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Ion Specific 2D To 3D Structural Modification Of Langmuir Monolayer At Lower Surface Pressure

机译:离子特异性2D在较低表面压力下Langmuir Monolayer的3D结构改性

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2D to 3D structural transformation of stearic acid Langmuir monolayer in presence of Ca~(2+) and Zn~(2+) ions at lower surface pressure (≈25 mN/m) has been studied at lower (pH≈ 6.8) and higher (pH≈ 9.5) subphase pH. Generally, 2D to 3D structural transformation of monolayer occurs at higher surface pressure (>50 mN/m) after collapse point which can be identified from surface pressure (π) vs. specific molecular area (A) isotherms. In presence of Ca~(2+) ions and for both lower and higher subphase pH, stearic acid monolayer remains as 2D monolayer at that lower surface pressure as confirmed from the Atomic Force Microscopy (AFM) studies on the films deposited at π≈ 25mN/m. However, in presence of Zn~(2+) at higher subphase pH, stearic acid monolayer shows 2D to 3D structural transformation where less covered bilayer-like structure forms on top of the monolayer as obtained from the AFM studies. Fourier transform infrared (FTIR) spectroscopy results reveal that formation of relatively more amount of bidentate bridging coordination of metal carboxylate headgroup may be the key reason of such 2D to 3D structural transformation for Zn~(2+).
机译:在下表面压力下在Ca〜(2+)和Zn〜(2+)离子存在下的硬脂酸Langmuir单层的3D结构转化(≈25mN/ m),以较低(ph≈6.8)和更高(pH≈1.5)子相pH。通常,在塌陷点之后的折射点在可以从表面压力(π)与特定分子面积(a)等温线识别,Monolayer的2D至3D结构转化发生在较高的折叠点。在Ca〜(2+)离子和较低且较高的子相pH的情况下,硬脂酸单层保持在该下表面压力下作为2D单层,从原子力显微镜(AFM)研究中沉积在π≈25Mn的薄膜上/ m。然而,在较高子相pH的Zn〜(2+)存在下,硬脂酸单层表示2D至3D结构变换,其中从AFM研究中获得的单层的顶部形成较少的覆盖的双层结构。傅里叶变换红外(FTIR)光谱结果表明,形成金属羧酸盐头组的相对较多的双齿桥接配位的形成可以是Zn〜(2+)的3D结构变换的关键原因。

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