Добірка наукової літератури з теми "MoS2-polymer"

Since discovery of graphene, great attention had been paid to other two dimensional (2D) layered materials. As a graphene-like layered nanomaterial, molybdenum disulfide (MoS2) had gained enormous attention from the materials fields which had been widely used in many areas such as solid lubricants, lithium ion batteries, photocatalysts, sensors or as conductive fillers in polymer composites. In this work, MoS2 nanosheets were incorporated into polymer matrix as nanofillers by three typical preparation methods, including solvent blending, in situ polymerization and melt blending method. The MoS2 nanosheets were dispersed well in the polymer matrices which improved the thermal stability, mechanical properties and reduced fire hazards of the composites obviously. The improvements in the thermal properties, fire resistance properties and mechanical properties of polymer/MoS2 nanocomposites were mainly attributed to good dispersion of MoS2, physical barrier effects of MoS2 and catalytic char function of MoS2 nanosheets.

The objective of this study was to investigate a mechanism for enhancing the tribological properties of a green polymer material using MoS2, which is a common material with good tribological qualities. In this study, MoS2 nanoparticles were added to the biopolymer hydroxypropyl methylcellulose, obtaining an evident enhancement of the tribological behavior. The suitable content of MoS2 can provide the best structure of the composite film and optimize the transfer layer, and further enhance the tribological properties. The addition of 5–10% MoS2 particles to the polymer can improve the surface roughness up to 60%, reduce the friction coefficient of the thin-film material by more than 40% and reduce the wear rate of the substrate by 65%. The mechanism by which MoS2 additives enhance the tribological properties of the biopolymer material lies in the reduction of the run-in time in the initial stage of wear by modifying the surface roughness. This effect accelerates the formation of a transfer layer of good quality and provides good tribological properties.

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.

Hybrids of fluorinated graphite/MoS2 (FGr@MoS2) were prepared via a hydrothermal method and used as lubricating additives to take full advantage of the synergy between FGr and MoS2 in carbon-fiber-reinforced polymer (CFRP). The results show a 21.6% reduction in the friction coefficient compared to the neat sample when the CFRP was filled with 1.2 wt.% FGr@MoS2 hybrids. The addition of 1.5 wt.% FGr@MoS2 resulted in a 60.9% reduction in the wear rate compared to neat CFRP. For the 1.2 wt.% FGr@MoS2-reinforced CFRP, the friction coefficient maintained a relatively steady value of approximately 0.46 at various temperatures, indicating frictional stability. However, the wear rate increased by 13.95% at 60 ℃ compared to that at room temperature. The interfacial bonding force between the FGr@MoS2 hybrid and the matrix, as well as the adhesive force with the surface of the counterpart ball, is improved, caused by the heterostructure of FGr@MoS2, resulting in enhanced mechanical properties and formation efficiency as well as the transfer film on the surface of the counterpart ball. The results suggest that an FGr@MoS2 micro-nano structure is a promising additive to be applied in polymer tribology.

The graphene-like two dimensional (2D) inorganic materials have been been shown great interest for a variety of applications. In this work, polymer composite nanofibres containing molybdenum disulfide (MoS2) nanosheets were obtained by electrospinning. The MoS2 nanosheets were well dispersed inside the fibres, and the nanofibres maintained the fibre morphology well with the MoS2 nanosheets embedded. The incorporation of MoS2 nanosheets changes polymer nanofibre morphology from round to ribbon-like. Moreover, through thermogravimetric (TG) analysis and dynamic mechanical thermal analysis (DMTA) measurements, it was found that the MoS2 nanosheets as an additive material led to an increase in thermal stability and in the storage modulus. This work comprises an extensive approach to producing a novel 2D inorganic-organic composite structure, which should be applicable for membrane engineering with enhanced thermal and mechanical stability.

The reinforcement effects of liquid exfoliated molybdenum disulphide (MoS2) nanosheets, dispersed in polystyrene (PS) matrix, are evaluated here. The range of composites (0~0.002 volume fraction (Vf) MoS2-PS) is prepared via solution casting. Size selected MoS2 nanosheets (3~4 layers), with a lateral dimension L 0.5~1 µm, have improved Young’s modulus up to 0.8 GPa for 0.0002 Vf MoS2-PS as compared to 0.2 GPa observed for PS only. The ultimate tensile strength (UTS) is improved considerably (~×3) with a minute addition of MoS2 nanosheets (0.00002 Vf). The MoS2 nanosheets lateral dimension and number of layers are approximated using atomic force microscopy (AFM). The composites formation is confirmed using X-ray diffraction (XRD) and scanning electron microscopy (SEM). Theoretical predicted results (Halpin-Tsai model) are well below the experimental findings, especially at lower concentrations. Only at maximum concentrations, the experimental and theoretical results coincide. The high aspect ratio of MoS2 nanosheets, homogeneous dispersion inside polymer, and their probable planar orientation are the possible reasons for the effective stress transfer, resulting in enhanced mechanical characteristics. Moreover, the micro-Vickers hardness (HV) of the MoS2-PS is also improved from 19 (PS) to 23 (0.002 Vf MoS2-PS) as MoS2 nanosheets inclusion may hinder the deformation more effectively.

In this work, improved fracture toughness of tetra-functional epoxy polymer was obtained using two-dimensional (2H polytype) molybdenum disulfide (MoS2) nano-platelets as a filler. Simultaneous in-situ exfoliation and functionalization of MoS2 were achieved in the presence of cetyltrimethylammonium bromide (CTAB) via sonication. The aim was to improve the dispersion of MoS2 nanoplatelets in epoxy and enhance the interfacial interaction between nanoplatelets and epoxy matrix. Epoxy nanocomposites with CTAB functionalized MoS2 (f-MoS2) nanoplatelets, ranging in content from 0.1 wt% up to 1 wt%, were fabricated. Modified MoS2 improved the fracture properties (81%) of tetrafunctional epoxy nanocomposites. The flexural strength and compressive strength improved by 64% and 47%, respectively, with 0.25 wt% loading of f-MoS2 nanoplatelets compared to neat epoxy. The addition of f-MoS2 nanoplatelets enhanced the thermomechanical properties of epoxy. This work demonstrated the potential of organically modified MoS2 nanoplatelets for improving the fracture and thermal behavior of tetrafunctional epoxy nanocomposites.

A model is developed for the dielectric permittivity of polymer nanocomposites reinforced with transition metal dichalcogenide fillers at microwave frequencies. The model takes into account aggregation of nanoparticles into clusters (that involve both filler and matrix components) and the aspect ratio of aggregates. The governing equations involve four material parameters that are found by matching observations on the real and imaginary parts of the dielectric permittivity of polymers reinforced with MoS2 and WS2 micro- and nanospheres, MoS2 nanosheets and nanoflowers, and composite heterostructures formed by MoS2 and MoS2-CoS2 nanoparticles with graphene and reduced graphene oxide. Good agreement is demonstrated between results of simulation and the experimental data at frequencies in the S, X, and Ku bands of the electromagnetic spectrum. It is shown that composite heterostructures have superior dielectric properties compared with those of neat transition metal dichalcogenide nanoparticles.

The ability to convert photons into mechanical motion is of significant importance for many energy conversion and reconfigurable technologies. Establishing an optical-mechanical interface has been attempted since 1881; nevertheless, only few materials exist that can convert photons of different wavelengths into mechanical motion that is large enough for practical import. Recently, various nanomaterials including nanoparticles, nanowires, carbon nanotubes, and graphene have been used as photo-thermal agents in different polymer systems and triggered using near infrared (NIR) light for photo-thermal actuation. In general, most photomechanical actuators based on sp bonded carbon namely nanotube and graphene are triggered mainly using near infra-red light and they do not exhibit wavelength selectivity. Layered transition metal dichalcogenides (TMDs) provide intriguing opportunities to develop low cost, light and wavelength tunable stimuli responsive systems that are not possible with their conventional macroscopic counterparts. Compared to graphene, which is just a layer of carbon atoms and has no bandgap, TMDs are stacks of triple layers with transition metal layer between two chalcogen layers and they also possess an intrinsic bandgap. While the atoms within the layers are chemically bonded using covalent bonds, the triple layers can be mechanically/chemically exfoliated due to weak van der Waals bonding between the layers. Due to the large optical absorption in these materials, they are already being exploited for photocatalytic, photoluminescence, photo-transistors, and solar cell applications. The large breaking strength together with large band gap and strong light- matter interaction in these materials have resulted in plethora of investigation on electronic, optical and magnetic properties of such layered ultra-thin semiconductors. This dissertation will go in depth in the synthesis, characterization, development, and application of two- dimensional (2D) nanomaterials, with an emphasis on TMDs and molybdenum disulfide (MoS2), when used as photo-thermal agents in photoactuation technologies. It will present a new class of photo-thermal actuators based on TMDs and hyperelastic elastomers with large opto-mechanical energy conversion, and investigate the layer-dependent optoelectronics and light-matter interaction in these nanomaterials and nanocomposites. Different attributes of semiconductive nanoparticles will be studied through different applications, and the possibility of globally/locally engineering the bandgap of such nanomaterials, along with its consequent effect on optomechanical properties of photo thermal actuators will be investigated. Using liquid phase exfoliation in deionized water, inks based on 2D- materials will be developed, and inkjet printing of 2D materials will be utilized as an efficient method for fast fabrication of functional devices based on nanomaterials, such as paper-graphene-based photo actuators. The scalability, simplicity, biocompatibility, and fast fabrication characteristics of the inkjet printing of 2D materials along with its applicability to a variety of substrates such as plastics and papers can potentially be implemented to fabricate high-performance devices with countless applications in soft robotics, wearable technologies, flexible electronics and optoelectronics, bio- sensing, photovoltaics, artificial skins/muscles, transparent displays and photo-detectors.

碩士
國立臺灣海洋大學
光電科學研究所
107
We study the use of quantum dots (QDs) based on two-dimensional materials to enhance the power conversion efficiency (PCE) of polymer solar cells. In this work, P3HT and PC61BM were used as the active layer of the polymer solar cells. Based on this structure, the p-type two-dimensional MoS2 QDs were added to the active layer precursor solution to form the ternary mixture for the active layer. We found that the ternary hybrid solar cell with p-type MoS2 QDs exhibited superior performance than that of the solar cells without MoS2 QDs. The best PCE was found to be 4.04 % for the solar cells with 4 vol% MoS2 QDs which was an increase of 8.60 % compared to that for the solar cells without MoS2 QDs (3.72%). The p-type MoS2 QDs as an additive were found to improve the short-circuit current of the polymer solar cell, and the short-circuit current was increased from 9.74 mA/cm2 to 10.49 mA/cm2. The overall improvement in performance was due to the increased crystallinity of P3HT, which is more orderly and thus improved the absorption of sunlight and the mobility of hole carriers.

This thesis deals with the research work carried out on the properties and applications such as GaN nanoparticles, Graphene etc. Chapter 1 of the thesis gives introduction to nanomaterials and various aspects of the thesis. Chapter 2 of the thesis describes the synthesis of GaN nanocrystals and their use as white light sources and as room temperature gas sensors. It also discusses negative differential resistance above room temperature exhibited by GaN. Electroluminescence from GaN-polymer heterojunction forms the last section of this chapter. Chapter 3 demonstrates the role of defect concentration on the photodetecting properties of ZnO nanorods with different defects prepared at different temperatures. Chapter 4 presents remarkable infrared and ultraviolet photodetector properties of reduced graphene oxide and graphene nanoribbons. Chapter 5 presents the infrared detecting properties of graphene-like few-layer MoS2. The summary of the thesis is given at the end of the thesis.

The ever increasing demand for energy due to over consumption of non-renewable fossil fuels has emphasized the need for alternate, sustainable and efficient energy conversion and storage systems. In this direction, electrochemical energy conversion and storage systems involving various fundamental electrochemical redox processes such as hydrogen evolution (HER), oxygen reduction (ORR), oxygen evolution (OER), hydrogen oxidation (HOR) reactions and others become highly important. Electrocatalysts are often used to accelerate the kinetics of these reactions. Platinum (Pt), ruthenium oxide and iridium oxide (RuO2 and IrO2) are known to be the state of the art catalysts for several of these reactions due to favouarable density of states (DOS) near the Fermi level, binding energy with the reactant species, chemical inertness etc. Apart from HER, OER and ORR, chlorine evolution reaction (Cl-ER) is another industrially important reaction associated with water purification, disinfection, bleaching, chemical weapons and pharmaceuticals. Dimensionally stable anodes (RuO2/IrO2 mixed with TiO2 on Ti) are the most commonly used catalysts for this process. Issues related to surface poisoning, corrosion and cost of the catalysts, in addition to selectivity and specificity towards a particular reaction are various aspects to be addressed. For example, Pt is not very specific for ORR in presence of methanol in addition to high cost and corrosion in certain media. On the other hand, DSA can efficiently catalyze both OER and Cl-ER, and hence there is overlap of the two processes in the potential range available. There is an on going search for efficient, cost-effective, stable catalysts that possess high specificity for a particular redox reaction. Towards this goal, the present study explores certain layered (phospho)chalcogenides for catalyzing HER, ORR, OER and Cl-ER. The present thesis is structured in two parts, where the first part explores the multi-functional catalytic aspects of new classes of compounds based on layered transition metal mixed chalcogenides (MoS2(1-x)Se2x) and ternary phosphochalcogenides (FePS3, FePSe3 and MoPS). In addition, lithium insertion and desinsertion has been studied with the aim of using the layered materials for rechargeable batteries. The second part of the thesis explores organic electrode materials with active carbonyl groups such as rufigallol, polydihydroxyanthrachene succinic anhydride (PDASA) as battery electrodes. Additionally, covalently functionalized transition metal phthalocyanines with reduced graphene oxide are studied as counter electrodes in dye sensitized solar cells (DSSCs). MoS2(1-x)Se2x (x = 0 to 1) compositions are solid solutions of MoS2 and MoSe2 in different ratios. They crystallize in hexagonal structure with space group P63/mmc (D6h4) having Mo in trigonal prismatic coordination like the pristine counterparts. X-Ray diffraction studies reveal that Vegard’s law (figure 1a) is followed and hence complete miscibility of MoS2 and MoSe2 is established. MoS2(1-x)Se2x (x = 0 to 1) are layered in nature and the layers are held together by long range, weak van der Waal’s forces. This gives us the flexibility of exfoliation to produce corresponding few-layer materials (figure 1b). Figure 1. (a) Variation of lattice parameter corresponding to (002) reflection of MoS2(1-x)Se2x with different x values. (b) Scanning electron micrograph of few-layer MoS2(1-x)Se2x (x = 0.5). The electrocatalytic activity of the few-layer sulphoselenides have been studied towards HER in aqueous 0.5 M H2SO4 and towards Cl-ER in 3 M aqueous NaCl (pH = 3) solution. The mixed chalcogenides exhibit very good activities for both HER and Cl-ER as compared to the activity of their pristine counter parts (i.e. MoS2 and MoSe2) (figures 2a and 2b). Electrocatalytic activity on different compositions reveal that MoS1.0Se1.0 exhibits the maximum activity. Additionally, it has been observed that MoS1.0Se1.0 shows high specificity for Cl-ER with negligible interference of OER. Figure 2. Voltammetric data for (a) hydrogen evolution reaction (in 0.5 M aqueous H2SO4) and (b) chlorine evolution reaction (in 3 M aqueous NaCl solution, pH = 3) on MoS2(1-x)Se2x (x = 0, 0.5, 1). Figure 3. (a) XRD pattern of MoS2(1-x)Se2x (x = 0.5) electrode after a cycle of Li insersion and deinsersion (red) along with as-synthesized material (black) (b) Cycling behaviour of rGO supported (black) and pristine (red) MoS2(1-x)Se2x (x = 0.5) as electrode in rechargeable lithium-ion battery. The equiatomic MoS1.0Se1.0 has also been studied as an anode material for rechargeable lithium batteries. The cyclic voltammogram and characterization after charge-discharge cycle (figure 3a) indicate intercalation of Li with in the layers followed by conversion type formation of Li-S and Li-Se type compounds. The pristine material shows continuous capacity fading while the composites of sulphoselenides functionalized with conducting carbon supports such as rGO, MWCNT, super P carbon, toray carbon show marked improvement in capacity as well as cycling behavior. The rGO functionalized MoS1.0Se1.0 reveals ~1000 mAh/g of stable specific discharge capacity for 500 cycles (figure 3b). In the next two chapters, new class of transition metal-based layered materials FePS3 and FePSe3, containing both P and chalcogen (S and Se) is indroduced for electrocatalysis. FePS3 crystallizes in monoclinic symmetry with an indirect band gap of ~1.55 eV while FePSe3 possesses rhombohedral crystal structure with comparatively low band gap (~1.3 eV) as shown in figure 4a. The FePS3 and FePSe3 have been exfoliated as has been done for MoS1.0Se1.0 (liquid exfoliation method) using acetone as the solvent. Stable colloids with few-layer nanosheets having lamellar morphology and lateral sizes of ~100 to 200 nm are obtained. Electrical characterization indicates that they are semiconducting and the conductivity of the Se analogue is ~50 times higher than that of the S analogue (figure 4b). Figure 4. (a) Catholuminescence of FePX3 ( X = S and Se) reveals the band gap of the material. Band gap of the S analogue is 1.52 eV and that of the Se analogue is 1.33 eV (b) Resistivity of FePX3 ( X = S and Se) as a function of temperature. The tri-functional electrocatalytic activities on rGO-few layer FePX3 (X = S and Se) have been evaluated for HER over a wide pH range (0.5 M H2SO4, 0.5 M KOH, phosphate Figure 5. Catalytic activity of rGO-few-layer FePX3 (X = S, Se) towards HER in (a) aqueous 0.5 M H2SO4 and (b) 3.5 wt % NaCl solutions. (c) ORR activity of the catalysts in oxygen saturated 0.5 M KOH (d) OER behaviour on the catalysts in 0.5 M KOH at a rotation speed of 1600 rpm. buffer, pH 7 and 3.5 % NaCl), ORR and OER in alkaline media (0.5 M KOH). The studies clearly reveal that both rGO-FePS3 and rGO-FePSe3 exhibit excellent HER activity in acidic media (figure 5a) with high stability. The HER studies in 3.5 wt % aqueous NaCl solution (figure 5b) suggests that the catalysts are effective in evolving hydrogen from sea-water environment. Studies on ORR activity (figure 5c) indicate that the rGO composites of both S and Se analogues follow 4-electron pathways to produce water as the final product. They are also found to be highly methanol tolerant. In the case of OER (figure 5d), XPS characterization of the electrodes after the voltammetric studies reveals the presence of very thin layer of Fe2O3 (not detectable by XRD). All the three reactions (HER, ORR and OER) catalyzed by the Se analogue are better than the S analogue (figure 5). This could be due to the low band gap and high conductivity of FePSe3 as compared to FePS3. The over potential to achieve 10 mAcm-2 current density is ~108 mV for rGO-few-layer FePS3 catalyst where in the case of rGO-few layer FePSe3, it is ~97 mV (table 1). Table 1. Catalytic activities of rGO-few layer FePS3 and rGO-few layer FePSe3 towards HER, ORR and OER. Reaction studied rGO-FePS3 rGO-FePSe3 HER (η @ 10mAcm-2) ~108 mV ~97 mV ORR (peak potential) ~0.81 V ~0.87 V OER (η @ 10mAcm-2) ~470 mV ~430 mV It is likely that there is a strong interaction between FePX3 (metal d-orbital) and rGO, as observed from the downward shift of Fe 2p peak in high resolution XPS studies. This interaction may extend the density of states of metal d-orbitals thereby improving the catalytic activities. The next chapter deals with molybdenum-based phosphosulphide compound (MoPS). Molybdenum-based phosphide catalysts have been explored recently as excellent catalysts for various electrochemical reactions such as HER. It is expected that the catalyst containing both S and P will show positive effects on catalytic activities due to the synergy between S and P. In the present study, P incorporated MoS2 is studied towards HER. The XRD pattern of the as-synthesized crystal suggests the presence of mixed phase of MoS2, MoP2 and MoP while the elemental mapping in microscopy indicates the ratio of Mo, P and S to be 1:1:1. The electrochemical HER in 0.5 M H2SO4 indicates that the activity is improved drastically as compared to bulk and few-layer MoS2. The next section explores the use of different organic electrode materials possessing active carbonyl groups for Li-storage studies. The advantage of the use of carbonyl-based compounds lies in the high reversible activity towards Li ion insersion and de-insersion. Rufigallol (figure 6a) exhibits very stable capacity of ~200 mAh/g (at C/20 rate) upto 500 Figure 6. (a) and (c) Schematic representation of rufigallol and poly-dihydroanthracene succinic anhydride (PDASA) respectively. (b) and (d) Cyclic behaviour of rufigallol (at C/20 rate) and PDASA (at 20 mAg-1 current rate) in Li-storage devices. (e) and (f) represent the coulombic efficiency of rufigallol (at C/20 rate) and PDASA (at 20 mAg-1 current rate) as a function of number of cycles. cycles along (figure 6b) and with very good rate capability. A triptycene-based mesoporous polymer, PDASA (figure 6c) is introduced and explored as efficient electrode material for Li-storage. PDASA exhibits very high capacity of ~1000 mAh/g at a current rate of 50 mA/g upto 1000 cycles (figure 6d). Even at very high current rates (3A/g) excellent cyclability is observed. The mechanistic details of lithium uptake and release are studied using various spectroscopic techniques. In both the cases the coulombic efficiency observed is ~80 to 90 % (figures 6e and f). Figure 7. (a) Digital photograph of the dye sensitized solar cell with rGO-Co-TAPc counter electrode. (b) Photoconversion efficiency of DSSCs with different counter electrodes as mentioned in the figure. (c) Photo conversion efficiency of Pt and rGO-Co-TAPc based DSSCs as function of storage time. (d) Schematic illustration of DSSC wherein the energy level of the counter electrodes and electrolyte are shown for different M-TAPcs. In a slightly different direction, metal phthalocyanine - rGO composites (rGO-M-TAPc; M = Co, Zn, Fe) have been explored as counter electrodes in DSSC. Figure 7a depicts the digital image of a DSSC constructed using rGO-Co-TAPc as the counter electrode. It has been observed that rGO-cobalt tetraamino phthalocyanine (rGO-Co-TAPc) counter electrode exhibits ~6.6 % of solar conversion efficiency (figure 7b) and is close to that of standard DSSC (Pt counter electrode) under identical experimental conditions and are highly stable (figure 7c). Other metal phthalocyanines show less efficiency and is analysed based on the relative positions of HOMO energy levels of the materials and the energy level of the redox system (I-/I3- system) as given in figure 7d. The thesis contains eight chapters on aspects discussed above along with summary and future perspectives given at the end. It is devided into various chapters in two sections, one comprising inorganic chalcogenide-based electrocatalysts and another comprising organic electrode materials. Appendix I discusses the Na-storage behaviour of MoS1.0Se1.0 and appendix II describes the Li-storage behaviour of rGO functionalized benzoquinone and diamino anthraquinone electrode materials.

AbstractThe aim of this work was to design and optimize compositions of three-component composites based on polyetheretherketone (PEEK) with enhanced tribological and mechanical properties. Initially, two-component PEEK-based composites loaded with molybdenum disulfide (MoS2) and polytetrafluoroethylene (PTFE) were investigated. It was shown that an increase in dry friction mode tribological characteristics in metal-polymer and ceramic-polymer tribological contacts was attained by loading with lubricant fluoroplastic particles. In addition, molybdenum disulfide homogenized permolecular structure and improved matrix strength properties. After that, a methodology for identifying composition of multicomponent PEEK-based composites having prescribed properties which based on a limited amount of experimental data was proposed and implemented. It was shown that wear rate of the “PEEK + 10% PTFE + 0.5% MoS2” composite decreased by 39 times when tested on the metal counterpart, and 15 times on the ceramic one compared with neat PEEK. However, in absolute terms, wear rate of the three-component composite on the metal counterpart was 1.5 times higher than on the ceramic one. A three-fold increase in wear resistance during friction on both the metal and ceramic counterparts was achieved for the “PEEK + 10% PTFE + 0.5% MoS2” three-component composite compared with the “PEEK + 10% PTFE”. Simultaneous loading with two types of fillers slightly deteriorated the polymer composite structure compared with neat PEEK. However, wear rate was many times reduced due to facilitation of transfer film formation. For this reason, there was no microabrasive wear on both metal and ceramic counterpart surfaces.

For an effective EMI shielding, materials should have high electrical conductivity as EMI attenuation is a sum of relfection, absorption, and multiple relfections which requires the existence of mobile charge carriers (electrons or holes), electric and/or magnetic dipoles, usually provided by materials having high dielectric constants (ε) or magnetic permeability (μ) and the large surface area or interface area. Until now, a metal shroud was the material of choice as an EMI shield. However, metal fillers add additional weight and are susceptible to corrosion, making them less desirable. Therefore, we have focused on new emerging two-dimensional 2D nanomaterials that are light in weight and have a low cost. Here, the focus is to address the challenges in their synthesis especially transition metal carbides (MXenes), MoS2, functionalized graphene/ferromagnetic conducting polymer composites, and their fabrication for EMI reductions. These articles also evaluate and explain the recent progress explicitly and underline the complex interplay of its intrinsic properties of 2D nanostructured materials (MXene, MoS2, Graphene/ferromagnetic polymer composite) as a potential candidate for EMI shielding and evaluate their electromagnetic compatibility. The chapter will cover the facets related to a newly emerging area of EMI shields in the automotive industry, especially lithium-ion battery-operated electric vehicles and self-driving cars, high-speed wireless communication devices, and next-generation mobile phones with 4G and 5G technology.

This chapter describes the use of Raman spectroscopy and mapping analysis for the characterization of low dimensional nanostructures, including 2D sheets (graphene oxide, graphene sheets, MoS2, siloxene), and one-dimensional carbyne chains. The Raman mapping analysis and their application towards understanding the molecular level interactions in these low dimensional materials, nanostructured polymer composites, and nanopaints are also discussed. The stoichiometric composition and structure of these low dimensional materials were correlated with the Raman spectral and mapping analysis. Further, Raman spectroscopy for understanding or probing the mechanism of mechanical to electrical energy harvesting properties of carbyne films via the structural transformation from cumulene to polynne networks of carbyne is demonstrated.

Abstract Infrared (IR) thermography is a non-contact method of measuring temperature that analyzes the infrared radiation emitted by an object. Properties of polymer composites are heavily influenced by the filler material, filler size, and filler dispersion, and thus thermographic analysis can be a useful tool to determine the curing and filler dispersion. In this study, we investigated the curing mechanisms of polymer composites at the microscale by capturing real-time temperature using an IR Thermal Camera. Silicone polymers with fillers of Graphene, Graphite powder, Graphite flake, and Molybdenum disulfide (MoS2) were subsequently poured into a customized 3D printed mold for thermography. The nanocomposites were microscopically heated with a Nichrome resistance wire, and real-time surface temperatures were measured using different Softwares. This infrared thermal camera divides the target area into 640 × 480 pixels, allowing measurement and analysis of the sample with a resolution of 65 micrometers. Depending on the filler material, the temperature rises to a certain maximum point before curing, and once curing is complete, polymer composites exhibit a rapid temperature change indicating a transition from viscous fluid to solid. MoS2, Polydimethylsiloxane (PDMS) without filler, and PDMS with larger filler are ranked in order of maximum constant temperature. PDMS (without filler) cures in 500s, while PDMS-Graphene and PDMS Graphite Powder cure in about 800s. The curing time for PDMS Graphite flake is slightly longer (950s), while MoS2 is around 520s. Therefore, this technique can indicate the influence of fillers on the curing of composites at the microscale, which is difficult to achieve by conventional methods such as differential scanning calorimetry. This nondestructive, low-cost, fast infrared thermography can be used to analyze the properties of polymer composites with different fillers and dispersion qualities in a variety of applications including precision additive manufacturing and quality control of curable composite inks.

MoS2 multi-component nanolubrication system showed significant friction and wear reduction (more than 30% in friction reduction and 50% in wear reduction) in sliding steel surfaces, especially under mixed and boundary lubrication conditions [1–3]. It is believed that the formation of tribofilms in MoS2 multi-component nanolubrication system under different lubrication regimes is the primary reason for reduced friction and wear. To investigate the in-depth science of the tribo-chemical interface formed by MoS2 multicomponent nanolubrication system, it is necessary to study the chemical states of tribofilm during its evolution (generation ↔ regeneration) process at tribo-interfaces. Tribofilms from various lubrication regimes were characterized by scanning electron microscope (SEM), energy dispersive X-ray spectroscopy (EDX), Raman microscope, and X-ray photoelectron spectroscopy (XPS) techniques to study the morphology, chemical composition, elemental distribution, and chemical bonding of tribo-chemical surface, respectively. Besides the evolution process, the characterization of tribofilms also reveals the possibility of forming new meta-stable phases (chemical compounds) after tribological testing. Patchy tribofilms and progressive tribofilms have been observed from the SEM analysis and the EDX results showed existence of Mo-S-P as the composition of tribo-chemical films. The Raman spectroscopy analysis of tribofilms showed significant difference (such as formation of poly-molybdates) in chemical information of nanolubricants and tribofilms, which is an indication of the formation of friction polymer [4–5]. Additionally, phosphates and oxides, acting as components of surface protecting layer of tribofilms, have been found on surface by XPS technique. Moreover, MoS2 nanoparticles are found to navigate into surface asperities to protect the contacting surfaces. The results (information about the chemical states of the tribofilm) obtained from different characterization techniques can be used to explain the mechanism of friction and wear reduction associated with MoS2 multi-component nanolubrication system that has been reported in the literature.

The friction and wear properties of polymer were investigated under a hydrogen atmosphere, by using PTFE (polytetrafluoroethylene) and two kinds of PTFE composites. Experiments were also conducted in air, nitrogen, and vacuum environment. The experiment carried out by pin-on-disk friction and wears apparatus in the vacuum chamber. Pin specimens are no filling PTFE, Gr-filled PTFE (Gr filled with 25 wt%) and MoS2–filled PTFE (MoS2 filled with 25 wt%). Friction disk is aluminum alloy 6061-T6 with 0.02μm surface roughness. Aluminum alloy 6061-T6 is able to use for apparatus for hydrogen. After experiments, specific wear rate was calculated, specimen surface, wear track and wear debris were observed, surface profile of the wear track were measured. The specific wear rate of unfilled PTFE and PTFE/MoS2 of in air was lower than the other atmospheres. The A6061-T6 disk was worn by PTFE pin specimens and in the case of wear track was much rougher, the specific wear rate of pin specimens tended to increase without unfilled PTFE in air and PTFE/Gr.

Abstract Climate change and its related effects are imposing severe stress on the current freshwater supplies. This has been exacerbated due to the growth in population, rapid industrialization, and increased energy demand. Increased water requirement is a global challenge. Although more than 70% of the Earth is covered by water, much of it is unusable for human use. Freshwater reservoirs, ponds, and subterranean aquifers account for just 2.5% of the world’s overall freshwater availability. Unfortunately, these water supplies are not very unevenly spread. Therefore, the need to augment these supplies through the desalination of seawater or brackish water. Reverse osmosis (RO) is currently the most widespread method of desalination. However, the unit cost of water is still high partly due to the thin-film composite (TFC) polymer membranes used in the current desalination system. Thus the need for low-cost nanomaterials for Water Desalination and Purification. A promising way to meet this demand is to use two-dimensional (2D) nanoporous materials such as graphene and MoS2 to minimize energy consumption during the desalination process. New nanotechnology methodologies that apply reverse osmosis have been developed. Among some of these technologies is using 2D materials such as graphene and MoS2, which have been studied extensively for water desalination. Single-layer nanoporous 2D materials such as graphene and MoS2 promises better filtrations in the water channel. Although single-layer MoS2 (SL_MoS2) membrane have much promise in the RO desalination membrane, multilayer MoS2 are simpler to make and more cost-efficient. Building on the SL_MoS2 membrane knowledge, we have used the molecular dynamics method (MD) to explore the effects of multilayer MoS2 in water desalination. This comparison is made as a function of the pore size, water flow rate and salt rejection. In addition, we also looked at the effect of the increased interlayer spacing between layers of the nanoporous 2D membrane and then made the comparison. The ions rejection follows the trend trilayer> bilayer> monolayer from results obtained, averaging over all three membrane types studied for the MoS2, the ions rejection follows the trend trilayer > bilayer > monolayer. We find that the thin, narrow layer separation plays a vital role in the successful rejection of salt ions in bilayers and trilayers membranes. These findings will help build and proliferate tunable nanodevices for filtration and other applications.

Fullerene-like WS2 (MoS2) nanoparticles (IF) have been studied in the past [1–3] Their efficacy as additives for lubrication fluids has been demonstrated. [4–5] Recently, IF-WS2 nanoparticles were confined inside a porous and densified bronze-graphite matrix, prepared by powder metallurgy (PM) technique. Substantial reduction in both friction and wear, and an increase in the critical load were observed [6]. New applications of IF nanopartcles as development of polymer nanocomposites, burnishing and friction of ceramic materials under severe contact conditions are presented in this work.

The surfaces of a ball-joint (diam. 10 m and weight 680 tons) used for the rotation of two retaining walls of a storm surge near Rotterdam are initially covered with a sliding spray of MoS2 and PTFE, but suffer wear. Lubricants in heavy-loaded constructions should most likely be avoided, implying a new design of the sliding surfaces by incorporation of polymer discs into holes (diam. 250 mm and depth 32 mm) tapped onto the back-scales of the joint. This study comprises theoretical and practical analysis of the contact situation, using FEM and full-scale test equipment for verification of the local static and dynamic behaviour of the polymer parts.