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Attosecond X-ray Molecular Dynamics and Strong-Field Control

Project description

Ultrashort light pulses reveal ultrafast dynamics of light-induced reactions

Ultrashort light sources enable scientists to study electron and nuclear dynamics in materials. The temporal resolution of these ultrafast pulses opens a window on chemical reactions and the interactions of biological molecules in real time. The EU-funded ATTO-CONTROL project will harness two of the most powerful experimental methods available to study and ultimately control important photochemical reactions of relevance to biology and technological development. Photochemical reactions are chemical reactions triggered when light energy is absorbed by one or more molecules, leading to a temporarily excited state that alters the physical and chemical properties of the molecules. ATTO-CONTROL will apply ultrashort light sources to observe and/or control these dynamics in real time.

Objective

The development in recent years of ultrashort light sources in the attosecond regime has opened new avenues for the investigation of electronic and nuclear dynamics. In particular, the current development of UV-XUV or UV-X-ray pump-probe schemes with subfemtosecond temporal resolution represents a doorway to study chemical reactions in excited states of molecules in real-time, including biological reactions, such as e.g. those related to DNA damage and mutations.
The aim of this project is to understand and ultimately control photochemical reactions in excited states of polyatomic molecules, especially relating to two fundamental processes in biology and chemistry: (i) cis-trans photoisomerization and (ii) the internal conversion of pi-pi*/n-pi* states in organic chromophores. Two top-notch experimental methods will be employed to achieve this goal: attosecond X-ray transient absorption (X-ATAS) at the University of California at Berkeley (United States), where the fellowship will be carried out under the supervision of Prof. S. Leone, and three-color femtosecond pump-probe velocity map imaging (fs-VMI) at Complutense University of Madrid (Spain), where the incoming phase will take place under the supervision of Prof. L. Bañares.
The project is divided in three specific objectives and work-packages. Firstly, the powerful X-ATAS method will be employed to observe dynamics in real-time through individual carbon atom spectra and disentangle the dynamics underlying these processes in two polyatomic targets –nitroethylene and transbutadiene– and two bio-relevant ones –thymine and citosine. Secondly, attosecond control in real-time using X-ATAS on the pi-pi*/ n-pi* internal conversion in thymine will be performed in a pioneering experiment. Finally, effective femtosecond control with fs-VMI of these processes in nitroethylene and trans-butadiene, molecules of interest for technologies, will be performed based on the relevant results from the X-ATAS experiments.

Fields of science (EuroSciVoc)

Keywords

Programme(s)

Topic(s)

Funding Scheme

MSCA-IF - Marie Skłodowska-Curie Individual Fellowships (IF)

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Call for proposal

(opens in new window) H2020-MSCA-IF-2018

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Coordinator

UNIVERSIDAD COMPLUTENSE DE MADRID
Net EU contribution
€ 245 732,16
Address
AVENIDA DE SENECA 2
28040 Madrid
Spain
Region
Comunidad de Madrid Comunidad de Madrid Madrid
Activity type
Higher or Secondary Education Establishments
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Total cost
€ 245 732,16

Partners (1)