In this paper, the potential of marine algae to act as sensitizers is systematically studied and presented. We aim to find a feasible financial strategy to enhance the global efficiency of dye-sensitized solar cells (DSSC). Algae are mainly composed of chlorophylls, carotenoids, flavonoids, and Betalains, which are essential pigments that confer unique characteristics that are required in natural sensitizers. Therefore, this review aims to unveil and understand the underlying mechanism between algae pigments and photoelectrodes and to conduct a comprehensive analysis to determine the effect of algae dye on light absorption efficiency and electron transport. The structural, morphological, optical, and electrochemical impedance properties are deeply analyzed, and we show the current opportunities for natural dyes to be used in energy technologies through DSSC. A comparison of several bibliographic sources dealing with DSSC based on algae provided a general overview of the improvements in factors such as the recombination times, the filling factor, and the Voc values. The contributions of this paper relate to the conversion efficiency and future applications in the DSSC field. Finally, this review exemplifies that the nature of the pigment affects the photophysical properties of the cell. Thus, this paper may contribute to future investigations of DSSC when choosing efficient natural dyes according to their optical and electronic properties. Therefore, this work provides the knowledge required to efficiently merge materials and dyes, in which photovoltaic energy systems’ reproducibility and scalability still represent a challenge. Lastly, this document discusses the natural pigments’ stability and the approaches to improve their chemical stability.

Materials known as Nd:YAG are crystalline materials of the cubic system made from the neodymium-doped yttrium aluminum garnet, which, among others, have excellent optical properties. Nd:YAG four-level laser devices are frequently used in both the health and industrial sectors. In this study, a simple and inexpensive alternative to manufacturing Nd:YAG materials through solid state reactions following powder processing routes was proposed. For this, an intense mixture of the precursor materials (Al₂O₃ and Y₂O₃) was carried out, followed by the addition of neodymium atoms to improve the optical properties of the resulting material. High-energy mechanical mixing of the precursor powders resulted in submicron particles with good size distributions of the powders. The advance of YAG formation was monitored by intermediate phase formation during heat treatment through interrupted tests at different temperatures and analysis by X-ray diffraction. From this analysis, it was found that reaction for the formation of the desired YAG is completed at 1500 °C. Fourier transform infrared spectroscopy analyses determined the presence of functional groups corresponding to the YAG. Finally, the study employing optical emission spectroscopy showed wavelengths in agreement with those of the electronic structure of the elements of the synthesized Nd:YAG.

High entropy alloys (HEAs) of the type CrCuFeNiTi-Alx were processed through mechanical alloying. The aluminum concentration was varied in the alloy, to determine its effect on the HEAs’ microstructure, phase formation, and chemical behavior. X-ray diffraction studies performed on the pressureless sintered samples revealed the presence of structures composed of face centered cubic (FCC) and body centered cubic (BCC) solid-solution phases. Since the valences of the elements that form the alloy are different, a nearly stoichiometric compound was obtained, increasing the final entropy of the alloy. The aluminum was partly responsible for this situation, which also favored transforming part of the FCC phase into BCC phase on the sintered bodies. X-ray diffraction also indicated the formation of different compounds with the alloy’s metals. Bulk samples exhibited microstructures with different phases. The presence of these phases and the results of the chemical analyses revealed the formation of alloying elements that, in turn, formed a solid solution and, consequently, had a high entropy. From the corrosion tests, it could be concluded that the samples with a lower aluminum content were the most resistant to corrosion.

Aluminum matrix composites have recently taken an important role in advanced applications because they have a good combination of physical and chemical properties. For this reason, in this work, aluminum composites, with additions of ceramic particles (mullite or tungsten carbide), were manufactured in order to determine the effect of those particles on the mechanical properties and microstructure of aluminum. The manufacture of the composites was carried out by means of powder metallurgy. We studied composites with additions of 0.5 and 1 vol.% of the respective ceramic. Composites were sintered at 580 and 601 °C, which corresponds to 88 and 91% of the melting point of aluminum, respectively. Observations in SEM, together with EDX analysis, confirm that mullite particles are located at intragranular and transgranular positions of the aluminum matrix, while tungsten carbide particles were found mostly at intragranular areas of the matrix. From the analysis of the studied ceramics, it was found that with the use of mullite, there are greater improvements in the hardness and elastic modulus of the manufactured composite.

Agave lechuguilla fibers exhibit high tensile strength, low density and durability, but their use in natural rubber composites is underexplored. This study investigates alkaline-treated fibers (149–180 µm) as reinforcements for natural latex. Fibers were pretreated with a methanol–acetone mixture, followed by immersion in 10% NaOH at 70 °C for 1 h, removing lignin and hemicellulose as confirmed by FTIR and SEM. Thermogravimetric analysis showed three weight-loss stages: moisture/volatiles (9.4%), hemicellulose (peak at 341 °C), and cellulose/lignin (peak at 482 °C), with <3% residue above 500 °C. Treated composites exhibited enhanced tensile strength (4.68 ± 1.2 MPa vs. 1.3 ± 0.8 MPa for untreated) and elongation at break (530 ± 51% vs. 452 ± 32%). Hardness increased from 21.8 (neat latex) to 30.3, and compression resistance was improved. Optical microscopy revealed strong fiber–matrix adhesion with uniform dispersion. Alkaline treatment enhances interfacial bonding and mechanical performance, making A. lechuguilla fibers a sustainable reinforcement for eco-friendly composites in automotive, construction, and packaging sectors.

Biomaterials have assumed a decisive role in modern medicine by enabling significant advancements in medical care practices. These materials are designed to interact with biological systems, offering substantial solutions for various medical needs. In this research, bioceramic materials consisting of a bioactive hydroxyapatite-based matrix with Ti nanoparticles, were processed as promising materials. These bioceramics were obtained using mechanical milling, uniaxial pressing, and sintering as powder processing techniques. This study evaluates the effect of Ti additions on the structural, electrochemical, and mechanical properties of the hydroxyapatite ceramic material. Titanium additions were about 1, 2 and 3 wt%. The experimental results demonstrate that the biocomposite's structure has two hexagonal phases: one corresponding to the hydroxyapatite matrix and the other to the Ti as a reinforced phase. The biomaterials' microstructure is completely fine and homogeneous. The biomaterial reinforced with 1wt. % Ti exhibits the best mechanical behavior. In this context, Electrochemical tests reveal that bio-ceramics can achieve stability through an ion adsorption mechanism when exposed to a physiological electrolyte. Bioceramics, particularly those containing 1%Ti, develop their bioactivity through the formation a high-density hydroxide film during a porous sealing process at potentials around −782.71 mV, with an ionic charge transfer of 0.43x10^-9 A/cm². Finally, this biofilm behaves as a capacitor Cc = 0.18 nF/cm², resulting in lower ionic charge transfer resistance (Rct = 1.526x106 Ω-cm²) at the interface. This mechanism promotes the material’s biocompatibility for bone integration as an implant material.