Related Experiment Video
Updated: Mar 13, 2026

Measurement of Ultrafast Vibrational Coherences in Polyatomic Radical Cations with Strong-Field Adiabatic Ionization
Published on: August 6, 2018
Interaction of Helium Rydberg State Molecules with Dense Helium
Nelly Bonifaci1, Zhiling Li2, Jussi Eloranta3
1G2ELab-GreEn-ER, Equipe MDE , 21 avenue des Martyrs, CS 90624, 38031 Grenoble Cedex 1, France.
Helium excimer potentials reveal unique interactions and solvation effects in dense helium. These findings help understand fluorescence spectroscopy limitations in probing discharge zones.
Area of Science:
- Atomic and Molecular Physics
- Quantum Chemistry
- Condensed Matter Physics
Background:
- The He2* excimer is crucial for understanding interactions in dense helium.
- Previous studies have explored its electronic states and interaction potentials.
Purpose of the Study:
- To present interaction potentials for He2* electronic states (a3Σu, b3Πg, c3Σg, d3Σu).
- To investigate the behavior of the 3d state excimer in dense helium.
- To compare calculated fluorescence shifts with experimental data.
Main Methods:
- Bosonic density functional calculations were employed.
- Interaction potentials were analyzed for symmetry and short-range features.
- Pressure-induced fluorescence band shifts were calculated and compared to experimental corona discharge results.
Main Results:
- Interaction potentials exhibit short-range minima and unusual long-range maxima due to electrostatic attraction and Pauli repulsion.
- The 3d state excimer forms localized solvation bubbles in dense helium (4.5 K), with radii decreasing under pressure.
- Calculated 3d → 3b fluorescence shifts align well with experimental data.
Conclusions:
- The study elucidates the complex interaction potentials of He2* excimers.
- Solvation effects significantly influence excimer behavior in dense helium.
- Fluorescence spectroscopy of this transition probes the surrounding dense helium, not the discharge zone itself.
Related Concept Videos
Molecular Orbital Theory II
Real Gases: Effects of Intermolecular Forces and Molecular Volume Deriving Van der Waals Equation
Spin–Spin Coupling Constant: Overview
Qualitatively, any spin plus-half nucleus polarizes the spins of its electrons to the minus-half state. Consequently, the paired electron in the hydrogen–carbon bond must...
Van der Waals Equation
First, the attractive forces between molecules, which are stronger at higher densities and reduce the pressure, are considered by adding to the pressure a term equal to the square of the molar density multiplied by a positive coefficient a. Second, the volume...
Emission Spectra
Behavior of Gas Molecules: Molecular Diffusion, Mean Free Path, and Effusion

