Cocrystallization tailoring radiative decay pathways for thermally activated delayed fluorescence and room-temperature phosphorescence emission. Issue 17 (14th April 2022)

• Record Type: Journal Article
• Authors: Liu, Kun; Li, Shuai; Fu, Liyuan; Lei, Yilong; Liao, Qing; Fu, Hongbing
• Is Part Of: Nanoscale. Volume 14:Issue 17(2022)
• Page Start: 6305
• Page End: 6311
• Publication Date: 2022-04-14
• Subjects: Nanoscience -- Periodicals; Nanotechnology -- Periodicals; 620.505
• DOI: 10.1039/d2nr00757f
• Languages: English
• ISSNs: 2040-3364

Abstract

Abstract : We achieve TADF or dual-emissive TADF/RTP by tailoring the substitution positions of bromine atoms in binary organic D–A-type CT cocrystals, which offers a wonderful insight in modulating radiative decay pathways of organic CT cocrystals. Abstract : Modulation of excited-state processes in binary organic cocrystals has been rarely explored so far. Here, we develop two charge-transfer (CT) cocrystal microrods with a 1 : 1 stoichiometric ratio where halogenated dibenzothiophene (DBT) compounds act as π-electron donors and 1, 2, 4, 5-tetracyanobenzene (TCNB) acts as an acceptor. Unexpectedly, the cocrystal containing one bromine (Br) atom at the 3-position of DBT (3-BrTC) presents thermally activated delayed fluorescence (TADF), while the other one comprising one Br atom at the 4-position of DBT (4-BrTC) exhibits both TADF and room-temperature phosphorescence (RTP). Experimental and theoretical calculation results reveal that CT interactions in 3- and 4-BrTC decrease the S1 –T2 energy gap, whereas abundant lone-pair electrons from the Br atom in 4-BrTC facilitate the n → π* transition. As a consequence, single TADF and dual-emissive TADF/RTP were realized, respectively. The present work offers wonderful insight into the effect of molecular structures on the excited-state pathways of organic CT cocrystals.