journal article·2016-04-20Open access

High-Performance Phototransistors Based on PDIF-CN2 Solution-Processed Single Fiber and Multifiber Assembly

Wassima Rekab, Marc-Antoine Stoeckel, Mirella El Gemayel, Marco Gobbi, Emanuele Orgiu, Paolo Samorì

Abstract

Here we describe the fabrication of organic phototransistors based on either single or multifibers integrated in three-terminal devices. These self-assembled fibers have been produced by solvent-induced precipitation of an air stable and solution-processable perylene di-imide derivative, i.e., PDIF-CN2. The optoelectronic properties of these devices were compared to devices incorporating more disordered spin-coated PDIF-CN2 thin-films. The single-fiber devices revealed significantly higher field-effect mobilities, compared to multifiber and thin-films, exceeding 2 cm(2) V(-1) s(-1). Such an efficient charge transport is the result of strong intermolecular coupling between closely packed PDIF-CN2 molecules and of a low density of structural defects. The improved crystallinity allows efficient collection of photogenerated Frenkel excitons, which results in the highest reported responsivity (R) for single-fiber PDI-based phototransistors, and photosensitivity (P) exceeding 2 × 10(3) AW(-1), and 5 × 10(3), respectively. These findings provide unambiguous evidence for the key role played by the high degree of order at the supramolecular level to leverage the material's properties toward the fabrication of light-sensitive organic field-effect transistors combining a good operational stability, high responsivity and photosensitivity. Our results show also that the air-stability performances are superior in devices where highly crystalline supramolecularly engineered architectures serve as the active layer.
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Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Advanced Memory and Neural Computing · Conducting polymers and applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Nanochemistry Laboratory, ISIS & icFRC, Université de Strasbourg & CNRS, 8 allée Gaspard Monge, 67000 Strasbourg, France

Funding

Agence Nationale de la Recherche · European Research Council · Centre International de Recherche aux Frontières de la Chimie

References (71)

Show source-provided references
1. 10.1002/1521-4095(20020116)14:2<99::AID-ADMA99>3.0.CO;2-910.1002/1521-4095(20020116)14:2<99::AID-ADMA99>3.0.CO;2-9 ↗
2. 10.1002/adma.20060017810.1002/adma.200600178 ↗
3. 10.1016/S1369-7021(07)70017-210.1016/S1369-7021(07)70017-2 ↗
4. 10.1021/cr050154310.1021/cr0501543 ↗
5. 10.1021/cr050138610.1021/cr0501386 ↗
6. 10.1039/b614393h10.1039/b614393h ↗
7. 10.1039/c1cc10321k10.1039/c1cc10321k ↗
8. 10.1063/1.151182610.1063/1.1511826 ↗
9. 10.1038/nmat216710.1038/nmat2167 ↗
10. 10.1109/JSEN.2009.203277910.1109/JSEN.2009.2032779 ↗
11. 10.1063/1.323225210.1063/1.3232252 ↗
12. 10.1021/ja910667y10.1021/ja910667y ↗
13. 10.1073/pnas.120054910910.1073/pnas.1200549109 ↗
14. 10.1021/nn503135y10.1021/nn503135y ↗
15. 10.1021/cr900150b10.1021/cr900150b ↗
16. 10.1002/adma.20130580910.1002/adma.201305809 ↗
17. 10.1038/347539a010.1038/347539a0 ↗
18. 10.1038/365628a010.1038/365628a0 ↗
19. 10.1002/1616-3028(200110)11:5<374::AID-ADFM374>3.0.CO;2-W10.1002/1616-3028(200110)11:5<374::AID-ADFM374>3.0.CO;2-W ↗
20. 10.1038/nprot.2012.09410.1038/nprot.2012.094 ↗
21. 10.1002/adma.20110343910.1002/adma.201103439 ↗
22. 10.1063/1.481726710.1063/1.4817267 ↗
23. 10.1002/adma.20140366410.1002/adma.201403664 ↗
24. 10.1016/j.orgel.2014.06.00710.1016/j.orgel.2014.06.007 ↗
25. 10.1016/j.orgel.2014.07.04110.1016/j.orgel.2014.07.041 ↗
26. 10.1002/pssa.20130039510.1002/pssa.201300395 ↗
27. 10.1109/LPT.2014.236549810.1109/LPT.2014.2365498 ↗
28. 10.1021/acs.chemmater.5b0034110.1021/acs.chemmater.5b00341 ↗
29. 10.1002/aelm.20150011910.1002/aelm.201500119 ↗
30. 10.1021/ja201494910.1021/ja2014949 ↗
31. 10.1039/c2jm33998f10.1039/c2jm33998f ↗
32. 10.1002/adma.20110094410.1002/adma.201100944 ↗
33. 10.1016/j.orgel.2014.02.02310.1016/j.orgel.2014.02.023 ↗
34. 10.1021/acsnano.5b0198210.1021/acsnano.5b01982 ↗
35. 10.1002/aelm.20150007110.1002/aelm.201500071 ↗
36. Wu G. · Adv. Electron. Mater. · 2015 · 1 · 150013610.1002/aelm.201500136 ↗
37. 10.1039/C5CC04711K10.1039/C5CC04711K ↗
38. 10.1039/C5RA14266K10.1039/C5RA14266K ↗
39. 10.1002/adfm.20090166210.1002/adfm.200901662 ↗
40. 10.1088/0957-4484/26/33/33520110.1088/0957-4484/26/33/335201 ↗
41. 10.1063/1.492291710.1063/1.4922917 ↗
42. 10.1016/S0040-6090(00)00719-710.1016/S0040-6090(00)00719-7 ↗
43. 10.1021/jp046246y10.1021/jp046246y ↗
44. 10.1039/b417320c10.1039/b417320c ↗
45. 10.1016/j.optmat.2007.03.00910.1016/j.optmat.2007.03.009 ↗
46. 10.1021/ja901077a10.1021/ja901077a ↗
47. 10.1002/adma.20090362810.1002/adma.200903628 ↗
48. 10.1021/ja211515b10.1021/ja211515b ↗
49. 10.1039/c2jm14179e10.1039/c2jm14179e ↗
50. 10.1002/adfm.20120184810.1002/adfm.201201848 ↗
51. 10.1039/c3tc30442f10.1039/c3tc30442f ↗
52. 10.1016/j.tsf.2014.07.05510.1016/j.tsf.2014.07.055 ↗
53. 10.1002/adom.20140034610.1002/adom.201400346 ↗
54. 10.1002/adma.20130341910.1002/adma.201303419 ↗
55. 10.1002/anie.20046132410.1002/anie.200461324 ↗
56. 10.1002/adma.20070147810.1002/adma.200701478 ↗
57. 10.1002/adfm.20070104510.1002/adfm.200701045 ↗
58. 10.1002/adfm.20110142710.1002/adfm.201101427 ↗
59. 10.1002/adma.20110396010.1002/adma.201103960 ↗
60. 10.1063/1.479861010.1063/1.4798610 ↗
61. 10.1002/adma.20040121610.1002/adma.200401216 ↗
62. 10.1038/nature0337610.1038/nature03376 ↗
63. 10.1103/PhysRevB.91.20530510.1103/PhysRevB.91.205305 ↗
64. 10.1073/pnas.17239099910.1073/pnas.172390999 ↗
65. 10.1103/PhysRevB.50.1076910.1103/PhysRevB.50.10769 ↗
66. 10.1021/ja074675e10.1021/ja074675e ↗
67. 10.1021/ja075242e10.1021/ja075242e ↗
68. 10.1002/adma.20080320710.1002/adma.200803207 ↗
69. 10.1016/j.orgel.2015.07.06010.1016/j.orgel.2015.07.060 ↗
70. 10.1021/ja809848y10.1021/ja809848y ↗
71. 10.1063/1.289085310.1063/1.2890853 ↗