Surface potential distribution, V(CPD), and evolution of atmospheric adsorbates on few and multiple layers (FLG and MLG) of graphene grown on SiC(0001) substrate have been investigated by electrostatic and Kelvin force microscopy techniques at T = 20-120 °C. The change of the surface potential distribution, ΔV(CPD), between FLG and MLG is shown to be temperature dependent. The enhanced ΔV(CPD) value at 120 °C is associated with desorption of adsorbates at high temperatures and the corresponding change of the carrier balance. The nature of the adsorbates and their evolution with temperature are considered to be related to the process of adsorption and desorption of the atmospheric water on MLG domains. We demonstrate that both the nano- and microscale wettability of the material are strongly dependent on the number of graphene layers.

MoS2 has been regarded as a promising addition for the preparation of epoxy-based coatings with high anticorrosion ability. However, its dispersion and compatibility remain significant challenges. In the present work, an organic thin layer was well coated on lamellar molybdenum disulfide (MoS2) via a simple modification of 3-aminopropyltriethoxysilane (APTES). The modification of hydrolyzing APTES on lamellar MoS2 effectively improved the dispersity of MoS2 in water-borne epoxy (WEP) and successfully enhanced the compatibility and crosslinking density of MoS2 with WEP. The influence of introducing MoS2-APTES into WEP coating on anticorrosion property for N80 steel was tested by electrochemical impedance spectroscopy (EIS), potentiodynamic polarization and salt spray test. The results exhibited that the |Z|0.01Hz value of MoS2-APTES/WEP still reached 3.647 × 107 Ω·cm2 even after the immersion time of 50 days in 3.5 wt.% NaCl solution, showing an extraordinary performance of corrosion resistance. The enhanced anticorrosion performance of composite coating could be resulted from the apparently increased dispersibility and compatibility of MoS2 in WEP.

Behavior of liquid crystal (LC) is a result of interaction between the geometrical shape restrictions of the adjacent surface and molecular forces among LCs or adjacent surface. For years, continuous efforts have been made to control LC orientation and anchoring with pretilt angle for modulating the electro‐optical characteristics. For now, diverse driving modes have been developed including twisted nematic, optically compensated bend, electrically controlled birefringence, and vertical alignment. However, it has the limitation that different fabrication process should be adopted in different driving mode such as materials of alignment layer and techniques for aligning the LCs. Herein, selective LC modes are achieved by controlling the LC pretilt angle using nanopatterned organic/inorganic hybrid thin films composed of polyimide (PI) and tin oxide (SnO). It is possible to control the surface wettability according to the composition ratio between PI and SnO, thereby adjusting the pretilt angle of the LCs. Fabrication of SnO combined with PI applied via embossing allows for the large‐scale replication for LC alignment and based on consumer demand, devices can be manufactured in various modes through simple configuration changes. Therefore, an inorganic compound combined with an organic one permits designing addressable LC driving modes.

No abstract

Sulfonated graphene had high solubility, broad pH stability and good antioxidative effect.