All‐Optical Switching and Two‐States Light‐Controlled Coherent‐Incoherent Random Lasing in a Thiophene‐Based Donor‐Acceptor System
We describe herein the synthesis and characterization of a thiophene‐based donor‐acceptor system, namely (E)‐2‐(4‐nitrostyryl)‐5‐phenylthiophene (Th‐pNO2), which was prepared under Horner‐Wadsworth‐Emmons conditions. The UV/Vis absorption bands, including the intramolecular charge transfer (ICT) ban...
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Published in: | Chemphyschem Vol. 19; no. 13; pp. 1605 - 1616 |
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Abstract | We describe herein the synthesis and characterization of a thiophene‐based donor‐acceptor system, namely (E)‐2‐(4‐nitrostyryl)‐5‐phenylthiophene (Th‐pNO2), which was prepared under Horner‐Wadsworth‐Emmons conditions. The UV/Vis absorption bands, including the intramolecular charge transfer (ICT) band, were fully assigned using DFT and TD‐DFT computations. The results of both efficient third‐order nonlinear optical properties and light‐amplification phenomena are presented. Investigations of photoinduced birefringence (PIB) in optical Kerr effect (OKE) experiments showed a great potential for this particular compound as an efficient, fully reversible, and fast optical switch. Time constants for the observed trans‐cis‐trans molecular transitions are in the range of microseconds and give a competitive experimental result for the well‐known and exploited azobenzene derivatives. Random lasing (RL) investigations confirmed that this organic system is potentially useful to achieve strong light enhancement, observed as a multimode lasing action. Both RL and OKE measurements indicate that this material is a representative of thiophene derivatives, which can be utilized to fabricate fast all‐optical switches or random lasers (light amplifiers).
A thiophene derivative, synthesized through the Horner‐Wadsworth‐Emmons (HWE) reaction, has been fully characterized in this study. The material exhibits efficient third‐order nonlinear optical properties and an attractive light‐amplification behavior. Photoinduced birefringence investigations suggest that it could be used as an efficient, fully reversible and fast optical switch. |
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AbstractList | We describe herein the synthesis and characterization of a thiophene‐based donor‐acceptor system, namely (E)‐2‐(4‐nitrostyryl)‐5‐phenylthiophene (Th‐pNO2), which was prepared under Horner‐Wadsworth‐Emmons conditions. The UV/Vis absorption bands, including the intramolecular charge transfer (ICT) band, were fully assigned using DFT and TD‐DFT computations. The results of both efficient third‐order nonlinear optical properties and light‐amplification phenomena are presented. Investigations of photoinduced birefringence (PIB) in optical Kerr effect (OKE) experiments showed a great potential for this particular compound as an efficient, fully reversible, and fast optical switch. Time constants for the observed trans‐cis‐trans molecular transitions are in the range of microseconds and give a competitive experimental result for the well‐known and exploited azobenzene derivatives. Random lasing (RL) investigations confirmed that this organic system is potentially useful to achieve strong light enhancement, observed as a multimode lasing action. Both RL and OKE measurements indicate that this material is a representative of thiophene derivatives, which can be utilized to fabricate fast all‐optical switches or random lasers (light amplifiers).
A thiophene derivative, synthesized through the Horner‐Wadsworth‐Emmons (HWE) reaction, has been fully characterized in this study. The material exhibits efficient third‐order nonlinear optical properties and an attractive light‐amplification behavior. Photoinduced birefringence investigations suggest that it could be used as an efficient, fully reversible and fast optical switch. We describe herein the synthesis and characterization of a thiophene-based donor-acceptor system, namely (E)-2-(4-nitrostyryl)-5-phenylthiophene (Th-pNO2 ), which was prepared under Horner-Wadsworth-Emmons conditions. The UV/Vis absorption bands, including the intramolecular charge transfer (ICT) band, were fully assigned using DFT and TD-DFT computations. The results of both efficient third-order nonlinear optical properties and light-amplification phenomena are presented. Investigations of photoinduced birefringence (PIB) in optical Kerr effect (OKE) experiments showed a great potential for this particular compound as an efficient, fully reversible, and fast optical switch. Time constants for the observed trans-cis-trans molecular transitions are in the range of microseconds and give a competitive experimental result for the well-known and exploited azobenzene derivatives. Random lasing (RL) investigations confirmed that this organic system is potentially useful to achieve strong light enhancement, observed as a multimode lasing action. Both RL and OKE measurements indicate that this material is a representative of thiophene derivatives, which can be utilized to fabricate fast all-optical switches or random lasers (light amplifiers). We describe herein the synthesis and characterization of a thiophene‐based donor‐acceptor system, namely (E)‐2‐(4‐nitrostyryl)‐5‐phenylthiophene (Th‐ p NO 2 ), which was prepared under Horner‐Wadsworth‐Emmons conditions. The UV/Vis absorption bands, including the intramolecular charge transfer (ICT) band, were fully assigned using DFT and TD‐DFT computations. The results of both efficient third‐order nonlinear optical properties and light‐amplification phenomena are presented. Investigations of photoinduced birefringence (PIB) in optical Kerr effect (OKE) experiments showed a great potential for this particular compound as an efficient, fully reversible, and fast optical switch. Time constants for the observed trans‐cis‐trans molecular transitions are in the range of microseconds and give a competitive experimental result for the well‐known and exploited azobenzene derivatives. Random lasing (RL) investigations confirmed that this organic system is potentially useful to achieve strong light enhancement, observed as a multimode lasing action. Both RL and OKE measurements indicate that this material is a representative of thiophene derivatives, which can be utilized to fabricate fast all‐optical switches or random lasers (light amplifiers). |
Author | Szukalski, Adam Mysliwiec, Jaroslaw Sahraoui, Bouchta Ayadi, Awatef Haupa, Karolina El‐Ghayoury, Abdelkrim |
Author_xml | – sequence: 1 givenname: Adam surname: Szukalski fullname: Szukalski, Adam email: adam.szukalski@pwr.edu.pl organization: Wroclaw University of Science and Technology, Wyb. Wyspianskiego 27, 50-320 – sequence: 2 givenname: Awatef surname: Ayadi fullname: Ayadi, Awatef organization: Université de Sfax – sequence: 3 givenname: Karolina surname: Haupa fullname: Haupa, Karolina organization: Department of Applied Chemistry and Institute of Molecular Science, National Chiao Tung – sequence: 4 givenname: Abdelkrim orcidid: 0000-0003-2787-3859 surname: El‐Ghayoury fullname: El‐Ghayoury, Abdelkrim email: abdelkrim.elghayoury@univ-angers.fr organization: Université d'Angers, UFR Sciences, UMR 6200, CNRS, Bât. K, 2 Bd. Lavoisier – sequence: 5 givenname: Bouchta surname: Sahraoui fullname: Sahraoui, Bouchta organization: Université d'Angers, UFR Sciences, UMR 6200, CNRS, Bât. K, 2 Bd. Lavoisier – sequence: 6 givenname: Jaroslaw surname: Mysliwiec fullname: Mysliwiec, Jaroslaw organization: Wroclaw University of Science and Technology, Wyb. Wyspianskiego 27, 50-320 |
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Cites_doi | 10.1002/adma.200500734 10.1016/S0379-6779(00)00595-6 10.1063/1.2159083 10.1016/j.physb.2003.08.031 10.1103/PhysRevLett.87.215503 10.1016/S0925-3467(97)00068-2 10.1088/1612-2011/11/4/045801 10.1063/1.1984106 10.1063/1.1862312 10.1016/S0379-6779(03)00298-4 10.1103/PhysRevB.71.045205 10.1016/j.cplett.2013.05.018 10.1109/JQE.1966.1074123 10.1063/1.1646440 10.1016/j.cplett.2004.06.011 10.1364/JOSAB.21.000208 10.1016/j.dyepig.2016.11.030 10.1103/PhysRevE.54.4256 10.1002/jcc.22885 10.1021/acs.jpcc.5b01947 10.1364/AO.47.005074 10.1021/jp510102q 10.1063/1.2173258 10.1063/1.464129 10.1063/1.124645 10.1038/373203b0 10.1103/PhysRevLett.82.2278 10.1016/j.tsf.2007.04.103 10.1364/JOSAB.27.001874 10.1021/jp054324r 10.1007/s00894-015-2651-z 10.1016/j.dyepig.2017.04.009 10.1002/adma.19970091508 10.1063/1.1782259 10.1021/jp3027447 10.1063/1.1605233 10.1016/j.cplett.2006.01.068 10.1021/acs.jpcc.6b03915 10.1038/368436a0 |
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References_xml | – volume: 119 start-page: 1347 year: 2015 end-page: 1358 publication-title: J. Phys. Chem. A – volume: 33 start-page: 580 year: 2012 end-page: 592 publication-title: J. Comput. Chem. – volume: 338 start-page: 212 year: 2003 end-page: 214 publication-title: Physica B – volume: 17 start-page: 2073 year: 2005 end-page: 2077 publication-title: Adv. Mater. – volume: 98 start-page: 3022 year: 1993 end-page: 3037 publication-title: J. Chem. Phys. – volume: 87 start-page: 215503 year: 2001 end-page: 4 publication-title: Phys. Rev. Lett. – volume: 71 start-page: 045205 year: 2005 end-page: 5 publication-title: Phys. Rev. B – volume: 9 start-page: 46 year: 1998 end-page: 52 publication-title: Opt. Mater. – volume: 116 start-page: 12434 year: 2012 end-page: 12442 publication-title: Nanomater Interfaces – volume: 373 start-page: 203 year: 1995 end-page: 204 publication-title: Nature – volume: 85 start-page: 1289 year: 2004 end-page: 1291 publication-title: Appl. Phys. Lett. – volume: 54 start-page: 4256 year: 1996 end-page: 4265 publication-title: Phys. Rev. E – year: 2007 – volume: 15 start-page: 1164 year: 1997 end-page: 1168 publication-title: Adv. Mater. – volume: 393 start-page: 51 year: 2004 end-page: 57 publication-title: Chem. Phys. Lett. – volume: 421 start-page: 272 year: 2006 end-page: 276 publication-title: Chem. Phys. Lett. – volume: 95 start-page: 3141 year: 2004 end-page: 3147 publication-title: J. Appl. Phys. – volume: 83 start-page: 1941 year: 2003 end-page: 1943 publication-title: Appl. Phys. Lett. – volume: 142 start-page: 507 year: 2017 end-page: 515 publication-title: Dyes Pigm. – volume: 139 start-page: 901 year: 2003 end-page: 903 publication-title: Synth. Met. – volume: 109 start-page: 21690 year: 2005 end-page: 21693 publication-title: J. Phys. Chem. B. – volume: 138 start-page: 255 year: 2017 end-page: 266 publication-title: Dyes Pigm. – volume: 21 start-page: 208 year: 2004 end-page: 213 publication-title: J. Opt. Soc. Am. B – volume: 576 start-page: 31 year: 2013 end-page: 34 publication-title: Chem. Phys. Lett. – volume: 516 start-page: 2700 year: 2008 end-page: 2703 publication-title: Thin Solid Films – volume: 87 start-page: 013104 year: 2005 end-page: 3 publication-title: Appl. Phys. Lett. – volume: 21 start-page: 1 year: 2015 end-page: 18 publication-title: J. Mol. Model. – volume: 119 start-page: 10007 year: 2015 end-page: 10014 publication-title: J. Phys. Chem. C – volume: 11 start-page: 045801 year: 2014 publication-title: Laser Phys. Lett. – volume: 368 start-page: 436 year: 1994 end-page: 438 publication-title: Nature – volume: 97 start-page: 064315 year: 2005 end-page: 4 publication-title: J. Appl. Phys. – volume: 47 start-page: 5074 year: 2008 end-page: 5077 publication-title: Appl. Opt. – volume: 82 start-page: 2278 year: 1999 end-page: 2281 publication-title: Phys. Rev. Lett. – volume: 2 start-page: 442 year: 1966 end-page: 446 publication-title: IEEE J. Quantum Electron. – volume: 119 start-page: 7 year: 2001 end-page: 12 publication-title: Synth. Met. – volume: 75 start-page: 1213 year: 1999 end-page: 1215 publication-title: Appl. Phys. Lett. – volume: 27 start-page: 1874 year: 2010 end-page: 1877 publication-title: J. Opt. Soc. Am. B – volume: 120 start-page: 14813 year: 2016 end-page: 14819 publication-title: J. Phys. Chem. C – volume: 99 start-page: 013518 year: 2006 end-page: 4 publication-title: J. Appl. Phys. – volume: 124 start-page: 1 year: 2006 end-page: 15 publication-title: J. Chem. Phys. – ident: e_1_2_10_21_1 doi: 10.1002/adma.200500734 – ident: e_1_2_10_14_1 doi: 10.1016/S0379-6779(00)00595-6 – ident: e_1_2_10_16_1 doi: 10.1063/1.2159083 – ident: e_1_2_10_3_1 doi: 10.1016/j.physb.2003.08.031 – ident: e_1_2_10_2_1 doi: 10.1103/PhysRevLett.87.215503 – ident: e_1_2_10_23_1 doi: 10.1016/S0925-3467(97)00068-2 – ident: e_1_2_10_38_1 doi: 10.1088/1612-2011/11/4/045801 – ident: e_1_2_10_10_1 doi: 10.1063/1.1984106 – ident: e_1_2_10_12_1 doi: 10.1063/1.1862312 – ident: e_1_2_10_18_1 doi: 10.1016/S0379-6779(03)00298-4 – ident: e_1_2_10_13_1 doi: 10.1103/PhysRevB.71.045205 – ident: e_1_2_10_37_1 doi: 10.1016/j.cplett.2013.05.018 – ident: e_1_2_10_1_1 doi: 10.1109/JQE.1966.1074123 – ident: e_1_2_10_11_1 doi: 10.1063/1.1646440 – ident: e_1_2_10_25_1 doi: 10.1016/j.cplett.2004.06.011 – ident: e_1_2_10_9_1 doi: 10.1364/JOSAB.21.000208 – ident: e_1_2_10_32_1 doi: 10.1016/j.dyepig.2016.11.030 – ident: e_1_2_10_7_1 doi: 10.1103/PhysRevE.54.4256 – ident: e_1_2_10_24_1 – ident: e_1_2_10_26_1 doi: 10.1002/jcc.22885 – ident: e_1_2_10_29_1 doi: 10.1021/acs.jpcc.5b01947 – ident: e_1_2_10_41_1 doi: 10.1364/AO.47.005074 – ident: e_1_2_10_39_1 doi: 10.1021/jp510102q – ident: e_1_2_10_31_1 doi: 10.1063/1.2173258 – ident: e_1_2_10_40_1 doi: 10.1063/1.464129 – ident: e_1_2_10_4_1 doi: 10.1063/1.124645 – ident: e_1_2_10_5_1 doi: 10.1038/373203b0 – ident: e_1_2_10_8_1 doi: 10.1103/PhysRevLett.82.2278 – ident: e_1_2_10_17_1 doi: 10.1016/j.tsf.2007.04.103 – ident: e_1_2_10_27_1 doi: 10.1364/JOSAB.27.001874 – ident: e_1_2_10_19_1 doi: 10.1021/jp054324r – ident: e_1_2_10_35_1 doi: 10.1007/s00894-015-2651-z – ident: e_1_2_10_33_1 doi: 10.1016/j.dyepig.2017.04.009 – ident: e_1_2_10_22_1 doi: 10.1002/adma.19970091508 – ident: e_1_2_10_15_1 doi: 10.1063/1.1782259 – volume-title: Nonlinear Optics – 3rd Edition year: 2007 ident: e_1_2_10_30_1 contributor: fullname: Boyd R. W. – ident: e_1_2_10_34_1 doi: 10.1021/jp3027447 – ident: e_1_2_10_20_1 doi: 10.1063/1.1605233 – ident: e_1_2_10_36_1 doi: 10.1016/j.cplett.2006.01.068 – ident: e_1_2_10_28_1 doi: 10.1021/acs.jpcc.6b03915 – ident: e_1_2_10_6_1 doi: 10.1038/368436a0 |
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Snippet | We describe herein the synthesis and characterization of a thiophene‐based donor‐acceptor system, namely (E)‐2‐(4‐nitrostyryl)‐5‐phenylthiophene (Th‐pNO2),... We describe herein the synthesis and characterization of a thiophene‐based donor‐acceptor system, namely (E)‐2‐(4‐nitrostyryl)‐5‐phenylthiophene (Th‐ p NO 2 ),... We describe herein the synthesis and characterization of a thiophene-based donor-acceptor system, namely (E)-2-(4-nitrostyryl)-5-phenylthiophene (Th-pNO2 ),... |
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SubjectTerms | Absorption spectra Birefringence Charge transfer Chemical Sciences Derivatives Information technology Lasing Light amplifiers Molecular chains nonlinear optics Optical properties optical switches Optical switching photoinduced birefringence Physics random lasing Switches thiophene derivatives |
Title | All‐Optical Switching and Two‐States Light‐Controlled Coherent‐Incoherent Random Lasing in a Thiophene‐Based Donor‐Acceptor System |
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