Founding offer · lifetime membership for a single £24, exclusive to our first members · closes 20 June Claim your place →
Global Research Partnerships £24 Lifetime Log inCreate free account

Funded Projects › FP7

XCHEM · XUV/X-ray lasers for ultrafast electronic control in chemistry

FP7Status: CLOSED1 January 201231 August 2017EU funding €2,447,736

Advances in generating controlled few-cycle laser pulses and novel ultrashort XUV/Xray sources, from free electron laser (FEL)-based to attosecond high harmonic generation (HHG)-based, have opened completely new avenues for imaging electronic and nuclear dynamics in molecules, with exciting applications in physics, chemistry and biology. Processes such as ionization and dissociation of simple diatomic molecules can now be monitored in real time, but the access to few-femtosecond or attosecond time scales in the XUV/X-ray domain may also allow one to uncover and control the dynamics of elementary chemical processes such as, e.g., ultrafast charge migration, proton transfer, isomerization or multiple ionization, and to address new key questions about the role of attosecond coherent electron dynamics in chemical reactivity. The success of current experimental efforts in explaining these phenomena, present in many biological processes, is seriously limited due to the difficulty in their interpretation. In this respect, the implementation by the applicant’s group of nearly exact theoretical methods in supercomputers has made it possible to guide experimental research on simple systems. Such theoretical methods lie outside the traditional quantum chemistry realm since, e.g., they must accurately reproduce the time evolution of the coupled electronic and nuclear motions in the electronic and dissociative continua, including electron correlation and non-adiabatic effects. The necessary extension to systems of chemical interest, the current bottleneck in this field, requires extensive and novel theoretical developments along a similar direction. The aim of this project is to study the electronic and coupled electronic-nuclear dynamics in complex molecules at the attosecond or few-femtosecond time-scales, developing concepts and accurate theoretical tools to interpret the new generation of time-resolved experiments and to achieve ultrafast electronic control in chemistry.

Consortium · 1 organisation

coordinator

UNIVERSIDAD AUTONOMA DE MADRID

ES · €2,447,736

Research fields

View the official record on CORDIS →

← Find collaborators and more funded projects

Source: CORDIS, Publications Office of the European Union. Global Research Partnerships surfaces open EU research data to help you find collaborators; we are not affiliated with the European Union.