Engineering functionalized low LUMO [1]benzothieno[3, 2-b][1]benzothiophenes (BTBTs): unusual molecular and charge transport properties. Issue 43 (21st August 2020)

• Record Type: Journal Article
• Authors: Ozdemir, Resul; Ahn, Kyunghan; Deneme, İbrahim; Zorlu, Yunus; Kim, Dojun; Kim, Myung-Gil; Usta, Hakan
• Is Part Of: Journal of materials chemistry. Volume 8:Issue 43(2020)
• Page Start: 15253
• Page End: 15267
• Publication Date: 2020-08-21
• Subjects: Materials -- Periodicals; Chemistry, Analytic -- Periodicals; Optical materials -- Research -- Periodicals; Electronics -- Materials -- Research -- Periodicals; 543.0284
• DOI: 10.1039/d0tc02945a
• Languages: English
• ISSNs: 2050-7526

Abstract

Abstract : A unique molecular library of functionalized low LUMO BTBT semiconductors was developed and studied in detail to reveal key design principles for electron transport in DAcTTs. Abstract : Diacene-fused thienothiophenes (DAcTTs) have provided an excellent π-framework for the development of high mobility p-type molecular semiconductors in the past decade. However, n-type DAcTTs are rare and their electron transport characteristics remain largely unexplored. Herein, a series of functionalized low LUMO (lowest unoccupied molecular orbital) [1]benzothieno[3, 2- b ][1]benzothiophene (BTBT)-based small molecules, D(C7 CO)-BTBT, C7 CO-BTBT-CC(CN)2 C7, and D(C7 CC(CN)2 )-BTBT, have been developed. Detailed structural, physicochemical, optoelectronic, and single-crystal characterization were performed. The new molecules exhibit large optical band gaps (∼2.8–3.1 eV) and highly stabilized (−Δ E LUMO = 1.2–1.4 eV)/π-delocalized LUMOs as compared to p-type DAcTTs. Symmetric functionalization is found to be important to enable strong intermolecular interactions in the solid-state. All molecules exhibit alternately stacked layers of "F–BTBT–F" and "S" (F: functional group/S: substituent) with strong herringbone-like interactions (2.8–3.6 Å distances) between π-cores. While carbonyls, regardless of the substituent, adopt nearly coplanar π-backbones with BTBT, dicyanovinylenes are found to be twisted (47.5°). The conformational difference at the molecular level has unusual effects on the π-electron deficiencies, frontier molecular orbital energetics, thermal/photophysical properties, and π-electronic structures. Dicyanovinylenes at the 2, 7 positions, despite twisted conformations, are shown for the first time to yield good electron transport in DAcTTs. The D(C7 CC(CN)2 )-BTBT thin film exhibits large 2D plate-like crystalline grains (∼1–2 μm sizes) of terraced islands and becomes a rare example of an n-type DAcTT in organic field-effect transistors (OFETs). Although a stabilized/π-delocalized LUMO, largely governed by functional groups and intramolecular twists, is essential for electron transport, our findings suggest that it should be combined with proper substituents to yield a favorable three-dimensional BTBT/functional group π-electronic structure and a low intramolecular reorganization energy. Combined with our first n-type DAcTT semiconductor D(PhF CO)-BTBT, a molecular library with systematically varied chemical structures has been studied herein for the first time for low LUMO DAcTTs. The molecular engineering perspectives presented in this study may give unique insights into the design of novel electron transporting thienoacenes for unconventional optoelectronics.