journal article·2017-02-01

Low-Temperature Solution-Processed Thiophene-Sulfur-Doped Planar ZnO Nanorods as Electron-Transporting Layers for Enhanced Performance of Organic Solar Cells

Swapnil B. Ambade, Rohan B. Ambade, Sushil S. Bagde, Seung Hun Eom, Rajaram S. Mane, Won Suk Shin, Soo-Hyoung Lee

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Abstract

1-D ZnO represents a fascinating class of nanostructures that are significant to optoelectronics. In this work, we investigated the use of an eco-friendly, metal free in situ doping through a pure thiophene-sulfur (S) on low temperature processed (<95 °C) and annealed (<170 °C), planar 1-D ZnO nanorods (ZnRs) spin-coated as a hole-blocking and electron transporting layer (ETL) for inverted organic solar cells ( i OSCs). The TEM, HRTEM, XPS, FT-IR, EDS and Raman studies clearly reveal that the thiophene-S (Thi-S) atom is incorporated on planar ZnRs. The investigations in electrical properties suggest the enhancement in conductivity after Thi-S doping on 1-D ZnRs. The i OSCs of poly(3-hexylthiophene-2,5-diyl) and phenyl-C 61 -butyric acid methyl ester (P3HT: PC 60 BM) photoactive layer containing thiophene-S doped planar ZnRs (Thi-S-PZnRs) as ETL exhibits power conversion efficiency (PCE) of 3.68% under simulated AM 1.5 G, 100 mW cm –2 illumination. The ∼47% enhancement in PCE compared with pristine planar ZnRs (PCE = 2.38%) ETL is attributed to a combination of desirable energy level alignment, morphological modification, increased conductivity and doping effect. The universality of Thi-S-PZnRs ETL is demonstrated by the highest PCE of 8.15% in contrast to 6.50% exhibited by the i OSCs of ZnRs ETL for the photoactive layer comprising of poly[4,8-bis(5-(2-ethylhexyl)thiophene-2-yl)benzo[1,2-b;4,5-b]dithiophene-2,6-diyl- alt -(4-(2-ethylhexyl)-3-fluorothieno[3,4- b ]thiophene-)-2-carboxylate-2–6-diyl)]: phenyl-C71-butyric acid methyl ester (PTB7-Th: PCB 71 M). This enhancement in PCE is observed to be driven mainly through improved photovoltaic parameters like fill factor (ff) as well as photocurrent density ( J sc ), which are assigned to increased conductivity, exciton dissociation, and effective charge extraction, while; better ohmic contact, reduced charge recombination, and low leakage current density resulted in increased V oc .
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Research context

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

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

Affiliations

School of Semiconductor and Chemical Engineering, Chonbuk National University, 567 Baekje-daero, Jeonju, 54896, Republic of Korea

Division of Advanced Materials, Korea Research Institute of Chemical Technology (KRICT), 141 Gajeong-ro, Yuseong-gu, Daejeon 34114, Republic of Korea

Centre for Nanomaterials & Energy Devices, School of Physical Sciences, SRTM, University, 431606, Nanded, India

Energy Materials Research Centre, Korea Research Institute of Chemical Technology, Daejeon, Korea

Funding

Korea Research Institute of Chemical Technology · National Research Foundation of Korea

References (57)

Show source-provided references
1. 10.1063/1.273075610.1063/1.2730756 ↗
2. 10.1038/nmat150010.1038/nmat1500 ↗
3. 10.1002/adfm.20050021110.1002/adfm.200500211 ↗
4. 10.1038/nmat192810.1038/nmat1928 ↗
5. 10.1038/nmat190910.1038/nmat1909 ↗
6. 10.1039/b921624c10.1039/b921624c ↗
7. 10.1039/C5CS00831J10.1039/C5CS00831J ↗
8. 10.1039/c3ta11998j10.1039/c3ta11998j ↗
9. 10.1039/C0EE00273A10.1039/C0EE00273A ↗
10. 10.1039/c2ee22296e10.1039/c2ee22296e ↗
11. 10.1039/c3ee42440e10.1039/c3ee42440e ↗
12. 10.1039/c1ee01873f10.1039/c1ee01873f ↗
13. 10.1002/adma.20100430110.1002/adma.201004301 ↗
14. 10.1002/adfm.20110296810.1002/adfm.201102968 ↗
15. 10.1002/adfm.20110191510.1002/adfm.201101915 ↗
16. 10.1016/j.orgel.2009.08.01110.1016/j.orgel.2009.08.011 ↗
17. 10.1021/am401448810.1021/am4014488 ↗
18. 10.1016/j.orgel.2012.01.01110.1016/j.orgel.2012.01.011 ↗
19. Thomas, S.; Kalarikkal, N.; Stephan, A. M.; Raneesh, B.Advanced Nanomaterials: Synthesis, Properties, and Applications;CRC Press, 2014; pp1–402.10.1201/b16966 ↗
20. 10.1021/am500783210.1021/am5007832 ↗
21. 10.1021/jp202356710.1021/jp2023567 ↗
22. 10.1016/j.solmat.2010.09.02010.1016/j.solmat.2010.09.020 ↗
23. 10.1021/jp045237m10.1021/jp045237m ↗
24. 10.1007/s10854-013-1566-710.1007/s10854-013-1566-7 ↗
25. 10.1016/j.matlet.2008.11.00610.1016/j.matlet.2008.11.006 ↗
26. 10.1016/j.mssp.2008.02.00310.1016/j.mssp.2008.02.003 ↗
27. 10.1063/1.152157710.1063/1.1521577 ↗
28. 10.1021/nl060204z10.1021/nl060204z ↗
29. 10.1016/j.jhazmat.2010.07.02610.1016/j.jhazmat.2010.07.026 ↗
30. 10.1039/c3nr05061k10.1039/c3nr05061k ↗
31. 10.1039/C4NR03080J10.1039/C4NR03080J ↗
32. 10.1021/am509125c10.1021/am509125c ↗
33. 10.1039/C5NR08849F10.1039/C5NR08849F ↗
34. 10.1021/jp910263n10.1021/jp910263n ↗
35. 10.1016/0379-6779(95)03470-510.1016/0379-6779(95)03470-5 ↗
36. 10.1021/cr00012a00910.1021/cr00012a009 ↗
37. 10.1039/c3ta14734g10.1039/c3ta14734g ↗
38. 10.1021/jp111472410.1021/jp1114724 ↗
39. 10.1016/0379-6779(95)03560-510.1016/0379-6779(95)03560-5 ↗
40. 10.1021/jp011577l10.1021/jp011577l ↗
41. 10.1021/jp800106v10.1021/jp800106v ↗
42. 10.1021/am300348g10.1021/am300348g ↗
43. 10.1021/jp308847g10.1021/jp308847g ↗
44. 10.1021/cg800629810.1021/cg8006298 ↗
45. 10.1021/la980909j10.1021/la980909j ↗
46. 10.1002/adfm.20120018610.1002/adfm.201200186 ↗
47. 10.1021/jp020482w10.1021/jp020482w ↗
48. 10.1021/nn100427f10.1021/nn100427f ↗
49. 10.1039/C0JM02184A10.1039/C0JM02184A ↗
50. 10.1021/nn800878c10.1021/nn800878c ↗
51. 10.1002/adma.20130332710.1002/adma.201303327 ↗
52. 10.1002/adma.20130284510.1002/adma.201302845 ↗
53. 10.1039/c2jm31277h10.1039/c2jm31277h ↗
54. 10.1002/adma.20120195810.1002/adma.201201958 ↗
55. 10.1021/jp108886p10.1021/jp108886p ↗
56. 10.1002/aenm.20110035710.1002/aenm.201100357 ↗
57. 10.1039/c3cc00310h10.1039/c3cc00310h ↗