首页> 外文会议>Proceedings vol.2004-18; International Symposium on Electrode Processes; 2004; Honolulu,HI(US) >DEMONSTRATION OF AN IN-SITU ELECTROCHEMICAL RBS SYSTEM TO STUDY ELECTRODE-ELECTROLYTE INTERFACES
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DEMONSTRATION OF AN IN-SITU ELECTROCHEMICAL RBS SYSTEM TO STUDY ELECTRODE-ELECTROLYTE INTERFACES

机译:用于研究电极与电解质界面的现场电化学RBS系统的演示

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摘要

An in-situ electrochemical Rutherford backscattering (ECRBS) system has been demonstrated that enables the investigation of electrode and solution composition, along with kinetics of nuclide adsorption and desorption, at an electrode-electrolyte interface (EEI) under potential control. In contrast to other in-situ electrochemical diffraction or spectroscopy techniques, ECRBS can provide quantitative elemental analysis over an area of ~0.25 mm~2. The probe depth of the RBS ion beam allows observation of the EEI through a thin-film electrode window assembly (~200 nm). The depth resolution of RBS (1-10 nm) allows for measurement of nuclide concentration of the surface and near-surface layers. In this first report, we seek to demonstrate elemental characterization using ECRBS by measuring iodine adsorption on a polycrystalline gold electrode as well as gold dissolution. We believe ECRBS will bring new insight to a wide range of electrochemical processes, in particular to investigations of corrosion, electrodeposition, and electrocatalysis.
机译:已经证明了原位电化学卢瑟福背散射(ECRBS)系统可以在电位控制下在电极-电解质界面(EEI)上研究电极和溶液的组成以及核素的吸附和解吸动力学。与其他原位电化学衍射或光谱技术相比,ECRBS可以在约0.25 mm〜2的面积上提供定量元素分析。 RBS离子束的探针深度允许通过薄膜电极窗组件(〜200 nm)观察EEI。 RBS的深度分辨率(1-10 nm)可以测量表面层和近表面层的核素浓度。在这份第一份报告中,我们试图通过测量多晶金电极上的碘吸附以及金的溶解来证明使用ECRBS进行元素表征。我们相信ECRBS将为广泛的电化学过程带来新的见解,尤其是对腐蚀,电沉积和电催化的研究。

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