Prabir Patra

Covalently Interconnected Three- Dimensional Graphene Oxide Solids

The creation of three-dimensionally engineered nanoporous architectures via covalently interconnected nanoscale building blocks remains one of the fundamental challenges in nanotechnology. Here we report the synthesis of ordered, stacked macroscopic three-dimensional (3D) solid scaffolds of graphene oxide (GO) fabricated via chemical cross-linking of two-dimensional GO building blocks. The resulting 3D GO network solids form highly porous interconnected structures, and the controlled reduction of these structures leads to formation of 3D conductive graphene scaffolds. These 3D architectures show promise for potential applications such as gas storage; CO2 gas adsorption measurements carried out under ambient conditions show high sorption capacity, demonstrating the possibility of creating new functional carbon solids starting with two-dimensional carbon layers.

In situ Synthesis of Metal Nanoparticle Embedded Free Standing Multifunctional PDMS Films

We demonstrate a simple one-step method for synthesizing noble metal nanoparticle embedded free standing polydimethylsiloxane (PDMS) composite films. The process involves preparing a homogenous mixture of metal salt (silver, gold and platinum), silicone elastomer and the curing agent (hardener) followed by curing. During the curing process, the hardener crosslinks the elastomer and simultaneously reduces the metal salt to form nanoparticles. This in situ method avoids the use of any external reducing agent/stabilizing agent and leads to a uniform distribution of nanoparticles in the PDMS matrix. The films were characterized using UV-Vis spectroscopy, transmission electron microscopy and X-ray photoemission spectroscopy. The nanoparticle-PDMS films have a higher Youngs modulus than pure PDMS films and also show enhanced antibacterial properties. The metal nanoparticle-PDMS films could be used for a number of applications such as for catalysis, optical and biomedical devices and gas separation membranes.

Graphene Oxide as a Quencher for Fluorescent Assay of Amino Acids, Peptides, and Proteins

Understanding the interaction between graphene oxide (GO) and the biomolecules is fundamentally essential, especially for disease- and drug-related peptides and proteins. In this study, GO was found to strongly interact with amino acids (tryptophan and tyrosine), peptides (Alzheimers disease related amyloid beta 1-40 and type 2 diabetes related human islet amyloid polypeptide), and proteins (drug-related bovine and human serum albumin) by fluorescence quenching, indicating GO was a universal quencher for tryptophan or tyrosine related peptides and proteins. The quenching mechanism between GO and tryptophan (Trp) or tyrosine (Tyr) was determined as mainly static quenching, combined with dynamic quenching (Förster resonance energy transfer). Different quenching efficiency between GO and Trp or Tyr at different pHs indicated the importance of electrostatic interaction during quenching. Hydrophobic interaction also participated in quenching, which was proved by the presence of nonionic amphiphilic copolymer Pluronic F127 (PF127) in GO dispersion. The strong hydrophobic interaction between GO and PF127 efficiently blocked the hydrophobic interaction between GO and Trp or Tyr, lowering the quenching efficiency.

Conducting Polymer and Conducting Composite Strain Sensors on Textiles

Metallic connections and polymer sensors have been printed onto textiles as a step toward the production of flexible printed electronics. We show that the strain response of conducting polymers and composites on woven textiles depends on the detailed distribution the sensor material on the yarn. The structure of most textiles, with strong fibers twisted into yarns, can provide a support which allows electronic materials, impregnated into the yarn, to stretch and bend without breaking.

Observation of Dynamic Strain Hardening in Polymer Nanocomposites

Most materials respond either elastically or inelastically to applied stress, while repeated loading can result in mechanical fatigue. Conversely, bones and other biomechanical tissues have the ability to strengthen when subjected to recurring elastic stress. The cyclic compressive loading of vertically aligned carbon nanotube/poly(dimethylsiloxane) nanocomposites has revealed a self-stiffening response previously unseen in synthetic materials. This behavior results in a permanent increase in stiffness that continues until the dynamic stress is removed and resumes when it is reapplied. The effect is also specific to dynamic loads, similar to the localized self-strengthening that occurs in biological structures. These observations help to elucidate the complex interactions between matrix materials and nanostructures, and control over this mechanism could lead to the development of adaptable structural materials and active, load-bearing artificial connective tissues.

Role of electrospun fibre diameter and corresponding specific surface area (SSA) on cell attachment

In order to develop scaffolds for tissue regeneration applications, it is important to develop an understanding of the kinetics of cell attachment as a function of scaffold geometry. In the present study, we investigated how the specific surface area of electrospun scaffolds affected cell attachment and spreading. Number of cells attached to the scaffold was measured by the relative intensity of a metabolic dye (MTS) and cell spreading was analysed for individual cells by measuring the area of projected F‐actin cytoskeleton. We varied the fibre diameter to obtain a specific surface area distribution in the range 2.24–18.79 µm−1. In addition, we had one case where the scaffolds had beads in them and therefore had non‐uniform fibres. For each of these different geometries, we varied the cell‐seeding density (0.5–1 × 105) and the serum concentration (0–12%) over the first 8 h in an electrospun polycaprolactone NIH 3T3 fibroblast system. Cells on beaded scaffolds showed the lowest attachment and almost no F‐actin spreading in all experiments indicating uniform fibre diameter is essential for electrospun scaffolds. For the uniform fibre scaffolds, cell attachment was a function of scaffold specific surface area (SSA) (18.79–2.24 µm−1) and followed two distinct trends: when scaffold SSA was < 7.13 µm−1, cell adhesion rate remained largely unchanged; however, for SSA > 7.13 µm−1 there was a significant increase in cellular attachment rate with increasing SSA. This indicated that nanofibrous scaffolds increased cellular adhesion compared to microfibrous scaffolds. This phenomenon is true for serum concentrations of 7.5% and higher. For 5% and lower serum concentration, cell attachment is low and higher SSA fails to make a significant improvement in cell attachment. When cell attachment was investigated at a single‐cell level by measuring the projected actin area, a similar trend was noted where the effect of higher SSA led to higher projected area for cells at 8 h. These results indicate that uniform electrospun scaffolds with SSA provide a faster cell attachment compared to lower SSA and beaded scaffolds. These results indicate that continuous electrospun nanofibrous scaffolds may be a good substrate for rapid tissue regeneration. Copyright

Dynamic self-stiffening in liquid crystal elastomers

Biological tissues have the remarkable ability to remodel and repair in response to disease, injury, and mechanical stresses. Synthetic materials lack the complexity of biological tissues, and man-made materials which respond to external stresses through a permanent increase in stiffness are uncommon. Here, we report that polydomain nematic liquid crystal elastomers increase in stiffness by up to 90% when subjected to a low-amplitude (5%), repetitive (dynamic) compression. Elastomer stiffening is influenced by liquid crystal content, the presence of a nematic liquid crystal phase and the use of a dynamic as opposed to static deformation. Through rheological and X-ray diffraction measurements, stiffening can be attributed to a nematic director which rotates in response to dynamic compression. Stiffening under dynamic compression has not been previously observed in liquid crystal elastomers and may be useful for the development of self-healing materials or for the development of biocompatible, adaptive materials for tissue replacement.

Water tribology on graphene

Classical experiments show that the force required to slide liquid drops on surfaces increases with the resting time of the drop, t(rest), and reaches a plateau typically after several minutes. Here we use the centrifugal adhesion balance to show that the lateral force required to slide a water drop on a graphene surface is practically invariant with t(rest). In addition, the drops three-phase contact line adopts a peculiar micrometric serrated form. These observations agree well with current theories that relate the time effect to deformation and molecular re-orientation of the substrate surface. Such molecular re-orientation is non-existent on graphene, which is chemically homogenous. Hence, graphene appears to provide a unique tribological surface test bed for a variety of liquid drop-surface interactions.

Hybrid Electrodes by In-Situ Integration of Graphene and Carbon-Nanotubes in Polypyrrole for Supercapacitors.

Supercapacitors also known as electrochemical capacitors, that store energy via either Faradaic or non-Faradaic processes, have recently grown popularity mainly because they complement, and can even replace, conventional energy storage systems in variety of applications. Supercapacitor performance can be improved significantly by developing new nanocomposite electrodes which utilizes both the energy storage processes simultaneously. Here we report, fabrication of the freestanding hybrid electrodes, by incorporating graphene and carbon nanotubes (CNT) in pyrrole monomer via its in-situ polymerization. At the scan rate of 5 mV s−1, the specific capacitance of the polypyrrole-CNT-graphene (PCG) electrode film was 453 F g−1 with ultrahigh energy and power density of 62.96 W h kg−1 and 566.66 W kg−1 respectively, as shown in the Ragone plot. A nanofibrous membrane was electrospun and effectively used as a separator in the supercapacitor. Four supercapacitors were assembled in series to demonstrate the device performance by lighting a 2.2 V LED.

OPTIMIZATION OF ELECTROSPINNING PROCESS PARAMETERS FOR TISSUE ENGINEERING SCAFFOLDS

The goal of the current study was to optimize important process parameters for electrospinning polycaprolactone (PCL) for growing 3T3 fibroblasts. We hypothesized that the smallest obtainable fiber diameter would provide the best cell growth kinetics and we tested this hypothesis for three different process parameters: solution concentration, voltage and collector screen distance. Beaded structures were formed when using low concentration electrospinning solutions (8 wt% to 13 wt%), in which the viscosity ranged from 16.0 cP to 340.0 cP. In this concentration range, cell growth kinetics was impeded when using a high concentration of cells (8–10 × 105). Higher PCL concentration led to an increase in the average fiber diameter from 400 nm to 1600 nm when PCL solution concentration changed from 15 wt% to 20 wt%. Although, the mean values indicated that cell growth kinetics were higher at the lower end of the concentration (15% as opposed to 20%) and this correlated with lower average fiber diameter, the results in this range were not statistically significant (p > 0.05). The average fiber diameter of scaffolds first decreased and then increased when electrospinning voltage was increased. The cell growth kinetics demonstrated that smaller average diameter PCL fiber scaffolds had higher growth kinetics than larger average diameter scaffolds with the best conditions obtained at 15 KV. By increasing the screen distance, the average fiber diameter decreased but had no significant impact on cell growth kinetics. In summary, the optimal parametric space for 3T3 fibroblast growth for our studies was electrospinning a 15 wt% PCL solution using 15 kV voltage and a 25 cm collector distance.