The growth of a thin gold film on a conducting polymer surface from nucleation to formation of a continuous layer with a thickness of several nanometers is investigated in situ with grazing incidence small-angle X-ray scattering (GISAXS). Time resolution is achieved by performing the experiment in cycles of gold deposition on poly(N-vinylcarbazole) (PVK) and subsequently recording the GISAXS data. The 2D GISAXS patterns are simulated, and morphological parameters of the gold film on PVK such as the cluster size, shape, and correlation distance are extracted. For the quantitative description of the cluster size evolution, scaling laws are applied. The time evolution of the cluster morphology is explained with a growth model, suggesting a cluster growth proceeding in four steps, each dominated by a characteristic kinetic process: nucleation, lateral growth, coarsening, and vertical growth. A very limited amount of 6.5 wt % gold is observed to be incorporated inside a 1.2-nm-thick enrichment layer in the PVK film.
We have studied the thermal behavior of amphiphilic, symmetric triblock copolymers having short, deuterated polystyrene (PS) end blocks and a large poly(N-isopropylacrylamide) (PNIPAM) middle block exhibiting a lower critical solution temperature (LCST) in aqueous solution. A wide range of concentrations (0.1−300 mg/mL) is investigated using a number of analytical methods such as fluorescence correlation spectroscopy (FCS), turbidimetry, dynamic light scattering (DLS), small-angle neutron scattering (SANS), and neutron spin-echo spectroscopy (NSE). The critical micelle concentration is determined using FCS to be 1 μM or less. The collapse of the micelles at the LCST is investigated using turbidimetry and DLS and shows a weak dependence on the degree of polymerization of the PNIPAM block. SANS with contrast matching allows us to reveal the core−shell structure of the micelles as well as their correlation as a function of temperature. The segmental dynamics of the PNIPAM shell are studied as a function of temperature and are found to be faster in the collapsed state than in the swollen state. The mode detected has a linear dispersion in q
2 and is found to be faster in the collapsed state as compared to the swollen state. We attribute this result to the averaging over mobile and immobilized segments.
Voltage source converter (VSC)-based high-voltage direct current (HVDC) and multi-terminal (MT)/DC grid technologies are the new HVDC transmission technologies after ultra-high voltage alternative current (UHVAC) and UHVDC transmission technologies which have been widely used in China. The application of the new technologies has resulted in a rapid increase in the number of schemes in construction and planning worldwide. This has been stimulated by the greater level of functionality available from the VSC technology, which makes it suitable for a wide variety of applications. These include the integration of offshore wind farms, embedded links within AC networks and interconnectors, especially where the AC networks are relatively 'weak'. VSC technology has renewed interest in MT DC systems, which may ultimately lead to wide area DC grids. This study outlines the research and application on MT and DC grids in China with respect to VSC-HVDC key technologies and DC grid key technologies based on the presentation given in the International Workshop on Next Generation Power Equipment held on 23 September 2016 in Xian, China. The briefing details of the VSC-HVDC projects constructed and to be constructed in China are summarised in this study.
We investigate a new type of thin film material which allows for water storage without an increase in film thickness, whereas typically water storage in polymers and polymer films is accompanied with a strong swelling of the film, i.e., a strong increase in the film thickness. So these films will avoid problems related to strains which are caused by swelling. The basic key for the preparation of such thin films is the installation of a glassy network by the use of an asymmetric diblock copolymer polystyrene-block-poly(N-isopropylacrylamide) [P(S-b-NIPAM)] with a long PS and short PNIPAM block in combination with a solvent which is more equal in interaction with both the blocks as compared to water. With in situ neutron reflectivity the water storage and removal are probed. The total film thickness increases only by 2.5% by allowing for a total water storage of 17.4%. Thus the material can be used for coatings to reduce humidity in nano-applications, which might suffer from changes in the water content of the surrounding environment.
The influence of nanoparticles on the domain orientation in a particle co-operated self-assembly process in thin diblock copolymer films is investigated toward the preparation of ordered magnetic nanoparticle arrays. Thin films are prepared from a mixture of chemically masked iron oxide nanoparticles and a polystyrene-block-poly (methyl methacrylate) diblock copolymer. The resulting nanostructures are investigated with grazing incidence small-angle X-ray scattering, atomic force microscopy and scanning electron microscopy. Nanoparticles arrange themselves spontaneously inside the upright cylindrical domains due to the selective affinity to the poly (methyl methacrylate) minority phase during the microphase separation process and due to the balance of the surface free energies between the polymers and the nanoparticle coating after annealing. The incorporation of the nanoparticles inside the cylindrical domains increases the diameter of the cylindrical domains and the distance between two neighboring domains. A spatially ordered arrangement of magnetic nanoparticles is observed below a critical concentration of 0.2 vol % for the investigated molecular weight of 77 kg/mol.
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