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J. C. J. Koelemeij

Publications and source records attributed to J. C. J. Koelemeij.

At least 19 recordsLinked to original sources

Spectroscopy of the Hyperfine Structure of HD$^+$ in Rotationally Excited States with 10-ppb Uncertainty

We report the first measurement of the total hyperfine interval in the manifold of the ($v=0,L=3$) rovibrational state of HD$^+$ using microwave spectroscopy of HD$^+$ ions in a linear Paul trap. To overcome the low (0.2%) occupancy of the quantum states involved, we employ a novel technique that combines intermittent Majorana depolarization of the HD$^+$ ensemble with redistribution of rotational-state population by blackbody radiation to effectively amplify the occupancy by a factor of 25. This enables the observation of a single field-insensitive magnetic subcomponent of the hyperfine transition, leading to a measured total hyperfine interval of ${1\,050\,804.511}\pm 0.011\,$kHz with an unprecedented relative uncertainty of 10 parts per billion. This differs from the theoretically predicted value ${1\,050\,802.78}\pm 0.89\,$kHz by 1.9$σ$. We show that our experimental value is consistent with the recently measured hyperfine structure of the ($v=0,L=0$) rovibrational state of HD$^+$ [C.M. König et al., High-precision Penning trap spectroscopy of the ground state spin structure of HD$^+$, Phys. Rev. Lett. $\mathbf{136}$,143002 (2026)], for which a similar deviation from theory was found. Our work may help resolve puzzling discrepancies between the theoretical and experimental hyperfine structure observed previously in optical rovibrational spectra of HD$^+$.

physics.atom-ph↗

Spectroscopy of $^4$He at 0.25 ppt Uncertainty and Improved Alpha-Helion Charge-Radius Difference Determination

High-precision spectroscopy of simple atomic systems can be used to advance the theory of atomic energy levels but can also serve as a sensitive probe of nuclear charge radii. For this last purpose, we report an improved measurement of the $2\,^3{S}_1 \to 2\,^1{S}_0$ transition frequency in $^4$He with 48 Hz uncertainty (0.25 ppt), using a Bose-Einstein condensed sample confined in a magic-wavelength optical dipole trap. A systematic Doppler shift from condensate motion is suppressed by time-resolved ion detection, and the transition frequency is calibrated via a White Rabbit link to a remote active hydrogen maser clock. Combined with previous $^3$He measurements and improved theory, we obtain the most precise determination to date of the charge-radius difference between the helion and alpha particle ($r_{h}^2 -r_α^2$) of $1.0676(10)\text{fm}^2$. This is consistent with other recent determinations and confirms that the current discrepancy between QED theory and experimentally observed ionization energies of excited states in helium is not apparent in the isotope shift.

physics.atom-ph↗

A hybrid optical-wireless network for decimetre-level terrestrial positioning

Global navigation satellite systems (GNSS) are widely used for navigation and time distribution, features indispensable for critical infrastructure such as mobile communication networks, as well as emerging technologies like automated driving and sustainable energy grids. While GNSS can provide centimetre-level precision, GNSS receivers are prone to many-metre errors due to multipath propagation and obstructed view of the sky, which occur especially in urban areas where accurate positioning is needed most. Moreover, the vulnerabilities of GNSS, combined with the lack of a back-up system, pose a severe risk to GNSS-dependent technologies. Here, we demonstrate a terrestrial positioning system which is independent of GNSS and offers superior performance through a constellation of radio transmitters, connected and time-synchronised at the sub-nanosecond level through a fibre-optic Ethernet network. Employing optical and wireless transmission schemes similar to those encountered in mobile communication networks, and exploiting spectrally efficient virtual wideband signals, the detrimental effects of multipath propagation are mitigated, thus enabling robust decimetre-level positioning and sub-nanosecond timing in a multipath-prone outdoor environment. This work provides a glimpse of a future in which telecommunication networks provide not only connectivity, but also GNSS-independent timing and positioning services with unprecedented accuracy and reliability.

physics.app-ph↗

Proton-Electron Mass Ratio from Laser Spectroscopy of HD$^+$ at the Part-Per-Trillion Level

Accepted values of the masses of several subatomic particles have been under debate since recent measurements in Penning traps produced more precise yet incompatible results, implying possible inconsistencies in closely related physical constants like the proton-electron and deuteron-proton mass ratios. These quantities also influence the predicted vibrational spectrum of the deuterated molecular hydrogen ion in its electronic ground state, of which we measured the v=0 - 9 overtone transition frequency with an uncertainty of 2.9 parts-per-trillion through Doppler-free two-photon laser spectroscopy. Leveraging high-precision ab initio calculations we convert our measurement to tight constraints on the proton-electron and deuteron-proton mass ratios, consistent with the most recent Penning-trap determinations of these quantities, and yielding a new value of the proton-electron mass ratio with an unprecedented precision of 21 parts-per-trillion.

physics.atom-ph↗

Measurement of optical to electrical and electrical to optical delays with ps-level uncertainty

We present a new measurement principle to determine the absolute time delay of a waveform from an optical reference plane to an electrical reference plane and vice versa. We demonstrate a method based on this principle with 2 ps uncertainty. This method can be used to perform accurate time delay determinations of optical transceivers used in fibre-optic time-dissemination equipment. As a result the time scales in optical and electrical domain can be related to each other with the same uncertainty. We expect this method to break new grounds in high-accuracy time transfer and absolute calibration of time-transfer equipment.

physics.optics↗

Proton-electron mass ratio from HD$^+$ revisited

We present a new derivation of the proton-electron mass ratio from the hydrogen molecular ion, HD$^+$. The derivation entails the adjustment of the mass ratio in highly precise theory so as to reproduce accurately measured ro-vibrational frequencies. This work is motivated by recent improvements of the theory, as well as the more accurate value of the electron mass in the recently published CODATA-14 set of fundamental constants, which justifies using it as input data in the adjustment, rather than the proton mass value as done in previous works. This leads to significantly different sensitivity coefficients and, consequently, a different value and larger uncertainty margin of the proton-electron mass ratio as obtained from HD$^+$.

physics.atom-ph↗

High-precision spectroscopy of the HD+ molecule at the 1-p.p.b. level

Recently we reported a high precision optical frequency measurement of the (v,L):(0,2)->(8,3) vibrational overtone transition in trapped deuterated molecular hydrogen (HD+) ions at 10 mK temperature. Achieving a resolution of 0.85 parts-per-billion (p.p.b.) we found the experimental value ($ν_0= 383,407,177.38(41)$ MHz) to be in agreement with the value from molecular theory ($ν_\text{th}=383,407,177.150(15)$ MHz) within 0.6(1.1) p.p.b. [Biesheuvel et al., Nat. Commun. 7, 10385 (2016)]. This enabled an improved test of molecular theory (including QED), new constraints on the size of possible effects due to 'new physics', and the first determination of the proton-electron mass ratio from a molecule. Here, we provide the details of the experimental procedure, spectral analysis, and the assessment of systematic frequency shifts. Our analysis focuses in particular on deviations of the HD+ velocity distribution from thermal (Gaussian) distributions under the influence of collisions with fast ions produced during (laser-induced) chemical reactions, as such deviations turn out to significantly shift the hyperfine-less vibrational frequency as inferred from the saturated and Doppler-broadened spectrum, which contains partly unresolved hyperfine structure.

physics.atom-ph↗

Ghost features in Doppler-broadened spectra of rovibrational transitions in trapped HD$^+$ ions

Doppler broadening plays an important role in laser rovibrational spectroscopy of trapped deuterated molecular hydrogen ions (HD$^+$), even at the millikelvin temperatures achieved through sympathetic cooling by laser-cooled beryllium ions. Recently, Biesheuvel \textit{et al.} \cite{Biesheuvel2016} presented a theoretical lineshape model for such transitions which not only considers linestrengths and Doppler broadening, but also the finite sample size and population redistribution by blackbody radiation, which are important in view of the long storage and probe times achievable in ion traps. Here, we employ the rate equation model developed by Biesheuvel \textit{et al.} to theoretically study the Doppler-broadened hyperfine structure of the $(v,L):(0,3)\rightarrow(4,2)$ rovibrational transition in HD$^+$ at 1442~nm. We observe prominent yet hitherto unrecognized ghost features in the simulated spectrum, whose positions depend on the Doppler width, transition rates, and saturation levels of the hyperfine components addressed by the laser. We explain the origin and behavior of such features, and we provide a simple quantitative guideline to assess whether ghost features may appear. As such ghost features may be common to saturated Doppler-broadened spectra of rotational and vibrational transitions in trapped ions composed of partly overlapping lines, our work illustrates the necessity to use lineshape models that take into account all the relevant physics.

physics.atom-ph↗

Probing QED and fundamental constants through laser spectroscopy of vibrational transitions in HD+

The simplest molecules in nature, molecular hydrogen ions in the form of H2+ and HD+, provide an important benchmark system for tests of quantum electrodynamics in complex forms of matter. Here, we report on such a test based on a frequency measurement of a vibrational overtone transition in HD+ by laser spectroscopy. We find that the theoretical and experimental frequencies are equal to within 0.6(1.1) parts per billion, which represents the most stringent test of molecular theory so far. Our measurement not only confirms the validity of high-order quantum electrodynamics in molecules, but also enables the long predicted determination of the proton-to-electron mass ratio from a molecular system, as well as improved constraints on hypothetical fifth forces and compactified higher dimensions at the molecular scale. With the perspective of comparisons between theory and experiment at the 0.01 part-per-billion level, our work demonstrates the potential of molecular hydrogen ions as a probe of fundamental physical constants and laws.

physics.atom-ph↗

Effect of soil temperature on one-way optical frequency transfer through dense-wavelength-division-multiplexing fibre links

Results of optical frequency transfer over a carrier-grade dense-wavelength-division-multiplexing (DWDM) optical fibre network are presented. The relation between soil temperature changes on a buried optical fibre and frequency changes of an optical carrier through the fibre is modelled. Soil temperatures, measured at various depths by the Royal Netherlands Meteorology Institute (KNMI) are compared with observed frequency variations through this model. A comparison of a nine-day record of optical frequency measurements through the 2 x 298 km fibre link with soil temperature data shows qualitative agreement. A soil temperature model is used to predict the link stability over longer periods (days-months-years). We show that one-way optical frequency dissemination is sufficiently stable to distribute and compare e.g. rubidium frequency standards over standard DWDM optical fibre networks.

physics.optics↗

Delivering 10 Gb/s optical data with picosecond timing uncertainty over 75 km distance

We report a method to determine propagation delays of optical 10 Gb/s data traveling through a 75 km long amplified fiber link with an uncertainty of 4 ps. The one-way propagation delay is determined by two-way exchange and cross correlation of short (< 1 ms) bursts of 10 Gb/s data, with a single-shot time resolution better than 2.5 ps. We thus achieve a novel optical communications link suited for both long-haul high-capacity data transfer and time transfer with picosecond-range uncertainty. This opens up the perspective of synchronized optical telecommunication networks allowing picosecond-range time distribution and millimeter-range positioning.

physics.optics↗

Bounds on fifth forces from precision measurements on molecules

Highly accurate results from frequency measurements on neutral hydrogen molecules H_2, HD and D_2 as well as the HD^+ ion can be interpreted in terms of constraints on possible fifth-force interactions. Where the hydrogen atom is a probe for yet unknown lepton-hadron interactions, and the helium atom is sensitive for lepton-lepton interactions, molecules open the domain to search for additional long-range hadron-hadron forces. First principles calculations in the framework of quantum electrodynamics have now advanced to the level that hydrogen molecules and hydrogen molecular ions have become calculable systems, making them a search-ground for fifth forces. Following a phenomenological treatment of unknown hadron-hadron interactions written in terms of a Yukawa potential of the form V_5(r)=βexp(-r/λ)/r current precision measurements on hydrogenic molecules yield a constraint β< 1 \times 10^{-7} eVÅfor long-range hadron-hadron interactions at typical force ranges commensurate with separations of a chemical bond, i.e. λ~1 Åand beyond.

physics.atom-ph↗

Infrared dynamic polarizability of HD+ rovibrational states

A calculation of dynamic polarizabilities of rovibrational states with vibrational quantum number $v=0-7$ and rotational quantum number $J=0,1$ in the 1s$σ_g$ ground-state potential of HD$^+$ is presented. Polarizability contributions by transitions involving other 1s$σ_g$ rovibrational states are explicitly calculated, whereas contributions by electronic transitions are treated quasi-statically and partially derived from existing data [R.E. Moss and L. Valenzano, \textit{Molec. Phys.}, 2002, \textbf{100}, 1527]. Our model is valid for wavelengths $>4~μ$m and is used to to assess level shifts due to the blackbody radiation (BBR) electric field encountered in experimental high-resolution laser spectroscopy of trapped HD$^+$ ions. Polarizabilities of 1s$σ_g$ rovibrational states obtained here agree with available existing accurate \textit{ab initio} results. It is shown that the Stark effect due to BBR is dynamic and cannot be treated quasi-statically, as is often done in the case of atomic ions. Furthermore it is pointed out that the dynamic Stark shifts have tensorial character and depend strongly on the polarization state of the electric field. Numerical results of BBR-induced Stark shifts are presented, showing that Lamb-Dicke spectroscopy of narrow vibrational optical lines ($\sim 10$ Hz natural linewidth) in HD$^+$ will become affected by BBR shifts only at the $10^{-16}$ level.

physics.atom-ph↗

Frequency Comparison of Two High-Accuracy Al+ Optical Clocks

We have constructed an optical clock with a fractional frequency inaccuracy of 8.6e-18, based on quantum logic spectroscopy of an Al+ ion. A simultaneously trapped Mg+ ion serves to sympathetically laser-cool the Al+ ion and detect its quantum state. The frequency of the 1S0->3P0 clock transition is compared to that of a previously constructed Al+ optical clock with a statistical measurement uncertainty of 7.0e-18. The two clocks exhibit a relative stability of 2.8e-15/ sqrt(tau), and a fractional frequency difference of -1.8e-17, consistent with the accuracy limit of the older clock.

quant-ph↗

Observation of the 1S0 - 3P0 clock transition in 27Al+

We report for the first time, laser spectroscopy of the 1S0 - 3P0 clock transition in 27Al+. A single aluminum ion and a single beryllium ion are simultaneously confined in a linear Paul trap, coupled by their mutual Coulomb repulsion. This coupling allows the beryllium ion to sympathetically cool the aluminum ion, and also enables transfer of the aluminum's electronic state to the beryllium's hyperfine state, which can be measured with high fidelity. These techniques are applied to a measurement of the clock transition frequency, ν= 1 121 015 393 207 851(8) Hz. They are also used to measure the lifetime of the metastable clock state, τ= 20.6 +/- 1.4 s, the ground state 1S0 g-factor, g_S = -0.00079248(14), and the excited state 3P0 g-factor, g_P = -0.00197686(21), in units of the Bohr magneton.

physics.atom-ph↗

Blackbody radiation shift of the 27Al+ 1S0 - 3P0 transition

The differential polarizability, due to near-infrared light at 1126 nm, of the 27Al+ 1S0 -> 3P0 clock transition is measured to be 4πε_0 x (1.6 +/- 0.5) x 10^{-31} m^3. This measurement is combined with experimental oscillator strengths to extrapolate the differential static polarizability of the clock transition as 4πε_0 x (1.5 +/- 0.5) x 10^{-31} m^3. The resulting room temperature blackbody fractional frequency shift of -8(3) x 10^{-18} is the lowest known shift of all atomic transitions under consideration for optical frequency standards. A method is presented to estimate the differential static polarizability of an optical transition, from a differential light shift measurement.

physics.atom-ph↗

Optical Clocks in Space

The performance of optical clocks has strongly progressed in recent years, and accuracies and instabilities of 1 part in 10^18 are expected in the near future. The operation of optical clocks in space provides new scientific and technological opportunities. In particular, an earth-orbiting satellite containing an ensemble of optical clocks would allow a precision measurement of the gravitational redshift, navigation with improved precision, mapping of the earth's gravitational potential by relativistic geodesy, and comparisons between ground clocks.

gr-qc↗

Prospects for measurement and control of the scattering length of metastable helium using photoassociation techniques

A numerical investigation of two-laser photoassociation (PA) spectroscopy on spin-polarized metastable helium (He*) atoms is presented within the context of experimental observation of the least-bound energy level in the scattering potential and subsequent determination of the s-wave scattering length. Starting out from the model developed by Bohn and Julienne [Phys. Rev. A \textbf{60}, (1999) 414], PA rate coefficients are obtained as a function of the parameters of the two lasers. The rate coefficients are used to simulate one- and two-laser PA spectra. The results demonstrate the feasibility of a spectroscopic determination of the binding energy of the least-bound level. The simulated spectra may be used as a guideline when designing such an experiment, whereas the model may also be employed for fitting experimentally obtained PA spectra. In addition, the prospects for substantial modification of the He* scattering length by means of optical Feshbach resonances are considered. Several experimental issues relating to the numerical investigation presented here are discussed.

cond-mat.other↗