Nanosized CeO2-CuO (CeCu, 2:1) and CeO2-CoO (CeCo, 2:1) were synthesized by co-precipitation from nitrate precursors using 25% ammonia solution (NH4OH) as the precipitating agent. The catalysts were calcined in air at 800°C for 4h to evaluate the thermal stability. Powder x-ray diffraction (XRD) and Dynamic Light Scattering (DLS) techniques were used for catalyst characterization. A Thermo Gravimetric/Differential Thermal Analyzer (TG/DTA) was used to determine the catalytic efficiency and soot oxidation activity. Ce-composite nanoparticles heightens the redox properties of the catalyst relative to undoped ceria. The Ce-composite samples exhibited excellent soot catalytic combustion performance by decreasing activation energy of soot oxidation.

Highly detailed structural characterization is required to understand the discharge mechanism in order to effectively investigate α-MnO2 structured lithium battery cathode materials. This paper discusses recent findings which elucidate the lithiation mechanism of silver-hollandite, AgxMn8O16. For Ag1.2Mn8O16, the structure is not significantly perturbed during the first 2 equivalents of lithiation and the electrochemistry is highly reversible. Upon 4 equivalents of lithiation, the structure becomes highly distorted, in correlation with capacity fade observed over 40 cycles. Notably, regarding capacity fade, modifications to Ag/Mn ratio are less impactful than modifications to the α-MnO2 crystallite size. This is shown in comparisons of two materials with the same stoichiometry (Ag1.4Mn8O16) and differing crystallite size (10 and 15 nm).

This work presents the study of the isolation of chitin from residues of the Patagonian shrimp (Pleoticus muelleri), and its subsequent conversion to chitosan under different reaction conditions. The obtained products were characterized by evaluating their molecular weight (Mw) and degree of deacetylation (DD). In addition, chitosan- glycerol films were prepared (5, 10 and 20% w/w of plasticizer content), using a neutralization process during the unmolding step. The films were characterized by infrared (FTIR) and UV-Visible spectroscopy and scanning electron microscopy (SEM). In addition, its behavior against water (contact angle and water sorption) and mechanical properties were also studied. It was observed that 72 hours of reaction time at 120 °C were necessary to obtain a chitosan sample with the desirable solubility properties from the chitin extracted from Pleoticus muelleri shells. The chitosan-glycerol films turned out to be systems of high transparency and their properties depended on the plasticizer content, obtaining homogeneous systems for concentrations up to 10% w/w. In addition, the films were found to be more hydrophilic than the reference material, with smaller contact angle and greater water absorption values, obtaining more flexible films in view of their mechanical properties.

Here we present an investigation into the phase change mechanism and detection methods of the metal-insulator transition of vanadium dioxide (VO2). We are able to detect the onset of the phase transition, and track it to completion using both the mechanical and electrical response by depositing VO2/TiO2 layers onto microcantilever devices by pulsed laser deposition. The resonance frequency of v-shaped cantilevers was shown to increase by up to 41 % upon deposition of VO2 as detected by laser Doppler vibrometry. Such a large increase in resonance frequency is ascribed to high tensile stress imparted onto the cantilever during the deposition process. The insulator-metal transition manifested as a 5 % increase in the resonance frequency as a result of lattice compression, resulting in additional tensile stress in the more ordered metallic phase. Electrically, the transition was confirmed by over three orders magnitude decrease in resistance upon heating past the transition. The metal-insulator transition was measured with an accuracy of a few °C when comparing the two methods, however, the transition was much sharper in the mechanical response.

The effects of different starting materials using nano-synthesis methodology on electrochemical performance of lithium manganese oxide (LixMn2O4) are studied. Four spinel-type LixMn2O4 (LMO) cathode materials were prepared with different lithium and manganese sources and were analyzed chemically and characterized by BET and XRD. The electrochemical performance of the cathodes at room temperature and elevated temperature was tested. The crystal structure was indexed to be a cubic system with lattice parameters of 8.2342 ±0.170 Å and defined to the space group Fd3m. There was no peak of impurity because the raw materials for Mn source were first treated with acid. Although the results showed that the structures of the samples were confirmed to be cubic spinel structure, the lattice parameter and specific surface area of the samples were different. The LiMn2O4 cathodes have an initial discharge capacity of over 120mAh/g and show an ordinary two-step voltage profile. The results demonstrated that the cathode materials prepared with LiNO3 as Li source have larger lattice parameters, than those prepared from LiOH·H2O as Li source. The cathode prepared from Electrochemical Manganese Dioxide (EMD) as Mn source have larger particle sizes, lower first charge and discharge capacity, better cyclic performance, whereas those from Chemical Manganese Dioxide (CMD) as Mn source have smaller particle size, higher first charge and discharge capacity, and poor cyclic stability at elevated temperature. The cell polarization of the cathode developed by LiOH•H2O and EMD was identified to be the least and the elevated temperature cycelability to be the best. These manifestations can be attributed to differences in Li and Mn sources, specific surface areas, purities of starting materials and synthesis conditions. Melt-impregnation as a nano-synthesis method proved to be an excellent method to synthesize LiMn2O4 cathode materials that can operate at elevated temperatures when using correct starting materials and good control of synthesis temperatures.

The design of the surface chemistry of colloidal semiconductor nanocrystals (NCs) presents a powerful synthetic approach that allows to tune the optical and electronic properties of the particles in independent and precisely desired manner, to provide chemical and colloidal stability in diverse media, and, finally, to control their targeted applicability ranging from catalysis, medicine to advanced electronic devices. In this article, we summarize the successful functionalization of colloidal NCs with specifically chosen ligands using a novel ligand-exchange strategy. To transform diverse colloidal NCs into a competitive class of solution-processed semiconductors for electronic applications, we replaced the pristine, insulating ligands with tiny inorganic and hybrid inorganic/organic species. The surface modification with inorganic ions modulates the charge carrier density in NC units and guarantees enhanced interparticle interactions. The subsequent functionalization of the all-inorganic-capped NCs with organic molecules leads to the formation of hybrid inorganic/organic-capped NCs. For example, the introduction of short amine molecules enables to preserve the optical and electronic characteristics of their all-inorganic counterparts, while extending the solubility range and improving the ability to form long-range ordered 2D and 3D superstructures. Moreover, these short amines can be further used as convenient axillary co-ligands facilitating the surface functionalization of all-inorganic NCs with other biocompatible molecules, such as polyethylene glycol (PEG). This opens further perspectives for NCs not only in optoelectronic but also in biological and medical applications.

ZnFe2O4 (ZFO) represents a promising anode material for lithium ion batteries, but there is still a lack of deep understanding of the fundamental reduction mechanism associated with this material. In this paper, the complete visualization of reduction/oxidation products irrespective of their crystallinity was achieved experimentally through a compilation of in situ X-ray diffraction, synchrotron based powder diffraction, and ex-situ X-ray absorption fine structure data. Complementary theoretical modelling study further shed light upon the fundamental understanding of the lithiation mechanism, especially at the early stage from ZnFe2O4 up to LixZnFe2O4 (x = 2).

The objective of this paper is to demonstrate that Ag readily diffuses into Sb2S3 and that electric fields can control the diffusion. Ag diffusion influences the crystallization temperature and electrical properties of Sb2S3. We studied the interface between Ag and Sb2S3 using X-ray reflectivity and show that the Ag cations can be controlled by applying an electric field. We believe this effect has technological applications in data storage devices.

This work presents the synthesis and characterization of TiO2 nanotubes (NTT) with chitosan (CS). In a first stage, electrochemical anodization of titanium foils was used to generate NTT in a membrane-type arrangement. From these experiments, suitable experimental conditions were selected. In a second stage, the synthesized NTT were detached from the titanium foils by sonication. In the third stage, the detached NTT were dispersed in an acid solution containing CS in various concentrations. Finally, the nanotubes-chitosan (NTT/CS) samples were characterized by Scanning Electron Microscopy (SEM), X-ray diffraction (XRD), and Fourier Transform Infrared Spectrometry (FTIR). Our results showed that the NTT presented very regular tube morphology with -OH and Ti-O- functional groups on the surface. The interaction of NTT and chitosan was enhanced by increasing the time of contact during the synthesis of the titanium composites.

Transition metal dichalcogenides (TMDC), such as MoS2, WS2 have attracted attention due to their mechanical and electronic properties in their two dimensional (2D) structures. Here, we report a facile growth of monolayer TMDC using oxide source materials with the assistant of NaCl. The addition of NaCl can enhance the lateral growth and widen the growth window of TMDC. Through carefully controlling the growth parameters, large area growth of TMDC can be achieved. Two steps E-beam lithography was utilized to fabricate electrodes of TMDC. The phototransistors made from the CVD grown TMDC show strong persistent photoconductivity (PPC). It was finally shown that TMDC device capping with h-BN could have suppressed PPC effects.