首页 | 本学科首页   官方微博 | 高级检索  
     


Electrochemical properties of LaFeO3-rGO composite
Authors:Yongjie Yuan  Zhentao Dong  Yuan Li  Lu Zhang  Yumeng Zhao  Bo Wang  Shumin Han
Affiliation:State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004, China;State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004, China;State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004, China;State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004, China;State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004, China;State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004, China;State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004, China
Abstract:
LaFeO3-xwt% rGO composite (x = 8, 10, 12) was synthesized by ultraphonic stirring and lyophilization method. SEM, TEM and XRD results show that the perovskite-type LaFeO3 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 LaFeO3, thus improving the electrical conductivity and appreciably enhancing the electrochemical properties of LaFeO3. As compared with LaFeO3, the maximum discharge capacity of the composite (x=10) increased from 209.5 mAh g–1 to 334.6 mAh g–1. The High rate dischargeability at a discharge current density of 1500 mA g–1 (HRD1500) and the capacity retention rate after 100 charge/discharge cycles (S100) of the composite increased by 9% and 17%, respectively.
Keywords:MH/Ni batteries   LaFeO3   RGO   Composite   Electrochemical property
本文献已被 CNKI ScienceDirect 等数据库收录!
点击此处可从《自然科学进展(英文版)》浏览原始摘要信息
点击此处可从《自然科学进展(英文版)》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号