摘要
本文在SnO2-Sb2O5氧化物为中间层的钛基体上,采用电沉积法制备了无掺杂的Ti/PbO2、掺杂F的Ti/PbO2(Ti/PbO2+F)和掺杂Co3O4纳米粒子的Ti/PbO2电极(Ti/PbO2+Nano-Co3O4).用X射线衍射(XRD)和扫描电镜(SEM)分析和观察了电极材料的组成、结构和形貌,并通过电化学方法研究了这三种电极对苯酚的电催化氧化性能.结果表明,Ti/PbO2+F电极的析氧电位较Ti/PbO2电极的发生明显正移,但其苯酚的氧化峰和析氧峰并不能分开;而Ti/PbO2+Nano-Co3O4电极虽然其析氧电位负移,但对苯酚的氧化峰出现在析氧峰之前.这一结果表明,体系存在着某种反应特别快的瞬态中间体,即在水分子被解离之前已与苯酚发生了反应,从而更有利于苯酚的转化和降解.
Three types of electrodes, namely, Ti/PbO2, F-doped PbO2 (Ti/PbO2-F) and nano-Co3O4-doped PbO2(Ti/PbO:+Nano- Co3O4) electrodes, were prepared by electro-deposition method on the Ti substrate with the interlayer of SnO2-Sb2O5. X-ray diffraction (XRD) and scanning electron microscopy (SEM) were used to study the compositions, structures and film morphologies of the electrodes. Electroeatalytic oxidation characteristics to phenol on the prepared electrodes were investigated by electrochemical method. The experimental results showed that compared with the Ti/PbO2 electrode, the potentials of oxygen evolution on the Ti/PbO2+F electrode apparently shifted more positively, while those of Ti/PbO2+Nano-Co3O4 electrode shifted negatively after the oxidation of phenol took place. This provided experimental evidence for the existence of some transient intermediates which underwent particularly fast reactions, i.e., the reaction of water molecule with phenol occurred before the dissociation of water molecule, which was more beneficial to the transformation and degradation of phenol.
出处
《电化学》
CAS
CSCD
北大核心
2013年第1期59-64,共6页
Journal of Electrochemistry
基金
国家自然科学基金(No.20873051)
吉林省科技发展计划重点项目(No.20100326)资助
关键词
PbO2
电极
掺杂
电催化氧化
苯酚
PbO2
electrode
doped
electrocatalytic oxidation
phenol