Vertical graphene nanowalls supported hybrid W2C/WOx composite material as an efficient non-noble metal electrocatalyst for hydrogen evolution.

Research for the development of noble metal-free electrodes for hydrogen evolution has blossomed in recent years. Transition metal carbides compounds, such as W2C, have been considered as a promising alternative to replace Pt-family metals as electrocatalysts towards hydrogen evolution reaction (HER). Moreover, hybridization of TMCs with graphene nanostructures has emerged as a reliable strategy for the preparation of compounds with high surface to volume ratio and abundant active sites. The present study focuses in the preparation of tungsten carbide/oxide compounds deposited in a three-dimensional vertical graphene nanowalls (VGNW) substrate via chemical vapor deposition, magnetron sputtering and thermal annealing processes. Structural and chemical characterization reveals the partial carburization and oxidation of the W film sputtered on the VGNWs, due to C and O migration from VGNWs towards W during the high temperature annealing process. Electrochemical characterization shows the enhanced performance of the nanostructured hybrid W2C/WOx on VGNW compound towards HER, when compared with planar W2C/WOx films. The W2C/WOx nanoparticles on VGNWs require an overpotential of -252 mV for the generation of 10 mA cm-2. Chronoamperometry tests in high overpotentials reveal the compounds stability while sustaining high currents, in the order of hundreds of mA. Post-chronoamperometry test XPS characterization unveils the formation of a W hydroxide layer which favours hydrogen evolution in acidic electrolytes. We aspire that the presented insights can be valuable for those working on the preparation of hybrid electrodes for electrochemical processes.

Processing and Functionalization of Vertical Graphene Nanowalls by Laser Irradiation.

The processing of vertical graphene nanowalls (VGNWs) via laser irradiation is proposed as a means to modulate their physicochemical properties. The effects of the number of applied pulses and fluence of each pulse are examined. Raman spectroscopy studies the effect of irradiation on the chemical structure of the VGNWs. Results show a decrease in density of defects and number of layers, which points toward a mechanism including evaporation of amorphous or loosely bonded C from defective points and recrystallization of graphene. Moreover, the effect of laser irradiation parameters on the morphology of Mo thin films deposited on VGNWs is investigated. The received thermal dosage results in the formation of particles. In this case, the number of pulses and pulse fluence are found to affect the size and distribution of these particles. The study provides a novel approach for the functionalization of VGNWs via laser irradiation, which can be extended to other graphene-based nanostructures.

Advancements in Plasma-Enhanced Chemical Vapor Deposition for Producing Vertical Graphene Nanowalls.

In recent years, vertical graphene nanowalls (VGNWs) have gained significant attention due to their exceptional properties, including their high specific surface area, excellent electrical conductivity, scalability, and compatibility with transition metal compounds. These attributes position VGNWs as a compelling choice for various applications, such as energy storage, catalysis, and sensing, driving interest in their integration into next-generation commercial graphene-based devices. Among the diverse graphene synthesis methods, plasma-enhanced chemical vapor deposition (PECVD) stands out for its ability to create large-scale graphene films and VGNWs on diverse substrates. However, despite progress in optimizing the growth conditions to achieve micrometer-sized graphene nanowalls, a comprehensive understanding of the underlying physicochemical mechanisms that govern nanostructure formation remains elusive. Specifically, a deeper exploration of nanometric-level phenomena like nucleation, carbon precursor adsorption, and adatom surface diffusion is crucial for gaining precise control over the growth process. Hydrogen's dual role as a co-catalyst and etchant in VGNW growth requires further investigation. This review aims to fill the knowledge gaps by investigating VGNW nucleation and growth using PECVD, with a focus on the impact of the temperature on the growth ratio and nucleation density across a broad temperature range. By providing insights into the PECVD process, this review aims to optimize the growth conditions for tailoring VGNW properties, facilitating applications in the fields of energy storage, catalysis, and sensing.

Hybrid Nanostructured Compounds of Mo2C on Vertical Graphene Nanoflakes for a Highly Efficient Hydrogen Evolution Reaction.

Organizing a post-fossil fuel economy requires the development of sustainable energy carriers. Hydrogen is expected to play a significant role as an alternative fuel as it is among the most efficient energy carriers. Therefore, nowadays, the demand for hydrogen production is increasing. Green hydrogen produced by water splitting produces zero carbon emissions but requires the use of expensive catalysts. Therefore, the demand for efficient and economical catalysts is constantly growing. Transition-metal carbides, and especially Mo2C, have attracted great attention from the scientific community since they are abundantly available and hold great promises for efficient performance toward the hydrogen evolution reaction (HER). This study presents a bottom-up approach for depositing Mo carbide nanostructures on vertical graphene nanowall templates via chemical vapor deposition, magnetron sputtering, and thermal annealing processes. Electrochemical results highlight the importance of adequate loading of graphene templates with the optimum amount of Mo carbides, controlled by both deposition and annealing time, to enrich the available active sites. The resulting compounds exhibit exceptional activities toward the HER in acidic media, requiring overpotentials of 82 mV at -10 mA/cm2 and demonstrating a Tafel slope of 56 mV/dec. The high double-layer capacitance and low charge transfer resistance of these Mo2C on GNW hybrid compounds are the main causes of the enhanced HER activity. This study is expected to pave the way for the design of hybrid nanostructures based on nanocatalyst deposition on three-dimensional graphene templates.

Homogeneous Fe2O3 coatings on carbon nanotube structures for supercapacitors.

The combination of carbon nanotubes with transition metal oxides can exhibit complementary charge storage properties for use as electrode materials for next generation energy storage devices. One of the biggest challenges so far is to synthesize homogeneous oxide coatings on carbon nanotube structures preserving their integrity. Here we present the formation of conformal coatings of Fe2O3 on vertically aligned carbon nanotubes obtained by atomic layer deposition. We investigate the effect of pristine, nitrogen plasma and water plasma treated carbon nanotube surfaces on the ALD-growth of Fe2O3 using ferrocene and ozone precursors. The surface morphology, coating thickness, microstructure and surface chemistry of iron oxide-carbon nanotube composites and their ultimate influence on the electrochemical behavior of the composites are evaluated. The most effective surface functionalization is that achieved by H2O plasma treatment, whereas untreated carbon nanotubes, despite the lack of active sites in the starting pristine surface, can be coated with an inhomogeneous Fe2O3 film.

Super-Capacitive Performance of Manganese Dioxide/Graphene Nano-Walls Electrodes Deposited on Stainless Steel Current Collectors.

Graphene nano-walls (GNWs) are promising materials that can be used as an electrode in electrochemical devices. We have grown GNWs by inductively-coupled plasma-enhanced chemical vapor deposition on stainless steel (AISI304) substrate. In order to enhance the super-capacitive properties of the electrodes, we have deposited a thin layer of MnO2 by electrodeposition method. We studied the effect of annealing temperature on the electrochemical properties of the samples between 70 °C and 600 °C. Best performance for supercapacitor applications was obtained after annealing at 70 °C with a specific capacitance of 104 F g-1 at 150 mV s-1 and a cycling stability of more than 14k cycles with excellent coulombic efficiency and 73% capacitance retention. Electrochemical impedance spectroscopy, cyclic voltammetry, and galvanostatic charge/discharge measurements reveal fast proton diffusion (1.3 × 10-13 cm²·s-1) and surface redox reaction after annealing at 70 °C.

New Three-Dimensional Porous Electrode Concept: Vertically-Aligned Carbon Nanotubes Directly Grown on Embroidered Copper Structures.

New three-dimensional (3D) porous electrode concepts are required to overcome limitations in Li-ion batteries in terms of morphology (e.g., shapes, dimensions), mechanical stability (e.g., flexibility, high electroactive mass loadings), and electrochemical performance (e.g., low volumetric energy densities and rate capabilities). Here a new electrode concept is introduced based on the direct growth of vertically-aligned carbon nanotubes (VA-CNTs) on embroidered Cu current collectors. The direct growth of VA-CNTs was achieved by plasma-enhanced chemical vapor deposition (PECVD), and there was no application of any post-treatment or cleaning procedure. The electrochemical behavior of the as-grown VA-CNTs was analyzed by charge/discharge cycles at different specific currents and with electrochemical impedance spectroscopy (EIS) measurements. The results were compared with values found in the literature. The as-grown VA-CNTs exhibit higher specific capacities than graphite and pristine VA-CNTs found in the literature. This together with the possibilities that the Cu embroidered structures offer in terms of specific surface area, total surface area, and designs provide a breakthrough in new 3D electrode concepts.

Evaluation of Graphene/WO3 and Graphene/CeO x Structures as Electrodes for Supercapacitor Applications.

The combination of graphene with transition metal oxides can result in very promising hybrid materials for use in energy storage applications thanks to its intriguing properties, i.e., highly tunable surface area, outstanding electrical conductivity, good chemical stability, and excellent mechanical behavior. In the present work, we evaluate the performance of graphene/metal oxide (WO3 and CeO x ) layered structures as potential electrodes in supercapacitor applications. Graphene layers were grown by chemical vapor deposition (CVD) on copper substrates. Single and layer-by-layer graphene stacks were fabricated combining graphene transfer techniques and metal oxides grown by magnetron sputtering. The electrochemical properties of the samples were analyzed and the results suggest an improvement in the performance of the device with the increase in the number of graphene layers. Furthermore, deposition of transition metal oxides within the stack of graphene layers further improves the areal capacitance of the device up to 4.55 mF/cm2, for the case of a three-layer stack. Such high values are interpreted as a result of the copper oxide grown between the copper substrate and the graphene layer. The electrodes present good stability for the first 850 cycles before degradation.

Water plasma functionalized CNTs/MnO2 composites for supercapacitors.

A water plasma treatment applied to vertically-aligned multiwall carbon nanotubes (CNTs) synthesized by plasma enhanced chemical vapour deposition gives rise to surface functionalization and purification of the CNTs, along with an improvement of their electrochemical properties. Additional increase of their charge storage capability is achieved by anodic deposition of manganese dioxide lining the surface of plasma-treated nanotubes. The morphology (nanoflower, layer, or needle-like structure) and oxidation state of manganese oxide depend on the voltage window applied during charge-discharge measurements and are found to be key points for improved efficiency of capacitor devices. MnO2/CNTs nanocomposites exhibit an increase in their specific capacitance from 678 Fg(-1), for untreated CNTs, up to 750 Fg(-1), for water plasma-treated CNTs.

Vertically aligned carbon nanotubes for microelectrode arrays applications.

In this work a methodology to fabricate carbon nanotube based electrodes using plasma enhanced chemical vapour deposition has been explored and defined. The final integrated microelectrode based devices should present specific properties that make them suitable for microelectrode arrays applications. The methodology studied has been focused on the preparation of highly regular and dense vertically aligned carbon nanotube (VACNT) mat compatible with the standard lithography used for microelectrode arrays technology.

Ultraslow Li diffusion in spinel-type structured Li4Ti5O12 - a comparison of results from solid state NMR and impedance spectroscopy.

The cubic spinel oxides Li(1+x)Ti(2-x)O(4) (0 < or =x< or = 1/3) are promising anode materials for lithium-ion rechargeable batteries. The end member of the Li-Ti-O series, Li(4)Ti(5)O(12), can accommodate Li ions up to the composition Li(7)Ti(5)O(12). Whereas a number of studies focus on the electrochemical behaviour of Li insertion into and Li diffusion in the Li intercalated material, only few investigations about low-temperature Li dynamics in the non-intercalated host material Li(4)Ti(5)O(12) have been reported so far. In the present paper, Li diffusion in pure-phase microcrystalline Li(4)Ti(5)O(12) with an average particle size in the microm range was probed by (7)Li solid state NMR spectroscopy using spin-alignment echo (SAE) and spin-lattice relaxation (SLR) measurements. Between T = 295 K and 400 K extremely slow Li jump rates tau(-1) ranging from 1 s(-1) to about 2200 s(-1) were directly measured by recording the decay of spin-alignment echoes as a function of mixing time and constant evolution time. The results point out the slow Li diffusion in non-intercalated Li(4)Ti(5)O(12) x tau(-1) (1/T) follows Arrhenius behaviour with an activation energy E(ASAE) of about 0.86 eV. Interestingly, E(ASAE) is comparable to activation energies deduced from conductivity measurements (0.94(1) eV) and from SLR measurements in the rotating frame (0.74(2) eV) rather than from those performed in the laboratory frame, E(A)(low-T) = 0.26(1) eV at low T.

Preparation by high-energy milling, characterization, and catalytic properties of nanocrystalline TiO2.

Titanium dioxide (TiO2) is widely used for applications in heterogeneous photocatalysis. We prepared nanocrystalline powders of the anatase as well as the rutile modification by high-energy ball milling of the coarse grained source materials for up to 4 h. The resulting average grain size was about 20 nm. The morphology of the powders was investigated with transmission electron microscopy, X-ray powder diffraction, and BET surface area determination. Measurements of the catalytic activity reveal a maximum as a function of the milling time at about 40 min. This maximum could be explained by a superposition of two counteracting effects. The first one is the increase of the specific surface area resulting in an increase of the catalytic activity, and the second one is a change of the electronic structure at the surface of the TiO2 particles corresponding to a reduction of the surface. The latter one was confirmed by light absorption experiments, X-ray photoelectron spectroscopy, and electron paramagnetic resonance spectroscopy.