A facile technique was developed for a long-term increase in silicone elastomer surface hydrophilicity, eliminating the need for post-cure surface treatment (e.g. oxygen plasma or surface grafting). Well-defined silicones (1-4 kDa) with a central vinyl functionality and discrete PEG2, PEG3 and tetrahydrofurfuryl (THF) pendant endgroups were synthesized, characterized and used as comonomers in addition-cure, platinum catalyzed 2-part silicone elastomer formulations. The modified silicone elastomers were optically clear and maintained the mechanical performance characteristic of this class of material with up to 20 wt.% comonomer in the 2-part formulation. Contact angle measurements of deionized water on the silicone elastomer surface showed improved wettability with comonomer content. The elastomer surface shifted from hydrophobic (contact angle ∼120°C) to hydrophilic (contact angle < 90°C) at ∼5 wt.% comonomer loadings for extended time frames (> 5 months). Coefficient of friction measurements of the modified silicone elastomers revealed an increase in surface lubricity with comonomer loadings.

Silver nanoparticle (AgNP) is one of the elegant material because its uses in various fields. In this study, AgNPs have been prepared by using Peltophorum pterocarpum (PP) flower extract as reducing and capping agent and aqueous silver nitrate (aq.AgNO3) as silver precursor. The synthesized nanoparticles were characterized using Ultra Violet - Visible (UV-Vis) spectroscopy, High Resolution Transmission Electron Microscope (HR-TEM) and Fourier Transform Infrared Spectroscopy (FT-IR), which reveals the formation of nanosized particles. The UV-Vis spectrum shows an absorption peak around 430nm. HR-TEM images of AgNPs with clear morphology and well dispersed prepared AgNPs.

Inkjet printing of TiO2 potentially offers a high degree of control over the deposition of TiO2 suspensions. Previous use of inkjet printing for TiO2 depositions have focused on producing TiO2 films with uniform density. A multi-ink printing system offers the possibility of depositing TiO2 films with variable density using a single deposition method.

For this research, inkjet printing of TiO2 films with a graded density profile was explored as a means of improving dye sensitized solar cells (DSSCs) performance. Varying pore volume as a means to produce density variations in TiO2 layers was explored. To control the pore volume, several TiO2 suspensions were developed with different pore-forming additives. DSSCs with printed TiO2 films having three density layers showed an average improvement in the conversion efficiency of 127% versus those with a single layer and 45% versus those with dual- layer TiO2. Short-circuit current densities of cells with tri-layer films increased an average of 62% over those with a single layer and 17% over those with dual-layer TiO2. It was also shown that DSSCs with inkjet printed TiO2 layers performed better than those with spin-coated TiO2 layers.

The results effectively demonstrated the potential for using inkjet printing as a sole deposition method to produce TiO2 films with non-uniform density leading to improved DSSC performance. One possibility for further study is to create further layer variations through simultaneous printing of different suspensions.

The synthesis of bimetallic magnetic nanoparticles is very challenging because of the agglomeration and non-uniform size. In this paper, we present the synthesis of monodispersed 3-5 nm sized thiolated bimetallic alloyed Au/Co nanoparticles with decahedral and icosahedral shape, their characterization using Cs-corrected scanning transmission electron microscopy (STEM) and magnetic measurements using superconducting quantum interference device (SQUID) magnetometer. The Z-contrast imaging and energy dispersive X-ray spectroscopy (EDS) mapping showed an inhomogeneous alloying with minor segregation between Au and Co at nanoscale and the SQUID measurement exhibited the ferromagnetic behavior.

We show that high-efficiency and low-degradation hydrogenated amorphous silicon (a-Si:H) p-i-n solar cells can be obtained by depositing absorber layers in a triode-type plasma-enhanced chemical vapor deposition (PECVD) process. Although the deposition rate is relatively low (0.01-0.03 nm/s) compared to the conventional diode-type PECVD process (∼0.2 nm/s), the light-induced degradation in conversion efficiency of single-junction solar cell is substantially reduced (Δη/ηini∼10%) due to the suppression of light-induced metastable defects in the a-Si:H absorber layer. So far, we have attained an independently-confirmed stabilized efficiency of 10.11% for a 220-nm-thick a-Si:H solar cell which was light soaked under 1 sun illumination for 1000 hours at cell temperature of 50°C. We further demonstrate that stabilized efficiencies as high as 10% can be maintained even when the solar cell is thickened to >300 nm.

Imprinting is a well-established technique to induce recognition features in both organic and inorganic materials for a variety of target analytes. In this study, ion imprinted polysiloxanes with varying percentage of coupling agent i.e. 3-chloro propyl trimethoxy silane (CPTM) were synthesized by sol-gel method for imprinting of Cr3+. The imprinting of Cr3+ in cross-linked siloxane network was investigated by FT-IR which indicates the metal ion is coordinated with oxygen atoms of polysiloxanes. SEM images revealed that imprinted polysiloxanes possess uniform particles of submicron size. It was experienced that by increasing the concentration of CPTM up to 10% (v/v) substantially improves the binding capacity of polysiloxanes which allows us to recognized Cr3+ down to 50µg/L. Furthermore, the selectivity of Cr3+-imprinted polysiloxanes was evaluated by treating them with other competing metal ions of same concentration i.e. Cr6+, Pb2+ and Ni2+. In this regard, polysiloxanes showed much higher binding for imprint ion i.e. Cr3+ in comparison to above mentioned metal ions. Finally, the regenerated polysiloxanes were studied in order to reuse them thus, developing cost effective biomimetic sensor coatings.

A hand operated benchtop stamping press was developed to conduct research on microscale hole fabrication in polymer membranes for applications as scaffolds in tissue engineering. A biocompatible and biodegradable polymer, poly(ε-caprolactone), was selected for micropunching. Membranes between 30 μm and 50 μm thick were fabricated by hot melt extrusion, but could not be stamped with a 200 μm circular punch at room temperature, regardless of die clearance due to excessive strain to fracture. This problem was overcome by cooling the membrane and die sets with liquid nitrogen to take advantage of induced brittle behavior below the polymer’s glass transition temperature. While cooled, 203 μm hole patterns were successfully punched in 33 μm thick poly(ε-caprolactone) membranes with 11% die clearance, achieving 71% porosity.

The current gold-standard therapeutic strategies for bone grafts in the patient population are to use either allograft or autograft bone. Although these approaches have a long track record of utilization, neither is without risk to the patient, and there remains a desire in the field to improve treatment options. While there have been treatments approved by the FDA for full length growth factors and calcium salt-laden collagen sponges, these are not available for the entire population of potential bone graft patients. One viable strategy to focus on these concerns is to design an implantable bone graft substitute that can address all the negative drawbacks of autograft bone, allograft bone, and full length proteins. The work provides a preliminary investigation of synthetic, nanofiber-permeated, composite polymer/ceramic scaffold for bone repair using thermally induced phase separation, PLLA microspheres, and hydroxyapatite. The scaffolds as described have fiber diameters that mimic natural collagen ECM networks in bone as determined by scanning electron microscopy and will serve as the basis for future studies in substrate-guided bone tissue regeneration.

The formation of misfit dislocations is an important issue for the performance of heteroepitaxial micro- and optoelectronic devices. We analyze three approaches that quantify the stability of misfit dislocations in axial-heteroepitaxial nanowires with respect to applicability and predictions of critical nanowire dimensions. The “nanoheteroepitaxy” approach of Zubia and Hersee proves suitable for determination of strain partitioning in the presence of an elastic mismatch. Concerning the critical thickness and diameter however the descriptions of Ertekin et al. and Glas respectively yield more reliable results, owing to the consideration of the total coherent and dislocation related energies plus the residual strain energy. In contrast to the model of Ertekin et al., which refers to infinitely long nanowires, the other two mentioned approaches allow predictions of the critical thickness of mismatched deposits on the nanowire axial face.

4H-SiC p+n photodiodes based on ultrathin-junctions have been fabricated with distinct processes for the p+-region creation: either with Aluminium conventional ion implantation, or with Boron Plasma Ion Immersion Implantation. Spectral sensitivity measurements were performed at several temperatures from room temperature up to 340°C, with incident wavelengths ranging from 200 to 400 nm. Both responses are characterized by a stability between 200 and 270 nm, and a important increase with temperature between 270 and 380 nm. This fact has to be related to the two different kinds of optical absorption phenomena in SiC with respect to the wavelength, which are direct and indirect (phonon assisted) transitions. When decreasing the temperature, we noticed a hysteresis effect, which could be due to charge trapping by temperature activated defects. After strong proton and electron irradiations, the diodes showed a stability of the response below 270 nm, making them suitable for use in harsh environments. Simulation was performed at room temperature, with a good correlation between simulated and experimental room temperature curves.

Silver nanoparticle inks are increasingly applied for the manufacture of inkjet-printed electrically conductive patterns. In order to obtain high conductivity, the printed liquid patterns have to be functionalized by an appropriate post- treatment step. Modern post-treatment methods using e.g. microwaves, intense pulsed light or adopted infrared radiation, are nevertheless the basis of the thermal process. The thermal treatment e.g. in furnaces or on heating plates, is applicable for a great variety of inks and ensures an efficient sintering without major technical efforts. It has been studied intensively wherein the reports mainly focus on reduction of the resistivity by controlling the parameters of the thermal treatment. Our researches exceed these comparative studies by investigating multi-layered patterns, their manufacturing and post-treatment.

Two silver nanoparticle inks were inkjet printed on a rigid and a flexible substrate. The geometry of the patterns was varied. The different drying behaviors of the inks were investigated. In addition, the number of layers which were printed on top of each other was varied. The sintering temperatures and time durations were varied.

The morphology of the patterns is investigated by profilometry and optical microscopy. The microstructure is analyzed by scanning electron microscope and X-ray diffraction. Furthermore, the electrical characteristics were determined by the measurement of the resistance. The results indicate the relation between the manufacture and the resulting microstructure and functionality of the patterns. The knowledge of these parameters enables us to control the industrial manufacturing of similar conductive patterns.

We report magneto-dielectric anomaly of the multiferroic (Bi0.95Nd0.05)(Fe0.97Mn0.03)O3 (BNFM) ceramic near Néel temperature. The ceramic pellets were synthesized by conventional solid state reaction route. X-ray diffraction patterns revealed that most of the peaks shifted slightly towards higher Bragg’s angle compared to those of pure BiFeO3 and also confirmed the formation of rhombohedral phase. It also suggests that the small chemical substitution of Nd and Mn atoms at Bi and Fe sites of BiFeO3 (BFO) perovskite respectively does not alter the crystal structure. Temperature and frequency dependent dielectric response indicate large dielectric anomaly at 620 K, slightly below the known Néel temperature of BFO. The enhancement in dielectric properties of BNFM ceramic was observed as compared to BFO due to suppression of oxygen vacancies by the doping. Temperature dependent dielectric response in conjunction with Raman and thermo-analytical data show that the BNFM sample presents significant magneto-dielectric response around Néel temperture TN ∼ 620 K.

We review an optofluidic waveguiding lab-on-a-chip used to sense bioparticles. The sensor uses a liquid filled Anti-Resonant Reflecting Optical Waveguide (ARROW) that is interfaced with standard ridge waveguides. The ridge waveguides are coupled to off-chip lasers and detectors via optical fiber. A perpendicular intersection between the ARROW and a ridge waveguide is especially useful for detecting fluorescently tagged particles. Light coupled into the ridge waveguide can fluorescently excite these particles within a very small volume. Fluorescent signal can then be guided within the ARROW and subsequently off chip to a detector.

We also discuss how such devices are fabricated. Both the ARROW and ridge waveguides are made using alternating thin films of tantalum oxide and silicon dioxide on silicon substrates. These thin films are deposited by either sputtering or plasma enhanced chemical vapor deposition (PECVD). The waveguides are patterned using a combination of standard photolithographic processes, reactive ion etching, and sacrificial etching. Low-loss optical guiding is very dependent on both the waveguide structure and the materials used. The latest processes for maximizing detection sensitivity are reviewed.

We also present results using the optofluidic waveguiding sensor for detecting a variety of different types of particles such as fluorescently labeled nanobeads, viruses, ribosomes, and RNA.

B-type carbonate apatite (B-CAp) powders were prepared by a wet method using Ca(OH)2 suspension and H3PO4 solution including NaHCO3 as a carbonate source, and porous B-CAp ceramics with two different amounts of carbonate contents were fabricated by sintering freeze-dried mixtures of the powders and gelatin composite. The porous B-CAp ceramics prepared had three-dimensionally interconnected pores. The sinterability of B-CAp ceramics was dependent on the chemical composition, especially sodium content and vacancy of OH site, and the carbonate contents did not directly influence the dissolution rate of porous B-CAp ceramics.

Our recent efforts using primarily nanodiamonds as lubricant additives are discussed. For traditional high performance engine oils, our results show a reduction in friction for steel surfaces for both laboratory experiments under controlled conditions and in a pilot study of passenger cars under typical driving conditions. Examination of the surfaces suggests that surface polishing at the sub-micron scale may be responsible for these results. A separate set of experiments using a quartz crystal microbalance to measure dissipation and drag due to friction has shown that when added to water the charge of the nanodiamond acquired from surface functionalization can have a large influence on uptake and friction at the water-metal interface. More importantly, these results suggest the possibility of creating nanodiamonds with controllable frictional drag at the solid-liquid interface through surface processing. Companion simulation results for nanodiamonds in water sliding between diamond surfaces are also presented. Future possibilities for further understanding and tuning the properties of nanodiamonds as lubricant additives through synergistic experiments and modeling are also discussed.

Two types of TiN/HfOx/TiN devices have been fabricated where the top 200nm TiN electrode has been deposited by two different sputtering methods; reactive, using a titanium target in a nitrogen environment, and non-reactive, using a titanium nitride target. Characterization of the materials shows that the reactive TiN is single-phase stoichiometric TiN with a sheet resistance of 7Ω/square. The non-reactive TiN has a sheet resistance of 300Ω/square and was found to contain significant amounts of oxygen. The resistive switching behavior differs for both devices. The reactive stoichiometric TiN device results in bipolar switching with a Roff/Ron ratio of 50. The non-reactive TiN results in unipolar switching with a Roff/Ron ratio of more than 103, however this device shows poor reproducibility. These results show that an oxygen rich layer between the top electrode and insulator affects the Roff value. It supports the theory of oxygen vacancies leading to the formation of conductive filaments.

Scanning electronic microscopy (SEM), X ray diffraction (XRD) and photoluminescence (PL) have been applied to the study of structural and optical properties of ZnO nanocrystals prepared by the ultrasonic spray pyrolysis (USP) at different temperatures. The variation of temperatures and times at the growth of ZnO films permits modifying the ZnO phase from the amorphous to crystalline, to change the size of ZnO nanocrystals (NCs), as well as to vary their photoluminescence spectra. The study has revealed three types of PL bands in ZnO NCs: defect related emission, the near-band-edge (NBE) PL, related to the LO phonon replica of free exciton (FE) recombination, and its second-order diffraction peaks. The PL bands, related to the LO phonon replica of FE, and its second-order diffraction in the room temperature Pl spectrum testify on the high quality of ZnO films prepared by the USP technology.

A new route to producing microcrystalline silicon (µc-Si) thin films by re-crystallizing Si nanoparticle films by flash lamp method is presented. High quality Si nanoparticle films with high uniformity and high particle packing density were obtained using a stable non-aqueous Si nanoparticle suspension and the electrophoretic deposition (EPD) method. Morphology and crystallinity of as-deposited and flash lamp re-crystallized Si nanoparticle films were studied.