Nonpolar Materials Research Articles

Nanoplastic Release from Disposable Plastics: Correlation with Maximum Service Temperature

The potential for bioaccumulation of nanoplastics (NPs, <1µm) increases as the particle size decreases. Since several disposable plastic products used daily may release NPs, their intake may be unavoidable. Therefore, it is crucial to examine the release patterns of NPs from these products. This study investigates the relationship between NP release and the Maximum Service Temperature (MST) of five plastic types, confirming the correlation under real-world conditions. The releasing tendencies of NPs were investigated using plastic pellets. We simulated the packaging of hot food in plastic containers, considering the physical dynamics of food delivery, and replicated cooking in an oven and microwave. We observed that the mass of NPs released tended to reach its maximum at the material's MST. In real-life conditions, the release of NP was found to increase with higher container content temperatures and longer packaging or cooking durations. Physical impacts were confirmed to be the most significant contributors to NP release. Moreover, Higher microwave power levels lead to greater NP release, with polar materials releasing more NPs compared to non-polar materials. Consequently, to minimize NP ingestion, it is recommended to use containers made from non-polar materials with a high MST.

Highly Responsive Polar Vortices in All-Ferroelectric Heterostructures.

The discovery of polar vortices and skyrmions in ferroelectric-dielectric superlattices [such as (PbTiO3)n/(SrTiO3)n] has ushered in an era of novel dipolar topologies and corresponding emergent phenomena. The key to creating such emergent features has generally been considered to be related to counterpoising strongly polar and non-polar materials thus creating the appropriate boundary conditions. This limits the utility these materials can have, however, by rendering (effectively) half of the structure unresponsive to applied stimuli. Here, using advanced thin-film deposition and an array of characterization and simulation approaches, polar vortices are realized in all-ferroelectric trilayers, multilayers, and superlattices built from the fundamental building block of (PbTiO3)n/(PbxSr1- xTiO3)n wherein in-plane ferroelectric polarization in the PbxSr1- xTiO3 provides the appropriate boundary conditions. These superlattices exhibit substantially enhanced electromechanical and ferroelectric responses in the out-of-plane direction that arise from the ability of the polarization in both layers to rotate to the out-of-plane direction under field. In the in-plane direction, the layers are found to be strongly coupled during switching and when heterostructured with ferroelectric-dielectric building blocks, it is possible to produce multistate switching. This approach expands the realm of systems supporting emergent dipolar texture formation and does so with entirely ferroelectric materials thus greatly improving their responses.

Enhanced oxygen evolution reaction in flexoelectric thin-film heterostructures

Recently, the flexoelectric effect has triggered considerable interest in energy-related applications, such as flexo-actuation, flexo-photovoltaic, and flexo-catalysis, because of its ubiquitous feature allowing the creation of electric polarity, i.e., the flexoelectric polarization (Pflexo), in non-polar materials by strain gradient. Here, we show a flexoelectric strategy in electrocatalytic water splitting. Remarkably enhanced oxygen evolution reaction (OER) properties are achieved in strain-gradient LaFeO3 (LFO) thin-film heterostructures owing to the promotion of kinetic processes by Pflexo. The improved OER is demonstrated by increased current density of ∼300% in linear sweep voltammetry and lowered charge transfer resistance by two orders of magnitude in electrochemical impedance spectroscopy. These are ascribed to the flexoelectric-induced downward bending of the LFO band, as revealed by density functional theory calculations and band structure measurements. With Pflexo in the thin-film heterostructure catalysts, the adsorption of hydroxyl ions is strengthened on the polar LFO surface, and the transfer of electrons is accelerated from the reactants/key intermediates to the catalyst across the band-tilted LFO layer. These findings indicate the significance of flexoelectric effect in OER kinetics and open a new perspective for exploiting catalytic mechanisms and performances in water splitting.

Mixed (NH4)2Mn0.47Cu0.53(SO4)2(H2O)6 Tutton salt: A novel optical material for solar-blind technology

In this paper, a novel mixed Tutton salt (NH4)2Mn0.47Cu0.53(SO4)2(H2O)6 obtained in single crystal form is described. Their structural, thermal, electrical, and spectroscopic properties have been examined, and their possible uses are discussed. The salt crystallizes in a monoclinic symmetry (P21/c) and exhibits thermal stability between 300-333 K. Above this temperature, the crystal undergoes phase changes associated with dehydration and crystallization processes. 231 optical phonons distributed between 50 and 4000 cm–1, calculated through density functional perturbation theory, were used to accurately assign vibrational modes in experimental FT-IR and Raman spectra. Additional computational studies using Hirshfeld surfaces have revealed that H···O/O···H and H···H intermolecular contacts are crucial interactions for stabilizing the crystal lattice. Electrical characteristics (resistivity = 1160 MΩ·cm; capacitance = 3.6 pF) and optical data (bandgap = 4.27 eV) depict a typical behavior of nonpolar dielectric materials. UV-Vis-NIR transmittance spectrum has shown deep light blocking in the UV-C and Vis/NIR spectral regions and high transmittance levels (reaching 98.5%) in the UV-B/-A/Vis range. The photoresponse findings point out that (NH4)2Mn0.47Cu0.53(SO4)2(H2O)6 is a promising light-absorbing material for solar-blind photodetection devices operating in the 200-280 nm interval. The crystal as a bandpass filter (280-615 nm) or a cut-off filter (615-1000 nm) are also excellent prospects for application.

Large depth-of-focus achievement based on an aspheric lens with a ring

Terahertz (THz) imaging technology has been widely studied because of its easy penetration of non-polar materials and low photon energy. To acquire a beam featuring both excellent transverse spatial resolution and a considerable depth-of-focus (DOF) to fulfill the demands of two-dimensional and three-dimensional THz imaging, this paper presents an aspheric lens with ring (ALR). The ALR has a controlled diameter of 50 mm, can be machined by 3D-printed technology, and does not need to use complex imaging optical paths to achieve the large DOF function. In a transmitted point-scan imaging system with a 140 GHz light source, the lens can achieve both a resolution of 6 mm and an effective DOF of 66.4 mm for objects greater than 27 mm from the lens surface.

Optimization of malic anhydrate concentration in manufacturing PP-g-MA compatibilizer on test percent of grafting degree

The difference in polarity means that two or more materials cannot react, a connecting material such as a compatibilizer is needed to react between polar and non-polar materials. This research aims to determine the effect of maleic anhydride (MA) concentration on the process of grafting MA onto polypropylene (PP) chains with the help of benzoyl peroxide (BPO) as an initiator. The method used to mix these two materials uses the blending method using an internal mixer instrument and testing the percent degree of grafting using the titration method with three repetitions of the test.The research results showed that the highest percent grafting degree occurred at a concentration of 86% PP, 11% MA, and 3% BPO, with a value of 10.28%. The Spectroscopy Fourier Transform Infrared (FTIR) analysis of Polypropylene grafted maleic anhydride (PP-g-MA) showed the presence of new peaks at wavenumbers 1707cm-1 and 1162 cm-1.Increasing the concentration of maleic anhydride had no effect on increasing the percent degree of grafting.

Optical Control of In-Plane Domain Configuration and Domain Wall Motion in Ferroelectric and Ferroelastic Materials.

The sensitivity of ferroelectric domain walls to external stimuli makes them functional entities in nanoelectronic devices. Specifically, optically driven domain reconfiguration with in-plane polarization is advantageous and thus is highly sought. Here, we show the existence of in-plane polarized subdomains imitating a single domain state and reversible optical control of its domain wall movement in a single-crystal of ferroelectric BaTiO3. Similar optical control in the domain configuration of nonpolar ferroelastic material indicates that long-range ferroelectric polarization is not essential for the optical control of domain wall movement. Instead, flexoelectricity is found to be an essential ingredient for the optical control of the domain configuration, and hence, ferroelastic materials would be another possible candidate for nanoelectronic device applications.

A Transformer-based neural network for automatic delamination characterization of quartz fiber-reinforced polymer curved structure using improved THz-TDS

Quartz fiber-reinforced polymer (QFRP) is a vital non-polar material used in aviation wave-transparent structural components. Automatic characterization of delamination defects in QFRP is critical to aviation structural component safety. Terahertz time-domain spectroscopy (THz-TDS) is one of the new non-destructive testing (NDT) methods with highly accurate characterization of internal defects in non-polar material. Hence, attempts to extract features of THz time-domain signals for automatic characterization have been made by using deep learning algorithms. In this work, a Transformer-based neural network to classify the THz time-domain signals collected from a QFRP curved structure for automatic characterization of pre-embedded delamination defects has been reported. A THz-TDS system combined with a collaborative robot for collecting the THz signals from QFRP curved structure has been built. An automatic characterization method framework is developed. Results show that the precision rates of Transformer-based neural network for 1st delamination to 5th delamination are 1.0, 1.0, 1.0, 0.985, 1.0, and F1 score of it is 0.982. During the process of testing, delamination defects inside the QFRP curved structure were visualized using pixels with different colors. Results indicate that the Transformer-based neural network can characterize all pre-embedded delamination defects while minimizing false identification of non-defective areas, performing outstanding generalization.

Flexoelectric Engineering of Bulk Photovoltaic Photodetector.

The bulk photovoltaic effect (BPVE) offers an interesting approach to generate a steady photocurrent in a single-phase material under homogeneous illumination, and it has been extensively investigated in ferroelectrics exhibiting spontaneous polarization that breaks inversion symmetry. Flexoelectricity breaks inversion symmetry via a strain gradient in the otherwise nonpolar materials, enabling manipulation of ferroelectric order without an electric field. Combining these two effects, we demonstrate active mechanical control of BPVE in suspended 2-dimensional CuInP2S6 (CIPS) that is ferroelectric yet sensitive to electric field, which enables practical photodetection with an order of magnitude enhancement in performance. The suspended CIPS exhibits a 20-fold increase in photocurrent, which can be continuously modulated by either mechanical force or light polarization. The flexoelectrically engineered photodetection device, activated by air pressure and without any optimization, possesses a responsivity of 2.45 × 10-2 A/W and a detectivity of 1.73 × 1011 jones, which are superior to those of ferroelectric-based photodetection and comparable to those of the commercial Si photodiode.

Ferroelastic Twin-Wall-Mediated Ferroelectriclike Behavior and Bulk Photovoltaic Effect in SrTiO_{3}.

Ferroelastic twin walls in nonpolar materials can give rise to a spontaneous polarization due to symmetry breaking. Nevertheless, the bistable polarity of twin walls and its reversal have not yet been demonstrated. Here, we report that the polarity of SrTiO_{3} twin walls can be switched by an ultralow strain gradient. Using first-principles-based machine-learning potential, we demonstrate that the twin walls can be deterministically rotated and realigned in specific directions under the strain gradient, which breaks the inversion symmetry of a sequence of walls and leads to a macroscopic polarization. The system can maintain polarity even after the constraint is removed. As a result, the polarization of twin walls can exhibit a ferroelectriclike hysteresis loop upon cyclic bending, namely flexoferroelectricity. Finally, we propose a scheme to experimentally detect the polarity of the twin wall by measuring the bulk photovoltaic responses. Our findings suggest a twin-wall-mediated flexoferroelectricity in SrTiO_{3}, which could be potentially exploited as functional elements in nanoelectronic devices design.

Experimental study of a thin thermally grown oxide layer in thermal barrier coatings based on the SWT-BP algorithm and terahertz technology

As a promising nondestructive testing (NDT) technique with a very adaptive physical modeling of wave transmission process, terahertz technology is used for the detection and characterization of nonpolar materials and the evaluation of layered and/or defective structures. THz-TDS can also be used to perform spectroscopic analysis and detect structural defects in thermal barrier coatings (TBCs) of aero-engines. Although it is generally difficult to measure the structure of the thin oxide layer of the thermal barrier coatings whose thickness is generally lower than 30 µm (the current axial resolution of the THz-TDS cannot exceed 30 µm). We were able to complete the detection of the oxide layer within 1–29 µm through simulation by using the SWT-BP algorithm. In this study, the analysis was performed on real-world samples, the fitting degree of the SWT-BP algorithm reached 0.77, and the minimum prediction error was less than 0.1 µm. The paper also put forward some improvement measures about the experimental results.

Control of Polarity in Kagome-NiAs Bismuthides.

A 2×2×1 superstructure of the P63/mmc NiAs structure is reported in which kagome nets are stabilized in the octahedral transition metal layers of the compounds Ni0.7Pd0.2Bi, Ni0.6Pt0.4Bi, and Mn0.99Pd0.01Bi. The ordered vacancies that yield the true hexagonal kagome motif lead to filling of trigonal bipyramidal interstitial sites with the transition metal in this family of "kagome-NiAs" type materials. Further ordering of vacancies within these interstitial layers can be compositionally driven to simultaneously yield kagome-connected layers and a net polarization along the c axes in Ni0.9Bi and Ni0.79Pd0.08Bi, which adopt Fmm2 symmetry. The polar and non-polar materials exhibit different electronic transport behaviour, reflecting the tuneability of both structure and properties within the NiAs-type bismuthide materials family.

Large Polarization Near 50 μC/cm2 in a Single Unit Cell Layer SrTiO3.

The generally nonpolar SrTiO3 has attracted more attention recently because of its possibly induced novel polar states and related paraelectric-ferroelectric phase transitions. By using controlled pulsed laser deposition, high-quality, ultrathin, and strained SrTiO3 layers were obtained. Here, transmission electron microscopy and theoretical simulations have unveiled highly polar states in SrTiO3 films even down to one unit cell at room temperature, which were stabilized in the PbTiO3/SrTiO3/PbTiO3 sandwich structures by in-plane tensile strain and interfacial coupling, as evidenced by large tetragonality (∼1.05), notable polar ion displacement (0.019 nm), and thus ultrahigh spontaneous polarization (up to ∼50 μC/cm2). These values are nearly comparable to those of the strong ferroelectrics as the PbZrxTi1-xO3 family. Our findings provide an effective and practical approach for integrating large strain states into oxide films and inducing polarization in nonpolar materials, which may broaden the functionality of nonpolar oxides and pave the way for the discovery of new electronic materials.

Ti2CTx MXene Cathode Host for Enhanced Zinc‐Bromine Battery Performance

AbstractAqueous zinc‐bromine batteries represent a promising large‐scale energy storage system, yet generally suffer from the dissolution of polybromides in the cathode. Currently, various nonpolar carbon materials are employed as hosts for the bromine cathode. Still, they typically exhibit weak adsorption capabilities toward polybromides. Here, a highly conductive Ti2CTx MXene synthesized through an eco‐friendly molten salt method is reported, serving as an ideal bromine cathode host material for the first time. Ti2CTx MXene shows strong chemisorptive capability to soluble polybromide species and can effectively immobilize them for enhanced coulombic efficiency and prolong cycling life of zinc‐bromine batteries. Additionally, Ti2CTx MXene enhances the reaction kinetics of the bromine cathode. Benefiting from the synergistic polybromide adsorption and catalysis effects of Ti2CTx, the dual‐plating zinc‐bromine batteries exhibit good cycle stability, with a capacity retention of 87% after 3000 cycles, outperforming traditional carbon host which fail after 2300 cycles. Meanwhile, Ti2CTx achieves a much lower polarization voltage of only 84 mV, significantly less than 240 mV observed with carbon hosts. This research highlights the potential of developing host materials with polybromide chemisorptive properties to advance the performance of zinc‐bromine batteries.

Polymerization of polar α-olefin with high activity and high syndiotactic selectivity catalyzed by scandium metal catalyst of fluorene coordination

High functional poly α-olefin can be synthesized from polar α-olefin containing heteroatomic groups by coordination polymerization. These highly functional poly α-olefin materials can obviously improve the non-polar poly α-olefin materials, such as the appearance, printability, adhesion, rheology, compatibility with other polymer materials and blending properties to improve their added value and expand their industrial application range. In this paper, a series of polymer materials with potential application value were prepared with a catalyst of scandium fluorene Flu-Sc(THF)n (CH2SiMe3)2 to achieve high reaction activity (63.1×103g/(molcath)) and high selectivity polymerization (rrrr>99%) of polar α-olefin with different heteroatoms and different chain lengths.

Theoretical investigation of synergistically boosting the anchoring and electrochemical performance of lithiophilic/sulfiphilic transition metal carbides for lithium-sulfur batteries.

Lithium-sulfur (Li-S) battery is one of the most promising next-generation energy-storage systems with a high energy density and low cost. However, their commercial applications face several challenges, such as the shuttle effect caused by the soluble lithium polysulfide (LiPSs) intermediates and the sluggish sulfur redox reaction. In this article, we systematically investigated the anchoring and electrochemical performance of a series of transition metal carbides (TMCs: TiC, VC, ZrC, NbC, HfC, TaC) as cathode materials for Li-S batteries by theoretical calculations. The lithiophilic/sulfiphilic non-polar (001) surfaces of TMCs can offer moderate binding strength with LiPS intermediates, ensuring good performance of sulfur immobilization. These TMCs can also facilitate lithium diffusion, indicating the good rate performance of Li-S batteries. We also demonstrated that the studied TMCs can be classified into two classes according to their catalytic activity for Li2S decomposition which originated from their different electronic structural features. Furthermore, TiC, ZrC, and HfC exhibited excellent bifunctional electrochemical activity through reducing the Gibbs free energy for sulfur reduction reactions (SRRs) and lowering the barrier for Li2S decomposition which facilitates accelerating electrode kinetics and elevating utilization of sulfur. Our results offer a systematic approach to designing and screening non-polar materials for high-performance Li-S batteries, based on the rational electronic structure and lattice match strategy.

Study on material structure design, selective adsorption mechanism, and application for adsorption recovery of oil substances in coal chemical wastewater

In response to the problem of high emulsified and dissolved oils being difficult to recovery from coal chemical wastewater (CCW), this study specifically constructed a non-polar, macropore, and hydrophobic adsorption material (pSt-X) based on the main components of these two oils (aromatics and phenols) for selective recovery. The results revealed that pSt-X had an adsorption capacity of 215.52 mg/g, which had remained stable for multiple recycling sessions, with an adsorption capacity constantly above 95 %. The pSt-X has significantly larger particle size (0.7 mm–1.2 mm), which simplifies the process of adsorption regeneration and effectively prevents the loss of the adsorbent powder problem. The pSt-X adsorbent demonstrated remarkable selectivity towards dissolved and emulsified oils, exhibiting removal rates of 90.2 % and 81.7 %, respectively. Moreover, pSt-X proved remarkable selectivity in removing aromatic hydrocarbons (AHs) and phenols, with impressive removal rates of 77.8 % and 85.9 %, respectively. The selective separation mechanism of pSt-X for oil substances was further analyzed, indicating that its selective adsorption of oils was primarily driven by hydrophobic, π-π, and hydrogen bonding interactions owing to its non-polar and macropore structure and hydrophobic properties. The results of this study provide solid theoretical support for green and low-carbon recovery of oil substances in CCW and are of positive practical importance for clean production in the coal chemical industry.

Silane Effects on Adhesion Enhancement of 2K Polyurethane Adhesives.

With excellent properties such as great flexibility, outstanding chemical resistance, and superb mechanical strength, two-part polyurethane (2K PU) adhesives have been widely applied in many applications, including those in transportation and construction. Despite the extensive use, their adhesion to nonpolar polymer substrates still needs to be improved and has been widely studied. The incorporation of silane molecules and the use of plasma treatment on substrate surfaces are two popular methods to increase the adhesion of 2K PU adhesives, but their detailed adhesion enhancement mechanisms are still largely unknown. In this research, sum frequency generation (SFG) vibrational spectroscopy was used to probe the influence of added or coated silanes on the interfacial structure at the buried polypropylene (PP)/2K PU adhesive interface in situ. How plasma treatment on PP could improve adhesion was also investigated. To achieve maximum adhesion, two methods to involve silanes were studied. In the first method, silanes were directly mixed with the 2K PU adhesive before use. In the second method, silane molecules were spin-coated onto the PP substrate before the PU adhesive applied. It was found that the first method could not improve the 2K PU adhesion to PP, while the second method could substantially enhance such adhesion. SFG studies demonstrated that with the second method silane molecules chemically reacted at the interface to connect PP and 2K PU adhesive to improve the adhesion. With the first method, silane molecules could not effectively diffuse to the interface to enhance adhesion. In this research, plasma treatment was also found to be a useful method to improve the adhesion of the 2K PU adhesive to nonpolar polymer materials.

Dehydration-triggered structural phase transition-associated ferroelectricity in a hybrid perovskite-type crystal

Since the appearance of Rochelle salt, ferroelectrics have received extensive attention from researchers due to they are playing an important role in sensors, memories, mechanical actuation, and so on. In recent years, with the rapid development of molecular ferroelectrics, high-performance molecular ferroelectrics have become effective complement to inorganic ferroelectrics. However, compared with inorganic ferroelectrics, the family of molecular ferroelectrics is relatively scarce, and exploring high-performance ferroelectric materials through new synthesis strategies has become the trend of molecular ferroelectrics. Here, we successfully transformed non-polar material 1 (2-H2PCA)2(H2O)CdCl6 (2-H2PCA = 2-picolylamine cation) into polar material 2 (2-H2PCA)2CdCl6 by single-crystal to single-crystal transformation (SCSCT). Meanwhile, 2 exhibits clear ferroelectricity with a high-temperature Tc of 378 K, a Ps of 1.18 µC/cm2 at 300 K. This work not only realizes the purpose of synthesizing ferroelectrics by forming polar structures by SCSCT, but also realizes the reversibility of SCSCT, which provides ideas for the construction and exploration of new molecular ferroelectrics.

Oxidization and Chain-Branching Reaction for Recycling HDPE and Mixed HDPE/PP with In-situ Compatibilization by Ozone-Induced Reactive Extrusion.

High-density polyethylene(HDPE)and isotactic polypropylene(iPP)are widely used in industrial and residential applications due to theirlow cost and chemical stability, thustheirrecycling process can contributeto a circular economy. However, both polymers are non-polar materials, and the incompatibility with most other materials leadsto substantially inferior properties of blends. In this work, we propose a flexible compatibilization strategy to improve the compatibility of HDPE/iPP blends. Ozone was adopted to induce reactive extrusion for rapid oxidation of HDPE and chain-branching reactions for bothHDPE and HDPE/iPP blends. During extrusion process, ozone oxidizesHDPE effectively in a short time and introducesoxygen-containing groupssuchas carbonyl and ester group, which improvesthe hydrophilicity.The addition of trimethylolpropane triacrylate (TMPTA) could promote branching reaction and facilitate the formation of HDPE-g-iPP copolymers, which improved the compatibility for HDPE/iPP. As a result, the impact strength of ozone-modified HDPE and HDPE/iPP blends increased by 22% and 82%, respectively, and the tensile strength also increased. This strategy would have potential applications in the field of sorting-free and solvent-free recycling of waste polyolefin plastics.