This paper presents a methodology for the optimal allocation and economic analysis of energy storage system (ESS) in microgrids (MGs) on the basis of net present value (NPV). As the performance of an MG strongly depends on the allocation and arrangement of its ESS, optimal allocation methods and economic operation strategies of the ESS devices are required for the MG. To optimize the operation strategies and capacities of ESS in MGs, the financial benefit and dynamic models of ESS are discussed. And then, a matrix real-coded genetic algorithm is applied to find maximal NPV, in which each GA chromosome consists of a 2-D real number matrix representing the generation schedule of ESS and distributed generation sources. This paper is to suggest, among those available ESS, the optimal sizes and types of them and their optimal arrangement, such that the total NPV achieved during the system operational lifetime period is maximized. Finally, some computational simulation results are presented to verify the effectiveness of the proposed method.
The formation of MoO(3) and its spontaneous spread over an Au (111) surface have been studied by X-ray photoelectron spectroscopy (XPS) and scanning tunneling microscopy (STM). Metallic Mo clusters grown by Mo(CO)(6) chemical vapor deposition (CVD) have a constant size independent of the Mo coverage. Molecular oxygen does not react with low coverage of Mo, probably due to the encapsulation of the Mo clusters by Au. At higher coverage, O(2) reacts with Mo, partially transforming the metallic Mo to Mo(4+). NO(2) can oxidize Mo efficiently to Mo(6+) and Mo(5+) species at all coverages investigated. XPS experiments show that the integrated intensity of the Mo 3d peaks increases by a factor of 2 upon the oxidation, suggesting the spread of the MoO(3) over the surface. The STM study confirms this suggestion and provides the mechanistic details of the spreading. Mo oxide forms ramified two-dimensional islands covering a substantially larger fraction of the Au surface than the metallic Mo. We propose that the morphology change starts with the diffusion of oxide clusters (ramified-cluster-diffusion mechanism), followed by their breakdown to highly disordered two-dimensional islands of molecular MoO(3).
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