The effects of carbon coating on the electrochemical performances of ZnO in Ni-Zn secondary batteries

摘要

The ZnO samples coated with carbon are successfully synthesized by using a high energy ball milling method. The scanning electron microscopy (SEM) images and energy dispersive spectrometer (EDS) spectra of the carbon-coated ZnO and pure ZnO show that the carbon-coated ZnO (carbon source: glucose, citric acid) samples and the untreated ZnO sample have similar particle size and crystal form. The particles have prismatic microstructure whose sizes are about 100-200 nm. However, the carbon-coated ZnO (carbon source: sucrose) sample has become agglomeration after calcination whose size has been increased to 2-6 μm. The uncoated ZnO powders have more complete crystal shape and they are glazed quadrangular materials, while the carbon coated ZnO particles has a rough surface, which resulted from the growth of carbon coating on ZnO particles. X-ray diffraction (XRD) patterns of the carbon-coated ZnO and the pure ZnO show carbon formed on the surface of ZnO is amorphous. Tafel plot, cyclic voltammetry (CV), AC impedance spectroscopy and galvanostatic charge-discharge measurement are utilized to examine the electrochemical performances of the carbon-coated ZnO. The carbon-coated ZnO (carbon source: glucose) have the most positive steady-state potential and lowest corrosion current density in the zinc electrodes which indicates that it has a good anticorrosion ability. A lower charge platform and a higher discharge platform of carbon-coated ZnO indicate that it have a better charge/discharge performance as anodic material for Ni/Zn cells. A smaller ohmic resistance and charge-transfer resistance imply that the carbon film upon ZnO could greatly decrease the impedance of the reaction process. Meanwhile, the carbon-coated ZnO also showed more excellent cycling performance than pure ZnO. The reason of improvement about electrochemical performance can be ascribed as the unique structure of amorphous carbon layer.