Effat Samir

This work focuses on improving the fluorescence intensity of cerium oxide (ceria) nanoparticles (NPs) through added plasmonic nanostructures. Ceria nanoparticles are fluorescent nanostructures which can emit visible fluorescence emissions under violet excitation. Here, we investigated different added plasmonic nanostructures, such as gold nanoparticles (Au NPs) and Cadmium sulfide/selenide quantum dots (CdS/CdSe QDs), to check the enhancement of fluorescence intensity emissions caused by ceria NPs. Different plasmonic resonances of both aforementioned nanostructures have been selected to develop optical coupling with both fluorescence excitation and emission wavelengths of ceria. In addition, different additions whether in-situ or post-synthesis have been investigated. We found that in-situ Au NPs of a 530 nm plasmonic resonance wavelength provides the highest fluorescence emissions of ceria NPs compared to other embedded plasmonic structures. In addition to the optical coupling between plasmonic resonance of Au with the visible emissions fluorescence spectrum of ceria nanoparticles, the 530 nm in-situ Au NPs were found to reduce the bandgap of ceria NPs. We suggest that the formation of more tri-valent cerium ions traps energy levels along with more associated oxygen vacancies, which is responsible for increasing the fluorescence visible emissions intensity caused by ceria. As an application, the gold-ceria NPs is shown to optically detect the varied concentration of iron tiny particles in aqueous medium based on a fluorescence quenching mechanism. This work is promising in different applications such as biomarkers, cancer treatments, and environmental pollution monitoring.

Cerium oxide (ceria) nanoparticles (NPs) have been proved to be an efficient optical fluorescent material through generating visible emission (~530 nm) under violet excitation. This feature allowed ceria NPs to be used as an optical sensor via the fluorescence quenching Technique. In this paper, the impact of in-situ embedded gold nanoparticles (Au NPs) inside ceria nanoparticles was studied. Then, gold–ceria NPs were used for sensing dissolved oxygen (DO) in aqueous media. It was observed that both fluorescence intensity and lifetime were changed due to increased concentration of DO. Added gold was found to enhance the sensitivity of ceria to DO quencher detection. This enhancement was due to optical coupling between the fluorescence emission spectrum of ceria with the surface plasmonic resonance of gold nanoparticles. In addition, gold caused the decrease of ceria nanoparticles’ bandgap, which indicates the formation of more oxygen vacancies inside the non-stoichiometric crystalline structure of ceria. The Stern–Volmer constant, which indicates the sensitivity of optical sensing material, of ceria–gold NPs with added DO was found to be 893.7 M⁻¹, compared to 184.6 M⁻¹ to in case of ceria nanoparticles only, which indicates a superior optical sensitivity to DO compared to other optical sensing materials used in the literature to detect DO. Moreover, the fluorescence lifetime was found to be changed according to the variation of added DO concentration. The optically-sensitivity-enhanced ceria nanoparticles due to embedded gold nanoparticles can be a promising sensing host for dissolved oxygen in a wide variety of applications including biomedicine and water quality monitoring.

Ceria nanoparticles have been recently used as an optical fluorescent material with visible emission under ultraviolet excitation, due to the formation of trivalent cerium ions with corresponding oxygen vacancies. This paper introduces the enhancement of both fluorescence emission and lifetime through adding gold nanoparticles. The reason is due to possible coupling between the plasmonic resonance of gold nanoparticles and the fluorescence emission of ceria that has been achieved, along with enhanced formation of trivalent cerium ions. Both factors lead to higher fluorescence intensity peaks and shorter fluorescence lifetimes. As an application, gold-ceria nanoparticles have been used as an optical sensing material for lead particles in aqueous media based on fluorescence quenching. Stern-Volmer constant of in-situ gold-ceria nanoparticles is found to be 2.424 M⁻¹, with a relative intensity change of up to 40% at 0.2 g/L.

This paper introduces electrospun nanofibers embedded with ceria nanoparticles as silicon solar cells coaters, showing their influence on the solar cells efficiency. Ceria nanoparticles can be synthesized to have formed oxygen vacancies (O-vacancies), which are associated with converting cerium ions from the Ce⁴⁺ state ions to the Ce³⁺ ones. These O-vacancies follow the rule of improving silicon solar cellconductivity through the hopping mechanism. Besides, under violet excitation, the reduced trivalent cerium Ce³⁺ ions are directly responsible for down-converting the un-absorbed violet or ultra-violet (UV) wavelengths to a resulted green fluorescence emission at ~520 nm. These are absorbed through the silicon solar cells active layer. When electrospun Poly(vinyl alcohol) (PVA) is embedded with ceria nanoparticles on the rear surface of silicon solar cell, a promising enhancement in the behavior of solar cells current–voltage (I–V) curve is observed. The efficiency has improved by about 24% of its initial value due to the mutual impact of improving both electrical conductivity and optical conversions from the higher surface-to-volume ratio of electrospun nanofibers embedded by ceria nanoparticles. The solar cell efficiency improvement is due to the mutual impact of both optical down-conversion and better electric paths via the used nanocomposite. The added nanostructures coating can utilize part of the transmitted UV or violet spectrum through the cell as optical conversion from violet to the visible region. In addition, the formed active tri-valent states are associated with O-vacancies which can help in a better conductivity of the generated photoelectrons from the cell through the hopping mechanism. The PVA nanofibers host offers a better distribution of ceria nanoparticles and better conductivity paths for the photoelectrons based on the better surface-to-volume ratio of the nanofibers.

This paper introduces lanthanide-doped ceria nanoparticles as silicon solar cell back-side coaters, showing their influence on the solar cell efficiency. Ceria nanoparticles can be synthesized to have formed oxygen vacancies (O-vacancies), which are associated with converting cerium ions from the Ce⁴⁺ state ions to the Ce³⁺ ones. These O-vacancies follow the rule of improving silicon solar cell conductivity through a hopping mechanism. Besides, under near-ultra violet (near-UV) excitation, the reduced trivalent cerium Ce³⁺ ions are directly responsible for down converting the un-absorbed UV wavelengths to a resultant green photo-luminescence emission at ~520 nm, which is absorbed through the silicon solar cell’s active layer. Adding lanthanide elements such as Neodymium “Nd” as ceria nanoparticle dopants helps in forming extra oxygen vacancies (O-vacancies), followed by an increase in the number of Ce⁴⁺ to Ce³⁺ ion reductions, thus enhancing the conductivity and photoluminescence down conversion mechanisms. After introducing lanthanide-doped ceria nanoparticles on a silicon solar cell surface, a promising enhancement in the behavior of the solar cell current-voltage curve is observed, and the efficiency is improved by about 25% of its initial value due to the mutual impact of improving both electric conductivity and optical conversions.

This work presents a new nanocomposite of cerium oxide (ceria) nanoparticles embedded in electrospun PVA nanofibers for optical sensing of radicals in solutions. Our ceria nanoparticles are synthesized to have O-vacancies which are the receptors for the radicals extracted from peroxide in water solution. Ceria nanoparticles are embedded insitu in PVA solution and then formed as nanofibers using an electrospinning technique. The formed nanocomposite emits visible fluorescent emissions under 430 nm excitation, due to the active ceria nanoparticles with fluorescent Ce³⁺ ionization states. When the formed nanocomposite is in contact with peroxide solution, the fluorescence emission intensity peak has been found to be reduced with increasing concentration of peroxide or the corresponding radicals through a fluorescence quenching mechanism. The fluorescence intensity peak is found to be reduced to more than 30% of its original value at a peroxide weight concentration up to 27%. This work could be helpful in further applications of radicals sensing using a solid mat through biomedical and environmental monitoring applications.

This paper introduces a new fluorescent nanocomposite of electrospun biodegradable nanofibers embedded with optical nanoparticles. In detail, this work introduces the fluorescence properties of PVA nanofibers generated by the electrospinning technique with embedded cerium oxide (ceria) nanoparticles. Under near-ultra violet excitation, the synthesized nanocomposite generates a visible fluorescent emission at 520 nm, varying its intensity peak according to the concentration of in situ embedded ceria nanoparticles. This is due to the fact that the embedded ceria nanoparticles have optical tri-valiant cerium ions, associated with formed oxygen vacancies, with a direct allowed bandgap around 3.5 eV. In addition, the impact of chemical crosslinking of the PVA on the fluorescence emission is studied in both cases of adding ceria nanoparticles in situ or of a post-synthesis addition via a spin-coating mechanism. Other optical and structural characteristics such as absorbance dispersion, direct bandgap, FTIR spectroscopy, and SEM analysis are presented. The synthesized optical nanocomposite could be helpful in different applications such as environmental monitoring and bioimaging.

This paper discusses the effect of adding reduced erbium-doped ceria nanoparticles (REDC NPs) as a coating on silicon solar cells. Reduced ceria nanoparticles doped with erbium have the advantages of both improving conductivity and optical conversion of solar cells. Oxygen vacancies in ceria nanoparticles reduce Ce⁴⁺ to Ce³⁺ which follow the rule of improving conductivity of solar cells through the hopping mechanism. The existence of Ce³⁺ helps in the down-conversion from 430 nm excitation to 530 nm emission. The erbium dopant forms energy levels inside the low-phonon ceria host to up-convert the 780 nm excitations into green and red emissions. When coating reduced erbium-doped ceria nanoparticles on the back side of a solar cell, a promising improvement in the solar cell efficiency has been observed from 15% to 16.5% due to the mutual impact of improved electric conductivity and multi-optical conversions. Finally, the impact of the added coater on the electric field distribution inside the solar cell has been studied.