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A study of the factors influencing the performance of ternary MEH-PPV:porphyrin:PCBM heterojunction devices: A steric approach to controlling charge recombination
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Ternary blends provide a potential pathway toward higher photovoltaic performance, while maintaining the simplicity of processing single junctions.
“Thus, ternary blends provide a potential pathway toward higher photovoltaic performance, while maintaining the simplicity of processing single junctions.”
From Recent progress in porphyrin-based materials for organic solar cells (2018) · cites this paper as [141]
Porphyrin broadened the absorption range, contributed to the photocurrent generation and initiated primary charge separation.
“The results indicate that porphyrin broadened the absorption range, contributed to the photocurrent generation and initiated primary charge separation.”
From Recent progress in porphyrin-based materials for organic solar cells (2018) · cites this paper as [141]
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Burke, K. B., Belcher, W. J., Thomsen, L., Watts, B., McNeill, C. R., Ade, H., & Dastoor, P. C. (2009) · Macromolecules · doi:10.1021/ma802632y · Cited by 44
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- Dastoor, 2007, Understanding and improving solid-state polymer/C-60-fullerene bulk-heterojunction solar cells using ternary porphyrin blends, Phys. Chem. C, 111, 15415, 10.1021/jp0748664 · DOI · Paper page
- Belcher, 2007, The effect of porphyrin inclusion on the spectral response of ternary P3HT:porphyrin:PCBM bulk heterojunction solar cells, Sol. Energy Mater. Sol. Cells, 91, 447, 10.1016/j.solmat.2006.09.007 · DOI · Paper page
- Schenning, 1996, Control of aggregation and tuning of the location of porphyrins in synthetic membranes as mimics for cytochrome P450, Langmuir, 12, 1572, 10.1021/la950486a · DOI
- Splan, 2004, Permeable nonaggregating porphyrin thin films that display enhanced photophysical properties, Langmuir, 20, 10560, 10.1021/la048465g · DOI
- Wagner, 1994, Synthesis of porphyrins tailored with 8 facially-encumbering groups—an approach to solid-state light-harvesting complexes, Tetrahedron, 50, 11097, 10.1016/S0040-4020(01)89413-8 · DOI
- Lee, 2009, Synthesis, optical and photovoltaic properties of porphyrin dyes, J. Macromol. Sci., Pure Appl. Chem., 46, 730, 10.1080/10601320902938558 · DOI
- Boyd, 1999, Selective supramolecular porphyrin/fullerene interactions, J. Am. Chem. Soc., 121, 10487, 10.1021/ja992165h · DOI
- Boyd, 2005, Fullerene–porphyrin constructs, Acc. Chem. Res., 38, 235, 10.1021/ar040168f · DOI
- Golder, 1988, Metal-complexes of sterically hindered porphyrins – crystal and molecular-structure of meso-tetrakis(3,5-di-tert-butyl-4-hydroxyphenyl)porphyrin-nickel(II), Inorg. Chim. Acta., 143, 71, 10.1016/S0020-1693(00)85847-8 · DOI
- Adler, 1967, A simplified synthesis for meso-tetraphenylporphyrin, J. Org. Chem., 32, 476, 10.1021/jo01288a053 · DOI
- Crossley, 1998, A convenient procedure for moderate-scale Rothemund synthesis of lipophilic porphyrins: an alternative to the Adler-Longo and Lindsey methodologies, J. Porphyrins Phthalocyanines, 2, 511, 10.1002/(SICI)1099-1409(199811/12)2:6<511::AID-JPP102>3.0.CO;2-E · DOI
- Frisch, 2004, Gaussian 03, Revision E.01, Gaussian, Inc., Wallingford, CT,
- Pavlishchuk, 2000, Conversion constants for redox potentials measured versus different reference electrodes in acetonitrile solutions at 25 degrees C, Inorg. Chim., 298, 97, 10.1016/S0020-1693(99)00407-7 · DOI
- Paliteiro, 2005, Electrochemical and spectroelectrochemical characterization of meso-tetra-alkyl porphyrins, Electrochim. Acta, 50, 2445, 10.1016/j.electacta.2004.10.070 · DOI
- R.W. Taft, Steric Effects in Organic Chemistry, in: M.S. Newman (Ed.), Wiley, New York, 1956, p. 556.
- Charton, 1975, Steric effects .1. Esterification and acid-catalyzed hydrolysis of esters, J. Am. Chem. Soc., 97, 1552, 10.1021/ja00839a047 · DOI
- Charton, 1975, Steric effects .2. Base-catalyzed ester hydrolysis, J. Am. Chem. Soc., 97, 3691, 10.1021/ja00846a022 · DOI
- Charton, 1975, Steric effects .3. Bimolecular nucleophilic-substitution, J. Am. Chem. Soc., 97, 3694, 10.1021/ja00846a023 · DOI
- Charton, 1975, Steric effects. 4. E1 and E2 eliminations, J. Am. Chem. Soc., 97, 6159, 10.1021/ja00854a034 · DOI
- Wienke, 1996, Adsorption of oriented methyl pyridinium porphyrins on solid substrates, Thin Solid Films, 279, 87, 10.1016/0040-6090(95)08155-0 · DOI
- Kasha, 1963, Energy transfer mechanisms and molecular exciton model for molecular aggregates, Radiat. Res., 20, 55, 10.2307/3571331 · DOI
- Krebs, 2005, Antibatic photovoltaic response in zinc-porphyrin-linked oligothiophenes, Sol. Energy Mater. Sol. Cells, 88, 363, 10.1016/j.solmat.2004.12.003 · DOI
- Belair, 2002, Photophysical characterization of free-base N-confused tetraphenylporphyrins, J. Phys. Chem. A, 106, 6445, 10.1021/jp025569w · DOI
- McNeill, 2009, Evolution of laterally phase-separated polyfluorene blend morphology studied by X-ray spectromicroscopy, Macromolecules, 42, 3347, 10.1021/ma801816r · DOI
- Koster, 2005, Device model for the operation of polymer/fullerene bulk heterojunction solar cells, Phys. Rev. B, 72, 085205-1, 10.1103/PhysRevB.72.085205 · DOI
- Shuttle, 2008, Bimolecular recombination losses in polythiophene: fullerene solar cells, Phys. Rev. B, 78, 113201-1, 10.1103/PhysRevB.78.113201 · DOI
- Ohkita, 2008, Charge carrier formation in polythiophene/fullerene blend films studied by transient absorption spectroscopy, J. Am. Chem. Soc., 130, 3030, 10.1021/ja076568q · DOI
- Mandoc, 2007, Effect of traps on the performance of bulk heterojunction organic solar cells, Appl. Phys. Lett., 91, 263505-1, 10.1063/1.2821368 · DOI
- Mandoc, 2007, Optimum charge carrier mobility in organic solar cells, Appl. Phys. Lett., 90, 133504-1, 10.1063/1.2711534 · DOI
- Braun, 1984, Electric field assisted dissociation of charge transfer states as a mechanism of photocarrier production, J. Chem. Phys., 80, 4157, 10.1063/1.447243 · DOI
- Mandoc, 2007, Origin of the reduced fill factor and photocurrent in MDMO-PPV: PCNEPV all polymer solar cells, Adv. Funct. Mater., 17, 2167, 10.1002/adfm.200601110 · DOI
- Morteani, 2004, Exciton regeneration at polymeric semiconductor heterojunctions, Phys. Rev. Lett., 92, 247402-1, 10.1103/PhysRevLett.92.247402 · DOI
- Mandoc, 2007, Origin of the efficiency improvement in all-polymer solar cells upon annealing, Appl. Phys. Lett., 91, 073518-1, 10.1063/1.2772185 · DOI
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Recent progress in porphyrin-based materials for organic solar cells
Mahmood, A., Hu, J.-Y., Xiao, B., Tang, A., Wang, X., & Zhou, E. (2018) · Journal of Materials Chemistry A · doi:10.1039/c8ta06392c · Cited by 311
Metadata
- Authors
- Cooling, N., Burke, K. B., Zhou, X., Lind, S. J., Gordon, K. C., Jones, T. W., Dastoor, P. C., & Belcher, W. J.
- Affiliations
- University of Newcastle Australia (AU)
- Commonwealth Scientific and Industrial Research Organisation (AU)
- University of Otago (NZ)
- Corresponding author
- Belcher, Warwick J.
- ORCID
- Venue
- Solar Energy Materials and Solar Cells
- Publisher
- Elsevier BV
- Published
- 2011-07
- Volume
- 95
- Issue
- 7
- Pages
- 1767-1774
- ISSN
- 0927-0248 (ISSN-L)
- OpenAlex
- W1975456562
- Cited by
- 38
- References
- 1
- Citations by year
- 2026: 1 · 2025: 1 · 2023: 1 · 2021: 1 · 2020: 1 · 2018: 2 · 2016: 4 · 2015: 7 · 2014: 4 · 2013: 8 · 2012: 5
- FWCI
- 4.47
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Solar Energy Materials and Solar Cells (publishedVersion)
- Topics
- Physical Sciences › Engineering › Electrical and Electronic Engineering › Organic Electronics and Photovoltaics
- Physical Sciences › Engineering › Electrical and Electronic Engineering › Organic Light-Emitting Diodes Research
- Physical Sciences › Materials Science › Materials Chemistry › Porphyrin and Phthalocyanine Chemistry
- Keywords
- porphyrins, steric bulk, charge recombination, bulk heterojunction solar cells, MEH-PPV, PCBM, organic solar cells, open-circuit voltage, bimolecular recombination, peripheral substituents, tetraphenylporphyrin, band gap, active layer morphology
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