...
首页> 外文期刊>International Journal of Electrochemical Science >EQCM Study of the Adsorption of Polyethyleneglycol With Different Molecular Weights and its Coadsorption With Cl- ions on Pt in Perchloric Acid Solution
【24h】

EQCM Study of the Adsorption of Polyethyleneglycol With Different Molecular Weights and its Coadsorption With Cl- ions on Pt in Perchloric Acid Solution

机译:EQCM研究不同分子量的聚乙二醇在高氯酸溶液中对Pt的吸附及其与Cl -离子的共吸附

获取原文
           

摘要

The adsorption of polyethyleneglycol with different molecular weights (PEGX; x = 400, 3000, 8000, or- 20000), and its coadsorption with Cl ions, was investigated using cyclic voltammetry (CV) inconjunction with simultaneous measurements of the frequency changes of an electrochemical quartzcrystal microbalance (EQCM). First we investigated the adsorption of PEGX on the surface of the Ptelectrode at the open circuit potential. The results obtained showed that the mass of PEGX adsorbed onthe Pt surface reaches a stationary value with time, and that this stationary value increases inproportion to the PEG molecular weight. The quantity of PEGX adsorbed on the Pt surface increased- when Cl ions were present. In addition, the adsorption of PEGX did not interfere with the oxidation ofthe Pt surface to form a PtO film. Analysis of simultaneously recorded voltammograms and- massograms revealed that during the potential scan in the negative direction in solutions without Cl ,- three processes involving the partial desorption of PEGX from the Pt surface. In the presence of Cl , bycontrast, one adsorption process and two partial desorption processes of PEGX occur. On the basis of- the CV and EQCM data, we propose that in the absence of Cl ions, the oxidation of PEGX in thepotential interval from 0.5 to 0.8 V form the corresponding aldehyde adsorbed on the Pt surface. In the- presence of Cl ions, however, the oxidation of PEGX was almost completely suppressed.
机译:使用循环伏安法(CV)结合同时测量电化学元件的频率变化,研究了不同分子量(PEGX; x = 400、3000、8000或20000)的聚乙二醇的吸附及其与Cl离子的共吸附。石英微量天平(EQCM)。首先,我们研究了开路电位下PEGX在Pt电极表面的吸附。获得的结果表明,吸附在Pt表面上的PEGX的质量随时间达到固定值,并且该固定值与PEG分子量成比例地增加。当存在Cl离子时,吸附在Pt表面上的PEGX的量增加。另外,PEGX的吸附不干扰Pt表面的氧化以形成PtO膜。对同时记录的伏安图和质谱图的分析显示,在没有Cl的溶液中,在负方向上进行电位扫描时,三个过程涉及PEGX从Pt表面部分解吸。相比之下,在Cl的存在下,发生了PEGX的一个吸附过程和两个部分解吸过程。根据CV和EQCM数据,我们建议在不存在Cl离子的情况下,在0.5至0.8 V的电位区间内PEGX的氧化形成吸附在Pt表面的相应醛。然而,在Cl离子存在下,PEGX的氧化几乎被完全抑制。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号