Patterned carbon dot-based thin films for solid-state devices.

Carbon dot-based fluorescent nanocomposite compounds were obtained following microwave assisted thermal treatment of an aqueous mixture consisting of citric acid and urea. Thin film deposition of nanocomposites on SiO2 (100) substrates is followed by annealing, in order to render the films dissolution-resistant and processable. Optical lithography and O2 plasma etching are utilized to pattern the deposited films in the desired shapes and dimensions and a solid-state relative humidity sensor is fabricated on the SiO2 substrate. Spectroscopy and microscopy techniques are employed to characterize and monitor the whole process throughout the fabrication steps. The patterned films retain the functional groups introduced during their synthesis and continue to display hydrophilicity and PL properties. Successful patterning of these nanocomposites opens the way for the fabrication of solid-state, carbon dot-based optical and electrical devices that take advantage of the properties of carbon quantum dots.

Magnetic fluid hyperthermia simulations in evaluation of SAR calculation methods.

PURPOSE: The purpose of this study is to employ magnetic fluid hyperthermia simulations in the precise computation of Specific Absorption Rate functions -SAR(T)-, and in the evaluation of the predictive capacity of different SAR calculation methods. METHODS: Magnetic fluid hyperthermia experiments were carried out using magnetite-based nanofluids. The respective SAR values were estimated through four different calculation methods including the initial slope method, the Box-Lucas method, the corrected slope method and the incremental analysis method (INCAM). A novel numerical model combining the heat transfer equations and the Navier-Stokes equations was developed to reproduce the experimental heating process. To address variations in heating efficiency with temperature, the expression of the power dissipation as a Gaussian function of temperature was introduced and the Levenberg-Marquardt optimization algorithm was employed to compute the function parameters and determine the function's effective branch within each measurement's temperature range. The power dissipation function was then reduced to the respective SAR function. RESULTS: The INCAM exhibited the lowest relative errors ranging between 0.62 and 15.03% with respect to the simulations. SAR(T) functions exhibited significant variations, up to 45%, within the MFH-relevant temperature range. CONCLUSIONS: The examined calculation methods are not suitable to accurately quantify the heating efficiency of a magnetic fluid. Numerical models can be exploited to effectively compute SAR(T) and contribute to the development of robust hyperthermia treatment planning applications.

Advanced Photocatalysts Based on Reduced Nanographene Oxide-TiO2 Photonic Crystal Films.

Surface functionalization of TiO2 inverse opals by graphene oxide nanocolloids (nanoGO) presents a promising modification for the development of advanced photocatalysts that combine slow photon-assisted light harvesting, surface area, and mass transport of macroporous photonic structures with the enhanced adsorption capability, surface reactivity, and charge separation of GO nanosheets. In this work, post-thermal reduction of nanoGO-TiO2 inverse opals was investigated in order to explore the role of interfacial electron transfer vs. pollutant adsorption and improve their photocatalytic activity. Photonic band gap-engineered TiO2 inverse opals were fabricated by the coassembly technique and were functionalized by GO nanosheets and reduced under He at 200 and 500 °C. Comparative performance evaluation of the nanoGO-TiO2 films on methylene blue photodegradation under UV-VIS and visible light showed that thermal reduction at 200 °C, in synergy with slow photon effects, improved the photocatalytic reaction rate despite the loss of nanoGO and oxygen functional groups, pointing to enhanced charge separation. This was further supported by photoluminescence spectroscopy and salicylic acid UV-VIS photodegradation, where, in the absence of photonic effects, the photocatalytic activity increased, confirming that fine-tuning of interfacial coupling between TiO2 and reduced nanoGO is a key factor for the development of highly efficient photocatalytic films.

Study of hybrid solar cells made of multilayer nanocrystalline titania and poly(3-octylthiophene) or poly-(3-(2-methylhex-2-yl)-oxy-carbonyldithiophene).

Hybrid solar cells have been constructed by using nanocrystalline titania and hole-transporting polymers. Titania was deposited on fluorine-doped tin-oxide transparent electrodes in three layers: a blocking layer and two nanostructured layers, giving densely packed or open structures. Open structures produced higher currents due to better polymer penetration and larger oxide-polymer interface. Cells based on the dithiophene-unit-containing polymer gave higher open-circuit voltage. Efficient cells could be made only in the presence of a dye sensitizer and a lithium salt. Cells were neither sealed nor encapsulated and their components were deposited under ambient conditions except for the metal back electrode, which was deposited under vacuum. Cells demonstrated a transient behavior in two stages: initially an increase of both current and voltage followed by an increase in voltage and a drop in current. Both quantities were stabilized at values approximately established within a few days. These values remained stable for several months when the cells were stored in the dark.

Effect of the conditions of platinum deposition on titania nanocrystalline films on the efficiency of photocatalytic oxidation of ethanol and production of hydrogen.

Titania nanocrystalline films have been deposited on glass slides and loaded with Pt nanoparticles by adsorption from aqueous solutions of sodium tetrachloroplatinate followed by UVA radiation or heat treatment. These metal/semiconductor combined photocatalysts have been used for photooxidation of aqueous ethanol and production of hydrogen. The efficiency of the photocatalytic process was associated with the metal load on the titania films and the size of the metal nanoparticles. Characterization of the combined photocatalyst has been made by X-ray photoelectron spectroscopy and transmission electron microscopy.