-of-flight tube were also performed, and excellent agreement between the simulated and experimental mass resolution was observed. Progress towards combining the buffer gas guide with the previously independent ion trap is also presented. It is anticipated that the combined buffer gas guide ion trap apparatus will enable the study of ion-molecule reactions at low temperatures with translationally and rotationally cold molecules. It is anticipated that the new digital ion trap mass spectrometry technique will simplify the study of reactions when multiple product ions whose masses are separated by only 1 AMU are formed.