Search Results (98)

Lead halide perovskite quantum dots, also known as perovskite nanocrystals, are considered one of the most promising photovoltaic materials for solar cells due to their outstanding optoelectronic properties and simple preparation techniques. The key factors restricting the photoelectric conversion efficiency of solar cell systems are the separation and transmission performances of charge carriers. Here, femtosecond time-resolved ultrafast spectroscopy was used to measure the interfacial charge transfer dynamics of different sizes of CsPbBr₃ assembled with TiO₂. The effect of perovskite size on the charge transfer is discussed. According to our experimental data analysis, the time constants of the interfacial electron transfer and charge recombination of the assembled systems of CsPbBr₃ and titanium dioxide become larger when the size of the CsPbBr₃ nanocrystals increases. We discuss the physical mechanism by which the size of perovskites affects the rate of charge transfer in detail. We expect that our experimental results provide experimental support for the application of novel quantum dots for solar cell materials. Full article

This research aimed to co-produce CQDs and hydrochar from natural sources to improve the photocatalytic properties of TiO₂. Juice extract from Citrus lemon fruits from south-eastern Spain was used as the carbon precursor. The synthesis strategy of the CQDs and hydrochar (Hc) was divided into different stages aimed at figuring out the role of the temperature (180, 220, 250 °C), the addition of TiO₂ nanoparticles, and the presence of N-/P-donor compounds (ethylenediamine and orto-phosphoric acid) in the photocatalytic properties of final composites. The results revealed that at 250 °C, using agro-carbon materials as Hc, and the addition of N-donor compounds, improved the photocatalytic activity and photodegradation rate of TiO₂ over methyl orange (MO) under blue light by 1000% and 2700%, respectively, with the parallel reduction of TiO₂ bandgap from 3.5 eV (Uv light) to 3.00 eV (visible light). These results are related to the ability of the carbon materials (electronegative) to enhance the formation of a Ti³⁺-active state. This study provides a landscape for a one-step method for the production of agro-carbon/TiO₂ photocatalysts with high activity under visible light as an efficient and sustainable strategy for applications such as energy generation and water purification under sunlight. Full article

The introduction of side-emitting lenses into white light-emitting diodes (LEDs) has enabled thin panel lighting technology based on LED technology, but also presents the disadvantage of low color rendering due to insufficient red components in the spectra of typical white LEDs. Additional application of remote quantum dot (QD) components such as QD films or caps presents the issues of increased numbers of components and higher costs. In this study, we incorporated red QDs directly into a lens placed on white LEDs and analyzed the effects of QD lenses on the optical characteristics of a lighting device through experiments and simulations. By incorporating red CdSe/ZnS QDs into UV-curable resin to fabricate QD lenses and applying them to white LEDs, we significantly improved the color rendering index and were able to adjust the correlated color temperature over a wide range between 2700 and 9900 K. However, as the concentration of QDs in the lens increased, scattering by the QD particles was enhanced, strengthening the Lambertian distribution in the intensity plot. Following the development of optical models for QD lenses under experimental conditions, comprehensive optical simulations of white LED lighting systems revealed that increasing the device height proved more effective than modifying TiO₂ scattering particle concentration in the diffuser plate for mitigating QD-induced bright spots and enhancing illumination uniformity. Full article

Colloidal copper-based chalcogenide quantum dots (QDs), particularly lead-free CuInSe₂ systems, have emerged as promising photosensitizers for optoelectronic de-vices due to their high extinction coefficients and solution processability. In this work, we demonstrate a TiO₂ photodetector enhanced through interfacial engineering with the size of 9.88 ± 2.49 nm CuInSe₂ QD_s, synthesized via controlled thermal injection. The optimized device architecture combines a 160 nm TiO₂ active layer with 60 μm horizontal channel electrodes, achieving high performance metrics. The QD-sensitized device demonstrates an impressive switching ratio of approximately 10⁵ in the 405 nm wavelength, a significant 34-times increase in responsivity at a 2 V bias, and a detection rate of 4.17 × 10⁸ Jones. Due to the limitations imposed by the TiO₂ bandgap, the TiO₂ photodetector exhibits a negligible increase in photocurrent at 565 nm. The engineered type-II heterostructure enables responsivity enhancement across an extended spectral range through sensitization while maintaining equivalent performance characteristics at both 405 nm and 565 nm wavelengths. Furthermore, the sensitized architecture demonstrates superior response kinetics, enhanced specific detectivity, and exceptional operational stability, establishing a universal design framework for broadband photodetection systems. Full article

Recently, the numerical simulation of solar cells has attracted tantamount scientific attention in the photovoltaic community because it saves on research time and resources before the actual fabrication of the devices in the laboratories. Despite significant advancements in the fabrication of quantum dot-sensitized solar cells (QDSSCs), the power conversion efficiency (PCE) is still low when compared to other solar cells such as perovskite. This efficiency gap poses a substantial challenge in harnessing the full potential of QDSSCs for widespread adoption in renewable energy applications. Enhancing the efficiency of QDSSCs is imperative for their commercial viability and widespread deployment. In this work, SCAPS-1D was used in the simulation of QDSSCs. The solar cell with a general configuration of FTO/TiO₂/PbS/HTL/Au was investigated. In the device, PbS quantum dots were inserted as the absorber layer, TiO₂ as the electron transport layer (ETL), gold as the back contact, and the following inorganic materials, i.e., copper (I) iodide (CuI), copper (I) oxide (Cu₂O), cadmium zinc telluride selenide (CZTSe), copper iron tin sulfide (CFTS), and copper zinc tin sulfide selenide (CZTSSe) were tested as HTL materials, and FTO acted as the conductive substrate. The best HTL material (CZTSSe) exhibited a PCE of 22.61%, with a fill factor (FF) of 84.67%, an open circuit voltage (V_oc) of 0.753 V, and a current density (J_sc) of 35.48 mA cm⁻². This study contributes to the field by employing SCAPS-1D simulations to optimize QDSSCs, exploring novel inorganic HTL materials for these solar cells and identifying CZTSSe as a promising low-cost HTL that significantly enhances both the performance and commercial viability of QDSSCs. Full article

Conventional wastewater treatment methods do not fully utilize the energy in wastewater. This study uses a photocatalytic fuel cell (PFC) to remove dye impurities and generate electricity with that energy. Pt serves as the PFC’s cathode, while the carbon quantum dots (CQDs)/anatase TiO₂ (A-TiO₂) serve as its photoanode. The visible light absorption range of A-TiO₂ can be increased by combining CQDs with A-TiO₂. The composite of CQD and A-TiO₂ broadens the absorption edge from 364 nm to 538 nm. TiO₂’s different crystal structures and particle sizes impact the PFC’s power generation and dye contaminant removal. The 30 min photodegradation rate of methylene blue by the 20 nm A-TiO₂ was 97.3%, higher than that of the 5 nm A-TiO₂ (75%), 100 nm A-TiO₂ (92.1%), and A-TiO₂ (93%). The photocurrent density of the 20 nm A-TiO₂ can reach 4.41 mA/cm², exceeding that of R-TiO₂ (0.64 mA/cm²), 5 nm A-TiO₂ (1.97 mA/cm²), and 100 nm A-TiO₂ (3.58 mA/cm²). The photodegradative and electrochemical test results show that the 20 nm A-TiO₂ delivers a better degradation and electrochemical performance than other samples. When the 20 nm A-TiO₂ was used in the PFC photoanode, the photocurrent density, open-circuit voltage, and maximum power density of the PFC were found to be 0.6 mA/cm², 0.41 V, and 0.1 mW/cm², respectively. The PFC prepared in this study shows a good level of performance compared to recent similar systems. Full article

Energy generation and storage are critical challenges for developing economies due to rising populations and limited access to clean energy resources. Fossil fuels, commonly used for energy production, are costly and contribute to environmental pollution through greenhouse gas emissions. Quantum dot-sensitized solar cells (QDSSCs) offer a promising alternative due to their stability, low cost, and high-power conversion efficiency (PCE) compared to other third-generation solar cells. Kesterite materials, known for their excellent optoelectronic properties and chemical stability, have gained attention for their potential as hole transport layer (HTL) materials in solar cells. In this study, the SCAPS-1D numerical simulator was used to analyze a solar cell with the configuration FTO/TiO₂/MoS₂/HTL/Ag. The electron transport layer (ETL) used was titanium dioxide (TiO₂), while Cu₂FeSnS₄ (CFTS), Cu₂ZnSnS₄ (CZTSe), Cu₂NiSnS₄ (CNTS), and Cu₂ZnSnSe₄ (CZTSSe) kesterite materials were evaluated as HTLs. MoS₂ quantum dot served as the absorber, with FTO as the anode and silver as the back metal contact. The CFTS material outperformed the others, yielding a PCE of 25.86%, a fill factor (FF) of 38.79%, a short-circuit current density (J_SC) of 34.52 mA cm⁻², and an open-circuit voltage (V_OC) of 1.93 V. This study contributes to the advancement of high-performance QDSSCs. Full article

In recent years, nanomaterials have gained special attention for removing contaminants from wastewater. Nanoparticles (NPs), such as carbon-based materials and metal oxides, exhibit exceptional adsorption capacity and antimicrobial properties for wastewater treatment. Their unique properties, including reactivity, high surface area, and tunable surface functionalities, make them highly effective adsorbents. They can remove contaminants such as organics, inorganics, pharmaceuticals, medicine, and dyes by adsorption mechanisms. In this review, the effectiveness of different types of carbon-based NPs, including carbon nanotubes (CNTs), graphene-based nanoparticles (GNPs), carbon quantum dots (CQDs), carbon nanofibers (CNFs), and carbon nanospheres (CNSs), and metal oxides, including copper oxide (CuO), zinc oxide (ZnO), iron oxide (Fe₂O₃), titanium oxide (TiO₂), and silver oxide (Ag₂O), in the removal of different contaminants from wastewater has been comprehensively evaluated. In addition, their synthesis methods, such as physical, chemical, and biological, have been described. Based on the findings, CNPs can remove 75 to 90% of pollutants within two hours, while MONPs can remove 60% to 99% of dye in 150 min, except iron oxide NPs. For future studies, the integration of NPs into existing treatment systems and the development of novel nanomaterials are recommended. Hence, the potential of NPs is promising, but challenges related to their environmental impact and their toxicity must be considered. Full article

Ammonia (NH₃) gas is prevalent in industrial production as a health hazardous gas. Consequently, it is essential to develop a straightforward, reliable, and stable NH₃ sensor capable of operating at room temperature. This paper presents an innovative approach to modifying SnO₂ colloidal quantum dots (CQDs) on the surface of Ti₃C₂T_x MXene to form a heterojunction, which introduces a significant number of adsorption sites and enhances the response of the sensor. Zero-dimensional (0D) SnO₂ quantum dots and two-dimensional (2D) Ti₃C₂T_x MXene were prepared by solvothermal and in situ etching methods, respectively. The impact of the mass ratio between two materials on the performance was assessed. The sensor based on 12 wt% Ti₃C₂T_x MXene/SnO₂ composites demonstrates excellent performance in terms of sensitivity and response/recovery speed. Upon exposure to 50 ppm NH₃, the frequency shift in the sensor is −1140 Hz, which is 5.6 times larger than that of pure Ti₃C₂T_x MXene and 2.8 times higher than that of SnO₂ CQDs. The response/recovery time of the sensor for 10 ppm NH₃ was 36/54 s, respectively. The sensor exhibited a theoretical detection limit of 73 ppb and good repeatability. Furthermore, a stable sensing performance can be maintained after 30 days. The enhanced sensor performance can be attributed to the abundant active sites provided by the accumulation/depletion layer in the Ti₃C₂T_x/SnO₂ heterojunction, which facilitates the adsorption of oxygen molecules. This work promotes the gas sensing application of MXenes and provides a way to improve gas sensing performance. Full article

Photocatalytic degradation of pollutants have a high potential for sustainable and renewable uses. TiO₂ is a widely studied photocatalyst due to its high chemical and photochemical stability and wide range of applications. However, the wide band gap and low capacity of photo-induced charge separation provide lower catalytic activity; thus, improvement of these properties must be found. The doping of TiO₂ with other elements, such as carbon nanoparticles (CNP) in a quantum dot form, offers a promising pathway to improve the aforementioned properties. In addition, in situ doping methods should be investigated for practical scalability, as they offer the advantage of integrating dopants directly during material synthesis, ensuring a more uniform distribution and better interaction between the dopant and the host material, in turn leading to more consistent photocatalytic properties. Current technologies primarily involve nanoparticle combinations. This work focuses on the development of a novel in situ synthesis methodology by the introduction of three different graphene-based quantum nanodots into anodic TiO₂ and the following investigation of structural, morphological, and photocatalytic properties. Results indicate that the introduction of CNP allows for the shift of a set of parameters, such as the optical band gap, increased photo-induced charge carrier density of TiO₂/CNP composite, and, most importantly, the change of crystalline phase composition depending on added CNP material. Research indicates that not only a higher concentration of added CNP enhances higher photocatalytic activity as tested by the degradation of methylene blue dye, but also the type of CNP determines final crystalline phase. For the first time brookite and rutile phases were obtained in anodic titania synthesized in inorganic electrolyte by introducing hydrothermally treated exfoliated graphene. Full article

The first part of this work evaluates Al-doped ZnO (AZO) as an optically transparent top-gate material for studies on semiconductor quantum dots. In comparison with conventional Ti gates, samples with AZO gates demonstrate a more than three times higher intensity in the quantum dot emission under comparable excitation conditions. On the other hand, charges inside a process-induced oxide layer at the interface to the semiconductor cause artifacts at gate voltages above $U\approx$ 1 V. The second part describes an optical and simulation study of a vertical electric-field (F)-induced switching from a strong to an asymmetric strong–weak confinement in GaAs cone-shell quantum dots (CSQDs), where the charge carrier probability densities are localized on the surface of a cone. These experiments are performed at low U and show no indications of an influence of interface charges. For a large F, the measured radiative lifetimes are substantially shorter compared with simulation results. We attribute this discrepancy to an F-induced transformation of the shape of the hole probability density. In detail, an increasing F pushes the hole into the wing part of a CSQD, where it forms a quantum ring. Accordingly, the confinement of the hole is changed from strong, which is assumed in the simulations, to weak, where the local radius is larger than the bulk exciton Bohr radius. In contrast to the hole, an increasing F pushes the electron into the CSQD tip, where it remains in a strong confinement. This means the radiative lifetime for large F is given by an asymmetric confinement with a strongly confined electron and a hole in a weak confinement. To our knowledge, this asymmetric strong–weak confinement represents a novel kind of quantum mechanical confinement and has not been observed so far. Furthermore, the observed weak confinement for the hole represents a confirmation of the theoretically predicted transformation of the hole probability density from a quantum dot into a quantum ring. For such quantum rings, application as storage for photo-excited charge carriers is predicted, which can be interesting for future quantum photonic integrated circuits. Full article

Novel photocatalysts were synthesized through the association of carbon quantum dots (CQDs) with commercial (P25) titanium dioxide (TiO₂) by sonication. The resulting TiO₂/CQDs composite was then incorporated into the polyamide 66 (PA66) biopolymer nanofibers using the electrospinning technique, considering a composite nanoparticles-to-polymer ratio of 1:2 in the electrospinning precursor solution. The produced nanofibers presented suitable morphology and were tested for the photocatalytic degradation under simulated solar radiation of 10 mg L⁻¹ of amoxicillin (AMX) and sulfadiazine (SDZ), in phosphate buffer solution (pH 8.06) and river water, using 1.5 g L⁻¹ of photocatalyst. The presence of the photocatalyst increased the removal of AMX in phosphate buffer solution by 30 times, reducing the AMX degradation half-life time from 62 ± 1 h (without catalyst) to 1.98 ± 0.06 h. Moreover, SDZ degradation half-life time in phosphate buffer solution was reduced from 5.4 ± 0.1 h (without catalyst) to 1.87 ± 0.05 h in the presence of the photocatalyst. Furthermore, the PA66/TiO₂/CQDs were also efficient in river water samples and maintained their performance in at least three cycles of SDZ photodegradation in river water. The presented results evidence that the produced photocatalyst can be a promising and sustainable solution for antibiotics’ efficient removal from water. Full article

Self-doped CuS nanoparticles (NPs) were successfully synthesized via microwave-assisted polyol process to act as co-catalysts to TiO₂ nanofiber (NF)-based photoanodes to achieve higher photocurrents on visible light-assisted water electrolysis. The strategy adopted to perform the copper cation sulfidation in polyol allowed us to overcome the challenges associated with the copper cation reactivity and particle size control. The impregnation of the CuS NPs on TiO₂ NFs synthesized via hydrothermal corrosion of a metallic Ti support resulted in composites with increased visible and near-infrared light absorption compared to the pristine support. This allows an improved overall efficiency of water oxidation (and consequently hydrogen generation at the Pt counter electrode) in passive electrolyte (pH = 7) even at 0 V bias. These low-cost and easy-to-achieve composite materials represent a promising alternative to those involving highly toxic co-catalysts. Full article

In this study, titanium oxide TiO₂ nanoparticles were produced using the sol–gel approach of green synthesis with pectin as the reducing agent. The synthetized TiO₂ nanoparticles with pectin were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), visible light absorption (UV–Vis) and the BET method. The structure and morphology of the TiO₂ powder were described with SEM, revealing uniform monodisperse grains with a distribution of 80% regarding sizes < 250 nm; the resulting crystal phase of synthetized TiO₂ was identified as an anatase and rutile phase with a crystallinity size estimated between 27 and 40 nm. Also, the surface area was determined by nitrogen adsorption–desorption using the Brown–Emmet–Teller method, with a surface area calculated as 19.56 m²/g, typical of an IV type isotherm, indicating mesoporous NPs. UV–Vis spectra showed that sol–gel synthesis reduced the band gap from the 3.2 eV common value to 2.22 eV after estimating the optical band gap energy using the adsorption coefficient; this translates to a possible extended photo response to the visible region, improving photoactivity. In addition, the power conversion of the photoelectrode was compared based on similar assembly techniques of TiO₂ electrode deposition. Quantum dot crystals were deposited ionically on the electrode surface, as two different paste formulations based on a pectin emulsifier were studied for layer deposition. The results confirm that the TiO₂ paste with TiO₂-synthesized powder maintained good connections between the nanocrystalline mesoporous grains and the deposited layers, with an efficiency of 1.23% with the transparent paste and 2.27% with the opaque paste. These results suggest that pectin could be used as a low-cost, functional sol–gel catalysis agent for the synthesis of controlled NPs of metal oxide. It demonstrates interesting optical properties, such as an increase in photo response, suggesting further applications to photocatalysts and biomedical features. Full article

In this study, carbon-quantum-dot (CQD)-decorated TiO₂ was prepared using an ultrasonic doping method and applied in the photocatalytic degradation of naphthalene under sunlight irradiation. The CQDs were synthesized from a typical macroalgae via diluted sulfuric acid pretreatment and hydrothermal synthesis using an optimal design, i.e., 3 wt% and 200 °C, respectively. The CQD/TiO₂ composite remarkably enhanced the photocatalytic activity. The degradation of naphthalene under a visible light environment indicated that there is a synergistic mechanism between the CQDs and TiO₂, in which the generation of reactive oxygen species is significantly triggered; in addition, the N that originated from the macroalgae accelerated the photocatalytic efficiency. Kinetic analysis showed that the photocatalytic behavior of the CQD/TiO₂ composite followed a pseudo-first-order equation. Consequently, our combined experimental approach not only provides a facile pretreatment process for bio-CQDs synthesis, but also delivers a suitable TiO₂ photocatalyst for the visible environment along with critical insights into the development of harmful macroalgae resources. Full article