RESUMEN
Two-dimensional MoS2 with a controllable morphology was prepared via a simple one-step hydrothermal method. Citric acid was used as a complexing agent and self-assembly inducer. The morphology of MoS2 changed from clusters to nanosheets, and, eventually, to stacked nanorods. A formation mechanism is proposed for the observed evolution of the morphology. The nanosheet structure presents a relatively large specific surface area, more exposed active sites and greater 1T phase content compared to the other morphologies. The electrochemical performance tests show that the MoS2 nanosheets exhibit excellent electrochemical behavior. Their specific capacitance is 320.5 F g-1, and their capacitance retention is up to 95% after 5000 cycles at 5 mA cm-2. This work provides a feasible approach for changing the morphology of MoS2 for high efficiency electrode materials for supercapacitors.
RESUMEN
Bismuth-based oxides exhibit outstanding oxygen ionic conductivity and fast oxygen surface kinetics and have shown great potential as a highly active component for electrode materials in solid oxide fuel cells (SOFCs). Herein, a Nb-doped La0.6Sr0.4Co0.2Fe0.7Nb0.1O3-δ (LSCFNb) electrode with 40% Er0.4Bi1.6O3 (ESB) composite electrode was successfully fabricated by decoration method and directly assembled on barrier-layer-free yttrium-stabilized zirconia (YSZ) electrolyte cells, achieving a peak power density of 1.32 W cm-2 and excellent stability at 750 °C and 250 mA cm-2 for 100 h. ESB decoration also significantly reduces the activation energy from 214 kJ mol-1 for the O2 reduction on pristine LSCFNb electrode to 98 kJ mol-1. Further microstructural analysis reveals that there is a redistribution and migration of the ESB phase in the ESB-LSCFNb composite toward the YSZ electrolyte under the influence of cathodic polarization, forming a thin ESB layer at the cathode/YSZ electrolyte interface. The in situ formed ESB layer not only prevents the direct contact and subsequent reaction between segregated SrO and YSZ electrolytes, but also remarkably promotes the oxygen migration/diffusion at the interface for O2 reduction reaction, resulting in a remarkable increase in power output and a decrease in activation energy. The present study clearly demonstrated the in situ formation of a highly functional and active ESB protective layer at LSCFNb cobaltite cathode and YSZ electrolyte interface via ESB-decorated LSCFNb composite cathode under SOFC operation conditions.
RESUMEN
TiO2 is usually used as a sintering aid to lower the sintering temperature of porous alumina membrane support. Two ways of the addition of TiO2 are chosen: in-situ precipitation and in-situ hydrolysis. The results show that the distribution status of TiO2 has an important effect on the property of porous alumina membrane support. In in-situ hydrolysis method, the nano-meter scale TiO2 distributes evenly on the alumina particles' surface. The bending strength of the support increases sharply and the pore size distribution changes more sharply along with the content of TiO2 which slightly increases from 0.3 wt.% to 0.4 wt.%. The distribution of the nano-meter scale TiO2 is not so even added by in-situ precipitation method. Neither the bending strength nor the pore size distribution of the support is worse than that of the support added by in-situ hydrolysis even if the content of TiO2 is high to 2 wt.%. The permeating flux has a similar tendency. Consequently, the porous alumina membrane support has the porosity of 30.01% and the bending strength of 77.33 MPa after sintering at 1650 °C for 2 h with the optimized TiO2 content of 0.4 wt.% added by the in-situ hydrolysis method.
