In situ synchrotron radiation grazing incidence X-ray diffraction—A powerful technique for the characterization of solid-state ion-selective electrode surfaces

An in situ surface study of the iron chalcogenide glass membrane ion-selective electrode (ISE) in aqueous media has been undertaken using a tandem technique of mixed potential/synchrotron radiation grazing incidence X-ray diffraction (SR-GIXRD) and atomic force microscopy (AFM). This work has simultaneously monitored the mixed potential and in situ surface diffraction patterns of this crystalline glassy material, showing that the observed gradual shift of the electrode potential in the anodic direction is linked to the preferential dissolution of the GeSe (1 1 1), GeSe (1 0 1) and GeSe (1 4 1) and/or Sb₂Se₃ (0 1 3), Sb₂Se₃ (2 2 1) and Sb₂Se₃ (0 2 0) surfaces. Expectedly, these observations are internally consistent with preferential oxidative attack of the crystalline regions of the membrane comprising GeSe and/or Sb₂Se₃, as evidenced by AFM imaging of the electrode surface. Clearly, this work corroborates the results of previous ex situ surface studies on the iron chalcogenide glass ISE, whereby it was shown that alkaline saline solutions have a tendency to alter the surface chemistry and concomitant response characteristics of the ISE.     

An in situ electrochemical impedance spectroscopy/synchrotron radiation grazing incidence X-ray diffraction study of the influence of acetate on the carbon dioxide corrosion of mild steel

A combination of electrochemical impedance spectroscopy (EIS) and in situ synchrotron radiation grazing incidence X-ray diffraction (SR-GIXRD) has been used to study the influence of acetate on the carbon dioxide corrosion of mild steel. The SR-GIXRD data demonstrated that normal corrosion - in a carbon dioxide saturated brine - induced the formation of a thick corrosion scale of Fe₂(OH)₂CO₃ and Fe₂O₂CO₃, and this totally obscured the α-Fe diffraction peaks of the underlying steel substrate after 24 h. On the other hand, the carbon dioxide corrosion of mild steel in the presence of acetate also detected the Bragg diffraction peaks for Fe₂(OH)₂CO₃ and Fe₂O₂CO₃; however, the α-Fe diffraction peaks of the underlying steel substrate were not extinguished with time, and there was a reversal in the pattern of evolution of the intensities of the Fe₂(OH)₂CO₃ and Fe₂O₂CO₃ phases in acetate. Accordingly, the EIS data showed a poorly defined medium frequency time constant for the corroded steel specimen in brine spiked with acetate, and this medium frequency time constant was extinguished as a function of time. Alternatively, EIS of the corroded specimen also revealed a medium frequency time constant after 24 h. In addition, EIS complex-plane impedance plots showed that the corroded electrode had become passivated in an acetate-spiked brine, as evidenced by a three-fold enhancement in the charge transfer resistance at low frequency. These EIS/SR-GIXRD outcomes suggest that acetate affects the crystallization chemistry of the Fe₂(OH)₂CO₃/Fe₂O₂CO₃ corrosion scale, and this causes a mild passivation of the corroded steel surface.     

A flow cell for transient voltammetry and in situ grazing incidence X-ray diffraction characterization of electrocrystallized cadmium(II) tetracyanoquinodimethane

An easy to fabricate and versatile cell that can be used with a variety of electrochemical techniques, also meeting the stringent requirement for undertaking cyclic voltammetry under transient conditions in in situ electrocrystallization studies and total external reflection X-ray analysis, has been developed. Application is demonstrated through an in situ synchrotron radiation-grazing incidence X-ray diffraction (SR-GIXRD) characterization of electrocrystallized cadmium (II)-tetracyanoquinodimethane material, Cd(TCNQ)₂, from acetonitrile (0.1 mol dm⁻³ [NBu₄][PF₆]). Importantly, this versatile cell design makes SR-GIXRD suitable for almost any combination of total external reflection X-ray analysis (e.g., GIXRF and GIXRD) and electrochemical perturbation, also allowing its application in acidic, basic, aqueous, non-aqueous, low and high flow pressure conditions. Nevertheless, the cell design separates the functions of transient voltammetry and SR-GIXRD measurements, viz., voltammetry is performed at high flow rates with a substantially distended window to minimize the IR (Ohmic) drop of the electrolyte, while SR-GIXRD is undertaken using stop-flow conditions with a very thin layer of electrolyte to minimize X-ray absorption and scattering by the solution.     

In situ X-ray analysis under controlled potential conditions: An innovative setup and its application to the investigation of ultrathin films electrodeposited on Ag(1 1 1)

An innovative setup to combine electrochemical and in situ surface X-ray diffraction (SXRD) measurements is described. This electrochemical cell has a different design from the other ones commonly used for X-ray diffraction studies. It allows the sample surface to stay always completely immersed into the solution under controlled potential conditions even during the SXRD measurements. The X-ray beam crosses the liquid (about 1 cm) and the cell walls. Because of the high X-ray energy, the beam attenuation is negligible and by an appropriate positioning of the detector arm slits it is possible to minimize the diffuse scattering induced by the liquid and cell walls in order to still detect the minima of the crystal truncation rods (CTRs). The liquid solution in the cell is managed by a special device, which allows the controlled exchange of the electrolyte solutions necessary in the electrochemical atomic layer epitaxy (ECALE) growth. The whole setup can be remotely controlled from outside the experimental hutch by a dedicated computer. As an example we report measurements on S layers deposited at underpotential on the Ag(1 1 1) surface, and on CdS films of increasing thickness.     

Ex situ and in situ characterization studies of spin-coated TiO2 film electrodes for the electrochemical ozone production process

An electrode composed of silicon/titanium oxide/platinum/titanium dioxide (Si/TiO_X/Pt/TiO₂) was fabricated by spin-coating TiO₂ multilayers on a Si/TiO_X/Pt substrate and was used in electrochemical ozone production (EOP). EOP was realized when the Si/TiO_X/Pt substrate was completely covered with the TiO₂ film and a current efficiency of 7% was achieved at a low current density of 26.7 mA cm⁻² in 0.01 M HClO₄ at 15 °C. The TiO₂ film was found to be of an anatase-type TiO₂ and that to comprise aperture structures from the X-ray diffraction (XRD) and transmission electron microscopy (TEM) observations. Moreover, the fabricated TiO₂ film was found to be an n-type semiconductor by photoelectrochemical measurements. The high efficiency at a low current density of EOP on the TiO₂ n-type semiconductor was explained to result from the electron transfer through the TiO₂/HClO₄ interface as tunneling current. When the tunneling current passes through a depletion layer of TiO₂, the electrode potential is necessarily high enough to facilitate EOP.     

Development of an environmentally friendly protective coating for the depleted uranium-0.75 wt.% titanium alloy: Part V. Electrochemical impedance spectroscopy of the coating

Molybdenum oxide based conversion coatings have been formed on the surface of the depleted uranium-0.75 wt.% titanium alloy. Electrochemical impedance spectroscopy (EIS) measurements have been performed on the as-made and aged coatings and compared with the untreated depleted uranium (DU) alloy. The Nyquist and Bode plots of the as-made coating were similar to the untreated samples and contained capacitive and inductive loops. The aged coating exhibits significantly different behavior from the as-made coating and has been modeled with a four element equivalent circuit that contains a constant phase element (CPE).     

Hydrothermal transformation of the calcium aluminum oxide hydrates CaAl2O4·10H2O and Ca2Al2O5·8H2O to Ca3Al2(OH)12 investigated by in situ synchrotron X-ray powder diffraction

The hydrothermal transformation of calcium aluminate hydrates were investigated by in situ synchrotron X-ray powder diffraction in the temperature range 25 to 170 °C. This technique allowed the study of the detailed reaction mechanism and identification of intermediate phases. The material CaAl₂O₄·10H₂O converted to Ca₃Al₂(OH)₁₂ and amorphous aluminum hydroxide. Ca₂Al₂O₅·8H₂O transformed via the intermediate phase Ca₄Al₂O₇·13H₂O to Ca₃Al₂(OH)₁₂ and gibbsite, Al(OH)₃. The phase Ca₄Al₂O₇·19H₂O reacted via the same intermediate phase to Ca₃Al₂(OH)₁₂ and mainly amorphous aluminum hydroxide. The powder pattern of the intermediate phase is reported.