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原位表面增强拉曼光谱研究纳滤膜在金和铂电极上的吸附。

In situ surface-enhanced Raman spectroscopic studies of nafion adsorption on Au and Pt electrodes.

机构信息

Department of Chemistry & Biochemistry, Miami University, Oxford, Ohio 45056, United States.

出版信息

Langmuir. 2012 Jan 10;28(1):957-64. doi: 10.1021/la2035455. Epub 2011 Dec 1.

Abstract

Understanding interactions between Nafion (perfluorosulfonic acid) and Pt catalysts is important for the development and deployment of proton exchange membrane fuel cells. However, study of such interactions is challenging and Nafion/Pt interfacial structure remains elusive. In this study, adsorption of Nafion ionomer on Au and Pt surfaces was investigated for the first time by in situ surface-enhanced Raman spectroscopy. The study is made possible by the use of uniform SiO(2)@Au core-shell particle arrays which provides very strong enhancement of Raman scattering. The high surface sensitivity offered by this approach yields insightful information on interfacial Nafion structure. Through spectral comparison of several model compounds, vibration assignments of SERS bands were made. The SER spectra suggest the direct interaction of sulfonate group with the metal surfaces, in accord with cyclic voltammetric results. Comparison of present SERS results with previous IR spectra was briefly made.

摘要

了解全氟磺酸(Nafion)与 Pt 催化剂之间的相互作用对于质子交换膜燃料电池的开发和应用至关重要。然而,此类相互作用的研究极具挑战性,Nafion/Pt 界面结构仍难以捉摸。在这项研究中,首次通过原位表面增强拉曼光谱研究了全氟磺酸离聚物在 Au 和 Pt 表面上的吸附。这项研究之所以成为可能,是因为使用了均匀的 SiO2@Au 核壳颗粒阵列,该阵列提供了非常强的拉曼散射增强。这种方法的高表面灵敏度提供了有关界面 Nafion 结构的有见地的信息。通过对几种模型化合物的光谱比较,确定了 SERS 带的振动分配。SER 谱表明,磺酸盐基团与金属表面的直接相互作用与循环伏安结果一致。简要比较了目前的 SERS 结果与以前的红外光谱。

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