Substitutional impurities in monolayer hexagonal boron nitride as single-photon emitters

Single-photon emitters in hexagonal boron nitride have attracted great attention over the last few years due to their excellent optoelectronical properties. Despite the vast range of results reported in the literature, studies on substitutional impurities belonging to the 13th and 15th groups have not been reported yet. Here, through theoretical modeling, we provide direct evidence that hexagonal boron nitride can be opportunely modified by introducing impurity atoms such as aluminum or phosphorus that may work as color centers for single-photon emission. By means of density functional theory, we focus on determining the structural stability, induced strain, and charge states of such defects and discuss their electronic properties. Nitrogen substitutions with heteroatoms of group 15 are shown to provide attractive features (e.g. deep defect levels and localized defect states) for single-photon emission. These results may open up new possibilities for employing innovative quantum emitters based on hexagonal boron nitride for emerging applications in nanophotonics and nanoscale sensing devices

Structure-property relations in amorphous carbon for photovoltaics

Carbon is emerging as a material with great potential for photovoltaics (PV). However, the amorphous form (a-C) has not been studied in detail as a PV material, even though it holds similarities with amorphous Silicon (a-Si) that is widely employed in efficient solar cells. In this work, we correlate the structure, bonding, stoichiometry, and hydrogen content of a-C with properties linked to PV performance such as the electronic structure and optical absorption. We employ first-principles molecular dynamics and density functional theory calculations to generate and analyze a set of a-C structures with a range of densities and hydrogen concentrations. We demonstrate that optical and electronic properties of interest in PV can be widely tuned by varying the density and hydrogen content. For example, sunlight absorption in a-C films can significantly exceed that of a same thickness of a-Si for a range of densities and H contents in a-C. Our results highlight promising features of a-C as the active layer material of thin-film solar cells

First-principles calculations of exciton radiative lifetimes in monolayer graphitic carbon nitride nanosheets: implications for photocatalysis

In this work, we report on the exciton radiative lifetimes of graphitic carbon nitride monolayers in the triazine-based (gC3N4-t) and heptazine-based (gC3N4-h) forms, as obtained by means of ground-state plus excited-state ab initio calculations. By analyzing the exciton fine structure, we highlight the presence of dark states and show that the photogenerated electron–hole (e-h) pairs in gC3N4-h are remarkably long-lived, with an effective radiative lifetime of 260 ns. This fosters the employment of gC3N4-h in photocatalysis and makes it attractive for the emerging field of exciton devices. Although very long intrinsic radiative lifetimes are an important prerequisite for several applications, pristine carbon nitride nanosheets show very low quantum photoconversion efficiency, mainly due to the lack of an efficient e-h separation mechanism. We then focus on a vertical heterostructure made of gC3N4-t and gC3N4-h layers, which shows a type-II band alignment and looks promising for achieving net charge separation

Stability and Bandgap Engineering of In1-{xGaxSe} Monolayer

Bandgap engineering of semiconductor materials represents a crucial step for their employment in optoelectronics and photonics. It offers the opportunity to tailor their electronic and optical properties, increasing the degree of freedom in designing new devices and widening the range of their possible applications. Here, we report the bandgap engineering of a layered InSe monolayer, a superior electronic and optical material, by substituting In atoms with Ga atoms. We developed a theoretical understanding of [Formula: see text] stability and electronic properties in its whole compositional range ([Formula: see text]) through first-principles density functional theory calculations, the cluster expansion method, and kinetic Monte Carlo simulations. Our findings highlight the possibility of modulating the InGaSe bandgap by ≈0.41 eV and reveal that this compound is an excellent candidate to be employed in many optoelectronic and photonic devices

Doped ordered mesoporous carbons as novel, selective electrocatalysts for the reduction of nitrobenzene to aniline

Ordered mesoporous carbons (OMCs) doped with nitrogen, phosphorus or boron were synthesised through a two-step nanocasting method and studied as electrocatalysts for the reduction of nitrobenzene to aniline in a half-cell setup. The nature of the dopant played a crucial role in the electrocatalytic performance of the doped OMCs, which was monitored by LSV with a rotating disk electrode setup. The incorporation of boron generated the electrocatalysts with the highest kinetic current density, whereas the incorporation of phosphorus led to the lowest overpotential. Doping with nitrogen led to intermediate behaviour in terms of onset potential and kinetic current density, but provided the highest selectivity towards aniline, thus resulting in the most promising electrocatalyst developed in this study. Density functional theory calculations allowed explaining the observed difference in the onset potentials between the various doped OMCs, and indicated that both graphiticN and pyrdinic N can generate active sites in the N-doped electrocatalyst. A chronoamperometric experiment over N-doped OMC performed at -0.75 V vs. Fc/Fc(+) in an acidic environment, resulted in a conversion of 61% with an overall selectivity of 87% to aniline. These are the highest activity and selectivity ever reported for an electrocatalyst for the reduction of nitrobenzene to aniline, making N-doped OMC a promising candidate for the electrochemical cogeneration of this industrially relevant product and electricity in a fuel cell setup

Facilely synthesized nitrogen-doped reduced graphene oxide functionalized and/or co-doped with metal ions as electrocatalyst for oxygen reduction reaction

Due to fossil fuels depletion and environmental pollution, clean and sustainable energy technologies, e.g. fuel cells and metal-air batteries, have attracted extensive attention. To push further the research on these electrochemical devices, low-cost, durable and efficient electrocatalysts alternative to platinum are required, to boost the oxygen reduction reaction (ORR). A microwave-assisted method has been optimized, to obtain effective heterogeneous catalyst for ORR, starting from graphene oxide (GO), urea and a transition metal (e.g. Mn and Cu) precursor. We have proved that our synthetic method originates porphyrin-like structures containing pyrrole rings within the reduced GO (rGO) basal plane which coordinate the Mn2+. In the case of copper, however, Cu2+ forms an ionic tetra coordinated structure anchored at the rGO surface via residual oxygen containing functional groups. In both cases, metal complex acts as an ORR highly efficient catalytic reaction center and their identification were strongly supported by several characterization techniques, such as X-ray Photoelectron Spectroscopy (XPS), X-ray absorption spectroscopies (XAS) and Transmission Electron Microscopy (TEM), together with Density Functional Theory (DFT) simulations. All synthesized materials exhibit outstanding catalytic properties toward ORR, as evidenced by electron transfer numbers larger than 3.8 and peroxide percentages lower than 7%, similar to Pt/C reference electrode

Understanding the role of imidazolium-based ionic liquids in the electrochemical CO2 reduction reaction

The development of efficient CO 2 capture and utilization technologies driven by renewable energy sources is mandatory to reduce the impact of climate change. Herein, seven imidazolium-based ionic liquids (ILs) with different anions and cations were tested as catholytes for the CO2 electrocatalytic reduction to CO over Ag electrode. Relevant activity and stability, but different selectivities for CO2 reduction or the side H 2 evolution were observed. Density functional theory results show that depending on the IL anions the CO 2 is captured or converted. Acetate anions (being strong Lewis bases) enhance CO2 capture and H2 evolution, while fluorinated anions (being weaker Lewis bases) favour the CO2 electroreduction. Differently from the hydrolytically unstable 1-butyl-3-methylimidazolium tetrafluoroborate, 1-Butyl-3-Methylimidazolium Triflate was the most promising IL, showing the highest Faradaic efficiency to CO (>95%), and up to 8 h of stable operation at high current rates (−20 mA & −60 mA), which opens the way for a prospective process scale-up

Facilely synthesized nitrogen-doped reduced graphene oxide functionalized with copper ions as electrocatalyst for oxygen reduction

Nitrogen-doped reduced graphene oxide is successfully synthesized and functionalized with hydroxylated copper ions via one-pot microwave-assisted route. The presence of cationic Cu coordinated to the graphene layer is fully elucidated through a set of experimental characterizations and theoretical calculations. Thanks to the presence of these hydroxyl-coordinated Cu2+ active sites, the proposed material shows good electrocatalytic performance for the oxygen reduction reaction, as evidenced by an electron transfer number of almost 4 and by high onset and half-wave potentials of 0.91 V and 0.78 V vs. the reversible hydrogen electrode, respectively. In addition, the N-doped Cu-functionalized graphene displays a superior current retention with respect to a commercial Pt/C catalyst during the stability test, implying its potential implementation in high-performance fuel cells and metal-air batteries