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Träfflista för sökning "WFRF:(Nazeeruddin M. K.) "

Search: WFRF:(Nazeeruddin M. K.)

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  • Agrios, Alexander George, et al. (author)
  • Nanostructured composite films for dye-sensitized solar cells by electrostatic layer-by-layer deposition
  • 2006
  • In: Chemistry of Materials. - : American Chemical Society (ACS). - 0897-4756 .- 1520-5002. ; 18:23, s. 5395-5397
  • Journal article (peer-reviewed)abstract
    • The possibilities for making nanocomposite semiconductor films for DSC using the ELBL method was investigated. Coated slides were cut in half vertically giving two strips that can be subjected to different treatments for comparison. The electrode was heated to 450 °C for 30 min and then Cooled to 80 °C. Scanning electron microscopy of a sintered film with 5 cycles of TiO2 nanoparticles shows that the particles are well distributed and completely cover the transparent conducting oxide substrate. Spectroscopic measurements of a dye-coated film in acetonitrile found a dye concentration within the film of 0.15 mM based on an extinction coefficient. The solar cell including a scattering layer had more than double the current of the transparent layer-only cell. It was observed that ELBL method can produce TiO2 films for DSC with high efficiencies at low thickness.
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  • Nazeeruddin, M. K., et al. (author)
  • DFT-INDO/S modeling of new high molar extinction coefficient charge-transfer sensitizers for solar cell applications
  • 2006
  • In: Inorganic Chemistry. - : American Chemical Society (ACS). - 0020-1669 .- 1520-510X. ; 45:2, s. 787-797
  • Journal article (peer-reviewed)abstract
    • A new ruthenium(II) complex, tetrabutylammonium [ruthenium (4-carboxylic acid-4'-carboxylate-2,2'-bipyridine)(4,4'-di(2-(3,6-dimethoxyphenyl)ethenyl)-2,2'-bipyridine)(NCS)(2)] (N945H), was synthesized and characterized by analytical, spectroscopic, and electrochemical techniques. The absorption spectrum of the N945H sensitizer is dominated by metal-to-ligand charge-transfer (MLCT) transitions in the visible region, with the lowest allowed MLCT bands appearing at 25 380 and 18 180 cm(-1). The molar extinction coefficients of these bands are 34 500 and 18 900 M-1 cm(-1), respectively, and are significantly higher when compared to than those of the standard sensitizer cis-dithiocyanatobis(4,4'-dicarboxylic acid-2,2'-bipyridine)ruthenium(II). An INDO/S and density functional theory study of the electronic and optical properties of N945H and of N945 adsorbed on TiO2 was performed. The calculations point out that the top three frontier-filled orbitals have essentially ruthenium 4d (t(2g) in the octahedral group) character with sizable contribution coming from the NCS ligand orbitals. Most critically the calculations reveal that, in the TiO2-bound N945 sensitizer, excitation directs charge into the carboxylbipyridine ligand bound to the TiO2 surface. The photovoltaic data of the N945 sensitizer using an electrolyte containing 0.60 M butylmethylimidazolium iodide, 0.03 M I-2, 0.10 M guanidinium thiocyanate, and 0.50 M tert-butylpyridine in a mixture of acetonitrile and valeronitrile (volume ratio = 85:15) exhibited a short-circuit photocurrent density of 16.50 +/- 0.2 mA cm(-2), an open-circuit voltage of 790 +/- 30 mV, and a fill factor of 0.72 +/- 0.03, corresponding to an overall conversion efficiency of 9.6% under standard AM (air mass) 1.5 sunlight, and demonstrated a stable performance under light and heat soaking at 80 degrees C.
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  • Kuang, Daibin, et al. (author)
  • Stable dye-sensitized solar cells based on organic chromophores and ionic liquid electrolyte
  • 2011
  • In: Solar Energy. - : Elsevier BV. - 0038-092X .- 1471-1257. ; 85:6, s. 1189-1194
  • Journal article (peer-reviewed)abstract
    • A series of polyene-diphenylaniline based organic dyes (coded as D5, D7, D9 and D11) have been reported for the application in ionic liquid electrolyte based dye-sensitized solar cells. The effects of substitution of organic dyes on the photovoltaic performance have been investigated, which show addition of methoxy groups on the triphenylamine donor group increases short-circuit current, open-circuit voltage and photovoltaic performance. A power conversion efficiency of 6.5% under AM 1.5 sunlight at 100 mW/cm(2) has been obtained with D11 dye in combination with a binary ionic liquid electrolyte, which when subjected to accelerated testing under one sun light soaking at 60 degrees C, the efficiency remained 90% of initial efficiency.
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  • Tress, Wolfgang, et al. (author)
  • The role of the hole-transport layer in perovskite solar cells - reducing recombination and increasing absorption
  • 2014
  • In: 2014 IEEE 40TH PHOTOVOLTAIC SPECIALIST CONFERENCE (PVSC). - : IEEE. - 9781479943982 ; , s. 1563-1566
  • Conference paper (peer-reviewed)abstract
    • The role of the hole-transport layer (HTL) in CH3NH3PbI3 perovskite solar cells is investigated. It is found that it mainly serves three purposes: First, deposited prior to the gold electrode, it avoids direct contact of the metal electrode with the meso porous TiO2-perovskite layer, and therefore increases the selectivity of the contact. This reduces recombination as evident from an increased open-circuit voltage and a higher luminescence efficiency. Second, the HTL increases the internal quantum efficiency independent of applied voltage and illumination wavelength by reducing (diffusion) losses of charges. Third, due to a smoothing of the TiO2-perovskite mesoscopic layer the HTL increases the reflectivity of the gold electrode, allowing for a second path of the light through the absorber. Both effects result in an enhancement of the short-circuit current density.
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