Search Results (38)

In a solid-state dye-sensitized solar cell, a fast-ion conducting (σ_25°C > 10⁻⁴ S cm⁻¹) solid redox mediator (SRM; electrolyte) helps in fast dye regeneration and back-electron transfer inhibition. In this work, we synthesized solid Co^2+/3+ redox mediators using a [(1 − x)succinonitrile: x poly(ethylene oxide)] matrix, LiX, Co(tris-2,2′-bipyridine)₃(bis(trifluoromethyl) sulfonylimide)₂, and Co(tris-2,2′-bipyridine)₃(bis(trifluoromethyl) sulfonylimide)₃ via the solution-cast method, and the results were compared with those of their acetonitrile-based liquid counterparts. The notation x is a weight fraction (=0, 0.5, and 1), and X represents an anion. The anion was either bis(trifluoromethyl) sulfonylimide [TFSI⁻; ionic size, 0.79 nm] or trifluoromethanesulfonate [Triflate⁻; ionic size, 0.44 nm]. The delocalized electrons and a low value of lattice energy for the anions made the lithium salts highly dissociable in the matrix. The electrolytes exhibited σ_25°C ≈ 2.1 × 10⁻³ (1.5 × 10⁻³), 7.2 × 10⁻⁴ (3.1 × 10⁻⁴), and 9.7 × 10⁻⁷ (6.3 × 10⁻⁷) S cm⁻¹ for x = 0, 0.5, and 1, respectively, with X = TFSI⁻ (Triflate⁻) ions. The log σ–T⁻¹ plot portrayed a linear curve for x = 0 and 1, and a downward curve for x = 0.5. The electrical transport study showed σ(TFSI⁻) > σ(Triflate⁻), with lower activation energy for TFSI⁻ ions. The anionic effect increased from x = 0 to 1. This effect was explained using conventional techniques, such as Fourier transform infrared spectroscopy (FT-IR), X-ray diffractometry (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), UV–visible spectroscopy (UV-vis), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). Full article

Redox mediators comprising I⁻, Co³⁺, and Ti₃C₂Tx MXene were applied to dye-sensitized solar cells (DSCs). In the as-prepared DSCs (I-DSCs), wherein hole conduction occurred via the redox reaction of I⁻/I₃⁻ ions, the power conversion efficiency (PCE) was not altered by the addition of Ti₃C₂Tx MXene. The I-DSCs were exposed to light to produce Co²⁺/Co³⁺-based cells (Co-DSCs), wherein the holes were transferred via the redox reaction of Co²⁺/Co³⁺ ions. A PCE of 9.01% was achieved in a Co-DSC with Ti₃C₂Tx MXene (Ti₃C₂Tx-Co-DSC), which indicated an improvement from the PCE of a bare Co-DSC without Ti₃C₂Tx MXene (7.27%). It was also found that the presence of Ti₃C₂Tx MXene in the redox mediator increased the hole collection, dye regeneration, and electron injection efficiencies of the Ti₃C₂Tx-Co-DSC, leading to an improvement in both the short-circuit current and the PCE when compared with those of the bare Co-DSC without MXene. Full article

Dyes have played a pivotal role in the advancement of modern dye-sensitized solar cells (DSCs), as they not only facilitate light harvesting, but also serve as blocking layers to impede recombination. In this study, we conducted a systematic investigation to elucidate the influence of dye coverage on the photovoltaic parameters of copper-electrolyte-based DSCs by precisely controlling the dye coverage on the TiO₂ substrate using D35 organic dye solutions with varying concentrations. The dye loading increased proportionally with the increase in dye concentrations until it reached saturation at a concentration of 0.2 mM. However, an optimal dye concentration of 0.1 mM was determined in terms of achieving the highest photovoltaic performance, under both outdoor and indoor light conditions. Notably, a maximum power conversion efficiency (PCE) of 6.50 ± 0.25% under outdoor illumination (100 mW/cm²) and 10.48 ± 0.30% under indoor light (1000 lux, WW CFL) was attained using a 0.1 mM D35 dye concentration. Additionally, the dark current and ideality factor (m) were found to be minimized at the 0.1 mM dye concentration. Furthermore, the ideality factor (m) exhibited disparities between indoor and outdoor light conditions. The lifetime obtained from electrochemical impedance spectroscopy (EIS) measurements correlated well with the ideality factor (m) and dark current. Notably, electron injection, dye regeneration, charge collection, and ion diffusion were observed to be independent of the dye coverage. Full article

Nanostructured metal sulfides such as copper sulfide (CUS) form from single-source precursors (SSPs) and are cost-friendly materials that can be used in a one-pot approach with potential applications in dye-sensitizer solar cells (DSCs). This is an attractive pathway that allows the careful control of tailoring the design of the nanostructures with slight variations in the mixture conditions to form uniform nanoparticles and enhance the performance of DSCs. We report on the optical, structural, and morphological properties of CuS as photosensitizers and their application in QDSCs using characterization techniques such as cyclic voltammetry (CV), current–voltage (I-V), UV-Vis spectroscopy (UV-Vis), X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), etc. The UV-Vis reveals that the band gap for the three samples is found at 2.05–2.87 eV, confirming them as suitable materials for solar cells. The XRD peaks for the three CuS nanoparticles harmonized very well with hexagonal CuS. The thermal gravimetric (TGA) suitability of the three complexes shows a two-step decomposition within the temperature range of 125–716 °C, with a final residue of 2–4%. CV curves for three samples show that none of the developed metal sulfides exhibits a peak indicative of limited catalytic activity in the iodine electrolyte. The I-V overall energy conversion efficiency (η%) of 4.63% for the CuSb photosensitizer is linked to the wide electronic absorption spectrum and better relative dye loading. The synthesis of photosensitizers from a trioctylphosphine oxide (TOPO) capping agent shows improved efficiency compared to our previous studies, which used hexadecylamine as a coordinating solvent. Full article

This work aimed to show the possibility of applying anthocyanins extracted from blueberries following a straightforward path as potential impregnation dyes in dye-sensitized solar cells (DSSCs), particularly in the presence of co-adsorbents, such as silver nanoparticles, as an alternative in order to profit from large amounts of discarded fruits. Following a simple procedure, anthocyanins (mainly delphinidin-3-glucoside) were obtained from blueberries (Southern Highbush type). Complete characterization was carried out in order to prove the utility of delphinidin-3-glucoside as a sensitizer in DSSCs. The analyzed anthocyanin is suitable for sensitizing because of its high molar absorptivity values within the visible region of the light spectra, the adsorption ability to a FTO/TiO₂ electrode (FTO, fluorine-doped tin oxide) as confirmed by Fourier transform infrared (FTIR) as well as thermogravimetry coupled to differential scanning calorimetry (TG-DSC), a potential oxidation value near 1 V, and adequate thermal as well as light stabilities. Moreover, the cell’s conversion efficiency is improved in the presence of silver nanoparticles, reaching 0.24% (nearly a 25% increase). The sum of all these characteristics points to the application of delphinidin-3-glucoside as a sensitizer in DSSCs, offering a technological use with potential interest for countries where agricultural production offers an abundant origin of extraction. Full article

Dye-sensitized solar cells (DSCs) remain an interesting photovoltaic concept, although recent times have seen their envisioned broad-scale applications being replaced with more niche ones. Nevertheless, as a key component of DSCs, titanium(IV) oxide (TiO₂) must be produced in a large volume, low cost, and highly reproducible manner. Degussa P25 remains a benchmark TiO₂ product, addressing the first two of the above points very well. Post-treatment processes that may also be carried out on a large scale give some hope to addressing the reproducibility issue. This paper builds on our previous works wherein mixed-phase P25 (anatase + rutile + amorphous TiO₂) was converted into an amorphous free form by selectively dissolving and recrystallizing the amorphous component. Here we investigated the performance of metal-free organic dye (D149)-based DSCs with three different TiO₂ films: (1) as-received P25 (TiO₂-P25), (2) amorphous-free P25 (TiO₂-HP25), and (3) anatase nanoparticles obtained from Dyesol (TiO₂-DSL). DSCs based on TiO₂-HP25 showed comparable performance (5.8 ± 0.2% PCE) to DSCs based on the TiO₂-DSL (5.8 ± 0.4% PCE) and substantially higher than for devices based on the as-obtained P25 nanoparticles (3.9 ± 0.4% PCE). The enhancement resulting from the post-processing of P25 derives from simultaneous increases in photo-current density (J_sc), open-circuit voltage (V_OC), and the fill factor (FF), due to enhancing the dye-loading capability and the charge-transport efficiency (suppressing the electron recombination) as a result of the removal of amorphous barriers and associated defect states. This is in line with enhancing DSC performance based on the organometallic N719 dye we reported previously. However, the photoanode material based on abundant P25 TiO₂ sensitized with high-extinction-coefficient organic D149 dye can be adopted as a cost-effective DSC as an alternative to relatively high-cost DSCs based on the commercial anatase TiO₂ sensitized with organometallic N719 dye. Full article

This work investigates an electrochemical impedance analysis based on synthesized TiO₂ nanofibers (NFs) photoanodes, which were fabricated via electrospinning and calcination. The investigated photoanode substrate NFs were studied in terms of physicochemical tools to investigate their morphological character, crystallinity, and chemical contents via scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS), and X-ray diffraction (XRD) analyses. As a result, the studied photoanode substrate NFs were applied to fabricate dye-sensitized solar cells (DSCs), and the electrochemical impedance analysis (EIS) was studied in terms of equivalent circuit fitting and impacts of N-doping, the latter of which was approved via XPS analysis. N-doping has a considerable role in the enhancement of charge transfers, which could be due to the strong interactions between active-site N atoms and the used photosensitizer. Full article

Perovskite solar cells (PSCs) and dye-sensitized solar cells (DSCs) both represent promising strategies for the sustainable conversion of sunlight into electricity and fuels. However, a few flaws of current devices hinder the large-scale establishment of such technologies. On one hand, PSCs suffer from instabilities and undesired phenomena mostly linked to the perovskite/hole transport layer (HTL) interface. Most of the currently employed organic HTL (e.g., Spiro-OMeTAD) are supposed to contribute to the perovskite decomposition and to be responsible for charge recombination processes and polarization barriers. On the other hand, power conversion efficiencies (PCEs) of DSCs are still too low to compete with other conversion technologies. Tandem cells are built by assembling p-type and n-type DSCs in a cascade architecture and, since each dye absorbs on a different portion of the solar spectrum, the harvesting window is increased and the theoretical efficiency limit for a single chromophore (i.e., the Shockley–Queisser limit) is overcome. However, such a strategy is hindered by the lack of a p-type semiconductor with optimal photocathode features. Nickel oxide has been, by far, the first-choice inorganic p-type semiconductor for both PV technologies, but its toxicity and non-optimal features (e.g., too low open circuit voltage and the presence of trap states) call for alternatives. Herein, we study of three p-type semiconductors as possible alternative to NiO, namely CuI, CuSCN and Cu₂O. To this aim, we compare the structural and electronic features of the three materials by means of a unified theoretical approach based on the state-of-the art density functional theory (DFT). We focus on the calculation of their valence band edge energies and compare such values with those of two widely employed photo-absorbers, i.e., methylammonium lead iodide (MAPI) and the triple cation MAFACsPbBrI in PSCs and P1 and Y123 dyes in DSCs, given that the band alignment and the energy offset are crucial for the charge transport at the interfaces and have direct implications on the final efficiency. We dissect the effect a copper vacancy (i.e., intrinsic p-type doping) on the alignment pattern and rationalize it from both a structural and an electronic perspective. Our data show how defects can represent a crucial degree of freedom to control the driving force for hole injection in these devices. Full article

ZnO nanorods were formed by chemical bath deposition on fluorine–doped tin oxide (FTO) glass and the photovoltaic performance of ZnO-based dye-sensitized solar cells (DSCs) was investigated. A DSC with 8 h-grown ZnO nanorods showed a higher power conversion efficiency (PCE) than devices with 4, 6, and 10 h-grown ones. Further improvement in PCE was achieved in a cell with a silver-ion-deposited ZnO/FTO electrode. By deposition of Ag⁺ on the surface of the 8 h-grown ZnO nanorods, the dye-loading amount increased by approximately 210%, compared to that of pristine ZnO nanorods, resulting in a 1.8-times higher PCE. A DSC with the pristine ZnO/FTO electrode showed a PCE of 0.629%, while in a device with the silver-ion-deposited ZnO/FTO, the PCE increased to 1.138%. In addition, interfacial resistance at the ZnO/dye/electrolyte was reduced to approximately 170 Ω from 460 Ω for the control cell with the pristine ZnO/FTO. We attributed the higher dye-loading amount in the silver-ion-deposited ZnO/FTO to the electrostatic attraction between the positively charged ZnO and carboxylate anions (–COO⁻) of the N719 dyes. Full article

The fabrication of colorless and see-through dye-sensitized solar cells (DSCs) requires the photosensitizers to have little or no absorption in the visible light region of the solar spectrum. However, a trade-off between transparency and power conversion efficiency (PCE) has to be tackled, since most transparent DSCs are showing low PCE when compared to colorful and opaque DSCs. One strategy to increase PCE is applying two cosensitizers with selective conversion of the UV and NIR radiation, therefore, the non-visible part only is absorbed. In this study, we report synthesis of novel five UV-selective absorbers, based on diimide and Schiff bases incorporating carboxyl and pyridyl anchoring groups. A systematic computational investigation using density functional theory (DFT) and time-dependent DFT approaches was employed to evaluate their prospect of application in transparent DSCs. Experimental UV/Vis absorption spectra showed that all dyes exhibit an absorption band covering the mid/near-UV region of solar spectrum, with a bathochromic shift and a hyperchromic shifts for Py-1 dye. Computational results showed that the studied dyes satisfied the basic photophysical and energetics requirements of operating DSC as well as the stability and thermodynamical spontaneity of adsorption onto surface of TiO₂. However, results revealed outperformance of the thienothiophene core-containing Py-1 UV-dye, owing to its advantageous structural attributes, improved conjugation, intense emission, large Stokes shift and maximum charge transferred to the anchor. Chemical compatibility of Py-1 dye was then theoretically investigated as a potential cosensitizer of a reference VG20-C2 NIR-dye. By the judicious selection of pyridyl anchor-based UV-absorber (Py-1) and carboxyl anchor-based NIR-absorber (VG20), the advantage of the optical complementarity and selectivity of different TiO₂-adsorption-site (Lewis- and Bronsted-acidic) can be achieved. An improved overall PCE is estimated accordingly. Full article

A dye-sensitized solar cell (DSC) is the third generation of solar technology, utilizing TiO₂ nanoparticles with sizes of 20–30 nm as the photoelectrode material. The integration of smaller nanoparticles has the advantage of providing a larger surface area, yet the presence of grain boundaries is inevitable, resulting in a higher probability of electron trapping. This study reports on the improvement of charge transport through the integration of quantum dot (QD) TiO₂ with a size of less than 10 nm as the dye absorption photoelectrode layer. The QD TiO₂ samples were synthesized through sol–gel and reflux methods in a controlled pH solution without surfactants. The synthesized samples were analyzed using microscopic, diffraction, absorption, as well as spectroscopic analyses. A current–voltage and impedance analysis was used to evaluate the performance of a DSC integrated with synthesized TiO₂ as the photoelectrode material. The sample with smaller crystallite structures led to a large surface area and exhibited a higher dye absorption capability. Interestingly, a DSC integrated with QD TiO₂ showed a higher steady-state electron density and a lower electron recombination rate. The shallow distribution of the trap state led to an improvement of the electron trapping/de-trapping process between the Fermi level and the conduction band of oxide photoelectrode material, hence improving the lifetime of generated electrons and the overall performance of the DSC. Full article

The effects of different I₂ concentrations and different ionic liquids (ILs) in the electrolyte on the performances of dye-sensitized solar cells (DSCs) containing an iron(II) N-heterocyclic carbene dye and containing the I^–/I₃^– redox shuttle have been investigated. Either no I₂ was added to the electrolyte, or the initial I₂ concentrations were 0.02, 0.05, 0.10, and 0.20 M. The short-circuit current density (J_SC), open-circuit voltage (V_OC), and the fill factor (ff) were influenced by changes in the I₂ concentration for all the ILs. For 1-hexyl-3-methylimidazole iodide (HMII), low V_OC and low ff values led to poor DSC performances. Electrochemical impedance spectroscopy (EIS) showed the causes to be increased electrolyte diffusion resistance and charge transfer resistance at the counter electrode. DSCs containing 1,3-dimethylimidazole iodide (DMII) and 1-ethyl-3-methylimidazole iodide (EMII) showed the highest J_SC values when 0.10 M I₂ was present initially. Short alkyl substituents (Me and Et) were more beneficial than longer chains. The lowest values of the transport resistance in the photoanode semiconductor were found for DMII, EMII, and 1-propyl-2,3-dimethylimidazole iodide (PDMII) when no I₂ was added to the initial electrolyte, or when [I₂] was less than 0.05 M. Higher [I₂] led to decreases in the diffusion resistance in the electrolyte and the counter electrode resistance. The electron lifetime and diffusion length depended upon the [I₂]. Overall, DMII was the most beneficial IL. A combination of DMII and 0.1 M I₂ in the electrolyte produced the best performing DSCs with an average maximum photoconversion efficiency of 0.65% for a series of fully-masked cells. Full article

The leakage and volatilization of liquid electrolytes limit the commercialization of dye-sensitized solar cells (DSCs). As solid-state (ss) hole-transporting materials, free from leakage and volatilization, biscarbazole-based polymers with different molecular weights (PBCzA-H (21,200 g/mol) and PBCzA-L (2450 g/mol)) were applied in combination with additives to produce ssDSCs. An ssDSC with PBCzA-H showed a better short-circuit current (J_sc), open-circuit voltage (V_oc), and fill factor (FF) than a device with PBCzA-L, resulting in 38% higher conversion efficiency. Compared to the PBCzA-L, the PBCzA-H with a higher molecular weight showed faster hole mobility and larger conductivity, leading to elevations in J_sc via rapid hole transport, V_oc via rapid hole extraction, and FF via lowered series and elevated shunt resistances. Thus, it is believed that PBCzA-H is a useful candidate for replacing liquid electrolytes. Full article

Most organic dyes synthesized for dye-sensitized solar cells (DSC) use a single linker group to bind to the metal oxide photo-anode. Here we describe the synthesis and testing of two new triphenylamine dyes containing either two carboxylic acids 5-[2-(4-diphenylamino-phenyl)-vinyl]-isophthalic acid (10) or two cyanoacrylic acids (2Z, 2′Z)-3, 3′-(5-((E)-4-(diphenylamino) styryl)-1, 3-phenylene) bis (2-cyanoacrylic acid) (8) as linker groups. Full characterization data are reported for these dyes and their synthetic intermediates. DSC devices have been prepared from these new dyes either by passive or fast dyeing and the dyes have also been tested in co-sensitized DSC devices leading to a PCE (η = 5.4%) for the double cyanoacrylate linker dye (8) co-sensitized with D149. The dye:TiO₂ surface interactions and dye excitations are interpreted using three modelling methods: density functional theory (at 0 K); molecular dynamics (at 298 K); time dependent density functional theory. The modelling results show the preferred orientation of both dyes on an anatase (1 0 1) TiO₂ surface to be horizontal, and both the simulated and experimental absorption spectra of the dye molecules indicate a red shifted band for (8) compared to (10). This is in line with broader light harvesting and J_sc for (8) compared to (10). Full article