Abstract:Assembled metal-insulator nanoparticles with a core-shell geometry provide access to materials containing a large number (>10(6)) of tunneling barriers. We demonstrate the production of ceramic coated metal nanoparticles exhibiting an exceptional pressure-sensitive conductivity. We further show that graphene bi- and trilayers on 20 nm copper nanoparticles are insulating in such a core-shell geometry and show a similar pressure-dependent conductivity. This demonstrates that core-shell metal-insulator assemblies… Show more
“…Recently we have used a wet-chemical method [7,10] to demonstrate the above concepts of chemically modifying graphene by covalently attaching organic moieties in a patterncontrolled way (lithography) onto a graphene model surface (highly oriented pyrolytic graphite (HOPG)). [11] More specifically, attachment of p-substituted benzene rings perpendicular to the graphene plain allowed to influence directly the surface potential by correctly choosing the benzene substituents.…”
Graphene modifications with oxygen or hydrogen are well known in contrast to carbon attachment to the graphene lattice. The chemical modification of graphene sheets with aromatic diazonium ions (carbon attachment) is analyzed by confocal Raman spectroscopy. The temporal and spatial evolution of surface-adsorbed species allows accurate tracking of the chemical reaction and identification of intermediates. The controlled transformation of sp(2) to sp(3) carbon proceeds in two separate steps. The presented derivatization is faster for single-layer graphene and allows controlled transformation of adsorbed diazonium reagents into covalently bound surface derivatives with enhanced reactivity at the edge of single-layer graphene. On bilayer graphene the derivatization proceeds to an adsorbed intermediate, which reacts slower to a covalently attached species on the carbon surface.
“…Recently we have used a wet-chemical method [7,10] to demonstrate the above concepts of chemically modifying graphene by covalently attaching organic moieties in a patterncontrolled way (lithography) onto a graphene model surface (highly oriented pyrolytic graphite (HOPG)). [11] More specifically, attachment of p-substituted benzene rings perpendicular to the graphene plain allowed to influence directly the surface potential by correctly choosing the benzene substituents.…”
Graphene modifications with oxygen or hydrogen are well known in contrast to carbon attachment to the graphene lattice. The chemical modification of graphene sheets with aromatic diazonium ions (carbon attachment) is analyzed by confocal Raman spectroscopy. The temporal and spatial evolution of surface-adsorbed species allows accurate tracking of the chemical reaction and identification of intermediates. The controlled transformation of sp(2) to sp(3) carbon proceeds in two separate steps. The presented derivatization is faster for single-layer graphene and allows controlled transformation of adsorbed diazonium reagents into covalently bound surface derivatives with enhanced reactivity at the edge of single-layer graphene. On bilayer graphene the derivatization proceeds to an adsorbed intermediate, which reacts slower to a covalently attached species on the carbon surface.
“…7 The conductivity across the gaps was explained by an electron hopping 16 or an electron tunnelling process. 17,18 Due to the many parameters influencing the percolation concentration, to which the filler distribution, filler shape, filler-matrix interactions and of course the synthesis method could be attributed as the most important ones, 12 the resulting system cannot easily be described by a theoretical model. Currently, most ceramic/metal composites (cermets) are obtained by hot-pressing, 11 sintering 4 or sputtering.…”
“…The temperature dependence, given by the negative temperature coefficient was similar or even enhanced when compared to commercial piezoelectric materials (Athanassiou et al 2006). The tunneling based conduction mechanism (Figure 4) showed that core/shell conductive/insulator materials offered a new and simple production route of highly sensitive pressure and temperature sensors (Athanassiou et al 2008;Athanassiou et al 2007b). Luechinger et al (2007) implemented carbon/copper nanoparticles in water based dispersions.…”
Section: Reducing Flames: From Oxides To Metal Nanoparticlesmentioning
Aerosol nanotechnology has rapidly evolved in the past years. This fascinating technology has resulted in the development of functional nanomaterials providing novel solutions in industrial applications. The extensive research on the physical understanding of gas phase processes has strongly contributed to the present industrial use of single and mixed oxides and the design of industrial aerosol reactors. Recent advances have shown that chemical aerosol engineering can be established on the interface between classical aerosol science and chemical engineering. The emerging new methods give access to a much broader class of functional materials including salt and metal nanoparticles. The latter implies that aerosol production units can now be considered as chemical reactors. The incorporation of thermodynamic considerations and chemical kinetics in the modelling of gas phase processes will further boost the development of aerosol engineering and will provide deeper understanding of the fundamentals of particle formation mechanisms. This will ultimately enable access to new multicomponent materials with various structures or morphologies and the development of more sustainable, energy efficient gas phase processes.
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