scholarly journals Amphiphilic Ruthenium(II) Terpyridine Sensitizers with Long Alkyl Chain Substituted β-Diketonato Ligands: An Efficient Coadsorbent-Free Dye-Sensitized Solar Cells

2011 ◽  
Vol 2011 ◽  
pp. 1-7 ◽  
Author(s):  
Ashraful Islam ◽  
Surya Prakash Singh ◽  
Masatoshi Yanagida ◽  
Mohammad Rezaul Karim ◽  
Liyuan Han

Three alkyl-substitutedβ-diketonato-ruthenium(II)-polypyridyl sensitizers with different alkyl chain lengths, [Ru(tctpy)(tfpd)(NCS)] (A1), [Ru(tctpy)(tfdd)(NCS)] (A2), and [Ru(tctpy)(tfid)(NCS)] (A3), were designed and synthesized for dye-sensitized solar cells (DSCs) to investigate the effect of bulky alkyl chain substituents on the photovoltaic performances (where tctpy = 4,4′,4′′-tricarboxy-2,2′:;6′,2′′-terpyridine, tfpd =1,1,1-trifluoropentane-2,4-dione, tfdd = 1,1,1-trifluorodecane-2,4-dione, and tfid =1,1,1-trifluoroicosane-2,4-dione). These complexes exhibit a broad metal-to-ligand charge transfer absorption band over the whole visible range extending up to 950 nm. All complexes were examined in the presence and absence of the coadsorbent deoxycholic acid (DCA) in dye-bath solutions. These sensitizers, when anchored to nanocrystalline TiO2films, achieve efficient sensitization to TiO2electrodes. Under standard AM 1.5 sunlight, the complexA3containing long alkyl chain length of C16yielded a short-circuit photocurrent density of 18.0 mA/cm2, an open-circuit voltage of 0.64 V, and a fill factor of 0.66, corresponding to an overall conversion efficiency of 7.6% in the absence of DCA. The power conversion efficiency ofA1sensitized DSCs was significantly increased upon the addition of DCA as compared to that in the absence of DCA. However, the photovoltaic performance ofA3was not dependent on DCA at all, probably due to the inherent structural nature of theA3molecule.

2011 ◽  
Vol 2011 ◽  
pp. 1-7 ◽  
Author(s):  
Joe Otsuki ◽  
Yusho Takaguchi ◽  
Daichi Takahashi ◽  
Palanisamy Kalimuthu ◽  
Surya Prakash Singh ◽  
...  

We have prepared a novel piperidine-donor-substituted perylene sensitizer, PK0002, and studied the photovoltaic performance in dye-sensitized solar cells (DSSCs). Physical properties and photovoltaic performance of this new perylene derivative PK0002 are reported and compared with those of unsubstituted perylene sensitizer, PK0003. PK0002, when anchored to nanocrystalline TiO2 films, achieves very efficient sensitization across the whole visible range extending up to 800 nm. The incident photon-to-current conversion efficiency (IPCE) spectrum was consistent with the absorption spectrum and resulted in a high short-circuit photocurrent density (Jsc) of 8.8 mA cm-2. PK0002 showed higher IPCE values than PK0003 in the 520–800 nm region. Under standard AM 1.5 irradiation (100 mW cm-2) and using an electrolyte consisting of 0.6 M dimethylpropyl-imidazolium iodide, 0.05 M I2, 0.1 M LiI, and 0.5 M tert-butylpyridine in acetonitrile, a solar cell containing sensitizer PK0002 yielded a short-circuit photocurrent density of 7.7 mA cm-2, an open-circuit photovoltage of 0.57 V, and a fill factor of 0.70, corresponding to an overall conversion efficiency of 3.1%.


Materials ◽  
2019 ◽  
Vol 12 (24) ◽  
pp. 4181 ◽  
Author(s):  
Mariia Karpacheva ◽  
Vanessa Wyss ◽  
Catherine E. Housecroft ◽  
Edwin C. Constable

By systematic tuning of the components of the electrolyte, the performances of dye-sensitized solar cells (DSCs) with an N-heterocyclic carbene iron(II) dye have been significantly improved. The beneficial effects of an increased Li+ ion concentration in the electrolyte lead to photoconversion efficiencies (PCEs) up to 0.66% for fully masked cells (representing 11.8% relative to 100% set for N719) and an external quantum efficiency maximum (EQEmax) up to approximately 25% due to an increased short-circuit current density (JSC). A study of the effects of varying the length of the alkyl chain in 1-alkyl-3-methylimidazolium iodide ionic liquids (ILs) shows that a longer chain results in an increase in JSC with an overall efficiency up to 0.61% (10.9% relative to N719 set at 100%) on going from n-methyl to n-butyl chain, although an n-hexyl chain leads to no further gain in PCE. The results of electrochemical impedance spectroscopy (EIS) support the trends in JSC and open-circuit voltage (VOC) parameters. A change in the counterion from I− to [BF4]− for 1-propyl-3-methylimidazolium iodide ionic liquid leads to DSCs with a remarkably high JSC value for an N-heterocyclic carbene iron(II) dye of 4.90 mA cm−2, but a low VOC of 244 mV. Our investigations have shown that an increased concentration of Li+ in combination with an optimized alkyl chain length in the 1-alkyl-3-methylimidazolium iodide IL in the electrolyte leads to iron(II)-sensitized DSC performances comparable with those of containing some copper(I)-based dyes.


Author(s):  
Sevil ŞENER

The synthesis and spectroscopic characterization of an innovative ball-type cobalt (II)  metallophthalocyanine 4, bridged by four 1,2-bis(2-hydroxymethyl)-O-carborane (HMOC) 1 units has been achieved. The structure of 4 was characterized via elemental analysis, UV–visible absorption spectroscopy, FT-IR spectroscopy, and MALDI-TOF mass spectrometry. The photovoltaic performance of the newly synthesized compound in dye-sensitized solar cells was investigated. In order to clarify the effect of dye-sensitization time on photovoltaic performance parameters, the sensitization time was varied from 12 to 60 h and the performance parameters were investigated. It was found that sensitization time had a strong effect on the main performance parameters. The best photovoltaic performance was achieved after sensitization for 36 h (short circuit current density, 6.41 mA cm−2; overall conversion efficiency, 3.42%). Geometry optimization of the molecule was performed using density functional theory and shows a peripheral structure.


RSC Advances ◽  
2015 ◽  
Vol 5 (62) ◽  
pp. 50483-50493 ◽  
Author(s):  
Malihe Afrooz ◽  
Hossein Dehghani

In this study, triphenyl phosphate (TPP) is applied as an effective and inexpensive additive in the dye sensitized solar cells (DSSCs) and an increase in the photoelectric conversion efficiency is obtained of almost 24%.


2008 ◽  
Vol 8 (9) ◽  
pp. 4761-4766 ◽  
Author(s):  
Dong Wook Kim ◽  
Jin Joo Choi ◽  
Man Ku Kang ◽  
Yongku Kang ◽  
Changjin Lee

We prepared organic sensitizers (S1 and S2) containing julolidine moiety as a donor, phenyl or phenylene thiophene units as a conjugation bridge, and cyano acetic acid as an acceptor for dye sensitized solar cells. S1 exhibited two absorption maxima at 441 nm (ε = 26 200) and 317 nm (ε = 15 500) due to the π–π* transition of the dye molecule. S2 dyes with an additional thiophene unit showed the absorption maximum extended by 18 nm. DSSCs based on S1 dye achieved 2.66% of power conversion efficiency with 8.3 mA cm−2 of short circuit current, 576 mV of open circuit voltage, and 0.56 of fill factor. DSSCs using S2 dye with a longer conjugation attained only 1.48% of power conversion efficiency. The 0.21 V lower driving force for regeneration of the S2 dye compared to the S1 dye is one of the reasons for low conversion efficiency of the S2 dye.


2015 ◽  
Vol 787 ◽  
pp. 3-7 ◽  
Author(s):  
S. Karuppuchamy ◽  
C. Brundha

We demonstrated the construction and performance of dye-sensitized solar cells (DSCs) based on nanoparticles of TiO2coated with thin shells of MgO by simple solution growth technique. The XRD patterns confirm the presence of both TiO2and MgO in the core-shell structure. The effect of varied shell thickness on the photovoltaic performance of the core-shell structured electrode is also investigated. We found that MgO shells of all thicknesses perform as barriers that improve open-circuit voltage (Voc) of the DSCs only at the expense of a larger decrease in short-circuit current density (Jsc). The energy conversion efficiency was greatly dependent on the thickness of MgO on TiO2film, and the highest efficiency of 4.1% was achieved at the optimum MgO shell layer.


2021 ◽  
Author(s):  
S. Revathi ◽  
A Pricilla Jeyakumari

Abstract Currently, the TiO2/CdS photoanodes based dye sensitized solar cells (DSSCs) have shown extraordinary developments in the photo conversion efficiency. In this report, pristine TiO2, CdS and various molar ratios of TiO2/CdS photoanodes were prepared by one step microwave irradiation route and followed by doctor blade method. The sheet like morphology of the TiO2 and CdS nanoparticles were clearly evident from the SEM and TEM images. A significant reduction band gap with enhanced light absorption and rapid prevention of electron hole pair was explored by UV-DRS and PL studies. The photocurrent density-voltage (J-V) and electrochemical impedance (EIS) characteristics were analyzed for assembled solar cell. The photo-conversion efficiency of 12.8% was obtained with the configuration TiO2/CdS (200 mg) that represent a 2.5 fold increment compared to bare TiO2 (5.33%) as well as commercial Pt (6.11%). The experimental results are discussed.


2015 ◽  
Vol 2015 ◽  
pp. 1-5 ◽  
Author(s):  
Mengmei Pan ◽  
Hanjun Liu ◽  
Zhongyu Yao ◽  
Xiaoli Zhong

Trace amount Ca-doped TiO2films were synthesized by the hydrothermal method and applied as photoanodes of dye-sensitized solar cells (DSSCs). To prepare Ca-doped TiO2film electrodes, several milliliters of Ca(NO3)2solution was added in TiO2solution during the hydrolysis process. The improvements of DSSCs were confirmed by photocurrent density-voltage (J-V) characteristics, electrochemical impedance spectroscopy (EIS) measurements. Owing to the doping effect of Ca, the Ca-doped TiO2thin film shows power conversion efficiency of 7.45% for 50 ppm Ca-doped TiO2electrode, which is higher than that of the undoped TiO2film (6.78%) and the short-circuit photocurrent density(Jsc)increases from 13.68 to 15.42 mA·cm−2. The energy conversion efficiency and short-circuit current density(Jsc)of DSSCs were increased due to the faster electron transport in the Ca-doped TiO2film. When Ca was incorporated into TiO2films, the electrons transport faster and the charge collection efficiencyηccis higher than that in the undoped TiO2films.


2012 ◽  
Vol 2012 ◽  
pp. 1-6 ◽  
Author(s):  
Yiming Chen ◽  
Haiyan Zhang ◽  
Yuting Chen ◽  
Jiapeng Lin

Carbon nanocomposite electrodes were prepared by adding carbon nanotubes (CNTs) into carbon black as counterelectrodes of dye-sensitized solar cells(DSSCs). The morphology and structure of carbon nanocomposite electrodes were studied by scanning electron microscopy. The influence of CNTs on the electrochemical performance of carbon nanocomposite electrodes is investigated by cyclic voltammetry and electrochemical impedance spectroscopy. Carbon nano composite electrodes with CNTs exhibit a highly interconnected network structure with high electrical conductivity and good catalytic activity. The influence of different CNTs content in carbon nanocomposite electrodes on the open-circuit voltage, short-circuit current, and filling factor of DSSCs is also investigated. DSSCs with 10% CNTs content exhibit the best photovoltaic performance in our experiments.


2020 ◽  
Vol 26 (1) ◽  
pp. 37-45
Author(s):  
Sevil Şener

AbstractThe synthesis and spectroscopic characterization of an innovative ball-type cobalt metallophthalocyanine 4, bridged by four 1,2-bis(2-hydroxymethyl)-O-carborane (HMOC) 1 units, has been achieved. The synthesized compound 4 was characterized structurally and electronically using elemental analysis, UV-Vis absorption spectroscopy, FT-IR spectroscopy, MALDI-TOF mass spectrometry, EPR spectroscopy and magnetic susceptibility. The photovoltaic performance of the newly synthesized compound in dye-sensitized solar cells was investigated. In order to clarify the effect of dye-sensitization time on photovoltaic performance parameters, the sensitization time was varied from 12 to 60 h and the performance parameters were investigated. It was found that sensitization time had a strong effect on the main performance parameters. The best photovoltaic performance was achieved after sensitization for 36 h (short circuit current density, 5.41 mA cm−2; overall conversion efficiency, 3.42%). Computational UV-Vis absorption spectra of the molecule was calculated using time dependent density functional theory and was found consistent with measured UV-Vis spectra.


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