Silicon electrodes with the columnar macroporous structure were investigated to determine the effect of variations in the columnar pore morphology on lithiation and energy storage capacity in Li-ion cells. Several variants of macroporous Si columnar electrodes were electrochemically cycled against the Li reference electrode. The changes in macro-pore size and Si wall thickness of the columnar architecture greatly affected the cyclic Li storage and discharge capacities. A strong correlation of the Li-storage capacity with the ratio of Si wall thickness to pore diameter is found to exist. Specifically, one columnar Si electrode with an optimum macroporous structure exhibited a very high reversible specific capacity of ~1250 mAh/g (total capacity 1.2 mAh/cm2) for over 200 cycles. Electron microscopy revealed that the high reversible Li-storage capacity is due to the macropores accommodating the change in volume of lithiation and providing nearly complete reconstruction of Si walls upon delithiation. The present observations can lead to practical, high-capacity, and damage-resistant Si electrodes for Li-ion batteries.

A comparison between electrochemical carbon dioxide conversion and reforestation is presented. By comparing thermodynamic and forestry data, recommendations for technology development can be made.

With the global average temperature steadily increasing due to anthropogenic emission of greenhouse gases into the atmosphere, there has been increasing interest worldwide in new technologies for carbon capture, utilization, and storage (CCUS). This coincides with the decrease in cost of deployment of intermittent renewable electricity sources, specifically solar energy, necessitating development of new methods for energy storage. Carbon dioxide conversion technologies driven by photovoltaics aim to address both these needs. To adequately contribute to greenhouse gas reduction, the carbon dioxide conversion technology deployed should have a substantially higher rate of carbon dioxide removal than planting an equivalent-sized forest. Using consistent methodologies, we analyze the effectiveness of model photovoltaic-driven carbon dioxide conversion technologies that produce liquid alcohols as compared to planting an equivalent forest. This analysis serves to establish an energy use boundary for carbon dioxide conversion technology, in order to be a viable alternative as a net carbon negative technology.

We continue to investigate the design, synthesis, and characterization of electrically and ionically active conjugated polythiophene copolymers for integrating a variety of biomedical devices with living tissue. This paper will describe some of our most recent results, including the development of several new monomers that can tailor the surface chemistry, adhesion, and biointegration of these materials with neural cells. Our efforts have focused on copolymers of 3,4 ethylenedioxythiophene (EDOT), functionalized variants of EDOT (including EDOT-acid and the trifunctional EPh), and dopamine (DOPA). The resulting PEDOT-based copolymers have electrical, optical, mechanical, and adhesive properties that can be precisely tailored by fine tuning the chemical composition and structure. Here we present results on EDOT-dopamine bifunctional monomers and their corresponding polymers. We discuss the design and synthesis of an EDOT-cholesterol that combines the thiophene with a biological moiety known to exhibit surface-active behaviour. We will also introduce EDOT-aldehyde and EDOT-maleimide monomers and show how they can be used as the starting point for a wide variety of functionalized monomers and polymers.

The binary metal oxides are increasingly used as supercapacitor electrode materials in energy storing devices. Particularly NiCo2O4 has shown promising electrocapacitive performance with high specific capacitance and energy density. The electrocapacitive performance of these oxides largely depends on their morphology and electrical properties governed by their energy band-gaps and defects. The morphological structure of NiCo2O4 can be altered via the synthesis route, while the energy band-gap could be altered by doping. Also, doping can enhance crystal stability and bring in grain refinement, which can further improve the much-needed surface area for high specific capacitance. Given the above, this study evaluates the electrochemical performance of Ca-doped Ni1-xCaxCo2O4 (0 ≤ x ≤ 0.8) compounds. This stipulates promising applications for electrodes in future supercapacitors.

The electrification of organic syntheses is a vividly growing research field and has attracted tremendous attention by the chemical industry. This review highlights aspects of electrosynthesis that are rarely addressed in other articles on the topic: the energy consumption and energy efficiency of technically relevant electro-organic syntheses.

Four examples on different scales are outlined.

Electro-organic synthesis has experienced a renaissance within the past years. This review addresses the energy efficiency or energy demand of electrochemically driven transformations as it is a key parameter taken into account by, for example, decision makers in industry. The influential factors are illustrated that determine the energy efficiency and discussed what it takes for an electrochemical process to be classified as “energy efficient.” Typical advantages of electrosynthetic approaches are summarized and characteristic aspects regarding the efficiency of electro-organic processes, such as electric energy consumption, are defined. Technically well-implemented examples are described to illustrate the possible benefits of electrochemical approaches. Further, promising research examples are highlighted and show that the conversion of fine chemicals is rather attractive than the electrochemical generation of synthetic fuels.

P-type NiO powders with an average crystallite size of 16 nm as shown by x-ray diffraction analysis were produced via biosynthesis using cactus plant extract. SEM showed that the NiO powders consisted of particles with sizes in the 20-35 nm range. A cyclic voltammetric study of the NiO nanopowders showed a quasi-reversible redox processes with the NiO powder showing potential for pseudo capacitance. Through these findings the use of natural Cactus extracts is hereby shown to be a cost-effective and environmentally friendly alternative for preparing Nickel oxide nanosized powders that can be of use in a variety of energy storage applications.

The activated carbon paper (ACP) has been designed as the active electrode material of supercapacitor to improve its capacitive performance. ACP is prepared by electrochemical nitrate ion–assisted exfoliation, sulfate ion–assisted exfoliation, and subsequent hydrothermal reduction processes. The as-prepared ACP shows obviously rougher surface along with the expanded layer distance. ACP exhibits higher specific capacitance of 380 mF/cm2 at 1 mA/cm2 than that of 21 mF/cm2 for carbon paper. ACP electrode shows the cycling capacitance retention of 98% after 5000 cycles at 10 mA/cm2. The symmetric ACP supercapacitor is constructed using ACP electrode and H2SO4 involved polyvinyl alcohol gel electrolyte. ACP supercapacitor presents the specific capacitance of 97 mF/cm2, the energy density of 0.343 mW h/cm3, and the output voltage of 1.6 V at 1 mA/cm2. ACP with high capacitance performance presents the promising supercapacitor application for the electrochemical energy storage.

Obtention of titanium (Ti)- and titanium dioxide (TiO2)–based nanocomposites is of great interest for biological nanomaterial applications, including for dental implants. Their mechanical properties can be improved by use of hydroxyapatite (HA) and chitosan through their biological anchorage with osseointegration and antibacterial activity. Electrochemical methods were chosen to obtain these composites in a quick and controllable way. In this work, electrochemical synthesis in one (alternated potential) or two steps (alternated or constant potential) was successfully applied. The single step (SS) obtained TiO2 + HA sample had different optical properties, as shown using ultraviolet–visible spectrometry, and the HA phase formation was proved using Raman spectroscopy. Thereby, SS_TiO2 + HA increased the corrosion resistance of titanium in artificial saliva medium, as shown by linear polarization and electrochemical impedance spectroscopy results. When using chitosan, the samples showed two corrosion interfaces, indicating its dissolution in human medium. These results indicate that the samples are excellent materials for dental implants.

In this work, the anodization of grade 2 titanium was performed using a HCl-based electrolyte in order to obtain Titania nanostructures. Different glycerol concentrations were added to the HCl electrolyte to study the effect it has on the shape and density of the nanostructures, additionally, anodization time and voltage was also varied. The anodized samples were observed by SEM microscopy and studied by Raman spectroscopy and X-ray diffraction. Raman spectroscopy and XRD showed the formation of the anatase phase of the TiO2. By SEM it was possible to observe several changes in the shape of the structures, by adding glycerol ball-like structures were visible, anodization time did not change the shape of the nanostructures. However, the voltage variation showed a clear control on the shape of the structures, forming nanotubes at higher voltages. It was concluded that a better control of the shape and density of the nanostructures is achieved by adding glycerol, however, in order to overcome the resistance that the electrolyte brings, higher voltages are required.

Electrochemical catalyst design and optimization primarily relies on understanding and facilitating interfacial charge transfer. Recently, piezotronics have emerged as a promising method for tuning the interfacial energetics. The unique band-engineering capability using piezoelectric or ferroelectric polarization could lead to performance gains for electrochemical catalysis beyond what can be achieved by chemical or structural optimization. This article addresses the fundamentals of surface polarization and corresponding band modulation at solid–liquid interfaces. The most recent advances in piezotronic modulations are discussed from multiple perspectives of catalysis, including photocatalytic, photoelectrochemical, and electrochemical processes, particularly for energy-related applications. The concept of piezocatalysis, a direct conversion of mechanical energy to chemical energy, is introduced with an example of mechanically driven water splitting. While still in the early stages, piezotronics is envisioned to become a powerful tool for revolutionizing electrochemical catalysis.

Solid-state batteries are considered the holy grail of next-generation battery technology, meeting the ever-increasing demand for energy storage that is affordable and safe, with high energy density and long cycle life. Materials and interfaces play a critical role for their eventual success and mass commercialization. This issue of MRS Bulletin focuses on the current state of the art of solid-state electrolytes and device architectures and provides a perspective into the various materials and interfacial challenges that limit its performance and stability.

This work presents a study about synthesis of polypyrrole films electrochemically doped with iodine by luminescent discharge plasma in aqueous sodium sulfate solution, and its structural, morphological and electrical characterization. The synthesis is carried out at atmospheric pressure with square pulse from -1.06 to 1.16 V for 120 minutes. Doping times of the films are 10, 30 and 50 minutes. The films have thicknesses of 6, 12.7, 20.32 and 25.4 μm, and linear growth trend according to the time exposure of their synthesis. The main chemical groups exhibited in the films are C-H, N-H and CH2I, which are characteristics of film doped with Iodine. The electrical conductivity calculated of polypyrrole films is in the range 10-5-10-3 S/cm, and its activation energy is between 0.052 and 1.77 eV.

The procedure proposed is the express method for the study of anion distribution profiles in the anodic aluminum oxide film. The method consists in measuring the variation of the steady-state electrode potential during the oxide etching. It allows the influence of the initial aluminum composition, the electrolyte composition, anodization regimes, etc. on the characteristics of dense anodic alumina films to be studied. The method developed can be used to study a chemical evolution in anodic alumina formed to correlate with modelling and simulations across materials science disciplines.

Hydroxyapatite (HA)/nanotubular titanium dioxide (TiO2) composite coatings loaded with antibiotics were developed to combine biocompatibility and antibacterial property. TiO2 nanotubes were first fabricated on Ti plates using anodization techniques. Then HA nanocrystals were synthesized on the TiO2 nanotubes by electrochemical deposition, followed by loading of a model drug compound, streptomycin. The streptomycin release profile of the composite coating was investigated. Bacterial tests demonstrate that the streptomycin-loaded composite coatings were highly effective in inhibiting bacterial growth. Simulated body fluid (SBF) experiments indicated that the composite coatings possessed good osseointegration capability.

Ti-based quasicrystals are well known to store a high capacity of hydrogen exceeding the density of liquid hydrogen. This fact is due to that TiZrNi contain a large number of tetrahedral sites formed with Ti and Zr atoms that are chemical affinity with hydrogen. TiZrNi quasicrystal absorbs hydrogen up to host metal ratio (H/M) value near to 2.0. The disadvantage is due to the low equilibrium pressure. To solve this problem, we substituted Ti with a small amount of vanadium (V), with the nominal composition Ti45−x VxZr38Ni17 (x = 5, 10, 15) and synthesized by mechanical alloying. The subsequent annealing in vacuum conditions converted the amorphous into an icosahedral quasicrystal (I-phase) with face-centered cubic (FCC) Ti2Ni-type crystal. As the results, we investigated the discharge capacity for both amorphous and quasicrystal electrodes using three electrodes system (working, reference and counter electrodes) at room temperature. The highest discharge capacities obtained were 81.45 mAh/g recorded for amorphous electrode and 318.4 mAh/g for quasicrystal whose compositions is Ti35V10Zr38Ni17 at discharge current density of 15 mA/g. X-ray diffraction measurement was performed to provide the structural information on materials before and after hydrogenation. Microstructures of the materials were studied using an electron scanning microscope and the chemical compositions were confirmed using an EDX-analysis.

This work presents a study of the chemical structure, morphology, electromagnetic absorption and electric conductivity of thin films. The electrochemical synthesis of polypyrrole/surfactant (PPy/SDS) films doped with iodine is carried out by glow discharge plasma in aqueous solution, at different reaction times. The morphology shows agglomerations of particles dispersed in the surface. Infrared spectroscopic analysis shows absorption on the wavenumbers 2915,2362 and 2082 cm-1 corresponding to chemical groups C-H, C=O and R/N=C=S, respectively. The electromagnetic absorption had higher response sensitivity between 340 to 800 nm in the visible region, and the electric conductivity of samples oscillated between 5.0x10-6 and 2.0x10-5 S/cm. The thickness films significantly increased when doping with iodine, reaching values up to 50 μm.

Three-dimensional nitrogen-doped graphene frameworks (3DNGFs) hold great promise in the application of supercapacitors for the advantages of superior conductivity, well-connected porous structure, and additional N-containing active sites for charge storage. Nevertheless, the developed techniques for preparing 3DNGFs always suffer from the drawbacks of high cost or complex processes for large-scale application. Herein, a new and cost-effective method has been developed to massively prepare monolithic 3DNGFs by a simple and scalable electrochemical oxidation process. Benefiting from the enhanced electrical conductivity, the increase in the pore volume for fast diffusion increased the electrode–electrolyte contact area and additional active sites resulting from the incorporation of nitrogen species, the 3DNGFs showed a high specific capacitance of 2250.3 mF/cm2 at 4 mA/cm2, with good rate capability. Furthermore, this 3DNGFs electrode also owns an excellent long-term cycling stability that can retain more than 97.5% of its original capacitance after 10,000 cycles.

Diketopyrrolopyrrole (DPP) is a critically important building block that has gained importance in the organic electronics community because of its wide applicability in various devices. In this work, the thiophene flanked DPP moiety attached to alkyl chains of various lengths (this includes straight octyl and branched ethyl hexyl units) has been used as the monomer for electropolymerization. This paper focuses on the study of optical, thermal, solid state ordering and electrochemical properties of these electron deficient monomers using various characterization techniques such as UV–Vis spectrometry (UV), photo-luminescence spectroscopy (PL), differential scanning calorimetry (DSC), thermal gravimetric analysis (TGA), X-ray diffraction (XRD), cyclic voltammetry (CV), as well as ab initio modeling. These monomers exhibit broad absorption spectra from the ultraviolet (280–400 nm) to visible (400–600 nm) regions and emission spectra between 560 and 610 nm. The band gaps of these monomers were calculated to be in the range of 2.00–2.20 eV. These monomers were electropolymerized by scanning the potential between −0.5 and 2.0 V versus ferrocene for up to 50 cycles on a glassy carbon electrode.

Composite copper oxide–copper bromide films were electrodeposited on gas diffusion layer (GDL) supports under controlled potential from aqueous copper salt solutions in the presence of a complexing/surfactant agent such as lactate. The solution pH was adjusted to target simultaneous deposition of cubic nanostructures composed of copper, oxygen, and bromine elements. The film composition and morphology were carefully tuned for enhanced electrochemical conversion of CO2 to hydrocarbons. Hydrocarbon products, predominantly ethylene and minor amounts of methane, ethane, and propylene were observed along with inevitable H2 co-generation. Importantly, CO gas was not detected during CO2 electrolyses. Low temperatures (3–5 °C) enhanced the conversion of CO intermediate to C2H4. The durability and electroactivity of these composite films were maintained for extended periods (up to 10 h) of CO2 electrolysis by periodic in situ application of anodic pulses to regenerate the cathode surface.

Electropolymerization is a promising approach to produce thin films of active organic conjugated materials on a desired conducting substrate. In this work, an electropolymerization study has been carried out on two diketopyrrolopyrrole (DPP)-based monomers 2,5-bis(2-butyloctyl)-3,6-di(furan-2-yl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione (BO-DPPF) and 2,5-bis(2-butyloctyl)-3,6-di(thiophen-2-yl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione (BO-DPPT). These monomers consist of thiophene and furan heterocyclic moieties attached to a DPP core with a common solubilizing alkyl chain (butyl-octyl). The properties of these monomers were analyzed via differential scanning calorimetry, thermogravimetric analysis, UV–Vis spectrometry (UV) and photoluminescence. Cyclic voltammetry (CV) studies indicate the presence of irreversible oxidation and reduction reactions. The electropolymerization of BO-DPPF and BO-DPPT electron-deficient monomers to form polymer films on a glassy carbon electrode is achieved by applying a potential between −2 V and 2 V versus ferrocene for up to 50 cycles. The properties of the polymers were investigated using the cyclic voltammetry (CV) technique.