Dye-sensitized Solar Cells Research Articles

Open-Cage Copper Complexes Modulate Coordination and Charge Transfer.

This study presents a novel copper-based redox shuttle that employs the PY5 pentadentate polypyridyl ligand in a dye-sensitized solar cell (DSSC). The [Cu(PY5)]2+ complex exhibits a unique five-coordinate square pyramidal geometry, characterized by a strategically labile axial position, to facilitate efficient dye regeneration while minimizing electron recombination, thereby enhancing DSSC performance. Notably, the inclusion of 4-tert-butylpyridine (TBP) as an additive is shown to significantly modulate the electrochemical and photophysical properties of the copper complexes, attributed to its coordination to the vacant axial site. This interaction leads to an improved open-circuit voltage and overall device efficiency, with the complexes achieving promising efficiencies under standard solar irradiance. The findings underscore the potential of utilizing copper-based redox shuttles with designed ligand geometries to overcome the limitations of current DSSC materials, opening new avenues for the design and optimization of solar energy conversion devices. This work not only contributes to the fundamental understanding of the behavior of copper complexes in DSSCs but also paves the way for future research aimed at exploiting the full potential of such geometrical and electronic configurations for the development of more robust and efficient solar energy solutions.

Dielectrically modified lanthanum (La3+) doped LaxCe2-xO3/ SnO2 nanocomposites for technological applications

Metal oxide nanocomposites are in high demand due to their versatile properties and wide range of applications in modern technology, including energy storage devices, electrode material design, and dye-sensitized solar cells (DSSCs). Nanocomposites of LaxCe2-xO3/SnO2 were prepared via sol-gel method. This research work has reported a detailed study of the dielectric properties of LaxCe2-xO3/SnO2 nanocomposites at high frequencies (1 MHz–3 GHz). After forming a mixed phase, the surface morphology was confirmed by HR-TEM, resulting in a significant change in particle size and distribution. Different polarization stages, the effect of grain boundaries and the relaxation phenomenon were discussed with the impact of La3+ contents. Relaxation behaviour at high frequency was examined due to strong polarization. In addition, a high dielectric constant value at high frequency shows that these nanocomposites are eligible to store more energy. At x = 0.6, the maximum value of the dielectric constant was observed. Results demonstrate that LaxCe2-xO3/SnO2 nanocomposites are competent for microwave, high-frequency devices and energy storage applications.

Perovskite-structured ceramic zinc titanate nanomaterials: A comparative study of photovoltaic and synthetic approaches

Ternary metal oxide materials are being explored as potential electrode materials for dye-sensitized solar cells due to their adjustable electronic band structures through elemental composition modifications. Perovskite materials based on zinc and titanium have been utilised in DSSC and show moderate performance. Considerable research has been dedicated to this field to improve their performances. The focus was primarily on the synthetic variabilities due to their impact on performance under varying synthetic conditions. According to this perspective, no comparative studies have found superior methodologies for utilising zinc titanate as a potential photoanode in DSSC. We synthesised a zinc titanate material using thermal, sol-gel, and plasma irradiation techniques. The materials' structural variability was analysed using PXRD and FT-IR techniques. A mixed-phase composition of spinel cubic and hexagonal has been identified. The SEM images provide insights into the particle distribution and morphology of the zinc titanate materials. Investigating absorption properties, band gap energy levels and aggregation behaviours provided initial insights into the potential use of the three zinc titanate materials. The DSSC devices were fabricated using zinc titanate materials with varying properties, and the results are detailed in this discussion. Based on the findings, the plasma and thermal irradiation techniques yielded more favourable zinc titanate materials for dye-sensitized solar cell use. The efficiency reached 0.04 % when operating with polymeric gel electrolytes.

The Effect of Mixed Dye Composition of Anthocyanin-Chlorophyll on DSSC Efficiency on TiO2/ZnO Semiconductors

The effect of mixed dye composition of anthocyanin-chlorophyll on DSSC efficiency on TiO2/ZnO semiconductors aims to determine the effect of using dye containing anthocyanin-chlorophyll on the absorbance value and work efficiency value of Dye Sensitized Solar Cell (DSSC). The TiO2/ZnO was deposited using the doctor blade method and the dye was made using the maceration method. The counter electrode was made on FTO glass coated by calcined battery carbon with temperature in 450°C. The DSSC assembly was arranged in a sandwich shape. Then electrolyte is dripped in the middle of the DSSC layer. Characterization tests were carried out to determine the dye absorbance value and gap energy value using a UV-Vis spectrophotometer. DSSC efficiency testing uses current and voltage (I-V) characterization. DSSC testing was carried out using a multimeter with a light source from sunlight. The results of UV-Vis characterization showed that the highest absorbance value was obtained for the kale-mangosteen peel dye at a wavelength of 530 nm with an absorbance of 5.234%. The TiO2/ZnO gap energy obtained using the touch plot method is 2.42 eV. The highest efficiency value was obtained from the kale-mangosteen peel dye mixture of 0.0286%. There was an increase in the DSSC efficiency value when the dyes were combined.

Enhancing Efficiency of Dye Sensitized Solar Cells by Coinage Metal Doping of Cyanidin-Silver Trimer Hybrids at TiO2 Support Based on Theoretical Study.

Identification of a natural-based sensitizer with optimal stability and efficiency for dye-sensitized solar cell (DSSC) application remains a challenging task. Previously, we proposed a new class of sensitizers based on bio-nano hybrids. These systems composed of natural cyanidin dyes interacting with silver nanoclusters (NCs) have demonstrated enhanced opto-electronic and photovoltaic properties. In this study, we explore the doping of silver nanocluster within a cyanidin-Ag3 hybrid employing Density Functional Theory (DFT) and its time-dependent counterpart (TDDFT). Specifically, we investigate the influence of coinage metal atoms (Au and Cu) on the properties of the cyanidin-Ag3 system. Our findings suggest that cyanidin-Ag2Au and cyanidin-AgAuCu emerge as the most promising candidates for improved light harvesting efficiency, increased two-photon absorption, and strong coupling to the TiO2 surface. These theoretical predictions suggest the viability of replacing larger silver NCs with heterometallic trimers such as Ag2Au or AgAuCu, presenting new avenues for utilizing bio-nano hybrids at the surface for DSSC application.

Synthesis and Performance Analysis of a Carbon-Doped Titania (C–TiO2) Counter Electrode (CE) for Dye-Sensitized Solar Cells (DSSCs)

Synthesis and Performance Analysis of a Carbon-Doped Titania (C–TiO2) Counter Electrode (CE) for Dye-Sensitized Solar Cells (DSSCs)

Fabrication of binder-free TiO2 P 25 films on flexible PET/ITO substrate for photoanode in dye-sensitized solar cells

In this work, TiO2 P 25 films for photoanode in dye-sensitized solar cells (DSSCs) have been fabricated using a flexible PET/ITO substrate with a low-temperature heating technique. Ammonium hydroxide/ethanol solution was used as an alternative binding agent to fabricate TiO2 paste, which can be removed at low-temperature heating. The conventional screen print method is still used in DSSC fabrication because it is a very cheap and easy technique. A hot-pressing method is also used to improve the quality of TiO2 films and the performance of DSSCs. The encapsulation technique used in the assembly of DSSC is expected to increase the stability of DSSC devices to prevent electrolyte leakage. The resulting TiO2 film shows the highest DSSC performance using the hot-pressing and encapsulation method with PCE 0.29%. The encapsulation technique increased the stability of DSSC devices with more extended durability than without encapsulation.

Exploring the Role of Central Metals in Bulky Phthalocyanines for Dye-Sensitized Solar Cells.

Two series of metallo-(Zn(II), Mg(II), and Ru(II)) and free-base phthalocyanines (Pcs) with a carboxyl anchoring group and well-established bulky peripheral substituents (either tert-butyl or bulky 2,6-diisopropylphenoxy) were synthesized and tested as sensitizers in dye-sensitized solar cells (DSSCs). The trend of photovoltaic efficiencies (PCEs) for free-base and metallo Pcs followed the order Zn(II)Pc>Mg(II)Pc≫H2Pc ≈ Ru(II)Pc regardless of the peripheral substitution. Higher efficiencies (4.95 versus 3.63 for the Zn(II) derivatives) were achieved with Pcs bearing the bulkier 2,6-diisopropylphenoxy group, indicating a lower aggregation and more suitable HOMO-LUMO levels. Furthermore, these derivatives showed a morelevant influence of the metal on the PCE values (from the highest 4.95 for the Zn(II)Pc to the lowest 0.23 for the Ru(II)Pc. In both series, the best PCEs observed with the Zn(II) derivatives were mainly due to their highest Jsc values. The lowest efficiencies found for the free-bases and Ru(II) derivatives were attributed to a mismatch between their LUMO levels and the conduction band of the TiO2,and lower light-harvesting capabilities, respectively. In conclusion, Zn(II) derivatives are still the best Pc candidates to use as sensitizers in molecular photovoltaics.

Thymus schimperi Ronniger plant flower extract dye-sensitized solar cells

The demand for energy is greatly increasing due to the world’s population growth and technological advancement. Natural dye-sensitized solar cells are attracting research as an alternative and renewable energy source due to their simple preparation technique, availability, cost effectiveness and environmental friendliness. In the present work, we have successfully fabricated dye-sensitized solar cells (DSSCs) from Thymus schimperi Ronniger plant flowers for the first time. The solvents used for extraction of the flower dye were deionized water and its mixture with ethanol. The T. schimperi Ronniger flower extract dye solutions and sensitized photoanodes were characterized by Fourier transform infrared and ultraviolet–visible techniques. The crystallinity of TiO2 films was analyzed by x-ray diffraction, and the films showed pure anatase phase behavior. The photoelectrochemical solar cell performance parameters, such as short circuit current density, open circuit voltage, fill factor and efficiency, were evaluated from current density–voltage measurements using a Keithley 2450 source meter. DSSCs sensitized with dye solution extracted by a mixture of water and ethanol showed better performance (1.37%) than those sensitized with dye solution extracted by deionized water alone (1.02%).

Theoretical, structural, and electronic analyses of pyridin-based dyes for dye-sensitized solar cells applications.

The new series of donor-π-acceptor dyes have been designed using pyridine derivatives as a donor group and thienothiophene as a π-spacer group, which were linked via 10acceptor groups. The highest occupied molecular orbital energies range from - 6.177 to - 5.786eV, whereas the lowest unoccupied molecular orbital energies range from - 2.181 to - 3.664eV. A6 dye has smaller energy gap, lower hardness, higher electrophilicity index, and good photovoltaic performance than other sensitizers. The lowest dihedral angle is observed in A1, A2, A6, A7, and A8 which are appropriate for intramolecular charge transfer between the molecules. The A8 has higher light harvesting efficiency, which increases the photovoltaic efficiency of the designed dye. The A6, A7, and A8 dyes spend less time in the excited state, which means they emit photons more efficiently than other dyes. The interaction between donor to π-spacer (red line) parts of the dyes has the bonding interaction (positive), and π-spacer to acceptor (blue line) parts of the dyes have the bonding and antibonding (negative) behaviours. The dyes A5 and A9 have 305.79 and 357.71 times higher β0 values than urea (0.781 × 10-30 esu) molecules. The spectral properties of the A6 dye strongly affect the structural modification. The density functional theory (DFT) and time-dependent DFT (TD-DFT) approach B3LYP/6-311G (d,p) basic set were used to optimize the designed dyes. All the calculations are performed using Gauss view 6.0 and Gaussian 09 software. The density of state spectrum is plotted using Gauss sum 2.6.

Robust carbon dots-wrapped NiCo flower-like nanostructures for enhanced triiodide reduction

Replacing traditional counter electrodes (CEs) with Pt-free electrodes is one of the challenges for developing dye-sensitized solar cells (DSCs). Herein, we successfully synthesized carbon dots-wrapped NiCo flower-like nanostructure (NiCo/Cdots) and evaluated its application as CEs for DSCs. To characterize as-prepared materials, we conducted FESEM and TEM-EDS. Cyclic Voltammetry (CV), electrochemical Impedance Spectroscopy (EIS), Bode, and Tafel plots were then used to investigate the electrocatalytic properties of NiCo/Cdots CE. As a result, the as-prepared sample exhibited high electrocatalytic activity, low charger-transfer resistance, and large exchange current density. DSC based on NiCo/Cdots CE was assembled and showed a slightly lower PCE than Pt CE-based DSCs (8.27 and 8.52 %, respectively). However, it provided excellent stability during a long-term performance. These results indicated that CoNi/Cdots is a low-cost, easy-to-fabricate material with high potential as a CE of DSCs.

Impedance spectroscopy using microscopic reference electrodes to analyze different rate-determining steps in aqueous dye-sensitized solar cells using nitroxide radicals as redox mediators

For new components in dye-sensitized solar cells (DSSCs), identification and quantification of rate-limiting steps is needed to evaluate their applicability. This is particularly important if fundamental changes are studied. In this work, the use of a micro-reference electrode in DSSCs is proposed to increase the significance of electrochemical impedance spectroscopy. The recombination of charge carriers at the photoanode and the regeneration of redox mediators at the counter electrode, which typically occur on similar timescales, could be studied separately but simultaneously in cells under operating conditions. This is particularly useful in the study of water-based DSSCs. Here, cells with 2,2,6,6-Tetramethylpiperidinoxyl (TEMPO) or 4-Hydroxy-TEMPO (OH-TEMPO) as redox mediators using additives like 1-Methylbenzimidazole (MBI) are discussed. It was revealed that the charge transfer resistance (RCE) for the reduction of the oxidized redox mediator at the counter electrode (CE) limits the fill factor (FF) of such DSSCs. TEMPO/MBI electrolytes yielded low RCE and high FF, whereas OH-TEMPO in otherwise identical cells resulted in large RCE, low FF, and low conversion efficiencies. This indicates that the interface between the CE and the electrolyte significantly influences the DSSC performance of these cells and strongly depends on the electrolyte composition. Important optimization strategies could be discussed based on the present results.

Geometry, reactivity descriptors, light harvesting efficiency, molecular radii, diffusion coefficient, and oxidation potential of RE(I)(CO)3Cl(TPA-2, 2′-bipyridine) in DSSC application: DFT/TDDFT study

Dye-sensitized solar cells (DSSCs) are an excellent alternative solar cell technology that is cost-effective and environmentally friendly. The geometry, reactivity descriptors, light-harvesting efficiency, molecular radii, diffusion coefficient, and excited oxidation state potential of the proposed complex were investigated. The calculations in this study were performed using DFT/TDDFT method with B3LYP functional employed on the Gaussian 09 software package. The calculations were used the 6–311 + + G(d, p) basis set for the C, H, N, O, Cl atoms and the LANL2DZ basis set for the Re atom, with the B3LYP functional.. The balance of hole and electron in this complex has increased the efficiency and lifetime of DSSCs for photovoltaic cell applications. The investigated compound shows that the addition of the TPA substituent marginally changes the geometric structures of the 2, 2′-bipyridine ligand in the T1 state. As EDsubstituents were added to the compound, the energy gap widened and moved from ELUMO (− 2.904 eV) (substituted TPA) to ELUMO (− 3.122 eV) (unsubstituted). In the studying of solvent affects; when the polarity of the solvent decreases, red shifts appears in the lowest energy an absorption and emission band. Good light-harvesting efficiency, molecular radii, diffusion coefficient, excited state oxidation potential, emission quantum yield, and DSSC reorganization energy, the complex is well suited for use as an emitter in dye-sensitized solar cells. Among the investigated complexes mentioned in literature, the proposed complex was a suitable candidate for phosphorescent DSSC.

Investigating the effect of nitrogen and chlorine Co–doped carbon quantum dots in phenazine and quinoxaline sensitized solar cells

We investigated five dyes for dye-sensitized solar cells (DSSCs) relying upon derivatives of phenazine and quinoxaline and also studied their optical characteristics and the influence of functional groups such as (-CH3, -NO2, -C = O, -CN, and -OH) on these characteristics. When the prepared dyes are directly used at DSSCs, 9-Nitrobenzo[a]phenazin-5-ol (3b) dye device showed an improved Jsc (0.288 mA cm−2), Voc (0.437 V), FF (0.446), and η (0.056 %) than the sensitized solar cells by other dyes. In the following, nitrogen-doped carbon quantum dot and nitrogen, chlorine co-doped carbon quantum dot are used to improve the performance of DSSCs. The results showed that the device sensitized using the sensitizer (5-hydroxybenzo[α]phenazin-9-yl)(phenyl) methanone (3c)/NCQD has the highest photovoltaic efficiency with Jsc (0.979 mA cm−2), Voc (0.465 V), FF (0.370), and η (0.168 %). The N and Cl co-doped carbon dots were synthesized with a green approach to improve the performance of solar cells by the co-sensitization method. This approach is improving the efficiency of DCSSs with a simple, eco-friendly, and low-cost technique. Among the prepared sensitizers, (5-hydroxybenzo[α]phenazin-9-yl)(phenyl) methanone (3c)/N, Cl-CQD demonstrates the highest photovoltaic efficiency with Jsc (1.31 mA cm−2), Voc (0.495 V), FF (0.466), and η (0.303 %). FT-IR, XRD, 13C NMR, 1H NMR, TEM, EDS-Map, AFM, DLS, and PL studies were used to confirm the structure of the synthesized dyes and quantum dots.

Quasi-Solid-State Dye-Sensitized Solar Cells by Mechanically Stable Semi-Interpenetrating Network Polymer Gel Electrolytes for Indoor Applications

Quasi-Solid-State Dye-Sensitized Solar Cells by Mechanically Stable Semi-Interpenetrating Network Polymer Gel Electrolytes for Indoor Applications

Computational study on metal-free dye-sensitized solar cells utilizing heterocyclic derivative π-spacers with open and fused rings: Design and analysis of D-π-A-π-A dye sensitizers

A series of metal-free dye-sensitized solar cells featuring a D-π-A-π-A configuration is devised, employing various heterocyclic derivative π-spacers in both open and fused configurations. Employing DFT and TD-DFT methods, the optoelectronic and photovoltaic characteristics of the dye are scrutinized. To evaluate the impact of diverse heterocyclic spacers, structural parameters such as distance and dihedral angle, alongside thermodynamic metrics including electron injection efficiency (ΔGinject), regeneration efficiency (ΔGreg), light harvesting efficiency (LHE), open-circuit photovoltage (VOC), and short-circuit current density (JSC) are assessed. Results indicate that selected dyes with open and fused configurations of heterocyclic π-spacers such as O-CNC-2, O-CNN-4, O-NNC-7, O-NNN-8, F-NNC-2, and F-NNN-1 exhibited superior electron density distribution, higher ΔGinject, lower ΔGreg, elevated VOC, and JSC compared to their counterparts based on open configurations. These D-π-A-π-A dyes can emerge as promising candidates for future applications in solar cells.

Unveiling the potential of TPA-based molecules to tune the optoelectronic properties and enhance the efficiency of dye-sensitized solar cells.

The world's energy and environmental requirements are changing due to rapid population growth and industrial growth, and solar cells can be used to meet these demands. Dye-sensitized solar cells (DSSCs) are solar cells in which energy conversion occurs via a process similar to photosynthesis in plants. DSSC development is still in its infancy. DSSCs can operate under cloudy conditions and indirect sunlight and have attracted considerable attention due to their low cost and high efficiency. We designed two metal-free TPA-based dyes (Dye2 and Dye3) based on the reference dye Mg207 (Dye1) by increasing the donor strength of the molecule, as such dyes have shown enhanced efficiency in DSSCs. Moreover, the triphenylamine (TPA) moiety has been demonstrated to be a good donor that prevents charge recombination. Intramolecular charge transfer (ICT) from the donor to acceptor moiety was found in the sensitizers, and electrons were promoted to the conduction band (CB) of the TiO2 semiconductor. The negative binding energy of the dye@TiO2 clusters indicated that dye adsorption on the semiconductor surface was stable. The double donor increased the electron injection and electronic coupling constants in Dye2 and Dye3, indicating that these newly designed dyes have superior charge injection capacity. Accordingly, the efficiencies of DSSCs with Dye2 and Dye3 were 9.77% and 9.62%, respectively, and substitution with the TPA unit at the -R1 and -R2 positions in Dye1 resulted in better power conversion compared to the parent compound (9.09%). Increased donor strength improved photovoltaic performance by increasing current density and light-harvesting efficiency. This is a good molecular design approach for preparing targeted donor- -acceptor (D- -A) organic dyes with high DSSC efficiency. To predict the charge transport and optoelectronic characteristics of the TPA dyes, quantum chemical calculations were carried out using Gaussian16. The ground-state (S0) optimized geometries of the sensitizers were computed by utilizing DFT at the B3LYP/6-31G** level. The absorption spectra ( max) were computed by employing TD-DFT with various functionals (B3LYP, PBE1PBE, CAM-B3LYP, and BHandHLYP) in the gas and solvent (DCM) phases. Among the studied functionals, BHandHLYP was found to be best at successfully reproducing the experimental data. Thus, the absorption spectra of the newly designed dyes and dye@TiO2 were calculated at the BHandHLYP/6-31G** level. The dye@TiO2 cluster optimizations were carried out at the B3LYP/6-31G**(LANL2DZ) level.

Characterization of graphene–TiO2-deposited semi-organic solar cell

High energy supply is critical, particularly in developing countries, to maintain lifestyles as the world's population and technological-economic metropolis grow. Solar photovoltaic cells have been used as an alternative to generate renewable, sustainable, and green energy for the past two decades. In general, the materials employed in the photoanode part are critical to manufacturing high-efficiency solar cells with 14–18% efficiency. A simple and successful method has been discovered for creating a film composed of graphene sheets and 99.8% pure anatase titanium oxide (TiO2) nanoparticles. After sensitization, the films were tested as photoelectrodes for dye-sensitized solar cells. The experimental results show that using an optimized graphene material considerably improves the power conversion efficiency of the cells, resulting in a 45% increase in short-circuit current density ( JSC). This study uses capsician as a bonding agent to enhance the current density of a graphene–TiO2 based semi-organic solar cell. The mechanical and electrical properties of the cell are investigated using a scanning electron microscope, energy dispersive X-ray, and Corescan.

Size controlled synthesis of hydrous TiO2 spheres by a thiol structure directing agent and its application in photocatalysis and efficient DSSC cells

In this work, hydrated TiO2 spheres (HTS) of the submicron order have been developed. Normally, the group of amines, such as dodecylamine, hexadecylamine, methylamine, and NH3, had been the main structure-directing agents (SDAs) used in the sol–gel process to obtain monodisperse hydrated TiO2 spheres. Even though progress has been made in the synthesis of HTS, it is crucial to include new SDAs capable of synthesizing monodisperse HTS with improved or new properties for practical applications. In this work, for the first time we demonstrate that a thiol, 3-mercaptopropionic acid (MPA), can be used as an effective SDA to synthesize monodisperse hydrous TiO2 spheres with a controllable particle diameter between 150 to 950 nm. Experimental preparation parameters such as Ti concentration, [MPA]/[Ti] and [Water]/[Ti] molar ratio in the precursor solution (Titanium (IV) butoxide—MPA—ethanol—water) were thoroughly optimized to get both high yield and high monodispersity. Remarkably, a wide range in the [Water]/[Ti] molar ratio, 17 to 118, was achieved, which is much wider than the typical Rw range of the amines group of 2 to 16, thus giving more control for choosing the HTS final size. The controlled growth of hydrated TiO2 nanospheres was explained according to the LaMer and DVLO theory. To demonstrate the applicability of the HTS synthesized using MPA as SDA, the development of efficient dye-sensitized solar cells getting an energy conversion greater than 9% as well as of an effective photocatalytic degradation process of the analgesic acetaminophen under concentrated solar radiation was conducted.

Synthesis of nanostructured zinc oxide and its composite with carbon dots for DSSCs applications using flexible electrode

ZnO nanowires (ZnO NWs), ZnO nanoparticles (ZnO NPs) and carbon dots (C-dots) were synthesized by hydrothermal, sol-gel and hydrothermal methods respectively. They were also characterized and applied for dye sensitized solar cells (DSSCs). The effects of C-dots on ZnO NWs and ZnO NPs have been evaluated. The C-dots were used at a mole ratio of citric acid (CA) to ethylene diamine (EDA) of 1 : 1.5. These C-dots were found to enhance the performance of the flexible electrode DSSCs. After the addition of C-dots, the power conversion efficiency (PCE) of ZnO NPs was boosted to be two times higher than that of ZnO NPs DSSCs without C-dots. Similarly, the ultraviolet (UV)-band revealed a blue shift, resulting in a lower band gap and a reduced charge transfer resistance, which can enhance the PCE of DSSCs. The loaded quantity on the flexible electrode substrate made of polyethylene terephthalate (PET) was optimized (50 mg). For DSSCs, the PET flexible electrode conductive polymer has produced positive outcomes. For ZnO NWs and ZnO NWs@C-dots, the PCE values were 1.45% and 4.25%; while for ZnO NPs and ZnO NPs@C-dots, they were 2.34% and 5.81%, respectively. This work achieved remarkable and competitive performance when compared to solid (indium tin oxides/glass)-based substrate.