Photosensitizer PCBM tuning of azo dyes-based composites: Third-order nonlinear optical properties
Source abstract
Abstract
Abstract New organic composites with significant third-order nonlinear optical properties have potential applications in photoelectronic and photonics, such as optical limiting and optical switching. Six new azo dye-based composites have been designed and prepared. The linear optical absorption properties were studied by the UV–Vis spectrum and the band-gaps of the samples were determined using the optical method. The third-order nonlinear optical (NLO) properties were investigated by standard Z-scan. The influence of the fullerene derivative (Iliopoulos et al., 2013; Iliopoulos et al., 2013) [6, 6] -phenyl C61 butyric acid methyl ester (PCBM) on the third-order NLO properties was discussed. The third-order NLO susceptibility χ(3) increases firstly with PCBM content, then decrease afterward, and the peak appears at about 0.30 wt%. The results revealed that the third-order nonlinear susceptibility χ(3) and the molecular second hyperpolarizability γ of these composites are of the order of 10−16 (m/V)2 and 10−40 m5V−2, respectively. And the Figures Merit T and W of 1, 2, 3, 4, 5, and 6 meet the all-optical switching requirements of T 1. Hence, 1, 2, 3, 4, 5, and 6 are promising candidates for applications in all-optical switching. This work can provide a reference for design new third-order NLO materials.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Nonlinear Optical Materials Research · Nonlinear Optical Materials Studies · Porphyrin and Phthalocyanine Chemistry
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (56)
Show source-provided references
1. Tan · J. Comput. Methods Sci. Eng. · 2019 · 19 · 427
2. Marder · Science · 1994 · 265 · 63210.1126/science.265.5172.632 ↗
3. Kulyk · RSC Adv. · 2016 · 6 · 1443910.1039/C5RA25889H ↗
4. Kulyk · Org. Electron. · 2016 · 36 · 110.1016/j.orgel.2016.05.028 ↗
5. Spiridon · Dyes Pigments · 2015 · 114 · 2410.1016/j.dyepig.2014.10.010 ↗
6. Iliopoulos · Appl. Phys. Lett. · 2013 · 10310.1063/1.4837055 ↗
7. Rau · J. Opt. Soc. Am. B · 2008 · 25 · 173810.1364/JOSAB.25.001738 ↗
8. Fuks-Janczarek · J. Phys. Chem. B · 2005 · 109 · 1017910.1021/jp0508711 ↗
9. Fuks-Janczarek · Optic Commun. · 2004 · 236 · 15910.1016/j.optcom.2004.03.022 ↗
10. Sahraoui · Chem. Phys. Lett. · 2002 · 365 · 32710.1016/S0009-2614(02)01477-X ↗
11. Sahraoui · Optic Commun. · 1997 · 138 · 10910.1016/S0030-4018(97)00033-3 ↗
12. Lee · ChemPhysChem · 2006 · 7 · 20610.1002/cphc.200500274 ↗
13. Yang · J. Am. Chem. Soc. · 2007 · 129 · 1318310.1021/ja0741022 ↗
14. Chen · Dyes Pigments · 2018 · 158 · 47410.1016/j.dyepig.2018.05.063 ↗
15. Zhao · Dyes Pigments · 2019 · 162 · 45110.1016/j.dyepig.2018.10.050 ↗
16. Mishra · Spectrochim. Acta Mol. Biomol. Spectrosc. · 2019 · 223 · 11735310.1016/j.saa.2019.117353 ↗
17. Zhang · RSC Adv. · 2019 · 9 · 925310.1039/C8RA07661H ↗
18. Zhao · Chemistry · 2005 · 11 · 364310.1002/chem.200401198 ↗
19. Chen · Mater. Res. Express · 2016 · 3 · 10510210.1088/2053-1591/3/10/105102 ↗
20. Nam · Nat. Commun. · 2015 · 6 · 892910.1038/ncomms9929 ↗
21. Liao · ChemSusChem · 2019 · 465 · 249
22. Chen · Optik · 2019 · 179 · 89510.1016/j.ijleo.2018.11.024 ↗
23. Chen · Opt. Mater. · 2019 · 91 · 8010.1016/j.optmat.2019.03.009 ↗
24. Wang · Dalton Trans. · 2015 · 44 · 1007810.1039/C5DT01134E ↗
25. Ma · Appl. Surf. Sci. · 2019 · 465 · 24910.1016/j.apsusc.2018.09.192 ↗
26. Ichida · J. Phys. Chem. B · 2000 · 104 · 708210.1021/jp0009453 ↗
27. Sarova · J. Phys. Chem. B · 2004 · 108 · 1726110.1021/jp047019z ↗
28. Divyasree · Opt. Mater. · 2018 · 79 · 7210.1016/j.optmat.2018.03.010 ↗
29. Yu · Opt. Mater. · 2019 · 97 · 10940010.1016/j.optmat.2019.109400 ↗
30. Wang · Results Phys. · 2019 · 15 · 10271110.1016/j.rinp.2019.102711 ↗
31. Tarwal · Appl. Surf. Sci. · 2011 · 257 · 1078910.1016/j.apsusc.2011.07.099 ↗
32. Senthil · RSC Adv. · 2014 · 4 · 5611210.1039/C4RA09112D ↗
33. Karthigha · RSC Adv. · 2016 · 6 · 3315910.1039/C6RA05055G ↗
34. Lubguban · J. Appl. Phys. · 2002 · 92 · 103310.1063/1.1483916 ↗
35. Kassem · Mater. Lett. · 1993 · 16 · 23610.1016/0167-577X(93)90171-S ↗
36. Tauc · Phys. Status Solidi · 1966 · 15 · 62710.1002/pssb.19660150224 ↗
37. Youssef · Appl. Phys. Lett. · 2013 · 103
38. Deng · Optic Commun. · 1999 · 168 · 20710.1016/S0030-4018(99)00297-7 ↗
39. Powell · 2010
40. Geskin · J. Am. Chem. Soc. · 2003 · 125 · 1565110.1021/ja035862p ↗
41. Shi · J. Phys. Chem. C · 2014 · 118 · 641310.1021/jp412500r ↗
42. Babeela · J. Phys. D Appl. Phys. · 2004 · 48 · 6510210.1088/0022-3727/48/6/065102 ↗
43. Walters · ACS Nano · 2015 · 9 · 934010.1021/acsnano.5b03308 ↗
44. Sheik-Bahae · IEEE J. Quant. Electron. · 1990 · 26 · 76010.1109/3.53394 ↗
45. Rao · Optic Commun. · 2013 · 287 · 22410.1016/j.optcom.2012.09.012 ↗
46. Arjonaesteban · J. Am. Chem. Soc. · 2015 · 137 · 1352410.1021/jacs.5b06722 ↗
47. Wang · RSC Adv. · 2016 · 6 · 1449010.1039/C5RA24761F ↗
48. Chen · J. Opt. Soc. Am. B: Optical Phys. · 1989 · 6 · 61610.1364/JOSAB.6.000616 ↗
49. Ganeev · Optic Commun. · 2004 · 229 · 40310.1016/j.optcom.2003.10.046 ↗
50. Szeremeta · J. Phys. Chem. C · 2013 · 117 · 2619710.1021/jp4051484 ↗
51. Hales · Science · 2010 · 327 · 148510.1126/science.1185117 ↗
52. Chen · Opt. Mater. · 2010 · 32 · 86810.1016/j.optmat.2010.01.003 ↗
53. Yang · Optic Commun. · 2005 · 256 · 25610.1016/j.optcom.2005.06.085 ↗
54. Remyamol · Mater. Res. Express · 2014 · 110.1088/2053-1591/1/3/035051 ↗
55. Narayanan · RSC Adv. · 2014 · 5 · 865710.1039/C4RA13024C ↗
56. Li · Dyes Pigments · 2015 · 119 · 7010.1016/j.dyepig.2015.03.025 ↗