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Electrochemical force spectroscopy

Self-assembly Electrochemical force spectroscopy Conclusions... [Pg.125]

Summary, Scanning probe microscopy studies of electrodes chemically modified with electroactive transition metal complexes are described. Emphasis is placed on scanning tunneling microscopy and electrochemical scanning tunneling microscopy studies of their structure and dynamics of formation and on electrochemical force spectroscopy studies of their electrochemical potential dependent chemical properties. [Pg.125]

Electrochemical impedance spectroscopy leads to information on surface states and representative circuits of electrode/electrolyte interfaces. Here, the measurement technique involves potential modulation and the detection of phase shifts with respect to the generated current. The driving force in a microwave measurement is the microwave power, which is proportional to E2 (E = electrical microwave field). Therefore, for a microwave impedance measurement, the microwave power P has to be modulated to observe a phase shift with respect to the flux, the transmitted or reflected microwave power APIP. Phase-sensitive microwave conductivity (impedance) measurements, again provided that a reliable theory is available for combining them with an electrochemical impedance measurement, should lead to information on the kinetics of surface states and defects and the polarizability of surface states, and may lead to more reliable information on real representative circuits of electrodes. We suspect that representative electrical circuits for electrode/electrolyte interfaces may become directly determinable by combining phase-sensitive electrical and microwave conductivity measurements. However, up to now, in this early stage of development of microwave electrochemistry, only comparatively simple measurements can be evaluated. [Pg.461]

BASIL CIS CV CVD DSSC ECALE EC-STM EDX, EDS, EDAX EIS EMF EQCM FAB MS FFG-NMR Biphasic Acid Scavenging Utilizing Ionic Liquids Copper-indium-selenide Cyclic Voltammetry Chemical Vapor Deposition Dye Sensitized Solar Cell Electrochemical Atomic Layer Epitaxy Electrochemical in situ scanning tunnelling microscopy Energy Dispersive X-ray analysis Electrochemical Impedance Spectroscopy Electromotive Force Electrochemical Quarz Crystal Microbalance Fast atom bombardment mass spectroscopy Fixed Field Gradient Nuclear Magnetic Resonance... [Pg.1]

Many techniques have been developed to characterize the properties of the SEI layer on the anodes, such as X-ray photoelectron spectroscopy (XPS), EELS and selected area electron diffraction (SAED) " as well as FTIR and HRTEM. Most of these techniques provide ex situ information on both the elechonic and crystalline stmctural variations of the electrode. Electrochemical impedance spectroscopy (EIS) and electrochemical quartz crystal microbalance (ECQCM) can provide in situ information of macro-scale properties of the SEI layers. Reflectance FTIR techniques and atomic force microscopy (AFM) have been used in situ to study the surface of metal lithium and electrochemically nonactive electrodes, such as Pt, Au and Ni as well. Nevertheless, it is still difficult to study rough electrode surfaces of composite materials in lithium ion batteries with these techniques. In addition, none of the above techniques, except for FTIR spectroscopy, can provide structural information at the molecular levels. [Pg.157]

Electrochemical Impedance Spectroscopy (EIS) under Forced Convection Conditions... [Pg.89]

SAMs of allgrlphosphonic acids (butylphosphonic acid, octylphosphonic acid, undecylphosphonic acid and octadecylphosphonic acid) on native niekel oxide allow substrates to be functionalized easily. Monolayer formation has been investigated by diffuse reflectance Fourier transform infrared spectroscopy, non-contact mode atomic force microscopy, contact angle measurements and matrix-assisted laser desorption ionization mass spectrometry. Cyclic voltammetry and electrochemical impedance spectroscopy studies showed that the monolayer increased surface resistance to oxidation. [Pg.291]

This conclusion falls in line with the fact that the anion radical could neither be detected after collision of the parent halide with alkali metal atoms in the gas phase (Compton et ai, 1978) nor upon y-irradiation in apolar or weakly polar solid matrixes at 77 K by esr spectroscopy (Symons, 1981). However, these observations are not absolute proofs that the anion radicals do not exist they might exist and be too short lived to be detectable. On the other hand, the reaction medium and the driving force conditions are quite different from those in the electrochemical experiments, which rendered necessary an independent investigation of the problem in the latter. [Pg.56]

A number of methods are available for the characterization and examination of SAMs as well as for the observation of the reactions with the immobilized biomolecules. Only some of these methods are mentioned briefly here. These include surface plasmon resonance (SPR) [46], quartz crystal microbalance (QCM) [47,48], ellipsometry [12,49], contact angle measurement [50], infrared spectroscopy (FT-IR) [51,52], Raman spectroscopy [53], scanning tunneling microscopy (STM) [54], atomic force microscopy (AFM) [55,56], sum frequency spectroscopy. X-ray photoelectron spectroscopy (XPS) [57, 58], surface acoustic wave and acoustic plate mode devices, confocal imaging and optical microscopy, low-angle X-ray reflectometry, electrochemical methods [59] and Raster electron microscopy [60]. [Pg.54]


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See also in sourсe #XX -- [ Pg.125 , Pg.126 , Pg.132 ]




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Electrochemical spectroscopy

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