Abstract

The B←N is isoelectronic to the C–C, with the former having stronger dipole moment and higher electron affinity. Replacing the C–C bonds in conjugated polymers with B←N bonds is an effective pathway toward novel polymers with strong electron affinity and adjustable optoelectronic properties. In this work, we synthesize a conjugated copolymer, namely, BNIDT-DPP, based on a B←N embedded unit, BNIDT, and a typical electron-deficient unit, diketopyrrolopyrrole (DPP). For comparison, the C–C counterpart, i.e., IDT-DPP, is also synthesized. In contrast to IDT-DPP, the B←N embedded polymer BNIDT-DPP shows an extended absorption edge (836 versus 978 nm), narrowed optical bandgap (1.48 versus 1.27 eV), and higher electron affinity (3.54 versus 3.74 eV). The Gaussian simulations reveal that the B←N embedded polymer BNIDT-DPP is more electron-deficient in contrast to IDT-DPP, supporting the decreased bandgap and energy levels of BNIDT-DPP. Organic thin-film transistor (OTFT) tests indicate a well-defined p-type characteristic for both IDT-DPP and BNIDT-DPP. The hole mobilities of IDT-DPP and BNIDT-DPP tested by OTFTs are 0.059 and 0.035 cm2/V·s, respectively. The preliminary fabrication of all-polymer solar cells based on BNIDT-DPP and PBDB-T affords a PCE of 0.12%. This work develops a novel B←N embedded polymer with strong electron affinity and extended absorption, which is potentially useful for electronic device application.

Highlights

  • IntroductionConjugated polymers have been intensively studied for application to organic electronics, e.g., organic field effect transistors (OFETs) and organic solar cells (OSCs) due to their light weight, flexibility, low cost, and easy processability [1,2,3,4,5,6]

  • Embedded polymer with strong electron affinity and extended absorption, which is potentially useful for electronic device application

  • Conjugated polymers have been intensively studied for application to organic electronics, e.g., organic field effect transistors (OFETs) and organic solar cells (OSCs) due to their light weight, flexibility, low cost, and easy processability [1,2,3,4,5,6]

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Summary

Introduction

Conjugated polymers have been intensively studied for application to organic electronics, e.g., organic field effect transistors (OFETs) and organic solar cells (OSCs) due to their light weight, flexibility, low cost, and easy processability [1,2,3,4,5,6]. B, the conjugated units containing bonds usually haveB←N to enhanced dipole–dipole interactions between the conjugated backbones To this end, most strong electron affinity with depressed energy levels in contrast to their. A–A phenyl copolymer, namely, DPP was stable BNIDT unit was obtained (Scheme 1b) This B←N embedded unit was copolymerized selected as the co-monomer owing to its rigid backbone, good co-planarity, strong electron deficiency, with another classic A unit, diketopyrrolopyrrole (DPP), to obtain an A–A copolymer, namely, and wide absorption spectra, which has been widely used for OFETs and OSC materials [42,43].

Results and Discussion
27.8 S1b in Supplementary
1.48 Absorption
Conclusions
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