Online Monitoring of Electrochemical Carbon Corrosion in Alkaline Electrolytes by Differential Electrochemical Mass Spectrometry.

Carbon corrosion at high anodic potentials is a major source of instability, especially in acidic electrolytes and impairs the long-term functionality of electrodes. In-depth investigation of carbon corrosion in alkaline environment by means of differential electrochemical mass spectrometry (DEMS) is prevented by the conversion of CO2 into CO3 2- . We report the adaptation of a DEMS system for online CO2 detection as the product of carbon corrosion in alkaline electrolytes. A new cell design allows for in situ acidification of the electrolyte to release initially dissolved CO3 2- as CO2 in front of the DEMS membrane and its subsequent detection by mass spectrometry. DEMS studies of a carbon-supported nickel boride (Nix B/C) catalyst and Vulcan XC 72 at high anodic potentials suggest protection of carbon in the presence of highly active oxygen evolution electrocatalysts. Most importantly, carbon corrosion is decreased in alkaline solution.

SLIM: A Short-Linked, Highly Redox-Stable Trityl Label for High-Sensitivity In-Cell EPR Distance Measurements.

The understanding of biomolecular function is coupled to knowledge about the structure and dynamics of these biomolecules, preferably acquired under native conditions. In this regard, pulsed dipolar EPR spectroscopy (PDS) in conjunction with site-directed spin labeling (SDSL) is an important method in the toolbox of biophysical chemistry. However, the currently available spin labels have diverse deficiencies for in-cell applications, for example, low radical stability or long bioconjugation linkers. In this work, a synthesis strategy is introduced for the derivatization of trityl radicals with a maleimide-functionalized methylene group. The resulting trityl spin label, called SLIM, yields narrow distance distributions, enables highly sensitive distance measurements down to concentrations of 90 nm, and shows high stability against reduction. Using this label, the guanine-nucleotide dissociation inhibitor (GDI) domain of Yersinia outer protein O (YopO) is shown to change its conformation within eukaryotic cells.

Role of Lattice Oxygen in the Oxygen Evolution Reaction on Co3O4: Isotope Exchange Determined Using a Small-Volume Differential Electrochemical Mass Spectrometry Cell Design.

This work demonstrates the role of lattice oxygen of metal oxide catalysts in the oxygen evolution reaction (OER) as evidenced by isotope labeling together with the differential electrochemical mass spectrometry (DEMS) method. Our recent report assessed this role for Co3O4 using a flow-through DEMS cell, which requires a large volume of electrolyte. Herein, we extend this procedure to different Co3O4 catalyst loadings and particle sizes as well as the mixed Ag + Co3O4 catalyst. We introduce, for the first time, a novel small-volume DEMS cell design capable of using disc electrodes and only <0.5 mL of electrolyte. The reliability of the cell is demonstrated by monitoring gas evolution during OER in real time. This cell shows high sensitivity, high collection efficiency, and very short delay time. DEMS results reveal that only the interfacial part (∼0.2% of the total loading or 25% of surface atoms) of the catalyst is active for OER. Interestingly, the amount of oxygen exchanged on the mixed Ag + Co3O4 catalyst is higher than that on the single Co3O4 catalyst, which illustrates the improved electrocatalytic activity previously reported on this mixed catalyst. Furthermore, the real surface area of the catalysts is estimated using different methods (namely, the ball model, double layer capacitance, isotope exchange, and redox peak methods). The surface areas estimated from the Brunauer-Emmett-Teller (BET) and ball models are comparable but roughly three times higher than that of the redox peak method. Our method represents an alternative approach for probing the mechanism and real surface area of catalysts.

K-O2 electrochemistry: achieving highly reversible peroxide formation.

Since the advent of the lithium-air battery, researchers have focused on understanding the underpinning mechanisms of the oxygen reduction and evolution reaction in aprotic solvents. In this work, the oxygen reaction in the presence of potassium ions in dimethyl sulfoxide was exploited as a model system to refine the present mechanistic picture of oxygen reduction in aprotic environments. In a combined approach utilizing differential electrochemical mass spectrometry in a generator-collector arrangement as well as classical electrochemical techniques, the reversible formation of insoluble peroxide as well as of slightly soluble superoxide is shown. As opposed to other peroxides in other non-aqueous metal-oxygen systems, potassium peroxide can be reoxidized to superoxide with an overpotential of as little as 100 mV. The investigation of the effect of the oxygen partial pressure between 0 and 1 atmosphere demonstrates how the precipitation of superoxide increases the oxidation overpotential of the peroxide and establishes a link between this work and other studies, in which the reversibility of the peroxide formation has not been identified.

Polyphenols from Rheum Roots Inhibit Growth of Fungal and Oomycete Phytopathogens and Induce Plant Disease Resistance.

A growing world population requires an increase in the quality and quantity of food production. However, field losses due to biotic stresses are currently estimated to be between 10 and 20% worldwide. The risk of resistance and strict pesticide legislation necessitate innovative agronomical practices to adequately protect crops in the future, such as the identification of new substances with novel modes of action. In the present study, liquid chromatography mass spectrometry was used to characterize Rheum rhabarbarum root extracts that were primarily composed of the stilbenes rhaponticin, desoxyrhaponticin, and resveratrol. Minor components were the flavonoids catechin, epicatechin gallate, and procyanidin B1. Specific polyphenolic mixtures inhibited mycelial growth of several phytopathogenic fungi and oomycetes. Foliar spray applications with fractions containing stilbenes and flavonoids inhibited spore germination of powdery mildew in Hordeum vulgare with indications of synergistic interactions. Formulated extracts led to a significant reduction in the incidence of brown rust in Triticum aestivum under field conditions. Arabidopsis thaliana mutant and quantitative reverse-transcription polymerase chain reaction studies suggested that the stilbenes induce salicylic acid-mediated resistance. Thus, the identified substances of Rheum roots represent an excellent source of antifungal agents that can be used in horticulture and agriculture.

Fast and Simultaneous Determination of Gas Diffusivities and Solubilities in Liquids Employing a Thin-Layer Cell Coupled to a Mass Spectrometer, Part II: Proof of Concept and Experimental Results.

A new method for simultaneously determining gas diffusivities and solubilities in liquids was presented and discussed in detail in Part I of this series. In this part of the series, the new measurement cell was employed to determine oxygen solubilities and diffusivities in 20 different dimethyl sulfoxide-based electrolytes. In addition, a comparison to values available in literature was made. From the temperature dependence of the diffusivity between 20 and 40 °C an activation barrier of 19 kJ mol-1 for the diffusion of oxygen in pure dimethyl sulfoxide was found. Moreover, qualitative agreement between Jones-Dole viscosity coefficients and the dependence of the diffusivity on the electrolyte concentration was confirmed. The temperature-dependent solubility measurements revealed an unexpected increase of the oxygen solubility for temperatures above 30 °C. While the oxygen solubility in the case of the alkali-perchlorates decreases with increasing electrolyte concentration, a pronounced salting-in effect for lithium bis(trifluoromethane)sulfonimide was observed.

Fast and Simultaneous Determination of Gas Diffusivities and Solubilities in Liquids Employing a Thin-Layer Cell Coupled to a Mass Spectrometer, Part I: Setup and Methodology.

Transport properties and solubilities of volatile species in liquid solutions are of high interest in different chemical, biological, and physical systems. In this work, a new approach for determining the diffusivity and solubility of gases in liquids simultaneously is presented. The method presented relies on the diffusion of a volatile species through a thin, liquid layer and the subsequent detection of the species using a mass spectrometer. Evaluation of the time development of the resulting transient yields the diffusion coefficient, while the concentration of the species in the liquid layer can be calculated from the steady-state value of the flux into the mass spectrometer. Apart from the geometry of the thin layer and the calibration constant of the mass spectrometer no additional or external data are required. Experimental results of the temperature-dependent solubility and diffusivity of oxygen in dimethyl sulfoxide are presented in our companion paper Part II and serve as a proof of concept.

Surface morphology and adlayer structure of Se on Rh(111).

The deposition of Se from SeO32- solutions was examined in the submonolayer regime by cyclic voltammetry, scanning tunneling microscopy and atomic force microscopy. Up to a coverage of ca. 0.5 (Se atoms to substrate atoms) a smooth adlayer is obtained with a 2 × âˆš3 structure. When the coverage is increased, at around 0.55 V further deposition is paralleled by a roughening starting at the monoatomic steps. The adsorbed Se is stable in the SeO32- free solution. For coverages below 0.25, separate domains for the Se covered regions and Se free regions were observed for potentials above 0.6 V. Since this is the potential of the spike corresponding to adsorption of OH at the clean Rh(111) surface in HClO4, we have to assume that Se and OH adsorb in separate domains. At lower potentials, where OH is desorbed, Se spreads over the complete surface which then appears completely smooth in the STM images. When the coverage is about 0.25 or above, the roughening is also observed in SeO32- free solution, demonstrating that the rough structures are not due to disordered deposition, but really due to a roughening by place exchange.

How many surface atoms in Co3O4 take part in oxygen evolution? Isotope labeling together with differential electrochemical mass spectrometry.

Understanding the mechanism underlying the oxygen evolution reaction (OER) on oxides is crucial for the development of many energy storage systems. Here, the mechanism of OER on a Co3O4 spinel catalyst is investigated in alkaline media using 18O-labeling combined with differential electrochemical mass spectrometry (DEMS). This work unravels the role of surface oxygen of the oxide in the OER. It is shown that in H218O-containing electrolyte the amount of 18O16O evolved increases from cycle to cycle together with a concomitant decrease of the amount of 16O2 with each cycle before reaching a steady-state value. 18O16O is also evolved from a H216O solution on a Co3O4 electrode pre-treated in H218O-containing solution, indicating the formation of the 18O-labeled oxide in the previous step. Therefore, the oxide layer takes part in OER via an oxygen exchange mechanism. The total number of oxygen atoms of the oxide participating in OER is 0.1 to 0.2% of the total oxide loading, corresponding to about 10-30% of the surface atoms; these represent the catalytically active sites. Moreover, the real surface area of the catalyst is estimated using different methods (namely the ball model, double layer capacitance method, redox peak method, isotope exchange), and compared to the BET data. The surface areas calculated from the BET data, ball model and redox peak method are similar for small particles, which indicates their smooth surface; however they are smaller than that estimated from double-layer capacitance. For larger particles, the much larger surface area estimated from the redox peak in comparison to that expected from the ball model seems to be due to their roughness. Thus, this work highlights the importance of probing the mechanism when investigating the OER activity of a catalyst.

Determining Solubility and Diffusivity by Using a Flow Cell Coupled to a Mass Spectrometer.

One of the main challenges in metal-air batteries is the selection of a suitable electrolyte that is characterized by high oxygen solubility, low viscosity, a liquid state and low vapor pressure across a wide temperature range, and stability across a wide potential window. Herein, a new method based on a thin layer flow through cell coupled to a mass spectrometer through a porous Teflon membrane is described that allows the determination of the solubility of volatile species and their diffusion coefficients in aqueous and nonaqueous solutions. The method makes use of the fact that at low flow rates the rate of species entering the vacuum system, and thus the ion current, is proportional to the concentration times the flow rate (c⋅u) and independent of the diffusion coefficient. The limit at high flow rates is proportional to D2/3·c·u1/3 . Oxygen concentrations and diffusion coefficients in aqueous electrolytes that contain Li(+) and K(+) and organic solvents that contain Li(+) , K(+) , and Mg(2+) , such as propylene carbonate, dimethyl sulfoxide tetraglyme, and N-methyl-2-pyrrolidone, have been determined by using different flow rates in the range of 0.1 to 80 µL s(-1) . This method appears to be quite reliable, as can be seen by a comparison of the results obtained herein with available literature data. The solubility and diffusion coefficient values of O2 decrease as the concentration of salt in the electrolyte was increased due to a "salting out" effect.

Electrocatalytic oxidation and adsorption rate of methanol at Pt stepped single-crystal electrodes and effect of Ru step decoration: a DEMS study.

The adsorption and oxidation of methanol at Pt(331) and Ru-step-decorated Pt(331) electrodes are studied recording currents and ion currents by online differential electrochemical mass spectrometry. The CO(2) current efficiencies and the degree of surface poisoning with CO(ad) formed during methanol oxidation are independent of the flow rate, confirming the parallel pathway mechanism. The CO(2) current efficiencies decrease with increasing methanol concentration and increase with increasing potential, whereas those of methyl formate show a reverse trend. At potentials higher than 0.6 V, neither the CO(2) current efficiencies nor the methanol oxidation currents increase with increasing Ru coverage. Instead, methanol oxidation is inhibited due to blocking of the most active platinum step sites. At potentials lower than 0.6 V, however, not only the onset of methanol oxidation shifts negatively, by about 0.1 V, but also the methanol oxidation current and the CO(2) current efficiencies increase. Crucial for the use in fuel cells is the complete oxidation to CO(2), which can be achieved if the reactants first adsorb at the electrode surface along the reaction path with adsorbed CO as an intermediate. Therefore, we directly determine the methanol adsorption rates at Pt(331) as well as at Ru-step-decorated Pt(331), Pt(332), Pt(100), and Pt(11,1,1) electrodes. The methanol adsorption rate is doubled by a double step density in the case of the Pt(331) and Pt(332) electrodes, higher at higher Ru coverages, and increases by a factor of three upon increasing the potential by 0.1 V (corresponding to a Tafel slope of approximately 200 mV dec(-1)). At Pt(331) electrodes with partial step decoration, stripping of adsorbed CO (from CO gas) reveals two adsorbate states, which are also discernable when the adsorbate formed from methanol dehydrogenation is stripped.

The mutualistic fungus Piriformospora indica protects barley roots from a loss of antioxidant capacity caused by the necrotrophic pathogen Fusarium culmorum.

Fusarium culmorum causes root rot in barley (Hordeum vulgare), resulting in severely reduced plant growth and yield. Pretreatment of roots with chlamydospores of the mutualistic root-colonizing basidiomycete Piriformospora indica (subdivision Agaricomycotina) prevented necrotization of root tissues and plant growth retardation commonly associated with Fusarium root rot. Quantification of Fusarium infections with a real-time polymerase chain reaction assay revealed a correlation between root rot symptoms and the relative amount of fungal DNA. Fusarium-infected roots showed reduced levels of ascorbate and glutathione (GSH), along with reduced activities of antioxidant enzymes such as superoxide dismutase, ascorbate peroxidase, GSH reductase, dehydroascorbate reductase, and monodehydroascorbate reductase. Consistent with this, Fusarium-infected roots showed elevated levels of lipid hydroperoxides and decreased ratios of reduced to oxidized forms of ascorbate and GSH. In clear contrast, roots treated with P. indica prior to inoculation with F. culmorum showed levels of ascorbate and GSH that were similar to controls. Likewise, lipid peroxidation and the overall reduction in antioxidant enzyme activities were largely attenuated by P. indica in roots challenged by F. culmorum. These results suggest that P. indica protects roots from necrotrophic pathogens, at least partly, through activating the plant's antioxidant capacity.

Oxidation of carbon monoxide, hydrogen peroxide and water at a boron doped diamond electrode: the competition for hydroxyl radicals.

Boron doped diamond (BDD) electrodes have an extremely high over-voltage for oxygen evolution from water, which favours its use in oxidation processes of other compounds at high potentials. We used a rotating ring disc (RRDE) assembly and differential electrochemical mass spectrometry (DEMS) in order to monitor the consumption or the production of species in the course of the electrode processes. By intercepting the intermediate of the electrochemical water oxidation with chemical reactions we demonstrate clearly, albeit indirectly, that in the water oxidation process at BDD above 2.5 V the first step is the formation of ˙OH radicals. The electro-oxidation of CO to CO2 at BDD electrodes proceeds only via a first attack by ˙OH radicals followed by a further electron transfer to the electrode. At potentials below the onset of oxygen evolution from water, H2O2 is oxidised by a direct electron transfer to the BDD electrode, while at higher potentials, two different reactions paths compete for the ˙OH radicals formed in the first electron transfer from water: one, where these ˙OH radicals react with each other followed by further electron transfers leading to O2 on the one hand and one, where ˙OH radicals react with other species like H2O2 or CO with subsequent electron transfers on the other hand.

Quantitative DEMS study of ethanol oxidation: effect of surface structure and Sn surface modification.

Using the dual thin layer flow through cell, a semi-quantitative analysis of the volatile products during the electrooxidation of adsorbed and bulk solution of 0.01 M ethanol at polycrystalline platinum, smooth, roughened and Sn modified Pt(11,1,1), Pt(311) electrodes has been done by on-line differential electrochemical mass spectroscopy (DEMS). In addition to the current efficiency of CO(2), that of acetaldehyde was determined as a function of the flow rate. At polycrystalline platinum, ethanol oxidation produces only acetaldehyde; the amount of acetaldehyde further oxidized to acetic acid is negligible due to convection conditions. For comparison and for calibration purposes, i-propanol oxidation was examined for which acetone is the only oxidation product. At Pt(11,1,1), the main oxidation product is acetaldehyde. At Pt(311), in addition to acetaldehyde, acetic acid was also formed. Surface modification with Sn did not increase the reactivity of Pt(11,1,1) instead it led to inhibition of the ethanol oxidation. In the case of Pt(311), the onset potential of oxidation was shifted negatively by 0.2 V in the presence of Sn. The results of the potentiostatic measurements showed that this shift is not associated with the production of CO(2); rather acetic acid and acetaldehyde are the main oxidation products.

Electrodeposited Cobalt Nanosheets on Smooth Silver as a Bifunctional Catalyst for OER and ORR: In Situ Structural and Catalytic Characterization.

Developing earth-abundant, cost-effective, and active bifunctional electrocatalysts for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is key to boosting sustainable energy systems such as electrolyzers and lithium-air batteries. However, the performance of promising cobalt-based materials is impaired by the external effects of binders and carbon additives as well as inhomogeneous electrode fabrication. In this work, binder- and carbon-free flower-like Co-decorated Ag catalytic nanosheets were in situ-synthesized via a simple electrodeposition approach. The morphology, composition, and structure of Co/Ag before and after OER were characterized using scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), X-ray photoelectron spectroscopy (XPS), and X-ray diffraction (XRD). Co/Ag thin film electrodes with various Co contents exhibited a bifunctional activity toward ORR and OER due to a synergistic effect. XPS analysis suggested the formation of Co3O4 as the main active species for OER. In particular, Co (83%)/Ag surface revealed a 60 mV lower ORR overpotential than a pure Ag surface and even lower than drop-casted Co3O4 nanoparticles on Ag surface. Only 1.5% peroxide was generated, suggesting a four-electron transfer ORR. In addition, the OER onset potential on Co/Ag is 60 mV less than Co3O4. Tafel slopes of 71 and 75 mV dec-1 were obtained for ORR and OER, respectively. Importantly, the three-dimensional (3D) growth mechanism of a cobalt layer (∼1 nm) on a well-defined atomic smooth Ag surface is unraveled by in situ electrochemical scanning tunneling microscopy (EC-STM). EC-STM suggests that Co prefers to nucleate at the step edges of Ag and grows in a 3D, forming nanoparticles, where the deposition/dissolution process of the Co adlayer on Ag is reversible. This investigation may provide insights into design strategies of efficient oxygen electrocatalysts.

Molecular adsorbates at single-crystal platinum-group metals and bimetallic surfaces.

The surface orientation of Pt-group metals determines the kind of organic species (such as CO, benzene and ethene) that will adsorb on them as well as the prevailing reaction channels. Pt and Pd as well as (sub)monolayers of them on Au are compared, including mono- and multiatomic rows of Pd on stepped Au surfaces. In general, Pd is less active for oxidation or hydrogenation of the adsorbates. Desorption of the intact molecule is favored because of a lower adsorption strength.

Electrochemical Reduction of O2 in Ca2+ -Containing DMSO: Role of Roughness and Single Crystal Structure.

In this study, the oxygen reduction reaction (ORR) in Ca2+ -containing dimethyl sulfoxide (DMSO) at well-ordered and rough electrode surfaces is compared by using cyclic voltammetry, differential electrochemical mass spectrometry, rotating ring disk electrode, and atomic force microscopy measurements. Slightly soluble CaO2 is the main product during early ORR on gold electrodes; after completion of a monolayer of CaO and/or CaO2 , which is formed in parallel and in competition to the peroxide, only superoxide is formed. When the monolayer is completely closed on smooth annealed Au, no further reduction occurs, whereas on rough Au a defect-rich layer allows for continuous formation of superoxide. CaO2 formed either via two subsequent 1  e - transfer steps or by disproportionation of superoxide may be deposited on top of the CaO/CaO2 adsorbate layer. The slow dissolution of the peroxide particles is demonstrated by AFM. Whereas a smooth CaO/CaO2 -covered electrode shows severe deactivation and a CaO/CaO2 -covered rough electrode allows for diffusion-limited superoxide formation, on single crystals peroxide formation is more pronounced. The reason is most likely the lack of nucleation sites for the blocking CaO/CaO2 layer. RRDE investigations showed sluggish reoxidation kinetics of the dissolved peroxide, which are most likely due to ion pairing with Ca2+ . The apparent transfer coefficient is estimated by using variation of the electrode roughness, confirming the result of the usual Tafel analysis and indicating an equilibrated first 1  e - transfer.

The Oxygen Reduction Reaction in Ca2+ -Containing DMSO: Reaction Mechanism, Electrode Surface Characterization, and Redox Mediation*.

In this study the fundamental understanding of the underlying reactions of a possible Ca-O2 battery using a DMSO-based electrolyte was strengthened. Employing the rotating ring disc electrode, a transition from a mixed process of O2 - and O2 2- formation to an exclusive O2 - formation at gold electrodes is observed. It is shown that in this system Ca-superoxide and Ca-peroxide are formed as soluble species. However, there is a strongly adsorbed layer of products of the oxygen reduction reaction (ORR) s on the electrode surface, which is blocking the electrode. Surprisingly the blockade is only a partial blockade for the formation of peroxide while the formation of superoxide is maintained. During an anodic sweep, the ORR product layer is stripped from the electrode surface. With X-ray photoelectron spectroscopy (XPS) the deposited ORR products were shown to be Ca(O2 )2 , CaO2 , and CaO as well as side-reaction products such as CO3 2- and other oxygen-containing carbon species. It is shown that the strongly attached layer on the electrocatalyst, that was partially blocking the electrode, could be adsorbed CaO. The disproportionation reaction of O2 - in presence of Ca2+ was demonstrated via mass spectrometry. Finally, the ORR mediated by 2,5-di-tert-1,4-benzoquinone (DBBQ) was investigated by differential electrochemical mass spectrometry (DEMS) and XPS. Similar products as without DBBQ are deposited on the electrode surface. The analysis of the DEMS experiments shows that DBBQ- reduces O2 to O2 - and O2 2- , whereas in the presence of DBBQ2- O2 2- is formed. The mechanism of the ORR with and without DBBQ is discussed.

Determination of the apparent transfer coefficient for CO oxidation on Pt(poly), Pt(111), Pt(665) and Pt(332) using a potential modulation technique.

The apparent transfer coefficient, which gives the magnitude of the potential dependence of the electrochemical reaction rates, is the key quantity for the elucidation of electrochemical reaction mechanisms. We introduce the application of an ac method to determine the apparent transfer coefficient alpha' for the oxidation of pre-adsorbed CO at polycrystalline and single-crystalline Pt electrodes in sulfuric acid. The method allows to record alpha' quasi continuously as a function of potential (and time) in cyclic voltammetry or at a fixed potential, with the reaction rate varying with time. At all surfaces (Pt(poly), Pt(111), Pt(665), and Pt(332)) we clearly observed a transition of the apparent transfer coefficient from values around 1.5 at low potentials to values around 0.5 at higher potentials. Changes of the apparent transfer coefficients for the CO oxidation with potential were observed previously, but only from around 0.7 to values as low as 0.2. In contrast, our experimental findings completely agree with the simulation by Koper et al., J. Chem. Phys., 1998, 109, 6051-6062. They can be understood in the framework of a Langmuir-Hinshelwood mechanism. The transition occurs when the sum of the rate constants for the forward reaction (first step: potential dependent OH adsorption, second step: potential dependent oxidation of CO(ad) with OH(ad)) exceeds the rate constant for the back-reaction of the first step. We expect that the ac method for the determination of the apparent transfer coefficient, which we used here, will be of great help also in many other cases, especially under steady conditions, where the major limitations of the method are avoided.

The 59th annual meeting of the International Society of Electrochemistry in Seville.

Electrochemistry down to the molecular level was the main theme of the 59th annual meeting of the International Society of Electrochemistry (ISE, see logo). Around 1400 scientists from all over the world met in Seville to discuss modern aspects, progress in methods and new mechanistic insights.