A key parametric study of ultrasonic exfoliation of 2D TiB2 using DI water as a unique medium.

Liquid Phase Exfoliation (LPE) is a very effective technique for the synthesis of few layered two dimensional (2D) nanosheets. There is a surge to find environment friendly solvents for efficient exfoliation of layered materials to produce 2D nanosheets. TiB2 is an important layered material with very little reported work on its 2D nanosheets. The present work is about successful LPE of TiB2 using deionized (DI) water as a clean, green and low cost dispersion medium to make TiB2 nanosheets. The impact of ultrasonication conditions i.e. input power and treatment duration for efficient synthesis of few layered 2D nanosheets in DI water is studied by Atomic Force Microscopy (AFM), X-Ray Diffraction (XRD) and Scanning Electron Microscopy (SEM). It is found that by increasing input power, the layer thickness is reduced from bulk to 34 nm with lateral dimensions as huge as up to 5 µm. The increased treatment duration has further reduced the layer thickness to 21 nm associated with a decrease in lateral dimensions to about 1 µm. The mechanism of variation in the aspect ratio of the 2D nanosheets with ultrasonication power and treatment duration is explained. The optimum conditions for the fabrication of high aspect ratio 2D nanosheets of TiB2 owe to a greater acoustic cavitation intensity, an optimum treatment duration and a homogenous distribution of the cavitation events while using an appropriate size of the sonotrode in the sonicated volume during ultrasonication.

Design of Multilayered 2D Nanomaterial Composite Structures for EMI Shielding Analysis.

It is still very challenging to effectively design nanocomposite microstructures with significantly improved electromagnetic interference shielding effectiveness (EMI SE). Herein, we developed a facile method for fabrication of molybdenum disulfide/graphene nanoplatelets (MoS2/GNPs) nanocomposites, in which GNPs are utilized as highly effective electrical transport materials, while MoS2 resolves the agglomeration problem of GNPs. GNPs also serve as an efficient cluster of electrical transport systems and dampen the incoming electromagnetic wave. Two types of samples are synthesized and compared in context of EMI SE values: physically mixed composite and layered samples. The sandwiched MoS2 between GNP layers showed an EMI SE of ∼24 dB, which was an almost 14% improvement relative to MoS2/GNPs nanocomposites exhibiting an EMI SE value of ∼21 dB, both containing 0.5 wt % GNPs. This work provides a new strategy for the design of multifunctional nanocomposites using the simple low-cost vacuum filtration method for EMI shielding for future applications.

Environmental treatment and remediation using h-BN based smart and hybrid membrane.

Corrosion is a major problem resulting from acid gases found in natural gas being transported in pipelines. To solve this problem, high aspect ratio h-BN nanosheets have been incorporated and are properly assimilated in the CA matrix, this led to an increase in tortuous path of flow for the gas resulting in smooth, dense membrane samples causing exceptional permeability reduction. Hexagonal Boron Nitride (h-BN) nanosheets have been synthesized and incorporated into cellulose acetate (CA) matrix using solution casting method. Nanosheets of various sizes, separated by varying centrifugation speeds (i.e. 500 rpm, 700 rpm, 1500 rpm, 2000 rpm and 2500 rpm), have been prepared and used for our work. The resulting nanocomposites, having thickness ranging between 40 and 60 µm, were then tested for CO2 gas permeability reduction using both short-term (8 h) tests as well as long-term (72-h tests). As a result of these tests, a maximum CO2 permeability reduction of 99.84% is found with a minimum CO2 permeability of 3.25 barrer. For dimensional analysis of both nanosheets and nanocomposites, scanning electron microscopy (SEM) analysis is used. For verifying the presence of the required functional groups in our synthesized samples, FT-IR spectroscopy is used. Moreover, to confirm the presence of crystalline phases, X-ray Diffraction (XRD) analysis is used. Also, tensile testing is used to analyze the mechanical robustness and it was found that nanocomposite samples exhibited higher tensile strength as compared to pristine samples. Furthermore, tribological property analysis was also carried out for adhesion testing of polymeric material with steel.

A flexible piezoresistive strain sensor based on laser scribed graphene oxide on polydimethylsiloxane.

Flexible strain sensors are an important constituent in soft robotics, health care devices, and in the defence industry. Strain sensors are characterized by their sensitivity (gauge factor-GF) and sensing range. In flexible strain sensors, simultaneously achieving consistency and high sensitivity has always been challenging. A number of materials and their derivatives have been explored to achieve balanced sensitivity with respect to sensing range with limited results. In this work, a low-cost flexible piezoresistive strain sensor has been developed using reduced graphene oxide (rGO) on polydimethylsiloxane (PDMS). The reduction has been performed using laser scribing, which enables the fabrication of arbitrary structures. After lead-out, the devices were again sandwiched in a layer of PDMS to secure the structures before performing their testing using a locally developed testing rig. Compared to previously reported graphene strain sensors, the devices fabricated in this work show relatively high GF with respect to sensing range. The GF calculated for stretching, bending and torsion was 12.1, 3.5, and 90.3 respectively, for the strain range of 0-140%, 0-130%, and 0-11.1%. A hand test was performed for the detection of joint movement. Change of resistance has been observed indicating muscle motion.

2D nanosheets and composites for EMI shielding analysis.

Liquid exfoliated, 2-dimensional (2D), few layered graphene and molybdenum disulfide nanosheets (GNS and MNS) are size selected for EMI shielding application. Scanning electron microscopy (SEM) has confirmed the lateral dimensions increase (1-2 µm for GNS and MNS) with lowering centrifugation speed (1000 to 500 rpm). The micron size (~ 15 µm) restacked structures of GNS and MNS (L ~ 2 µm) over a nylon membrane have shown ~ 16 dB and ~ 6 dB EMI shielding effectiveness (1-8 GHz frequency), respectively. The enhanced EMI shielding effectiveness for GNS-500 may be credited to its high carrier mobility as well as high aspect ratio of nanosheets. The GNS-500 are further dispersed (0.3 wt.%) in thermoplastic polyurethane for their applicability as flexible EMI shielding material. The dielectric characteristics predicted an enhancement for the attenuation (200 MHz-1 GHz). The experimental results (1-8 GHz) suggested the maximum attenuation ~ 18 dB showing the composite applicability as a broadband EMI shielding material.

PS/PANI/MoS2 Hybrid Polymer Composites with High Dielectric Behavior and Electrical Conductivity for EMI Shielding Effectiveness.

Liquid exfoliated molybdenum disulfide (MoS2) nanosheets and polyaniline (PANI) nanoparticles are dispersed in polystyrene (PS) matrix to fabricate hybrid polymer composites with high dielectric and electromagnetic interference (EMI) shielding behavior. A phase-separated morphology is formed when PANI and MoS2 are incorporated into polystyrene (PS) matrix. An increasing concentration of MoS2 nanoparticles inside PS/PANI (5 wt %) polymer blend forms an interconnected network, resulting in high electrical conductivity and dielectric behavior, making them a suitable candidate for EMI shielding application. An increment in dielectric constant and loss, up to four and five orders of magnitude, respectively, is recorded at a maximum concentration of 1 wt % of MoS2 in PS/PANI-5 polymer blend at 100 Hz. The enhanced dielectric characteristics for PS/PANI/MoS2 composites are then theoretically evaluated for the estimation of EMI shielding effectiveness in the frequency range of 100 Hz to 5 MHz. The maximum dielectric constant and loss achieved for PS/PANI-5 wt %/MoS2-1 wt % are responsible for estimated shielding effectiveness of around 92 dB at 100 Hz. The increase in dielectric behavior and shielding effectiveness is probably due to the increased number of charged dipoles accumulated at the insulator-conductor interface.

Self-assembly and wetting properties of gold nanorod-CTAB molecules on HOPG.

The formation of self-assembled superstructures of cetyltrimethylammonium bromide (CTAB) after drying on a nonwetting highly ordered pyrolytic graphite (HOPG) surface have been investigated using scanning electron microscopy (SEM) and atomic force microscopy (AFM). Although SEM did not reveal coverage of CTAB layers, AFM showed not only CTAB assembly, but also the dynamics of the process on the surface. The self-assembled layers of CTAB molecules on the HOPG terraces prior to nanorod deposition were shown to change the wettability of the surface, and as a result, gold nanorod deposition takes place on nonwetting HOPG terraces.

Uniaxial Drawing of Graphene-PVA Nanocomposites: Improvement in Mechanical Characteristics via Strain-Induced Exfoliation of Graphene.

Polyvinyl alcohol (PVA)-stabilized graphene nanosheets (GNS) of lateral dimension (L) ~1 µm are obtained via liquid phase exfoliation technique to prepare its composites in the PVA matrix. These composites show low levels of reinforcements due to poor alignment of GNS within the matrix as predicted by the modified Halpin-Tsai model. Drawing these composites up to 200 % strain, a significant improvement in mechanical properties is observed. Maximum values for Young's modulus and strength are ~×4 and ~×2 higher respectively than that of neat PVA. Moreover, the rate of increase of the modulus with GNS volume fraction is up to 700 GPa, higher than the values predicted using the Halpin-Tsai theory. However, alignment along with strain-induced de-aggregation of GNS within composites accounts well for the obtained results as confirmed by X-ray diffraction (XRD) characterization.

Enhancing the mechanical properties of BN nanosheet-polymer composites by uniaxial drawing.

We have used liquid exfoliation of hexagonal Boron-Nitride (BN) to prepare composites of BN nanosheets of three different sizes in polyvinylchloride matrices. These composites show low levels of reinforcement, consistent with poor alignment of the nanosheets as-described by a modified version of Halpin-Tsai theory. However, drawing of the composites to 300% strain results in a considerable increase in mechanical properties with the maximum composite modulus and strength both ∼×3 higher than that of the pristine polymer. In addition, the rate of increase of modulus with BN volume fraction was up to 3-fold larger than for the unstrained composites. This is higher than can be explained by drawing-induced alignment using Halpin-Tsai theory. However, the data was consistent with a combination of alignment and strain-induced de-aggregation of BN multilayers.