Dynamics and Vector Correlations of Vacuum Ultraviolet (VUV) Photodissociation of CO2 at 155 nm

Author(s):  
Evangelia Sakkoula ◽  
Gautam Sarma ◽  
Xingan Wang ◽  
Simon W. North ◽  
David H Parker ◽  
...  

In this work, the CO2 Vacuum Ultraviolet (VUV) photodissociation dynamics of the dominant O(1D) channel near 155 nm have been studied using Velocity Map Imaging (VMI) technique. Correlations among the...

2020 ◽  
Vol 637 ◽  
pp. A37 ◽  
Author(s):  
Xiaoping Chi ◽  
Pan Jiang ◽  
Qihe Zhu ◽  
Min Cheng ◽  
Hong Gao

In this study, we present C+ ion photofragment spectroscopic studies and photodissociation branching ratio measurements for two CO isotopologs, 13C16O and 12C18O, in the vacuum ultraviolet (VUV) region from 107 800 cm−1 (92.76 nm) to 109 700 cm−1 (91.16 nm) using a time-slice velocity-map imaging setup and a tunable VUV laser radiation source generated by the two-photon resonance-enhanced four-wave mixing technique. Several absorption bands of 12C16O in the above energy region are reinvestigated up to higher rotational levels compared with previous studies. The results are compared among 12C16O, 13C16O, and 12C18O on a state-by-state basis, and the photodissociation branching ratios for channels C(1D) + O(3P), and C(3P) + O(1D) are dramatically changed for most of the absorption bands due to the substitutions of 12C by 13C and 16O by 18O. The branching ratios of 13C16O and 12C18O are close to each other due to their similar reduced masses. The strong and selective isotope effects obtained here not only provide useful information for understanding the complicated predissociation dynamics of CO, but are also important for developing a comprehensive photochemical model for explaining the C and O isotope heterogeneities as observed in the Solar System.


Science ◽  
2014 ◽  
Vol 346 (6205) ◽  
pp. 61-64 ◽  
Author(s):  
Zhou Lu ◽  
Yih Chung Chang ◽  
Qing-Zhu Yin ◽  
C. Y. Ng ◽  
William M. Jackson

Photodissociation of carbon dioxide (CO2) has long been assumed to proceed exclusively to carbon monoxide (CO) and oxygen atom (O) primary products. However, recent theoretical calculations suggested that an exit channel to produce C + O2 should also be energetically accessible. Here we report the direct experimental evidence for the C + O2 channel in CO2 photodissociation near the energetic threshold of the C(3P) + O2(X3Σg–) channel with a yield of 5 ± 2% using vacuum ultraviolet laser pump-probe spectroscopy and velocity-map imaging detection of the C(3PJ) product between 101.5 and 107.2 nanometers. Our results may have implications for nonbiological oxygen production in CO2-heavy atmospheres.


1988 ◽  
Vol 102 ◽  
pp. 353-356
Author(s):  
C. Goldbach ◽  
G. Nollez

AbstractThe principles and the realization of an experiment devoted to oscillator strength measurements in the vacuum-ultraviolet by the emission method are briefly presented. The results obtained for the strong multiplets of neutral nitrogen and carbon in the 1200-2000 Å range yield an absolute scale of oscillator strengths in good agreement with the most recent calculations.


1978 ◽  
Vol 39 (C4) ◽  
pp. C4-227-C4-232 ◽  
Author(s):  
JAMES A. R. SAMSON
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document