Highly soluble small-molecule organic semiconductor with trihexylsilyloxy side chain for high-performance organic field-effect transistors with mobility of up to 3.10 cm2 V−1 s−1
A donor–acceptor type small molecule organic semiconductor with a trihexylsilyloxy bulky side chain, coded LGC-D127, was synthesized, and its electronic, electrochemical, and electrical properties were investigated for use as the active layer of solution-processable organic field-effect transistors....
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Lim, Bogyu [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2017transfer abstract |
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| Schlagwörter: |
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| Umfang: |
7 |
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| Übergeordnetes Werk: |
Enthalten in: A multiscale analysis for free vibration of fuzzy fiber-reinforced nanocomposite conical shells - Haghgoo, M. ELSEVIER, 2020, Amsterdam [u.a.] |
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| Übergeordnetes Werk: |
volume:142 ; year:2017 ; pages:17-23 ; extent:7 |
| Links: |
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| DOI / URN: |
10.1016/j.dyepig.2017.03.025 |
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ELV014836572 |
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| 245 | 1 | 0 | |a Highly soluble small-molecule organic semiconductor with trihexylsilyloxy side chain for high-performance organic field-effect transistors with mobility of up to 3.10 cm2 V−1 s−1 |
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| 520 | |a A donor–acceptor type small molecule organic semiconductor with a trihexylsilyloxy bulky side chain, coded LGC-D127, was synthesized, and its electronic, electrochemical, and electrical properties were investigated for use as the active layer of solution-processable organic field-effect transistors. LGC-D127 consisted of a phenylene–dithiophene moiety with a bulky trihexylsilyloxy side chain as the electron-donating core, diketopyrrolopyrrole as the electron-accepting linker, and octylrhodanine as the electron-accepting end group. In spite of bulky trihexylsilyloxy side chains, LGC-D127 film was highly crystalline. The charge-carrier transport properties of the LGC-D127 was investigated through the fabrication and characterization of field-effect transistor via solution process. LGC-D127 showed significantly high field-effect hole mobility of 3.16 cm2 V−1 s−1 after thermal annealing due to the large crystalline nanostructure and the small grain boundaries. In particular, LGC-D127 had good solubility in the environmentally friendly solvent such as 2-methyltetrahydrofuran due to the bulky trihexylsilyloxy side chain, and its high hole mobility (max. 3.06 cm2 V−1 s−1) was sustained from the LGC-D127 solution in 2-methyltetrahydrofuran. | ||
| 520 | |a A donor–acceptor type small molecule organic semiconductor with a trihexylsilyloxy bulky side chain, coded LGC-D127, was synthesized, and its electronic, electrochemical, and electrical properties were investigated for use as the active layer of solution-processable organic field-effect transistors. LGC-D127 consisted of a phenylene–dithiophene moiety with a bulky trihexylsilyloxy side chain as the electron-donating core, diketopyrrolopyrrole as the electron-accepting linker, and octylrhodanine as the electron-accepting end group. In spite of bulky trihexylsilyloxy side chains, LGC-D127 film was highly crystalline. The charge-carrier transport properties of the LGC-D127 was investigated through the fabrication and characterization of field-effect transistor via solution process. LGC-D127 showed significantly high field-effect hole mobility of 3.16 cm2 V−1 s−1 after thermal annealing due to the large crystalline nanostructure and the small grain boundaries. In particular, LGC-D127 had good solubility in the environmentally friendly solvent such as 2-methyltetrahydrofuran due to the bulky trihexylsilyloxy side chain, and its high hole mobility (max. 3.06 cm2 V−1 s−1) was sustained from the LGC-D127 solution in 2-methyltetrahydrofuran. | ||
| 650 | 7 | |a Donor-acceptor |2 Elsevier | |
| 650 | 7 | |a Trihexylsilyloxy side chain |2 Elsevier | |
| 650 | 7 | |a Small-molecule semiconductor |2 Elsevier | |
| 650 | 7 | |a Green solvent |2 Elsevier | |
| 650 | 7 | |a Organic field-effect transistors |2 Elsevier | |
| 700 | 1 | |a Sun, Huabin |4 oth | |
| 700 | 1 | |a Noh, Yong-Young |4 oth | |
| 773 | 0 | 8 | |i Enthalten in |n Elsevier Science |a Haghgoo, M. ELSEVIER |t A multiscale analysis for free vibration of fuzzy fiber-reinforced nanocomposite conical shells |d 2020 |g Amsterdam [u.a.] |w (DE-627)ELV004269640 |
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10.1016/j.dyepig.2017.03.025 doi GBVA2017003000018.pica (DE-627)ELV014836572 (ELSEVIER)S0143-7208(17)30273-5 DE-627 ger DE-627 rakwb eng 660 660 DE-600 690 VZ 50.31 bkl 56.11 bkl Lim, Bogyu verfasserin aut Highly soluble small-molecule organic semiconductor with trihexylsilyloxy side chain for high-performance organic field-effect transistors with mobility of up to 3.10 cm2 V−1 s−1 2017transfer abstract 7 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier A donor–acceptor type small molecule organic semiconductor with a trihexylsilyloxy bulky side chain, coded LGC-D127, was synthesized, and its electronic, electrochemical, and electrical properties were investigated for use as the active layer of solution-processable organic field-effect transistors. LGC-D127 consisted of a phenylene–dithiophene moiety with a bulky trihexylsilyloxy side chain as the electron-donating core, diketopyrrolopyrrole as the electron-accepting linker, and octylrhodanine as the electron-accepting end group. In spite of bulky trihexylsilyloxy side chains, LGC-D127 film was highly crystalline. The charge-carrier transport properties of the LGC-D127 was investigated through the fabrication and characterization of field-effect transistor via solution process. LGC-D127 showed significantly high field-effect hole mobility of 3.16 cm2 V−1 s−1 after thermal annealing due to the large crystalline nanostructure and the small grain boundaries. In particular, LGC-D127 had good solubility in the environmentally friendly solvent such as 2-methyltetrahydrofuran due to the bulky trihexylsilyloxy side chain, and its high hole mobility (max. 3.06 cm2 V−1 s−1) was sustained from the LGC-D127 solution in 2-methyltetrahydrofuran. A donor–acceptor type small molecule organic semiconductor with a trihexylsilyloxy bulky side chain, coded LGC-D127, was synthesized, and its electronic, electrochemical, and electrical properties were investigated for use as the active layer of solution-processable organic field-effect transistors. LGC-D127 consisted of a phenylene–dithiophene moiety with a bulky trihexylsilyloxy side chain as the electron-donating core, diketopyrrolopyrrole as the electron-accepting linker, and octylrhodanine as the electron-accepting end group. In spite of bulky trihexylsilyloxy side chains, LGC-D127 film was highly crystalline. The charge-carrier transport properties of the LGC-D127 was investigated through the fabrication and characterization of field-effect transistor via solution process. LGC-D127 showed significantly high field-effect hole mobility of 3.16 cm2 V−1 s−1 after thermal annealing due to the large crystalline nanostructure and the small grain boundaries. In particular, LGC-D127 had good solubility in the environmentally friendly solvent such as 2-methyltetrahydrofuran due to the bulky trihexylsilyloxy side chain, and its high hole mobility (max. 3.06 cm2 V−1 s−1) was sustained from the LGC-D127 solution in 2-methyltetrahydrofuran. Donor-acceptor Elsevier Trihexylsilyloxy side chain Elsevier Small-molecule semiconductor Elsevier Green solvent Elsevier Organic field-effect transistors Elsevier Sun, Huabin oth Noh, Yong-Young oth Enthalten in Elsevier Science Haghgoo, M. ELSEVIER A multiscale analysis for free vibration of fuzzy fiber-reinforced nanocomposite conical shells 2020 Amsterdam [u.a.] (DE-627)ELV004269640 volume:142 year:2017 pages:17-23 extent:7 https://doi.org/10.1016/j.dyepig.2017.03.025 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 50.31 Technische Mechanik VZ 56.11 Baukonstruktion VZ AR 142 2017 17-23 7 045F 660 |
| spelling |
10.1016/j.dyepig.2017.03.025 doi GBVA2017003000018.pica (DE-627)ELV014836572 (ELSEVIER)S0143-7208(17)30273-5 DE-627 ger DE-627 rakwb eng 660 660 DE-600 690 VZ 50.31 bkl 56.11 bkl Lim, Bogyu verfasserin aut Highly soluble small-molecule organic semiconductor with trihexylsilyloxy side chain for high-performance organic field-effect transistors with mobility of up to 3.10 cm2 V−1 s−1 2017transfer abstract 7 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier A donor–acceptor type small molecule organic semiconductor with a trihexylsilyloxy bulky side chain, coded LGC-D127, was synthesized, and its electronic, electrochemical, and electrical properties were investigated for use as the active layer of solution-processable organic field-effect transistors. LGC-D127 consisted of a phenylene–dithiophene moiety with a bulky trihexylsilyloxy side chain as the electron-donating core, diketopyrrolopyrrole as the electron-accepting linker, and octylrhodanine as the electron-accepting end group. In spite of bulky trihexylsilyloxy side chains, LGC-D127 film was highly crystalline. The charge-carrier transport properties of the LGC-D127 was investigated through the fabrication and characterization of field-effect transistor via solution process. LGC-D127 showed significantly high field-effect hole mobility of 3.16 cm2 V−1 s−1 after thermal annealing due to the large crystalline nanostructure and the small grain boundaries. In particular, LGC-D127 had good solubility in the environmentally friendly solvent such as 2-methyltetrahydrofuran due to the bulky trihexylsilyloxy side chain, and its high hole mobility (max. 3.06 cm2 V−1 s−1) was sustained from the LGC-D127 solution in 2-methyltetrahydrofuran. A donor–acceptor type small molecule organic semiconductor with a trihexylsilyloxy bulky side chain, coded LGC-D127, was synthesized, and its electronic, electrochemical, and electrical properties were investigated for use as the active layer of solution-processable organic field-effect transistors. LGC-D127 consisted of a phenylene–dithiophene moiety with a bulky trihexylsilyloxy side chain as the electron-donating core, diketopyrrolopyrrole as the electron-accepting linker, and octylrhodanine as the electron-accepting end group. In spite of bulky trihexylsilyloxy side chains, LGC-D127 film was highly crystalline. The charge-carrier transport properties of the LGC-D127 was investigated through the fabrication and characterization of field-effect transistor via solution process. LGC-D127 showed significantly high field-effect hole mobility of 3.16 cm2 V−1 s−1 after thermal annealing due to the large crystalline nanostructure and the small grain boundaries. In particular, LGC-D127 had good solubility in the environmentally friendly solvent such as 2-methyltetrahydrofuran due to the bulky trihexylsilyloxy side chain, and its high hole mobility (max. 3.06 cm2 V−1 s−1) was sustained from the LGC-D127 solution in 2-methyltetrahydrofuran. Donor-acceptor Elsevier Trihexylsilyloxy side chain Elsevier Small-molecule semiconductor Elsevier Green solvent Elsevier Organic field-effect transistors Elsevier Sun, Huabin oth Noh, Yong-Young oth Enthalten in Elsevier Science Haghgoo, M. ELSEVIER A multiscale analysis for free vibration of fuzzy fiber-reinforced nanocomposite conical shells 2020 Amsterdam [u.a.] (DE-627)ELV004269640 volume:142 year:2017 pages:17-23 extent:7 https://doi.org/10.1016/j.dyepig.2017.03.025 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 50.31 Technische Mechanik VZ 56.11 Baukonstruktion VZ AR 142 2017 17-23 7 045F 660 |
| allfields_unstemmed |
10.1016/j.dyepig.2017.03.025 doi GBVA2017003000018.pica (DE-627)ELV014836572 (ELSEVIER)S0143-7208(17)30273-5 DE-627 ger DE-627 rakwb eng 660 660 DE-600 690 VZ 50.31 bkl 56.11 bkl Lim, Bogyu verfasserin aut Highly soluble small-molecule organic semiconductor with trihexylsilyloxy side chain for high-performance organic field-effect transistors with mobility of up to 3.10 cm2 V−1 s−1 2017transfer abstract 7 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier A donor–acceptor type small molecule organic semiconductor with a trihexylsilyloxy bulky side chain, coded LGC-D127, was synthesized, and its electronic, electrochemical, and electrical properties were investigated for use as the active layer of solution-processable organic field-effect transistors. LGC-D127 consisted of a phenylene–dithiophene moiety with a bulky trihexylsilyloxy side chain as the electron-donating core, diketopyrrolopyrrole as the electron-accepting linker, and octylrhodanine as the electron-accepting end group. In spite of bulky trihexylsilyloxy side chains, LGC-D127 film was highly crystalline. The charge-carrier transport properties of the LGC-D127 was investigated through the fabrication and characterization of field-effect transistor via solution process. LGC-D127 showed significantly high field-effect hole mobility of 3.16 cm2 V−1 s−1 after thermal annealing due to the large crystalline nanostructure and the small grain boundaries. In particular, LGC-D127 had good solubility in the environmentally friendly solvent such as 2-methyltetrahydrofuran due to the bulky trihexylsilyloxy side chain, and its high hole mobility (max. 3.06 cm2 V−1 s−1) was sustained from the LGC-D127 solution in 2-methyltetrahydrofuran. A donor–acceptor type small molecule organic semiconductor with a trihexylsilyloxy bulky side chain, coded LGC-D127, was synthesized, and its electronic, electrochemical, and electrical properties were investigated for use as the active layer of solution-processable organic field-effect transistors. LGC-D127 consisted of a phenylene–dithiophene moiety with a bulky trihexylsilyloxy side chain as the electron-donating core, diketopyrrolopyrrole as the electron-accepting linker, and octylrhodanine as the electron-accepting end group. In spite of bulky trihexylsilyloxy side chains, LGC-D127 film was highly crystalline. The charge-carrier transport properties of the LGC-D127 was investigated through the fabrication and characterization of field-effect transistor via solution process. LGC-D127 showed significantly high field-effect hole mobility of 3.16 cm2 V−1 s−1 after thermal annealing due to the large crystalline nanostructure and the small grain boundaries. In particular, LGC-D127 had good solubility in the environmentally friendly solvent such as 2-methyltetrahydrofuran due to the bulky trihexylsilyloxy side chain, and its high hole mobility (max. 3.06 cm2 V−1 s−1) was sustained from the LGC-D127 solution in 2-methyltetrahydrofuran. Donor-acceptor Elsevier Trihexylsilyloxy side chain Elsevier Small-molecule semiconductor Elsevier Green solvent Elsevier Organic field-effect transistors Elsevier Sun, Huabin oth Noh, Yong-Young oth Enthalten in Elsevier Science Haghgoo, M. ELSEVIER A multiscale analysis for free vibration of fuzzy fiber-reinforced nanocomposite conical shells 2020 Amsterdam [u.a.] (DE-627)ELV004269640 volume:142 year:2017 pages:17-23 extent:7 https://doi.org/10.1016/j.dyepig.2017.03.025 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 50.31 Technische Mechanik VZ 56.11 Baukonstruktion VZ AR 142 2017 17-23 7 045F 660 |
| allfieldsGer |
10.1016/j.dyepig.2017.03.025 doi GBVA2017003000018.pica (DE-627)ELV014836572 (ELSEVIER)S0143-7208(17)30273-5 DE-627 ger DE-627 rakwb eng 660 660 DE-600 690 VZ 50.31 bkl 56.11 bkl Lim, Bogyu verfasserin aut Highly soluble small-molecule organic semiconductor with trihexylsilyloxy side chain for high-performance organic field-effect transistors with mobility of up to 3.10 cm2 V−1 s−1 2017transfer abstract 7 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier A donor–acceptor type small molecule organic semiconductor with a trihexylsilyloxy bulky side chain, coded LGC-D127, was synthesized, and its electronic, electrochemical, and electrical properties were investigated for use as the active layer of solution-processable organic field-effect transistors. LGC-D127 consisted of a phenylene–dithiophene moiety with a bulky trihexylsilyloxy side chain as the electron-donating core, diketopyrrolopyrrole as the electron-accepting linker, and octylrhodanine as the electron-accepting end group. In spite of bulky trihexylsilyloxy side chains, LGC-D127 film was highly crystalline. The charge-carrier transport properties of the LGC-D127 was investigated through the fabrication and characterization of field-effect transistor via solution process. LGC-D127 showed significantly high field-effect hole mobility of 3.16 cm2 V−1 s−1 after thermal annealing due to the large crystalline nanostructure and the small grain boundaries. In particular, LGC-D127 had good solubility in the environmentally friendly solvent such as 2-methyltetrahydrofuran due to the bulky trihexylsilyloxy side chain, and its high hole mobility (max. 3.06 cm2 V−1 s−1) was sustained from the LGC-D127 solution in 2-methyltetrahydrofuran. A donor–acceptor type small molecule organic semiconductor with a trihexylsilyloxy bulky side chain, coded LGC-D127, was synthesized, and its electronic, electrochemical, and electrical properties were investigated for use as the active layer of solution-processable organic field-effect transistors. LGC-D127 consisted of a phenylene–dithiophene moiety with a bulky trihexylsilyloxy side chain as the electron-donating core, diketopyrrolopyrrole as the electron-accepting linker, and octylrhodanine as the electron-accepting end group. In spite of bulky trihexylsilyloxy side chains, LGC-D127 film was highly crystalline. The charge-carrier transport properties of the LGC-D127 was investigated through the fabrication and characterization of field-effect transistor via solution process. LGC-D127 showed significantly high field-effect hole mobility of 3.16 cm2 V−1 s−1 after thermal annealing due to the large crystalline nanostructure and the small grain boundaries. In particular, LGC-D127 had good solubility in the environmentally friendly solvent such as 2-methyltetrahydrofuran due to the bulky trihexylsilyloxy side chain, and its high hole mobility (max. 3.06 cm2 V−1 s−1) was sustained from the LGC-D127 solution in 2-methyltetrahydrofuran. Donor-acceptor Elsevier Trihexylsilyloxy side chain Elsevier Small-molecule semiconductor Elsevier Green solvent Elsevier Organic field-effect transistors Elsevier Sun, Huabin oth Noh, Yong-Young oth Enthalten in Elsevier Science Haghgoo, M. ELSEVIER A multiscale analysis for free vibration of fuzzy fiber-reinforced nanocomposite conical shells 2020 Amsterdam [u.a.] (DE-627)ELV004269640 volume:142 year:2017 pages:17-23 extent:7 https://doi.org/10.1016/j.dyepig.2017.03.025 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 50.31 Technische Mechanik VZ 56.11 Baukonstruktion VZ AR 142 2017 17-23 7 045F 660 |
| allfieldsSound |
10.1016/j.dyepig.2017.03.025 doi GBVA2017003000018.pica (DE-627)ELV014836572 (ELSEVIER)S0143-7208(17)30273-5 DE-627 ger DE-627 rakwb eng 660 660 DE-600 690 VZ 50.31 bkl 56.11 bkl Lim, Bogyu verfasserin aut Highly soluble small-molecule organic semiconductor with trihexylsilyloxy side chain for high-performance organic field-effect transistors with mobility of up to 3.10 cm2 V−1 s−1 2017transfer abstract 7 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier A donor–acceptor type small molecule organic semiconductor with a trihexylsilyloxy bulky side chain, coded LGC-D127, was synthesized, and its electronic, electrochemical, and electrical properties were investigated for use as the active layer of solution-processable organic field-effect transistors. LGC-D127 consisted of a phenylene–dithiophene moiety with a bulky trihexylsilyloxy side chain as the electron-donating core, diketopyrrolopyrrole as the electron-accepting linker, and octylrhodanine as the electron-accepting end group. In spite of bulky trihexylsilyloxy side chains, LGC-D127 film was highly crystalline. The charge-carrier transport properties of the LGC-D127 was investigated through the fabrication and characterization of field-effect transistor via solution process. LGC-D127 showed significantly high field-effect hole mobility of 3.16 cm2 V−1 s−1 after thermal annealing due to the large crystalline nanostructure and the small grain boundaries. In particular, LGC-D127 had good solubility in the environmentally friendly solvent such as 2-methyltetrahydrofuran due to the bulky trihexylsilyloxy side chain, and its high hole mobility (max. 3.06 cm2 V−1 s−1) was sustained from the LGC-D127 solution in 2-methyltetrahydrofuran. A donor–acceptor type small molecule organic semiconductor with a trihexylsilyloxy bulky side chain, coded LGC-D127, was synthesized, and its electronic, electrochemical, and electrical properties were investigated for use as the active layer of solution-processable organic field-effect transistors. LGC-D127 consisted of a phenylene–dithiophene moiety with a bulky trihexylsilyloxy side chain as the electron-donating core, diketopyrrolopyrrole as the electron-accepting linker, and octylrhodanine as the electron-accepting end group. In spite of bulky trihexylsilyloxy side chains, LGC-D127 film was highly crystalline. The charge-carrier transport properties of the LGC-D127 was investigated through the fabrication and characterization of field-effect transistor via solution process. LGC-D127 showed significantly high field-effect hole mobility of 3.16 cm2 V−1 s−1 after thermal annealing due to the large crystalline nanostructure and the small grain boundaries. In particular, LGC-D127 had good solubility in the environmentally friendly solvent such as 2-methyltetrahydrofuran due to the bulky trihexylsilyloxy side chain, and its high hole mobility (max. 3.06 cm2 V−1 s−1) was sustained from the LGC-D127 solution in 2-methyltetrahydrofuran. Donor-acceptor Elsevier Trihexylsilyloxy side chain Elsevier Small-molecule semiconductor Elsevier Green solvent Elsevier Organic field-effect transistors Elsevier Sun, Huabin oth Noh, Yong-Young oth Enthalten in Elsevier Science Haghgoo, M. ELSEVIER A multiscale analysis for free vibration of fuzzy fiber-reinforced nanocomposite conical shells 2020 Amsterdam [u.a.] (DE-627)ELV004269640 volume:142 year:2017 pages:17-23 extent:7 https://doi.org/10.1016/j.dyepig.2017.03.025 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 50.31 Technische Mechanik VZ 56.11 Baukonstruktion VZ AR 142 2017 17-23 7 045F 660 |
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Enthalten in A multiscale analysis for free vibration of fuzzy fiber-reinforced nanocomposite conical shells Amsterdam [u.a.] volume:142 year:2017 pages:17-23 extent:7 |
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highly soluble small-molecule organic semiconductor with trihexylsilyloxy side chain for high-performance organic field-effect transistors with mobility of up to 3.10 cm2 v−1 s−1 |
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Highly soluble small-molecule organic semiconductor with trihexylsilyloxy side chain for high-performance organic field-effect transistors with mobility of up to 3.10 cm2 V−1 s−1 |
| abstract |
A donor–acceptor type small molecule organic semiconductor with a trihexylsilyloxy bulky side chain, coded LGC-D127, was synthesized, and its electronic, electrochemical, and electrical properties were investigated for use as the active layer of solution-processable organic field-effect transistors. LGC-D127 consisted of a phenylene–dithiophene moiety with a bulky trihexylsilyloxy side chain as the electron-donating core, diketopyrrolopyrrole as the electron-accepting linker, and octylrhodanine as the electron-accepting end group. In spite of bulky trihexylsilyloxy side chains, LGC-D127 film was highly crystalline. The charge-carrier transport properties of the LGC-D127 was investigated through the fabrication and characterization of field-effect transistor via solution process. LGC-D127 showed significantly high field-effect hole mobility of 3.16 cm2 V−1 s−1 after thermal annealing due to the large crystalline nanostructure and the small grain boundaries. In particular, LGC-D127 had good solubility in the environmentally friendly solvent such as 2-methyltetrahydrofuran due to the bulky trihexylsilyloxy side chain, and its high hole mobility (max. 3.06 cm2 V−1 s−1) was sustained from the LGC-D127 solution in 2-methyltetrahydrofuran. |
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A donor–acceptor type small molecule organic semiconductor with a trihexylsilyloxy bulky side chain, coded LGC-D127, was synthesized, and its electronic, electrochemical, and electrical properties were investigated for use as the active layer of solution-processable organic field-effect transistors. LGC-D127 consisted of a phenylene–dithiophene moiety with a bulky trihexylsilyloxy side chain as the electron-donating core, diketopyrrolopyrrole as the electron-accepting linker, and octylrhodanine as the electron-accepting end group. In spite of bulky trihexylsilyloxy side chains, LGC-D127 film was highly crystalline. The charge-carrier transport properties of the LGC-D127 was investigated through the fabrication and characterization of field-effect transistor via solution process. LGC-D127 showed significantly high field-effect hole mobility of 3.16 cm2 V−1 s−1 after thermal annealing due to the large crystalline nanostructure and the small grain boundaries. In particular, LGC-D127 had good solubility in the environmentally friendly solvent such as 2-methyltetrahydrofuran due to the bulky trihexylsilyloxy side chain, and its high hole mobility (max. 3.06 cm2 V−1 s−1) was sustained from the LGC-D127 solution in 2-methyltetrahydrofuran. |
| abstract_unstemmed |
A donor–acceptor type small molecule organic semiconductor with a trihexylsilyloxy bulky side chain, coded LGC-D127, was synthesized, and its electronic, electrochemical, and electrical properties were investigated for use as the active layer of solution-processable organic field-effect transistors. LGC-D127 consisted of a phenylene–dithiophene moiety with a bulky trihexylsilyloxy side chain as the electron-donating core, diketopyrrolopyrrole as the electron-accepting linker, and octylrhodanine as the electron-accepting end group. In spite of bulky trihexylsilyloxy side chains, LGC-D127 film was highly crystalline. The charge-carrier transport properties of the LGC-D127 was investigated through the fabrication and characterization of field-effect transistor via solution process. LGC-D127 showed significantly high field-effect hole mobility of 3.16 cm2 V−1 s−1 after thermal annealing due to the large crystalline nanostructure and the small grain boundaries. In particular, LGC-D127 had good solubility in the environmentally friendly solvent such as 2-methyltetrahydrofuran due to the bulky trihexylsilyloxy side chain, and its high hole mobility (max. 3.06 cm2 V−1 s−1) was sustained from the LGC-D127 solution in 2-methyltetrahydrofuran. |
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