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材料研究学报  2011, Vol. 25 Issue (2): 199-204    
  研究论文 本期目录 | 过刊浏览 |
聚乙烯吡咯烷酮对PbO2电极微结构和性能的影响
杨卫华, 付芳, 杨武涛
华侨大学材料科学与工程学院 厦门 361021
Effect of Polyvinylpyrrolidone on the Microstructure and Properties of PbO2 Electrode
YANG Weihua, FU Fang, YANG Wutao
College of Material Science and Engineering, Huaqiao University, Xiamen 361021
引用本文:

杨卫华 付芳 杨武涛. 聚乙烯吡咯烷酮对PbO2电极微结构和性能的影响[J]. 材料研究学报, 2011, 25(2): 199-204.
, . Effect of Polyvinylpyrrolidone on the Microstructure and Properties of PbO2 Electrode[J]. Chin J Mater Res, 2011, 25(2): 199-204.

全文: PDF(1017 KB)  
摘要: 采用电沉积法制备不同浓度聚乙烯吡咯烷酮(PVP)改性PbO2电极, 通过SEM、XRD、电化学阻抗谱(EIS)和线性极化(VA)等方法表征其微结构和电化学性能, 研究了PVP对电极电化学性能的影响。结果表明, PVP的包覆和空间位阻作用可抑制晶粒生长速度和团聚作用, 使电极表面晶粒细化均匀, 微结构得以改善; 改性PbO2电极具有更低的电化学反应电阻和更高的析氧电位; 适量的PVP掺杂可有效提高电极的电催化性能, 其中0.4 g ? L-1PVP改性电极的电催化活性最佳。最佳改性PbO2电极显示了良好的耐腐蚀性和电催化稳定性, 使用90 h后其降解率仍能达到81.5%。
关键词 材料表面与界面改性二氧化铅电极聚乙烯吡咯烷酮(PVP)电化学性能    
Abstract:PbO2electrodes modified with different concentrations of polyvinylpyrrolidone (PVP) were prepared using electrodeposition method. The microstructure and electrochemical properties of the modified electrode were investigated using SEM, XRD, electrochemical impedance spectroscopy (EIS) and liner sweep voltammetry (VA) techniques. Results show that PVP molecules can be coated around PbO2 particles and can restrict their further growth and polymerization, which lead to a uniform and fine crystalline grains. The modified electrode presents a relatively lower charge transfer resistance as well as a higher oxygen evolution potential. Appropriate amount of PVP can enhance the electrocatalytic activity of electrode and the optimum doped concentration is 0.4 g·L−1. The modified electrode also exhibit excellent corrosion resistance and electrocatalytic stability. After having been used for 90 h, the degradation ratio of phenol can still reach 81.5%.
Key wordssurface and interface in the materials    modified lead dioxide electrode    polyvinylpyrrolidone(PVP)    electrochemical properties
收稿日期: 2010-08-27     
ZTFLH: 

O646

 
基金资助:

福建省自然科学基金D0540003资助项目。

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