Study on CaCO3-coated ZnO nanoparticles based dye sensitized solar cell

Dye sensitized solar cells (DSSCs) have been fabricated using ZnO and CaCO₃-coated ZnO nanoparticles. The effect of CaCO₃ coating on the performance of DSSC has been investigated. CaCO₃-coated ZnO nanoparticles have been synthesized by hydrothermal method. X-ray diffraction patterns of synthesized nanoparticles reveal that the ZnO and CaCO₃-coated ZnO nanoparticles have respectively wurtzite and rhomb-centred structure and both having hexagonal phase. Transmission electron microscopy study reveal that ZnO and CaCO₃-coated ZnO nanoparticles possess spherical symmetry and have average particle size respectively 6.2 and 6.7 nm. In case of CaCO₃/ZnO nanoparticles, the quenching in photoluminescence emission intensity has been attributed to the decrease in recombination rate of photo-generated electron–hole pairs. UV–Vis absorption spectra, confirms that the electrodes fabricated from the CaCO₃-coated ZnO nanoparticles have higher absorbance that shows their higher dye adsorbing power. The use of CaCO₃ coating has been found to enhance the efficiency of DSSC by over 100 %.     

Dye-sensitized solar cells based on ZnO nanoflowers and TiO2 nanoparticles composite photoanodes

ZnO nanoflowers were synthesized by low temperature solution-phase method. ZnO nanoflowers/TiO₂ nanoparticles composite photoanodes with various mass ratios were prepared on transparent conductive fluorine-doped tin oxide substrates by doctor-blade technique. The dye-sensitized solar cells (DSSCs) were assembled. The morphology characteristics of ZnO nanoflowers and ZnO/TiO₂ composite photoanodes have been analyzed by scanning electron microscopy. The effect of the ZnO nanoflowers/TiO₂ nanoparticles mass ratio on the performance of DSSCs was systematically investigated by I–V characteristics and electrochemical impedance spectroscopy. Results show that the conversion efficiency of the dye-sensitized solar cell with a ZnO/TiO₂ mass ratio of 25:75 was increased by about 35 % compared to that of pure TiO₂-based solar cell. Addition of ZnO nanoflowers can enhance the light harvesting and improve electron transport.     

Analyzing the efficiency of nanostructured Sm3+- and Gd3+-doped TiO2 and constructing DSSCs using efficacious photoanodes

The rare earth elements, gadolinium and samarium, are doped with TiO₂ by hydrothermal synthesis technique to study the photoconversion performance of a photoanode in a dye-sensitized solar cell (DSSC). The obtained materials are subjected to the characterizations XRD, HR-TEM, UV–Vis spectroscopy, and XPS. DSSCs are fabricated using N719 dye, redox electrolyte, and platinum counter electrode. Charge-transfer ability was investigated using electrochemical impedance spectroscopy (EIS) on DSSCs. The efficiencies of DSSCs are influenced by the electron transport within the TiO₂–dye–electrolyte system. After the fabrication and simulation, among the two, Gd³⁺-doped TiO₂ gives the desired outcomes and higher efficiency (5.542%) than the pure and Sm³⁺-doped TiO₂ and thus it proves to be a superior solar cell anode material.

     

Microstructural and chemical variation of TiO2 electrodes in DSSCs after ethanol vapour treatment

TiO₂ based dye-sensitized solar cells (DSSCs) have great potential to solve many energy challenges, however, their low energy conversion rate is still a barrier for further applications. Ethanol vapour post-treatment can improve the DSSC's conversion efficiency without changing its architecture, and a stable 2–3% improvement was found in our experiments. Microstructural and chemical factors were investigated using scanning electron microscopy and analytical electron microscopy on treated and untreated electrodes. The vapour treatment improved the porosity and surface-to-volume ratio of the TiO₂ particles, decreased electron transport loss between TiO₂ and fluorine doped tin oxide, and increased hydroxyl sites on the TiO₂ particle's surface. The modification therefore enhanced the dye uptake and dye–TiO₂ coupling, and it reduced the energy loss during the carrier transfer.     

Performance of Eu2O3 coated ZnO nanoparticles-based DSSC

To provide an inherent energy barrier between the electrode and electrolyte interface, the surface of the ZnO nanoparticles has been modified by Eu₂O₃ layer. The synthesis of ZnO, Eu₂O₃ coated ZnO nanoparticles have been carried out by chemical precipitation method and solvothermal treatment. The synthesized samples were characterized by XRD and the diffraction plane (222) of Eu₂O₃ detected, demonstrating the existence of Eu₂O₃ on the surface of ZnO, which is further verified using energy dispersive X-ray spectroscopy and Fourier transform infrared spectroscopy. The strong quenching in photoluminescence emission, in case of Eu₂O₃/ZnO nanoparticles, has been attributed to the decrease in recombination rate of photo-generated electron–hole pairs. Compared to ZnO electrodes, Eu₂O₃ coated ZnO electrodes adsorbed more dye. The photoelectrochemical properties of the Eu₂O₃/ZnO electrodes have been found to improve and the energy conversion efficiency increase from 0.44 to 1.45 % under the illumination of simulated light of 100 mW/cm².     

Improved performance of dye-sensitized solar cells with surface-treated TiO2 as a photoelectrode

We report on the effects of surface-modified TiO₂ on the performance of dye-sensitized solar cells (DSSCs). TiO₂ surface was modified with Na₂CO₃ via a simple dip coating process and the modified TiO₂ was applied to photoelectrodes of DSSCs. By dipping of TiO₂ layer into aqueous Na₂CO₃ solution, the DSSC showed a power conversion efficiency of 9.98%, compared to that (7.75%) of the reference device without surface treatment. The UV–vis absorption spectra, the impedance spectra and the dark current studies revealed that the increase of all parameters was attributed to the enhanced dye adsorption, the prolonged electron lifetime and the reduced interfacial resistance.     

Fabrication and properties of meso-macroporous electrodes screen-printed from mesoporous titania nanoparticles for dye-sensitized solar cells

A meso-macroporous TiO₂ film electrode was fabricated by using mesoporous TiO₂ (m-TiO₂) nanoparticles through a screen-printing technique in order to efficiently control the main fabrication step of dye-sensitized solar cells (DSSCs). The qualities of the screen-printed m-TiO₂ films were characterized by means of spectroscopy, electron microscopy, nitrogen adsorption–desorption and photoelectrochemical measurements. Under the optimal paste composition and printing conditions, the DSSC based on the meso-macroporous m-TiO₂ film electrode exhibits an energy conversion efficiency of 4.14%, which is improved by 1.70% in comparison with DSSC made with commercially available nonporous TiO₂ nanoparticles (P25, Degussa) electrode printed with a similar paste composition. The meso-macroporous structure within the m-TiO₂ film is of great benefit to the dye adsorption, light absorption and the electrolyte transportation, and then to the improvement of the overall energy conversion efficiency of DSSC.     

Synthesis and characterization of anatase TiO2 nanotubes and their use in dye-sensitized solar cells

Anatase TiO₂ nanotubes (NTs) with the diameter of about 12 nm and the length of several hundreds nanometers were synthesized by hydrothermal method. The samples were characterized by X-ray diffraction (XRD), transmitting electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and Brunauer–Emmet–Teller (BET) measurements. The NTs are used to make composites photoanode with pristine TiO₂ nanoparticles in dye-sensitized solar cells (DSSCs). It was found that the NT/nanoparticle ratio had a pronounced impact on the performance of solar cells. The electrode composite has better photoelectric properties than the full nanoparticle and NTs solar cells. The optimum content NTs, was found to be 5%, at which content the incident photon to current efficiency was about 63.1%, an 13.8% increment compared to that using full P25 under the same condition.     

LiFePO<Subscript>4</Subscript>/TiO<Subscript>2</Subscript>/Pt composite film used as effective and robust counter electrode for dye sensitized solar cells

A series of composite films based on LiFePO₄/TiO₂/Pt were synthesized and used as counter electrodes for dye sensitized solar cells (DSSCs). The composites are characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and Brunauer–Emmett–Teller (BET). These analysis results demonstrate that the crystal structure of LiFePO₄ in composite is not changed, and the prepared LiFePO₄/TiO₂/Pt composite films hold a rough surface and porous structure which provide more catalytic activity sites for I₃ ^? reduction and more space for I^?/I₃ ^? diffusion. The DSSC based on LiFePO₄/TiO₂/Pt composite CEs shows a high power conversion efficiency of 6.23% at a low Pt dosage of 2%, comparable to the conventional magnetron sputtering Pt CE (6.31%). The electrochemical analysis reveals that the presented composite CEs have good electrocatalytic activity and low charge transfer resistance. Furthermore, the DSSCs based on LiFePO₄/TiO₂/Pt composite CE exhibit high stability under the continuous tests condition and electrolyte soaking. The results suggest that this LiFePO₄-based composite film could be a perspective electrode for practical application of DSSCs and it maybe provide a potential for further research about photo-charging lithium-ion batteries.     

Progress in nanostructured photoanodes for dye-sensitized solar cells

Solar cells represent a principal energy technology to convert light into electricity. Commercial solar cells are at present predominately produced by single- or multi-crystalline silicon wafers. The main drawback to silicon-based solar cells, however, is high material and manufacturing costs. Dye-sensitized solar cells (DSSCs) have attracted much attention during recent years because of the low production cost and other advantages. The photoanode (working electrode) plays a key role in determining the performance of DSSCs. In particular, nanostructured photoanodes with a large surface area, high electron transfer efficiency, and low electron recombination facilitate to prepare DSSCs with high energy conversion efficiency. In this review article, we summarize recent progress in the development of novel photoanodes for DSSCs. Effect of semiconductor material (e.g. TiO₂, ZnO, SnO₂, N₂O₅, and nano carbon), preparation, morphology and structure (e.g. nanoparticles, nanorods, nanofibers, nanotubes, fiber/particle composites, and hierarchical structure) on photovoltaic performance of DSSCs is described. The possibility of replacing silicon-based solar cells with DSSCs is discussed.     

Ultrafast Flame Annealing of TiO2 Paste for Fabricating Dye‐Sensitized and Perovskite Solar Cells with Enhanced Efficiency

Mesoporous TiO₂ nanoparticle (NP) films are broadly used as electrodes in photoelectrochemical cells, dye‐sensitized solar cells (DSSCs), and perovskite solar cells (PSCs). State‐of‐the‐art mesoporous TiO₂ NP films for these solar cells are fabricated by annealing TiO₂ paste‐coated fluorine‐doped tin oxide glass in a box furnace at 500 °C for ≈30 min. Here, the use of a nontraditional reactor, i.e., flame, is reported for the high throughput and ultrafast annealing of TiO₂ paste (≈1 min). This flame‐annealing method, compared to conventional furnace annealing, exhibits three distinct benefits. First, flame removes polymeric binders in the initial TiO₂ paste more completely because of its high temperature (≈1000 °C). Second, flame induces strong interconnections between TiO₂ nanoparticles without affecting the underlying transparent conducting oxide substrate. Third, the flame‐induced carbothermic reduction on the TiO₂ surface facilitates charge injection from the dye/perovskite to TiO₂. Consequently, when the flame‐annealed mesoporous TiO₂ film is used to fabricate DSSCs and PSCs, both exhibit enhanced charge transport and higher power conversion efficiencies than those fabricated using furnace‐annealed TiO₂ films. Finally, when the ultrafast flame‐annealing method is combined with a fast dye‐coating method to fabricate DSSC devices, its total fabrication time is reduced from over 3 h to ≈10 min.     

Dye-sensitized solar cells based on composite TiO<Subscript>2</Subscript> nanoparticle–nanorod single and bi-layer photoelectrodes

TiO₂ nanoparticle (NP), composite TiO₂ nanoparticle–nanorod (NP–NR) and bi-layer TiO₂ nanoparticle/nanorod (NP/NR) with the optimized diameter of NRs had been prepared as anode layer in dye-sensitized solar cells (DSSCs). Morphology and thickness of anode layers were provided by field emission scanning electron microscope (FE-SEM) and scanning electron microscopy (SEM) devices. Current density–voltage diagrams were prepared by potentiostat and solar simulator devices at air mass (AM) 1.5. It is determined that DSSCs based on composite NP–NR photoelectrode had the best conversion efficiency of 5.07%. Also, the results of the electrochemical modelling of these DSSCs indicated that solar cells based on NP–NR electrode had the highest electron transport time (τ _d) of 312.87 ms, electrons’ recombination lifetime (τ _n) of 130.4 ms and the lowest transfer resistance (R _ct) as well as transport resistance (R _t) of 22.46 and 9.4 Ω, respectively.     

Effect of TiO2 nanotube length and lateral tubular spacing on photovoltaic properties of back illuminated dye sensitized solar cell

The main objective of this study is to show the effect of TiO₂ nanotube length, diameter and intertubular lateral spacings on the performance of back illuminated dye sensitized solar cells (DSSCs). The present study shows that processing short TiO₂ nanotubes with good lateral spacings could significantly improve the performance of back illuminated DSSCs. Vertically aligned, uniform sized diameter TiO₂ nanotube arrays of different tube lengths have been fabricated on Ti plates by a controlled anodization technique at different times of 24, 36, 48 and 72?h using ethylene glycol and ammonium fluoride as an electrolyte medium. Scanning electron microscopy (SEM) showed formation of nanotube arrays spread uniformly over a large area. X-ray diffraction (XRD) of TiO₂ nanotube layer revealed the presence of crystalline anatase phases. By employing the TiO₂ nanotube array anodized at 24?h showing a diameter ??80?nm and length ??1·5???m as the photo-anode for back illuminated DSSCs, a full-sun conversion efficiency (??) of 3·5 % was achieved, the highest value reported for this length of nanotubes.     

Rutile TiO2 microspheres with exposed nano-acicular single crystals for dye-sensitized solar cells

Uniquely structured rutile TiO₂ microspheres with exposed nano-acicular single crystals have been successfully synthesized via a facile hydrothermal method. After calcination at 450 °C for 2 h, the rutile TiO₂ microspheres with a high surface area of 132 m²/g have been utilized as a light harvesting enhancement material for dye-sensitized solar cells (DSSCs). The resultant DSSCs exhibit an overall light conversion efficiency of 8.41% for TiO₂ photoanodes made of rutile TiO₂ microspheres and anatase TiO₂ nanoparticles (mass ratio of 1:1), significantly higher than that of pure anatase TiO₂ nanoparticle photoanodes of similar thickness (6.74%). Such a significant improvement in performance can be attributed to the enhanced light harvesting capability and synergetic electron transfer effect. This is because the photoanodes made of rutile TiO₂ microsphere possess high refractive index which improves the light utilisation efficiency, suitable microsphere core sizes (450–800 nm) to effectively scatter visible light, high surface area for dye loading, and synergetic electron transfer effects between nanoparticulate anatase and nano-acicular rutile single crystals phases giving high electron collection efficiency.      

Ionic liquid-assisted hydrothermal synthesis of TiO2 nanoparticles and its applications towards the photocatalytic activity and electrochemical sensor

This work reports the synthesis of TiO₂ nanoparticles via ionic liquid-assisted hydrothermal method at 130?°C for two days. The obtained product was characterised by various techniques. The X-ray diffraction data reveal the anatase phase TiO₂ nanoparticles with crystallite size 37 nm. The Fourier transform infrared spectrum shows a band at 400 cm^?1 due to Ti–O–Ti stretching vibration, in addition to the presence of ionic liquid. The UV–Vis spectrum of TiO₂ nanoparticles shows an absorption band at 314 nm which indicates a blueshift compared with that of bulk TiO_2. The transmission electron microscopy images show almost spherical-shaped nanoparticles with an average diameter of 40–80 nm. TiO₂ nanoparticles exhibit excellent photocatalytic activity for the degradation of trypan blue, and also help in the reduction of Cr⁺⁶ to Cr⁺³. TiO₂ nanoparticles modified glassy carbon electrode exhibits better electrocatalytic oxidation towards dopamine compared with bare glassy carbon electrode.     

Rapid thermal melted TiO2 nano-particles into ZnO nano-rod and its application for dye sensitized solar cells

TiO₂ nano-particles with an anchored ZnO nano-rod structure were synthesized using the hydrothermal method to grow ZnO nano-rods and coated TiO₂ nano-particles on ZnO nano-rods using the rapid thermal annealing method on ITO conducting glass pre-coated with nano porous TiO₂ film. The XRD study showed that there was little difference in crystal composition for various types of TiO₂ nano-particles anchored to ZnO nano-rods. The as-prepared architecture was characterized using field-emission scanning electron microscopy (FE-SEM). Films with TiO₂ nano-particles anchored to ZnO nano-rods were used as electrode materials to fabricate dye sensitized solar cells (DSSCs). The best solar energy conversion efficiency of 2.397% was obtained by modified electrode material, under AM 1.5 illumination, achieved up to J_sc = 15.382 mA/cm², V_oc = 0.479 V and fill factor = 32.8%.     

Effect of atomic layer deposited ultra thin HfO2 and Al2O3 interfacial layers on the performance of dye sensitized solar cells

The objective of this work was to investigate the improvement in performance of dye sensitized solar cells (DSSCs) by depositing ultra thin metal oxides (hafnium oxide (HfO₂) and aluminum oxide (Al₂O₃)) on mesoporous TiO₂ photoelectrode using atomic layer deposition (ALD) method. Different thicknesses of HfO₂ and Al₂O₃ layers (5, 10 and 20 ALD cycles) were deposited on the mesoporous TiO₂ surface prior to dye loading process used for fabrication of DSSCs. It was observed that the ALD deposition of ultrathin oxides significantly improved the performance of DSSCs and that the improvement in the DSSC performance depends on the thickness of the deposited HfO₂ and Al₂O₃ films. Compared to a reference DSSC the incorporation of a HfO₂ layer resulted in 69% improvement (from 4.2 to 7.1%) in the efficiency of the cell and incorporation of Al₂O₃ (20 cycles) resulted in 19% improvement (from 4.2 to 5.0%) in the efficiency of the cell. These results suggest that ultrathin metal oxide layers affect the density and the distribution of interface states at the TiO₂/organic dye and TiO₂/liquid electrolyte interfaces and hence can be utilized to treat these interfaces in DSSCs.     

Tuning the dye aerosol impaction and TiO2 nanoparticle stacking structures for High-Efficiency Dye-Sensitized solar cells

The rapid manufacturing of high-efficiency dye-sensitized solar cells (DSSCs) is limited by the slow dye adsorption on TiO₂ nanoparticles (NPs)-accumulated photoelectrode using conventional dip-coating process. Therefore, we aim to accelerate the adsorption of dyes that are attached on TiO₂ NPs by employing an aerosol impactor. Herein the aerosolized dyes are designed to get deposited rapidly on the TiO₂ NPs-accumulated photoelectrode. In addition, to effectively trap the irradiated sunlight in DSSCs, we assemble the photoelectrodes incorporated with bilayered TiO₂ thin films comprising small TiO₂ NPs-based underlayer and large TiO₂ NPs-based overlayer as dye-supporting and light-scattering mediums, respectively. Furthermore, the effects of dye aerosol impaction and TiO₂ stacking structures on the efficiency of DSSCs are examined. The power conversion efficiency (PCE) of DSSCs comprising a N719 dye-supporting layer treated with dip-coating process was determined as ～ 5.67%; however, when the bilayered TiO₂ thin films with an optimized thickness ratio of light-scattering overlayer and dye-supporting underlayer were coated with N719 dyes using dye aerosol impactor, the resulting PCE increased to ～ 7.46%. This suggests that the photovoltaic characteristics of DSSCs can be enhanced considerably using the effective TiO₂ NP stacking structures coated with rapid, uniform, and strong aerosol dye adsorption throughout the TiO₂-based photoelectrodes.     

Rose bengal-sensitized nanocrystalline ceria photoanode for dye-sensitized solar cell application

For efficient charge injection and transportation, wide bandgap nanostructured metal oxide semiconductors with dye adsorption surface and higher electron mobility are essential properties for photoanode in dye-sensitized solar cells (DSSCs). TiO₂-based DSSCs are well established and so far have demonstrated maximum power conversion efficiency when sensitized with ruthenium-based dyes. Quest for new materials and/or methods is continuous process in scientific investigation, for getting desired comparative results. The conduction band (CB) position of CeO₂ photoanode lies below lowest unoccupied molecular orbital level (LUMO) of rose bengal (RB) dye. Due to this, faster electron transfer from LUMO level of RB dye to CB of CeO₂ is facilitated. Recombination rate of electrons is less in CeO₂ photoanode than that of TiO₂ photoanode. Hence, the lifetime of electrons is more in CeO₂ photoanode. Therefore, we have replaced TiO₂ by ceria (CeO₂) and expensive ruthenium-based dye by a low cost RB dye. In this study, we have synthesized CeO₂ nanoparticles. X-ray diffraction (XRD) analysis confirms the formation of CeO₂ with particle size ～7 nm by Scherrer formula. The bandgap of 2.93 eV is calculated using UV–visible absorption data. The scanning electron microscopy (SEM) images show formation of porous structure of photoanode, which is useful for dye adsorption. The energy dispersive spectroscopy is in confirmation with XRD results, confirming the presence of Ce and O in the ratio of 1:2. UV–visible absorption under diffused reflectance spectra of dye-loaded photoanode confirms the successful dye loading. UV–visible transmission spectrum of CeO₂ photoanode confirms the transparency of photoanode in visible region. The electrochemical impedance spectroscopy analysis confirms less recombination rate and more electron lifetime in RB-sensitized CeO₂ than TiO₂ photoanode. We found that CeO₂ also showed with considerable difference between dark and light DSSCs performance, when loaded with RB dye. The working mechanism of solar cells with fluorine-doped tin oxide (FTO)/CeO₂/RB dye/carbon-coated FTO is discussed. These solar cells show V _OC ～360 mV, J _SC ～0.25 mA cm ^?2 and fill factor ～63% with efficiency of 0.23%. These results are better as compared to costly ruthenium dye-sensitized CeO₂ photoanode.     

Preparation and characterization of TiO2 anode film with spinodal phase separation structure in dye-sensitized solar cells

Low electronic transmission efficiency and high charge recombination are the existing problems of photoanode film in traditional dye sensitized solar cells (DSSCs). This paper put forward the photoanode TiO₂ films with spinodal phase separation structure (SPSS) and continuous TiO₂ skeleton which were triggered by the photopolymerization of organic monomers in a photomonomer-inorganic precursor system. The photoanode TiO₂ films fabricated by different precursor solution compositions and different coating layers were characterized mainly by scanning electron microscopy (SEM), photocatalysis and photoelectric performance test. The results indicated that, the as-prepared TiO₂ anode film with seven coating layers and heat treated at 500 °C showed higher photoelectric conversion efficiency at about 2% than that of other samples with less coating layers and lower heat treatment temperature. The film also showed excellent photocatalytic activity by using methylene blue (MB) dye as a model organic substrate under fluorescent lamp irradiation. It is suggested that the film with SPSS structure has the potential to improve the electronic transmission efficiency and reduce the carrier recombination due to its particular structure, higher surface area, and lack of bottleneck in electronic transmission. It is worth noting that the SPSS structure provides new ideas to develop new photoanode films and further improve the photoelectric conversion performance of the DSSC in future.