Search

Organic semiconductor molecules possess chemical tunability and large stimulated emission cross section, representing a promising candidate for laser gain medium. However, for the pursuit of telecom‐wavelength organic lasers, one of the major obstacles is the lack of effective energy‐level systems with high optical gain to compensate the exciton deactivation losses. Herein, the effects of molecular conformation‐dependent distinct cascaded proton‐transfer six‐level energy gain systems on lasing emission properties are systematically investigated based on organic polymorphs, proving that an energy‐level gain system without reversible transition channels is more conducive to the formation of efficient population inversion and high optical gain. Notably, the one‐way irreversible six‐level energy system of β‐phase polymorph supports more favorable population inversions than the two‐way reversible six‐level system of α‐phase polymorph due to the irreversible excited‐state second proton transfer and the irreversible ground‐state recovery, achieving the amplified spontaneous emission at telecom‐wavelength of ≈850 nm. This study provides useful guidelines for constructing efficient energy‐level gain systems, promoting the exploration of high‐gain organic semiconductor laser materials from visible to near‐infrared region. [ABSTRACT FROM AUTHOR]

Organic molecules which can undergo excited‐state intramolecular proton transfer (ESIPT) process have been considered as ideal gain materials for near‐infrared organic lasers owing to their effective four‐level systems. However, extending lasing wavelength beyond 800 nm with present ESIPT‐active gain materials is still in challenge. Herein, we established a molecular design strategy that operates via extending the π‐conjugated system of the ESIPT parent core to enhance the cascaded double ESIPT process and thus to achieve the red‐shifted six‐level system lasing. Concretely, a model molecule with 1,9‐dihydroxyanthracene as the ESIPT parent core was designed and synthesized, which was proved to undergo twice cascaded ESIPT processes while the 1,8‐dihydroxynaphthalene‐based analogue can only undergo once ESIPT process based on DFT calculations and ultrafast dynamics analyses. Finally, a six‐level system lasing toward 900 nm was achieved with a low threshold of 27.4 μJ cm−2. [ABSTRACT FROM AUTHOR]

Excited‐state intramolecular proton transfer (ESIPT)‐active organic semiconductor materials, characterized by a or several resonance‐assisted hydrogen bonds (RAHBs), are supposed to be ideal candidates for achieving high‐performance near‐infrared (NIR) lasers. However, according to the energy gap law, the development of ESIPT‐active gain materials is still limited by the serious nonradiative decays. Herein, it is demonstrated that RAHBs can activate ESIPT lasing by inhibiting nonradiative decays. A new ESIPT‐active material 1,5‐dihydroxy‐2,6‐diphenylanthraquinone (DP‐DHAQ) containing two centrosymmetric RAHBs is developed, which exhibits a ≈100‐fold higher radiative decay rate (kr = 1.1 × 1010 s–1) in doped polystyrene (PS) film than that of 1‐hydroxy‐5‐methoxy‐2,6‐diphenylanthraquinone (DP‐HMAQ) and 1,5‐dimethoxy‐2,6‐diphenylanthraquinone (DP‐DMAQ), in which one and two RAHBs are broken, respectively, by introducing methyl groups. Both DP‐DHAQ and DP‐HMAQ can form four‐level systems based on the ESIPT processes, but only DP‐DHAQ doped PS microspheres exhibit laser emission at 710 nm under the test conditions. It is worth mentioning that single‐crystal microplates of DP‐DHAQ can realize NIR laser emission at 725 nm. The results suggest that RAHBs can effectively activate the gain property of ESIPT‐active materials, which deepens insights into NIR ESIPT lasing and provides a new proposal for the design of organic laser‐active molecules. [ABSTRACT FROM AUTHOR]

Near‐infrared (NIR) organic solid‐state lasers play an essential role in applications ranging from laser communication to infrared night vision, but progress in this area is restricted by the lack of effective excited‐state gain processes. Herein, we originally proposed and demonstrated the cascaded occurrence of excited‐state intramolecular proton transfer for constructing the completely new energy‐level systems. Cascading by the first ultrafast proton transfer of <430 fs and the subsequent irreversible second proton transfer of ca. 1.6 ps, the stepwise proton transfer process favors the true six‐level photophysical cycle, which supports efficient population inversion and thus NIR single‐mode lasing at 854 nm. This work realizes longest wavelength beyond 850 nm of organic single‐crystal lasing to date and originally exploits the cascaded excited‐state molecular proton transfer energy‐level systems for organic solid‐state lasers. [ABSTRACT FROM AUTHOR]