TY - JOUR
T1 - Development of a Multitimescale Time-Resolved Electron Diffraction Setup
T2 - Photoinduced Dynamics of Oxygen Radicals on Graphene Oxide
AU - Saida, Yuri
AU - Shikata, Ryo
AU - En-Ya, Kaito
AU - Ohmura, Satoshi
AU - Nishina, Yuta
AU - Hada, Masaki
N1 - Funding Information:
This work was supported by Kakenhi Grants-in-Aid (Nos. JP18H05208, JP20H01832, and JP20H04657) and the Leading Initiative for Excellent Young Researchers of the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan. This work was also supported by JST FOREST Program, Grant Number JPMJFR211V. A part of this work was supported by “Advanced Research Infrastructure for Materials and Nanotechnology in Japan (ARIM)” of the Ministry of Education, Culture, Sports, Science and Technology (MEXT). Grant Number JPMXP1222BA0009.
Publisher Copyright:
© 2022 American Chemical Society.
PY - 2022
Y1 - 2022
N2 - We developed a multitimescale time-resolved electron diffraction setup by electrically synchronizing a nanosecond laser with our table-top picosecond time-resolved electron diffractometer. The setup covers the photoinduced structural dynamics of target materials at timescales ranging from picoseconds to submilliseconds. Using this setup, we sequentially observed the ultraviolet (UV) photoinduced bond dissociation, radical formation, and relaxation dynamics of the oxygen atoms in the epoxy functional group on the basal plane of graphene oxide (GO). The results show that oxygen radicals formed via UV photoexcitation on the basal plane of GO in several tens of picoseconds and then relaxed back to the initial state on the microsecond timescale. The results of first-principles calculations also support the formation of oxygen radicals in the excited state on an early timescale. These results are essential for the further discussion of the reactivities on the basal plane of GO, such as catalytic reactions and antibacterial and antiviral activities. The results also suggest that the multitimescale time-resolved electron diffraction system is a promising tool for laboratory-based molecular dynamics studies of materials and chemical systems.
AB - We developed a multitimescale time-resolved electron diffraction setup by electrically synchronizing a nanosecond laser with our table-top picosecond time-resolved electron diffractometer. The setup covers the photoinduced structural dynamics of target materials at timescales ranging from picoseconds to submilliseconds. Using this setup, we sequentially observed the ultraviolet (UV) photoinduced bond dissociation, radical formation, and relaxation dynamics of the oxygen atoms in the epoxy functional group on the basal plane of graphene oxide (GO). The results show that oxygen radicals formed via UV photoexcitation on the basal plane of GO in several tens of picoseconds and then relaxed back to the initial state on the microsecond timescale. The results of first-principles calculations also support the formation of oxygen radicals in the excited state on an early timescale. These results are essential for the further discussion of the reactivities on the basal plane of GO, such as catalytic reactions and antibacterial and antiviral activities. The results also suggest that the multitimescale time-resolved electron diffraction system is a promising tool for laboratory-based molecular dynamics studies of materials and chemical systems.
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U2 - 10.1021/acs.jpca.2c04075
DO - 10.1021/acs.jpca.2c04075
M3 - Article
C2 - 36063425
AN - SCOPUS:85137883444
SN - 1089-5639
JO - Journal of Physical Chemistry A
JF - Journal of Physical Chemistry A
ER -