RESUMO
The hydrogen evolution reaction (HER) in alkaline electrolytes using transition metal dichalcogenides is a research area that is not tapped into. Alkaline HER ( 2 H 2 O + 2 e - â H 2 + O H - ${{2H}_{2}O+2{e\ }^{-}\to {H}_{2}+{OH}^{-}{\rm \ }}$ ) is harder to achieve relative to acidic HER ( H + + 2 e - â H 2 ${{H}^{+}+2{e\ }^{-}\to \ {H}_{2}}$ ), this is attributed to the additional water dissociation step that occurs in basic HER to generate H+ ions. In fact, for most catalysts, their HER activity decreases tremendously when the electrolyte is changed from acidic to basic conditions. Platinum dichalcogenides, PtX2 (X=S, Se, Te), are an interesting member of transition metal dichalcogenides (TMDs) as these show an immense hybridization of the Pt d orbitals and chalcogen p orbitals because of closely correlated orbital energies. The trend in electronic properties of these materials changes drastically as the chalcogen is changed, with PtS2 reported to exhibit semi-conductor properties, PtSe2 is semi-metallic or semi-conductive, depending on the number of layers, while PtTe2 is metallic. The effect of varying the chalcogen atom on the HER activity of Pt dichalcogenides will be studied. Pt dichalcogenides have previously been prepared by direct high-temperature chalcogen deposition of Pt substrate and evaluated as electrocatalysts for HER in H2SO4. The previously employed synthesis procedures for PtX2 limit these compounds' mass production and post-synthesis treatment. In this study, we demonstrated, for the first time the preparation of PtSe2 and PtTe2 by colloidal synthesis. Colloidal synthesis offers the possibility of large-scale synthesis of materials and affords the employment of the colloids at various concentrations in ink formulation. The electrochemical HER results acquired in 1â M KOH indicate that PtTe2 has a superior HER catalytic activity to PtSe2. A potential of 108â mV for PtTe2 and 161â mV for PtSe2 is required to produce a current density of -10â mA cm-2 from these catalysts. PtTe2 has a low Tafel slope of 79â mVdec-1, indicating faster HER kinetics on PtTe2. Nonetheless, the stability of these catalysts in an alkaline medium needs to be improved to render them excellent HER electrocatalysts.
RESUMO
Herein we report on the use of different metal precursors in the synthesis of MoSe2 nanomaterials in order to control their morphology. The use of Mo(CO)6 as the metal precursor resulted in the formation of wrinkled few-layer nanosheets, while the use of H2MoO4 as the metal precursor resulted in the formation of nanoflowers. To investigate the effect of the morphologies on their performance as catalysts in the hydrogen evolution reaction, electrochemical characterization was done using linear sweep voltammetry (LSV), cyclic voltammetry (CV), and electrical impedance spectroscopy (EIS). The MoSe2 nanoflowers were found to have superior electrochemical performance towards the hydrogen evolution reaction with a lower Tafel slope, on-set potential, and overpotential at 10 mA/cm2 compared to the wrinkled few-layer nanosheets. This was found to be due to the higher effective electrochemical surface area of the nanoflowers compared to the nanosheets which suggests a higher number of exposed edge sites in the nanoflowers.
RESUMO
We report the preparation of write-once-read-many times memory devices using composites of carbon nanotubes and poly(vinyl phenol) sandwiched between Al electrodes. Three types of nanotubes (undoped multiwalled carbon nanotubes, nitrogen-doped multiwalled carbon nanotubes and boron-doped multiwalled carbon nanotubes) are investigated for this application. The OFF to ON state switching threshold is only slightly dependent on nanotube type, but the ON/OFF current ratio depends on both nanotube type and concentration and varies up to 10(6), decreasing for nanotube concentrations larger than 0.50 wt% in the composite.