Nitrogen doped graphene with diamond-like bonds achieves unprecedented energy density at high power in a symmetric sustainable supercapacitor

Supercapacitors have attracted great interest because of their fast, reversible operation and sustainability. However, their energy densities remain lower than those of batteries. In the last decade, supercapacitors with an energy content of similar to 110 W h L-1 at a power of similar to 1 kW L-1 were developed by leveraging the open framework structure of graphene-related architectures. Here, we report that the reaction of fluorographene with azide anions enables the preparation of a material combining graphene-type sp(2) layers with tetrahedral carbon-carbon bonds and nitrogen (pyridinic and pyrrolic) superdoping (16%). Theoretical investigations showed that the C-C bonds develop between carbon-centered radicals, which emerge in the vicinity of the nitrogen dopants. This material, with diamond-like bonds and an ultra-high mass density of 2.8 g cm(-3), is an excellent host for the ions, delivering unprecedented energy densities of 200 W h L-1 at a power of 2.6 kW L-1 and 143 W h L-1 at 52 kW L-1. These findings open a route to materials whose properties may enable a transformative improvement in the performance of supercapacitor components.Web of Science15274874

Hematene: A sustainable 2D conductive platform for visible-light-driven photocatalytic ammonia decomposition

The emerging class of 2D non-van der Waals (n-vdW) materials, including 2D iron oxides, possesses unique properties and high applicability, making them attractive for various technological applications. However, the synthesis of these materials through a scalable and eco-friendly method remains a challenge, as most known chemical exfoliation processes require toxic organic solvents. In this study, we report a green synthesis of 2D hematene (α-Fe2O3) using an ultrasound-supported exfoliation method of earth-abundant iron oxide ore in a pure aqueous solution. The resulting hematene sheets, only a few nanometers thick, exhibit superior electrochemical performance in terms of charge transfer processes, making them ideal for photocatalytic applications. By doping a conductive hematene substrate with ruthenium, we demonstrate a synergistic effect for generating electrons and holes under visible light irradiation. Using this approach, we successfully decomposed ammonia into hydrogen and nitrogen, highlighting the potential of this novel class of environmentally-friendly photocatalysts for clean energy production. Overall, our water-assisted scalable synthesis of hematene offers a promising strategy for producing efficient and sustainable photocatalysts.Web of Science34art. no. 10188

Probing the effect of a glass network on the synthesis and luminescence properties of composite perovskite glasses [Invited]

All-inorganic cesium lead bromide perovskite nanocrystals (PNCs) are highly promising candidates for various optoelectronic and photonic devices. However, poor stability upon exposure to moisture and lead toxicity issues significantly limit their applications. A modern and promising strategy on resolving these issues is the encapsulation of highly luminescent (PNCs) within transparent inorganic oxide glasses. While the encapsulation procedure effect on the development and properties of the so-formed PV-Glasses has been explored in detail, there is lack of understanding the influence of the selected glass composition and network type on the outcome of the synthesis. Herein we report on the synthesis and photoluminescence properties of composite perovskite-glasses upon growing all-inorganic lead halide perovskites within three different types of inorganic oxide glasses. When a silver metaphosphate glass matrix is used it is revealed that the low glass transition temperature of the phosphate glass limits significantly the temperature range of the required post-melting annealing treatment, while the lead salt precursors react with the phosphate entities of the network destroying the stoichiometry of the PNCs. As a result the formation of PNCs is hindered. As a consequence, a double network former borophosphate glass was employed as a suitable host. While annealing treatments at higher temperature were facilitated in this case, it is found that the high silver content becomes an obstacle for the perovskite formation. In view of these findings, cesium lead bromide (CsPbBr3) and cesium lead iodide (CsPbI3) composite perovskite borate glasses were synthesized and found to be suitable hosts. Indeed, such composite glasses exhibit interesting photoluminescence properties that are compared with those of PNCs outside the glass matrix.Web of Science12283482

Unveiling the true band gap of fluorographene and its origins by teaming theory and experiment

Fluorographene is a fully fluorinated derivative of graphene. Unlike graphene, fluorographene is a wide gap semiconductor/insulator that holds great potential for applications requiring two-dimensional dielectric nano materials. Despite growing interest and a well-defined structure, the basic questions of fluorographene's band gap nature and value remain a conundrum. Here, we resolve this long-standing issue, demonstrating a direct optical band gap at 5.75 eV by means of diffuse reflectance spectroscopy. The nature of the band gap and the factors contributing to earlier controversies are explained by combining spectroscopic methods, ab initio calculations based on the finite momentum Bethe-Salpeter equation, and structural characterization via x-ray diffraction and Raman scattering. Ab initio calculations complement the experimental results by showing an excitonic peak at 5.65 eV of a Frenkel exciton bound to a single atom. The calculations also reveal that the absorption bands at lower energies arise from the presence of fluorine vacancies in the material, which explains earlier controversies in the literature about the band gap of fluorographene.Web of Science587art. no. 15283