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Observing the primary steps of ion solvation in helium droplets.
Albrechtsen, Simon H; Schouder, Constant A; Viñas Muñoz, Alberto; Christensen, Jeppe K; Engelbrecht Petersen, Christian; Pi, Martí; Barranco, Manuel; Stapelfeldt, Henrik.
Afiliación
  • Albrechtsen SH; Department of Physics and Astronomy, Aarhus University, Aarhus, Denmark.
  • Schouder CA; Department of Chemistry, Aarhus University, Aarhus, Denmark.
  • Viñas Muñoz A; Université Paris-Saclay, CEA, CNRS, LIDYL, Gif-sur-Yvette, France.
  • Christensen JK; Department of Chemistry, Aarhus University, Aarhus, Denmark.
  • Engelbrecht Petersen C; Department of Chemistry, Aarhus University, Aarhus, Denmark.
  • Pi M; Department of Physics and Astronomy, Aarhus University, Aarhus, Denmark.
  • Barranco M; Departament FQA, Facultat de Física, Universitat de Barcelona, Barcelona, Spain.
  • Stapelfeldt H; Institute of Nanoscience and Nanotechnology (IN2UB), Universitat de Barcelona, Barcelona, Spain.
Nature ; 623(7986): 319-323, 2023 Nov.
Article en En | MEDLINE | ID: mdl-37938709
ABSTRACT
Solvation is a ubiquitous phenomenon in the natural sciences. At the macroscopic level, it is well understood through thermodynamics and chemical reaction kinetics1,2. At the atomic level, the primary steps of solvation are the attraction and binding of individual molecules or atoms of a solvent to molecules or ions of a solute1. These steps have, however, never been observed in real time. Here we instantly create a single sodium ion at the surface of a liquid helium nanodroplet3,4, and measure the number of solvent atoms that successively attach to the ion as a function of time. We found that the binding dynamics of the first five helium atoms is well described by a Poissonian process with a binding rate of 2.0 atoms per picosecond. This rate is consistent with time-dependent density-functional-theory simulations of the solvation process. Furthermore, our measurements enable an estimate of the energy removed from the region around the sodium ion as a function of time, revealing that half of the total solvation energy is dissipated after four picoseconds. Our experimental method opens possibilities for benchmarking theoretical models of ion solvation and for time-resolved measurements of cation-molecule complex formation.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Nature Año: 2023 Tipo del documento: Article País de afiliación: Dinamarca

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Nature Año: 2023 Tipo del documento: Article País de afiliación: Dinamarca