450 related articles for article (PubMed ID: 23085169)
1. Toward panchromatic organic functional molecules: density functional theory study on the nature of the broad UV-Vis-NIR spectra of substituted tetra(azulene)porphyrins.
Qi D; Zhang L; Jiang J
J Mol Graph Model; 2012 Sep; 38():304-13. PubMed ID: 23085169
[TBL] [Abstract][Full Text] [Related]
2. Toward panchromatic organic functional molecules: density functional theory study on the electronic absorption spectra of substituted tetraanthracenylporphyrins.
Qi D; Jiang J
J Phys Chem A; 2011 Dec; 115(47):13811-20. PubMed ID: 22029274
[TBL] [Abstract][Full Text] [Related]
3. Nature of the intense near-IR absorption and unusual broad UV-visible-NIR spectra of azulenocyanines: density functional theory studies.
Qi D; Zhang L; Zhang Y; Bian Y; Jiang J
J Phys Chem A; 2010 Dec; 114(51):13411-7. PubMed ID: 21141865
[TBL] [Abstract][Full Text] [Related]
4. Electronic structures of azulene-fused porphyrins as seen by magnetic circular dichroism and TD-DFT calculations.
Nakai K; Kurotobi K; Osuka A; Uchiyama M; Kobayashi N
J Inorg Biochem; 2008 Mar; 102(3):466-71. PubMed ID: 18180040
[TBL] [Abstract][Full Text] [Related]
5. Toward rational design of organic dye sensitized solar cells (DSSCs): an application to the TA-St-CA dye.
Mohammadi N; Mahon PJ; Wang F
J Mol Graph Model; 2013 Mar; 40():64-71. PubMed ID: 23353583
[TBL] [Abstract][Full Text] [Related]
6. Diketopyrrolopyrrole-porphyrin conjugates as broadly absorbing sensitizers for dye-sensitized solar cells.
Warnan J; Favereau L; Meslin F; Severac M; Blart E; Pellegrin Y; Jacquemin D; Odobel F
ChemSusChem; 2012 Aug; 5(8):1568-77. PubMed ID: 22791585
[TBL] [Abstract][Full Text] [Related]
7. Quantum chemistry calculations of 3-Phenoxyphthalonitrile dye sensitizer for solar cells.
Kumar PS; Vasudevan K; Prakasam A; Geetha M; Anbarasan PM
Spectrochim Acta A Mol Biomol Spectrosc; 2010 Sep; 77(1):45-50. PubMed ID: 20537937
[TBL] [Abstract][Full Text] [Related]
8. Electronic structures and absorption properties of three kinds of ruthenium dye sensitizers containing bipyridine-pyrazolate for solar cells.
Zhang CR; Liu ZJ; Sun YT; Shen YL; Chen YH; Liu YJ; Wang W; Zhang HM
Spectrochim Acta A Mol Biomol Spectrosc; 2011 Sep; 79(5):1843-8. PubMed ID: 21684807
[TBL] [Abstract][Full Text] [Related]
9. Molecular Docking toward Panchromatic Dye Sensitizers for Solar Cells Based upon Tetraazulenylporphyrin and Tetraanthracenylporphyrin.
Zhang CR; Li XY; Shen YL; Wu YZ; Liu ZJ; Chen HS
J Phys Chem A; 2017 Apr; 121(13):2655-2664. PubMed ID: 28319383
[TBL] [Abstract][Full Text] [Related]
10. DFT and TD-DFT study on geometries, electronic structures and electronic absorption of some metal free dye sensitizers for dye sensitized solar cells.
Mohr T; Aroulmoji V; Ravindran RS; Müller M; Ranjitha S; Rajarajan G; Anbarasan PM
Spectrochim Acta A Mol Biomol Spectrosc; 2015 Jan; 135():1066-73. PubMed ID: 25173523
[TBL] [Abstract][Full Text] [Related]
11. Theoretical study of electronic structure and absorption spectra of diacid and zinc species of series of meso-phenylporphyrins.
Zhang YH; Zhao LH; Ruan WJ; Xu Y
Spectrochim Acta A Mol Biomol Spectrosc; 2011 Sep; 79(5):1449-60. PubMed ID: 21620760
[TBL] [Abstract][Full Text] [Related]
12. Theoretical study of carbazole-triphenylamine-based dyes for dye-sensitized solar cells.
Jia C; Wan Z; Zhang J; Li Z; Yao X; Shi Y
Spectrochim Acta A Mol Biomol Spectrosc; 2012 Feb; 86():387-91. PubMed ID: 22093522
[TBL] [Abstract][Full Text] [Related]
13. UV-vis spectroscopy and semiempirical quantum chemical studies on methyl derivatives of annulated analogues of azafluoranthene and azulene dyes.
Danel KS; Gasiorski P; Matusiewicz M; Całus S; Uchacz T; Kityk AV
Spectrochim Acta A Mol Biomol Spectrosc; 2010 Sep; 77(1):16-23. PubMed ID: 20510645
[TBL] [Abstract][Full Text] [Related]
14. Computational study of diketopyrrolopyrrole-based organic dyes for dye sensitized solar cell applications.
Fan W; Tan D; Zhang Q; Wang H
J Mol Graph Model; 2015 Apr; 57():62-9. PubMed ID: 25662565
[TBL] [Abstract][Full Text] [Related]
15. Cosensitizers for simultaneous filling up of both absorption valleys of porphyrins: a novel approach for developing efficient panchromatic dye-sensitized solar cells.
Sun X; Wang Y; Li X; Ågren H; Zhu W; Tian H; Xie Y
Chem Commun (Camb); 2014 Dec; 50(98):15609-12. PubMed ID: 25358496
[TBL] [Abstract][Full Text] [Related]
16. Synthesis and photophysical properties of stilbeneoctasilsesquioxanes. Emission behavior coupled with theoretical modeling studies suggest a 3-D excited state involving the silica core.
Laine RM; Sulaiman S; Brick C; Roll M; Tamaki R; Asuncion MZ; Neurock M; Filhol JS; Lee CY; Zhang J; Goodson T; Ronchi M; Pizzotti M; Rand SC; Li Y
J Am Chem Soc; 2010 Mar; 132(11):3708-22. PubMed ID: 20187633
[TBL] [Abstract][Full Text] [Related]
17. Theoretical investigation of phenothiazine-triphenylamine-based organic dyes with different π spacers for dye-sensitized solar cells.
Chen X; Jia C; Wan Z; Zhang J; Yao X
Spectrochim Acta A Mol Biomol Spectrosc; 2014 Apr; 123():282-9. PubMed ID: 24398472
[TBL] [Abstract][Full Text] [Related]
18. 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; 124():646-54. PubMed ID: 24513712
[TBL] [Abstract][Full Text] [Related]
19. Near-Infrared-Absorbing Metal-Free Organic, Porphyrin, and Phthalocyanine Sensitizers for Panchromatic Dye-Sensitized Solar Cells.
Brogdon P; Cheema H; Delcamp JH
ChemSusChem; 2018 Jan; 11(1):86-103. PubMed ID: 28926685
[TBL] [Abstract][Full Text] [Related]
20. Large pi-aromatic molecules as potential sensitizers for highly efficient dye-sensitized solar cells.
Imahori H; Umeyama T; Ito S
Acc Chem Res; 2009 Nov; 42(11):1809-18. PubMed ID: 19408942
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]