期刊文献+

新型多孔Ti/Sb2O4-SnO2电极的制备及性能 被引量:2

Preparation and Performance of Novel Porous Ti/Sb 2O 4-SnO 2 Electrode
下载PDF
导出
摘要 以采用脱合金方法制备的具有纳米多孔结构的钛板为基体,通过电沉积方法和热分解法成功制备了锡锑氧化物电极(Ti/Sb2O4-SnO2)。利用X射线衍射、扫描电子显微镜、透射电子显微镜对电极的相组成、微观形貌进行表征。应用电化学工作站测试电极的电化学性能,并研究了电极对苯酚的电催化氧化降解能力。通过调节钛基体热处理温度来优化电极性能,结果表明:多孔钛基体热处理温度为300℃时,制备的Ti/Sb2O4-SnO2电极多孔网状结构明显清晰,电流密度最大,导电性最好,电极实际寿命达到251.6 h,电极电阻最小,约为14.5Ω,90 min对苯酚的降解效率最高,约为97%。 Ti with nanoporous structure was prepared by dealloying method,and then it was used as a substrate for preparing a tin antimony oxide electrode(Ti/Sb 2O 4-SnO 2)by electrodeposition and thermal decomposition.The phase composition,microstructure and surface morphology of the electrode were analyzed by X-ray diffraction,scanning electron microscopy and transmission electron microscopy.The electrochemical performance of the electrode was tested by using an electrochemical workstation.The electrocatalytic oxidation property of the electrode as anode for the degradation of phenol was studied.The electrode performance was optimized by adjusting the heat treatment temperature of the Ti substrate.The results show that when the heat treatment temperature of the porous Ti substrate is 300℃,the porous network structure of the prepared Ti/Sb 2O 4-SnO 2 electrodeis clear,the electrode has maximum current density,best conductivity,its actual life reaches up to 251.6 h,it has minimum electrode resistance,approximately 14.5Ω.The degradation efficiency of phenol is the highest at 90 min,it is about 97%.
作者 刘洪浩 戴磊 陈钊 韩利华 王岭 LIU Hong-Hao;DAI Lei;CHEN Zhao;HAN Li-Hua;WANG Ling(College of Chemical Engineering,North China University of Science and Technology,Tangshan Hebei 063210,China;Hebei Province Key Laboratory of Photocatalytic and Electrocatalytic Materials for Environment,Tangshan Hebei 063210,China)
出处 《华北理工大学学报(自然科学版)》 CAS 2020年第3期40-48,共9页 Journal of North China University of Science and Technology:Natural Science Edition
基金 国家自然科学基金项目(50672080)。
关键词 SnO 2电极 多孔 电催化氧化 苯酚 SnO 2 electrode porous electrocatalytic oxidation phenol
  • 相关文献

同被引文献17

引证文献2

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部