Abstract
Ultrafast spectroscopic techniques in the electronic and vibrational domains have enabled the real-time tracking of molecular motions from electrons to atoms in naturally sourced organic chromophores, powering their intrinsic photoresponse and excited-state mechanisms that could be rationally tuned and designed for versatile optoelectronic applications. An interplay between charge/proton/energy transfer across singlet and triplet states has been highlighted as these organic optoelectronic materials represent a sustainable and efficient route to meet the growing energy and technological demands. Read more in the Review by T. D. Krueger and C. Fang on page 17736 ff.
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