The Science
The Impact
This research demonstrated that ETPA can obtain different information about molecules than OPA and TPA techniques can obtain. EPTA appears to be more efficient and to operate under lower photon intensity. This will allow scientists to use non-classical light to study states of molecules that are fundamentally different compared to states they can study with classical light techniques.
Summary
Scientists have often assumed that the colors of two-photon absorption from quantum light and classical light are the same. In this study, researchers from the University of Michigan and Northwestern University revealed through a combined experimental and theoretical study of an important organic molecule, zinc tetraphenyl porphyrin, that the colors of entangled two-photon absorption are remarkably different from the corresponding classical counterpart and also from one-photon resonant absorption with photons of doubled frequency (see “a” in the image above). This is due to the involvement of distinct electronic excited states. The results show that the most important excited states for both classical and quantum light excitation possess high electronic entanglements. The results also show that ETPA provides the opportunity to probe molecules with non-classical light that are inaccessible with classical light or to enhance their quantum light response under extremely low excitation intensity.
ETPA may be particularly useful for solving the long-standing challenge of photodamage and phototoxicity in bioimaging, especially in complex biological molecules. This would expand researchers’ ability to conduct non-destructive imaging of complex biomolecules. Of particular interest is the implementation of the ETPA imaging modality to monitor long-term spatial and temporal dynamics of bacterial gene expression in the sub-soil rhizosphere (see “b-c” in the image above). In addition, identifying the colors of such an entangled two-photon absorption could lead to reduction in data acquisition time while maintaining an extremely low excitation intensity.
Funding
This research was supported by the Department of Energy Office of Science, Biological and Environmental Research program.