ABSTRACT
Wheat straw-derived carbon from the Wheatbelt region in Western Australia was subjected to chemical activation in an electrolyte containing either acid or base treatment. The findings showed an increase in electron/hole mobility towards the interfaces due to the presence of different surface functional groups such as C-SOx -C and S=C in the carbon framework for acid activation. Likewise, the galvanostatic capacitance measured at a current density of 2â mA cm-2 in a three-electrode configuration for acid-activated wheat straw exhibited 162â F g-1 , while that for base-activated wheat straw exhibited 106â F g-1 . An increase of 34.5 % more capacitance was achieved for acid-treated wheat straw. This improvement is attributed to the synergistic effects between surface functional groups and electrolyte ions, as well as the electronic structure of the porous electrode.
Subject(s)
Carbon , Carbon/chemistry , Electric Capacitance , Electrodes , PorosityABSTRACT
The ability to tune the interfacial region in core-shell nanocomposites with a surface reconstruction as a source for surface energy (de)stabilization is presented. We consider Zn-doped nickel molybdate (NiMoO4) (ZNM) as a core crystal structure and AWO4 (A = Co or Mg) as a shell surface. Based on the density-functional theory method, the interfacial models of Zn-doped NiMoO4@AWO4 (ZNM@AW) core@shell structures are simulated and revealed to undergo surface reconstruction on the (-110) and (-202) surfaces of the AW shells, where the surface degradation of ZNM@MW(-110) is observed. The theoretical simulation is validated against the electrochemical performance of supercapacitor studies. To verify, we synthesize the hierarchical ZNM@AW core@shell semiconductor structured nanocomposites grown on a nickel foam conductive substrate using a facile and green two-step hydrothermal method. The morphology and chemical and electrochemical properties of the hierarchically structured nanocomposites are characterized in detail. The performance of the core@shell is significantly affected by the chosen intrinsic properties of metal oxides and exhibited high performance compared to a single-component system in supercapacitors. The proposed asymmetric device, Zn-doped NiMoO4@CoWO4 (ZNM@CW)||activated carbon, exhibits a superior pseudo-capacitance, delivering a high areal capacitance of 0.892 F cm-2 at a current density of 2 mA cm-2 and an excellent cycling stability of 96% retention of its initial capacitance after 1000 charge-discharge cycles. These fundamental theoretical and experimental insights with the extent of the surface reconstruction sufficiently explain the storage properties of the studied materials.
ABSTRACT
Nickel-based bimetallic oxides (BMOs) have shown significant potential in battery-type electrodes for pseudo-capacitors given their ability to facilitate redox reactions. In this work, two bimetallic oxides, NiMoO4 and NiWO4, were synthesized using a wet chemical route. The structure and electrochemical properties of the pseudo-capacitor cathode materials were characterized. NiMoO4 showed superior charge storage performance in comparison to NiWO4, exhibiting a discharge capacitance of 124 and 77 F.g-1, respectively. NiMoO4, moreover, demonstrates better capacity retention after 1000 cycles with 87.14% compared to 82.22% for NiWO4. The lower electrochemical performance of the latter was identified to result from the redox behavior during cycling. NiWO4 reacts in the alkaline solution and forms a passivation layer composed of WO3 on the electrode, while in contrast, the redox behavior of NiMoO4 is fully reversible.
ABSTRACT
The effect of zinc (Zn) doping and defect formation on the surface of nickel molybdate (NiMoO4) structures with varying Zn content has been studied to produce one-dimensional electrodes and catalysts for electrochemical energy storage and ethanol oxidation, respectively. Zn-doped nickel molybdate (Ni1-xZnxMoO4, where x = 0.1, 0.2, 0.4, and 0.6) nanorods were synthesized by a simple wet chemical route. The optimal amount of Zn is found to be around 0.25 above which the NiMoO4 becomes unstable, resulting in poor electrochemical activity. This result agrees with our density functional theory calculations in which the thermodynamic stability reveals that Ni1-xZnxMoO4 crystallized in the ß-NiMoO4 phase and is found to be stable for x≤0.25. Analytical techniques show direct evidence of the presence of Zn in the NiMoO4 nanorods, which subtly alter the electrocatalytic activity. Compared with pristine NiMoO4, Zn-doped NiMoO4 with the optimized Zn content was tested as an electrode for an asymmetric supercapacitor and demonstrated an enhanced specific capacitance of 122 F g-1 with a high specific energy density of 43 W h kg-1 at a high power density of 384 W kg-1. Our calculations suggest that the good conductivity from Zn doping is attributed to the formation of excess oxygen vacancies and dopants play an important role in enhancing the charge transfer between the surface and OH- ions from the electrolyte. We report electrochemical testing, material characterization, and computational insights and demonstrate that the appropriate amount of Zn in NiMoO4 can improve the storage capacity (â¼15%) due to oxygen vacancy interactions.
