Organic Single Crystals with High Photoluminescence Quantum Yields Close to 100% and High Mobility for Optoelectronic Devices

Abstract

Organic single crystals with excellent optical and electrical properties are critical for the development of organic optoelectronics. Herein, two compounds 9,10-bis([N,N-diphenyl]-4'-phenylethynyl)anthracene (TPA-An) and 9,10-bis([1',3'-diphenyl]-5'-phenylethynyl)anthracene (TBA-An) are synthesized by introducing two different luminescent groups, triphenylamine and 1,3-diphenylbenzene, at the 9,10 positions of anthracene via triple bond connection. Single crystals based on TPA-An and TBA-An with a ribbon morphology obtained through the slow solvent-evaporation method exhibit high photoluminescence quantum yields (PLQYs) of 98% and 99% at room temperature, and remarkable hole mobilities of 0.45 and 0.15 cm² V^-1 s^-1 in single-crystal organic field-effect transistors (SC-OFETs). Furthermore, UV phototransistors based on the two single crystals obtain photosensitivities of 1.03 × 10³ and 3.45 × 10⁴ , ultrahigh photoresponsivities of 7.19 × 10⁵ and 1.50 × 10⁵ A W^-1 , and the detectivities exceeding 1.40 × 10¹⁶ and 1.60 × 10¹⁷ Jones.

Keywords: 9,10-substituted anthracene derivatives; high mobility; organic phototransistors; organic single crystals; strong fluorescence emission.