Nanocomposite Structure Research Articles

Investigation of tribological behavior of MOFs/g-C3N4 nanocomposite for insight into effect of flake-on-sheet and ball-on-sheet nanostructure

Herein, we designed two catalogs of metal organic frame materials (MOF)/carbon nitride(g-C3N4) composite nanostructures (flake-on-sheet and ball-on-sheet nanostructure appearances) to probe the effect of composite nanostructures on the cooperative friction mechanism. The tribological behaviors of MOF/g-C3N4 composite nanostructures were extensively investigated in base oil on the four-ball friction tester. The results showed that the anti-wear ability of flake-on-sheet shaped MOF/g-C3N4 in oil was superior to the ball-on-sheet shaped MOF/g-C3N4, whereas the anti-friction and load-bearing ability of latter was preferable to the former. The flake-on-sheet shaped MOF/g-C3N4 enabled the friction coefficient (COF) and wear scar diameter (WSD) of oil to reduce 31.90% and 45.46%, while the ball-on-sheet shaped MOF/g-C3N4 enabled the friction coefficient (COF) and wear scar diameter (WSD) of oil to decrease 37.07% and 42.15%, respectively. Due to the morphology difference, the anti-frition and anti-wear mechanism of the flake-on-sheet shaped MOF/g-C3N4 were reliable to the tribo-film consisting of adsorption film and tribochemical film, whereas that of ball-on-sheet shaped MOF/g-C3N4 depended on the synergistic effect of the tribo-film and the ball bearing effect of MOF nanospehere in composite structure. Moreover, the interface interaction in composite structure also had a underlying influence in the friction behavior of nanoadditive.

Advanced composite material for high-performance supercapacitors: integrating graphene oxide and barium chromate

Graphene oxide-based Barium chromate (BaCr2O4@GO) composites were successfully synthesized through sonication assisted by a hydrothermal process designed for supercapacitor applications. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and morphological analyses were employed to characterize the nanostructured composites. The XRD and FTIR results reveal that the GO nanoparticles are arranged in a honeycomb-like configuration. Moreover, the TEM images reveal the presence of cauliflower-like structures in the morphology of the composites, which is attributed to the effective intercalation of GO during the thermal reduction process. The electrochemical properties of the nanocomposite were compared to those reported in previous studies on metal chromite materials aimed at enhancing supercapacity applications. The analysis of Galvanostatic Charge–Discharge (GCD) data indicates a significant increase in power density values from 292 W kg−1 to 495.5 W kg−1 for the Nanocomposites. The ability to achieve a balance between enhanced power density and efficient ion transport positions the -nanocomposites as a valuable candidate for advancing the performance of supercapacitors.

Investigations to intensified hydrogen production via sorption enhanced water gas shift reaction

Sorption enhanced water gas shift (SEWGS) reaction for the equilibrium enhanced hydrogen production is investigated using lithium orthosilicate (Li4SiO4) sorbents mixed with 1 wt% Pt/Al2O3 catalysts. The Li4SiO4 sorbents, synthesized using novel surfactant-mediated method, are characterized by ultra-fast CO2 capture rates with CO2 absorption capacity in the range of 319–333 mgCO2·g−s1. The thermogravimetric analysis results show ∼ 26 wt% of the carbonation sites are participating in the fast CO2 absorption (∼ 298 mgCO2·g−s1·min−1). The use of these sorbents with 1 wt% Pt/Al2O3 catalysts in the water gas shift reaction show a 103% increase in the hydrogen yield compared to the equilibrium concentration at 600◦C. The Li4SiO4 sorbent-catalyst combination show a shift in the equilibrium by preventing the reverse reaction in the temperature range of 600–650◦C. The SEWGS experiments show that the CO2 absorption capacities, and consequently the hydrogen yields, are affected by the diffusional resistance across Li2CO3 and Li2SiO3 product domains in the sorbent. The Li4SiO4 conversion rates during the SEWGS reaction are measured by sampling at different points in the SEWGS reaction and subsequent Rietveld analysis of the XRD patterns. The XRD results suggest the decrease in CO2 absorption rates as a result of the formation of additional Li2CO3 and Li2SiO3 fractions with decreasing Li4SiO4 phase in this nano-structured composite.

Structure and Mechanical Properties of iPP-Based Nanocomposites Crystallized under High Pressure.

The unique nonparallel chain arrangement in the orthorhombic γ-form lamellae of isotactic polypropylene (iPP) results in the enhancement of the mechanical properties of γ-iPP. Our study aimed at the investigation of the mechanical properties of γ-iPP nanocomposites with 1-5 wt.% multiwall carbon nanotubes (MWCNT) and 5 wt.% organo-modified montmorillonite prepared by melt-mixing and high-pressure crystallization. Neat iPP and the nanocomposites were crystallized under high pressures of 200 MPa and 300 MPa, and for comparison under 1.4 MPa, in a custom-built high-pressure cell. The structure of the materials was studied using WAXS, SAXS, DSC, and SEM, whereas their mechanical properties were tested in plane-strain compression. Under a small pressure of 1.4 MPa, polymer matrix in all materials crystallized predominantly in the α-form, the most common monoclinic form of iPP, whereas under high pressure it crystallized in the γ-form. This caused a significant increase in the elastic modulus, yield stress, and stress at break. Moreover, due to the presence of MWCNT, these parameters of the nanocomposites exceeded those of the neat polymer. As a result, a 60-70% increase in the elastic modulus, yield stress, and stress at break was achieved by filling of iPP with MWCNT and high-pressure crystallization.

Composition, Structure, and Wear Resistance of Surface Nanostructures Obtained by Electric Spark Alloying of 65G Steel

Composition, Structure, and Wear Resistance of Surface Nanostructures Obtained by Electric Spark Alloying of 65G Steel

Amorphous electrocatalysts for urea oxidation reaction

Electrochemical urea oxidation reaction (UOR) is a promising alternative to oxygen evolution reaction (OER) for realizing energy-saving hydrogen production. Developing efficient electrocatalysts for UOR becomes a central challenge. Recently, amorphous materials have been extensively used as UOR catalysts because of their numerous defective sites and flexible electronic properties. In this review, recent advancements in the development of amorphous UOR electrocatalysts are analyzed. The UOR mechanism is discussed, and the design of amorphous catalysts is then analyzed. The main catalyst design strategies are illustrated, including nanostructure control, heteroatom doping, composition regulation, and heterostructure construction. Also, electrocatalysts’ structure-performance correlation is interpreted. Perspectives in this field are proposed for guiding future studies on the development of high-performance amorphous catalysts towards energy sustainability.

Development of a novel pH-Responsive PVA/GO-Glu/TiO2 nanocomposite hydrogel for efficient degradation of organic pollutants

Water pollution poses a grave threat to public health and the environment. There is an urgent need for sustainable remediation strategies to remove toxic contaminants from water sources. In this study, we report the development of a novel pH-responsive nanocomposite hydrogel for the effective degradation of organic pollutants. The hydrogel was synthesized using polyvinyl alcohol, graphene oxide, glutamic acid, and titanium dioxide through an in-situ crosslinking method. Characterization using SEM, FTIR and UV–vis spectroscopy confirmed the successful formation of the nanocomposite structure. Batch experiments demonstrated that the hydrogel was able to degrade over 90% of methylene blue dye within 35 min under sunlight irradiation, owing to the synergistic effect of pH-sensitivity and the photocatalytic activity of titanium dioxide. Degradation efficiency increased with rising pH, reaching a maximum at pH 11. This eco-friendly nanohybrid holds tremendous potential for water remediation applications through low-cost, solar-powered degradation of toxic pollutants.

Black TiO2@Ag core-shell nanoparticles combined with WO3 nanorods on rGO nanosheets for PEC analysis

Well-coated black TiO2 and Ag core-shell nanoparticles (NPs) were prepared using a simple wet-chemical approach, which is combined with the WO3 nanorods over rGO nanosheets. The inherent properties of the composite nanostructures were examined thoroughly by diffuse reflectance spectroscopy, X-ray diffraction, Raman scattering, X-ray photoelectron spectroscopy, transmission electron microscopy, and photoelectrochemical (PEC) analysis. The formation of surface oxygen vacancies in the black TiO2 NPs facilitated tuning the optical properties in the visible region, which was enhanced by the surface plasmon resonance behavior of the Ag NPs. While combining the black TiO2@Ag core-shell NPs with intermediate bandgap WO3 nanorods and rGO nanosheets promoted PEC performance in the visible light irradiation. The composite nanostructure exhibited enhanced PEC efficiency (Jp=0.97 mAcm−2 and ABPE=0.62%) compared to the bare NPs. This work discusses the possible PEC mechanism based on the change in optical and structural properties.

Effect of Phosphorus-Nitrogen based Flame-Retardant Combined with Zinc Borate on Thermal Stability and Flame Retardancy of Epoxy Clay Nanocomposites

A phosphorus-nitrogen containing 6,6'-(piperazine-1,4-diyl)bis(6H-dibenzo[c,e][1,2]oxaphosphinine 6-oxide) (DOPO-PZ) flame-retardant was synthesized and its effect combined with zinc borate (ZnB) and nanoclay (NC) on thermal stability and flame retardancy of epoxy resin was studied. Various epoxy composites containing DOPO, DOPO-PZ, ZnB and NC using curing agent diaminodiphenylsulfone (DDS) were prepared. The X-ray diffraction (XRD) and transmission electron microscope (TEM) micrographs of the composites showed intercalated nanostructure of epoxy-clay nanocomposites. In thermogravimetric analysis (TGA), pure epoxy gave 3.4% char yield at 700 ºC in nitrogen atmosphere, while in case of EP/DOPO-PZ/ZnB/NC sample having 1% phosphorus content, 5 wt.% zinc borate (ZnB) and 3 wt.% nanoclay (NC), the char yield is increased to 24.0%. Differential scanning calorimetry (DSC) study showed decrease in the glass transition temperature (Tg) on the addition of flame-retardant due to plasticization effect and increase in Tg on addition of nanoclay due to formation of nanostructure of epoxy composites. The EP/DOPO-PZ/ZnB/NC nanocomposite sample exhibited a limiting oxygen index (LOI) value of 29.2% and passed the UL-94 test with a V-0 rating and thus achieved a sufficient flame retardancy.

Nanostructured Materials for Enhanced Performance of Solid Oxide Fuel Cells: A Comprehensive Review

Solid oxide fuel cells (SOFCs) have emerged as promising candidates for efficient and environmentally friendly energy conversion technologies. Their high energy conversion efficiency and fuel flexibility make them particularly attractive for various applications, ranging from stationary power generation to portable electronic devices. Recently, research has focused on utilizing nanostructured materials to enhance the performance of SOFCs. This comprehensive review summarizes the latest advancements in the design, fabrication, and characterization of nanostructured materials integrated in SOFC. The review begins by elucidating the fundamental principles underlying SOFC operation, emphasizing the critical role of electrode materials, electrolytes, and interfacial interactions in overall cell performance, and the importance of nanostructured materials in addressing key challenges. It provides an in-depth analysis of various types of nanostructures, highlighting their roles in improving the electrochemical performance, stability, and durability of SOFCs. Furthermore, this review delves into the fabrication techniques that enable precise control over nanostructure morphology, composition, and architecture. The influence of nanoscale effects on ionic and electronic transport within the electrolyte and electrodes is thoroughly explored, shedding light on the mechanisms behind enhanced performance. By providing a comprehensive overview of the current state of research on nanostructured materials for SOFCs, this review aims to guide researchers, engineers, and policymakers toward the development of high-performance, cost-effective, and sustainable energy conversion systems.

Investigation of mechanical properties of graphene-CNT reinforced nickel metal matrix nanocomposite structure

Nickel is a metal widely used in many industrial applications, but despite its superior properties, it also has some shortcomings. Carbon-based structures can be important reinforcement elements in improving the properties of metals. By providing a balance between the high corrosion resistance, high electrical conductivity and good magnetic properties of the nickel material and the lightness and high strength of carbon-based structures, a material with advanced properties can be obtained. Therefore, in this study, a new Nickel-Carbon nanostructure supported by a covalently bonded graphene-carbon nanotube (CNT) skeleton structure is presented. Additionally, three material designs with different geometric dimensions (Ni-G-CNT(5,5), Ni-G-CNT(10,10) and Ni-G-CNT(15,15)) were designed to determine the mechanical properties and properties of the structures in all directions. is to investigate the underlying deformation mechanisms. According to the results, it was observed that G-CNT structures increased the tensile and compressive behavior of the Ni structure in the CNT direction. For tensile loading in the CNT direction, as the CNT diameter decreases, the elastic modulus of the hybrid structures increases, while the maximum stress values are independent of the CNT diameter. As the CNT diameter increases, the ductility of the structures increases. In terms of compressive strength, it has been observed that in the linear region, as the CNT diameter increases, the strength generally increases and in the condensation region, it exhibits better compressive strength. With this study, an anisotropic nanostructure that is lighter and can exhibit higher tensile strength compared to the Ni structure is presented.

Synthesis and Characterization of B4C-Based Multifunctional Nanoparticles for Boron Neutron Capture Therapy Applications

Nanoparticles composed of inorganic boron-containing compounds represent a promising candidate as 10B carriers for BNCT. This study focuses on the synthesis, characterization, and assessment of the biological activity of composite nanomaterials based on boron carbide (B4C). Boron carbide is a compelling alternative to borated molecules due to its high volumetric B content, prolonged retention in biological systems, and low toxicity. These attributes lead to a substantial accumulation of B in tissues, eliminating the need for isotopically enriched compounds. In our approach, B4C nanoparticles were included in composite nanostructures with ultrasmall superparamagnetic nanoparticles (SPIONs), coated with poly (acrylic acid), and further functionalized with the fluorophore DiI. The successful internalization of these nanoparticles in HeLa cells was confirmed, and a significant uptake of 10B was observed. Micro-distribution studies were conducted using intracellular neutron autoradiography, providing valuable insights into the spatial distribution of the nanoparticles within cells. These findings strongly indicate that the developed nanomaterials hold significant promise as effective carriers for 10B in BNCT, showcasing their potential for advancing cancer treatment methodologies.

Enhancement of magnetization and optical properties of CuFe2O4/ZnFe2O4 core/shell nanostructure

In this work, core/shell of CuFe2O4/ZnFe2O4 nanostructure composite was prepared by hydrothermal method. X-ray diffraction (XRD) analysis, transmission electron microscope imaging, energy dispersive X-ray (EDX), and Fourier transform infrared techniques were used to prove the phase formation, morphology, elemental analysis, and cation distribution of core/shell structure, respectively. Furthermore, measurement of the optical properties proved the decrease of photoluminescence (PL) efficiency. The magnetic measurements showed an enhancement of the magnetization by about 63% relative to pure Cu ferrite, and the magnetization curve exhibited superparamagnetic behavior. These results were explained in terms of the depression of the magnetic dead layer thickness in the core/shell structure. The results unleash the promising applications of the prepared samples as transformer cores in the high frequency range and as a photocatalytic agent for water purification and hydrogen production.

Physics mechanisms underlying the optimization of coherent heat transfer across width-modulated nanowaveguides with calculations and machine learning

Optimization of heat transfer at the nanoscale is necessary for efficient modern technology applications in nanoelectronics, energy conversion, and quantum technologies. In such applications, phonons dominate thermal transport and optimal performance requires minimum phonon conduction. Coherent phonon conduction is minimized by maximum disorder in the aperiodic modulation profile of width-modulated nanowaveguides, according to a physics rule. It is minimized for moderate disorder against physics intuition in composite nanostructures. Such counter behaviors call for a better understanding of the optimization of phonon transport in non-uniform nanostructures. We have explored mechanisms underlying the optimization of width-modulated nanowaveguides with calculations and machine learning, and we report on generic behavior. We show that the distribution of the thermal conductance among the aperiodic width-modulation configurations is controlled by the modulation degree irrespective of choices of constituent material, width-modulation-geometry, and composition constraints. The efficiency of Bayesian optimization is evaluated against increasing temperature and sample size. It is found that it decreases with increasing temperature due to thermal broadening of the thermal conductance distribution. It shows weak dependence on temperature in samples with high discreteness in the distribution spectrum. Our work provides new physics insight and indicates research pathways to optimize heat transfer in non-uniform nanostructures.

High-pressure study of synthesized α-Bi2O3/NiBi3 nanostructured composite: In-situ synchrotron XRD measurements, DFT calculations and PDF approach

We investigated a nanostructured composite of α-Bi2O3/NiBi3, which was synthesized through high-energy milling, under high-pressure conditions of up to 30 GPa. To track its structural changes, we employed in-situ synchrotron angle-dispersive X-ray diffraction measurements in conjunction with density functional theory calculations. Crystallographic information was derived using the Rietveld method and DFT computations. Additionally, we examined the chemical short-range order using pair distribution functions and determined the compressibility parameters through the Birch-Murnaghan equation of state.We explored the high-pressure behavior of a nanostructured composite of α-Bi2O3/NiBi3, applying pressures up to 30 GPa. The composite sample, synthesized by mechanical alloying, underwent thorough structural characterization by X-ray diffraction, high-resolution transmission electron microscopy and Raman spectroscopy. The sample's response to applied pressure was studied by analyzing crystallographic data obtained from in-situ synchrotron angle-dispersive X-ray diffraction measurements and density functional theory calculations. Crystallographic information from experiments was refined using the Rietveld method. Additionally, chemical short-range order was examined using pair distribution functions, and compressibility parameters were determined via the Birch-Murnaghan equation of state. This investigation into the high-pressure behavior of NiBi3 provides valuable insights for future studies and potential applications of similar materials in extreme pressure environments.

NbC thin films via reactive DC sputtering in a CH4/Ar atmosphere

We have demonstrated the growth of NbC-Amorphous C films that manifest a well-known nanocomposite structure (Klages and Memming, 1990; Nedfors et al., 2011; Sala et al., 2021). The films were deposited using reactive DC sputtering in a CH4/Ar atmosphere using an insulating substrate near room temperature. A metallic Nb sputtering target was sputtered in an argon/CH4 atmosphere with a pressure range of 5.9 to 8.5 mTorr as the CH4 flow was also varied. Crystalline NbC films were deposited at room temperature at the lowest CH4 flow rate. The films exhibited ohmic electrical response at room temperature. The DC electrical resistivity scaled almost 4 orders of magnitude from 4.39 × 10−4 Ω-cm to 1.08 × 10−1 Ω-cm through changes in CH4 flow rates and the resultant C content of the films. The large variation in resistivity cannot be attributed to the changes in sample composition, e.g. volumetric mixing. It is postulated from XRD and TEM results that the large change in resistivity is due to the decreasing NbC crystallite size with increasing CH4. This leads to additional three-dimensional nanoscale intragranular interfaces and results in increased resistivity. X-ray reflectivity measurements were conducted, and the modelled film density was found to match the expected density for the film compositions as measured using X-ray photoelectron spectroscopy. Elastic recoil detection analysis (ERDA) was used to quantify H content of the films. The H content increased from 5.5 to 22 atomic percent with corresponding increase in CH4 flow. Transmission electron microscopy utilizing precession electron diffraction (PED) was conducted and showed a strong dependence of crystallinity on CH4 flow. A multilayer layer sample with varying CH4 flowrates was examined with TEM and showed that films were amorphous in nature for flow rates above 10 SCCM CH4; in agreement with XRD results.

Novel Nanocomposites for Luminescent Thermometry with Two Different Modalities.

In this work, we successfully integrated fluorescent nanodiamonds (FNDs) and lanthanide ion-doped upconversion nanoparticles (UCNPs) in a nanocomposite structure for simultaneous optical temperature sensing. The effective integration of FND and UCNP shells was confirmed by employing high-resolution TEM imaging, X-ray diffraction, and dual-excitation optical spectroscopy. Furthermore, the synthesized ND@UCNP nanocomposites were tested by making simultaneous optical temperature measurements, and the detected temperatures showed excellent agreement within their sensitivity limit. The simultaneous measurement of temperature using two different modalities having different sensing physics but with the same composite nanoparticles inside is expected to greatly improve the confidence of nanoscale temperature measurements. This should resolve some of the controversy surrounding nanoscale temperature measurements in biological applications.

Construction of a nanostructured NiCo2S4/Ni/Ni9S8 composite for energy storage applications

It is necessary to investigate and develop nickel-cobalt sulfide electrodes with superior electrochemical behavior. This work produced the NiCo2S4/Ni/Ni9S8 nanostructure composite (NCS/N/NS) for energy storage in supercapacitors using a solvothermal technique with polyethyleneimine (PEI) as a carbon source, followed by an hour of annealing in an argon atmosphere, and a hydrothermal method with thiourea as a sulfur and nitrogen source. Outstanding electrochemical energy storage properties are provided by NCS/N/NS. The produced electrode material, NCS/N/NS, demonstrated an exceptional capacitance of 1620 F g−1 (696 C g−1) at 1 A g−1 when employed for SCs. An NCS/N/NS was used as the positively charged electrode and the opposite electrode of commercial AC to build an NCS/N/NS//activated carbon (AC) asymmetric device for practical usage. At 1 A g−1, the asymmetric device produced a specific power of 887 W kg−1 and a unique specific energy of 53 Wh kg−1. Moreover, it exhibits a 100% coulombic efficacy and a 95% capacity retention after 3000 cycles, respectively.

Surface Plasmonic Core-Shell Nanostructures in Surface Enhanced Raman Scattering and Photocatalysis.

Core-shell nanostructures are a typical material design. Usually, it consists of a core wrapped in a shell. It has attracted much attention due to its tunable structure and composition, high surface area, and high programmability. The properties and resonance frequency of their surface plasmons can be adjusted by regulating the shape, size, and composition of metal core-shell nanostructures. This interaction makes core-shell nanostructures an excellent platform for plasmon-enhanced optical effects. This Perspective explores the categories of core-shell nanostructures, their exchanges with excitons in two-dimensional materials, their spectrum-enhanced aspects, and prospects for future applications of core-shell nanostructures.

Innovative multiwall carbon nanotubes synthesis on 3D nickel surface: a comparative study

The article presents the synthesis of multi-walled carbon nanotubes (MWCNTs) on the porous nickel foam (3D-Ni) surface using the chemical vapor deposition (CVD) method, followed by the field emission characteristics of the resulting 3D-Ni/MWCNT nanocomposite structures. The characterization of the 3D-Ni/MWCNT morphology showed a uniform distribution of the “moss-like” CNT coating on the walls of the porous 3D-Ni. TEM images showed a high number of walls in MWCNTs, which made such a material resistant to destruction under conditions of strong electric fields during the field emission process. The studies also showed a high degree of chemical purity of the synthesized MWCNTs under the presented technological conditions. An increase in the emission current due to the introduction of CNTs into the structure of porous 3D-Ni is shown. 3D-Ni/MWCNTs field emitter showed a low turn-on field of 5.41 V/μm; a field enhancement factor of 915; and high operating stability. For the first time, the current mode of 3D-Ni-MWCNTs cathode was tested for compliance with the classical field emission law using the Forbes “orthodoxy” test.