Minhua Zhao

Subsurface characterization of carbon nanotubes in polymer composites via quantitative electric force microscopy

Subsurface characterization of carbon nanotubes (CNTs) dispersed in free-standing polymer composite films was achieved via quantitative electric force microscopy (EFM). The effects of relative humidity, EFM probe geometry, tip-sample distance and bias voltage on the EFM contrast were studied. Non-parabolic voltage dependence of the EFM signal of subsurface CNTs in polymer composites was observed and a new mechanism was proposed taking consideration of capacitive coupling as well as coulombic coupling. We anticipate that this quantitative EFM technique will be a useful tool for non-destructive subsurface characterization of high dielectric constant nanostructures in low dielectric constant matrices.

Water-soluble DNA-wrapped single-walled carbon-nanotube/quantum-dot complexes.

In recent years, carbon nanotubes (CNTs), especially singlewalled carbon nanotubes (SWCNTs), have attracted much attention due to their unique properties and potential towards broad real-world applications. The integration of SWCNTs with other unique nanoscale luminescent materials, such as quantum dots (QDs), has enabled the manufacture of many novel nanocomposite materials with enhanced structural, mechanical, optical, and chemical properties. The performance of these composite materials strongly depends upon the properties of the individual components and additives as well as the conjugation chemistry required to assemble them into composite hybrids. Therefore, a variety of new techniques have been developed to modify the optical, mechanical, chemical, and electrical properties of SWCNTs to control the properties of the final composite materials. Among the additives to SWCNT-based composites, novel nanoparticles (NPs) have been increasingly employed. Functionalized NPs can be designed to covalently bind to the functional groups expressed on the sidewalls or ends of

Fate of graphene in polymer nanocomposite exposed to UV radiation

Graphene is increasingly incorporated in polymers to enhance their mechanical, thermal and electrical properties. However, organic polymers are prone to degrade when exposed to UV radiation. Therefore, graphene in polymer nanocomposites could eventually be released into the environment during their life cycle, which might have a negative impact on the environment and thus presents a roadblock to their use. This study investigates the degradation of a graphene/polyurethane composite and characterizes the graphene concentration at the nanocomposite surfaces during exposure to UV radiation. The polyurethane was a one-component, water-borne polyurethane and graphene material was graphene oxide (GO) sheets. GO/WBPU composites having a thickness between 105 μm and 150 μm were exposed to 75% RH, 50°C, and UV radiation between 290 nm and 400 nm in a NIST-developed UV chamber. Chemical degradation, mass loss, and surface morphology were measured at specified exposure time using FTIR, gravimetry, SEM, AFM and LCSM techniques. Results showed that, when exposed to UV radiation having wavelengths similar to those of the sunlight, the polyurethane matrix underwent photodegradation, subsequent mass loss and accumulation of a large amount of graphene on the composite surface.

Critical role of particle/polymer interface in photostability of nano-filled polymeric coatings

Nanoparticle-filled polymeric coatings have attracted great interest in recent years because the incorporation of nanofillers can significantly enhance the mechanical, electrical, optical, thermal, and antimicrobial properties of coatings. Due to the small size of the fillers, the volume fraction of the nanoparticle/polymer interfacial area in nano-filled systems is drastically increased, and the interfacial region becomes important in the performance of the nano-filled system. However, techniques used for characterizing nanoparticle/polymer interfaces are limited, and thus, the mechanism by which interfacial properties affect the photostability and the long-term performance of nano-filled polymeric coatings is not well understood. In this study, the role of the nanoparticle/polymer interface on the ultraviolet (UV) stability of a nano-ZnO-filled polyurethane (PU) coating system was investigated. The effects of parameters influencing the particle/polymer interfacial properties, such as size, loading, surface modification of the nanoparticles, on photodegradation of ZnO/PU films were evaluated. The nature of the interfacial regions before and after UV exposures were characterized by atomic force microscopy (AFM)-based techniques. Results have shown that the interfacial properties strongly affect chemical, thermo-mechanical, and morphological properties of the UV-exposed ZnO/PU films. By combining tapping mode AFM and novel electric force microscopy (EFM), the particle/polymer interfacial regions have been successfully detected directly from the surface of the ZnO/PU films. Further, our results indicate that ZnO nanoparticles can function as a photocatalyst or a photostabilizer, depending on the UV exposure conditions. A hypothesis is proposed that the polymers in the vicinity of the ZnO/PU interface are preferentially degraded or protected, depending on whether ZnO nanoparticles act as a photocatalyst or a photostabilizer in the polymers. This study clearly demonstrates that the particle/polymer interface plays a critical role in the photostability of nano-filled polymeric coatings.

Impact of UV irradiation on multiwall carbon nanotubes in nanocomposites: Formation of entangled surface layer and mechanisms of release resistance

Multiwall carbon nanotubes (MWCNTs) are nanofillers used in consumer and structural polymeric products to enhance a variety of properties. Under weathering, the polymer matrix will degrade and the nanofillers may be released from the products potentially impacting ecological or human health. In this study, we investigated the degradation of a 0.72 % (by mass) MWCNT/amine-cured epoxy nanocomposite irradiated with high intensity ultraviolet (UV) light at various doses, the effects of UV exposure on the surface accumulation and potential release of MWCNTs, and possible mechanisms for the release resistance of the MWCNT surface layer formed on nanocomposites by UV irradiation. Irradiated samples were characterized for chemical degradation, mass loss, surface morphological changes, and MWCNT release using a variety of analytical techniques. Under 295 nm to 400 nm UV radiation up to a dose of 4865 MJ/m2, the nanocomposite matrix underwent photodegradation, resulting in formation of a dense, entangled MWCNT network structure on the surface. However, no MWCNT release was detected, even at very high UV doses, suggesting that the MWCNT surface layer formed from UV irradiation of polymer nanocomposites resist release. Four possible release resistance mechanisms of the UV-induced MWCNT surface layer are presented and discussed.