Non-local X-ray intermolecular radiative decay probes solvation shell of ions in water

J Johan Söderström L Lucas M. Cornetta V Victor Ekholm V Vincenzo Carravetta A Arnaldo Naves de Brito R Ricardo Marinho M Marcus Agåker T Takashi Tokushima (MAX IV Laboratory) C Conny Såthe (MAX IV Laboratory) A Anirudha Ghosh D Dana Bloß (Institut für Physik und CINSaT, Universität Kassel, Heinrich-Plett-Str. 40, 34132 Kassel, Germany) A Andreas Hans (Institut für Physik und CINSaT, Universität Kassel, Heinrich-Plett-Str. 40, 34132 Kassel, Germany) F Florian Trinter (Fritz-Haber-Institut der Max-Planck-Gesellschaft , , Faradayweg 4-6 , ,) I Iyas Ismail (CNRS, UMR 7614, Sorbonne Université , , 4 Place Jussieu , ,) D Debora Vasconcelos J Joel Pinheiro Y Yi-Ping Chang (European XFEL, Holzkoppel 4, 22869 Schenefeld, Germany) M Manuel Harder (European XFEL, Holzkoppel 4, 22869 Schenefeld, Germany) Z Zhong Yin (International Center for Synchrotron Radiation Innovation Smart) J Joseph Nordgren G Gunnar Öhrwall (MAX IV Laboratory, Lund University, Box 118, 22100 Lund, Sweden) H Hans Ågren (School of Chemistry and Chemical Engineering) J Jan-Erik Rubensson O Olle Björneholm (Department of Physics and Astronomy, Uppsala University, Box 516, 75120 Uppsala, Sweden)

Abstract

Abstract Aqueous solutions are crucial in chemistry, biology, environmental science, and technology. The chemistry of solutes is influenced by the surrounding solvation shell of water molecules, which have different chemical properties than bulk water due to their different electronic and geometric structure. It is experimentally challenging to selectively investigate this property-determining electronic and geometric structure. Here, we report experimental results on the non-local X-ray emission process Intermolecular Radiative Decay, for the prototypical ions Na + and Mg 2+ in water. We show that, in Intermolecular Radiative Decay, an electron from the solvation shell fills a core hole in the solute, and the released energy is emitted as an X-ray photon. We interpret the underlying mechanism using theoretical calculations, and show how Intermolecular Radiative Decay will allow us to meet the challenge of selectively probing the solvation shell from within.

Article Details

Volume / Issue Vol. 16, Issue 1
Published November 17, 2025
ISSN 2041-1723
Publisher Nature Portfolio

Journal Info

Nature Communications

Nature Portfolio

ISSN: 2041-1723 Open Access Life Sciences

Authors (24)

J

Johan Söderström

L

Lucas M. Cornetta

V

Victor Ekholm

V

Vincenzo Carravetta

A

Arnaldo Naves de Brito

R

Ricardo Marinho

M

Marcus Agåker

T

Takashi Tokushima

MAX IV Laboratory

C

Conny Såthe

MAX IV Laboratory

A

Anirudha Ghosh

D

Dana Bloß

Institut für Physik und CINSaT, Universität Kassel, Heinrich-Plett-Str. 40, 34132 Kassel, Germany

A

Andreas Hans

Institut für Physik und CINSaT, Universität Kassel, Heinrich-Plett-Str. 40, 34132 Kassel, Germany

F

Florian Trinter

Fritz-Haber-Institut der Max-Planck-Gesellschaft , , Faradayweg 4-6 , ,

I

Iyas Ismail

CNRS, UMR 7614, Sorbonne Université , , 4 Place Jussieu , ,

D

Debora Vasconcelos

J

Joel Pinheiro

Y

Yi-Ping Chang

European XFEL, Holzkoppel 4, 22869 Schenefeld, Germany

M

Manuel Harder

European XFEL, Holzkoppel 4, 22869 Schenefeld, Germany

Z

Zhong Yin

International Center for Synchrotron Radiation Innovation Smart

J

Joseph Nordgren

G

Gunnar Öhrwall

MAX IV Laboratory, Lund University, Box 118, 22100 Lund, Sweden

H

Hans Ågren

School of Chemistry and Chemical Engineering

J

Jan-Erik Rubensson

O

Olle Björneholm

Department of Physics and Astronomy, Uppsala University, Box 516, 75120 Uppsala, Sweden