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Calibration of the scanning Kelvin probe force microscope under controlled environmental conditions

机译:在受控环境条件下对扫描Kelvin探针力显微镜的校准

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摘要

Local Volta potential differences (Δψ) between a platinum coated AFM tip and various pure metal specimens with a thin humidity induced surface electrolyte layer have been determined via scanning Kelvin probe force microscopy (SKPFM). SKPFM derived Δψ display a linear correlation with the same quantities obtained under nominally identical environmental conditions using a scanning Kelvin probe (SKP); the slope is within experimental error one. By exploiting this correlation and using a SKP previously calibrated versus a series of metal/aqueous metal ion redox couples it is possible to indirectly calibrate atmospheric SKPFM derived Δψ with electrochemical potential. Good correlation is also obtained between immersion corrosion potential (E_(corr)) in NaCl electrolyte and SKP determined Δψ in the presence of a NaCl dosed humidity layer. This implies that SKPFM may be calibrated directly against immersion E_(corr) provided SKPFM measurements are performed under suitably controlled conditions of atmospheric relative humidity and surface electrolyte dosing.
机译:已通过扫描开尔文探针力显微镜(SKPFM)确定了镀铂的AFM电极头和带有薄薄的湿度感应表面电解质层的各种纯金属样品之间的局部伏特电位差(Δψ)。 SKPFM得出的Δψ与使用扫描开尔文探针(SKP)在名义上相同的环境条件下所获得的相同数量显示出线性相关性;斜率在实验误差1之内。通过利用这种相关性,并使用先前已校准的SKP与一系列金属/水性金属离子氧化还原对进行比较,可以间接校准具有化学势的大气SKPFM衍生的Δψ。在存在NaCl的湿润层中,NaCl电解液中的浸入腐蚀电位(E_(corr))与SKP测定的Δψ之间也获得了良好的相关性。这意味着只要在适当控制的大气相对湿度和表面电解质剂量条件下执行SKPFM测量,就可以直接针对浸没E_(corr)校准SKPFM。

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