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We present a method for probing the quantum capacitance associated with the Rydberg transition of surface electrons on liquid helium using radio-frequency (rf) reflectometry. Resonant microwave excitation of the Rydberg transition induces a redistribution of image charges on capacitively coupled electrodes, giving rise to a quantum capacitance originating from adiabatic state transitions and the finite curvature of the energy bands. By applying frequency-modulated resonant microwaves to drive the Rydberg transition, we systematically measured a capacitance sensitivity of 0.34 aF/sqrt[Hz] for our rf reflectometry scheme. This sensitivity is sufficient to detect the Rydberg transition of a single electron, offering a scalable pathway toward qubit readout schemes based on surface electrons on helium.
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http://dx.doi.org/10.1103/5y8p-qhb4 | DOI Listing |
Phys Rev Lett
August 2025
RIKEN Center for Quantum Computing, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.
We present a method for probing the quantum capacitance associated with the Rydberg transition of surface electrons on liquid helium using radio-frequency (rf) reflectometry. Resonant microwave excitation of the Rydberg transition induces a redistribution of image charges on capacitively coupled electrodes, giving rise to a quantum capacitance originating from adiabatic state transitions and the finite curvature of the energy bands. By applying frequency-modulated resonant microwaves to drive the Rydberg transition, we systematically measured a capacitance sensitivity of 0.
View Article and Find Full Text PDFInorg Chem
September 2025
Laboratoire de Chimie Physique Matière et Rayonnement (LCPMR), CNRS UMR 7614, Sorbonne Université (SU), 4 place Jussieu, Paris 75005, France.
The one-photon KV X-ray photoelectron spectra of Na and its hydrated clusters [Na(HO)] ( = 1-6) are dominated by the unusual 1s → 1s3s transition. KV spectroscopy also reveals a pronounced redistribution of the 1s → 1s3p transition cross sections, directly correlated with hydration number and molecular arrangement. Its intrinsic two-step nature, involving simultaneous core ionization and core excitation, enables detailed investigation of solvation-induced electronic structure changes, including dipole-forbidden excitations, core-valence charge transfer, and subtle 1s → V energy shifts.
View Article and Find Full Text PDFJ Chem Phys
September 2025
Smoluchowski Institute of Physics, Faculty of Physics, Astronomy and Applied Computer Science, Jagiellonian University, Łojasiewicza 11, 30-348 Kraków, Poland.
An improved rotational characterization of the E3Σ1+(63S1) Rydberg state of the CdAr diatom produced in a supersonic beam and studied using laser induced fluorescence (LIF) excitation spectra is presented. As an example, the spectra of the E3Σ1+←A3Π0+(53P1) transition, originating from the excitation of a single 116Cd40Ar isotopologue, are recorded and analyzed. In the experiment, the optical-optical double resonance method is employed, utilizing the E3Σ1+(υ')←A3Π0+(53P1)(υ″=6)←X1Σ0+(υ=0) scheme.
View Article and Find Full Text PDFJ Phys Chem Lett
September 2025
Sorbonne Université, CNRS, UMR 7614, Laboratoire de Chimie Physique-Matière et Rayonnement, F-75005 Paris, France.
We report carbon and fluorine KV double core hole (DCH) spectra of CHF, recorded by single-photon hard X-ray photoelectron spectroscopy. A striking inversion in intensity between the and K7(3) resonances reflects a polarity switch in bonding character depending on the K-shell vacancy site. Within the Brillouin Inverse Theorem (BIT) framework, the transition strengths are shown to depend on the bielectronic integral (V = σ*, 3).
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2025
Institute of Astronomy Space and Earth Science, Kolkata 700054, India.
We report for the first time the ultraviolet-vacuum ultraviolet absorption spectrum of -propylamine in the wavenumber range 40 000 to 75 000 cm (5.0-9.3 eV) using synchrotron radiation.
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