Organic Single Crystals with High Photoluminescence Quantum Yields Close to 100% and High Mobility for Optoelectronic Devices.
basic_science · Level V
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- Record sourced from PubMed, PMID 34617639.
- Also identified by DOI 10.1002/adma.202105466.
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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 cm<sup>2</sup> V<sup>-1</sup> s<sup>-1</sup> in single-crystal organic field-effect transistors (SC-OFETs). Furthermore, UV phototransistors based on the two single crystals obtain photosensitivities of 1.03 × 10<sup>3</sup> and 3.45 × 10<sup>4</sup> , ultrahigh photoresponsivities of 7.19 × 10<sup>5</sup> and 1.50 × 10<sup>5</sup> A W<sup>-1</sup> , and the detectivities exceeding 1.40 × 10<sup>16</sup> and 1.60 × 10<sup>17</sup> Jones.