Greater than 10 cm2 V−1 s−1: A breakthrough of organic semiconductors for field‐effect transistors
Source abstract
Abstract
Abstract Organic semiconductors have been receiving intensive attention due to the specific advantages of low‐temperature processing ability, low‐fabrication cost, flexibility, and so forth. The charge carrier mobility of higher than 10 cm2 V−1 s−1 for organic semiconductors is of great importance to be studied since it presents a future promising research direction toward commercial microelectronic applications. With the significant progress of the discovery of novel organic molecules and the further improvements of device fabrication technology, some organic molecules can break the limit of our knowledge and show very high mobilities. In this review, organic polymers and small molecules with mobilities above 10 cm2 V−1 s−1 are first introduced to provide the readers with a general understanding of the features and characteristics of high‐performance organic semiconductors. Then, some important parameters, including the molecular structures, the device configurations, and the performance, are discussed in detail. Finally, the clues to obtain high mobility are summarized, and the perspective toward the future possible research directions are also provided. image
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Advanced Memory and Neural Computing · Nanowire Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Physics Northwest University Xi'an People's Republic of China
School of Materials Science and Engineering Shaanxi Normal University Xi'an People's Republic of China
School of Materials Science and Engineering Tianjin University Tianjin People's Republic of China
Funding
National Natural Science Foundation of China · Tianjin University
References (100+)
Show source-provided references
1. 10.1002/anie.20181443910.1002/anie.201814439 ↗
2. 10.1021/ja039393310.1021/ja0393933 ↗
3. 10.1126/science.290.5499.212310.1126/science.290.5499.2123 ↗
4. 10.1002/adma.20160316710.1002/adma.201603167 ↗
5. 10.1039/C6TC05346G10.1039/C6TC05346G ↗
6. 10.1016/j.jnoncrysol.2005.11.12210.1016/j.jnoncrysol.2005.11.122 ↗
7. 10.1002/adma.20100458810.1002/adma.201004588 ↗
8. 10.1016/S1369-7021(07)70016-010.1016/S1369-7021(07)70016-0 ↗
9. 10.1002/adma.20130251410.1002/adma.201302514 ↗
10. 10.1039/c3cs60127g10.1039/c3cs60127g ↗
11. 10.1002/adma.20130434610.1002/adma.201304346 ↗
12. 10.1039/C7TC04389A10.1039/C7TC04389A ↗
13. 10.1039/C9TC01268K10.1039/C9TC01268K ↗
14. 10.1063/1.9741710.1063/1.97417 ↗
15. 10.1557/jmr.2018.17110.1557/jmr.2018.171 ↗
16. 10.1002/adma.20180346710.1002/adma.201803467 ↗
17. 10.1002/adma.20130256310.1002/adma.201302563 ↗
18. 10.1038/nmat153710.1038/nmat1537 ↗
19. 10.1038/ncomms726910.1038/ncomms7269 ↗
20. 10.1002/adma.20110452210.1002/adma.201104522 ↗
21. 10.1002/adma.20090355910.1002/adma.200903559 ↗
22. 10.1038/nature0772710.1038/nature07727 ↗
23. 10.1021/ja210284s10.1021/ja210284s ↗
24. 10.1039/C7TC04982J10.1039/C7TC04982J ↗
25. 10.3390/cryst1011099310.3390/cryst10110993 ↗
26. 10.1039/c3977000057810.1039/c39770000578 ↗
27. 10.1063/1.11783410.1063/1.117834 ↗
28. 10.1021/ma021607y10.1021/ma021607y ↗
29. 10.1021/ma961121f10.1021/ma961121f ↗
30. 10.1038/372344a010.1038/372344a0 ↗
31. 10.1039/c3ee00015j10.1039/c3ee00015j ↗
32. 10.1038/s41570-019-0152-910.1038/s41570-019-0152-9 ↗
33. 10.1002/adma.20120179510.1002/adma.201201795 ↗
34. 10.1002/adma.20130494510.1002/adma.201304945 ↗
35. 10.1021/acs.accounts.8b0002510.1021/acs.accounts.8b00025 ↗
36. 10.1016/j.chempr.2018.08.00510.1016/j.chempr.2018.08.005 ↗
37. 10.1038/srep0075410.1038/srep00754 ↗
38. 10.1002/adma.20130608410.1002/adma.201306084 ↗
39. 10.1002/adma.20150427210.1002/adma.201504272 ↗
40. 10.1021/ja504537v10.1021/ja504537v ↗
41. 10.1002/adma.20130220410.1002/adma.201302204 ↗
42. 10.1021/acsnano.5b0198210.1021/acsnano.5b01982 ↗
43. 10.1002/adma.20130508410.1002/adma.201305084 ↗
44. 10.1038/ncomms840810.1038/ncomms8408 ↗
45. 10.1002/adma.20170125110.1002/adma.201701251 ↗
46. 10.1021/ar500278w10.1021/ar500278w ↗
47. 10.1021/acs.accounts.5b0011810.1021/acs.accounts.5b00118 ↗
48. 10.1021/cr050966z10.1021/cr050966z ↗
49. 10.1002/adma.20110200710.1002/adma.201102007 ↗
50. 10.1002/adma.20130549710.1002/adma.201305497 ↗
51. 10.1063/1.176728210.1063/1.1767282 ↗
52. 10.1016/j.jcrysgro.2012.10.00210.1016/j.jcrysgro.2012.10.002 ↗
53. 10.1002/pssa.20062223310.1002/pssa.200622233 ↗
54. 10.1016/j.progpolymsci.2018.02.00210.1016/j.progpolymsci.2018.02.002 ↗
55. 10.1080/1058725010802365910.1080/10587250108023659 ↗
56. 10.1002/anie.20039030510.1002/anie.200390305 ↗
57. 10.1021/cr100380z10.1021/cr100380z ↗
58. 10.1002/adma.20060216210.1002/adma.200602162 ↗
59. 10.1021/cm801896r10.1021/cm801896r ↗
60. 10.1038/ncomms1003210.1038/ncomms10032 ↗
61. 10.1021/jacs.7b0938110.1021/jacs.7b09381 ↗
62. 10.1002/adma.20040186610.1002/adma.200401866 ↗
63. 10.1063/1.147137810.1063/1.1471378 ↗
64. 10.1063/1.272489510.1063/1.2724895 ↗
65. 10.1063/1.238815110.1063/1.2388151 ↗
66. 10.1143/JJAP.49.08550210.1143/JJAP.49.085502 ↗
67. 10.1107/S010876810600305310.1107/S0108768106003053 ↗
68. 10.1126/science.109419610.1126/science.1094196 ↗
69. 10.1021/cm050262610.1021/cm0502626 ↗
70. 10.1002/adma.20040101710.1002/adma.200401017 ↗
71. 10.1063/1.216669810.1063/1.2166698 ↗
72. 10.1063/1.236394010.1063/1.2363940 ↗
73. 10.1016/j.orgel.2015.02.00310.1016/j.orgel.2015.02.003 ↗
74. 10.1109/55.64408510.1109/55.644085 ↗
75. 10.1557/PROC-771-L6.510.1557/PROC-771-L6.5 ↗
76. 10.1021/ja044586r10.1021/ja044586r ↗
77. 10.1063/1.170487410.1063/1.1704874 ↗
78. 10.1002/adma.20060092910.1002/adma.200600929 ↗
79. 10.1021/ja803291a10.1021/ja803291a ↗
80. 10.1021/jp300052p10.1021/jp300052p ↗
81. 10.1063/1.307612410.1063/1.3076124 ↗
82. 10.1038/srep0504810.1038/srep05048 ↗
83. 10.1002/adma.20160241010.1002/adma.201602410 ↗
84. 10.1063/1.312076910.1063/1.3120769 ↗
85. 10.1039/b809228c10.1039/b809228c ↗
86. 10.1021/ja068079g10.1021/ja068079g ↗
87. 10.1021/nl062703610.1021/nl0627036 ↗
88. 10.1021/ja107599r10.1021/ja107599r ↗
89. Synthesis and reactions of 2,7‐disubstituted benzothieno[3,2‐b]benzothiophenes
90. 10.1021/ar400282g10.1021/ar400282g ↗
91. 10.1038/nature1031310.1038/nature10313 ↗
92. 10.1038/ncomms616210.1038/ncomms6162 ↗
93. 10.1063/1.492134310.1063/1.4921343 ↗
94. 10.1002/aelm.20180007610.1002/aelm.201800076 ↗
95. 10.1038/ncomms400510.1038/ncomms4005 ↗
96. 10.1002/adma.20100438710.1002/adma.201004387 ↗
97. 10.1039/C5CC03305E10.1039/C5CC03305E ↗
98. 10.1021/ja307802q10.1021/ja307802q ↗
99. 10.1038/ncomms782810.1038/ncomms7828 ↗
100. 10.1002/adma.20140028910.1002/adma.201400289 ↗