Toward a better understanding of multifunctional cement-based materials: The impact of graphite nanoplatelets (GNPs)

The impact of graphite nanoplatelets (GNPs) on the physical and mechanical properties of cementitious nanocomposites was investigated. A market-available premixed mortar was modified with 0.01% by weight of cement of commercial GNPs characterized by two distinctively different aspect ratios.The rheological behavior of the GNP-modified fresh admixtures was thoroughly evaluated. Hardened cementitious nanocomposites were investigated in terms of density, microstructure (Scanning Electron Microscopy, SEM and micro–Computed Tomography, μ-CT), mechanical properties (three-point bending and compression tests), and physical properties (electrochemical impedance spectroscopy, EIS and thermal conductivity measurements). At 28 days, all GNP-modified mortars showed about 12% increased density. Mortars reinforced with high aspect ratio GNPs exhibited the highest compressive and flexural strength: about 14% and 4% improvements compared to control sample, respectively. Conversely, low aspect ratio GNPs led to cementitious nanocomposites characterized by 36% decreased electrical resistivity combined with 60% increased thermal conductivity with respect to the control sample.     

Poly(lactide)/cellulose nanocrystal nanocomposites by high-shear mixing

There is currently considerable interest in developing stiff, strong, tough, and heat resistant poly(lactide) (PLA) based materials with improved melt elasticity in response to the increasing demand for sustainable plastics. However, simultaneous optimization of stiffness, strength, and toughness is a challenge for any material, and commercial PLA is well-known to be inherently brittle and temperature-sensitive and to show poor melt elasticity. In this study, we report that high-shear mixing with cellulose nanocrystals (CNC) leads to significant improvements in the toughness, heat resistance, and melt elasticity of PLA while further enhancing its already outstanding room temperature stiffness and strength. This is evidenced by (i) one-fold increase in the elastic modulus (6.48 GPa), (ii) 43% increase in the tensile strength (87.1 MPa), (iii) one-fold increase in the strain at break (∼6%), (iv) two-fold increase in the impact strength (44.2 kJ/m²), (v) 113-fold increase in the storage modulus at 90°C (787.8 MPa), and (vi) 10³-fold increase in the melt elasticity at 190°C and 1 rad/s (∼10⁵ Pa) via the addition of 30 wt% CNC. It is hence possible to produce industrially viable, stiff, strong, tough, and heat resistant green materials with improved melt elasticity through high-shear mixing.     

Surface modification of cellulose nanocrystals towards new materials development

Cellulose nanocrystals (CNCs) are a kind of sustainable nanoparticle from biomass, which are widely used as reinforcing filler and assembly building block for high-performance composites and function materials including biomaterial, optics, and so forth. Here, their unique advantages in material applications were reviewed based on their rod-like morphology, crystalline structure, dimension-related effects, and multi-level order structure. Then, we focused on the molecular engineering of CNCs, including the structure and physicochemical properties of their surface, along with surface modification methods and steric effects. We further discussed the performance-improvement and functionalization methods based on multi-component complex systems, together with the effects of surface molecular engineering on the performance and functions. Meanwhile, methods of optimizing orientation in uniaxial arrays were discussed along with those of enhancing photoluminescence efficiency via surface chemical modification and substance coordination. In the end, we prospected the design, development, and construction methods of new CNCs materials.     

Mechanical Properties of Single-Layer Diamond Reinforced Poly(vinyl alcohol) Nanocomposites through Atomistic Simulation

Low-dimensional carbon nanostructures are ideal nanofillers to reinforce the mechanical performance of polymer nanocomposites due to their excellent mechanical properties. Through molecular dynamics simulations, the mechanical performance of poly(vinyl alchohol) (PVA) nanocomposites reinforced with a single-layer diamond – diamane is investigated. It is found the PVA/diamane exhibits similar interfacial strengths and pull-out characteristics with the PVA/bilayer-graphene counterpart. Specifically, when the nanofiller is fully embedded in the nanocomposite, it is unable to deform simultaneously with the PVA matrix due to the weak interfacial load transfer efficiency, thus the enhancement effect is not significant. In comparison, diamane can effectively promote the tensile properties of the nanocomposite when it has a laminated structure as it deforms simultaneously with the matrix. With this configuration, the interlayer sp³ bonds endows diamane with a much higher resistance under compression and shear tests, thus the nanocomposite can reach very high compressive and shear stress. Overall, enhancement on the mechanical interlocking at the interface as triggered by surface functionalization is only effective for the fully embedded nanofiller. This work provides a fundamental understanding of the mechanical properties of PVA nanocomposites reinforced by diamane, which can shed lights on the design and preparation of next generation high-performance nanocomposites.     

Fabrication of Anticounterfeiting Nanocomposites with Multiple Security Features via Integration of a Photoresponsive Polymer and Upconverting Nanoparticles

Anticounterfeiting materials are used to distinguish real banknotes, products, and documents from counterfeits, fakes, or unauthorized replicas. However, conventional anticounterfeiting materials generally exhibit a single anticounterfeiting function, resulting in a low level of security. Herein, a novel anticounterfeiting nanocomposite is demonstrated with numerous prominent security features. The nanocomposite is fabricated by doping upconverting nanoparticles (UCNPs) in a photoresponsive azobenzene-containing polymer (azopolymer). Because of the cis–trans photoisomerization of the azopolymer, the nanocomposite exhibits photoinduced reversible color changes suitable for anticounterfeiting applications. Additionally, the hard nanocomposite can be converted to a rubber-like soft solid by light irradiation. Imprinted microstructures are fabricated on the photosoftened nanocomposite, which result in photonic colors. Moreover, polarization-dependent structures are fabricated on the nanocomposite via photoinduced orientation for encryption. Importantly, UCNPs in the nanocomposite emit visible light upon excitation by near-infrared light, enabling the observation of various anticounterfeiting structures with high contrast. An advantage of the anticounterfeiting nanocomposite is that the security features can be observed by the naked eye for quick discrimination and can be analyzed using laboratory equipment for higher accuracy. The anticounterfeiting nanocomposite is easily processed on paper, glass, and plastic, which demonstrates its potential anticounterfeiting functions for banknotes, wines, and medicines.     

Single chamber Solid Oxide Fuel Cells selective electrodes: A real chance with brownmillerite-based nanocomposites

In this contribution brownmillerite-based nanocomposite cathode for Single-Chamber Solid Oxide Fuel Cells is developed. These cells can be very attractive especially for small and cheap devices because of the absence of seals. The efficiency of SC-SOFCs is strictly connected to the selectivity of anode and cathode, the bottleneck for this technology. The development of a cathode inert in fuel oxidation is particularly challenging. Our strategy is to start from a catalytically un-active support (CFA = Ca₂FeAl_0.95Mg_0.05O₅) and induce the formation of iron oxide based nanoparticles, expected to activate oxygen. Symmetric (CFA + FeO_x/CGO/CFA + FeO_x) and complete cells (CFA + FeO_x/CGO/Ni-CGO) are studied in air and methane/oxygen 2:1 mixture. The Area Specific Resistance of CFA + FeO_x is less than 1/3 that of CFA. The high selectivity allows to reach an efficiency of 25%; power still needs to be increased but we demonstrated the possibility to develop selective low cost electrodes. The effect of air, methane/oxygen exposure and the heat treatments were carefully investigated.     

Enhanced airborne sound absorption effect in poly(vinylidene fluoride)/(K0.5Na0.5)NbO3-nanofiber composite foams

Introducing electrical conductive function to discharge local piezoelectric effect is found effective for improving airborne sound absorption performance. In this work, instead of conductive fillers, a composite with two piezoelectric materials with opposite piezoelectric responses was explored aiming at enhanced sound absorption effect. Open-cell poly(vinylidene fluoride)/(K_0.5Na_0.5)NbO₃ (PVDF/KNN)-nanofiber composite foams were proposed and investigated for airborne sound absorption purpose. Structural and thermal analyses showed that the KNN nanofibers were well dispersed in the PVDF matrix and enhanced the degree of crystallinity of polar phase of PVDF. Significantly enhanced airborne sound absorption over a broad frequency range was observed in the PVDF/KNN-nanofiber composite foams, with increasing KNN nanofibers. One possible mechanism for the improved sound absorption with the piezoelectric KNN nanofibers with positive piezoelectric coefficient added in the PVDF matrix with negative piezoelectric coefficient is that electrical discharge could be facilitated for energy dissipation with the opposite charges generated through the piezoelectric effects in the two phases with opposite polarity. The experimental results show that the open-cell PVDF/KNN-nanofiber composite foams are promising for broadband airborne sound absorption application, and our analysis shed a light on the strategy in designing piezoelectric composite foam with high sound absorption performance.     

Enhanced hydrogen storage performance of three-dimensional hierarchical porous graphene with nickel nanoparticles

Three-dimensional hierarchical porous graphene with nickel nanoparticles (3DHPG-Ni) was synthesized through electrostatic assembly method with the assistance of poly (methyl methacrylate) (PMMA) template and subsequent removal of PMMA template by calcination. The morphology, microstructure and hydrogen adsorption properties of 3DHPG-Ni nanocomposites were examined in detail. The obtained 3DHPG-Ni nanocomposite exhibited hierarchical porous structure composed of macro-, meso- and micropores, high specific surface area (925 m² g^?1), large pore volume (0.58 cm³ g^?1) and excellent hydrogen storage capacity. Under the pressure of 5 bar, 3DHPG-Ni nanocomposite showed a maximum hydrogen capacity of 4.22 wt% and 1.95 wt% at 77 K and 298 K, respectively, demonstrating that the as-prepared 3DHPG-Ni nanocomposite was supposed to be a promising material with outstanding properties for practical applications in the field of hydrogen storage. The three-dimensional hierarchical porous structure, evenly distributed Ni nanoparticles and hydrogen spillover effect were responsible for the enhanced hydrogen storage capacities.     

二维层状Ni/β-Ni(OH)2纳米复合材料的制备及其摩擦学性能研究

采用水热反应制备出β-Ni(OH)2,然后通过水热还原得到Ni/β-Ni(OH)2纳米复合粉体材料,采用X射线衍射仪(XRD)和扫描电子显微镜(SEM)对复合材料的相结构、成分及形貌进行表征分析。采用四球摩擦磨损试验机评价制备的Ni/β-Ni(OH)2作为润滑油添加剂的摩擦学性能,基础油为PAO6。摩擦试验后,采用SEM分析典型试验钢球磨斑的表面形貌,利用能谱仪(EDS)研究磨斑表面化学元素的组成,探讨Ni/β-Ni(OH)2纳米复合润滑添加剂的减摩抗磨机制。结果表明:Ni/β-Ni(OH)2纳米复合材料作为润滑添加剂具有极好的减摩抗磨性能,显著优于基础油PAO6和未负载纳米Ni的二维β-Ni(OH)2层状材料;与基础油相比,添加0.1%质量分数Ni/β-Ni(OH)2添加剂的油样的摩擦因数和磨斑直径分别降低了17.6%和41.5%;Ni/β-Ni(OH)2纳米复合粉体综合了纳米Ni及层状β-Ni(OH)2两部分结构特性,在摩擦过程中,复合材料中的纳米金属粒子Ni与层状结构材料β-Ni(OH)2能够相互增强起到协同润滑作用。