Copper Oxide-Based Photocatalysts and Photocathodes: Fundamentals and Recent Advances.

This work aims at reviewing the most impactful results obtained on the development of Cu-based photocathodes. The need of a sustainable exploitation of renewable energy sources and the parallel request of reducing pollutant emissions in airborne streams and in waters call for new technologies based on the use of efficient, abundant, low-toxicity and low-cost materials. Photoelectrochemical devices that adopts abundant element-based photoelectrodes might respond to these requests being an enabling technology for the direct use of sunlight to the production of energy fuels form water electrolysis (H2) and CO2 reduction (to alcohols, light hydrocarbons), as well as for the degradation of pollutants. This review analyses the physical chemical properties of Cu2O (and CuO) and the possible strategies to tune them (doping, lattice strain). Combining Cu with other elements in multinary oxides or in composite photoelectrodes is also discussed in detail. Finally, a short overview on the possible applications of these materials is presented.

Chlorine Dioxide Degradation Issues on Metal and Plastic Water Pipes Tested in Parallel in a Semi-Closed System.

Chlorine dioxide (ClO2) has been widely used as a disinfectant in drinking water in the past but its effects on water pipes have not been investigated deeply, mainly due to the difficult experimental set-up required to simulate real-life water pipe conditions. In the present paper, four different kinds of water pipes, two based on plastics, namely random polypropylene (PPR) and polyethylene of raised temperature (PERT/aluminum multilayer), and two made of metals, i.e., copper and galvanized steel, were put in a semi-closed system where ClO2 was dosed continuously. The semi-closed system allowed for the simulation of real ClO2 concentrations in common water distribution systems and to simulate the presence of pipes made with different materials from the source of water to the tap. Results show that ClO2 has a deep effect on all the materials tested (plastics and metals) and that severe damage occurs due to its strong oxidizing power in terms of surface chemical modification of metals and progressive cracking of plastics. These phenomena could in turn become an issue for the health and safety of drinking water due to progressive leakage of degraded products in the water.

Structure and Stability of a Copper(II) Lactate Complex in Alkaline Solution: a Case Study by Energy-Dispersive X-ray Absorption Spectroscopy.

Energy-dispersive X-ray absorption spectroscopy was applied, aimed at solving the problem of the structure and stability of a copper(II) lactate complex in alkaline solution, used as a precursor for the electrodeposition of Cu2O. The application of multiple scattering calculations to the simulation of the X-ray absorption near-edge structure part of the spectra allowed an accurate resolution of the structure: the copper(II) cation is surrounded by four lactate ions in a distorted tetrahedral environment, with the lactate anions acting as monodentate ligands. This results in an atomic arrangement where copper is surrounded by four oxygen atoms located at quite a short distance (ca. 1.87 Å) and four oxygen atoms located quite far apart (ca. 3.1-3.2 Å). The complex was finally found to be stable in a wide range of applied potentials.

Observation of charge transfer cascades in α-Fe2O3/IrOx photoanodes by operando X-ray absorption spectroscopy.

Electrochemical devices for energy conversion and storage are central for a sustainable economy. The performance of electrodes is driven by charge transfer across different layer materials and an understanding of the mechanistics is pivotal to gain improved efficiency. Here, we directly observe the transfer of photogenerated charge carriers in a photoanode made of hematite (α-Fe2O3) and a hydrous iridium oxide (IrOx) overlayer, which plays a key role in photoelectrochemical water oxidation. Through the use of operando X-ray absorption spectroscopy (XAS), we probe the change in occupancy of the Ir 5d levels during optical band gap excitation of α-Fe2O3. At potentials where no photocurrent is observed, electrons flow from the α-Fe2O3 photoanode to the IrOx overlayer. In contrast, when the composite electrode produces a sustained photocurrent (i.e., 1.4 V vs. RHE), a significant transfer of holes from the illuminated α-Fe2O3 to the IrOx layer is clearly demonstrated. The analysis of the operando XAS spectra further suggests that oxygen evolution actually occurs both at the α-Fe2O3/electrolyte and α-Fe2O3/IrOx interfaces. These findings represent an important outcome for a better understanding of composite photoelectrodes and their use in photoelectrochemical systems, such as hydrogen generation or CO2 reduction from sunlight.

An Efficient CuxO Photocathode for Hydrogen Production at Neutral pH: New Insights from Combined Spectroscopy and Electrochemistry.

Light-driven water splitting is one of the most promising approaches for using solar energy in light of more sustainable development. In this paper, a highly efficient p-type copper(II) oxide photocathode is studied. The material, prepared by thermal treatment of CuI nanoparticles, is initially partially reduced upon working conditions and soon reaches a stable form. Upon visible-light illumination, the material yields a photocurrent of 1.3 mA cm(-2) at a potential of 0.2 V vs a reversible hydrogen electrode at mild pH under illumination by AM 1.5 G and retains 30% of its photoactivity after 6 h. This represents an unprecedented result for a nonprotected Cu oxide photocathode at neutral pH. The photocurrent efficiency as a function of the applied potential was determined using scanning electrochemical microscopy. The material was characterized in terms of photoelectrochemical features; X-ray photoelectron spectroscopy, X-ray absorption near-edge structure, fixed-energy X-ray absorption voltammetry, and extended X-ray absorption fine structure analyses were carried out on pristine and used samples, which were used to explain the photoelectrochemical behavior. The optical features of the oxide are evidenced by direct reflectance spectroscopy and fluorescence spectroscopy, and Mott-Schottky analysis at different pH values explains the exceptional activity at neutral pH.

3D-printed photo-spectroelectrochemical devices for in situ and in operando X-ray absorption spectroscopy investigation.

Three-dimensional printed multi-purpose electrochemical devices for X-ray absorption spectroscopy are presented in this paper. The aim of this work is to show how three-dimensional printing can be a strategy for the creation of electrochemical cells for in situ and in operando experiments by means of synchrotron radiation. As a case study, the description of two cells which have been employed in experiments on photoanodes for photoelectrochemical water splitting are presented. The main advantages of these electrochemical devices are associated with their compactness and with the precision of the three-dimensional printing systems which allows details to be obtained that would otherwise be difficult. Thanks to these systems it was possible to combine synchrotron-based methods with complementary techniques in order to study the mechanism of the photoelectrocatalytic process.

The Influence of Carbonaceous Matrices and Electrocatalytic MnO2 Nanopowders on Lithium-Air Battery Performances.

Here, we report new gas diffusion electrodes (GDEs) prepared by mixing two different pore size carbonaceous matrices and pure and silver-doped manganese dioxide nanopowders, used as electrode supports and electrocatalytic materials, respectively. MnO2 nanoparticles are finely characterized in terms of structural (X-ray powder diffraction (XRPD), energy dispersive X-ray (EDX)), morphological (SEM, high-angle annular dark field (HAADF)-scanning transmission electron microscopy (STEM)/TEM), surface (Brunauer Emmet Teller (BET)-Barrett Joyner Halenda (BJH) method) and electrochemical properties. Two mesoporous carbons, showing diverse surface areas and pore volume distributions, have been employed. The GDE performances are evaluated by chronopotentiometric measurements to highlight the effects induced by the adopted materials. The best combination, hollow core mesoporous shell carbon (HCMSC) with 1.0% Ag-doped hydrothermal MnO2 (M_hydro_1.0%Ag) allows reaching very high specific capacity close to 1400 mAh·g-1. Considerably high charge retention through cycles is also observed, due to the presence of silver as a dopant for the electrocatalytic MnO2 nanoparticles.

Fixed energy X-ray absorption voltammetry.

In this paper, the fixed energy X-ray absorption voltammetry (FEXRAV) is introduced. FEXRAV represents a novel in situ X-ray absorption technique for fast and easy preliminary characterization of electrode materials and consists of recording the absorption coefficient at a fixed energy while varying at will the electrode potential. The energy is chosen close to an X-ray absorption edge, in order to give the maximum contrast between different oxidation states of an element. It follows that any shift from the original oxidation state determines a variation of the absorption coefficient. Although the information given by FEXRAV obviously does not supply the detailed information of X-ray absorption near edge structure (XANES) or extended X-ray absorption fine structure (EXAFS), it allows to quickly map the oxidation states of the element under consideration within the selected potential windows. This leads to the rapid screening of several systems under different experimental conditions (e.g., nature of the electrolyte, potential window) and is preliminary to more deep X-ray absorption spectroscopy (XAS) characterizations, like XANES or EXAFS. In addition, the time-length of the experiment is much shorter than a series of XAS spectra and opens the door to kinetic analysis.

IrO2-based disperse-phase electrocatalysts: a complementary study by means of the cavity-microelectrode and ex-situ X-ray absorption spectroscopy.

In this work, IrO(2)-based powders are screened by cyclic voltammetry for the determination of the electrochemical active sites and for the qualitative evaluation of the iridium atoms speciation. All results are obtained using a cavity-microelectrode as powder holder, thus exploiting the features of this innovative tool, whose best potentialities have been recently introduced by our group. All the studied materials have been prepared by the sol-gel technique and differ in calcination temperature and method of mixing the metal oxide precursors. The electrochemical results are complemented with the information obtained by X-ray absorption spectroscopy (XAS), that give insights on the local structure of each selected sample, confirming the trends found by cyclic voltammetry and give new and unexpected insights on the powder structural features.

Quantitative studies on electrode material properties by means of the cavity microelectrode.

The determination of the number of active sites is a key issue in the evaluation of electrode materials for any electrochemical application. Nonetheless, and particularly in the case of powder materials, a commonly accepted method to determine the actual density of active sites is not yet available, mainly because a method to quantify the amount of material under investigation is missing. In this study, we propose the use of the cavity microelectrode (C-ME, i.e., a cylindrical recessed microdisk) of known volume, which enables the study of a known amount of material, thus allowing the quantitative evaluation of its properties. The validation of the method implied (i) the preparation of C-MEs with different radii and depths; (ii) the calibration of the relevant volumes by means of a "standard" powder, whose number of active sites can be easily determined by cyclic voltammetry; and (iii) their use for the quantification of specific parameters that identify the electrochemical properties of mixed IrO(2)-SnO(2) powders. The results evidence that the quantity of charge relative to the number of pseudocapacitance sites and the currents for the oxygen evolution reaction are proportional to the cavity volumes. This strategy allows the direct comparison of different materials for their rapid and accurate screening. In addition, thanks to the small amount of material required for the sample (typically 10-100 ng), the method can be safely listed among the nondestructive techniques.

Bridging the gap between electrochemical and organometallic activation: benzyl chloride reduction at silver cathodes.

Integration of voltammetry, surface-enhanced Raman spectroscopy (SERS), and density functional theory (DFT) has allowed unraveling the mechanistic origin of the exceptional electrocatalytic properties of silver cathodes during the reduction of benzyl chloride. At inert electrodes the initial reduction proceeds through a concerted direct electron transfer yielding a benzyl radical as the first intermediate. Conversely, at silver electrodes it involves an uphill preadsorption of benzyl chloride onto the silver cathode. Reduction of this adduct affords a species tentatively described as a distorted benzyl radical anion stabilized by the silver surface. This transient species rapidly evolves to yield ultimately a benzyl radical bound onto the silver surface, the latter being reduced into a benzyl-silver anionic adduct which eventually dissociates into a free benzyl anion at more negative potentials. Within this framework, the exceptional electrocatalytic properties of silver cathodes stem from the fact that they drastically modify the mechanism of the 2e-reduction pathway through a direct consequence of the electrophilicity of silver cathode surfaces toward organic halides. This mechanism contrasts drastically with any of those tentatively invoked previously, and bridges classical electroreduction mechanisms and oxidative additions similar to those occurring during organometallic homogeneous activation of organic halides by low-valent transition-metal complexes.

In situ identification of intermediates of benzyl chloride reduction at a silver electrode by SERS coupled with DFT calculations.

Aiming to deeply understand the electrocatalytic mechanism of silver on reduction of benzyl chloride, we carried out an in situ electrochemical surface-enhanced Raman spectroscopic study to characterize various surface species in different electrode potential regions. A further analysis with DFT calculation reveals that the benzyl radical and its anionic derivate bonded on a silver electrode are the key intermediates, implying that the pathway could drastically differ from the outer sphere concerted electron reduction at inert electrodes.

Screening of oxygen evolution electrocatalysts by scanning electrochemical microscopy using a shielded tip approach.

Oxygen evolution electrocatalysts in acidic media were studied by scanning electrochemical microscopy (SECM) in the substrate generation-tip collection (SG-TC) imaging mode with a 100 microm diam tip. Pure IrO2 and Sn(1-x)Ir(x)O2 combinatorial mixtures were prepared by a sol-gel route to form arrays of electrocatalyst spots. The experimental setup has been developed to optimize screening of electrocatalyst libraries under conditions where the entire array is capable of the oxygen evolution reaction (OER). The activity of individual spots was determined by reducing the interference from the reaction products of neighboring spots diffusing to the tip over the spot of interest. A gold layer deposited on the external wall of the SECM tip was used as a tip shield. In this study the shield was kept at a constant potential to reduce oxygen under mass transfer controlled conditions. The tip shield consumes oxygen coming from the neighbor spots in the array and enables the tip to correctly detect the activity of the spot below the tip. Simulations and experimental results are shown, demonstrating the effectiveness of the tip shield with the SG-TC setup in determining the properties of the composite materials and imaging arrays.

Impact of self-assembly composition on the alternate interfacial electron transfer for electrostatically immobilized cytochrome c.

We report on the effects of self-assembled monolayer (SAM) dilution and thickness on the electron transfer (ET) event for cytochrome c (CytC) electrostatically immobilized on carboxyl terminated groups. We observed biphasic kinetic behavior for a logarithmic dependence of the rate constant on the SAM carbon number (ET distance) within the series of mixed SAMs of C(5)COOH/C(2)OH, C(10)COOH/C(6)OH, and C(15)COOH/C(11)OH that is in overall similar to that found earlier for the undiluted SAM assemblies. However, in the case of C(15)COOH/C(11)OH and C(10)COOH/C(6)OH mixed SAMs a notable increase of the ET standard rate constant was observed, in comparison with the corresponding unicomponent (omega-COOH) SAMs. In the case of the C(5)COOH/C(2)OH composite SAM a decrease of the rate constant versus the unicomponent analogue was observed. The value of the reorganization free energy deduced through the Marcus-like data analysis did not change throughout the series; this fact along with the other observations indicates uncomplicated rate-determining unimolecular ET in all cases. Our results are consistent with a model that considers a changeover between the alternate, tunneling and adiabatic intrinsic ET mechanisms. The physical mechanism behind the observed fine kinetic effects in terms of the protein-rigidifying omega-COOH/CytC interactions arising in the case of mixed SAMs are also discussed.

Ion-channel sensors based on ETH 1001 ionophore embedded in charged-alkanethiol self-assembled monolayers on gold electrode surfaces.

An ion-channel sensor was demonstrated by immobilizing ETH 1001, an ionophore for ion-selective electrodes, on a gold electrode surface. The approach for preparing the sensor was to incorporate the ionophore into a mixed self-assembled monolayer of 10-mercaptodecanesulfonate and 11-hydroxy-1-undecanethiol formed on the surface. The voltammetric responses for the thus prepared sensor to the primary cation Ca(2+) were observed by using [Fe(CN)(6)](3-/4-) as an electroactive marker. The ionophore was stably immobilized on the electrode surface with the hydrophobic interaction between its alkyl chains and those of the alkanethiol. The introduction of a proper charge density to the electrode surface improved the sensor sensitivity with retaining the selective response to Ca(2+) against Mg(2+) with concentrations above 10(-4) M.

Selective electrodehalogenation of bromophenols on Ag electrocatalyst.

Among the innovative technologies for the detoxification and disposal of industrial effluents, our recently described electroreductive dehalogenation of organic halides on silver electrocatalyst provides a promising route, to be easily "plugged-in" into integrated waste treatments. Although electroreductions do not lead to total substrate mineralization, complete and selective dehalogenation may be achieved by the appropriate choice of the cathode material, thus decreasing the biotoxicity of the waste. In particular the use of silver as electrocatalyst greatly reduces the energy demand, and ensures higher yields and no by-products also when treating highly toxic aromatic halides. In the present work the electrocatalytic role of silver in the electroreductive dehalogenation process has been studied on mono- and polyhalogenated bromophenols, taken as model substrates, both in terms of selectivity of the reaction pathway and of reactivity of the position on the aromatic ring of the bromo leaving group. The results point to the possibility of effectively extending the methodology also to the more common and less reactive chlorinated derivatives.

pH measurements in non-aqueous and aqueous-organic solvents - definition of standard procedures.

pH standardisation procedures in non-aqueous and aqueous-organic solvents are discussed in the light of the newly prepared IUPAC recommendation on measurement of pH in dilute aqueous solutions. Both scientific and metrological aspects are considered, as required by the definitions of primary and secondary methods of measurements recently endorsed by BIPM (Bureau International de Poids et de Mesures, France).