RESUMEN
Solid-solid phase-change materials have great potential for developing compact and low-cost thermal storage systems. The solid-state nature of these materials enables the design of systems analogous to those based on natural rocks but with an extraordinarily higher energy density. In this scenario, the evaluation and improvement of the mechanical and thermophysical properties of these solid-solid PCMs are key to exploiting their full potential. In this study, LiNaSO4-based composites, comprising porous MgO and expanded graphite (EG) as the dispersed phases and LiNaSO4 as the matrix, have been prepared with the aim of enhancing the thermophysical and mechanical properties of LiNaSO4. The characteristic structure of MgO and the high degree of crystallinity of the EG600 confer on the LiNaSO4 sample mechanical stability, which leads to an increase in the Young's modulus (almost three times higher) compared to the pure LiNaSO4 sample. These materials are proposed as a suitable candidate for thermal energy storage applications at high temperatures (400-550 °C). The addition of 5 wt.% of MgO or 5% of EG had a minor influence on the solid-solid phase change temperature and enthalpy; however, other thermal properties such as thermal conductivity or specific heat capacity were increased, extending the scope of PCMs use.
RESUMEN
Achieving nanostructures with high surface area is one of the most challenging tasks as this metric usually plays a key role in technological applications, such as energy storage, gas sensing or photocatalysis, fields in which NiO is gaining increasing attention recently. Furthermore, the advent of modern NiO-based devices can take advantage of a deeper knowledge of the doping process in NiO, and the fabrication of p-n heterojunctions. By controlling experimental conditions such as dopant concentration, reaction time, temperature or pH, NiO morphology and doping mechanisms can be modulated. In this work, undoped and Sn doped nanoparticles and NiO/SnO2 nanostructures with high surface areas were obtained as a result of Sn incorporation. We demonstrate that Sn incorporation leads to the formation of nanosticks morphology, not previously observed for undoped NiO, promoting p-n heterostructures. Consequently, a surface area value around 340 m2/g was obtained for NiO nanoparticles with 4.7 at.% of Sn, which is nearly nine times higher than that of undoped NiO. The presence of Sn with different oxidation states and variable Ni3+/Ni2+ ratio as a function of the Sn content were also verified by XPS, suggesting a combination of two charge compensation mechanisms (electronic and ionic) for the substitution of Ni2+ by Sn4+. These results make Sn doped NiO nanostructures a potential candidate for a high number of technological applications, in which implementations can be achieved in the form of NiO-SnO2 p-n heterostructures.
RESUMEN
Transition metal oxides potentially present higher specific capacities than the current anodes based on carbon, providing an increasing energy density as compared to commercial Li-ion batteries. However, many parameters could influence the performance of the batteries, which depend on the processing of the electrode materials leading to different surface properties, sizes or crystalline phases. In this work a comparative study of tin and titanium oxide nanoparticles synthesized by different methods, undoped or Li doped, used as single components or in mixed ratio, or alternatively forming a composite with graphene oxide have been tested demonstrating an enhancement in capacity with Li doping and better cyclability for mixed phases and composite anodes.
