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https://www.selleckchem.com/products/ssr128129e.html Liquid water confined within nanometer-sized channels exhibits a surprisingly low dielectric constant along the direction orthogonal to the channel walls. This is typically assumed to result from a pronounced heterogeneity across the sample the dielectric constant would be bulk-like everywhere except at the interface, where it would be dramatically reduced by strong restrictions on interfacial molecules. Here we study the dielectric properties of water confined within graphene slit channels via classical molecular dynamics simulations. We show that the permittivity reduction is not due to any important alignment of interfacial water molecules, but instead to the long-ranged anisotropic dipole correlations combined with an excluded-volume effect of the low-dielectric confining material. The bulk permittivity is gradually recovered only over several nanometers due to the impact of long-range electrostatics, rather than structural features. This has important consequences for the control of, e.g., ion transport and chemical reactivity in nanoscopic channels and droplets.Holes in nanowires have drawn significant attention in recent years because of the strong spin-orbit interaction, which plays an important role in constructing Majorana zero modes and manipulating spin-orbit qubits. Here, from the strongly anisotropic leakage current in the spin blockade regime for a double dot, we extract the full g-tensor and find that the spin-orbit field is in plane with an azimuthal angle of 59° to the axis of the nanowire. The direction of the spin-orbit field indicates a strong spin-orbit interaction along the nanowire, which may have originated from the interface inversion asymmetry in Ge hut wires. We also demonstrate two different spin relaxation mechanisms for the holes in the Ge hut wire double dot spin-flip co-tunneling to the leads, and spin-orbit interaction within the double dot. These results help establish feasibilit

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