journal article·2013-12-26

Green-Sensitive Organic Photodetectors with High Sensitivity and Spectral Selectivity Using Subphthalocyanine Derivatives

Kwang-Hee Lee, Dong-Seok Leem, Jeffrey S. Castrucci, Kyung-Bae Park, Xavier Bulliard, Kyu-Sik Kim, Yong Wan Jin, Sangyoon Lee, Timothy P. Bender, Soo Young Park

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Abstract

Green-sensitive organic photodetectors (OPDs) with high sensitivity and spectral selectivity using boron subphthalocyanine chloride (SubPc) derivatives are reported. The OPDs composed of SubPc and dicyanovinyl terthiophene derivative (DCV3T) demonstrated the highest green-sensitivity with maximum external quantum efficiency (EQE) of 62.6 % at an applied voltage of -5 V, but wide full-width-at-half-maximum (FWHM) of 211 nm. The optimized performance considering spectral selectivity was achieved from the composition of N,N-dimethyl quinacridone (DMQA) and SubPc showing the high specific detectivity (D*) of 2.34 × 10(12) cm Hz(1/2)/W, the EQE value of 60.1% at -5 V, and narrow FWHM of 131 nm. In spite of the sharp absorption property of SubPc with the maximum wavelength (λmax) at 586 nm, the EQE spectrum showed favorable green-sensitivity characterized by smooth waveform with λmax at 560 nm, which is induced from the high reflectance of SubPc centered at 605 nm. The photoresponsivity of the OPD devices was found to be consistent with their absorptance. Optimized DMQA/SubPc device showed the lowest value of blue crosstalk (0.42) and moderate red crosstalk (0.37), suggesting its promising application as a green-sensitive OPD.
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Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Perovskite Materials and Applications

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Affiliations

Emerging Materials Center, Samsung Advanced Institute of Technology, Samsung Electronics Co., Yongin 446-712, Republic of Korea

Center for Supramolecular Optoelectronic Materials, Department of Materials Science and Engineering, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 151-744, Republic of Korea

Department of Chemical Engineering and Applied Chemistry, University of Toronto, 200 College Street, Toronto, Ontario M5S 3E5, Canada

References (38)

Show source-provided references
1. Martino N. · J. Mater. Chem. B · 2013 · 1 · 376810.1039/c3tb20213e ↗
2. Xu X. · Org. Electron. · 2008 · 9 · 112210.1016/j.orgel.2008.07.011 ↗
3. Someya T. · IEEE Trans. Electron Devices · 2005 · 52 · 250210.1109/TED.2005.857935 ↗
4. El Gamal A. · IEEE Circuits Devices Mag. · 2005 · 21 · 610.1109/MCD.2005.1438751 ↗
5. El-Desouki M. · Sensors · 2009 · 9 · 43010.3390/s90100430 ↗
6. Konstantatos G. · Nat. Photonics · 2007 · 1 · 53110.1038/nphoton.2007.147 ↗
7. Ihama M. · IDW 09, Proc. 16th Int. Display Workshops · 2009 · INP1
8. Agranov G. · IEEE Trans. Electron Devices · 2003 · 50 · 410.1109/TED.2002.806473 ↗
9. Theil J. A. · J. Non-Cryst. Solids · 2002 · 299 · 123410.1016/S0022-3093(01)01144-9 ↗
10. Vygranenko Y. · IEEE J. Quantum Electron. · 2005 · 41 · 69710.1109/JQE.2005.845029 ↗
11. Barton J. B. · Proc. SPIE · 2002 · 4721 · 3710.1117/12.478858 ↗
12. Konstantatos G. · Nat. Nanotechnol. · 2010 · 5 · 39110.1038/nnano.2010.78 ↗
13. Rauch T. · Nat. Photonics · 2009 · 3 · 33210.1038/nphoton.2009.72 ↗
14. Gan X. · Nat. Photonics · 2013 · 7 · 88310.1038/nphoton.2013.253 ↗
15. Baierl D. · Nat. Commun. · 2012 · 3 · 117510.1038/ncomms2180 ↗
16. Lin Y. · Chem. Soc. Rev. · 2012 · 41 · 424510.1039/c2cs15313k ↗
17. Baeg K.-J. · Adv. Mater. · 2013 · 25 · 426710.1002/adma.201204979 ↗
18. Gommans H. · Adv. Funct. Mater. · 2007 · 17 · 265310.1002/adfm.200700398 ↗
19. Gommans H. · Adv. Funct. Mater. · 2009 · 19 · 343510.1002/adfm.200900524 ↗
20. Beaumont N. · Adv. Funct. Mater. · 2012 · 22 · 56110.1002/adfm.201101782 ↗
21. Pandey R. · Adv. Funct. Mater. · 2012 · 22 · 61710.1002/adfm.201101948 ↗
22. Sullivan P. · Adv. Funct. Mater. · 2011 · 21 · 352
23. Lee K.-H. · J. Mater. Chem. C · 2013 · 1 · 266610.1039/c3tc00809f ↗
24. Morse G. E. · ACS Appl. Mater. Interfaces · 2010 · 2 · 193410.1021/am1002603 ↗
25. Uhrich C. · Adv. Funct. Mater. · 2007 · 17 · 299110.1002/adfm.200600917 ↗
26. Morse E. · ACS Appl. Mater. Interfaces · 2012 · 4 · 505510.1021/am3015197 ↗
27. Claessens C. G. · Chem. Rev. · 2012 · 102 · 83510.1021/cr0101454 ↗
28. Mizuguchi J. · J. Phys. Chem. B · 2006 · 110 · 1915410.1021/jp060915l ↗
29. Ziehlke H. · J. Phys. Chem. A · 2011 · 115 · 843710.1021/jp203420m ↗
30. Dennler G. · Adv. Mater. · 2009 · 21 · 132310.1002/adma.200801283 ↗
31. Mihailetchi V. D. · Adv. Funct. Mater. · 2006 · 16 · 69910.1002/adfm.200500420 ↗
32. Lenes M. · Adv. Funct. Mater. · 2009 · 19 · 110610.1002/adfm.200801514 ↗
33. Gong X. · Science · 2009 · 325 · 166510.1126/science.1176706 ↗
34. Tedde S. F. · Nano Lett. · 2009 · 9 · 98010.1021/nl803386y ↗
35. Vuuren R. D. J. · J. Mater. Chem. C · 2013 · 1 · 353210.1039/c3tc30472h ↗
36. Bass M. · 1995
37. Leem D.-S. · Appl. Phys. Lett. · 2013 · 103 · 04330510.1063/1.4816502 ↗
38. Fukuda T. · Jpn. J. Appl. Phys. · 2009 · 48 · 04C16210.1143/JJAP.48.04C162 ↗