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Based on the integrated consideration and engineering of both conjugated backbones and flexible side chains, solution‐processable polymeric semiconductors consisting of a diketopyrrolopyrrole (DPP) backbone and a finely modulated branching side chain (ε‐branched chain) are reported. The subtle change in the branching point from the backbone alters the π?π stacking and the lamellar distances between polymer backbones, which has a significant influence on the charge‐transport properties and in turn the performances of field‐effect transistors (FETs). In addition to their excellent electron mobilities (up to 2.25 cm2 V?1 s?1), ultra‐high hole mobilities (up to 12.25 cm2 V?1 s?1) with an on/off ratio (Ion/Ioff) of at least 106 are achieved in the FETs fabricated using the polymers. The developed polymers exhibit extraordinarily high electrical performance with both hole and electron mobilities superior to that of unipolar amorphous silicon.  相似文献   
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Tailoring the surface of the dielectric layer is of critical importance to form a good interface with the following channel layer for organic thin film transistors (OTFTs). Here, a simple surface treatment method is applied onto an ultrathin (<15 nm) organosilicon‐based dielectric layer via the initiated chemical vapor deposition (iCVD) to make it compatible with organic semiconductors without degrading its insulating property. A molecular‐thin oxide capping layer is formed on a 15 nm thick poly(1,3,5‐trimetyl‐1,3,5‐trivinyl cyclotrisiloxane) (pV3D3) by a brief oxygen plasma treatment. The capping layer greatly enhances the thermal stability of the dielectrics, without degrading the original mechanical flexibility and insulating performance of the dielectrics. Moreover, the surface silanol functionalities formed by the plasma treatment can also be utilized for the surface modification with silane compounds. The surface‐modified dielectrics are applied to fabricate low‐voltage operating (<5 V) pentacene‐based OTFTs. The highest field‐effect mobility of the device with the surface‐treated 15 nm thick pV3D3 is 0.59 cm2 V?1 s?1, which is improved up to two times compared to the TFT with the pristine pV3D3. It is believed that the simple surface treatment method can widely extend the applicability of the highly robust, ultrathin, and flexible pV3D3 gate dielectrics to design the surface of the dielectrics to match well various kinds of organic semiconductors.  相似文献   
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《Polymer》2014,55(26):6708-6716
Novel wide band-gap polymer of PBTFT containing dibenzosexithiophene-alt-bithiophene backbone was designed and synthesized via the Stille cross-coupling reaction. This polymer exhibited good thermal stability, well coplanar backbone and a broad absorption band from 350 nm to 610 nm with a wide optical band-gap of 2.02 eV. The polymer solar cells (PSCs) based on the PBTFT:PC71BM active layer showed the power conversion efficiency of 3.0% with an open circuit voltage of 0.70 V, a short-circuit current of 7.94 mA cm−2 and a fill factor of 53.98% under the illumination of AM.1.5, 100 mW cm−2. Holes mobility up to 0.028 cm2 V−1 s−1 with an on-off ratio of 1.0 × 106 was obtained in the PBTFT-based organic field-effect transistors (OFETs). Our work indicates that the dibenzosexithiophene-alt-bithiophene based copolymer can be efficiently applied in PSCs and OFETs.  相似文献   
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