4.8 Article

Multifunctional Benzo[4,5]thieno[3,2-b]benzofuran Derivative with High Mobility and Luminescent Properties

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 10, Pages 12250-12258

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c21286

Keywords

OLED; OFET; OPT; mobility; luminescence; multifunctionality

Funding

  1. Key-Area Research and Development Program of Guangdong Province [2019B010924003, 2020B010178001]
  2. Guangdong Basic and Applied Basic Research Foundation [2020B1515120030, 2020A1515010449]
  3. Shenzhen Science and Technology Research Grant [JCYJ20170412151139619, JCYJ20200109140425347]
  4. Shenzhen OLED Materials and Devices Technology Engineering Research Center (Shenzhen development and reform commission) [[2018] 1410]
  5. Natural Science Basic Research Program of Shaanxi [2019JLP-11]

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The research team successfully synthesized a new multifunctional semiconductor molecule, BTBF-DPh, which combines high charge transporting benzothieno[3,2-b][1]benzothiophene with strong emissive furan group, and applied it in devices including OLEDs, OFETs, and OPTs. Experimental results demonstrate the promising potential of BTBF-DPh in these devices, showing high performance.
Development of multifunctional materials and devices has garnered enormous attention in the field of organic optoelectronics; nevertheless, achieving high mobility together with strong luminescence in a single semiconductor remains a major bottleneck. Here, a new multifunctional semiconductor molecule, 2,7-diphenylbenzo[4,5]thieno[3,2-b]benzofuran (BTBF-DPh), that integrates high charge transporting [1]benzothieno[3,2-b][1]benzothiophene with a strongly emissive furan group, is synthesized and applied in three types of optoelectronic devices, including organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs), and organic phototransistors (OPTs). OLEDs based on BTBF-DPh as the emissive layer showed a blue emission with CIE coordinates of (0.151, 0.069) and a maximum current efficiency of 2.96 cd A(-1) with an external quantum efficiency of 4.23%. Meanwhile, OFETs fabricated with BTBF-DPh thin film manifested a carrier mobility of 0.181 cm(2) V-1 s(-1), which is comparable to that of thiophene-based counterparts. Additionally, BTBF-DPh-based OPTs exhibited a maximum responsivity and detectivity of 2.07 x 10(3) A W-1 and of 5.6 x 10(15) Jones, respectively. On the one hand, our rationally designed material, BTBF-DPh, has a dense and close-packed structure with an extended pi-conjugation, facilitating charge transport through adjacent molecules. On the other hand, the weakened dipole-dipole interactions between BTBF-DPh molecules that resulted from the unambiguous J-aggregation and reduced spin-orbit coupling caused by replacing sulfur atom significantly suppress the exciton quenching, contributing to the improved photoluminescence performance. These results validate that our newly developed BTBF-DPh is a promising multifunctional organic semiconductor for optoelectronic devices.

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