https://ogma.newcastle.edu.au/vital/access/ /manager/Index en-au 5 Consolidation of non-colloidal spherical particles at low particle Reynolds numbers https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:27376 Wed 11 Apr 2018 12:37:45 AEST ]]> Consolidation of large spherical particles at low Reynolds numbers https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:21617 Wed 11 Apr 2018 11:07:56 AEST ]]> Semiconductor Properties of Electrodeposited Manganese Dioxide for Electrochemical Capacitors: Mott-Schottky Analysis https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:39450 Wed 08 Jun 2022 09:41:19 AEST ]]> In situ investigation of the electrodeposition mechanism of manganese dioxide from a citrate electrolyte: the effect of intermediate stabilization on material morphology https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:40006 4, 0.1 M Na2SO4 and manganese citrate concentrations of 0, 0.5, 2 or 4 mM. It was found that varying the citrate concentration changed the deposition mechanism by stabilising the Mn3+ intermediate formed by the oxidation of Mn2+. The different stability of the Mn3+ ion affects the rate of nucleation on the surface and subsequent growth of the film. This in turn, affects the morphology of the deposited material. Understanding the effects of the deposition mechanism on the resultant film morphology is necessary to optimise the properties of electrodeposited films for their various applications.]]> Tue 21 Mar 2023 18:27:28 AEDT ]]> Duty cycle effects on the step potential electrochemical spectroscopy (SPECS) analysis of the aqueous manganese dioxide electrode https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:36942 -1/2), as well as the residual capacitance and the inverse of the scan rate (v-1).]]> Tue 21 Jul 2020 11:33:42 AEST ]]> Method comparison for deconvoluting capacitive and pseudo-capacitive contributions to electrochemical capacitor electrode behavior https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:36941 2SO4 between 0.0-0.8 V (vs SCE). It was found that in all cases, the specific capacitance was decreased by increasing the sweep rate. The capacitance-sweep rate dependence was only found to be accurate in a short range of low sweep rates. Overall there was good agreement between the SPECS and current-sweep rate dependence models over the full range of sweep rates. However, the SPECS method provided more precise information about the kinetic behavior of the electrochemical cell through a full range of sweep rates.]]> Tue 21 Jul 2020 11:26:42 AEST ]]> Complications when differentiating charge transfer processes in electrochemical capacitor materials: assessment of cyclic voltammetry data https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:36940 1v + k2v1/2, where k1 and k2 are constants. Outcomes from the analysis indicate that this approach is complicated by the resistance associated with double layer formation, electrode instabilities in the electrolyte under study, and also increased electrode resistance.]]> Tue 21 Jul 2020 11:19:42 AEST ]]> Modification of the step potential electrochemical spectroscopy analysis protocol to improve outcomes https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:36939 Tue 21 Jul 2020 11:19:41 AEST ]]> Electroanalytical characterization of electrochemical capacitor systems https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:36938 + (0.01 M AgNO3 in ACN) reference electrode. Situated between the opposing AC electrodes, between two separators, is a Pt sensing electrode, the potential of which is either monitored or controlled to explore either electrolyte fluxes during cycling, or the formation of soluble species in the electrolyte, respectively. It was deduced that electrolyte ions are strongly associated with the AC electrodes rather than between the electrodes even without an applied potential. Furthermore, aging of the electrochemical system with cycling (cyclic voltammetry) is also explored. Even with identical electrodes it is noted that the individual electrodes behaved differently as a result of anion versus cation association. Finally, at cell voltages approaching 2 V, oxidation of the positive electrode is observed, liberating species into the electrolyte. The implications of these observations have been discussed.]]> Tue 21 Jul 2020 11:05:42 AEST ]]> Oscillatory current behavior in energy storage electrode materials https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:36937 Tue 21 Jul 2020 10:51:42 AEST ]]> Redox mechanism contributions to the behaviour of electrochemical capacitor materials https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:39605 Thu 16 Jun 2022 09:54:02 AEST ]]> Influence of counter ions of ammonium for nitrogen doping and carbon properties in hydrothermal carbonization: characterization and supercapacitor performance https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:43377 Thu 15 Sep 2022 16:14:33 AEST ]]> Analysis of voltametric data from electrochemical capacitor electrode materials: Method refinement for improved outcomes https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:54296 Thu 15 Feb 2024 14:52:06 AEDT ]]> Electroanalytical characterization of electrochemical capacitor systems using step potential electrochemical spectroscopy https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:46822 + reference electrode, individual electrode potentials were measured showing that even though it is a symmetrical device, polarization on the positive electrode was always greater than the negative electrode, implying that the negative electrode capacitance is greater. Deconvolution of the i-t transients from the SPECS experiment across the device voltage window can be accomplished in a similar fashion to the study of a single electrode, in which case geometric and porous capacitances, as well as diffusion and residual processes are identified. Similarly, the components of the i-t transients can be converted into voltametric data, providing access to individual electrode performance over a wide range of sweep rates in the device. The inclusion of a sensing electrode between he positive and negative electrodes is also described, providing insight into electrolyte fluxes and electrode stability within the device.]]> Thu 01 Dec 2022 10:00:23 AEDT ]]> Modelling voltametric data from electrochemical capacitors https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:47594 Mon 23 Jan 2023 14:56:26 AEDT ]]> Development of electrochemical characterization methods and advanced capacitor materials https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:36935 Mon 20 Jul 2020 13:56:55 AEST ]]> Effect of electrolyte cation on the charge storage mechanism of manganese dioxide for electrochemical capacitors https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:48830 Mon 10 Apr 2023 10:35:30 AEST ]]> Carbon hollow spheres as electrochemical capacitors: mechanistic insights https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:37206 2SO4 electrolyte carbon hollow spheres provide much better overall capacitance values as compared to high surface area activated carbon due to the better surface area utilization particularly at large scan rates. Carbon hollow spheres exhibited 74% more specific surface area utilization for energy storage as an electrode material in comparison to activated carbon in 0.5 M Na2SO4 solution. When, overall capacitance is divided in to the fragment capacitances in terms of geometric, porous and diffusional contents; morphology of hollow spheres played an important role while in the non-aqueous solutions specific capacitance values remained dependent on the specific surface area of the carbon material. Diffusional fragment of capacitance values in carbon hollow spheres remained limited because of limited thickness of the hollow shells. In this study, at 1 mV s−1 carbon hollow spheres with 29 nm shell thickness and with a specific surface area of 1523 m2 g−1 exhibited a specific capacitance values of 105 F g−1 and 127 F g−1 as compared to 85 and 121 F g−1 for activated carbon with a specific surface area of 1895 m2 g−1 in 0.5 M sodium sulfate and 1.0 M TEABF4 respectively.]]> Mon 03 Apr 2023 11:52:29 AEST ]]>