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Spectroelectrochemical study of the electrosynthesis of Pt nanoparticles/poly(3,4-(ethylenedioxythiophene) composite

机译:铂纳米粒子/聚(3,4-(乙撑二氧噻吩)复合材料的电合成的光谱电化学研究

摘要

UV-Visible, NIR and Raman spectroelectrochemistry techniques have been used for the in-situ study of Pt nanoparticles (PtNPs) electrosynthesis on an electrochemically generated poly(3,4-ethylenedioxythiophene) film. Two electrochemical steps have been used to obtain in a reproducible way PtNPs with catalytic properties towards methanol oxidation: 1) deposition of Pt nuclei on the polymer modified electrode, 2) growth of these nuclei to form nanoparticles yielding drastic changes in the spectroscopic signal and a significant increase of the amount of Pt. A two steps procedure facilitates an interfacial growth mechanism of the nuclei over a diffusion controlled growth. Evolution of UV-Visible and NIR spectra during these two PtNPs synthesis steps helps to understand and explain the mechanism of generation of these nanoparticles. Besides, Energy Dispersive X-Ray analysis and Scanning Electron Microscopy images registered of the composite after each step of synthesis confirm the conclusions extracted from spectroelectrochemistry data
机译:紫外可见,近红外和拉曼光谱电化学技术已用于在电化学生成的聚(3,4-乙撑二氧噻吩)薄膜上电合成Pt纳米颗粒(PtNPs)的原位研究。已使用两个电化学步骤以可重现的方式获得对甲醇氧化具有催化性能的PtNP:1)Pt核在聚合物修饰电极上的沉积,2)这些核的生长以形成纳米粒子,从而产生光谱信号的急剧变化,并且铂含量显着增加。两步过程促进了核的界面生长机制超过了扩散控制的生长。在这两个PtNP合成步骤中,紫外可见光谱和近红外光谱的演变有助于理解和解释这些纳米粒子的生成机理。此外,在合成的每个步骤之后,复合材料的能量色散X射线分析和扫描电镜图像证实了从光谱电化学数据中提取的结论

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