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. 2017 May 25;13:39–59. doi: 10.1016/j.redox.2017.05.011

Table 1.

Molecular oxygen optical transitions between the ground state (O2 X3Σg-) and the first two electronic excited states (O2 a1Δg) and (O2 b1Σg+). The transitions are listed in order of increasing energy (eV) (decreasing wavelength in nm). Both monomol (M) and dimol (D) transitions are shown. Data based on [35], [99], [100], [101], [102], [103], [104], [107].

Wavelength Photon energy Type Electronic transition
(M-Monomol;
D-Dimol)
1270 nm 0.97 eV M O2 X3Σg- → O2 a1Δg v = 0
1065 nm 1.16 eV M O2 X3Σg- → O2 a1Δg v = 1
920 nm 1.35 eV M O2 X3Σg- → O2 a1Δg v = 2
810 nm 1.53 eV M O2 X3Σg- → O2 a1Δg v = 3
760 nm 1.63 eV M O2 X3Σg- → O2 b1Σg+ v = 0
690 nm 1.80 eV M O2 X3Σg- → O2 b1Σg+ v = 1
633 nm 1.96 eV D [O2 X3Σg- - O2 X3Σg-] → [O2 a1Δg v = 0 - O2 a1Δg v = 0]
627 nma 1.98 eV M O2 X3Σg- → O2 b1Σg+ v = 2
580 nma 2.14 eV M O2 X3Σg- → O2 b1Σg+ v = 3
577 nm 2.15 eV D [O2 X3Σg- - O2 X3Σg-] → [O2 a1Δg v = 1 - O2 a1Δg v = 0]
532 nma 2.33 eV D [O2 X3Σg- - O2 X3Σg-] → [O2 a1Δg v = 2 - O2 a1Δg v = 0]
495 nma 2.50 eV D [O2 X3Σg- - O2 X3Σg-] → [O2 a1Δg v = 3 - O2 a1Δg v = 0]
477 nma 2.60 eV D [O2 X3Σg- - O2 X3Σg-] → [O2 a1Δg v = 0 - O2 b1Σg+ v = 0]
446 nma 2.78 eV D [O2 X3Σg- - O2 X3Σg-] → [O2 a1Δg v = 1 - O2 b1Σg+ v = 0]
420 nma 2.95 eV D [O2 X3Σg- - O2 X3Σg-] → [O2 a1Δg v = 2 - O2 b1Σg+ v = 0]
395 nma 3.14 eV D [O2 X3Σg- - O2 X3Σg-] → [O2 a1Δg v = 3 - O2 b1Σg+ v = 0]
380 nma 3.26 eV D [O2 X3Σg- - O2 X3Σg-] → [O2 b1Σg+ v = 0 - O2 b1Σg+ v = 0]
360 nma 3.44 eV D [O2 X3Σg- - O2 X3Σg-] → [O2 b1Σg+ v = 1 - O2 b1Σg+ v = 0]
344 nma 3.60 eV D [O2 X3Σg- - O2 X3Σg-] → [O2 b1Σg+ v = 2 - O2 b1Σg+ v = 0]
a

Transitions included for completeness but not discussed in depth in the text.