An access to an increase in the information storage capacity is to reduce memory units to a nano-scale. There fore, we used carboxylized phenyl-capped polyaniline tetramer (PCAT) as the functional component and silica...An access to an increase in the information storage capacity is to reduce memory units to a nano-scale. There fore, we used carboxylized phenyl-capped polyaniline tetramer (PCAT) as the functional component and silica as the carrier to prepare PCAT/silica composite nano-particles (= 60 nm) with a structure of core-shell. The functionalized particles were two-dimensionally arrayed on substrates such as silicon, glass and ITO glass at pH 3.SEM and AFM results proved the arraying regularity of these particles under any given conditions, and the electrostatic force microscopy showed their response to +3 V bias applied.展开更多
The preparation and formation mechanism of silica/polyvinylpyrrolidone（PVP）-polyacrylonitrile（PAN） coaxial nanofibers were presented in this paper. The PVP-PAN composite nanofibers were obtained via an electrospin...The preparation and formation mechanism of silica/polyvinylpyrrolidone（PVP）-polyacrylonitrile（PAN） coaxial nanofibers were presented in this paper. The PVP-PAN composite nanofibers were obtained via an electrospinning technique, while SiO2 nanoparticles were prepared according to a Stber method. The measurements of water contact angle（WCA）, the compared results of silica coating PVP-PAN composite nanofibers with PAN nanofibers indicate that much PVP resided on the composite nanofiber surface, which results in the occurrence of SiO2@polymer coaxial nanofibers due to the formation of hydrogen bonding between silica and composite nanofibers and subsequent adsorption of silica on the fiber surface.展开更多
文摘An access to an increase in the information storage capacity is to reduce memory units to a nano-scale. There fore, we used carboxylized phenyl-capped polyaniline tetramer (PCAT) as the functional component and silica as the carrier to prepare PCAT/silica composite nano-particles (= 60 nm) with a structure of core-shell. The functionalized particles were two-dimensionally arrayed on substrates such as silicon, glass and ITO glass at pH 3.SEM and AFM results proved the arraying regularity of these particles under any given conditions, and the electrostatic force microscopy showed their response to +3 V bias applied.
文摘The preparation and formation mechanism of silica/polyvinylpyrrolidone（PVP）-polyacrylonitrile（PAN） coaxial nanofibers were presented in this paper. The PVP-PAN composite nanofibers were obtained via an electrospinning technique, while SiO2 nanoparticles were prepared according to a Stber method. The measurements of water contact angle（WCA）, the compared results of silica coating PVP-PAN composite nanofibers with PAN nanofibers indicate that much PVP resided on the composite nanofiber surface, which results in the occurrence of SiO2@polymer coaxial nanofibers due to the formation of hydrogen bonding between silica and composite nanofibers and subsequent adsorption of silica on the fiber surface.
