RESUMEN
Due to their high-power density and long lifetime, microsupercapacitors have been considered as an efficient energy supply/storage solution for the operation of small electronic devices. However, their fabrication remains confined to 2D thin-film microdevices with limited areal energy. In this study, the integration of all-solid-state 3D interdigitated microsupercapacitors on 4 in. silicon wafers with record energy density is demonstrated. The device electrodes are composed of a pseudocapacitive hydrated ruthenium dioxide RuO2 deposited onto highly porous current collectors. The encapsulated devices exhibit cell capacitance of 812 mF cm-2 per footprint area at an energy density of 329 mJ cm-2 , which is the highest value ever reported for planar configuration. These components achieve one of the highest surface energy/power density trade-offs and address the issue of electrical energy storage of modern electronics.
RESUMEN
Large areal capacitance electrodes made of ruthenium oxide on highly porous gold current collectors are realized by an attractive approach. The hybrid structure exhibits a capacitance in excess of 3 F cm(-2) and an areal energy density for all-solid-state microsupercapacitors that is comparable to those of microbatteries.
RESUMEN
We developed a stripping chronopotentiometric method (constant current stripping analysis, CCSA) with a mercury film electrode for selenium quantification in seawater. A sensitivity and detection limit of 222 ms ng(-1) l and 4 ng l(-1) (50 pM), respectively, were accomplished for a 3-min electrolysis time. Compared to the other chronopotentiometric methods available for a single selenium measurement only in natural waters, our procedure exhibits a ten times better sensitivity. It, therefore, allows one to reach the current concentration thresholds found in coastal and oceanic waters (30-200 ng l(-1)). Moreover, a simple change in operating conditions enables one to also quantify Se(IV), a toxic dissolved species. With respect to the other electrochemical methods of current use, our procedure is beneficial because of its ease-of-use: it needs neither degassing step, nor catalyser.
