Imaging intramolecular hydrogen migration with time- and momentum-resolved photoelectron diffraction
Entity
UAM. Departamento de QuímicaPublisher
Royal Society of ChemistryDate
2021-07-28Citation
10.1039/d1cp02055b
Physical Chemistry Chemical Physics 23.36 (2021): 20174-20182
ISSN
1463-9076 (print); 1463-9084 (online)DOI
10.1039/d1cp02055bFunded by
This work was performed under the European COST Action CA18222 AttoChem and Cooperative Research Program of ‘‘Network Joint Research Center for Materials and Devices.’’ K. H. acknowledges funding by JSPS KAKENHI under Grant No. 18K05027 and 17K04980. This work was partially funded by the Spanish Ministry of Science and Innovation – Ministerio Español de Ciencia e Innovación MICINN – projects PID2019-105458RB-I00 and PID2019-110091GB-I00, the Severo Ochoa Programme for Centres of Excellence in R & D (SEV-2016-0686) and the María de Maeztu Programme for Units of Excellence in R & D (CEX2018-000805-M)Project
Gobierno de España. PID2019-105458RB-I00; Gobierno de España. PID2019-110091GB-I00; Gobierno de España. SEV-2016-0686; Gobierno de España. CEX2018-000805-MEditor's Version
https://doi.org/10.1039/d1cp02055bSubjects
Chiral; Photoionization; Angular Distribution; QuímicaRights
© the Owner Societies 2021Abstract
Imaging ultrafast hydrogen migration with few- or sub-femtosecond time resolution is a challenge for ultrafast spectroscopy due to the lightness and small scattering cross-section of the moving hydrogen atom. Here we propose time- and momentum-resolved photoelectron diffraction (TMR-PED) as a way to overcome limitations of existing methodologies and illustrate its performance in the ethanol molecule. By combining different theoretical methods, namely molecular dynamics and electron scattering methods, we show that TMR-PED, along with a judicious choice of the reference frame for multi-coincidence detection, allows for direct imaging of single and double hydrogen migration in doubly-charged ethanol with both few-fs and Å resolutions, all the way from its birth to the very end. It also provides hints of proton extraction following H2 roaming. The signature of hydrogen dynamics shows up in polarization-averaged molecular-frame photoelectron angular distributions (PA-MFPADs) as moving features that allow for a straightforward visualization in space
Files in this item
Google Scholar:Ota, Fukiko
-
Abe, Shigeru
-
Hatada, Keisuke
-
Ueda, Kiyoshi
-
Díaz-Tendero Victoria, Sergio
-
Martín García, Fernando
This item appears in the following Collection(s)
Related items
Showing items related by title, author, creator and subject.