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[en] Highlights: • A single energy storage can always be split into two hybrid energy storages. • These hybrid storages have the same total energy and power as the single storage. • The potential for storage hybridisation depends on the shape of the power profile. • A higher potential allows a higher spread of the power/energy-ratios of the storages. • Automobile and pulsed power applications are well suited for storage hybridisation. - Abstract: Aim of a storage hybridisation is a beneficial usage or combination of different storage technologies with various characteristics to downsize the overall system, decrease the costs or to increase the lifetime, system efficiency or performance. In this paper, the point of interest is a different ratio of power to energy (specific power) of two storages to create a hybrid energy storage system (HESS) with a resulting specific power that better matches the requirements of the application. The approach enables a downsizing of the overall system compared to a single storage system and consequently decreases costs. The paper presents a theoretical and analytical benchmark calculation that determines the maximum achievable hybridisation, i.e. possible spread in specific power, while retaining the original total energy and power capacities of an equivalent single storage system. The theory is independent from technology, topology, control strategy, and application and provides a unified view on hybrid energy storage systems. It serves as a pre-dimensioning tool and first step within a larger design process. Furthermore, it presents a general approach to choose storage combinations and to characterize the potential of an application for hybridisation. In this context, a Hybridisation Diagram is proposed and integral Hybridisation Parameters are introduced.
[en] We report on strategies for characterizing hexagonal coincidence phases by analyzing the involved spatial moiré beating frequencies of the pattern. We derive general properties of the moiré regarding its symmetry and construct the spatial beating frequency as the difference between two reciprocal lattice vectors of the two coinciding lattices. Considering reciprocal lattice vectors , with lengths of up to n times the respective (1, 0) beams of the two lattices, readily increases the number of beating frequencies of the nth-order moiré pattern. We predict how many beating frequencies occur in nth-order moirés and show that for one hexagonal lattice rotating above another the involved beating frequencies follow circular trajectories in reciprocal-space. The radius and lateral displacement of such circles are defined by the order n and the ratio x of the two lattice constants. The question of whether the moiré pattern is commensurate or not is addressed by using our derived concept of commensurability plots. When searching potential commensurate phases we introduce a method, which we call cell augmentation, and which avoids the need to consider high-order beating frequencies as discussed using the reported moiré of graphene on SiC(0001). We also show how to apply our model for the characterization of hexagonal moiré phases, found for transition metal-supported graphene and related systems. We explicitly treat surface x-ray diffraction-, scanning tunneling microscopy- and low-energy electron diffraction data to extract the unit cell of commensurate phases or to find evidence for incommensurability. For each data type, analysis strategies are outlined and avoidable pitfalls are discussed. We also point out the close relation of spatial beating frequencies in a moiré and multiple scattering in electron diffraction data and show how this fact can be explicitly used to extract high-precision data. (paper)
[en] Understanding and controlling the growth kinetics of graphene is a prerequisite to synthesize this highly wanted material by chemical vapor deposition on Cu, e.g. for the construction of ultra-stable electron transparent membranes. It is reviewed that Cu foils contain a considerable amount of carbon in the bulk which significantly exceeds the expected amount of thermally equilibrated dissolved carbon in Cu and that this carbon must be removed before any high quality graphene may be grown. Starting with such conditioned Cu foils, systematic studies of the graphene growth kinetics in a reactive CH4/H2 atmosphere allow to extract the following meaningful data: prediction of the equilibrium constant of the graphene formation reaction within a precision of a factor of two, the confirmation that the graphene growth proceeds from a C(ad)-phase on Cu which is in thermal equilibrium with the reactive gas phase, its apparent activation barrier and finally the prediction of the achievable growth velocity of the growing graphene flakes during chemical vapor deposition. As a result of the performed study, growth parameters are identified for the synthesis of high quality monolayer graphene with single crystalline domains of 100-1000 μm in diameter within a reasonable growth time. (copyright 2017 by WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)