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It is found that despite of the variation of V/III ratios, GaSb always forms a shell layer instead of an axial NW segment on GaAs NWs.
The formation of SiC as a shell layer can limit the radial growth of Si nanocolumns as reported in our previous works [28, 29].
Many literatures reported that the products with tubular structures could be obtained when calcinating the polymer fiber templates coated with a shell layer of inorganic precursors [28, 29].
The abundant hydroxyl groups on Zn(OH 2 afford strong coordination ability with cations and help to the coating of a shell layer.
Furthermore, a shell layer made of organic molecules coated to a shell-core structurally functionalized iron oxide NPs that will form the shella-core-shellbstructure, which occurs in many current reports and generally obtained bylayer-by-layer technology.
The introduction of pH-responsive PAH polymer as a shell layer can endow Ag NPs a controllable localized surface plasmon resonance by adjusting the shell thickness under pH stimuli, resulting in tunable SERS effects.
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PANI/C/TiN NWA has unique shell/shell/core architecture, including a core layer of TiN NWA with a diameter of 40 160 nm and a length of 1.5 μm, a middle shell layer of carbon with a thickness of about 6.0 nm and an external surface layer of PANI with a thickness of 20 50 nm.
A thermodynamic model is developed to investigate the extent to which a free polymer, B, can be solubilized into a thin shell layer of grafted A chains of core-shell impact modifier particles.
Here, we propose manganese cobalt sulfide (MnCo2S4) nanowire wrapping by a flocculent shell layer using a facile hydrothermal method with post-sulfurization treatment.
In general, the model predicts that solubilization is favoured when the B chains are small and the A chains are large and initially exist in a thin shell layer.
A nanoindentation study was performed on a novel type of core shell nanostructure (CSN) that consists of a nanostructured core layer covered by a nanoscale shell layer.
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