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In this study, we implemented a functionalization process on the surface of silicon nanowires (SiNWs) which were fabricated by chemical vapour deposition (CVD) method in a low-pressure CVD (LPCVD) chamber. Surface functionalization was carried out in three stages: hydroxylation of the surface with piranha solution, silanization with a solution of 3-Aminopropyl triethoxysilane (APTES) in n-hexane, and finally functionalization with folic acid as a detection agent. Optical spectroscopy and electron microscopy techniques were used to experimentally characterize materials. Surface functionalization was evaluated using Attenuated Total Reflectance Fourier-Transform Infrared spectroscopy (FTIR-ATR), Field Emission Scanning Electron Miscoscopy (FESEM), and Transmission Electron Microscopy (TEM). Cell adhesion to functionalized and non-functionalized silicon nanowires was compared; a cell assay analysis on lung metastatic cells was conducted. Lung cancer metastatic QUDB cells were seeded on a SiNWs surface in RPMI1640 complete medium. To evaluate the adhesion of cancer cells to these surfaces FESEM imaging was used. The number of cancer cells trapped on the folic acid functionalized SiNWs was found to be approximately 3 times higher than that of the non-functionalized ones. This article is protected by copyright. All rights reserved

Hydrophobic mica particles were prepared by piranha solution activation, silanization, and copolymerization with acrylate monomers. Its surface morphology, hydrophilic properties, and thermogravimetric analysis changed differently in comparison with those of pristine mica. Scanning electron microscopy (SEM) showed that the modified (001) mica surface changed from flat to coarse. Thermogravimetric curves demonstrated that silane coupling agents and the grafted polymer were anchored on the modified-mica surface. The alternating surface polarity state was verified by different dispersion performances in the solvents. SEM images showed that the polypropylene (PP)/modified-mica composites had a better quality compatibility than the PP/untreated-mica composites. The PP/polymer-grafted-mica composites had improved mechanical properties, including stretching, tension, and impact properties. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017, 134, 44985.

Purpose The purpose of this in vitro study was to compare the shear bond strength of an airborne-particle abraded zirconia, an acid-etched zirconia (Piranha solution), an Alloy Primer treated zirconia, and a silaned zirconia to enamel, all bonded with a phosphate-methacrylate resin luting agent. Materials and Methods Seventy extracted intact human molars were collected, cleaned, and mounted in autopolymerizing acrylic resin, with the experimental surface of the teeth exposed. The specimens were randomly divided into seven groups of zirconia specimens (4 mm diameter, 2 mm thick). Group 1: Airborne-particle abrasion; group 2: Airborne-particle abrasion and Z-PRIME Plus; group 3: Airborne-particle abrasion and alloy primer; group 4: Piranha solution 7:1; group 5: Piranha solution 7:1 and Z-PRIME Plus; group 6: Piranha solution 7:1 and Alloy primer; group 7: CoJet and silane. All specimens were luted with a phosphate-methacrylate resin luting agent (Panavia F2.0) and stored in distilled water for 1 day, then thermocycled (5°C and 55°C) for 500 cycles and tested for shear bond strength (SBS), measured in MPa, with a universal testing machine at a 0.55 mm/min crosshead speed. All specimens were inspected under a scanning electron microscope to determine mode of failure. The mean values and standard deviations of all specimens were calculated for each group. A one-way ANOVA was performed, and multiple pairwise comparisons were then completed with post hoc Tukey test (alpha = 0.05). Results The airborne-particle abrasion and Z-PRIME Plus group resulted in a significantly higher SBS than the other groups (21.11 ± 6.32 MPa) (p < 0.001). The CoJet and silane group (15.99 ± 8.92 MPa) and airborne-particle abrasion and alloy primer group (11.07 ± 4.34 MPa) showed high shear bond strength but not statistically significant from the airborne-particle abrasion group (14.23 ± 5.68 MPa). Failure mode was predominately mixed in groups 1, 2, 3, and 7 with islands of retained resin on the zirconia and enamel surfaces; however, groups 4, 5, and 6 showed mostly adhesive failures, which left the zirconia surface free of the adhesive materials. No cohesive failures of the substrates (ceramic, resin, or enamel) were observed. Conclusion Airborne-particle abrasion followed by the application of a zirconia primer produced the highest bond strength to enamel. Therefore, it can be recommended as a promising surface treatment method to achieve a durable bond to densely sintered zirconia ceramics.

Successful realization of various BioMEMS devices demands effective surface modification techniques of PDMS elastomer. This paper presents a detailed report on a simple and cost effective approach for surface modification of PDMS films involving wet chemical treatment in two-step processes: primarily involving piranha solution followed by KOH dip to improve hydrophilicity and stability of PDMS surface. Chemical composition of the solution and surface treatment condition have been varied and optimized to significantly increase the surface energy. The effect of surface modification of the elastomer after wet chemical treatment is analyzed using contact angle measurement and FTIR-ATR study. PDMS surface treated in piranha solution with H2O2 and H2SO4 in the ratio of 2:3 followed by a dip in KOH solution for 15 min duration each, demonstrated a maximum reduction of contact angle to ∼27° as compared to untreated sample having a contact angle of ∼110°. The removal of hydrophobic methyl group from elastomer surface and subsequent hydrophilization of surface by wet chemical process was confirmed from FTIR-ATR spectra. This result is also supported by improved adhesion and electrical continuity of deposited aluminum metal film over the modified PDMS surface. Copyright © 2011 John Wiley & Sons, Ltd.

Nanoscale changes to the surface of polymeric materials enables changes in materials' adhesion, wettability, printability, chemical functionality, and bioactivity, while maintaining desirable bulk properties. Polymer surface modification is therefore used in applications such as antimicrobial or non-fouling materials, biosensors, and active packaging. The range of available modification and analytical techniques used across laboratories prevents accurate comparison of techniques in terms of their effects on surface chemistry and topography. It was therefore our goal to evaluate the effects of four surface modification techniques (chromic acid, piranha solution, ultraviolet irradiation, and oxygen plasma) on polyethylene films. Changes in surface chemistry and topography were quantified using attenuated total reflectance (ATR) Fourier transform infrared (FTIR) spectroscopy, atomic force microscopy (AFM), contact angle measurement, and direct measurement of available surface carboxylic acids. Roughness increased in the order: piranha (57.7 nm); oxygen plasma (76.3 nm); UV irradiation (76.4 nm); chromic acid (120 nm). Hydrophobicity decreased in the order: piranha (77.20), chromic acid (73.50), oxygen plasma (61.70), UV irradiation (58.70). Functionalization (by IR absorbance intensity between 1680–1780 cm−1) increased in the order: oxygen plasma (0.06), piranha (0.09), chromic acid (0.34), UV irradiation (0.50). By analyzing these methods using consistent analytical techniques, side-by-side comparisons have been accurately made. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011

Chemical modifications on the surface of optical fibers have played an important role in the immobilization of biological recognition molecules. In this article, the specific goal was to characterize the covalent bond on the surface of optical fiber by scanning electron microscopy and energy dispersive X-ray spectrometry (EDS) and chemical analysis after silanization. Optical fibers pretreated with hydrofluoric acid and piranha solution were silanized in the 3-aminopropyltriethoxysilane solution, then microscopic components of silanized optical fibers were determined to validate the silanization. Results showed that carbon atom was measured with EDS, and the ratio of silicon and oxygen atom was 1:3.6 on its surface by calculation. Fluorescence experiments on the short silanized optical fiber segments indicated that the intensity of fluorescence was relatively weak and reached equilibrium after 3 h. Both methods, EDS and fluorescence test, were effective to characterize the covalent bond of different silanes and biological recognition molecules on the optical fibers for biosensor applications. Copyright © 2009 John Wiley & Sons, Ltd.

Pseudo-one dimensional (pseudo-1D) materials are a new-class of materials where atoms are arranged in chain like structures in two-dimensions (2D). Examples include recently discovered black phosphorus, ReS2 and ReSe2 from transition metal dichalcogenides, TiS3 and ZrS3 from transition metal trichalcogenides and most recently GaTe. The presence of structural anisotropy impacts their physical properties and leads to direction dependent light-matter interactions, dichroic optical responses, high mobility channels, and anisotropic thermal conduction. Despite the numerous reports on the vapor phase growth of isotropic TMDCs and post transition metal chalcogenides such as MoS2 and GaSe, the synthesis of pseudo-1D materials is particularly difficult due to the anisotropy in interfacial energy, which stabilizes dendritic growth rather than single crystalline growth with well-defined orientation. The growth of monoclinic GaTe has been demonstrated on flexible mica substrates with superior photodetecting performance. In this work, we demonstrate that pseudo-1D monoclinic GaTe layers can be synthesized on a variety of other substrates including GaAs (111), Si (111) and c-cut sapphire by physical vapor transport techniques. High resolution transmission electron microscopy (HRTEM) measurements, together with angle resolved micro-PL and micro-Raman techniques, provide for the very first time atomic scale resolution experiments on pseudo-1D structures in monoclinic GaTe and anisotropic properties. Interestingly, GaTe nanomaterials grown on sapphire exhibit highly efficient and narrow localized emission peaks below the band gap energy, which are found to be related to select types of line and point defects as evidenced by PL and Raman mapping scans. It makes the samples grown on sapphire more prominent than those grown on GaAs and Si, which demonstrate more regular properties., 15 pages, 3 figures, supplement (submitted version)