Publications

Graphene oxide (GO) derived from the oxidization of graphite exhibits high specific surface area with potential in electrochemical applications. Furthermore, silver and zinc oxide nanoparticles, further denoted as AgNPs and ZnONPs, respectively, display superior physicochemical and electronic properties, that would significantly improve the electrocatalytic properties by being applied in electrochemical sensing. Consequently, in the present work, three different hybrid nanomaterials consisting of reduced graphene oxide (rGO) modified with either AgNPs, ZnONPs, or combined AgZnONPs were synthesized and characterized. The synthesis of GO was performed by a modified Hummer's method, while the decoration of GO with the nanoparticles was carried out by self-assembly solvothermal processes. The Ag-rGO, ZnO-rGO, and AgZnO-rGO nanocomposite hybrid materials were characterized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), Raman spectroscopy, scanning electron microscopy (SEM), and transmission electron microscopy (TEM) combined with energy-dispersive X-ray spectroscopy (EDX). Furthermore, the electrochemical responses of the fabricated nanocomposites towards the standard ferrocyanide/ferricyanide [Fe(CN)6]3-/4- redox system were investigated using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) techniques. The results have been explained in terms of structural differences between the nanoparticles formed on the surface of the fabricated nanocomposite materials. Namely, the improved electrochemical performance of ZnO-rGO can be attributed to the high surface to volume ratio of ZnO, which provides greater area of electrode/electrolyte junction and consequently, large number of sites at the electrolyte-ZnO interface. The aim of the present work is the fabrication of novel high-performance rGO-based nanomaterials for applications in electrochemical sensing.

As a potential anode material for potassium-ion batteries (PIBs), bimetallic sulfides are favored by researchers for their high specific capacity, low cost, and long cycle life. However, the non-ideal diffusion rate and poor cycle stability pose significant challenges in practical applications. In this work, bimetallic sulfide CuSbSyC with a yolk-shell structure was synthesized by in situ precipitation and carbonization. When CuSbSy is applied in the anode of PIBs, it can provide the desired capacity and reduce the volume expansion of the compound through the synergistic effect between copper and antimony. At the same time, the existence of the nitrogen-doped carbon shell confines the material within the shell while improving its electrical conductivity, inhibiting its volume expansion and aggregation. Therefore, CuSbSy@C exhibits a satisfactory capacity (438.8 mAh g^-1 at 100 mA g^-1 after 60 cycles) and an excellent long cycle life (174.5 mAh g^-1 at 1000 mA g^-1 after 1000 cycles).

Attributed to its environmental friendliness, high theoretical energy density, and abundant sodium resource, rechargeable hybrid sodium-air batteries (HSABs) are expected to become a promising pioneer of the new-generation green energy storage device. However, HSABs suffer from the high voltage gap, low energy conversion efficiency, and poor cycle stability due to the low catalytic activity of catalysts caused by the degradation of polymer binders. Herein, hierarchical mesoporous NiO nanosheet arrays grown on carbon papers (CP) (NiO NACP) were synthesized by a facile and efficient hydrothermal route and calcination process, which acts as an integrated electrode for HSABs. Compared with traditional air electrodes that contain a polymer binder and conductive carbon, the integrated NiO NA@CP electrode prevents the aggregation of catalysts, improves the electronic conductivity by good electric contact and ensures its robust mechanical stability. In addition, NiO NA@CP electrode with the abundant porosity and large specific area offers plenty of active sites and shortens ion transfer length and rapid mass transport in ORR/OER process, leading to excellent oxygen catalytic activities. HSABs with NiO NA@CP electrode show a low overpotential of 0.65 V, a state-of-the-art power density (7.53 mW cm^-2), as well as an excellent cyclability of 170 cycles (over 170 h) at a current density of 0.1 mA cm^-2.

Alkyd resins are oil-based polymers that have been widely used for generations in the surface coating industry and beyond. Characterization of these resins is of high importance to understand the influence of its components on its behavior, compatibility with other resins, and final quality to ensure high durability. Here, NMR spectroscopy and GPC were used for characterizing differences in the chemical structure, molecular distribution, and dispersity between oil-based and fatty acid-based alkyd polymers made from sacha inchi and linseed oils. Sancha inchi (Plukentia volubilis L.) is a fruit-bearing plant native to South America and the Caribbean, and has a rich unsaturated fatty acid content. The effect of vegetable oil and polyol selection on the synthesis of alkyd resins for coating applications was analyzed. The influence of two different synthesis methods, monoglyceride and fatty acid processes, was also compared. Important structural differences were observed using NMR: one-dimensional spectra revealed the degree of unsaturated fatty acid chains along the polyester backbone, whereas, 2D NMR experiments facilitated chemical shift assignments of all signals. GPC analysis suggested that alkyd resins with homogeneous and high molecular weights can be obtained with the fatty acid process, and that resins containing pentaerythritol may have uniform chain lengths.

We analyze the coupling between double nanowire cavities for both photonic modes and plasmonic modes. When the spacing between nanowires reduces, a redshift of the resonant frequency of the symmetric mode and a blueshift of the resonant frequency of the antisymmetric mode are observed. Compared to single nanowire cavity modes, the Q factors of antisymmetric supermodes of double nanowires can be improved by 51% for photonic modes and by 24% for plasmonic modes. The mechanisms of Q factor improvement for photonic modes and plasmonic modes are studied based on the field distribution of radiations from the modes. This paper may contribute to research and applications for double nanowire lasers and nanowire laser arrays.