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      Highlighting the processing versatility of a silicon phthalocyanine derivative for organic thin-film transistors

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          Abstract

          Silicon phthalocyanine (SiPc) derivatives have recently emerged as promising materials for n-type organic thin-film transistors (OTFTs) with the ability to be fabricated either by solid state or solution processes through axial functionalization.

          Abstract

          Silicon phthalocyanine (SiPc) derivatives have recently emerged as promising materials for n-type organic thin-film transistors (OTFTs) with the ability to be fabricated either by solid state or solution processes through axial functionalization. Among those, bis(tri- n-propylsilyl oxide) SiPc ((3PS) 2-SiPc) is unique as it can be processed by sublimation, while being soluble enough for solution processing. In this work, the charge transport properties of (3PS) 2-SiPc and its polymorphic forms were studied through Kinetic Monte Carlo (KMC) simulations and density functional theory (DFT) calculations along with the characterization of (3PS) 2-SiPc in n-type OTFTs fabricated by physical vapour deposition (PVD) and spin coating. Post-deposition thin-film characterization by X-ray diffraction (XRD), atomic force microscopy (AFM), and scanning transmission X-ray microscopy (STXM) was used to assess film morphology and microstructure in relation to the electrical performance of OTFTs. The differences in film formation by PVD and solution fabrication had little effect on OTFT performance with comparable field-effect mobility and threshold voltage ranging between 0.01–0.04 cm 2 V −1 s −1 and 18–36 V respectively. Consistent charge transport properties of (3PS) 2-SiPc OTFTs achieved at different fabrication conditions highlights the processing versatility of this material.

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            Non-fullerene acceptors for organic solar cells

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                Author and article information

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                Journal
                JMCCCX
                Journal of Materials Chemistry C
                J. Mater. Chem. C
                Royal Society of Chemistry (RSC)
                2050-7526
                2050-7534
                January 07 2022
                2022
                : 10
                : 2
                : 485-495
                Affiliations
                [1 ]Department of Chemical and Biological Engineering, University of Ottawa, 161 Louis Pasteur, Ottawa, ON, K1N 6N5, Canada
                [2 ]Donostia International Physics Center, 4 Paseo Manuel de Lardizabal, 20018 Donostia, Euskadi, Spain
                [3 ]Univ. Bordeaux, CNRS, Bordeaux INP, ISM, UMR 5255, F-33400 Talence, France
                [4 ]University of Bologna, Department of Industrial Chemistry, 4 Viale Risorgimento, 40136 Bologna, Italy
                [5 ]SOLEIL Synchrotron, L’Orme des Merisiers, Saint-Aubin, P.O. Box 48, CEDEX, FR-91192 Gif-Sur-Yvette, France
                [6 ]School of Electrical Engineering and Computer Science, University of Ottawa, 800 King Edward, Ottawa, ON, K1N 6N5, Canada
                Article
                10.1039/D1TC05238A
                3298cc56-1cf2-4005-8b3f-60c333e8f87c
                © 2022

                http://rsc.li/journals-terms-of-use

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