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Lothar Maisenbacher

Publications and source records attributed to Lothar Maisenbacher.

10 recordsLinked to original sources

Microscopy of Bioelectric Potentials using Electrochromism

Studying the electrical signals generated by living cells is key to understanding numerous biological phenomena. Electrochromic optical recording (ECORE) uses the electrochromism exhibited by certain materials to noninvasively measure these signals in real time. In this work, we report on the development of ECORE based on a high-NA microscope objective. We demonstrate the recording of extracellular action potentials from cardiomyocytes with single-cell resolution and a high sensitivity of 6.3 μV. Combining ECORE with microscopy simplifies the optical setup, allows for the simultaneous imaging of specimens, and makes ECORE accessible to a broader community of researchers, allowing for a better understanding of the biological processes that are integral to life.

physics.optics↗

A thermoelastic limit on the focal intensity in Fabry-Pérot cavities

Light in the mode of a Fabry-Pérot cavity heats the mirror surfaces via optical absorption, causing thermoelastic deformation of the mirror substrates, which in turn dictates the shape of the mode. We develop an analytical model which predicts that this effect limits the maximum focal intensity of the mode. Using two near-concentric Fabry-Pérot cavities -- one with 4.5-fold higher mirror absorption than the other -- we measure the thermoelastic properties of the cavity mirrors and demonstrate that it is possible to achieve at least 70% of this predicted limit (in the high-absorption cavity), and that the predicted limit is 2.9 TW/cm^2 (in the low-absorption cavity).

physics.optics↗

Sub-part-per-trillion test of the Standard Model with atomic hydrogen

Quantum electrodynamics (QED), the first relativistic quantum field theory, describes light-matter interactions at a fundamental level and is one of the pillars of the Standard Model (SM). Through the extraordinary precision of QED, the SM predicts the energy levels of simple systems such as the hydrogen atom with up to 13 significant digits, making hydrogen spectroscopy an ideal test bed. The consistency of physical constants extracted from different transitions in hydrogen using QED, such as the proton charge radius $r_\mathrm{p}$, constitutes a test of the theory. However, values of $r_\mathrm{p}$ from recent measurements of atomic hydrogen are partly discrepant with each other and with a more precise value from spectroscopy of muonic hydrogen. This prevents a test of QED at the level of experimental uncertainties. Here we present a measurement of the 2S-6P transition in atomic hydrogen with sufficient precision to distinguish between the discrepant values of $r_\mathrm{p}$ and enable rigorous testing of QED and the SM overall. Our result $ν^{}_{\text{2S-6P}}$ = 730,690,248,610.79(48) kHz gives a value of $r_\mathrm{p}$ = 0.8406(15) fm at least 2.5-fold more precise than from other atomic hydrogen determinations and in excellent agreement with the muonic value. The SM prediction of the transition frequency (730,690,248,610.79(23) kHz) is in excellent agreement with our result, testing the SM to 0.7 parts per trillion (ppt) and, specifically, bound-state QED corrections to 0.5 parts per million (ppm), their most precise test so far.

physics.atom-ph↗

Precision spectroscopy of the 2S-$n$P transitions in atomic hydrogen

Precision spectroscopy of atomic hydrogen is an important way to test bound-state quantum electrodynamics (QED), one of the building blocks of the Standard Model. In its simplest form, such a test consists of the comparison of a measured transition frequency with its QED prediction, which can be calculated with very high precision for the hydrogen atom. However, these calculations require some input in the form of physical constants, such as the Rydberg constant $R_\infty$ and the proton charge radius $r_\mathrm{p}$, both of which are currently determined to a large degree by hydrogen spectroscopy itself. Therefore, the frequency of at least three different transitions needs to be measured in order to test QED. Equivalently, a comparison of the values of $R_\infty$ and $r_\mathrm{p}$ determined from measurements of different transitions constitutes a test of QED. To this end, laser spectroscopy of optical 2S-$n$P transitions has been performed in this work. As these transitions are one-photon transitions, they are affected by a different set of systematic effects than the two-photon transitions on which most other spectroscopic measurements of hydrogen are based. In order to contribute to the test of QED, their transition frequencies must be determined with a relative uncertainty on the order of one part in $10^{12}$, corresponding to approximately 1 kHz in absolute terms. This is in turn approximately a factor of 10000 smaller than the relatively broad natural linewidth of the 2S-$n$P transitions, and a successful measurement requires both a very large experimental signal-to-noise ratio and a detailed theoretical understanding of the line shape of the observed resonance. The 2S-$n$P transitions were probed on a cryogenic beam of hydrogen atoms, which were optically excited to the metastable 2S level. The atomic beam was crossed at right angles with counter-propagating spectroscopy laser beams, which further excited the atoms to the $n$P level. The fluorescence from the subsequent rapid spontaneous decay served as experimental signal. The excitation with two counter-propagating beams led to two Doppler shifts of equal magnitude, but opposite sign, which thus canceled each other out. A velocity-resolved detection was used to determine any residual Doppler shifts, which could be excluded within the measurement uncertainty for both of the measurements discussed below. In a first experiment, the 2S-4P transition was probed. Quantum interference of neighboring atomic resonances produced subtle distortions of the line shape, which were found to be significant because of the very large resolution relative to the linewidth. The line shifts caused by the distortions were directly observed and could be removed by use of a line shape model based on perturbative calculations. With this, the transition frequency was determined with a relative uncertainty of 4 parts in $10^{12}$. In combination with the very precisely measured 1S-2S transition frequency, this allowed the, at the time, most precise determination of $R_\infty$ and $r_\mathrm{p}$ from atomic hydrogen. Moreover, good agreement was found with the much more precise value of $r_\mathrm{p}$ extracted from spectroscopy of muonic hydrogen, which had been in significant disagreement with previous data from (electronic) hydrogen, causing concern about the validity of QED. This result has since been confirmed by other experiments. The 2S-4P measurement is treated in the appendix of this thesis. The 2S-4P measurement, despite its large signal-to-noise ratio, was limited by counting statistics. To improve precision, a transition with a narrower linewidth and an improved experimental signal was necessary. Hence, the study of the 2S-6P transition, which offers a three times smaller natural linewidth, was begun. The atomic beam apparatus was upgraded, resulting in a corresponding decrease of the experimentally observed linewidth, and a close to an order of magnitude larger flux of atoms in the low-velocity tail of the atomic beam. Together with a detector redesign, this led to an up to 16 times larger signal than for the 2S-4P measurement, opening the path to increased precision. The Doppler-shift suppression was also rebuilt to support such precision, including a fiber collimator developed for this purpose, which provides high-quality spectroscopy beams at the new transition wavelength of 410 nm. This enabled a measurement of the 2S-6P transition frequency with a statistical uncertainty of 430 Hz, five times lower than for the 2S-4P measurement and corresponding to a suppression of the Doppler shift by six orders of magnitude. At this level of precision, the light force shift from the diffraction of atoms at the light grating formed by the counter-propagating spectroscopy beams becomes significant. This light force shift was directly observed for the first time for the 2S-$n$P transitions and found to be well-described by a model derived for this purpose. The size of all other systematic effects, except the very precisely known recoil shift, is estimated to be below 500 Hz each. The blind data analysis is ongoing at the time of writing and thus no transition frequencies can yet be given. However, a preliminary analysis suggests a five-fold improvement in the determination of $R_\infty$ and $r_\mathrm{p}$ as compared to the 2S-4P measurement, and a two-fold improvement over the currently most precise determination from atomic hydrogen. This places the uncertainty of the determined value of $r_\mathrm{p}$ within a factor of five of that of the muonic value. The 2S-6P measurement is treated in the main text of this thesis.

physics.atom-ph↗

Compact Electrochromic Optical Recording of Bioelectric Potentials

Electrochromic optical recording (ECORE) is a label-free method that utilizes electrochromism to optically detect electrical signals in biological cells with a high signal-to-noise ratio and is suitable for long-term recording. However, ECORE usually requires a large and intricate optical setup, making it relatively difficult to transport and to study specimens on a large scale. Here, we present a compact ECORE apparatus that drastically reduces the spatial footprint and complexity of the ECORE setup whilst maintaining high sensitivity. An autobalancing differential photodetector automates common-mode noise rejection, removing the need for manually adjustable optics, and a compact laser module conserves space compared to a typical laser mount. The result is a simple, easy-to-use, and relatively low cost system that achieves a sensitivity of 16.7 μV (within a factor of 5 of the shot noise limit), and reliably detects action potentials from Human-induced pluripotent stem cell (HiPSC) derived cardiomyocytes. This setup can be further improved to within 1.5 dB of the shot noise limit by filtering out power-line interference.

physics.optics↗

Dynamics of a buffer-gas-loaded, deep optical trap for molecules

We describe an approach to optically trapping small, chemically stable molecules at cryogenic temperatures by buffer-gas loading a deep optical dipole trap. The ~10 K trap depth will be produced by a tightly-focused, 1064-nm cavity capable of reaching intensities of hundreds of GW/cm$^2$. Molecules will be directly buffer-gas loaded into the trap using a helium buffer gas at 1.5 K. The very far-off-resonant, quasielectrostatic trapping mechanism is insensitive to a molecule's internal state, energy level structure, and its electric and magnetic dipole moment. Here, we theoretically investigate the trapping and loading dynamics, as well as the heating and loss rates, and conclude that $10^4$-$10^6$ molecules are likely to be trapped. Our trap would open new possibilities in molecular spectroscopy, studies of cold chemical reactions, and precision measurement, amongst other fields of physics.

physics.atom-ph↗

A nanoscale vacuum-tube diode triggered by few-cycle laser pulses

We propose and demonstrate a nanoscale vacuum-tube diode triggered by few-cycle near-infrared laser pulses. It represents an ultrafast electronic device based on light fields, exploiting near-field optical enhancement at surfaces of two metal nanotips. The sharper of the two tips displays a stronger field-enhancement, resulting in larger photoemission yields at its surface. One laser pulse with a peak intensity of $4.7\times 10^{11}$ W/cm$^2$ triggers photoemission of ${\sim }16$ electrons from the sharper cathode tip, while emission from the blunter anode tip is suppressed by $19$ dB to ${\sim }0.2$ electrons per pulse. Thus, the laser-triggered current between two tips exhibit a rectifying behavior, in analogy to classical vacuum-tube diodes. According to the kinetic energy of the emitted electrons and the distance between tips, the total operation time of this laser-triggered nanoscale diode is estimated to be below 1 ps.

physics.optics↗

Tracing the phase of focused broadband laser pulses

Precise knowledge of the behaviour of the phase of light in a focused beam is fundamental to understanding and controlling laser-driven processes. More than a hundred years ago an axial phase anomaly for focused monochromatic light beams was discovered and is now commonly known as the Gouy phase. Recent theoretical work has brought into question the validity of applying this monochromatic phase formulation to the broadband pulses becoming ubiquitous today. Based on electron back-scattering at sharp nanometre-scale metal tips, a method is available to measure light fields with sub-wavelength spatial resolution and sub-optical cycle time resolution. Here we report such a direct, three-dimensional measurement of the spatial dependence of the optical phase of a focused, 4-fs, near-infrared laser pulse. The observed optical phase deviates substantially from the monochromatic Gouy phase - exhibiting a much more complex spatial dependence, both along the propagation axis and in the radial direction. In our measurements, these significant deviations are the rule and not the exception for focused, broadband laser pulses. Therefore, we expect wide ramifications for all broadband laser-matter interactions, such as in high-harmonic and attosecond pulse generation, femtochemistry, ophthalmological optical coherence tomography and light-wave electronics.

physics.optics↗

Deuteron charge radius and Rydberg constant from spectroscopy data in atomic deuterium

We give a pedagogical description of the method to extract the charge radii and Rydberg constant from laser spectroscopy in regular hydrogen (H) and deuterium (D) atoms, that is part of the CODATA least-squares adjustment (LSA) of the fundamental physical constants. We give a deuteron charge radius Rd from D spectroscopy alone of 2.1415(45) fm. This value is independent of the measurements that lead to the proton charge radius, and five times more accurate than the value found in the CODATA Adjustment 10. The improvement is due to the use of a value for the 1S->2S transition in atomic deuterium which can be inferred from published data or found in a PhD thesis.

physics.atom-ph↗

Atom interferometry in an optical cavity

We propose and demonstrate a new scheme for atom interferometry, using light pulses inside an optical cavity as matter wave beamsplitters. The cavity provides power enhancement, spatial filtering, and a precise beam geometry, enabling new techniques such as low power beamsplitters ($<100 \mathrm{μW}$), large momentum transfer beamsplitters with modest power, or new self-aligned interferometer geometries utilizing the transverse modes of the optical cavity. As a first demonstration, we obtain Ramsey-Raman fringes with $>75\%$ contrast and measure the acceleration due to gravity, $\mathit{g}$, to $60 \mathrm{μ\mathit{g} / \sqrt{Hz}}$ resolution in a Mach-Zehnder geometry. We use $>10^7$ cesium atoms in the compact mode volume ($600 \mathrm{μm}$ $1/e^2$ waist) of the cavity and show trapping of atoms in higher transverse modes. This work paves the way toward compact, high sensitivity, multi-axis interferometry.

physics.atom-ph↗