Miguel Tinoco

Layered double hydroxides (LDH) based on transition metals are highly flexible in tailoring their dimensionality, lattice, and electronic structures, making them promising candidates as multifunctional 2D materials for the development of clean energy technologies and boosting the use of hydrogen as an energy vector. In this paper, strategic anion substitution in cobalt LDH is an appealing strategy to produce a material with two‐fold functionality, electrochemical and magnetocaloric response, offering a sustainable alternative to existing electrocatalysts and cryogenic refrigerants. It is unambiguously demonstrated that (poly)oxomolybdate‐based specimens interleave in Co LDH nanosheets up to a Co:Mo = 1:0.4 ratio, leading to an interstratified material. This intercalation greatly benefits the kinetics of the oxygen evolution reaction for H ₂ production, boosting the catalytic sites due to the expansion of the interlayer space, induced by the bulky molybdates which also partially modify the Co oxidation state of αCo(OH) ₂ nanolayers, favoring charge transfer. In parallel, the interleaved Mo species strengthen superexchange interactions compared with pristine α‐Co(OH) ₂ , effectively adjusting the operating temperature toward the liquid hydrogen range (2030 K). This specific temperature range allows to fill a critical gap in magnetocaloric materials, as few systems can simultaneously achieve both large magnetic entropy changes and structural stability.

This study presents groundbreaking results in the field of rechargeable aluminium‐ion batteries, achieving stable capacities exceeding 300 mAh g⁻¹ for more than 300 cycles. The key to this achievement lies in the utilization of tailor‐made carbon materials and a urea‐AlCl₃‐based electrolyte. The article investigates the optimal physicochemical properties of the active material necessary for effective electrodes for these aluminium‐ion batteries. This investigation employs a wide range of materials characterization techniques (XRD, SEM‐EDX, N₂ adsorption‐desorption isotherms, Hg porosimetry, XPS, FTIR, Raman and TEM‐EDX) and electrochemical performance analyses to delve into the subject. These findings represent a significant improvement in the capacity of aluminium‐ion batteries, bringing us closer to their implementation and commercialization. This achievement is attributed to the utilization of readily available, cost‐effective, and non‐corrosive materials. The ability to customize carbon xerogels and the use of the urea‐AlCl₃ electrolyte offer promising avenues for the practical implementation of these advanced battery technologies, leading to further enhancements in their performance and widespread adoption in various applications.

The hydrothermal synthesis of short Zn₂GeO₄ nanorods for light-emitting applications is reported, with structural, morphological and luminescence characterization, allowing correlation of the optoelectronic properties with the morphological aspects.

Zn2GeO4 is considered a very promising alternative to current luminescent semiconductors. Previous results suggest that its emitted wavelength may depend on different variables, such as particle size and morphology, among others. In this work, we have prepared pure and highly homogeneous Zn2GeO4 nanorods under hydrothermal synthesis conditions with a willemite-like structure. Their luminescent properties have been explored and their band gap estimated, which are distinct to previously reported Zn2GeO4 bulk particles. Therefore, our results identify particle morphology as a crucial factor for maximizing and fine-tuning the luminesce of Zn2GeO4 nano-phosphors.

The present work aims to assess the impact of morphology and reducibility on lanthanum-doped ceria nanocatalysts with controlled morphology on the NO oxidation reaction. Specifically, samples were prepared using a hydrothermal method incorporating lanthanum at varying molar concentrations (0, 5, 10, and 15 mol.%) into ceria with a controlled morphology (nanocubes and nanorods). The structural, compositional, and redox characterization of these catalysts has been performed via scanning transmission electron microscopy (STEM), X-ray diffraction (XRD), X-ray energy dispersive spectroscopy (X-EDS), inductively coupled plasma (ICP), hydrogen temperature-programmed reduction (H₂-TPR), and oxygen storage capacity (OSC). NO oxidation catalytic tests were conducted, and the results were compared with estimated curves (obtained by considering the proportions of the corresponding components), which revealed the presence of a synergistic effect between lanthanum and ceria. The degree of enhancement was found to depend on both the morphology and the amount of lanthanum incorporated into CeO₂. These findings may facilitate the optimization of features concerning ceria-based nanocatalysts for the removal of NO_x emissions from exhaust gases.

The frequently mutated phosphatidylinositol 3-kinase catalytic subunit alpha (PIK3CA) gene is associated with multiple tumors and endocytosis of viruses. Identification of muted nucleotides at the hotspot can help in finding the susceptible people who are vulnerable to cancers and viruses. Herein, a simple enzyme-free colorimetric method is developed for the quick detection of PIK3CA gene mutations. The main mechanism lies in the dissimilar interactions between praseodymia nanorods and different nucleotides, as well as the underlying oxidase-mimicking characteristics of praseodymia. With rational designs of probes and processes, this method has great potential for expanded applications in the screening of mutations in other genes of interest.

Ag₂S nanoparticles are near-infrared (NIR) probes providing emission in a specific spectral range (~1200 nm), and superparamagnetic iron oxide nanoparticles (SPION) are colloidal systems able to respond to an external magnetic field. A disadvantage of Ag₂S NPs is the attenuated luminescent properties are reduced in aqueous media and human fluids. Concerning SPION, the main drawback is the generation of undesirable clusters that reduce particle stability. Here, we fabricate biocompatible hybrid nanosystems combining Ag₂S NPs and SPION by the electrospraying technique for drug delivery purposes. These nanostructures are composed of poly(lactic-co-glycolic acid) (PLGA) as the polymeric matrix in connection with both Ag₂S NPs and SPIONs. Initially, we fabricate a hybrid colloidal nanosystem composed of Ag₂S NPs in connection with PLGA (PLGA@Ag₂S) by three different routes, showing good photoluminescent (PL) properties with relatively high average decay times. Then, we incorporate SPIONs, obtaining a PLGA polymeric matrix containing both Ag₂S NPs and SPION (PLGA@Ag₂S@SPION). Interestingly, in this hybrid system, the location of Ag₂S NPs and SPIONs depends on the synthesis route performed during electrospraying. After a detailed characterization, we demonstrate the encapsulation and release capabilities, obtaining the kinetic release using a model chemotherapeutic drug (maslinic acid). Finally, we perform in vitro cytotoxicity assays using drug-loaded hybrid systems against several tumor cell lines.

In this work, a simple one-step thermal oxidation process was established to achieve a significant surface increase in {110} and {111} nanofacets on well-defined, pure and Pr-doped, ceria nanocubes. More importantly, without changing most of the bulk properties, this treatment leads to a remarkable boost of their enzymatic activities: from the oxidant (oxidase-like) to antioxidant (hydroxyl radical scavenging) as well as the paraoxon degradation (phosphatase-like) activities. Such performance improvement might be due to the thermally generated sawtoothlike {111} nanofacets and defects, which facilitate the oxygen mobility and the formation of oxygen vacancies on the surface. Finally, possible mechanisms of nanoceria as artificial enzymes have been proposed in this manuscript. Considering the potential application of ceria as artificial enzymes, this thermal treatment may enable the future design of highly efficient nanozymes without changing the bulk composition.