Two-photon dissociation dynamics of N2O: The N(2P <i>J</i> ) and N(2D <i>J</i> ) atom channels

S Shuaikang Yang (Department of Chemical Physics, School of Chemistry and Materials Science, University of Science and Technology of China 1 , Hefei, Anhui 230026,) Y Yongxin Dong (State Key Laboratory of Chemical Reaction Dynamics and Dalian Coherent Light Source, Dalian Institute of Chemical Physics, Chinese Academy of Sciences 2 , Dalian, Liaoning 116023,) Z Zhiguo Zhang (Key Laboratory of Biomass Chemical Engineering of Ministry of Education, College of Chemical and Biological Engineering) Z Zijie Luo (State Key Laboratory of Chemical Reaction Dynamics and Dalian Coherent Light Source, Dalian Institute of Chemical Physics, Chinese Academy of Sciences 2 , Dalian, Liaoning 116023,) W Wei Hua Z Zhenxing Li (State Key Laboratory of Heavy Oil Processing, College of New Energy and Materials) Q Quan Shuai (State Key Laboratory of Chemical Reaction Dynamics and Dalian Coherent Light Source, Dalian Institute of Chemical Physics, Chinese Academy of Sciences 2 , Dalian, Liaoning 116023,) X Xingan Wang (State Key Laboratory of Chemical Reaction Dynamics and Department of Chemical Physics, University of Science and Technology of China 1 , Hefei 230026,) K Kaijun Yuan (State Key Laboratory of Chemical Reaction Dynamics and Dalian Coherent Light Source, Dalian Institute of Chemical Physics, Chinese Academy of Sciences 2 , Dalian, Liaoning 116023,) X Xueming Yang (State Key Laboratory of Chemical Reaction Dynamics and Dalian Coherent Light Source, Dalian Institute of Chemical Physics)

Abstract

Two-photon dissociation dynamics of N2O were investigated by means of the time-sliced velocity map ion imaging technique. The N(2PJ) + NO(X2Π) and N(2DJ) + NO(X2Π) channels were accessed via two-photon excitation in the wavelength range of 218–236 nm. The four lobes in the angular distributions were clearly observed in both N-atom product channels, implying that the coherence between the two sequential transitions in the overall two-photon photodissociation process at the energies investigated has a significant influence on the angular distribution of the products. In addition, the translational energy distributions have been determined from the recorded images, revealing highly inverted vibrational populations of both NO products. In the N(2PJ) channel, initial vibrational excitation has a significant impact on the photodissociation dynamics of N2O via 3pσ1Π states. According to experimental results, the N(2PJ) channel may proceed via a bent configuration dissociation pathway involving coupling to an A′ symmetry potential energy surface that has not yet been theoretically reported. While the N(2DJ) channel may be preferentially formed via triplet and singlet Rydberg states that couple to the 43A′ and 51A′ states, followed by dissociation in a bent geometry.

Article Details

Volume / Issue Vol. 163, Issue 23
Published December 21, 2025
ISSN 0021-9606
Publisher American Institute of Physics

Journal Info

The Journal of Chemical Physics

American Institute of Physics

ISSN: 0021-9606 Physical Sciences

Authors (10)

S

Shuaikang Yang

Department of Chemical Physics, School of Chemistry and Materials Science, University of Science and Technology of China 1 , Hefei, Anhui 230026,

Y

Yongxin Dong

State Key Laboratory of Chemical Reaction Dynamics and Dalian Coherent Light Source, Dalian Institute of Chemical Physics, Chinese Academy of Sciences 2 , Dalian, Liaoning 116023,

Z

Zhiguo Zhang

Key Laboratory of Biomass Chemical Engineering of Ministry of Education, College of Chemical and Biological Engineering

Z

Zijie Luo

State Key Laboratory of Chemical Reaction Dynamics and Dalian Coherent Light Source, Dalian Institute of Chemical Physics, Chinese Academy of Sciences 2 , Dalian, Liaoning 116023,

W

Wei Hua

Z

Zhenxing Li

State Key Laboratory of Heavy Oil Processing, College of New Energy and Materials

Q

Quan Shuai

State Key Laboratory of Chemical Reaction Dynamics and Dalian Coherent Light Source, Dalian Institute of Chemical Physics, Chinese Academy of Sciences 2 , Dalian, Liaoning 116023,

X

Xingan Wang

State Key Laboratory of Chemical Reaction Dynamics and Department of Chemical Physics, University of Science and Technology of China 1 , Hefei 230026,

K

Kaijun Yuan

State Key Laboratory of Chemical Reaction Dynamics and Dalian Coherent Light Source, Dalian Institute of Chemical Physics, Chinese Academy of Sciences 2 , Dalian, Liaoning 116023,

X

Xueming Yang

State Key Laboratory of Chemical Reaction Dynamics and Dalian Coherent Light Source, Dalian Institute of Chemical Physics