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Layered materials are of high importance because of their anisotropy and as a source of 2D materials. Whilst there is a plethora of multi-elemental 2D materials, the number mono-elemental 2D materials is rather limited. Herein, we demonstrate that aqueous shear exfoliation can be used to obtain As, Sb, and Bi exfoliated nanosheets. Morphological and chemical characterization of the exfoliated materials shows a decrease in thickness, sheet-to-nanosheet scale, and partial oxidation owing to a higher surface area. The electrochemical performance is tested in terms of inherent electrochemistry, electron transfer, and sensing applications as demonstrated with ascorbic acid. Potential energy-related applications are evaluated in the hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and oxygen reduction reaction (ORR), with shear-exfoliated Sb having the best electrochemical performance overall. These findings will have a profound impact on the preparation and application of 2D mono-elemental materials. [ABSTRACT FROM AUTHOR]

Graphane, the hydrogenated counterpart of graphene, was shown to exhibit properties such as tunable band gaps through varied degrees of hydrogenation, fluorescence, or ferromagnetism. Graphane nanostripe properties have also been theoretically predicted. Herein, we show that graphane nanostripes can be prepared by opening carbon nanotubes using Birch reduction in liquid ammonia utilizing potassium as a reducing agent and water as a proton donor. The prepared graphane nanostripes exhibit several exceptional properties when coupled with trace metal dopants. The interplay of metallic nanoparticles and defects lead to a spin polarization and induction of ferromagnetic moment, as well as to enhanced electrocatalytic properties in the hydrogen evolution reaction when compared to non-hydrogenated carbon nanotubes. [ABSTRACT FROM AUTHOR]

Partially hydrogenated graphene materials, synthesized by the chemical reduction/hydrogenation of two different graphene oxides using zinc powder in acidic environment or aluminum powder in alkaline environment, exhibit high electrocatalytic activities, as well as electrochemical sensing properties. The starting graphene oxides and the resultant hydrogenated graphenes were characterized in detail. Their electrocatalytic activity was examined in the oxygen reduction reaction, whereas sensing properties towards explosives were tested by using picric acid as a redox probe. Findings indicate that the high electrocatalytic performance originates not only from the hydrogenation of graphene, but also from unintentional contamination of graphene with manganese and other metals during synthesis. A careful evaluation of the obtained data and a detailed chemical analysis are necessary to identify the origin of this anomalous electrocatalytic activity. [ABSTRACT FROM AUTHOR]

Layered transition-metal dichalcogenides (TMDs) show promising electrocatalytic properties towards the hydrogen evolution reaction (HER). A series of graphene-amorphous TMD composites were prepared under hydrothermal conditions. Materials with varying contents of MoS x and WS x were synthesized from ammonium tetrathiomolybdate and ammonium tetrathiotungstate precursors in the presence of graphene oxide and diethylene glycol as a reducing agent. The synthesized materials exhibit not only a homogeneous distribution over the graphene surface, but also high electrocatalytic activity towards the HER. These findings are highly promising for industrial electrocatalysis, because the onset potential is close to the HER potential of industrially used platinum catalysts. [ABSTRACT FROM AUTHOR]

Interest in chemical functionalisation of graphenes today is largely driven by associated changes to its physical and material properties. Functionalisation with hydrogen was employed to obtain hydrogenated graphenes (also termed graphane if fully hydrogenated), which exhibited properties including fluorescence, magnetism and a tuneable band gap. Although the classical Birch reduction has been employed for hydrogenation of graphite oxide, variation exists between the choice of alkali metals and alcohols/water as quenching agents. A systematic study of electron (Li, Na, K, Cs) and proton sources ( tBuOH, iPrOH, MeOH, H2O) has been performed to identify optimal conditions. The proton source exerted a great influence on the resulting hydrogenation with water and out-performed alcohols, and the lowest carbon-to-hydrogen ratio was observed with sodium and water with composition of C1.4H1O0.3. Although ferromagnetism at room temperature correlates well with increasing hydrogen concentrations, small contributions from trace iron impurities cannot be completely eliminated. In contrast, hydrogenated graphenes exhibit a significant paramagnetic moment at low temperatures that has no correlation with impurities, and therefore, originates from the carbon system. This is in comparison to graphene, which is strongly diamagnetic, and concentrations of paramagnetic centres in hydrogenated graphenes are one order of magnitude larger than that in graphite. Nonetheless, hydrogenation over a particular level might also excessively disrupt intrinsic sp2 conjugation, resulting in unintended reduction of electrochemical properties. This was observed with heterogeneous electron-transfer rates and it was postulated that hydrogenated graphenes should generally have high defect densities, but only moderately high hydrogenation, should they be employed as electrode materials. [ABSTRACT FROM AUTHOR]

Group 5 elements (pnictogens) are attracting attention as mono‐elemental 2D materials with semiconducting properties. In their Communication on page 14417 ff., M. Pumera et al. present a green, scalable method for the aqueous shear‐force exfoliation of pnictogens using household kitchen blenders. The exfoliated nanosheets were evaluated in water‐splitting reactions, in which Sb showed the best performance. These results are significant for future electrochemical applications of pnictogens. [ABSTRACT FROM AUTHOR]