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LaFeO_3-xwt% r GO composite(x = 8, 10, 12) was synthesized by ultraphonic stirring and lyophilization method.SEM, TEM and XRD results show that the perovskite-type LaFeO_3 was dispersed by rGO to form special porous structure due to the gauze-shaped wrinkles and folds structure of rGO. It was found that the special porous structure can effectively increase the specific surface area and suppress particle aggregation of LaFeO_3, thus improving the electrical conductivity and appreciably enhancing the electrochemical properties of LaFeO_3. As compared with LaFeO_3, the maximum discharge capacity of the composite(x=10) increased from 209.5 mAhg~(–1) to 334.6 mAhg~(–1).The High rate dischargeability at a discharge current density of 1500 mAg~(–1)(HRD1500) and the capacity retention rate after 100 charge/discharge cycles(S100) of the composite increased by 9% and 17%, respectively.
LaFeO_3-xwt% r GO composite (x = 8, 10, 12) was synthesized by ultraphonic stirring and lyophilization method. SEM, TEM and XRD results show that the perovskite-type LaFeO_3 was dispersed by rGO to form special porous structure due to the It was found that the special porous structure could effectively increase the specific surface area and suppress particle aggregation of LaFeO 3, thus improving the electrical conductivity and appreciably enhancing the electrochemical properties of LaFeO 3. As compared with LaFeO 3 , the maximum discharge capacity of the composite (x = 10) increased from 209.5 mAhg -1 to 334.6 mAhg -1. The high rate dischargeability at a discharge current density of 1500 mAg -1 (HRD 1500 ) and the capacity retention rate after 100 charge / discharge cycles (S100) of the composite increased by 9% and 17%, respectively.