Nanoscale Dynamics and Structure of SAILs at Electrodes. This project will produce new, high performance, surface active ionic liquids. Surface active ionic liquids are pure salts in which one of the ions is based on a surfactant molecule. Surface active ionic liquids are much more effective than conventional electrolytes for some applications, but only at elevated temperature; at low temperature, ion dynamics are too slow. We will use cutting edge techniques to probe ion dynamics in surface act ....Nanoscale Dynamics and Structure of SAILs at Electrodes. This project will produce new, high performance, surface active ionic liquids. Surface active ionic liquids are pure salts in which one of the ions is based on a surfactant molecule. Surface active ionic liquids are much more effective than conventional electrolytes for some applications, but only at elevated temperature; at low temperature, ion dynamics are too slow. We will use cutting edge techniques to probe ion dynamics in surface active ionic liquids in the bulk and at electrode surfaces, and use this to elucidate rules for the rational design of new surface active ionic liquids with fast dynamics at low temperature, towards their use at room temperature in diverse areas; this project will target capacitors and gas sensors. Read moreRead less
Nanoparticles with structures that mimic enzymes for electrocatalysis. This project aims to create a new class of electrocatalysts with architectures inspired by enzymes. Electrocatalysts are the backbone of the modern energy economy. In the new electrocatalysts developed by the project, the intention is the active sites will be spatially separated from the bulk solution by nanopores, as enzymes do. This architecture allows the reaction environment to be altered from the bulk solution, active tr ....Nanoparticles with structures that mimic enzymes for electrocatalysis. This project aims to create a new class of electrocatalysts with architectures inspired by enzymes. Electrocatalysts are the backbone of the modern energy economy. In the new electrocatalysts developed by the project, the intention is the active sites will be spatially separated from the bulk solution by nanopores, as enzymes do. This architecture allows the reaction environment to be altered from the bulk solution, active transport of species to the active site and cascade reactions to be performed. This should give advantages in activity, selectivity and the ability to perform multistep reactions. The intended outcomes are better performing hydrogen fuel cells and more effective conversion of carbon dioxide into useful organic compounds.Read moreRead less
Special Research Initiatives - Grant ID: SR180200015
Funder
Australian Research Council
Funding Amount
$589,007.00
Summary
Combination of electrochemistry with sono to destroy and detoxify PFAS. Previously the major means of dealing with per- and poly-fluoroalkyl substances (PFAS) is by adsorption, to collect and remove PFAS from contaminated sites. However, PFAS still exist, non-degraded and waiting for destruction. Targeting slurry waste from current remediation / adsorption plants, this project aims to efficiently degrade PFAS by combining electrochemical oxidation with sono-chemistry to enhance degradation capac ....Combination of electrochemistry with sono to destroy and detoxify PFAS. Previously the major means of dealing with per- and poly-fluoroalkyl substances (PFAS) is by adsorption, to collect and remove PFAS from contaminated sites. However, PFAS still exist, non-degraded and waiting for destruction. Targeting slurry waste from current remediation / adsorption plants, this project aims to efficiently degrade PFAS by combining electrochemical oxidation with sono-chemistry to enhance degradation capacity, to accelerate PFAS desorption / transportation from slurry waste, to avoid electrode fouling and to detoxify PFAS. The expected outcome of this project is to clean up contaminated sites, including PFAS / precursors and other persistent organic pollutants, leading to significant environmental benefits.Read moreRead less