Related Experiment Video
Updated: Sep 18, 2025

Photoelectron Imaging of Anions Illustrated by 310 Nm Detachment of F−
Published on: July 27, 2018
Ionization Energy of Metastable ^{3}He (2 ^{3}S_{1}) and the Alpha- and Helion-Particle Charge-Radius Difference from
Gloria Clausen1, Frédéric Merkt1,2,3
1ETH Zurich, Department of Chemistry and Applied Biosciences, CH-8093 Zurich, Switzerland.
Abstract:
The current experimental and theoretical values of the ionization energy of metastable ^{4}He [(1s)(2s) ^{3}S_{1}] differ by 9σ, which prevents the determination of the alpha-particle charge radius from spectroscopic measurements in ^{4}He. To help clarify the origin of this discrepancy, we report on a precision measurement of hyperfine-resolved transitions from the (1s)(2s) ^{3}S_{1} metastable state of ^{3}He to high np Rydberg states converging on the F^{+}=0, 1 hyperfine levels of the ^{3}He^{+} (1s) ^{2}S_{1/2} ground state. Rydberg-series extrapolation using multichannel quantum-defect theory (MQDT) enabled the determination of the ionization energy of the (1s)(2s) ^{3}S_{1} state of ^{3}He [E_{I}(^{3}He)/h=1 152 788 844.6154(77)_{stat}(25)_{sys} MHz] and of the corresponding isotopic shift [(E_{I}(^{4}He)-E_{I}(^{3}He))/h=53 898.093(9) MHz]. The MQDT analysis also permitted the quantification of singlet-triplet mixing in the np series induced by the hyperfine interaction. From the isotopic shift of the ionization energy of He, the difference δr^{2} between the squared charge radii of the helion and alpha particles is determined to be 1.060(10) fm^{2}.
Related Concept Videos
The Bohr Model
Ionization Energy
The Energies of Atomic Orbitals
Emission Spectra
Electron Configurations
The relative energies of the subshells determine the order in which atomic orbitals are filled (1s, 2s, 2p, 3s, 3p,...
Electron Paramagnetic Resonance (EPR) Spectroscopy: Organic Radicals

