Metastable Copper‐Phthalocyanine Single‐Crystal Nanowires and Their Use in Fabricating High‐Performance Field‐Effect Transistors
Source abstract
Abstract
Abstract This paper describes a simple, vapor‐phase route for the synthesis of metastable α‐phase copper‐phthalocyanine (CuPc) single‐crystal nanowires through control of the growth temperature. The influence of the growth temperature on the crystal structures, morphology, and size of the CuPc nanostructures is explored using X‐ray diffraction (XRD), optical absorption, and transmission electron microscopy (TEM). α‐CuPc nanowires are successfully incorporated as active semiconductors in field‐effect transistors (FETs). Single nanowire devices exhibit carrier mobilities and current on/off ratios as high as 0.4 cm2 V−1 s−1 and >104, respectively.
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Research context
OpenAlex topics: ZnO doping and properties · Nanowire Synthesis and Applications · Organic Electronics and Photovoltaics
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References (51)
Show source-provided references
1. 10.1016/S1369-7021(08)70055-510.1016/S1369-7021(08)70055-5 ↗
2. 10.1002/adma.20080066910.1002/adma.200800669 ↗
3. 10.1002/adma.20080060410.1002/adma.200800604 ↗
4. 10.1021/ja064236010.1021/ja0642360 ↗
5. 10.1021/nl071495u10.1021/nl071495u ↗
6. 10.1002/adma.20060125910.1002/adma.200601259 ↗
7. 10.1021/ja068079g10.1021/ja068079g ↗
8. 10.1039/B614234F10.1039/B614234F ↗
9. Leznoff C. C · 1989
10. 10.1021/cr030206t10.1021/cr030206t ↗
11. 10.1016/S0925-4005(98)00070-710.1016/S0925-4005(98)00070-7 ↗
12. 10.1364/JOSAB.14.00060210.1364/JOSAB.14.000602 ↗
13. 10.1002/(SICI)1099-1409(199908/10)3:6/7<592::AID-JPP180>3.0.CO;2-G10.1002/(SICI)1099-1409(199908/10)3:6/7<592::AID-JPP180>3.0.CO;2-G ↗
14. 10.1063/1.134384910.1063/1.1343849 ↗
15. 10.1063/1.11684110.1063/1.116841 ↗
16. 10.1063/1.151537310.1063/1.1515373 ↗
17. 10.1007/s00339-003-2398-810.1007/s00339-003-2398-8 ↗
18. 10.1016/S0379-6779(02)01067-610.1016/S0379-6779(02)01067-6 ↗
19. 10.1063/1.12198210.1063/1.121982 ↗
20. 10.1021/ja052940v10.1021/ja052940v ↗
21. 10.1021/ja039791610.1021/ja0397916 ↗
22. 10.1002/anie.20079005810.1002/anie.200790058 ↗
23. 10.1039/jr935000061510.1039/jr9350000615 ↗
24. 10.1039/J1968000248810.1039/J19680002488 ↗
25. 10.1016/0022-0248(71)90021-210.1016/0022-0248(71)90021-2 ↗
26. 10.1002/adfm.20030518010.1002/adfm.200305180 ↗
27. 10.1063/1.184943810.1063/1.1849438 ↗
28. 10.1021/jp062951q10.1021/jp062951q ↗
29. 10.1166/jnn.2008.N1110.1166/jnn.2008.N11 ↗
30. 10.1002/adma.20060054210.1002/adma.200600542 ↗
31. 10.1002/adma.20070214510.1002/adma.200702145 ↗
32. 10.1007/s00339-003-2169-610.1007/s00339-003-2169-6 ↗
33. 10.1038/nmat128510.1038/nmat1285 ↗
34. Singh V. · Mater. Res. Soc. Symp. Proc. · 2008 · 1031 · H13
35. 10.1002/pssa.221132011010.1002/pssa.2211320110 ↗
36. 10.1002/1521-3951(200202)229:3<1175::AID-PSSB1175>3.0.CO;2-K10.1002/1521-3951(200202)229:3<1175::AID-PSSB1175>3.0.CO;2-K ↗
37. 10.1016/j.tsf.2006.12.18410.1016/j.tsf.2006.12.184 ↗
38. 10.1139/v93-23710.1139/v93-237 ↗
39. 10.1021/ic000982910.1021/ic0009829 ↗
40. Misra T. N. · Rev. Pure. Appl. Chem. · 1965 · 15 · 39
41. 10.1016/j.cplett.2006.12.00710.1016/j.cplett.2006.12.007 ↗
42. 10.1021/jp709780a10.1021/jp709780a ↗
43. 10.1016/S0169-4332(02)01115-710.1016/S0169-4332(02)01115-7 ↗
44. 10.1021/jp070302o10.1021/jp070302o ↗
45. 10.1002/anie.20050080510.1002/anie.200500805 ↗
46. 10.1039/tf955510106510.1039/tf9555101065 ↗
47. 10.1002/adma.20080034110.1002/adma.200800341 ↗
48. 10.1002/adma.20050165410.1002/adma.200501654 ↗
49. Tang Q. · J. Am. Chem. Soc. · 2006 · 128 · 4634
50. 10.1002/adma.20050244210.1002/adma.200502442 ↗
51. 10.1021/ja075045f10.1021/ja075045f ↗