Repositori URV

Autor segons l'article: Linnenberg O; Moors M; Solé-Daura A; López X; Bäumer C; Kentzinger E; Pyckhout-Hintzen W; Monakhov K

Departament: Química Física i Inorgànica

Autor/s de la URV: López Fernández, Javier / Solé Daura, Albert

Paraules clau: Clean water and sanitation

Resum: © 2017 American Chemical Society. The understanding of the molecular state of vanadium-oxo clusters (polyoxovanadates, POVs) in solution and on surface is a key to their target application in catalysis as well as molecular electronics and spintronics. We here report the results of a combined experimental and computational study of the behavior of nucleophilic polyoxoanions [VIV10VV8O42(I)]5- charged balanced by Et4N+ in water, in a one-phase organic solution of N,N-dimethylformamid (DMF) or acetonitrile (MeCN), in a mixed solution of MeCN-water, and at the hybrid liquid-surface interface. The molecular characteristics of the compound (NEt4)5[V18O42(I)] (1) in the given environments were studied by microspectroscopic, electrochemical, scattering, and molecular mechanics methods. Contrary to the situation in pure water, where we observe great agglomeration with a number of intercalated H2O molecules between POVs that are surrounded by the Et4N+ ions, no or only minor agglomeration of redox-active POVs in an unprecedented cation-mediated fashion was detected in pure DMF and MeCN, respectively. An inclusion of 1% water in the MeCN solution does not have an effect significant enough to reinforce agglomeration; however, this leads to the POV⋯POV interface characterized by the presence of the Et4N+ ions and a small number of H2O molecules. Water amounts of ≥5% trigger the formation of higher oligomers. The deposition of compound 1 from MeCN onto an Au(111) surface affords nearly round-shaped particles (∼10 nm). The use of DMF instead of MeCN results in bigger, irregularly shaped particles (∼30 nm). This change of solvent gives rise to more extensive intermolecular interactions between polyoxoanions and their countercations as well as weaker binding of ion-pairing induced agglomerates to the metallic substrate. Lower concentration of adsorbed molecules leads to a submonolayer coverage and an accompanied change of the POV's redox state, whereas their higher concentration results in a multilayer coverage that offers the pristine mixed-valence structure of the polyoxoanion. Our study provides first important insights into the reactivity peculiarities of this redox-responsive material class on a solid support.

Àrees temàtiques: Surfaces, coatings and films Química Physical and theoretical chemistry Nanoscience and nanotechnology Nanoscience & nanotechnology Medicina ii Medicina i Materials science, multidisciplinary Materiais Interdisciplinar General energy Farmacia Ensino Engenharias iv Engenharias iii Engenharias ii Engenharias i Energy (miscellaneous) Energy (all) Electronic, optical and magnetic materials Ciências biológicas iii Ciências biológicas ii Ciências biológicas i Ciências ambientais Ciências agrárias i Chemistry, physical Biotecnología Biodiversidade Astronomia / física

Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/

ISSN: 19327447

Adreça de correu electrònic de l'autor: javier.lopez@urv.cat

Identificador de l'autor: 0000-0003-0322-6796

Data d'alta del registre: 2024-11-16

Versió de l'article dipositat: info:eu-repo/semantics/acceptedVersion

Enllaç font original: https://pubs.acs.org/doi/10.1021/acs.jpcc.7b02138

URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/

Referència a l'article segons font original: Journal Of Physical Chemistry c. 121 (19): 10419-10429

Referència de l'ítem segons les normes APA: Linnenberg O; Moors M; Solé-Daura A; López X; Bäumer C; Kentzinger E; Pyckhout-Hintzen W; Monakhov K (2017). Molecular Characteristics of a Mixed-Valence Polyoxovanadate {VIV/V18O42} in Solution and at the Liquid-Surface Interface. Journal Of Physical Chemistry c, 121(19), 10419-10429. DOI: 10.1021/acs.jpcc.7b02138

DOI de l'article: 10.1021/acs.jpcc.7b02138

Entitat: Universitat Rovira i Virgili

Any de publicació de la revista: 2017

Tipus de publicació: Journal Publications