Charge Conduction Properties at the Contact Interface between (Phthalocyaninato)nickel(II) and Electron Acceptor Single Crystals
Source abstract
Abstract
Single-component crystals of both (phthalocyaninato)nickel(II) (Ni( Pc )) and 2,5-difluoro-7,7,8,8-tetracyanoquinodimethane (F 2 TCNQ) are typical band insulators. However, the contact interface between them demonstrates metal-like transport properties. Although Ni( Pc ) and F 2 TCNQ are an electron donor and an acceptor, respectively, the combination of these two components does not yield any charge transfer (CT) complex crystals. Infrared spectra show that the highly conductive feature originates from charge injection at the contact interface. The thermoelectric power of the mixed powder reveals that the transport at the contact interface is dominated by the holes in the Ni( Pc ) crystal.
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Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Organic and Molecular Conductors Research · Porphyrin and Phthalocyanine Chemistry
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Faculty of Science, ‡Graduate School of Chemical Sciences and Engineering, and §JST, CREST, Faculty of Science, Hokkaido University, Sapporo 060-0810, Japan
References (23)
Show source-provided references
1. Dimitrakopoulos C. D. · Adv. Mater. · 2002 · 14 · 9910.1002/1521-4095(20020116)14:2<99::AID-ADMA99>3.0.CO;2-9 ↗
2. Sunrar V. C. · Science · 2004 · 303 · 164410.1126/science.1094196 ↗
3. Roncali J. · Adv. Mater. · 2007 · 19 · 204510.1002/adma.200700135 ↗
4. Liu S. H. · Adv. Mater. · 2009 · 21 · 121710.1002/adma.200802202 ↗
5. Usta H. · Acc. Chem. Res. · 2011 · 7 · 50110.1021/ar200006r ↗
6. Gutmann F. · 1976
7. Wright J. D. · 1987
8. Epstein A. J. · Solid State Commun. · 1978 · 27 · 32510.1016/0038-1098(78)90046-7 ↗
9. Kumai R. · J. Am. Chem. Soc. · 1998 · 120 · 826310.1021/ja9816178 ↗
10. Gaudiello J. G. · J. Am. Chem. Soc. · 1989 · 111 · 525910.1021/ja00196a037 ↗
11. Alves H. · Nat. Mater. · 2008 · 7 · 57410.1038/nmat2205 ↗
12. Nakano M. · Appl. Phys. Lett. · 2010 · 96 · 23210210.1063/1.3449558 ↗
13. Wang H. · NPG Asia Mater. · 2010 · 2 · 6910.1038/asiamat.2010.44 ↗
14. Lezana I. G. · Nat. Mater. · 2012 · 11 · 78810.1038/nmat3383 ↗
15. Takahashi Y. · J. Phys. Chem. C. · 2012 · 116 · 70010.1021/jp2074368 ↗
16. Mochida T. · Synth. Met. · 1997 · 86 · 179710.1016/S0379-6779(97)80908-3 ↗
17. Robertson J. M. · J. Chem. Soc. · 1937 · 86 · 21910.1039/jr9370000219 ↗
18. Wiygul F. M. · Mol. Cryst. Liq. Cryst. · 1981 · 78 · 27910.1080/00268948108082165 ↗
19. Chaikin P. M. · Rev. Sci. Instrum. · 1975 · 46 · 21810.1063/1.1134171 ↗
20. Epstein A. J. · Ann. N.Y. Acad. Sci. · 1978 · 313 · 18310.1111/j.1749-6632.1978.tb39417.x ↗
21. Takahashi Y. · Dalton Trans. · 2011 · 40 · 556310.1039/c0dt01601b ↗
22. Emge T. J. · Mol. Cryst. Liq. Cryst. · 1981 · 78 · 29510.1080/00268948108082166 ↗
23. Mori T. · Bull. Chem. Soc. Jpn. · 1984 · 57 · 62710.1246/bcsj.57.627 ↗