Generation of highly porous silver nanowire networks by plasma treatment and their direct application as supercapacitor electrodes.

Exposure to plasma can significantly increase the surface area of silver species and their resistance to oxidation. While some work investigating plasma-treated silver has been done, limited morphologies and applications have been explored. We hereby explore this effect on silver nanowires (AgNWs) through medium-vacuum air plasma exposure time ranging between 30 s to 60 min. These plasma-treated AgNW networks are directly applied as supercapacitor electrodes, without any carbon or polymer additives that are typically employed alongside silver in energy storage applications. The plasma treatment consequently affected the electrochemical performance of AgNWs, where longer treatment times resulted in higher energy storage capacity. An increase in resistance was observed for plasma treatment times greater than or equal to 5 min, due to the switch from the percolation threshold of the metallic Ag phase to the Ag2O phase. Despite an initial drop in stored energy, an overall improvement in energy storage capacity was observed throughout cycling, where the optimal plasma treatment time of 5 min resulted in an increase of 320% of its starting value with near 100% coulombic efficiency, through the development of stable redox-active surface nanostructures.

Enhanced Flocculation Efficiency in a High-Ionic-Strength Environment by the Aid of Anionic ABA Triblock Copolymers.

The flocculation efficiency of polyelectrolytes in a high-ionic-strength environment is often affected and reduced due to shielding of the active ionizable functional groups, as well as changes in the surface chemistry of the solid slurry. To address this problem, a series of well-defined novel ABA triblock copolymers were employed for the flocculation of high-ionic-strength kaolin slurries at three different Ca2+ concentrations (0.05, 0.10, and 0.50 M). The primary focus was on the advancement in the polymer architecture, where the anionic functionalities were localized at the terminal ends. Typical commercial flocculants tend to have anionic functionalities randomly distributed throughout the polymer chain and hence a higher propensity toward condensed conformation and formation of insoluble species. In comparison to a control random copolymer, the ABA triblock copolymers were able to flocculate kaolin slurries to give faster settlement rates, particularly at the high Ca2+ concentrations of 0.10 and 0.50 M. In addition, these polymers had significantly better clarification ability at higher Ca2+ concentrations compared to the control random copolymer. The ABA triblock copolymer architecture may therefore have potential as a flocculant in high-ionic-strength applications.