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Quantification of porosity in extensively nanoporous thin films in contact with gases and liquids

机译:定量分析与气体和液体接触的纳米多孔薄膜的孔隙率

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摘要

Nanoporous layers are widely spread in nature and among artificial devices. However, complex characterization of extensively nanoporous thin films showing porosity-dependent softening lacks consistency and reliability when using different analytical techniques. We introduce herein, a facile and precise method of such complex characterization by multi-harmonic QCM-D (Quartz Crystal Microbalance with Dissipation Monitoring) measurements performed both in the air and liquids (Au-Zn alloy was used as a typical example). The porosity values determined by QCM-D in air and different liquids are entirely consistent with that obtained from parallel RBS (Rutherford Backscattering Spectroscopy) and GISAXS (Grazing-Incidence Small-Angle Scattering) characterizations. This ensures precise quantification of the nanolayer porosity simultaneously with tracking their viscoelastic properties in liquids, significantly increasing sensitivity of the viscoelastic detection (viscoelastic contrast principle). Our approach is in high demand for quantifying potential-induced changes in nanoporous layers of complex architectures fabricated for various electrocatalytic energy storage and analytical devices.
机译:纳米多孔层在自然界和人工装置中广泛分布。然而,当使用不同的分析技术时,显示出取决于孔隙率的软化作用的大量纳米多孔薄膜的复杂表征缺乏一致性和可靠性。我们在此介绍一种通过在空气和液体中均进行的多谐波QCM-D(带耗散监测的石英晶体微天平)测量来进行此类复杂表征的简便而精确的方法(以Au-Zn合金为典型示例)。由QCM-D在空气和不同液体中确定的孔隙率值与通过平行RBS(卢瑟福反向散射光谱法)和GISAXS(掠入射小角度散射)表征获得的孔隙率完全一致。这可以确保在对纳米层孔隙率进行精确定量的同时跟踪其在液体中的粘弹性,从而显着提高了粘弹性检测的灵敏度(粘弹性对比原理)。我们的方法迫切需要量化为各种电催化能量存储和分析设备制造的复杂体系结构的纳米孔层中的电势诱导变化。

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