journal article·2009-12-09

Metastable Copper‐Phthalocyanine Single‐Crystal Nanowires and Their Use in Fabricating High‐Performance Field‐Effect Transistors

Kai Xiao, Rongjin Li, Jing Tao, Edward A. Payzant, Ilia N. Ivanov, Alex A. Puretzky, Wenping Hu, David B. Geohegan

Advanced Functional Materials· Volume 19· Issue 23
Publisher page

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.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: ZnO doping and properties · Nanowire Synthesis and Applications · Organic Electronics and Photovoltaics

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

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 ↗