Hydroxylamine Oxidation on Polycrystalline Gold Electrodes in Aqueous Electrolytes: Quantitative On-Line Mass Spectrometry under Forced Convection.

Herein, a method is presented that allows quantitative determination of faradaic efficiencies for dinitrogen (N2 ) generation during the electrochemical oxidation of hydroxylamine (NH2 OH), fN2NH2OH , on a polycrystalline gold Au(poly) disk electrode in aqueous electrolytes over a wide pH range. This tactic involves the use of an impinging jet electrolyte configuration incorporating a gas porous ring connected in turn to a mass spectrometer. The actual amount of N2 generated at the Au(poly) disk was assayed using the oxidation of hydrazine (N2 H4 ) in aqueous phosphate buffer (pH 7). This redox process yields N2 as the only product, allowing a direct correlation to be established between the changes in the partial pressures of N2 and the current flowing through the disk electrode. An analysis of the data collected revealed a strong dependence of fN2NH2OH both on pH and the applied potential. Although values of fN2NH2OH as high as 20 to 30 % were found in acid and neutral media over a narrow potential region, those in alkaline solution were far smaller in the entire potential range examined.

Rotating Ring-Disk Electrode Method for the Detection of Solution Phase Superoxide as a Reaction Intermediate of Oxygen Reduction in Neutral Aqueous Solutions.

A method is herein described that allows for solution phase superoxide generated via the reduction of dioxygen in neutral aqueous solutions at a rotating disk electrode to be oxidized at a concentric Au ring electrode bearing a covalently linked monolayer of 3-mercapto-1-propanol, a modified surface that blocks the oxidation of solution phase of hydrogen peroxide. Experiments were performed in which the potential of a glassy carbon disk electrode was linearly scanned in the oxygen reduction region and the ring voltage was poised at a value at which superoxide oxidation ensued yielded bell-shaped ring currents. This behavior is consistent with changes in the relative rates constant for the processes involved in the mechanism of oxygen reduction on this carbonaceous material induced by the applied potential which so far had remained undetected using other techniques.

Quantitative aspects of normalized differential reflectance spectroscopy: Pt(111) in aqueous electrolytes.

A theoretical model is herein proposed to account for changes in the normalized differential reflectance, ΔR/R, of well-defined single crystal Pt(111) surfaces|aqueous electrolyte interfaces. It assumes that ΔR/R is proportional to the area of the electrode either bare or covered by neutral and/or nominally charged species and, for a specific type of site, is modulated by the applied potential, E. Correlations between the coverage of the various species and E were obtained from data reported in the literature or by coulometric analysis of linear voltammetric scans. Excellent agreement was found for the adsorption/desorption of hydrogen and that of bisulfate from acidic electrolytes both on bare, and cyanide-modified Pt(111). Also discussed are extensions of this technique in the transient mode involving the reduction of adsorbed nitric oxide, NO, on Pt(111).

Microparticle electrodes and single particle microbatteries: electrochemical and in situ microRaman spectroscopic studies.

Studies of the intrinsic electrochemical, structural, and electronic propertiesof microparticles of energy storage materials can provide much needed insight into the factors that control various aspects of the performance of technical electrodes for battery applications. This Account summarizes efforts made in our laboratories toward the development and implementation of methods for the in situ electrical, optical, and spectroscopic characterization of microparticles of a variety of such materials, including Ni hydroxide, Zn, carbon, and lithiated Mn and Co oxides. In the case of Ni hydroxide, the much darker appearance of NiOOH compared to the virtually translucent character of virgin Ni(OH)2 allowed for the spatial and temporal evolution of charge flow within spherical microparticles of Ni(OH)2 to be monitored in real time during the first scan toward positive potentials using computer-controlled video imaging. In situ Raman scattering measurements involving single microparticles of Zn harvested from a commercial Zn|MnO2 battery revealed that passive films formed in strongly alkaline solutions by stepping the potential from 1.55 V to either 0.7 or 0.8 V vs SCE displayed a largely enhanced feature at ca. 565 cm(-1) ascribed to a longitudinal optical phonon mode of ZnO, an effect associated with the presence of interstitial Zn and oxygen deficiencies in the lattice. In addition, significant amounts of crystalline ZnO could be detected only for passive films formed at the same two potentials after the electrodes had been roughened by a single passivation-reduction step. Quantitative correlations were found in the case of LiMn2O4 and KS-44 graphite between the Raman spectral properties and the state of charge. In the case of KS-44, a chemometrics analysis of the spectroscopic data in the potential region in which the transition between dilute phase 1 and phase 4 of lithiated graphite is known to occur made it possible to determine independently the fraction of each of the two phases present as a function of potential without relying on the coulometric information. Also featured in this Account are methods we developed for the assembly and electrochemical characterization of Zn|MnO2 and nickel|metal-hydride Ni|MH alkaline batteries incorporating single microparticles of the active materials. As evidenced from the data collected, the voltage-time profiles for constant current operation for both types of devices were found to be similar to those of commercially available batteries involving the same chemistries. The ability to monitor the state of charge of individual particles based strictly on spectroscopic data is expected to open exciting new prospects for visualizing the flow of charge within electrodes in Li-ion batteries, an area that is being vigorously pursued in our laboratories.

Quantitative correlations between the normal incidence differential reflectance and the coverage of adsorbed bromide on a polycrystalline platinum rotating disk electrode.

Normal incidence reflectance spectra (λ = 635 nm) data were acquired from a Pt disk of a rotating Pt

Quantitative aspects of ohmic microscopy.

The potential difference between two microreference electrodes, Δφ(sol), immersed in an aqueous sulfuric acid solution was monitored while performing conventional cyclic voltammetric experiments with a Pt disk electrode embedded in an insulating surface in an axisymmetric cell configuration. The resulting Δφ(sol) vs E curves, where E is the potential applied to the Pt disk electrode were remarkably similar to the voltammograms regardless of the position of the microreference probes. Most importantly, the actual values of Δφ(sol) were in very good agreement with those predicted by the primary current distribution using Newman's formalism (Newman, J. J. Electrochem. Soc. 1966, 113, 501-502). These findings afford a solid basis for the development of ohmic microscopy as a quantitative tool for obtaining spatially resolved images of electrodes displaying nonhomogenous surfaces.

Porous Teflon ring-solid disk electrode arrangement for differential mass spectrometry measurements in the presence of convective flow generated by a jet impinging electrode in the wall-jet configuration.

A porous Teflon ring|solid disk electrode is herein described specifically designed for acquiring online mass spectrometric measurements under well-defined forced convection created by liquid emerging from a circular nozzle impinging on the disk under wall-jet conditions. Measurements were performed for the oxidation of hydrazine, N(2)H(4), in a deaerated phosphate buffer electrolyte (pH 7) on Au, a process known to yield dinitrogen as the product. The N(2)(+) ion currents, measured by the mass spectrometer, i(N(2)(+)), as well as the corresponding polarization curves recorded simultaneously displayed very similar s-like shapes when plotted as a function of the potential applied to the Au disk. In fact, the limiting currents observed both electrochemically and spectrometrically were found to be proportional to [N(2)H(4)]. However, the limiting values of i(N(2)(+)) did not increase monotonically with the flow rate, ν(f), reaching instead a maximum and then decreasing to values independent of ν(f). This behavior has been attributed in part to hindrances in the mass transport of gases through the porous materials.

Adsorption of Cd2+ on carboxyl-terminated superparamagnetic iron oxide nanoparticles.

The affinity of Cd(2+) toward carboxyl-terminated species covalently bound to monodisperse superparamagnetic iron oxide nanoparticles, Fe(3)O(4)(np)-COOH, was investigated in situ in aqueous electrolytes using rotating disk electrode techniques. Strong evidence that the presence of dispersed Fe(3)O(4)(np)-COOH does not affect the diffusion limiting currents was obtained using negatively and positively charged redox active species in buffered aqueous media (pH = 7) devoid of Cd(2+). This finding made it possible to determine the concentration of unbound Cd(2+) in solutions containing dispersed Fe(3)O(4)(np)-COOH, 8 and 17 nm in diameter, directly from the Levich equation. The results obtained yielded Cd(2+) adsorption efficiencies of ~20 µg of Cd/mg of Fe(3)O(4)(np)-COOH, which are among the highest reported in the literature employing ex situ methods. Desorption of Cd(2+) from Fe(3)O(4)(np)-COOH, as monitored by the same forced convection method, could be accomplished by lowering the pH, a process found to be highly reversible.

An implantable biofuel cell for a live insect.

A biofuel cell incorporating a bienzymatic trehalase|glucose oxidase trehalose anode and a bilirubin oxidase dioxygen cathode using Os complexes grafted to a polymeric backbone as electron relays was designed and constructed. The specific power densities of the biofuel cell implanted in a female Blaberus discoidalis through incisions into its abdomen yielded maximum values of ca. 55 µW/cm(2) at 0.2 V that decreased by only ca. 5% after ca. 2.5 h of operation.

Bifunctional trehalose anode incorporating two covalently linked enzymes acting in series.

A bienzymatic electrode incorporating trehalase (Tre) and glucose oxidase (GOx) covalently bound to the surface of Pt through a functionalized thiol linker (Tre|GOx|Pt) has been designed and assembled and its catalytic properties examined by chemical and electrochemical methods in aqueous phosphate buffer solutions (PBS, pH 7.4). Exposure of Tre|GOx|Pt to PBS containing trehalose (Tr) and subsequent polarization at 0.6 V versus Ag/AgCl yielded after a few minutes well-defined steady-state currents ascribed to the oxidation of hydrogen peroxide generated by the GOx-mediated oxidation of glucose (Gl) produced by the Tre-mediated dissociation of Tr. Plots of the steady-state currents versus [Tr] over the range examined, i.e., 5-25 mM, were found to be linear. Implications of these results toward the development of an implantable biofuel cell as an autonomous energy conversion device for insects are discussed.

A hybrid lithium oxalate-phosphinate salt.

The novel organophosphorus-containing lithium salt Li(THF)[(C(2)O(4))B(O(2)PPh(2))(2)] (1; THF = tetrahydrofuran) was synthesized and characterized using a variety of spectroscopic techniques. An X-ray structural analysis on crystals of 1 grown from THF reveals a dimeric structure [Li(THF)(C(2)O(4))B(O(2)PPh(2))(2)](2)·THF, whereby the two units of 1 are bridged via P-O···Li interactions. Compound 1 displays high air and water stability and is also thermally robust, properties needed of electrolytes for their possible use as electrolytes and/or additives in lithium-ion battery applications.

Electrochemical oxidation of hydroxylamine on gold in aqueous acidic electrolytes: an in situ SERS investigation.

The electrooxidation of hydroxylamine (HAM) on roughened Au electrodes has been examined in aqueous buffered electrolytes (pH 3) using in situ surface-enhanced Raman scattering (SERS). Two distinct spectral features were observed at potentials, E, within the range in which HAM oxidation was found to ensue, centered at 803 cm(-1) for 0.55 < E < 0.8 V and at 826 cm(-1) for 1.0 < E < 1.40 V versus SCE, attributed, respectively, to adsorbed nitrite and adsorbed NO(2). Similar experiments performed in solutions containing nitrite instead of HAM under otherwise identical conditions displayed only the peak ascribed to adsorbed nitrite over the range of 0.1 < E < 0.8 V versus SCE with no additional features at higher potentials. These observations strongly suggest that under the conditions selected for these studies the oxidation of HAM on Au proceeds at least in part through a pathway that does not involve nitrite as a solution-phase intermediate.

Surface dynamics at well-defined single crystal microfacetted Pt(111) electrodes: in situ optical studies.

The assembly and electrochemical oxidation of well-defined CO adlayers on Pt(111) microfacets in aqueous CO-saturated 0.1 M H2SO4 were examined by a combination of in situ, simultaneous, time-resolved, reflectance spectroscopy (RS) and second harmonic generation (SHG), and potential step and linear scan techniques. Optical transients were collected following potential steps from a value high enough for a full monolayer of bisulfate (theta = 0.2) to adsorb on the Pt(111) facet, E(ox), to potentials E(ads), at which either the c(2 x 2)-3CO or square root of 19 x square root of 19R23.4 degrees-13CO phase is expected to form once surface saturation is achieved. Similar experiments involving subsequent steps from E(ads) to E(ox) provided unambiguous evidence that the rates of oxidation of c(2 x 2)-3CO on such quasi-perfect Pt(111) facet at constant overpotential are much slower than those of square root of 19 x square root of 19R23.4 degrees -13CO, an effect attributed to the presence of intrinsic vacant sites within the latter, more dilute phase, which are required for oxidation of adsorbed CO to ensue. Furthermore, continuous CO adsorption-oxidation cycles were found to increase the rate of oxidation of the c(2 x 2)-3CO phase. This phenomenon was tentatively ascribed to the progressive emergence of defects along the edge of the facet (and/or within the facet itself) which serve as nucleation sites for the oxidation of adsorbed CO.

In situ solution-phase Raman spectroscopy under forced convection.

In situ Raman spectra of solution-phase electrogenerated species have been recorded in a channel-type electrochemical cell incorporating a flat optically transparent window placed parallel to the channel plane that contains the embedded working electrode. A microscope objective with its main axis (Z) aligned normal to the direction of flow was used to focus the excitation laser beam (lambda exc = 532 nm) in the solution and also to collect the Raman scattered light from species present therein. Judicious adjustment of the cell position along Z allowed the depth of focus to overlap the diffusion boundary layer to achieve maximum detection sensitivity. Measurements were performed using a Au working electrode in iron hexacyanoferrate(II), [Fe(CN)6]4-, and nitrite, NO2-, containing aqueous solutions as a function of the applied potential, E. Linear correlations were found between both the gain and the loss of the integrated Raman intensity, IR, of bands, attributed to [Fe(CN)6]3- and [Fe(CN)6]4-, respectively, recorded downstream from the edge of the working electrode, and the current measured at the Au electrode as a function of E. The same overall trend was found for the gain in the IR of the NO3- band in the nitrite solution. Also included in this work is a ray trace analysis of the optical system.

Simultaneous in situ reflectance and probe beam deflection measurements at solid electrode-aqueous electrolyte interfaces.

A method is herein described for performing simultaneous in situ normal incidence reflectance spectroscopy (DeltaR/R, lambda = 633 nm) and probe beam deflection (PBD) measurements at solid electrodes in aqueous electrolytes, while scanning the potential linearly between two prescribed limits. Results obtained for Au in 0.1 M HClO4 and for Pt in both 0.1 M HClO4 and 0.1 M NaOH were found to be in excellent agreement with those reported in the literature for each individual spectroelectrochemical technique under otherwise similar conditions. Data collected for Pt electrodes in CO-saturated 0.1 M HClO4 revealed rather sudden changes in both DeltaR/R and PBD signals in the voltammetric region where the characteristic sharp peak associated with the oxidation of adsorbed CO occurs. This behavior was ascribed, respectively, to oxide formation (DeltaR/R) and to changes in the electrolyte composition in region neighboring the electrode, involving predominantly the acid concentration (PBD). In contrast, CO oxidation on Pt in 0.1 M NaOH yielded a PBD response consistent with formation of solution-phase carbonate via the reaction of the product, CO2, with hydroxyl ion. The exquisite sensitivity of DeltaR/R and PBD to interfacial phenomena was further illustrated using a monolayer of hemin irreversibly adsorbed on glassy carbon surfaces in 0.1 M Na2B4O7 (pH approximately 9.2). For this system, DeltaR/R was found to be proportional to the relative fractions of hemin and its reduced counterpart, while the PBD signal could be correlated with corresponding variations in the electrolyte concentration induced by the surface-bound redox process.

In situ, time-resolved reflectance spectroscopy in the microsecond domain: oxidation of adsorbed carbon monoxide on polycrystalline pt microelectrodes in aqueous solutions.

The dynamics of the electrooxidation of adsorbed CO, COads, on polycrystalline Pt microelectrodes has been examined in CO-saturated 0.5 M H2SO4 and 0.5 M HClO4 aqueous solutions, using in situ, time-resolved, normalized differential reflectance spectroscopy lambda = 633 nm). Attention was focused on the unique dependence of COads oxidation on the potential at which the adsorbed full CO monolayer is assembled (i.e., hydrogen adsorption/desorption vs the double-layer region) using both fast linear scan voltammetry and potential step techniques. As evidenced from the data collected, COads oxidation at a fixed potential proceeds at slower rates when the monolayer is formed in the double- layer region compared to when it is formed in the hydrogen adsorption/desorption region. Possible explanations for this effect are discussed.

Oxidation of adsorbed CO on Pt(111) in CO-saturated perchloric acid aqueous solutions: simultaneous in situ time-resolved reflectance spectroscopy and second harmonic generation studies.

Simultaneous normalized differential reflectance spectroscopy (DeltaR/R) and second harmonic generation (SHG) has been employed to follow, independently, OH and adsorbed CO (CO(ads)) on a single Pt(111) microfacet in CO-saturated aqueous perchloric acidic solutions during voltammetric cycles, leading to the oxidation of CO(ads) and subsequent readsorption of CO on the surface. The results obtained are consistent with the disruption of the radical19 x radical19R19.1 degrees phase just prior to the oxidation of adsorbed CO.

Assembly and electrochemical characterization of nanometer-scale electrode|solid electrolyte interfaces.

A technique is herein described for the assembly and characterization of nanometer-scale metal electrode|solid electrolyte interfaces of variable dimensions. The specific system examined in this work involves a sharp Pt tip attached to the piezo-driven head of a scanning tunneling microscope (STM) allowing the tip to be inserted into (or retrieved from) a Nafion membrane placed normal to the direction of tip travel. The actual Pt|Nafion area of contact was determined by coulometric analysis of the characteristic voltammetric features of Pt, using the tip as the working electrode and a much larger Pt gauze attached to the other side of the Nafion as a counter-reference electrode, yielding for some of the interfaces examined values equivalent to as low as 35 000 Pt surface atoms. This rather versatile arrangement allows experiments to be performed in both inert (Ar) and reactive atmospheres, such as oxygen or hydrogen on either or both sides of the membrane, under controlled humidity conditions, and thus sheds light into such phenomena as changes in the overall faradaic currents induced by plastic deformations of the Nafion as well as fundamental aspects of mass transport at reactant gas|Pt|Nafion three-boundary interfaces of relevance to polymer electrolyte fuel cells (PEFCs).

Hydration of CO adsorbed on Pt(100) at cryogenic temperatures in UHV environments.

Adsorption of small amounts of D(2)O (ca. 0.01 L exposure) on CO(sat)/Pt(100) surfaces in ultrahigh vacuum at 105 K was found to split the asymmetric peak at 2100 cm(-1) in the infrared reflection absorption spectra attributed to the stretching of CO adsorbed on atop sites into two clearly defined features: an intense component, which shifted toward lower energies due to surface hydration of adsorbed CO (originally at 2100 cm(-1), peak a), and a smaller peak centered at 2094 cm(-1) (peak b), which remained fixed in position even after closing the D(2)O dosing valve. The energies of peaks a and b, as determined by statistical analyses, correlated very well with those reported in the literature for CO adsorbed at high coverages on Pt(100) originally in the (5 x 20) or (hex) reconstruction, and on the unreconstructed Pt(100)-(1 x 1), respectively, at 90 K. On these bases, the asymmetry of the peak observed for CO(sat)/Pt(100) (no D(2)O dosing) is ascribed to the presence of CO linearly adsorbed on these two different sites on the surface, for which the rate of hydration is larger for the (5 x 20) compared to the (1 x 1) phases.

Optical determination of differential coverage-potential relations of redox-active species immobilized on electrode surfaces.

Single-wavelength (HeNe laser, lambda = 633 nm), normal incidence UV-visible reflectance spectroscopy was used to monitor the optical properties of the glassy carbon (GC)|0.2 M NaOH(aq) interface as a function of the applied potential, E. Whereas the electroreflectance coefficient for bare GC was found to be small and potential independent, surface functionalization by an irreversibly adsorbed layer of tetrasulfonated cobalt phthalocyanine (CoTSPc) yielded a clearly defined sigmoidally shaped normalized reflectance change (DeltaR/R) vs E curve over the potential region in which the adsorbate displayed redox peaks. Assuming DeltaR/R is proportional to the extent of redox conversion, as has been reported for macrocycles adsorbed on other types of carbon (e.g., Kim, S.; Xu, X.; Bae, I. T.; Wang, Z.; Scherson, D. A. Anal. Chem. 1990, 62, 2647-2650), differential coverage-potential relations were determined based purely on the optical data collected. A similar optical behavior was found for irreversible adsorbed CoPc and tetraamino CoPc (CoTAPc) adsorbed on GC, for which the voltammetric peaks were ill-defined, too small for coulometric analyses to be reliably performed, or both. No detectable changes in the DeltaR/R vs E profiles of either bare or macrocyclic-functionalized surfaces were observed upon addition of hydrazine to the neat 0.2 M NaOH solution at potentials at which these surfaces display electrocatalytic properties for its oxidation. Possible factors responsible for this behavior are discussed.