RESUMEN

Encapsulants based on ethylene-vinyl acetate copolymers (EVA) or polyolefin elastomers (POE) are essential for glass or photovoltaic module laminates. To improve their multi-functional property profile and their durability, the encapsulants are frequently peroxide crosslinked. The crosslinking kinetics are affected by the macromolecular structure and the formulation with stabilizers such as phenolic antioxidants, hindered amine light stabilizers or aromatic ultraviolet (UV) absorbers. The main objective of this study was to implement temperature-rise and isothermal dynamic mechanical analysis (DMA) approaches in torsional mode and to assess and compare the crosslinking kinetics of novel UV-transparent encapsulants based on EVA and POE. The gelation time was evaluated from the crossover of the storage and loss shear modulus. While the investigated EVA and POE encapsulants revealed quite similar activation energy values of 155 kJ/moles, the storage modulus and complex viscosity in the rubbery state were significantly higher for EVA. Moreover, the gelation of the polar EVA grade was about four times faster than for the less polar POE encapsulant. Accordingly, the curing reaction of POE was retarded up to a factor of 1.6 to achieve a progress of crosslinking of 95%. Hence, distinct differences in the crosslinking kinetics of the UV-transparent EVA and POE grades were ascertained, which is highly relevant for the lamination of modules.

RESUMEN

The integration of dye-sensitized solar cells (DSSCs) with building roof panels, windows, and various decorative outdoor installations is presently an important research topic for their immediate commercialization potential because of their power generation capability, sustainability, and aesthetic appearance. For industrial applications, Pt counter electrodes (CEs) need to be replaced with Pt-free CEs because of their limited sources and cost. An ideal CE should be economical, abundant, and have excellent electrochemical stability and activity, with easy processing in bulk. As an alternative practical CE, we introduce for the first time a carbon nano-onion (CNO)-based CE for transparent DSSCs. We developed a simple, energy-efficient one-step synthesis technique for fabricating high-quality CNOs in bulk quantities without any sophisticated instrumentation and expensive nanodiamond precursors. CNO CEs proved to be promising in terms of optical transparency, reasonable electrochemical redox activity for the I-/I3- redox couple, and exchange current density comparable to Pt CEs. CNO-powered DSSCs demonstrated an optical transparency of >55% with a significant solar energy conversion efficiency of 5.17%. The intrinsic hydrophilicity of the as-synthesized CNO eliminates the use of a binder or an additive, unlike in the case of other carbon allotropes. Our results demonstrate the possibility of using CNO-based CEs as promising substitutes for scarce and expensive Pt-based CEs for low-cost DSSCs.

RESUMEN

Graphene nanoplatelets (GNPs) are prepared from natural graphite by a simple and low-cost liquid phase high shear exfoliation method. The as-prepared GNPs are used as a counter electrode (CE) material for dye-sensitized solar cells (DSSCs). To confirm the Exfoliated GNPs, structural and morphological studies are carried out using X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM) and selected area electron diffraction (SAED) studies. The electrochemical behaviour of GNPs as a counter electrode material is evaluated and compared with standard Platinum (Pt) electrode using cyclic-voltammetry (CV) and electrochemical impedance spectroscopy (EIS). These studies indicated that electrocatalytic activity towards I-/I3- redox mediator exhibited by the GNPs based electrode is comparable to standard Pt counter electrodes. DSSCs are fabricated using the counter electrodes made of GNPs and the photo-conversion efficiency is found to be 6.23% under standard test conditions, which is comparable to Pt based DSSCs proving them as potential alternative materials for counter electrodes.

RESUMEN

In this study, we present the preparation of graphene quantum dots (GQDs) and graphene oxide quantum dots (GOQDs). GQDs/GOQDs are prepared by an easy electrochemical exfoliation method, in which two graphite rods are used as electrodes. The electrolyte used is a combination of citric acid and alkali hydroxide in water. Four types of quantum dots, GQD1-GQD4, are prepared by varying alkali hydroxide concentration in the electrolyte, while keeping the citric acid concentration fixed. Variation of alkali hydroxide concentration in the electrolyte results in the production of GOQDs. Balanced reaction of citric acid and alkali hydroxide results in the production of GQDs (GQD3). However, three variations in alkali hydroxide concentration result in GOQDs (GQD1, GQD2, and GQD4). GOQDs show tunable oxygen functional groups, which are confirmed by X-ray photoelectron spectroscopy. GQDs/GOQDs show absorption in the UV region and show excitation-dependent photoluminescence behavior. The obtained average size is 2-3 nm, as revealed by transmission electron microscopy. X-ray diffraction peak at around 10° and broad D band peak at 1350 cm-1 in Raman spectra confirm the presence of oxygen-rich functional groups on the surface of GOQDs. These GQDs and GOQDs show blue to green luminescence under 365 nm UV irradiation.

RESUMEN

Contact layers play an important role in thin film solar cells, but new material development and optimization of its thickness is usually a long and tedious process. A high-throughput experimental approach has been used to accelerate the rate of research in photovoltaic (PV) light absorbers and transparent conductive electrodes, however the combinatorial research on contact layers is less common. Here, we report on the chemical bath deposition (CBD) of CdS thin films by combinatorial dip coating technique and apply these contact layers to Cu(In,Ga)Se2 (CIGSe) and Cu2ZnSnSe4 (CZTSe) light absorbers in PV devices. Combinatorial thickness steps of CdS thin films were achieved by removal of the substrate from the chemical bath, at regular intervals of time, and in equal distance increments. The trends in the photoconversion efficiency and in the spectral response of the PV devices as a function of thickness of CdS contacts were explained with the help of optical and morphological characterization of the CdS thin films. The maximum PV efficiency achieved for the combinatorial dip-coating CBD was similar to that for the PV devices processed using conventional CBD. The results of this study lead to the conclusion that combinatorial dip-coating can be used to accelerate the optimization of PV device performance of CdS and other candidate contact layers for a wide range of emerging absorbers.

Asunto(s)

RESUMEN

ABSTRACT: The paper reports the fabrication of Zn-doped TiO2 nanotubes (Zn-TONT)/ZnO nanoflakes heterostructure for the first time, which shows improved performance as a photoanode in dye-sensitized solar cell (DSSC). The layered structure of this novel nanoporous structure has been analyzed unambiguously by Rutherford backscattering spectroscopy, scanning electron microscopy, and X-ray diffractometer. The cell using the heterostructure as photoanode manifests an enhancement of about an order in the magnitude of the short circuit current and a seven-fold increase in efficiency, over pure TiO2 photoanodes. Characterizations further reveal that the Zn-TONT is preferentially oriented in [001] direction and there is a Ti metal-depleted interface layer which leads to better band alignment in DSSC.

RESUMEN

Single crystal like TiO(2) nanotubes with preferential orientation along the [001] direction, parallel to the growth direction of nanotubes, that offer ease of charge transport much higher than reported so far, are fabricated using a cost effective two step technique. The success of this method to grow the nanotubes with the anomalous intense [001] preferential orientation is attributed to the zinc assisted minimization of the (001) surface energy. The single crystal like TiO(2) nanotubes show superior performance as supercapacitor electrodes compared to the normal polycrystalline titanium dioxide nanotubes.

RESUMEN

Dye sensitized solar cells (DSSCs) have attracted much attention in recent years due to low cost fabrication as compared to silicon-based and thin film solar cells. Though, platinum is an excellent catalytic material for use in preparation of counter electrodes (CEs) for DSSCs it is expensive. Alternatives to replacement of platinum (Pt) that have been examined are carbon materials, conductive polymers and hybrids. In this work, counter electrode for DSSCs was fabricated using carbon material obtained from graphitization of sucrose at high temperature. A slurry of the carbon produced from sucrose graphitization was made with polyvinylpyrrolidone (PVP) as a surfactant and a coating was obtained by doctor blading the slurry over the FTO glass substrate. The current density (Jsc) and open circuit voltage (V(OC)) of fabricated cell (area 0.25 cm(2)) was 10.28 mAc m(-2) and 0.76 V respectively. The efficiency of the cell was 4.33% which was just slightly lower than that obtained for similar cells using platinum based counter electrode.