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Title: Understanding how Lewis acids dope organic semiconductors: a “complex” story
We report on computational studies of the potential of three borane Lewis acids (LAs) (B(C 6 F 5 ) 3 (BCF), BF 3 , and BBr 3 ) to form stable adducts and/or to generate positive polarons with three different semiconducting π-conjugated polymers (PFPT, PCPDTPT and PCPDTBT). Density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations based on range-separated hybrid (RSH) functionals provide insight into changes in the electronic structure and optical properties upon adduct formation between LAs and the two polymers containing pyridine moieties, PFPT and PCPDTPT, unravelling the complex interplay between partial hybridization, charge transfer and changes in the polymer backbone conformation. We then assess the potential of BCF to induce p-doping in PCPDTBT, which does not contain pyridine groups, by computing the energetics of various reaction mechanisms proposed in the literature. We find that reaction of BCF(OH 2 ) to form protonated PCPDTBT and [BCF(OH)] − , followed by electron transfer from a pristine to a protonated PCPDTBT chain is highly endergonic, and thus unlikely at low doping concentration. The theoretical and experimental data can, however, be reconciled if one considers the formation of [BCF(OH)BCF] − or [BCF(OH)(OH 2 )BCF] − counterions rather than [BCF(OH)] − and invokes subsequent reactions resulting in the elimination of H 2 .  more » « less
Award ID(s):
1729737
PAR ID:
10296338
Author(s) / Creator(s):
; ; ; ; ; ;
Date Published:
Journal Name:
Chemical Science
Volume:
12
Issue:
20
ISSN:
2041-6520
Page Range / eLocation ID:
7012 to 7022
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
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