Abstract
Solution-processed organic field-effect transistors (OFETs) have great potential for next-generation "plastic electronics". The development of n-type polymer semiconductors still lags far behind that of p-type polymer semiconductors, including material number and device performance. Moreover, the reported high-performance n-type polymer semiconductors are mostly based on amide and imide units. To enrich the family of n-type polymers and promote the development of OFETs, we have proposed using a boron-nitrogen coordination bond (B←N) to develop n-type polymer semiconductors. In this work, we report a B←N-containing conjugated polymer, PBN-13, which is an alternating polymer of a double B←N-bridged bipyridine unit and a 5,6-difluoro-4,7-di(thiophen-2-yl)benzo[c][1,2,5]thiadiazole unit. This polymer exhibits strong aggregation ability in solution and good crystallinity in a thin film, which are very desirable for achieving good electron-transporting properties. The OFET device based on PBN-13 shows unipolar n-type behavior with an electron mobility of 0.19 cm2 V-1 s-1. The electron mobility is enhanced ∼10-fold compared to those of other n-type polymer semiconductors containing a B←N unit. This study thus not only provides an efficient n-type polymer semiconductor but also proves that the B←N unit is a promising candidate for the development of n-type polymer materials for OFETs.
| Original language | English |
|---|---|
| Pages (from-to) | 19-25 |
| Number of pages | 7 |
| Journal | ACS Applied Polymer Materials |
| Volume | 2 |
| Issue number | 1 |
| DOIs | |
| State | Published - 10 Jan 2020 |
Keywords
- boron-nitrogen coordination bond
- crystallinity
- fluorination strategy
- n-type polymer semiconductors
- organic field-effect transistors
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