Ongoing technological advances in diverse fields including portable electronics, transportation, and green energy are often hindered by the insufficient capability of energy-storage devices. By taking advantage of two different electrode materials, asymmetric supercapacitors can extend their operating voltage window beyond the thermodynamic decomposition voltage of electrolytes while enabling a solution to the energy storage limitations of symmetric supercapacitors. This review provides comprehensive knowledge to this field. We first look at the essential energy-storage mechanisms and performance evaluation criteria for asymmetric supercapacitors to understand the wide-ranging research conducted in this area. Then we move to the recent progress made for the design and fabrication of electrode materials and the overall structure of asymmetric supercapacitors in different categories. We also highlight several key scientific challenges and present our perspectives on enhancing the electrochemical performance of future asymmetric supercapacitors.
The demand for flexible/wearable electronic devices that have aesthetic appeal and multi-functionality has stimulated the rapid development of flexible supercapacitors with enhanced electrochemical performance and mechanical flexibility. After a brief introduction to flexible supercapacitors, we summarize current progress made with graphene-based electrodes. Two recently proposed prototypes for flexible supercapacitors, known as micro-supercapacitors and fiber-type supercapacitors, are then discussed. We also present our perspective on the development of graphene-based electrodes for flexible supercapacitors.
Anion
exchange membrane (AEM) electrolysis is a promising technology
to produce hydrogen through the splitting of pure water. In contrast
to proton-exchange-membrane (PEM) technology, which requires precious-metal
oxide anodes, AEM systems allow for the use of earth-abundant anode
catalysts. Here we report a study of first-row transition-metal (oxy)hydroxide/oxide
catalyst powders for application in AEM devices and compare physical
properties and performance to benchmark IrO
x
catalysts as well as typical catalysts for alkaline electrolyzers.
We show that the catalysts’ oxygen-evolution activity measured
in alkaline electrolyte using a typical three-electrode cell is a
poor indicator of performance in the AEM system. The best oxygen-evolution-reaction
(OER) catalysts in alkaline electrolyte, NiFeO
x
H
y
oxyhydroxides, are the worst
in AEM electrolysis devices where a solid alkaline electrolyte is
used along with a pure water feed. NiCoO
x
-based catalysts show the best performance in AEM electrolysis. The
performance can be further improved by adding Fe species to the particle
surface. We attribute the differences in performance in part to differences
in the electrical conductivity of the catalyst phases, which are also
measured and reported.
A facile and passive multiply flexible thin-film sensor is demonstrated based on thermoelectric effects in graphene. The sensor is highly conductive, free-standing, flexible, and elastic. It senses heat and cold, and measures heated/cooled areas; it also discerns human touch from other pressures, locates human touch, and measures pressure levels. All of these sensing abilities are demonstrated without any internal/external power supply.
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