Since 2000, there has been an explosion of activity in the field of plasmon-enhanced Raman spectroscopy (PERS), including surface-enhanced Raman spectroscopy (SERS), tip-enhanced Raman spectroscopy (TERS) and shell-isolated nanoparticle-enhanced Raman spectroscopy (SHINERS). In this Review, we explore the mechanism of PERS and discuss PERS hotspots — nanoscale regions with a strongly enhanced local electromagnetic field — that allow trace-molecule detection, biomolecule analysis and surface characterization of various materials. In particular, we discuss a new generation of hotspots that are generated from hybrid structures combining PERS-active nanostructures and probe materials, which feature a strong local electromagnetic field on the surface of the probe material. Enhancement of surface Raman signals up to five orders of magnitude can be obtained from materials that are weakly SERS active or SERS inactive. We provide a detailed overview of future research directions in the field of PERS, focusing on new PERS-active nanomaterials and nanostructures and the broad application prospect for materials science and technology. Assisted by rationally designed novel plasmonic nanostructures, surface-enhanced Raman spectroscopy has presented a new generation of analytical tools (that is, tip-enhanced Raman spectroscopy and shell-isolated nanoparticle-enhanced Raman spectroscopy) with an extremely high surface sensitivity, spatial resolution and broad application for materials science and technology.

Nanostructure-based plasmon-enhanced Raman spectroscopy for surface analysis of materials

Electrospun polyimide nanofibers and their applications

The well-defined silver (Ag) nanowires with five-twinned structure have been prepared by polyol reduction in the presence of poly(vinylpyrrolidone) (PVP K-30, 40 000). The obtained Ag nanowires are nearly monodispersed with an average diameter of 70 nm and length of 6 μm. It is confirmed from the results of thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS), and Fourier transform Raman spectra (FT-Raman) that one monolayer of the PVP molecules might be absorbed on the surface of the Ag nanowires through Ag−O coordination. On the basis of the experimental analysis, the probable spatial conformation of the PVP molecules is supposed to be that the CH skeleton chain of the PVP is close to the surface of the Ag nanowires. The pyrrolidone ring might be tilted on the surface of the Ag nanowires through Ag:O coordination. These results may provide direct evidence for the role of the PVP molecules in the formation of the Ag nanowires.

Evidence for the Monolayer Assembly of Poly(vinylpyrrolidone) on the Surfaces of Silver Nanowires

Learning polymer crystallization with the aid of linear, branched and cyclic model compounds.

Covalent attachment of a non-fluorinated polyetherimide onto the surface of carboxylic acid-functionalized multiwalled carbon nanotubes (MWNTs) has been achieved via grafting reactions. This confirms for the first time that the grafting reaction occurs at the nanotube surface when the carboxylic acid-functionalized MWNTs react with the polyetherimide with amine-terminated groups, through both amide and imide linkages formed at the interface between the carbon nanotubes and the polyetherimide. Additionally, an increase in the average molecular weight is detected in gel permeation chromatography when the polyetherimide is chemically attached onto the nanotubes. More interestingly, the chemical bonding at the interface provides much better interfacial adhesion and mechanical stress transfer, evidenced by a significant improvement in mechanical properties. As a result of the chemical attachment, the carbon nanotube-reinforced polyetherimide composite films have enhanced electrical conductivity, thermal deform...

Multiwalled Carbon Nanotubes with Chemically Grafted Polyetherimides

Surface lamellar decoration (SLD), surface enhanced Raman scattering (SERS) and optical second harmonic generation (SHG) experiments have been utilized to study the molecular orientation and conformation changes at a rubbed polyimide alignment-layer surface. This aromatic polyimide containing pendent cyanobiphenyl mesogens was synthesized via a polycondensation of 2,2'-bis(3,4-dicarboxy-phenyl)hexafluoropropane dianhydride (6FDA) with bis[omega-[4-(4-cyanophenyl)phenoxy]hexyl] 4,4'-diamino-2,2'-biphenyldicarboxylate (nCBBP, n = 6), abbreviated as 6FDA--6CBBP. Uniform alignment layers, possessing high pretilt angles ranging from 39 degrees to 43 degrees, have been achieved after mechanical rubbing of the polyimide thin film surface at room temperature and subsequent annealing. This is the first time that high pretilt angles have been detected to possess a negative angle (-theta(c)) with respect to the rubbing direction (i.e., opposite to the rubbing direction), considerably different from the conventional pretilt angle (theta(c)) observed along the rubbing direction. This observation is confirmed using magnetic null and SHG methods. Combined polyethylene (PE) SLD and atomic force microscopy experiments reveal that the azimuthal orientation distribution of the long axis of the edge-on PE lamellar crystals is oriented normal to the rubbing direction, indicating that the PE chains are aligned parallel to the rubbing direction. This SLD technique probes the anisotropic surface orientation of the outermost molecules of the rubbed polyimide layer. The SERS results show that prior to rubbing the surface, both the pendent cyanobiphenyls in the side chains and backbones possess nearly planar chain conformations at the polyimide surface. Mechanical rubbing causes not only tilting of the backbone moieties, such as imide-phenylene structure, but also significant conformational rearrangements of the pendent side chains at the surfaces. The molecular mechanism of this unusual alignment is due to the fact that the pendent cyanobiphenyls forms a uniformly tilted conformation on the rubbed surface, and the polar cyano groups point down toward the layer surface deduced from SHG phase measurements. This conformational rearrangement of the side chains results in the formation of fold-like bent structures on the surface, which directly leads to the long axis of cyanobiphenyls having the -theta(c) pretilt angle with respect to the rubbing direction.

Rubbing-induced molecular reorientation on an alignment surface of an aromatic polyimide containing cyanobiphenyl side chains.

Waveplates formed of mesogen-containing polymers and planar lightwave circuits containing such waveplates. Polymers have sidechains containing mesogens such as biphenyl-containing groups. Polymers may have a glass transition temperature between 100 °C and 300 °C, and polymers may be stretched in excess of 150% to increase birefringence of polymer and provide thin films. Waveplates formed of stretched polymer films may have high biaxial birefringence.

Waveplate and optical circuit formed from mesogen-containing polymer

A process for preparing polyimide fibers involves the preparation of a polymer in p-chlorophenol from reactants comprising 2,2'-dimethyl-4,4'-diaminobiphenyl and a tetracarboxylic anhydride. Following its preparation, the polyimide fibers can be spun directly from the reaction mixture. In a preferred embodiment, the dianhydride comprises 3,3',4,4'-biphenyltetracarboxylic dianhydride.

Process for preparing aromatic polyimide fibers

A polyimide comprises a reaction product of at least one dianhydride and at least one diamine, wherein the at least one diamine contains a pendent mesogenic group. A method for inducing a predetermined orientation of a liquid crystal material is also disclosed. The method includes applying an alignment layer material to a substrate and buffing the alignment layer material, thereby providing an alignment layer with a pre-tilt angle, wherein the alignment layer material is a reaction product of at least one dianhydride and at least one diamine, wherein the at least one diamine contains a pendent mesogenic group.

Polymide lcd alignment layer

Isothermal Thickening and Thinning Processes in Low Molecular Weight Poly(ethylene oxide) Fractions Crystallized from the Melt: Effects of Molecular Configurational Defects on Crystallization, Melting, and Annealing

Stephen Z. D. Cheng

Papers

Rubbing-induced molecular reorientation on an alignment surface of an aromatic polyimide containing cyanobiphenyl side chains.

Waveplate and optical circuit formed from mesogen-containing polymer

Process for preparing aromatic polyimide fibers

Polymide lcd alignment layer

Isothermal Thickening and Thinning Processes in Low Molecular Weight Poly(ethylene oxide) Fractions Crystallized from the Melt: Effects of Molecular Configurational Defects on Crystallization, Melting, and Annealing