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Thin film characterization quartz crystal microbalance

Such approximation is valid when the thickness of the polymeric layer is small compared to die thickness of die crystal, and the measured frequency change is small with respect to the resonant frequency of the unloaded crystal. Mass changes up to 0.05% of die crystal mass commonly meet this approximation. In die absence of molecular specificity, EQCM cannot be used for molecular-level characterization of surfaces. Electrochemical quartz crystal microbalance devices also hold promise for the task of affinity-based chemical sensing, as they allow simultaneous measurements of both tile mass and die current. The principles and capabilities of EQCM have been reviewed (67,68). The combination of EQCM widi scanning electrochemical microscopy has also been reported recently for studying die dissolution and etching of various thin films (69). The recent development of a multichannel quartz crystal microbalance (70), based on arrays of resonators, should further enhance die scope and power of EQCM. [Pg.54]

Film electrodes have been essential components of quartz microbalance studies of stoichiometry of many electrodeposition and dissolution experiments as well as polymer electrode characterization [25]. In the quartz microbalance, changes in mass are detected by measurement of changes in the resonant frequency of a quartz crystal oscillator as the mass adhering to the surface changes. The oscillation is feasible because thin-film metal electrodes (typically gold) applied to opposing faces of a piezoelectric quartz crystal serve both to induce the oscillation and to provide a site for electrochemical reaction. [Pg.336]


See other pages where Thin film characterization quartz crystal microbalance is mentioned: [Pg.86]    [Pg.58]    [Pg.260]    [Pg.199]    [Pg.604]    [Pg.160]    [Pg.241]    [Pg.210]    [Pg.390]    [Pg.331]    [Pg.380]    [Pg.651]    [Pg.217]    [Pg.217]   
See also in sourсe #XX -- [ Pg.86 , Pg.89 ]




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