Carregant...
Miniatura

Tipus de document

Article

Versió

Versió publicada

Data de publicació

Llicència de publicació

cc-by-nc (c) Hernández-Rodríguez, Javier et al., 2023
Si us plau utilitzeu sempre aquest identificador per citar o enllaçar aquest document: https://hdl.handle.net/2445/216980

Potential energy surfaces for singlet and triplet states of the LiH2+ system and quasi-classical trajectory cross sections for H + LiH+ and H+ + LiH

Títol de la revista

Director/Tutor

ISSN de la revista

Títol del volum

Resum

A new set of six accurate ab initio potential energy surfaces (PESs) is presented for the first three singlet and triplet states of LiH2+ (1,21A′, 11A′′, 1,23A′, and 13A′′ states, where four of them are investigated for the first time), which have allowed new detailed studies gaining a global view on this interesting system. These states are relevant for the study of the most important reactions of lithium chemistry in the early universe. More than 45 000 energy points were calculated using the multi-reference configuration interaction level of theory using explicitly correlated methods (ic-MRCI-F12), and the results obtained for each individual electronic state were fitted to an analytical function. Using quasiclassical trajectories and considering the initial diatomic fragment in the ground rovibrational state, we have determined the integral cross sections for the H + LiH+(X2Σ+, C2Π) and H+ + LiH(X1Σ+, B1Π) reactions. In these calculations all available reaction channels were considered: the chemically most important H or H+ transfer/abstraction as well as atom exchange and collision induced dissociation for up to 1.0 eV of collision energy.

Citació

Citació

HERNÁNDEZ-RODRÍGUEZ, Javier, SANZ-SANZ, Cristina, ENRÍQUEZ, Pedro alberto, GONZÁLEZ PÉREZ, Miguel, PANIAGUA, Miguel. Potential energy surfaces for singlet and triplet states of the LiH2+ system and quasi-classical trajectory cross sections for H + LiH+ and H+ + LiH. _Physical Chemistry Chemical Physics_. 2023. Vol. 25, núm. 28052-28062. [consulta: 23 de gener de 2026]. ISSN: 1463-9076. [Disponible a: https://hdl.handle.net/2445/216980]

Exportar metadades

JSON - METS

Compartir registre