Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

arXiv:2008.11407 · Physical Review Applied

Trapping, Cooling, and Photodissociation Analysis of State-Selected H2+ Ions Produced by ( 3+1 ) Multiphoton Ionization

Julian Schmidt, Thomas Louvradoux, Johannes Heinrich, Nicolas Sillitoe, Malcolm Simpson, Jean‐Philippe Karr, Laurent Hilico

Published Aug 19, 2020• 31 citations
arXivHTMLPDF

Abstract

We report on the production of cold, state-selected ${\mathrm{H}}_{2}^{+}$ molecular ions in a linear rf trap. The ions are produced by ($3+1$) resonance-enhanced multiphoton ionization (REMPI) of ${\mathrm{H}}_{2}$, and sympathetically cooled by laser-cooled ${\mathrm{Be}}^{+}$ ions. After demonstrating and characterizing the REMPI process, we use photodissociation by a deep UV laser at 213 nm to verify the high vibrational purity of the produced ${\mathrm{H}}_{2}^{+}$ ion samples. Moreover, the large difference between the photodissociation efficiencies of ions created in the $v=0$ and $v=1$ levels provides a way to detect a $v=0\ensuremath{\rightarrow}1$ transition. These results pave the way towards high-resolution vibrational spectroscopy of ${\mathrm{H}}_{2}^{+}$ for fundamental metrology applications.

DOI
10.1103/physrevapplied.14.024053

Related papers

An efficient preparation of HD+ molecular ions in an ion trap by REMPI

Yong Zhang, Qian-Yu Zhang, Wen-Li Bai +3 more

We report a method of efficiently generating ultracold hydrogen molecular ions HD+ in a segmented linear ion trap. HD+ ions are created by [2+1′] resonance-enhanced multiphoton ionization (REMPI) of an HD supersonic molecular beam, and sympathetically cooled by laser-cooled Be+ ions. The HD+ ions are generated species-selectively using 201 nm and 395 nm pulse lasers with energies of 0.08 mJ (5.1 × 106 W/cm2) and 1.5 mJ (9.5 × 107 W/cm2) respectively. The average loading rate of 4.3(2) HD+ ions per second in the ion trap is determined by comparing the experimental images with the simulated images of Be+-HD+ bi-component Coulomb crystals. This method paves a way to produce the state-selected HD+ ions, which can improve the signal strengths of the selected rovibrational transitions of HD+ ions.

Chinese Journal of Physics•Jan 13, 2023•7 citations

Production de source sélectives des ions H2+ et simulations numériques de refroidissement sympathique dans les pièges de radio fréquence

Nicolas Sillitoe

The high-resolution ro-vibrational spectroscopy of the H2+ molecular ion by resonance-enhanced multiphoton dissociation (REMPD) requires a state-selective source of H2+. In this thesis we present work on a functional state selective H2+ ion source using resonance enhanced multiphoton ionisation (REMPI) with a 303 nm pulsed laser.The second part of the thesis presents numerical simulations of sympathetic cooling in linear RF traps, whose main application is the GBAR project (Gravitational Behaviour of Antihydrogen at Rest) which involves sympathetic cooling of an antimatter H̄+ ion by laser-cooled Be+ ions. We developed a GPU code using a variable timestep technique enabling a fast description of Coulomb interactions. We discuss the influence of RF heating and scaling laws between cooling times, initial energy and ion numbers in the cooling crystal. We show that the H̄ sympathetic cooling step of GBAR could be feasible using a rotationally asymmetric two-component Be+/HD+ crystal which appears more effective than a single-component Be+ crystal. We find that the H̄+ ion’s capture by this crystal could be detected experimentally by Fourier analysis of the fluorescence data.

•Nov 16, 2017•0 citations

Rovibrational spectroscopy of trapped molecular hydrogen ions at millikelvin temperatures

Bernhard Roth, Jeroen C. J. Koelemeij, H. Daerr +1 more

We report a high-resolution spectroscopic study of molecular ions at millikelvin temperatures. We measured several rovibrational infrared transitions in $\mathrm{H}{\mathrm{D}}^{+}$ molecular ions, stored in a radio-frequency trap and sympathetically cooled to $\ensuremath{\approx}20\phantom{\rule{0.3em}{0ex}}\mathrm{mK}$ by laser-cooled ${\mathrm{Be}}^{+}$ ions. We observed hyperfine splitting of the lines, in good agreement with theoretical predictions. The transitions were detected by monitoring the decrease in ion number after selective photodissociation of $\mathrm{H}{\mathrm{D}}^{+}$ ions in the upper vibrational state. The method described here is expected to be generally applicable.

Physical Review A•Oct 6, 2006•74 citations

A Be+ Ion Trap for H2+ Spectroscopy

Johannes Heinrich

The objective of the project is to perform high-resolution Doppler-free two-photon vibrational spectroscopy of the H2+ molecular ion for accurate electron to proton mass ratio determination. Trapping and laser-cooling of the H2+ ions is necessary. Since H2+ molecular ions cannot be directly laser cooled, a solution is the implementation of sympathetic cooling via a laser cooled Be+ ions. In the first part of this thesis the design and implementation of a linear Paul trap is presented. This trap is suitable to confine H2+ and Be+ ions while allowing good optical access for multiple laser sources and the imaging system. The second part describes a low power, diode based laser system to provide narrow linewidth 626nm light, and a high power, fiber laser based laser system. Subsequently, a bow-tie cavity is presented to frequency double the 626nm light to obtain 313nm light for Be+ Doppler-cooling. In the last part the operational readiness of the trap and the fiber laser based 313nm laser source is demonstrated by the observation of Be+ Coulomb crystals. Electron impact ionization of H2 present in the residual gas allows to observe sympathetic cooling and shows that the developed setup can provide the experimental conditions for precision spectroscopy of H2+.

•Apr 13, 2018•1 citation

Ultracold molecular hydrogen ions in a linear radiofrequency trap: Novel systems for molecular frequency metrology

Bernhard Roth, H. Daerr, Jeroen C. J. Koelemeij +2 more

We have measured the ro-vibrational infrared transition (v = 0, J = 2) → (v = 4, J = 1) in ultracold HD+ molecular ions embedded inside Be+ Coulomb crystals, by 1+1 REMPI spectroscopy. The molecular ions, trapped in a linear radiofrequency trap, were cooled to temperatures of few tens of mK, via sympathetic cooling using laser-cooled Be+ ions. For detection, we have used secular excitation of the HD+ ions to monitor their loss rate. The transition frequency agrees with a theoretical prediction.

European Frequency and Time Forum•Mar 27, 2006•1 citation

Blackbody-radiation mediated quantum state preparation by dissociation and two-photon rotational spectroscopy scheme with cold HD+ ions

Florin Lucian Constantin

Hydrogen molecular ions play an important role for accurate quantum electrodynamics calculations of rovibrational energy levels [1] and the comparison with laser spectroscopy results [2] allowed probing fundamental physics constants and laws. Advances are driven by an accurate control of the external and internal molecular degrees of freedom with a wide range of techniques [3]. Experimental setups with HD+ions are based on ions in a linear Paul trap and sympathetically cooled to the Lamb-Dick confinement regime by a laser-cooled atomic ion (Be+). Optical transitions allowed rotational cooling [4] and state-resolved detection by resonant-enhanced-multiphoton dissociation (REMPD) [5]. This contribution reports numerical results on the use of a two-photon rotational transition in the terahertz frequency range for preparation of trapped HD+ions in the rovibrational ground state and for high-resolution spectroscopy.

Conference on Lasers and Electro-Optics Europe & European Quantum Electronics Conference (CLEO/Europe-EQEC)•Jun 1, 2017•0 citations
We report on the production of cold, state-selected H2+{\mathrm{H}}_{2}^{+}H2+​ molecular ions in a linear rf trap. The ions are produced by (3+13+13+1) resonance-enhanced multiphoton ionization (REMPI) of H2{\mathrm{H}}_{2}H2​, and sympathetically cooled by laser-cooled Be+{\mathrm{Be}}^{+}Be+ ions. After demonstrating and characterizing the REMPI process, we use photodissociation by a deep UV laser at 213 nm to verify the high vibrational purity of the produced H2+{\mathrm{H}}_{2}^{+}H2+​ ion samples. Moreover, the large difference between the photodissociation efficiencies of ions created in the v=0v=0v=0 and v=1v=1v=1 levels provides a way to detect a v=0\ensuremath→1v=0\ensuremath{\rightarrow}1v=0\ensuremath→1 transition. These results pave the way towards high-resolution vibrational spectroscopy of H2+{\mathrm{H}}_{2}^{+}H2+​ for fundamental metrology applications.
We report a method of efficiently generating ultracold hydrogen molecular ions HD+ in a segmented linear ion trap. HD+ ions are created by [2+1′] resonance-enhanced multiphoton ionization (REMPI) of an HD supersonic molecular beam, and sympathetically cooled by laser-cooled Be+ ions. The HD+ ions are generated species-selectively using 201 nm and 395 nm pulse lasers with energies of 0.08 mJ (5.1 × 106 W/cm2) and 1.5 mJ (9.5 × 107 W/cm2) respectively. The average loading rate of 4.3(2) HD+ ions per second in the ion trap is determined by comparing the experimental images with the simulated images of Be+-HD+ bi-component Coulomb crystals. This method paves a way to produce the state-selected HD+ ions, which can improve the signal strengths of the selected rovibrational transitions of HD+ ions.
The high-resolution ro-vibrational spectroscopy of the H2+ molecular ion by resonance-enhanced multiphoton dissociation (REMPD) requires a state-selective source of H2+. In this thesis we present work on a functional state selective H2+ ion source using resonance enhanced multiphoton ionisation (REMPI) with a 303 nm pulsed laser.The second part of the thesis presents numerical simulations of sympathetic cooling in linear RF traps, whose main application is the GBAR project (Gravitational Behaviour of Antihydrogen at Rest) which involves sympathetic cooling of an antimatter H̄+ ion by laser-cooled Be+ ions. We developed a GPU code using a variable timestep technique enabling a fast description of Coulomb interactions. We discuss the influence of RF heating and scaling laws between cooling times, initial energy and ion numbers in the cooling crystal. We show that the H̄ sympathetic cooling step of GBAR could be feasible using a rotationally asymmetric two-component Be+/HD+ crystal which appears more effective than a single-component Be+ crystal. We find that the H̄+ ion’s capture by this crystal could be detected experimentally by Fourier analysis of the fluorescence data.
We report a high-resolution spectroscopic study of molecular ions at millikelvin temperatures. We measured several rovibrational infrared transitions in HD+\mathrm{H}{\mathrm{D}}^{+}HD+ molecular ions, stored in a radio-frequency trap and sympathetically cooled to $\ensuremath{\approx}20\phantom{\rule{0.3em}{0ex}}\mathrm{mK}$ by laser-cooled Be+{\mathrm{Be}}^{+}Be+ ions. We observed hyperfine splitting of the lines, in good agreement with theoretical predictions. The transitions were detected by monitoring the decrease in ion number after selective photodissociation of HD+\mathrm{H}{\mathrm{D}}^{+}HD+ ions in the upper vibrational state. The method described here is expected to be generally applicable.
The objective of the project is to perform high-resolution Doppler-free two-photon vibrational spectroscopy of the H2+ molecular ion for accurate electron to proton mass ratio determination. Trapping and laser-cooling of the H2+ ions is necessary. Since H2+ molecular ions cannot be directly laser cooled, a solution is the implementation of sympathetic cooling via a laser cooled Be+ ions. In the first part of this thesis the design and implementation of a linear Paul trap is presented. This trap is suitable to confine H2+ and Be+ ions while allowing good optical access for multiple laser sources and the imaging system. The second part describes a low power, diode based laser system to provide narrow linewidth 626nm light, and a high power, fiber laser based laser system. Subsequently, a bow-tie cavity is presented to frequency double the 626nm light to obtain 313nm light for Be+ Doppler-cooling. In the last part the operational readiness of the trap and the fiber laser based 313nm laser source is demonstrated by the observation of Be+ Coulomb crystals. Electron impact ionization of H2 present in the residual gas allows to observe sympathetic cooling and shows that the developed setup can provide the experimental conditions for precision spectroscopy of H2+.
We have measured the ro-vibrational infrared transition (v = 0, J = 2) → (v = 4, J = 1) in ultracold HD+ molecular ions embedded inside Be+ Coulomb crystals, by 1+1 REMPI spectroscopy. The molecular ions, trapped in a linear radiofrequency trap, were cooled to temperatures of few tens of mK, via sympathetic cooling using laser-cooled Be+ ions. For detection, we have used secular excitation of the HD+ ions to monitor their loss rate. The transition frequency agrees with a theoretical prediction.
Hydrogen molecular ions play an important role for accurate quantum electrodynamics calculations of rovibrational energy levels [1] and the comparison with laser spectroscopy results [2] allowed probing fundamental physics constants and laws. Advances are driven by an accurate control of the external and internal molecular degrees of freedom with a wide range of techniques [3]. Experimental setups with HD+ions are based on ions in a linear Paul trap and sympathetically cooled to the Lamb-Dick confinement regime by a laser-cooled atomic ion (Be+). Optical transitions allowed rotational cooling [4] and state-resolved detection by resonant-enhanced-multiphoton dissociation (REMPD) [5]. This contribution reports numerical results on the use of a two-photon rotational transition in the terahertz frequency range for preparation of trapped HD+ions in the rovibrational ground state and for high-resolution spectroscopy.