Reaction dynamics and isotope effects in the D + CD4 → D2 + CD3 reaction

Y Yuxin Tan (State Key Laboratory of Chemical Reaction Dynamics and Department of Chemical Physics, University of Science and Technology of China 1 , Hefei 230026,) C Chang Luo M Mengda Jin (State Key Laboratory of Chemical Reaction Dynamics and Department of Chemical Physics, University of Science and Technology of China 1 , Hefei 230026,) Y Yu Zhang (Xiangya Hospital, Central South University Changsha China) F Fan Li S Shanshan Yu W Wentao Chen (Key Laboratory for Soft Chemistry and Functional Materials of Ministry Education, School of Chemistry and Chemical Engineering) D Daofu Yuan (Hefei National Research Center for Physical Sciences at Microscale, University of Science and Technology of China 2 , Hefei 230026,) X Xueming Yang (State Key Laboratory of Chemical Reaction Dynamics and Dalian Coherent Light Source, Dalian Institute of Chemical Physics) 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,)

Abstract

The H + CH4 reaction and its isotopic variant reactions serve as a benchmark reaction system to understand the dynamics of polyatomic reactions. In this paper, we report a vibrationally state-resolved crossed molecular beam study on the D + CD4 → D2 + CD3 reaction using the time-sliced velocity map ion imaging method. Pronounced collision energy dependence is found in product kinetic energy distributions and angular distributions. At 0.67 eV, CD3 products are dominantly distributed in the backward direction with D2 products in the vibrational ground state. As collision energy increases, the angular distributions of CD3 products shift from the backward direction to the sideways and forward directions, and vibrational excited D2 appears and intensifies. By comparing our result of the D + CD4 → D2 + CD3 reaction with previous studies on the D + CH4 → HD + CH3 and H + CD4 → HD + CD3 reactions, isotope effects have been discussed. The product kinetic energy and angular distributions vary significantly among the three isotopic variant reactions.

Article Details

Volume / Issue Vol. 163, Issue 20
Published November 28, 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)

Y

Yuxin Tan

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

C

Chang Luo

M

Mengda Jin

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

Y

Yu Zhang

Xiangya Hospital, Central South University Changsha China

F

Fan Li

S

Shanshan Yu

W

Wentao Chen

Key Laboratory for Soft Chemistry and Functional Materials of Ministry Education, School of Chemistry and Chemical Engineering

D

Daofu Yuan

Hefei National Research Center for Physical Sciences at Microscale, University of Science and Technology of China 2 , Hefei 230026,

X

Xueming Yang

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

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,