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Functionalization of nanocarbon materials with heteroatoms is of paramount interest as doping of carbon with electron withdrawing groups results in change of electrochemical properties of the potential catalyst. Adding fluorine, as the most electronegative element into the doping process next to boron is expected to have significant effect on the design of novel nanocarbon‐based electrocatalysts. In this paper boron and fluorine co‐doped reduced graphene oxide/few‐walled carbon nanotube (BF‐rGO/FWCNT) catalysts are synthesized via simple and low‐cost direct pyrolysis method using boron trifluoride diethyl etherate (BTDE). Composition analysis confirmed that boron and fluorine have been grafted onto the carbon support. Rotating disk electrode (RDE) measurements revealed that BF‐rGO/FWCNT has remarkable electrocatalytic activity toward the oxygen reduction reaction (ORR) both in alkaline and acid media. The onset potential of the best BF‐rGO/FWCNT catalyst was 50 mV more positive in alkaline and 600 mV more positive in acidic media compared with un‐doped rGO/FWCNT. The half‐wave potential was 100 mV more positive in alkaline media and 700 mV more positive in acidic media in comparison with un‐doped rGO/FWCNT. [ABSTRACT FROM AUTHOR]

Tin oxide (SnO2) is a versatile n-type semiconductor with a wide bandgap of 3.6 eV that varies as a function of its polymorph, i.e., rutile, cubic or orthorhombic. In this review, we survey the crystal and electronic structures, bandgap and defect states of SnO2. Subsequently, the significance of the defect states on the optical properties of SnO2 is overviewed. Furthermore, we examine the influence of growth methods on the morphology and phase stabilization of SnO2 for both thin-film deposition and nanoparticle synthesis. In general, thin-film growth techniques allow the stabilization of high-pressure SnO2 phases via substrate-induced strain or doping. On the other hand, sol–gel synthesis allows precipitating rutile-SnO2 nanostructures with high specific surfaces. These nanostructures display interesting electrochemical properties that are systematically examined in terms of their applicability to Li-ion battery anodes. Finally, the outlook provides the perspectives of SnO2 as a candidate material for Li-ion batteries, while addressing its sustainability. [ABSTRACT FROM AUTHOR]

Sunlight-driven photocatalytic degradation is an effective and eco-friendly technology for the removal of organic pollutants from contaminated water. Herein, we describe the one-step synthesis of Cu-Cu2O-Cu3N nanoparticle mixtures using a novel non-aqueous, sol-gel route and their application in the solar-driven photocatalytic degradation of methylene blue. The crystalline structure and morphology were investigated with XRD, SEM and TEM. The optical properties of the as-prepared photocatalysts were investigated with Raman, FTIR, UV-Vis and photoluminescence spectroscopies. The influence of the phase proportions of Cu, Cu2O and Cu3N in the nanoparticle mixtures on the photocatalytic activity was also investigated. Overall, the sample containing the highest quantity of Cu3N exhibits the highest photocatalytic degradation efficiency (95%). This enhancement is attributed to factors such as absorption range broadening, increased specific surface of the photocatalysts and the downward band bending in the p-type semiconductors, i.e., Cu3N and Cu2O. Two different catalytic dosages were studied, i.e., 5 mg and 10 mg. The higher catalytic dosage exhibited lower photocatalytic degradation efficiency owing to the increase in the turbidity of the solution. [ABSTRACT FROM AUTHOR]

This review addresses the most recent advances in the synthesis approaches, fundamental properties and photocatalytic activity of Cu3N nanostructures. Herein, the effect of synthesis conditions, such as solvent, temperature, time and precursor on the precipitation of Cu3N and the formation of secondary phases of Cu and Cu2O are surveyed, with emphasis on shape and size control. Furthermore, Cu3N nanostructures possess excellent optical properties, including a narrow bandgap in the range of 0.2 eV–2 eV for visible light absorption. In that regard, understanding the effect of the electronic structure on the bandgap and on the optical properties of Cu3N is therefore of interest. In fact, the density of states in the d-band of Cu has an influence on the band gap of Cu3N. Moreover, the potential of Cu3N nanomaterials for photocatalytic dye-degradation originates from the presence of active sites, i.e., Cu and N vacancies on the surface of the nanoparticles. Plasmonic nanoparticles tend to enhance the efficiency of photocatalytic dye degradation of Cu3N. Nevertheless, combining them with other potent photocatalysts, such as TiO2 and MoS2, augments the efficiency to 99%. Finally, the review concludes with perspectives and future research opportunities for Cu3N-based nanostructures. [ABSTRACT FROM AUTHOR]

Potentially, group-Ib elements (Cu, Ag, and Au) incorporated on Zn sites can be used for p-type doping of ZnO, and in the present paper, we use ion implantation to introduce Ag atoms in wurtzite ZnO single crystals. Monitoring the Li behavior, being a residual impurity in the crystals, as a tracer, we demonstrate that Zn interstitials assist the Ag diffusion and lead to Ag pile-up behind the implanted region after annealing above 800 °C. At even higher temperatures, a pronounced Ag loss from the sample surface occurs and concurrently the Ag atoms exhibit a trap-limited diffusion into the crystal bulk with an activation energy of ∼2.6 eV. The dominant traps are most likely Zn vacancies and substitutional Li atoms, yielding substitutional Ag atoms. In addition, formation of an anomalous multipeak Ag distribution in the implanted near-surface region after annealing can be attributed to local implantation-induced stoichiometry disturbances leading to trapping of the Ag atoms by O and Zn vacancies in the vicinity of the surface and in the end-of-range region, respectively. [ABSTRACT FROM AUTHOR]

Core‐shell Co@Co(OH)2 nanoparticles are characterised electrochemically with particular focus on the thin shell of cobalt (II) hydroxide which stabilises the metallic cobalt core against further oxidation in the presence of air. Voltammetric characterisation allows insights into the nature of the shell so both complementing and providing information unavailable using electron microscopy and X‐ray diffraction. Moreover, the electrode reactions, occurring at particle ensembles, of the further oxidation of surface Co(OH)2 to CoOOH under alkaline conditions are further evidenced at the single particle level using electrochemical particle‐electrode impacts (or 'nano‐impacts'). On this basis, the large extent of particle agglomeration/aggregation of Co@Co(OH)2 nanoparticles while suspended in the solutions is inferred. [ABSTRACT FROM AUTHOR]