We synthesized nano-ZnCo 2 O 4 using molten salt method at low temperature 280°C for 30 min or 3h in air, at a heating and cooling rate of 3°C/min and quenching. Reported are the effects of Co-sulphate, hydroxide and Zn-sulphate salt combinations, and heating, cooling rate on morphology and crystal structure of the ZnCo 2 O 4 . ZnCo 2 O 4 -I to IV phases were characterized by X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Density and Brunauer-Emmett-Teller (BET) surface area methods. All samples (ZnCo 2 O 4 -I to III) showed single phase materials with a lattice parameter values of ∼8.102–8.126 Å and surface area are in the range of 5 to 32 m 2 g −1 . Electrochemical properties were evaluated via cyclic voltammetry (CV) and galvanostatic cycling studies. CV studies showed a minor differences in the peak potentials depending on preparation method, and all compounds exhibits a main anodic peaks to occur at ∼1.65 V and ∼2.1 V and cathodic peaks at ∼0.95V, ∼1.25 V. Nano-ZnCo 2 O 4 -II prepared using Zn-sulphate and Co-hydroxide source showed a high and stable capacity of ∼974 mAh g −1 at the end of 40 th cycle, at a current rate of 60 mA g −1 in the voltage range, 0.005V–3.0 V. Heat treated electrode of ZnCo 2 O 4 - III showed improved cycling stability up to 30 cycles.
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Reddy et al. (2011) studied this question.
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