Hybrid Structure of TiO2 Nanofiber and Nanoparticle for Dye-Sensitized Solar Cells

2014 ◽  
Vol 922 ◽  
pp. 356-359
Author(s):  
Ji Sun Kim ◽  
Seong Cheol Shim ◽  
Tae Hwan Hwang ◽  
Won Youl Choi

Hybrid structure of TiO2nanofiber and nanoparticle as a photoelectrode was very attractive in dye-sensitized solar cells (DSCs) because TiO2nanoparticle provided a high specific surface area to adsorb the N719 dye and TiO2nanofiber was a direct path to transfer photoelectron from dye to electrode. TiO2nanofiber film was prepared with titanium-tetraisopropoxide (TTIP) and polyvinylpyrrolidone (PVP) based precursor by electro-spinning process. To fabricate the hybrid structure, TiO2nanoparticular paste was screen printed on the TiO2nanofiber film. Electrospun TiO2nanofiber film and screen printed TiO2nanoparticular film were combined in layer by layer method. These films were observed as an anatase phase by X-ray diffraction pattern. Thickness and diameter of TiO2nanofibers were ~5μm and ~400nm, respectively. Thickness and particle size of TiO2particles were ~5μm and ~20nm, respectively. Compared to conventional DSCs, higher short circuit current densities (Jsc) of 6.47 mA/cm2and higher power conversion efficiency of 3.06 % were measured in DSCs having hybrid structure of TiO2nanofiber and nanoparticle. Electrochemical impedance spectroscopy (EIS) was observed to understand an electron transfer and life time.

2014 ◽  
Vol 922 ◽  
pp. 67-70
Author(s):  
Ji Sun Kim ◽  
Seong Cheol Shim ◽  
Tae Hwan Hwang ◽  
Won Youl Choi

Hybrid structure of TiO2nanofiber and nanoparticle as a photoelectrode was very attractive in dye-sensitized solar cells (DSCs) because TiO2nanoparticle provided a high specific surface area to adsorb the N719 dye and TiO2nanofiber was a direct path to transfer photoelectron from dye to electrode. TiO2nanofiber film was prepared with titanium-tetraisopropoxide (TTIP) and polyvinylpyrrolidone (PVP) based precursor by electro-spinning process. To fabricate the hybrid structure, TiO2nanoparticular paste was screen printed on the TiO2nanofiber film. Electrospun TiO2nanofiber film and screen printed TiO2nanoparticular film were combined in layer by layer method. These films were observed as an anatase phase by X-ray diffraction pattern. Thickness and diameter of TiO2nanofibers were ~5μm and ~400nm, respectively. Thickness and particle size of TiO2particles were ~5μm and ~20nm, respectively. Compared to conventional DSCs, higher short circuit current densities (Jsc) of 6.47 mA/cm2and higher power conversion efficiency of 3.06 % were measured in DSCs having hybrid structure of TiO2nanofiber and nanoparticle. Electrochemical impedance spectroscopy (EIS) was observed to understand an electron transfer and life time.


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.


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.


2011 ◽  
Vol 1327 ◽  
Author(s):  
Liyuan Han ◽  
Ashraful Islam

ABSTRACTThe present paper discusses the principle of dye-sensitized solar cells (DSCs) in terms of equivalent circuit model and the key issues to improve the device efficiency. Equivalent circuit model is proposed following analysis by electrochemical impedance spectroscopy of the voltage dependence of the internal resistance elements of DSCs. The influence of these elements upon cell performance in areas such as short circuit current density (Jsc), open circuit voltage (Voc), and fill factor (FF) was examined based on the equivalent circuit. Efficient sensitization of nanocrystalline TiO2 film was observed across the whole visible range and into the near-IR region as far as 1000 nm with a new panchromatic substituted β-diketonato Ru(II)-terpyridine dye (HIG1). Introduction of bulky alkyl substituent group in a β-diketonato Ru(II)-terpyridine dye (A3) suppress aggregate formation result in an improved performance of DSCs and the performance is independent of the additive added during the dye adsorption process. The haze factor of TiO2 electrodes is a useful index when fabricating light-confined TiO2 electrodes to improve Jsc. It was demonstrated that blocking of bare TiO2 surface with small molecules is an effective way of suppress interfacial charge recombination at the TiO2-dye/electrolyte interface and of improving shunt resistance and Voc. FF was also improved by reduction of the internal series resistance, which is composed of the following three elements: the redox reaction resistance at the platinum counter electrode, the resistance of carrier transport by ions in the electrolyte, and resistance due to the sheet resistance of the transparent conducting oxide. Finally, the highest efficiency scores of 10.4% and 11.1% (aperture illumination area 1.004cm2 and 0.219cm2, respectively) were confirmed by a public test center.


2011 ◽  
Vol 383-390 ◽  
pp. 5510-5515
Author(s):  
Tien Tsan Hung

Novel phthalocyanine derivative and azo derivative have been synthesized as photosensitizers for the dye-sensitized solar cells (DSSCs). We used sol-gel method to prepare the titanium oxide (TiO2) membrane electrode of the DSSCs. The crystalline phase and surface morphology of TiO2 were characterized by using X-ray diffraction (XRD), and field emission scanning electron microscopy (FE-SEM) to investigate the effects of processing parameters on the films characteristic, microstructure and thickness. The performance of DSSCs was characterized by using electrochemical impedance spectroscopy (EIS) and current-voltage curve analysis. The sensitizing properties of phthalocyanine derivative, azo derivative and mixed dyes were studied, and it was found that the cell consisted of mixed dyes generated the highest power conversion efficiency () of 2.3 %, short circuit photocurrent density (Jsc) of 13.6 mA cm-2, open circuit photovoltage (Voc) of 0.46 V and fill factor (FF) of 0.37 under simulated AM 1.5 irradiation (100 mW cm-2) with a active area of 0.25 cm2.


2010 ◽  
Vol 93-94 ◽  
pp. 31-34 ◽  
Author(s):  
A. Chindaduang ◽  
Pattasuda Duangkaew ◽  
Sirapat Pratontep ◽  
Gamolwan Tumcharern

We focus on the energy conversion improvement of dye-sensitized solar cells by using poly(ethylene oxide)-multi-walled carbon nanotube (PEO-MWCNT) electrolyte. Compared with the MWCNT-free solar cells, the addition of 0.05 wt.% MWCNTs in the polymer electrolyte results in a dramatic increase of the short-circuit current (Jsc), consequently raising the device performance by approximately 9% under a direct light of the Air Mass 1.5 irradiation at 100 mW cm-2. The role of the conductive carbon materials in the polymer electrolyte have been investigated by means of ionic conductometry, electrochemical impedance spectroscopy and UV-visible spectroscopy. This work demonstrates that MWCNT additives in polymer electrolytes is a convenient yet effective strategy for improving the performance of photovoltaic devices.


2021 ◽  
Vol 2 (2) ◽  
pp. 222-236
Author(s):  
Hugo Cruz ◽  
Ana Lucia Pinto ◽  
Noémi Jordão ◽  
Luísa A. Neves ◽  
Luís C. Branco

Different alkali deep eutectic solvents (DES), such as LiI:nEG, NaI:nEG, and KI:nEG, have been tested as electrolytes for dye sensitized solar cells (DSSCs). These DSSCs were prepared using pure DES or, alternatively, DES combined with different amounts of iodine (I2). The most important parameters, such as open circuit voltage (VOC), short circuit current density (JSC), fill factor (FF), and the overall conversion efficiency (η), were evaluated. Some DES seem to be promising candidates for DSSC applications, since they present higher VOC (up to 140 mV), similar FF values but less current density values, when compared with a reference electrolyte in the same experimental conditions. Additionally, electrochemical impedance spectroscopy (EIS) has been performed to elucidate the charge transfer and transport processes that occur in DSSCs. The values of different resistance (Ω·cm2) phenomena and recombination/relaxation time (s) for each process have been calculated. The best-performance was obtained for DES-based electrolyte, KI:EG (containing 0.5 mol% I2) showing an efficiency of 2.3%. The efficiency of this DES-based electrolyte is comparable to other literature systems, but the device stability is higher (only after seven months the performance of the device drop to 60%).


Molecules ◽  
2020 ◽  
Vol 25 (7) ◽  
pp. 1528 ◽  
Author(s):  
Guglielmo Risi ◽  
Mariia Becker ◽  
Catherine E. Housecroft ◽  
Edwin C. Constable

The syntheses of 4,4′-bis(4-dimethylaminophenyl)-6,6′-dimethyl-2,2′-bipyridine (1), 4,4′-bis(4-dimethylaminophenylethynyl)-6,6′-dimethyl-2,2′-bipyridine (2), 4,4′-bis(4-diphenylaminophenyl)-6,6′-dimethyl-2,2′-bipyridine (3), and 4,4′-bis(4-diphenylaminophenylethynyl)-6,6′-dimethyl-2,2′-bipyridine (4) are reported along with the preparations and characterisations of their homoleptic copper(I) complexes [CuL2][PF6] (L = 1–4). The solution absorption spectra of the complexes exhibit ligand-centred absorptions in addition to absorptions in the visible region assigned to a combination of intra-ligand and metal-to-ligand charge-transfer. Heteroleptic [Cu(5)(Lancillary)]+ dyes in which 5 is the anchoring ligand ((6,6′-dimethyl-[2,2′-bipyridine]-4,4′-diyl)bis(4,1-phenylene))bis(phosphonic acid) and Lancillary = 1–4 have been assembled on fluorine-doped tin oxide (FTO)-TiO2 electrodes in dye-sensitized solar cells (DSCs). Performance parameters and external quantum efficiency (EQE) spectra of the DSCs (four fully-masked cells for each dye) reveal that the best performing dyes are [Cu(5)(1)]+ and [Cu(5)(3)]+. The alkynyl spacers are not beneficial, leading to a decrease in the short-circuit current density (JSC), confirmed by lower values of EQEmax. Addition of a co-absorbent (n-decylphosphonic acid) to [Cu(5)(1)]+ lead to no significant enhancement of performance for DSCs sensitized with [Cu(5)(1)]+. Electrochemical impedance spectroscopy (EIS) has been used to investigate the interfaces in DSCs; the analysis shows that more favourable electron injection into TiO2 is observed for sensitizers without the alkynyl spacer and confirms higher JSC values for [Cu(5)(1)]+.


2011 ◽  
Vol 347-353 ◽  
pp. 390-393 ◽  
Author(s):  
Shun Jian Xu ◽  
Yu Feng Luo ◽  
Wei Zhong ◽  
Guan Jun Qiao

A novel counter electrode has been fabricated at low temperature using nanoporous carbon (NC) with about 35 nm pore size as based catalysis materials and silver conductor paste (SCP) as connecting adhesive. The efficiency of dye-sensitized solar cells (DSCs) employing this SCP/NC electrode reaches to 5.91%, which is 15% higher than that of DSCs with NC electrode. The improved efficiency is attributed to the enhancement in the fill factor and the short circuit photocurrent density. Electrochemical impedance spectroscopy reveals that all of charge transfer resistance, ohmic serial resistance and Nernst diffusion impedance of SCP/NC electrode decrease compared with NC electrode. Especially, the efficiency of 5.91% is comparable to that of DSCs with Pt electrode.


2018 ◽  
Vol 9 ◽  
pp. 3069-3078 ◽  
Author(s):  
Mariia Karpacheva ◽  
Catherine E Housecroft ◽  
Edwin C Constable

We demonstrate that the performances of dye-sensitized solar cells (DSCs) sensitized with a previously reported N-heterocyclic carbene iron(II) dye in the presence of chenodeoxycholic acid co-adsorbant, can be considerably improved by altering the composition of the electrolyte while retaining an I−/I3 − redox shuttle. Critical factors are the solvent, presence of ionic liquid, and the use of the additives 1-methylbenzimidazole (MBI) and 4-tert-butylpyridine (TBP). For the electrolyte solvent, 3-methoxypropionitrile (MPN) is preferable to acetonitrile, leading to a higher short-circuit current density (J SC) with little change in the open-circuit voltage (V OC). For electrolytes containing MPN, an ionic liquid and MBI (0.5 M), DSC performance depended on the ionic liquid with 1-ethyl-3-methylimidazolium hexafluoridophosphate (EMIMPF) > 1,2-dimethyl-3-propylimidazolium iodide (DMPII) > 1-butyl-3-methylimidazolium iodide (BMII) ≈ 1-butyl-3-methylimidazolium hexafluoridophosphate (BMIMPF). Omitting the MBI leads to a significant improvement in J SC when the ionic liquid is DMPII, BMII or BMIMPF, but with EMIMPF the removal of the MBI additive results in a dramatic decrease in V OC (542 to 42 mV). For electrolytes containing MPN and DMPII, the effects of altering the MBI concentration have also been investigated. Although the addition of TBP improves V OC, it causes significant decreases in J SC. The best performing DSCs with the NHC-iron(II) dye employ an I−/I3 −-based electrolyte with MPN as solvent, DMPII ionic liquid (0.6 M) with no or 0.01 M MBI; values of J SC = 2.31 to 2.78 mA cm−2, V OC = 292 to 374 mV have been achieved giving η in the range of 0.47 to 0.57% which represents 7.8 to 9.3% relative to an N719 reference DSC set at 100%. Electrochemical impedance spectroscopy has been used to understand the role of the MBI additive in the electrolytes.


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