Li(OH2)1,2−: Two double-Rydberg anion (DRA) derivatives of OH3− and O2H5−

For several years, experimentalists have been searching for the double-Rydberg anions (DRAs), OH3- and O2H5-; however, no positive results have been reported other than those due to their theoretical prediction. By substituting one H atom in OH3- and O2H5- with an Li atom, we have successfully characterized the DRA's, Li(OH2)1,2- via anion photoelectron spectroscopy and ab initio calculations. The photoelectron spectra of [Li(OH2)1,2]- exhibited peaks with vertical detachment energy values at lower electron binding energies (EBE) than that of atomic Li-. Those observations showed that these anions are not the simple solvation complexes, Li-(H2O)1,2. Instead, their sharp, dominant peaks at EBE = 0.56 eV indicated that these are double-Rydberg anions. The geometrical structures and relevant Dyson orbitals, determined via our combined experimental and computational results, further demonstrated that these are the double-Rydberg anions, Li(OH2)1,2-. In LiOH2-, the Li atom and the H atoms are bound to the O atom, resulting in a pyramidal structure that resembles the predicted structure of OH3-. Moreover, Li(OH2)2- has the connectivity, H2O-Li-OH2-, with a bent O-Li-O sub-structure that resembles the predicted structure of O2H5-.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2026-08-24
DOI
https://doi.org/10.1063/5.0349796
Primary Topic
Advanced Chemical Physics Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Li(OH2)1,2−: Two double-Rydberg anion (DRA) derivatives of OH3− and O2H5−

Mary Marshall, Kiyokazu Fuke, Héctor H. Corzo, J. V. Ortiz et al.
The Journal of Chemical Physics
Advanced Chemical Physics Studies
article

Li(OH2)1,2−: Two double-Rydberg anion (DRA) derivatives of OH3− and O2H5−

Mary Marshall, Kiyokazu Fuke, Héctor H. Corzo, J. V. Ortiz, Tatsuya Chiba, Zhen Zeng, Kit H. Bowen, Sandra M. Ciborowski, Gaoxiang Liu, Wei‐Jun Zheng, Kenro Hashimoto, Xinxing Zhang
article en

Abstract

For several years, experimentalists have been searching for the double-Rydberg anions (DRAs), OH3- and O2H5-; however, no positive results have been reported other than those due to their theoretical prediction. By substituting one H atom in OH3- and O2H5- with an Li atom, we have successfully characterized the DRA's, Li(OH2)1,2- via anion photoelectron spectroscopy and ab initio calculations. The photoelectron spectra of [Li(OH2)1,2]- exhibited peaks with vertical detachment energy values at lower electron binding energies (EBE) than that of atomic Li-. Those observations showed that these anions are not the simple solvation complexes, Li-(H2O)1,2. Instead, their sharp, dominant peaks at EBE = 0.56 eV indicated that these are double-Rydberg anions. The geometrical structures and relevant Dyson orbitals, determined via our combined experimental and computational results, further demonstrated that these are the double-Rydberg anions, Li(OH2)1,2-. In LiOH2-, the Li atom and the H atoms are bound to the O atom, resulting in a pyramidal structure that resembles the predicted structure of OH3-. Moreover, Li(OH2)2- has the connectivity, H2O-Li-OH2-, with a bent O-Li-O sub-structure that resembles the predicted structure of O2H5-.

The Journal of Chemical PhysicsVol. 165(8)
Johns Hopkins University (US), The Open University of Japan (JP), Beijing National Laboratory for Molecular Sciences (CN), Kobe University (JP), Auburn University (US)
National Science Foundation
Affordable and clean energy
Openalex Percentile: Top 12%
Advanced Chemical Physics Studies
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