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Journal Abstract Search

792 related items for PubMed ID: 25042065

  • 21. D-D-π-A organic dyes containing 4,4'-di(2-thienyl)triphenylamine moiety for efficient dye-sensitized solar cells.
    Zhang MD, Xie HX, Ju XH, Qin L, Yang QX, Zheng HG, Zhou XF.
    Phys Chem Chem Phys; 2013 Jan 14; 15(2):634-41. PubMed ID: 23187831
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  • 22. Unveiling the potential of TPA-based molecules to tune the optoelectronic properties and enhance the efficiency of dye-sensitized solar cells.
    Al-Atawi FH, Irfan A, Al-Sehemi AG.
    J Mol Model; 2024 Jun 05; 30(7):197. PubMed ID: 38836952
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  • 23. Synthesis and photovoltaic properties of organic sensitizers incorporating a thieno[3,4-c]pyrrole-4,6-dione moiety.
    Feng Q, Lu X, Zhou G, Wang ZS.
    Phys Chem Chem Phys; 2012 Jun 14; 14(22):7993-9. PubMed ID: 22555312
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  • 24. Structural Engineering of Organic D-A-π-A Dyes Incorporated with a Dibutyl-Fluorene Moiety for High-Performance Dye-Sensitized Solar Cells.
    Wubie GZ, Lu MN, Desta MA, Weldekirstos HD, Lee MM, Wu WT, Li SR, Wei TC, Sun SS.
    ACS Appl Mater Interfaces; 2021 May 26; 13(20):23513-23522. PubMed ID: 33840194
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  • 25. 2,7-Diaminofluorene-based organic dyes for dye-sensitized solar cells: effect of auxiliary donor on optical and electrochemical properties.
    Baheti A, Singh P, Lee CP, Thomas KR, Ho KC.
    J Org Chem; 2011 Jun 17; 76(12):4910-20. PubMed ID: 21557605
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  • 26. Bi-anchoring Organic Dyes that Contain Benzimidazole Branches for Dye-Sensitized Solar Cells: Effects of π Spacer and Peripheral Donor Groups.
    Bodedla GB, Thomas KR, Fan MS, Ho KC.
    Chem Asian J; 2016 Sep 20; 11(18):2564-77. PubMed ID: 27434835
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  • 27. Dipolar compounds containing fluorene and a heteroaromatic ring as the conjugating bridge for high-performance dye-sensitized solar cells.
    Chen CH, Hsu YC, Chou HH, Thomas KR, Lin JT, Hsu CP.
    Chemistry; 2010 Mar 08; 16(10):3184-93. PubMed ID: 20119994
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  • 28. Substituent effect on the π linkers in triphenylamine dyes for sensitized solar cells: a DFT/TDDFT study.
    Xu J, Zhu L, Fang D, Chen B, Liu L, Wang L, Xu W.
    Chemphyschem; 2012 Oct 08; 13(14):3320-9. PubMed ID: 22763917
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  • 29. TD-DFT investigation of D-π-A organic dyes with thiophene moieties as π-spacers for use as sensitizers in DSSCs.
    Hasanein AA, Elmarassi YR, Kassem EN.
    J Mol Model; 2016 May 08; 22(5):115. PubMed ID: 27126050
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  • 30. Femtosecond to millisecond studies of electron transfer processes in a donor-(π-spacer)-acceptor series of organic dyes for solar cells interacting with titania nanoparticles and ordered nanotube array films.
    Ziółek M, Cohen B, Yang X, Sun L, Paulose M, Varghese OK, Grimes CA, Douhal A.
    Phys Chem Chem Phys; 2012 Feb 28; 14(8):2816-31. PubMed ID: 22258566
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  • 31. Organic Dyes with Well-Defined Structures for Highly Efficient Dye-Sensitised Solar Cells Based on a Cobalt Electrolyte.
    Seo KD, Choi IT, Kim HK.
    Chemistry; 2015 Oct 12; 21(42):14804-11. PubMed ID: 26332091
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  • 32. Theoretical investigation of new thiazolothiazole-based D-π-A organic dyes for efficient dye-sensitized solar cell.
    Fitri A, Benjelloun AT, Benzakour M, Mcharfi M, Hamidi M, Bouachrine M.
    Spectrochim Acta A Mol Biomol Spectrosc; 2014 Apr 24; 124():646-54. PubMed ID: 24513712
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  • 33. Synthesis and characterization of organic dyes with various electron-accepting substituents for p-type dye-sensitized solar cells.
    Weidelener M, Powar S, Kast H, Yu Z, Boix PP, Li C, Müllen K, Geiger T, Kuster S, Nüesch F, Bach U, Mishra A, Bäuerle P.
    Chem Asian J; 2014 Nov 24; 9(11):3251-63. PubMed ID: 25234556
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  • 34. Structure-property relationship of extended π-conjugation of ancillary ligands with and without an electron donor of heteroleptic Ru(II) bipyridyl complexes for high efficiency dye-sensitized solar cells.
    Hussain M, El-Shafei A, Islam A, Han L.
    Phys Chem Chem Phys; 2013 Jun 07; 15(21):8401-8. PubMed ID: 23629009
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  • 35. Kinetics of electron recombination of dye-sensitized solar cells based on TiO2 nanorod arrays sensitized with different dyes.
    Wang H, Liu M, Zhang M, Wang P, Miura H, Cheng Y, Bell J.
    Phys Chem Chem Phys; 2011 Oct 14; 13(38):17359-66. PubMed ID: 21881630
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  • 36. Harvesting UV photons for solar energy conversion applications.
    Wielopolski M, Linton KE, Marszałek M, Gulcur M, Bryce MR, Moser JE.
    Phys Chem Chem Phys; 2014 Feb 07; 16(5):2090-9. PubMed ID: 24343589
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  • 37. Long-Range π-Conjugation in Phenothiazine-containing Donor-Acceptor Dyes for Application in Dye-Sensitized Solar Cells.
    Antony MP, Moehl T, Wielopolski M, Moser JE, Nair S, Yu YJ, Kim JH, Kay KY, Jung YS, Yoon KB, Grätzel C, Zakeeruddin SM, Grätzel M.
    ChemSusChem; 2015 Nov 07; 8(22):3859-68. PubMed ID: 26616683
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  • 38. Facile and selective synthesis of oligothiophene-based sensitizer isomers: an approach toward efficient dye-sensitized solar cells.
    Feng Q, Zhang Q, Lu X, Wang H, Zhou G, Wang ZS.
    ACS Appl Mater Interfaces; 2013 Sep 25; 5(18):8982-90. PubMed ID: 23981089
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  • 39. Efficient organic dye-sensitized solar cells: molecular engineering of donor-acceptor-acceptor cationic dyes.
    Cheng M, Yang X, Zhao J, Chen C, Tan Q, Zhang F, Sun L.
    ChemSusChem; 2013 Dec 25; 6(12):2322-9. PubMed ID: 24039097
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  • 40. Theoretical investigation of triphenylamine-based sensitizers with different π-spacers for DSSC.
    Li W, Wang J, Chen J, Bai FQ, Zhang HX.
    Spectrochim Acta A Mol Biomol Spectrosc; 2014 Jan 24; 118():1144-51. PubMed ID: 24184585
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