Synthesis, Characterization and Electronic Properties of trans-[4-(Alkoxycarbonyl)phenyl]porphyrin-[Ru-II(bpy)(3)](2) Complexes or Boron-Dipyrrin Conjugates as Panchromatic Sensitizers for DSSCs
dc.contributor.author | Stangel, C. | en |
dc.contributor.author | Ladomenou, K. | en |
dc.contributor.author | Charalambidis, G. | en |
dc.contributor.author | Panda, M. K. | en |
dc.contributor.author | Lazarides, T. | en |
dc.contributor.author | Coutsolelos, A. G. | en |
dc.date.accessioned | 2015-11-24T16:49:28Z | |
dc.date.available | 2015-11-24T16:49:28Z | |
dc.identifier.issn | 1434-1948 | - |
dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/9490 | |
dc.rights | Default Licence | - |
dc.subject | energy transfer | en |
dc.subject | solar cells | en |
dc.subject | sensitizers | en |
dc.subject | dyes | en |
dc.subject | pigments | en |
dc.subject | porphyrinoids | en |
dc.subject | ruthenium | en |
dc.subject | boron | en |
dc.subject | nanocrystalline tio2 electrodes | en |
dc.subject | efficient co-sensitization | en |
dc.subject | solar-cells | en |
dc.subject | ruthenium sensitizers | en |
dc.subject | energy-transfer | en |
dc.subject | photoelectrochemical properties | en |
dc.subject | conversion-efficiency | en |
dc.subject | quantum yields | en |
dc.subject | excited-state | en |
dc.subject | organic-dyes | en |
dc.title | Synthesis, Characterization and Electronic Properties of trans-[4-(Alkoxycarbonyl)phenyl]porphyrin-[Ru-II(bpy)(3)](2) Complexes or Boron-Dipyrrin Conjugates as Panchromatic Sensitizers for DSSCs | en |
heal.abstract | Two porphyrin-based dyes were synthesized that incorporate two additional chromophores to absorb in a wider UV/Vis region. In the first dye, a porphyrin ring is linked through an amide bond to two [Ru(bpy)(3)](2+) units, forming a symmetric [Ru(bpy)(3)]-porphyrin-[Ru(bpy)(3)] {Por(COOH)(2)[Ru(bpy)(3)](2)} system. The second porphyrin is trans substituted through a triple bond to the meso position with two boron dipyrrin (BDP) molecules {Por(COOH)(2)(BDP)(2)}. Both porphyrins bear two carboxylic groups capable of binding onto a TiO2 surface, with potential applications in dye-sensitized solar cells (DSSCs). The title dyes were characterized by means of H-1 and C-13 NMR spectroscopy, elemental analysis, MALDI-TOF, UV/Vis absorption and emission studies. | en |
heal.access | campus | - |
heal.fullTextAvailability | TRUE | - |
heal.identifier.primary | DOI 10.1002/ejic.201201248 | - |
heal.identifier.secondary | <Go to ISI>://000316395600005 | - |
heal.identifier.secondary | http://onlinelibrary.wiley.com/store/10.1002/ejic.201201248/asset/1275_ftp.pdf?v=1&t=hmri99fy&s=1691899cde6d48593d1d1f1b07f16b2badce2a7c | - |
heal.journalName | European Journal of Inorganic Chemistry | en |
heal.journalType | peer reviewed | - |
heal.language | en | - |
heal.publicationDate | 2013 | - |
heal.publisher | Wiley-VCH Verlag | en |
heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας | el |
heal.type | journalArticle | - |
heal.type.el | Άρθρο Περιοδικού | el |
heal.type.en | Journal article | en |
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