The probability of ND-TPA is quantified as the non-degenerate two-photon absorption cross section (ND-TPACS) and is an inherent property of molecules. ND-TPACS has been measured using Z-scan (pump-probe) techniques,[3] which measure the laser intensity decrease due to absorption, and fluorescence-based techniques,[4] which measure the fluorescence generated by the fluorophores upon ND-TPA.
In ND-TPA, by absorbing the first photon, the molecule makes a transition to a virtual state and stays in the virtual state for an extremely short period of time (virtual state lifetime, VSL). If a second photon is absorbed during the VSL, the molecule makes a transition to the excited electronic state, otherwise it will relax back to the ground state. Therefore, the two photons are "almost" simultaneously absorbed in two-photon absorption. Based on the time–energy uncertainty relation, VSL is inversely proportional to the energy difference between the virtual state and the nearest real electronic state (i.e. the ground or a nearby excited state). Therefore, the closer the virtual state to the real state, the longer the VSL and the higher the probability of TPA. This means that in comparison to degenerate TPA, where the virtual state is in the middle of the ground and the excited state, ND-TPA has a larger absorption cross-section. This phenomenon is known as the resonance enhancement and is the main mechanism behind the observed increase in ND-TPACS of semiconductors [5] and fluorophores[6][7] in comparison to their degenerate TPA cross-sections.
ND-TPA has also been explored in two-photon microscopy for decreasing out-of-focus excitation, increasing penetration depth, increasing spatial resolution, and extending the excitation wavelength range.
^Hutchings, DC; Van Stryland, Eric W (1992). "Nondegenerate two-photon absorption in zinc blende semiconductors". JOSA B. 9 (11): 2065–2074. doi:10.1364/JOSAB.9.002065.
^Lakowicz, Joseph R; Gryczynski, Ignacy; Malak, Henryk; Gryczynski, Zygmunt (1996). "Two‐Color Two‐Photon Excitation of Fluorescence". Photochemistry and Photobiology. 64 (4): 632–635. doi:10.1111/j.1751-1097.1996.tb03116.x. PMID8863469. S2CID29680279.
^Negres, Raluca A; Hales, Joel M; Kobyakov, Andrey; Hagan, David J; Van Stryland, Eric W (2002). "Two-photon spectroscopy and analysis with a white-light continuum probe". Optics Letters. 27 (4): 270–272. doi:10.1364/OL.27.000270. PMID18007776.