SOLVE

"Solvated Electrons in Water: Structure, Dynamics and Reactivity at Interfaces"

Coordinatore	UNIVERSITY OF DURHAM    more Spiacenti, non ci sono informazioni su questo coordinatore. Contattare Fabio per maggiori infomrazioni, grazie.
Nazionalità Coordinatore	United Kingdom [UK]
Totale costo	1˙839˙322 €
EC contributo	1˙839˙322 €
Programma	FP7-IDEAS-ERC Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
Code Call	ERC-2012-StG_20111012
Funding Scheme	ERC-SG
Anno di inizio	2013
Periodo (anno-mese-giorno)	2013-01-01   -   2017-12-31

 Partecipanti

#	participant	country	role	EC contrib. [€]
1	UNIVERSITY OF DURHAM  Organization address address: STOCKTON ROAD THE PALATINE CENTRE city: DURHAM postcode: DH1 3LE contact info Titolo: Dr. Nome: Jan Raf Rogier Cognome: Verlet Email: send email Telefono: +44 191 3342159 Fax: +44 191 334 2051	UK (DURHAM)	hostInstitution	1˙839˙322.00
2	UNIVERSITY OF DURHAM  Organization address address: STOCKTON ROAD THE PALATINE CENTRE city: DURHAM postcode: DH1 3LE contact info Titolo: Ms. Nome: Wendy Cognome: Harle Email: send email Telefono: +44 191 3344635 Fax: +44 191 3344634	UK (DURHAM)	hostInstitution	1˙839˙322.00

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 Obiettivo del progetto (Objective)

'Understanding the solvation of an ion at the molecular level is a cornerstone of physical chemistry. For anions in water, the interactions are particularly complex, with some simple anions exhibiting surface activity. The most fundamental aqueous anion is the hydrated electron and it represents a benchmark for understanding solvation and electron-water interactions in solution. However, despite the hydrated electron’s apparent simplicity and its technological and scientific importance, it remains at the centre of much debate. Questions concerning its structure and solvation at interfaces are currently highly contentious. In this proposal, a number of complementary approaches are applied to the study of aqueous interfacial electrons with the aim of gaining a new understanding of the solvation structure, dynamics and reactivity of this species. Specifically, gas-phase clusters will be used as molecular-level laboratories to gain a fundamental understanding of the electron-water interactions as well as solvation motifs and dynamics. These will also be used to explore the reactivity of electrons bound at the interface of water with atmospheric and biologically pertinent molecules. In parallel to the cluster studies, dynamics and reactivity of the electron at the ambient water interface will also be studied using non-linear spectroscopy. Together, these studies will provide an in depth understanding of electron solvation and its importance as a reactive species at aqueous interfaces.'