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Table B.1

Photodissociation pathways, cross-sections, and quantum yields used in this study.

Species Products Cross sections Quantum yields
H2O H + OH Chan et al. (1993c); Fillion et al. (2004); Heays et al. (2017)
H2 + O(1D) Mota et al. (2005); Ranjan et al. (2020)
H + H + O(3P)
CO + O(1D) Stark et al. (2007); Huestis & Berkowitz (2010); Heays et al. (2017)
CO + O(3P) Venot et al. (2018)
H2CO H2 + CO Cooper et al. (1996); Meller & Moortgat (2000) Heays et al. (2017)
H + HCO
H + H + CO
OH O(1D) + H Huebner et al. (1992) Heays et al. (2017)
O(3P) + H
OOH OH + O(3P) Heays et al. (2017)
CO C + O(3P) Olney et al. (1997) Heays et al. (2017)
C + O(1D)
H2 H + H Samson & Haddad (1994); Heays et al. (2017)
Chan et al. (1992); Olney et al. (1997)
HCO H + CO Loison et al. (1991); Hochanadel et al. (1980)
CH3OH H2CO + H2 Burton et al. (1992); Cheng et al. (2002) Heays et al. (2017)
CH3 + OH
CH3OOH CH3O + OH Vaghjiani & Ravishankara (1989); Matthews et al. (2005)
CH2CO 3CH2 + CO Laufer & Keller (1971)
CH3CHO CH4 + CO Limão-Vieira et al. (2003); Burkholder et al. (2020) Heays et al. (2017)
CH3 + HCO
CH3 1CH2 + H Heays et al. (2017) Heays et al. (2017)
CH4 CH3 + H Au et al. (1993); Lee et al. (2001); Peng et al. (2014)
1CH2 + H2 Kameta et al. (2002); Chen & Wu (2004)
1CH2 + H + H
3CH2 + H + H
CH + H2 + H
C2H C + C + H Heays et al. (2017); Fahr (2003)
C2H2 C2H + H Cooper et al. (1995a); Wu et al. (2001) Heays et al. (2017); Hébrard et al. (2013)
C2H3 C2H2 + H Fahr et al. (1998)
C2H4 C2H2 + H2 Cooper et al. (1995b); Orkin et al. (1997); Heays et al. (2017)
C2H2 + H + H Wu et al. (2004)
C2H6 C2H4 + H2 Au et al. (1993); Kameta et al. (1996); Heays et al. (2017); Hébrard et al. (2006)
C2H4 + H + H Lee et al. (2001); Chen & Wu (2004)
C2H2 + H2 + H2
CH4 + 1CH2
CH3 + CH3
N2 N(2D) + N(4S) Samson & Cairns (1964); Huffman (1969);
Stark et al. (1992); Chan et al. (1993d)
NH2 NH + H Heays et al. (2017) Heays et al. (2017)
NH2 + H Burton et al. (1993); Chen et al. (1998); Heays et al. (2017)
NH + H2 Cheng et al. (2006)
NH + H + H
N2H4 N2H3 + H Vaghjiani (1993); Biehl & Stuhl (1991)
HCN, HNC CN + H Nuth & Glicker (1982);Bénilan et al. (in prep.); Heays et al. (2017)
Venot et al. (in prep.)
H2CN HCN + H Nizamov & Dagdigian (2003); Teslja et al. (2006)
C2N2 CN + CN Bénilan et al. (in prep.)
NO N(4S) + O(3P) Iida et al. (1986); Chan et al. (1993b) Heays et al. (2017)
NO2 NO + O(3P) Au & Brion (1997); Vandaele et al. (2002) Heays et al. (2017)
NO + O(1D)
NO3 NO2 + O(3P) Orphal & Chance (2003); Sander (1986) Heays et al. (2017)
NO + O2 Yokelson et al. (1994)
HNO2 NO + OH Burkholder et al. (2020)
HNO3 NO2 + OH Burkholder et al. (2020)
N2O N2 + O(1D) Burkholder et al. (2020); Hubrich & Stuhl (1980) Heays et al. (2017)
O2 O(3P) + O(3P) Brion et al. (1979); Yoshino et al. (2005) Heays et al. (2017)
O(1D) + O(3P) Fally et al. (2000); Chan et al. (1993a)
O(1D) + O(1D)

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