Shawn Bourdo

Graphene supports in vitro proliferation and osteogenic differentiation of goat adult mesenchymal stem cells: potential for bone tissue engineering

Current treatments for bone loss injuries involve autologous and allogenic bone grafts, metal alloys and ceramics. Although these therapies have proved useful, they suffer from inherent challenges, and hence, an adequate bone replacement therapy has not yet been found. We hypothesize that graphene may be a useful nanoscaffold for mesenchymal stem cells and will promote proliferation and differentiation into bone progenitor cells. In this study, we evaluate graphene, a biocompatible inert nanomaterial, for its effect on in vitro growth and differentiation of goat adult mesenchymal stem cells. Cell proliferation and differentiation are compared between polystyrene‐coated tissue culture plates and graphene‐coated plates. Graphitic materials are cytocompatible and support cell adhesion and proliferation. Importantly, cells seeded on to oxidized graphene films undergo osteogenic differentiation in fetal bovine serum‐containing medium without the addition of any glucocorticoid or specific growth factors. These findings support graphenes potential to act as an osteoinducer and a vehicle to deliver mesenchymal stem cells, and suggest that the combination of graphene and goat mesenchymal stem cells provides a promising construct for bone tissue engineering. Copyright

Organic Solar Cells: A Review of Materials, Limitations, and Possibilities for Improvement

Significant attention has been given during the last few years to overcome technological and material barriers in order to develop organic photovoltaic devices (OPVs) with comparable cost efficiency similar to the inorganic photovoltaics (PVs) and to make them commercially viable. To take advantage of the low cost for such devices, major improvements are necessary which include: an efficiency of around 10%, high stability from degradation under real-world conditions, novel optically active materials, and development of novel fabrication approaches. In order to meet such stringent requirements, the research and development in OPVs need to improve upon the short diffusion length of excitons, which is one of the factors that are responsible for their low power conversion efficiency. This review discusses some of the most significant technological developments that were presented in the literature and helped improve photovoltaic performance, such as tandem architectures, plasmonics, and use of graphitic nanostructural materials, among others. Tandem organic solar cells with embedded plasmonics are a promising approach to further increase the power conversion efficiency of organic solar cells, by harvesting complementary spectral regions with high quantum efficiencies. Polymeric nanocomposites incorporating graphitic nanostructures were extensively investigated for the next generation of efficient and low-cost solar cells, since such nanomaterials show excellent electrical and mechanical properties, excellent carrier transport capabilities, and provide an efficient pathway to the dissociated charge carriers.

Structural and optoelectronic properties of P3HT-graphene composites prepared by in situ oxidative polymerization

Poly(3-hexylthiophene) (P3HT)-graphene nanocomposites were synthesized via in situ oxidative polymerization of 3-hexylthiophene monomer in the presence of graphene. The main thrust was to investigate the structural and optoelectronic properties of P3HT-graphene nanocomposites with various graphene concentrations. NMR spectroscopy was used to determine the regioregularity of the polymer composites, whereas Fourier transform infrared spectroscopy and differential scanning calorimetry were used to study their structural and thermal properties. Moreover, cyclic voltammetry was employed to evaluate the HOMO levels of the nanocomposites, while optical spectrophotometry (UV-Vis-NIR) was utilized to determine the optical bandgap of the composites. The information from the aforementioned techniques was used to estimate the HOMO-LUMO energy levels. The results revealed changes in the optical bandgap of P3HT with increasing graphene content. Furthermore, an extensive study aiming at the effect of graphene content on...

Catalytic Conversion of Graphene into Carbon Nanotubes via Gold Nanoclusters at Low Temperatures

Here, we present the catalytic conversion of graphene layers into carbon nanotubes (CNTs), in the presence of Au nanoparticles (AuNPs) without the need for an additional carbon source. We have demonstrated that this catalytic process takes place at temperatures as low as 500 °C. No other oxide supports decorated with AuNPs were found to grow CNTs at this temperature. These findings highlight the high activity of graphene when used as a support for catalytic reactions.

Comparative Aging Study of Organic Solar Cells Utilizing Polyaniline and PEDOT:PSS as Hole Transport Layers.

UNLABELLED The aging effect on P3HT:PCBM organic solar cells was investigated with camphorsulfonic doped polyaniline (PANI:CSA) or poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) ( PEDOT PSS) used as the hole transport layer (HTL). The cells were encapsulated and exposed to a continuous normal atmosphere on a dark shelf and then characterized intermittently for more than two years. The photovoltaic results revealed that the cells with PEDOT PSS HTL showed better initial results than the cells with PANI:CSA HTL. Over time, PEDOT PSS-based cells exhibited faster degradation than PANI:CSA-based cells, where the average efficiency of six cells dropped to zero in less than one and a half years. On the other hand, PANI:CSA-based cells exhibited a much more stable performance with an average efficiency drop of only 15% of their initial values after one and a half years and 63% after two years. A single-diode model was utilized to fit the experimental data with the theoretical curve to extract the diode parameters, such as the ideality factor, to explain the effect of aging on the diodes performance.

Photovoltaic devices based on high density boron-doped single-walled carbon nanotube/n-Si heterojunctions

A simple and easily processible photovoltaic device has been developed based on boron-doped single-walled carbon nanotubes (B-SWNTs) and n-type silicon (n-Si) heterojunctions. The SWNTs were substitutionally doped with boron atoms by thermal annealing, in the presence of B2O3. The samples used for these studies were characterized by Raman spectroscopy, thermal gravimetric analysis, transmission electron microscopy, and x-ray photoelectron spectroscopy. The fully functional solar cell devices were fabricated by airbrush deposition that generated uniform B-SWNT films on top of the n-Si substrates. The carbon nanotube films acted as exciton-generation sites, charge collection, and transportation while the heterojunctions formed between B-SWNTs and n-Si acted as charge dissociation centers. The current-voltage characteristics in the absence of light and under illumination, as well as optical transmittance spectrum are reported here. It should be noted that the device fabrication process can be made amenable t...

Single-walled carbon nanotubes as specific targeting and Raman spectroscopic agents for detection and discrimination of single human breast cancer cells

Abstract. Raman active nano-complex agents based on single-walled carbon nanotubes (SWCNTs) are prepared and used for the swift and specific detection of breast cancer cells. SWCNTs are functionalized to bond covalently with the anti-epithelial cell adhesion molecule (anti-EpCAM) antibody, which is specific to the highly expressed EpCAM antigen on the surface of breast cancer cells (MCF-7), but not on normal cells. The Raman nano-complexes demonstrate excellent ability to detect in vitro single breast cancer cells (MCF-7) and discriminate between them and normal fibroblast cells during the first 30 min of the targeting process. Raman linearity scanning is collected from a monolayer cell mixture, including both cancer cells and normal cells incubated with anti-EpCAM-SWCNTs, using a 633-nm laser excitation. The results shows that the Raman signal collected from targeted MCF-7 cells is extremely high, whereas there is little signal from the normal cells.

Ammonia Gas Sensing Behavior of Tanninsulfonic Acid Doped Polyaniline-TiO2 Composite

A highly active tannin doped polyaniline-TiO2 composite ammonia gas sensor was developed and the mechanism behind the gas sensing activity was reported for the first time. A tanninsulfonic acid doped polyaniline (TANIPANI)-titanium dioxide nanocomposite was synthesized by an in situ polymerization of aniline in the presence of tanninsulfonic acid and titanium dioxide nanoparticles. X-ray diffraction and thermogravimetric analysis were utilized to determine the incorporation of TiO2 in TANIPANI matrix. UV-Visible and infrared spectroscopy studies provided information about the electronic interactions among tannin, polyaniline, and TiO2. Scanning electron microscopy (SEM) along with energy dispersive X-ray spectroscopy (EDS) and atomic force microscopy (AFM) surface analysis techniques were used to investigate the metal oxide dispersions inside polyaniline matrix. Gas sensors were prepared by spin coating solutions of TANIPANI-TiO2 and TANIPANI composites onto glass slides. Sensors were tested at three different concentrations (20 ppm, 40 ppm, and 60 ppm) of ammonia gas at ambient temperature conditions by measuring the changes in surface resistivity of the films with respect to time. Ammonia gas sensing plots are presented showing the response values, response times and recovery times. The TANIPANI-TiO2 composite exhibited better response and shorter recovery times when compared to TANIPANI control and other polyaniline composites that have been reported in the literature. For the first time a proposed mechanism of gas sensing basing on the polaron band localization and its effects on the gas sensing behavior of polyaniline are reported.

Tuning the work function of polyaniline via camphorsulfonic acid: an X-ray photoelectron spectroscopy investigation

In this work, we present the first demonstration of tuning the work function of polyaniline by controlling the concentration level of camphorsulfonic acid as a protonic acid dopant and m-cresol as a solvent. Optical, thermal, structural, and electronic properties, along with surface topography and elemental analysis of protonated polyaniline, were studied in detail to investigate the effect of camphorsulfonic acid on the work function of polyaniline. The results showed that an increase in camphorsulfonic acid content induces a gradual transformation in the polyaniline structure from an emeraldine base to an emeraldine salt phase, which is associated with an increase in electrical conductivity and an improvement in crystallinity. X-ray photoelectron spectroscopy was used to evaluate the work function and to determine the elemental composition of the surface and several atomic layers beneath the surface. The results showed that increasing the camphorsulfonic acid content from quarter protonated to fully protonated leads to an increase in the work function of polyaniline from 4.42 ± 0.14 eV to 4.78 ± 0.13 eV.

The role of surface chemistry in the cytotoxicity profile of graphene.

Graphene and its derivative, because of their unique physical, electrical and chemical properties, are an important class of nanomaterials being proposed as foundational materials in nanomedicine as well as for a variety of industrial applications. A major limitation for graphene, when used in biomedical applications, is its poor solubility due to its rather hydrophobic nature. Therefore, chemical functionalities are commonly introduced to alter both its surface chemistry and biochemical activity. Here, we show that surface chemistry plays a major role in the toxicological profile of the graphene structures. To demonstrate this, we chemically increased the oxidation level of the pristine graphene and compared the corresponding toxicological effects along with those for the graphene oxide. X‐ray photoelectron spectroscopy revealed that pristine graphene had the lowest amount of surface oxygen, while graphene oxide had the highest at 2.5% and 31%, respectively. Low and high oxygen functionalized graphene samples were found to have 6.6% and 24% surface oxygen, respectively. Our results showed a dose‐dependent trend in the cytotoxicity profile, where pristine graphene was the most cytotoxic, with decreasing toxicity observed with increasing oxygen content. Increased surface oxygen also played a role in nanomaterial dispersion in water or cell culture medium over longer periods. It is likely that higher dispersity might result in graphene entering into cells as individual flakes ~1 nm thick rather than as more cytotoxic aggregates. In conclusion, changes in graphenes surface chemistry resulted in altered solubility and toxicity, suggesting that a generalized toxicity profile would be rather misleading. Copyright