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Erschienen in: Polymer Bulletin 9/2023

02.11.2022 | Original Paper

Synthesis of bis(thiophen-2-yl)benzothiadiazole scaffold donor-acceptor polymers: studies of polymerization, electrical, optical, and photovoltaic properties

verfasst von: Anamika Mishra, Sonal Gupta, Asit Patra

Erschienen in: Polymer Bulletin | Ausgabe 9/2023

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Abstract

Facile and efficient synthesis of conjugated donor-acceptor polymers via direct C-H arylation polymerization has received significant interest in organic electronic applications. We report here a one-pot synthesis of a series of bis(thiophen-2-yl)benzothiadiazole-based donor-acceptor polymers P1-4 via direct C-H arylation polymerization in excellent yield. Two donor moieties [3-hexylthiophene and 1,4-bis(dodecyloxy)benzene], and one acceptor unit 4,7-bis(thiophen-2-yl)benzo[c][1,2,5]thiadiazole were used for direct C-H arylation polymerization. The prowess of the methodology was applied to synthesis of polymer by adding one donor unit followed by a second donor unit after the due course. The resulting polymers are soluble and characterized. Optical and electrochemical properties were carried out by UV-Vis-NIR and cyclic voltammetry, respectively. A temperature-dependent absorption of the polymer films blended with PC71BM was studied for photovoltaic application. Devices were fabricated by solution-processable deposition of active layer and a PCE of 3.82% was achieved.

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Literatur
1.
Zurück zum Zitat Pankow RM, Thompson BC (2020) The development of conjugated polymers as the cornerstone of organic electronics. Polymer 207:122874 Pankow RM, Thompson BC (2020) The development of conjugated polymers as the cornerstone of organic electronics. Polymer 207:122874
2.
Zurück zum Zitat Dudnik AS, Aldrich TJ, Eastham ND, Chang RPH, Facchetti A, Marks TJ (2016) Tin-Free direct C-H arylation polymerization for high photovoltaic efficiency conjugated copolymers. J Am Chem Soc 138:15699–15709PubMed Dudnik AS, Aldrich TJ, Eastham ND, Chang RPH, Facchetti A, Marks TJ (2016) Tin-Free direct C-H arylation polymerization for high photovoltaic efficiency conjugated copolymers. J Am Chem Soc 138:15699–15709PubMed
3.
Zurück zum Zitat Lu L, Zheng T, Wu Q, Schneider AM, Zhao D, Yu L (2015) Recent advances in bulk heterojunction polymer solar cells. Chem Rev 115:12666PubMed Lu L, Zheng T, Wu Q, Schneider AM, Zhao D, Yu L (2015) Recent advances in bulk heterojunction polymer solar cells. Chem Rev 115:12666PubMed
4.
Zurück zum Zitat Truong NTT, Nguyen LT, Mai HLT, Mai HLT, Doan BK, Tran DH, Truong KT, Nguyen VQ, Nguyen LTT, Hoang MH, Pham TV, Nguyen VM, Huynh TM, Doan TCD, Nguyen HT (2020) Phenothiazine derivatives, diketopyrrolopyrrole-based conjugated polymers: synthesis, optical and organic field effect transistor properties. J Polym Res 27:223 Truong NTT, Nguyen LT, Mai HLT, Mai HLT, Doan BK, Tran DH, Truong KT, Nguyen VQ, Nguyen LTT, Hoang MH, Pham TV, Nguyen VM, Huynh TM, Doan TCD, Nguyen HT (2020) Phenothiazine derivatives, diketopyrrolopyrrole-based conjugated polymers: synthesis, optical and organic field effect transistor properties. J Polym Res 27:223
5.
Zurück zum Zitat Zhang L, Liu C, Zhang J, Li X, Cheng C, Tian Y, Jen AKY, Xu B (2018) Intensive exposure of functional rings of a polymeric hole-transporting material enables efficient perovskite solar cells. Adv Mater 30:1804028 Zhang L, Liu C, Zhang J, Li X, Cheng C, Tian Y, Jen AKY, Xu B (2018) Intensive exposure of functional rings of a polymeric hole-transporting material enables efficient perovskite solar cells. Adv Mater 30:1804028
6.
Zurück zum Zitat Hou P, Oechsle P, Paradies KD, J, (2020) Palladium-catalyzepolycondensation for the synthesisof poly(Aryl)sulfides. Macromol Rapid Commun 41:2000067 Hou P, Oechsle P, Paradies KD, J, (2020) Palladium-catalyzepolycondensation for the synthesisof poly(Aryl)sulfides. Macromol Rapid Commun 41:2000067
7.
Zurück zum Zitat Patra A, Kumar R, Chand S (2014) Selenium-containing π-conjugated polymers for organic solar cells. Isr J Chem 54:621–641 Patra A, Kumar R, Chand S (2014) Selenium-containing π-conjugated polymers for organic solar cells. Isr J Chem 54:621–641
8.
Zurück zum Zitat Zhao C, Guo Y, Zhang Y, Yan N, You S, Li W (2019) Diketopyrrolopyrrole-based conjugated materials for non-fullerene organic solar cells. J Mater Chem A 7:10174 Zhao C, Guo Y, Zhang Y, Yan N, You S, Li W (2019) Diketopyrrolopyrrole-based conjugated materials for non-fullerene organic solar cells. J Mater Chem A 7:10174
9.
Zurück zum Zitat Heinrichová P, Pospíšil J, Stříteský S, Vala M, Weiter M, Toman P, Rais D, Pfleger J, Vondráček M, Šimek D, Fekete L, Horáková P, Dokládalová L, Kubáč L, Kratochvílová I (2019) Diketopyrrolopyrrole-based organic solar cells functionality: the role of orbital energy and crystallinity. J Phys Chem C 123(18):11447–11463. https://doi.org/10.1021/acs.jpcc.9b01328CrossRef Heinrichová P, Pospíšil J, Stříteský S, Vala M, Weiter M, Toman P, Rais D, Pfleger J, Vondráček M, Šimek D, Fekete L, Horáková P, Dokládalová L, Kubáč L, Kratochvílová I (2019) Diketopyrrolopyrrole-based organic solar cells functionality: the role of orbital energy and crystallinity. J Phys Chem C 123(18):11447–11463. https://​doi.​org/​10.​1021/​acs.​jpcc.​9b01328CrossRef
10.
Zurück zum Zitat Fusco S, Barra M, Bonomo M, Cassinese A, Centore R, Chiarella F, Senneca F, Carella A (2021) Novel DPP derivatives functionalized with auxiliary electron-acceptor groups and characterized by narrow bandgap and ambipolar charge transport properties. Dyes Pigm 186:109026 Fusco S, Barra M, Bonomo M, Cassinese A, Centore R, Chiarella F, Senneca F, Carella A (2021) Novel DPP derivatives functionalized with auxiliary electron-acceptor groups and characterized by narrow bandgap and ambipolar charge transport properties. Dyes Pigm 186:109026
11.
Zurück zum Zitat Holliday S, Ashraf RS, Wadsworth A, Baran D, Yousaf SA, Nielsen CB, Tan CH, Dimitrov SD, Shang Z, Gasparini N, Alamoudi M, Laquai F, Brabec CJ, Salleo A, Durrant JR, McCulloch I (2016) High-efficiency and air-stable P3HT-based polymer solar cells with a new non-fullerene acceptor. Nat Commun 7:11585PubMedPubMedCentral Holliday S, Ashraf RS, Wadsworth A, Baran D, Yousaf SA, Nielsen CB, Tan CH, Dimitrov SD, Shang Z, Gasparini N, Alamoudi M, Laquai F, Brabec CJ, Salleo A, Durrant JR, McCulloch I (2016) High-efficiency and air-stable P3HT-based polymer solar cells with a new non-fullerene acceptor. Nat Commun 7:11585PubMedPubMedCentral
12.
Zurück zum Zitat Farinhas J, Oliveira R, Ferreira Q, Morgado J, Charas A (2017) Enhanced efficiency of PTB7: PC61BM organic solar cells by adding a low efficient polymer donor. Int J Photoenergy 2017:4501758 Farinhas J, Oliveira R, Ferreira Q, Morgado J, Charas A (2017) Enhanced efficiency of PTB7: PC61BM organic solar cells by adding a low efficient polymer donor. Int J Photoenergy 2017:4501758
13.
Zurück zum Zitat Yadav P, Patra A (2020) Recent advances in poly(3,4-ethylenedioxyselenophene) and related polymers. Polym Chem 11:7275–7292 Yadav P, Patra A (2020) Recent advances in poly(3,4-ethylenedioxyselenophene) and related polymers. Polym Chem 11:7275–7292
14.
Zurück zum Zitat Le DT, Truong NT, Luu TH, Nguyen LT, Hoang MH, Huynh HPK, Cu ST, Nguyen QT, Nguyen HT (2022) Donor – acceptor and donor – donor alternating conjugated polymers based on dithieno[3,2-b:2’,3’-d]pyrrole: synthesis, optical properties and organic solar cells applications. J Polym Res 29:111 Le DT, Truong NT, Luu TH, Nguyen LT, Hoang MH, Huynh HPK, Cu ST, Nguyen QT, Nguyen HT (2022) Donor – acceptor and donor – donor alternating conjugated polymers based on dithieno[3,2-b:2’,3’-d]pyrrole: synthesis, optical properties and organic solar cells applications. J Polym Res 29:111
15.
Zurück zum Zitat Amiel DBA, Ck K, Gidron O (2021) Oligofuran-benzothiadiazole Co-oligomers: synthesis. Optoelectron Proper React, Org Mater 03:303–308 Amiel DBA, Ck K, Gidron O (2021) Oligofuran-benzothiadiazole Co-oligomers: synthesis. Optoelectron Proper React, Org Mater 03:303–308
16.
Zurück zum Zitat Tomar M, Ashar AZ, Narayan KS, Müllen K, Jacob J (2016) Tuning the HOMO energy levels in quinoline and biquinoline based donor-acceptor polymers. J Polym Res 23:50 Tomar M, Ashar AZ, Narayan KS, Müllen K, Jacob J (2016) Tuning the HOMO energy levels in quinoline and biquinoline based donor-acceptor polymers. J Polym Res 23:50
17.
Zurück zum Zitat Singhal S, Patra A (2020) Benzothiadiazole bridged EDOT based donor–acceptor polymers with tunable optical, electrochemical, morphological and electrochromic performance: effects of solvents and electrolytes. Phys Chem Chem Phys 22:14527–14536PubMed Singhal S, Patra A (2020) Benzothiadiazole bridged EDOT based donor–acceptor polymers with tunable optical, electrochemical, morphological and electrochromic performance: effects of solvents and electrolytes. Phys Chem Chem Phys 22:14527–14536PubMed
18.
Zurück zum Zitat Patra A, Agrawal V, Bhargav R, Shahjad BD, Chand S, Sheynin Y, Bendikov M (2015) Metal free conducting PEDOS, PEDOT, and their analogues via an unusual bromine-catalyzed polymerization. Macromolecules 48:8760–8764 Patra A, Agrawal V, Bhargav R, Shahjad BD, Chand S, Sheynin Y, Bendikov M (2015) Metal free conducting PEDOS, PEDOT, and their analogues via an unusual bromine-catalyzed polymerization. Macromolecules 48:8760–8764
19.
Zurück zum Zitat Gupta S, Patra A (2020) Facile polymerization method for poly(3,4-ethylenedioxythiophene) and related polymers using iodine vapour. New J Chem 44:6883–6888 Gupta S, Patra A (2020) Facile polymerization method for poly(3,4-ethylenedioxythiophene) and related polymers using iodine vapour. New J Chem 44:6883–6888
20.
Zurück zum Zitat Bhardwaj D, Shahjad GS, Yadav P, Bhargav R, Patra A (2017) All Conjugated Poly(3-hexylthiophene)-block-poly (hexyl-3,4-ethylenedioxythiophene) Copolymers. ChemistrySelect 2:9557–9562 Bhardwaj D, Shahjad GS, Yadav P, Bhargav R, Patra A (2017) All Conjugated Poly(3-hexylthiophene)-block-poly (hexyl-3,4-ethylenedioxythiophene) Copolymers. ChemistrySelect 2:9557–9562
21.
Zurück zum Zitat Bura T, Blaskovits JT, Leclerc M (2016) Direct (hetero)arylation polymerization: toward defect-free conjugated polymers. J Am Chem Soc 138:10056PubMed Bura T, Blaskovits JT, Leclerc M (2016) Direct (hetero)arylation polymerization: toward defect-free conjugated polymers. J Am Chem Soc 138:10056PubMed
22.
Zurück zum Zitat Mercier LG, Leclerc M (2013) Direct (Hetero)Arylation: a new tool for polymer chemists. Acc Chem Res 46:1597PubMed Mercier LG, Leclerc M (2013) Direct (Hetero)Arylation: a new tool for polymer chemists. Acc Chem Res 46:1597PubMed
23.
Zurück zum Zitat Suraru SL, Lee JA, Luscombe CK (2016) C-H arylation in the synthesis of π-conjugated polymers. ACS Macro Lett 5:724PubMed Suraru SL, Lee JA, Luscombe CK (2016) C-H arylation in the synthesis of π-conjugated polymers. ACS Macro Lett 5:724PubMed
24.
Zurück zum Zitat Leclerc M, Brassard S, Beaupré S (2020) Direct (hetero) arylation polymerization: toward defect-free conjugated polymers. Polym J 52:13–20 Leclerc M, Brassard S, Beaupré S (2020) Direct (hetero) arylation polymerization: toward defect-free conjugated polymers. Polym J 52:13–20
25.
Zurück zum Zitat Rao GH, Rana PJS, Islam A, Singh SP (2018) Synthesis of multichromophoric asymmetrical squaraine sensitizer via C-H arylation for see-through photovoltaic. ACS Appl Energy Mater 1:4786–4793 Rao GH, Rana PJS, Islam A, Singh SP (2018) Synthesis of multichromophoric asymmetrical squaraine sensitizer via C-H arylation for see-through photovoltaic. ACS Appl Energy Mater 1:4786–4793
26.
Zurück zum Zitat Liu SY, Fu WF, Xu JQ, Fan CC, Jiang H, Shi M, Li HY, Chen HZ (2013) A direct arylation-derived DPP-based small molecule for solution-processed organic solar cells. Nanotechnology 25:014006PubMed Liu SY, Fu WF, Xu JQ, Fan CC, Jiang H, Shi M, Li HY, Chen HZ (2013) A direct arylation-derived DPP-based small molecule for solution-processed organic solar cells. Nanotechnology 25:014006PubMed
27.
Zurück zum Zitat Liu SY, Shi MM, Huang JC, Jin ZN, Hu XL, Pan JY, Li HY, Jen AKY, Chen HZ (2013) C-H activation: making diketopyrrolopyrrole derivatives easily accessible. J Mater Chem A 1:2795–2805 Liu SY, Shi MM, Huang JC, Jin ZN, Hu XL, Pan JY, Li HY, Jen AKY, Chen HZ (2013) C-H activation: making diketopyrrolopyrrole derivatives easily accessible. J Mater Chem A 1:2795–2805
28.
Zurück zum Zitat Liu SY, Wang DG, Zhong AG, Wen HR (2018) One-step rapid synthesis of π-conjugated large oligomers via C-H activation coupling. Org Chem Front 5:653–661 Liu SY, Wang DG, Zhong AG, Wen HR (2018) One-step rapid synthesis of π-conjugated large oligomers via C-H activation coupling. Org Chem Front 5:653–661
29.
Zurück zum Zitat Huang WY, Shen ZQ, Cheng JZ, Liu LL, Yang K, Chen X, Wen HR, Liu SY (2019) C-H activation derived CPPs for photocatalytic hydrogen production excellently accelerated by a DMF cosolvent. J Mater Chem A 7:24222–24230 Huang WY, Shen ZQ, Cheng JZ, Liu LL, Yang K, Chen X, Wen HR, Liu SY (2019) C-H activation derived CPPs for photocatalytic hydrogen production excellently accelerated by a DMF cosolvent. J Mater Chem A 7:24222–24230
30.
Zurück zum Zitat Govindan V, Wu CG (2017) Facile synthesis of low band-gap DPP–EDOT containing small molecules for solar cell applications. RSC Adv 7:28788–28796 Govindan V, Wu CG (2017) Facile synthesis of low band-gap DPP–EDOT containing small molecules for solar cell applications. RSC Adv 7:28788–28796
31.
Zurück zum Zitat Wang S, Hu J, Wang J, Huang W (2019) Direct CH arylation for small molecules composed of diketopyrrolopyrrole and benzothiadiazole as organic semiconductor materials. Synth Met 250:94–98 Wang S, Hu J, Wang J, Huang W (2019) Direct CH arylation for small molecules composed of diketopyrrolopyrrole and benzothiadiazole as organic semiconductor materials. Synth Met 250:94–98
32.
Zurück zum Zitat Wang S, Yang J, Broch K, Novoák J, Cao X, Shaw J, Tao Y, Hu Y, Huang W (2016) Direct C-H arylation for various Ar-cored diketopyrrolopyrrole containing small molecules in solution-processed field-effect transistor. RSC Adv 6:57163–57173 Wang S, Yang J, Broch K, Novoák J, Cao X, Shaw J, Tao Y, Hu Y, Huang W (2016) Direct C-H arylation for various Ar-cored diketopyrrolopyrrole containing small molecules in solution-processed field-effect transistor. RSC Adv 6:57163–57173
33.
Zurück zum Zitat Nitti A, Debattista F, Abbondanza L, Bianchi G, Po R, Pasini D (2017) Donor–acceptor conjugated copolymers incorporating tetrafluorobenzene as the π-electron deficient unit. J Polym Sci Part A: Polym Chem 55:1601–1610 Nitti A, Debattista F, Abbondanza L, Bianchi G, Po R, Pasini D (2017) Donor–acceptor conjugated copolymers incorporating tetrafluorobenzene as the π-electron deficient unit. J Polym Sci Part A: Polym Chem 55:1601–1610
34.
Zurück zum Zitat Chang SW, Waters H, Kettle J, Kuo ZR, Li CH, Yu CY, Horie M (2012) Pd-catalysed direct arylation polymerisation for synthesis of low-bandgap conjugated polymers and photovoltaic performance. Macromol rapid commun 33:1927–1932PubMed Chang SW, Waters H, Kettle J, Kuo ZR, Li CH, Yu CY, Horie M (2012) Pd-catalysed direct arylation polymerisation for synthesis of low-bandgap conjugated polymers and photovoltaic performance. Macromol rapid commun 33:1927–1932PubMed
35.
Zurück zum Zitat Choi SJ, Kuwabara J, Kanbara T (2013) Microwave-assisted polycondensation via direct arylation of 3, 4-ethylenedioxythiophene with 9, 9-dioctyl-2, 7-dibromofluorene. ACS Sustain Chem Eng 1:878–882 Choi SJ, Kuwabara J, Kanbara T (2013) Microwave-assisted polycondensation via direct arylation of 3, 4-ethylenedioxythiophene with 9, 9-dioctyl-2, 7-dibromofluorene. ACS Sustain Chem Eng 1:878–882
36.
Zurück zum Zitat Chen S, Lee KC, Zhang ZG, Kim DS, Li Y, Yang C (2016) An indacenodithiophene–quinoxaline polymer prepared by direct arylation polymerization for organic photovoltaics. Macromolecules 49:527–536 Chen S, Lee KC, Zhang ZG, Kim DS, Li Y, Yang C (2016) An indacenodithiophene–quinoxaline polymer prepared by direct arylation polymerization for organic photovoltaics. Macromolecules 49:527–536
37.
Zurück zum Zitat Estrada LA, Deininger JJ, Kamenov GD, Reynolds JR (2013) Direct (hetero) arylation polymerization: an effective route to 3, 4-propylenedioxythiophene-based polymers with low residual metal content. ACS Macro Lett 2:869–873PubMed Estrada LA, Deininger JJ, Kamenov GD, Reynolds JR (2013) Direct (hetero) arylation polymerization: an effective route to 3, 4-propylenedioxythiophene-based polymers with low residual metal content. ACS Macro Lett 2:869–873PubMed
38.
Zurück zum Zitat Nitti A, Signorile M, Boiocchi M, Bianchi G, Po R, Pasini D (2016) Conjugated thiophene-fused isatin dyes through intramolecular direct arylation. J Org Chem 81:11035PubMed Nitti A, Signorile M, Boiocchi M, Bianchi G, Po R, Pasini D (2016) Conjugated thiophene-fused isatin dyes through intramolecular direct arylation. J Org Chem 81:11035PubMed
39.
Zurück zum Zitat Nitti A, Bianchi G, Po R, Swager TM, Pasini D (2017) Domino direct arylation and cross-aldol for rapid construction of extended polycyclic π-scaffolds. J Am Chem Soc 139:8788PubMed Nitti A, Bianchi G, Po R, Swager TM, Pasini D (2017) Domino direct arylation and cross-aldol for rapid construction of extended polycyclic π-scaffolds. J Am Chem Soc 139:8788PubMed
40.
Zurück zum Zitat Areephong J, Hendsbee AD, Welch GC (2015) Facile synthesis of unsymmetrical and π-extended furan-diketopyrrolopyrrole derivatives through C-H direct (hetero) arylation using a heterogeneous catalyst system. New J Chem 39:6714 Areephong J, Hendsbee AD, Welch GC (2015) Facile synthesis of unsymmetrical and π-extended furan-diketopyrrolopyrrole derivatives through C-H direct (hetero) arylation using a heterogeneous catalyst system. New J Chem 39:6714
41.
Zurück zum Zitat Matsidik R, Martin J, Schmidt S, Obermayer LF, Nübling F, Komber H, Fazzi D, Sommer M (2015) C-H arylation of unsubstituted furan and thiophene with acceptor bromides: access to donor–acceptor–donor-type building blocks for organic electronics. J Org Chem 80(2):980PubMed Matsidik R, Martin J, Schmidt S, Obermayer LF, Nübling F, Komber H, Fazzi D, Sommer M (2015) C-H arylation of unsubstituted furan and thiophene with acceptor bromides: access to donor–acceptor–donor-type building blocks for organic electronics. J Org Chem 80(2):980PubMed
42.
Zurück zum Zitat Hendsbee AD, Li Y (2018) Performance comparisons of polymer semiconductors synthesized by direct (Hetero) arylation Polymerization (DHAP) and conventional methods for organic thin film transistors and organic photovoltaics. Molecules 23:1255PubMedPubMedCentral Hendsbee AD, Li Y (2018) Performance comparisons of polymer semiconductors synthesized by direct (Hetero) arylation Polymerization (DHAP) and conventional methods for organic thin film transistors and organic photovoltaics. Molecules 23:1255PubMedPubMedCentral
43.
Zurück zum Zitat Shahjad BR, Bhardwaj D, Mishra A, Patra A (2017) Synthesis and characterization of benzodithiophene-chalcogenophene based copolymers: a comparative study of optoelectronic properties and photovoltaic applications. Macromol Chem Phys 218:1700038 Shahjad BR, Bhardwaj D, Mishra A, Patra A (2017) Synthesis and characterization of benzodithiophene-chalcogenophene based copolymers: a comparative study of optoelectronic properties and photovoltaic applications. Macromol Chem Phys 218:1700038
44.
Zurück zum Zitat Mishra A, Gupta S, Patra A (2021) Synthesis and properties of 3,4-dioxythiophene and 1,4-dialkoxybenzene based copolymers via direct C H arylation: dopant-free hole transport material for perovskite solar cells. J Polym Sci 60:975–984 Mishra A, Gupta S, Patra A (2021) Synthesis and properties of 3,4-dioxythiophene and 1,4-dialkoxybenzene based copolymers via direct C H arylation: dopant-free hole transport material for perovskite solar cells. J Polym Sci 60:975–984
45.
Zurück zum Zitat Naqvi S, Chaudhary N, Singhal S, Yadav P, Patra A (2021) Hole transport materials by direct C-H arylation for organic solar cells: effect of structure and conjugation on electrical, optical and computational properties. ChemistrySelect 6:131–139 Naqvi S, Chaudhary N, Singhal S, Yadav P, Patra A (2021) Hole transport materials by direct C-H arylation for organic solar cells: effect of structure and conjugation on electrical, optical and computational properties. ChemistrySelect 6:131–139
46.
Zurück zum Zitat Naqvi S, Yadav P, Pahari P, Patra A (2021) Synthesis and properties of 3,4-dioxythiophene and1,4-dialkoxybenzene based copolymers via direct C-H arylation: dopant-free hole transport materialfor perovskite solar cells. J Polym Res 28:250 Naqvi S, Yadav P, Pahari P, Patra A (2021) Synthesis and properties of 3,4-dioxythiophene and1,4-dialkoxybenzene based copolymers via direct C-H arylation: dopant-free hole transport materialfor perovskite solar cells. J Polym Res 28:250
47.
Zurück zum Zitat Cong S, Chen J, Wang L, Lan L, Wang Y, Dai H, Liao H, Zhou Y, Yu Y, Duan J, Li Z (2022) Donor functionalization tuning the N-type performance of Donor-acceptor copolymers for Aqueous-based electrochemical devices. Adv Funct Mater 2022:2201821 Cong S, Chen J, Wang L, Lan L, Wang Y, Dai H, Liao H, Zhou Y, Yu Y, Duan J, Li Z (2022) Donor functionalization tuning the N-type performance of Donor-acceptor copolymers for Aqueous-based electrochemical devices. Adv Funct Mater 2022:2201821
48.
Zurück zum Zitat Singhal S, Yadav P, Naqvi S, Gupta S, Patra A (2019) Donor–acceptor–donor copolymers with 3, 4-ethylenedioxythiophene moiety: electropolymerization and effect on optoelectronic and electrochromic properties. ACS Omega 4:3484–3492PubMedPubMedCentral Singhal S, Yadav P, Naqvi S, Gupta S, Patra A (2019) Donor–acceptor–donor copolymers with 3, 4-ethylenedioxythiophene moiety: electropolymerization and effect on optoelectronic and electrochromic properties. ACS Omega 4:3484–3492PubMedPubMedCentral
49.
Zurück zum Zitat Chaudhary N, Kesari JP, Chaudhary R, Patra A (2016) Low band gap polymeric solar cells using solution-processable copper iodide as hole transporting layer. Opt Mater 58:116–120 Chaudhary N, Kesari JP, Chaudhary R, Patra A (2016) Low band gap polymeric solar cells using solution-processable copper iodide as hole transporting layer. Opt Mater 58:116–120
50.
Zurück zum Zitat Chaudhary N, Chaudhary R, Kesari JP, Patra A (2017) An eco-friendly and inexpensive solvent for solution processable CuSCN as a hole transporting layer in organic solar cells. Opt Mater 69:367–371 Chaudhary N, Chaudhary R, Kesari JP, Patra A (2017) An eco-friendly and inexpensive solvent for solution processable CuSCN as a hole transporting layer in organic solar cells. Opt Mater 69:367–371
Metadaten
Titel
Synthesis of bis(thiophen-2-yl)benzothiadiazole scaffold donor-acceptor polymers: studies of polymerization, electrical, optical, and photovoltaic properties
verfasst von
Anamika Mishra
Sonal Gupta
Asit Patra
Publikationsdatum
02.11.2022
Verlag
Springer Berlin Heidelberg
Erschienen in
Polymer Bulletin / Ausgabe 9/2023
Print ISSN: 0170-0839
Elektronische ISSN: 1436-2449
DOI
https://doi.org/10.1007/s00289-022-04535-1

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