Organic/inorganic thermoelectric composites have played an important role in the development of new, green, and renewable energy sources with potential applications in efficient thermal management, flexible electronics, and bioelectronics. Electrochemical syntheses, including electropolymerization, electrochemical deposition, electrochemical doping, electrochemical post-processing, etc., require no addition of surfactants or oxidants, the products of which are easy to separate and purify, providing clean, efficient, and facile routes for the preparation of organic thermoelectric materials and their composites. In this review, the preparation, properties, and applications of organic/inorganic thermoelectric composites from electrochemical synthesis were reviewed in detail, offering a perspective on the recent advances in the field.
Graphical abstractIn this study, poly(L-lactic acid) (PLA)/low molar mass alkali lignin (aL) (1%, 5% and 10% w/w) composites were prepared primarily for a comprehensive understanding of the effect of aL on their antimicrobial properties, biocompatibility and cytotoxic behavior. The properties were evaluated by Fourier transform infrared spectroscopy, scanning electron microscopy, differential scanning calorimetry, thermogravimetry and X-ray diffraction. The mechanical, water vapor barrier properties and photodegradability were analyzed as well. The results showed a significant inhibiting effect of aL on the crystallization behavior of PLA, increased water barrier properties (up to 73%) and photodegradability. PLA/aL composites showed a tenfold reduction in Gram-positive bacteria viability, very good cellular response and very low cytotoxicity levels, thus validating these materials as non-cytotoxic and with high potential to be used as food packaging.
Graphical abstractThe properties of nanoparticle–polymer composites strongly depend on the network structure of the polymer matrix. By introducing nanoparticles into a monomer (solution) and subsequently polymerizing it, the formation of the polymer phase influences the mechanical and physicochemical properties of the composite. In this study, semi-conducting indium tin oxide (ITO) nanoparticles were prepared to form a rigid nanoparticle scaffold in which 1,6-hexanediol diacrylate (HDDA), together with an initiator for photo-polymerization, was infiltrated and subsequently polymerized by UV light. During this process, the polymerization reaction was characterized using rapid scan Kubelka–Munk FT-IR spectroscopy and compared to bulk HDDA. The conductivity change of the ITO nanoparticles was monitored and correlated with the polymerization process. It was revealed that the reaction rates of the radical initiation and chain propagation are reduced when cured inside the voids of the nanoparticle scaffold. The degree of conversion is lower for HDDA infiltrated into the mesoporous ITO nanoparticle scaffold compared to purely bulk-polymerized HDDA.
Graphical abstractAquivion membrane displays improved properties as compared to Nafion membrane, partly due to shorter side chains. However, some improvements are still necessary for proton exchange membrane fuel cell to operate at low relative humidity. To overcome this drawback, the addition of clay nanoparticle into the Aquivion matrix can be considered. In this study, different composite membranes have been prepared mixing short-side-chain PFSA (perfluorosulfonic acid) Aquivion and selectively modified halloysite nanotubes for PEMFC low relative humidity operation. Halloysites were grafted with fluorinated groups, sulfonated groups, or perfluoro-sulfonated groups on inner or outer surface of the tubes. The obtained composite membranes showed improved properties, especially higher water uptake associated with reduced swelling and better mechanical strength compared to pristine Aquivion membrane and commercially available Nafion HP used as reference. The best performance in this study was obtained with Aquivion loaded with 5 wt% of pretreated perfluoro-sulfonated halloysite. The composite membrane, referred to as Aq/pHNT-SF5, displayed the largest water uptake and proton conductivity among the panel of membranes tested. The chemical stability was not affected by the presence of halloysite in the Aquivion matrix.
Graphical abstractIn this critical note, the thermal stability behavior of ultra-fine grained (UFG) and nano-structured (NS) metals and alloys produced through severe plastic deformation (SPD) techniques is reviewed. For this case, the common engineering metals with body-centered cubic (BCC), face-centered cubic (FCC), and hexagonal close-packed (HCP) crystal structures such as aluminum, copper, nickel, magnesium, steel, titanium, and their relating alloys were assessed. Microstructural evolution in these severely deformed materials following post-processing annealing treatment was investigated for various times and temperatures below the recrystallization point. The microstructure development reported in the literature was studied in terms of the stable grain structures correlated with different levels of plastic straining. The stacking fault energy (SFE) is noted to be a key issue which has a critical influence in predicting the coalescence or coarsening behavior of ultra-fine and nanoscale grains after SPD treatment by controlling the cross-slip phenomenon for screw dislocations.
Graphical AbstractExtension of corrosion inhibitors from traditional molecular-scale to nanoscale will not only be significant to develop green and efficient inhibitors, but also supplement the discipline system of corrosion inhibitors. However, many research on the interfacial behavior of nano-inhibitors have ignored the special colloidal properties of nanoparticles and show no obvious differences with traditional inhibitors. In this study, graphene oxide (GO) was functionalized with polydopamine (PDA) via covalent modifications and self-polymerization, and GO-PDA was studied as a corrosion inhibitor of carbon steel in HCl solution. Diversified measurements confirmed that GO-PDA can effectively protect carbon steel from corrosion, and the inhibition efficiency almost reached 90% at 100 mg/L. Interfering factors including immersion time and concentration were investigated. The lamellar nanoparticles adsorbed on the surface of carbon steel have formed a hydrophobic film in micro-nano structures. The transition from a negative charge on the GO surface to a positively charged GO-PDA contributed to adsorption at the interface. An initial model of nano-inhibitor was established to explicate the inhibition mechanism.
Graphical abstractCold welding technique at room temperature is the preferred option in nano-assembly and nano-jointing. In this study, the cold welding behavior and mechanical strength of Cu50Zr50 metallic glass nanowires (MGNWs) in head-to-head contact are investigated by molecular dynamics simulation based on the embedded atom method potential. Effects of welding velocity, operating temperature, and size of nanowires are discussed with the consideration of stress, shear strain, atomic deformation processes, and weld quality. Our simulation results demonstrate that a desirable weld quality can be obtained at room temperature. With an increase in welding velocity, the shear deformation zones of the welded MGNWs increase, leading to a decrease in mechanical strength. However, the effect of temperature on the weld quality is not pronounced. Besides, the elongation ability of the welded MGNWs increases with increasing diameters of nanowires. Smaller diameter results in better weld quality due to the size effect of metallic glass. For a pair of MGNWs with different diameters, the necking and fracture of the welded MGNWs occur in the regions of the nanowire with a relatively smaller diameter. This study carries major implications for the fabrication and structural assembly of metallic glass-based nanomaterials.
Graphical AbstractSilica aerogel composites reinforced with different aramid fibres have been synthesized and compared considering their potential use in thermal protection systems of Space devices. These composites were prepared from tetraethoxysilane and vinyltrimethoxysilane and the network was strengthened with aramid fibres. The results showed that the physical and chemical properties of the fibres were relevant, leading to composites with different properties/performance. In general, the obtained values for bulk density were low, down to 150 kg m?3. Very good thermal properties were achieved, reaching thermal conductivities bellow 30 mW m?1 K?1, and thermal stability up to 550 °C in all cases. Short length fibres produce stiffer composites with lower thermal conductivities, while among longer fibres, meta-aramid-containing fibres lead to nanocomposites with best insulation performance. Standard tests for Space materials qualification, as thermal cycling and outgassing, were conducted to assess the compliance with Space conditions, confirming the suitability of these aerogel composites for this application.
Graphical abstractOxygen-containing carbon materials have been studied extensively because of their excellent dispersibility, absorptivity, separability, and supportability of catalysts. However, structural control by existing top-down methods is almost impossible. Our group has demonstrated that phloroglucinol (PG, 1,3,5-trihydroxybenzene) can be a promising raw material to synthesize structurally controlled oxygen-containing carbon materials. In this study, in addition to PG, hexahydroxybenzene (HHB), which has more oxygen and high symmetry, was used as the raw material, and a Lewis acid catalyst, tris (pentafluorophenyl) borane (TPB), was used to enhance the structural control rate and the removability of catalysts from the carbonized samples. The solubility of heat-treated HHB was lower than that of heat-treated PG, but the oxygen content of heat-treated HHB was higher than that of heat-treated PG even at 673 K. By adding TPB to PG, dibenzofuran-like structures formed, and the structural control rate increased up to 93.6%. Besides, the content of fluorine in the catalyst was reduced to 0%, indicating that TPB can be a promising recyclable catalyst to promote the structural control rate of carbonized PG.
Graphical abstractNon-dendritic microstructures are generally obtained in metals after semi-solid deformation (deformation during solidification); however, dendritic growth is preferred without deformation. The fragmentation of dendrites is recognized as an essential contributing factor to non-dendritic microstructures. However, the underlying mechanism of fragmentation needs to be clarified in depth. It is infamously hard for researchers to carry out a direct observation of this process. Moreover, a comprehensive numerical survey of this process is not trivial. The present research reported a new method to model dendritic growth during semi-solid deformation. The motion and deformation of the solid coupled with liquid flow in the melt were treated as the two-phase flow because plastic materials could be formulated as non-Newtonian fluids. The vector-valued phase-field formulation and the self-constructed Navier–Stokes solver made it possible to simulate the growth, motion, deformation, fragmentation and agglomeration of two dendrites coupled with liquid flow in the melt. Computational results suggest that fragmentation can occur when the grain boundary is wet and penetrated by the melt, giving new supporting evidence to a previously proposed mechanism for the fragmentation of dendrites.
Graphical abstractSilver nanowires find use in a myriad of applications, including communication systems, sensors, medical devices and electrical equipment. Temperature-dependent electrical and thermal properties of chemically derived silver nanowires are rarely explored. In the present work, seed-mediated synthesis of silver nanowires has been carried out, and their electrical and thermal conductivity at 300 K is found to be 1.848?×?107 S/m and 64.8 W/mK, respectively. A screen-printable ink of silver nanowires is formulated and printed on low-cost and widely used substrates like paper and cotton fabrics. Flexible printed electrodes could be made possible with uniform printed structures obtained in cotton fabric and paper substrate. The printed pattern exhibited sheet resistance of 0.7 Ω/sq. Screen-printed silver nanowires on paper show shielding efficiency of 99.9% in X band, which promotes them as excellent candidates in fabricating lightweight electronic devices by a one-step printing process.
Graphical abstractWO3, a visible light reaction catalyst, absorbs light at a wavelength of 470 nm and has many advantages, such as strong stability, long life, non-toxicity, low cost, and suitable band edges. In this review, the photocatalytic mechanism of WO3 in water pollution treatment is introduced, as well as a systematic summary, and some main strategies for improving the photocatalytic activity of WO3 in water pollution treatment are introduced, for example surface and morphology control, synthetic heterojunctions, and doping element. Finally, the main conclusions and prospects of WO3-based photocatalysts are pointed out. It can be expected that this review can provide guidance for designing low-cost, high-efficiency new WO3-based photocatalysts in the process of water pollution treatment and can meet the application prospects of efficient utilization of solar degradation in the field of environmental purification.
Graphical abstractSilicon has become one of the most emerging anode materials in Li-ion batteries due to its excellent specific capacity. The incorporation of binders can significantly reduce the volume expansion of silicon during the cycling process. In this work, a novel type of cross-linked siloxane-based copolymer, poly (tert-butyl acrylate-co-vinyl tri-lactate ethyl silane) (TBA-VTLES) was designed and utilized as the binder for the silicon anode in Li-ion batteries to alleviate the inner stress of adverse volume changes and improve the electrochemical performance. The hard TBA and soft VTLES were interwoven into a 3D network to achieve the adhesive action via free radical polymerization. The soft chains in TBA-VTLES can enhance the cohesion of the copolymer to disperse residual stress, and thus avoid structural damage during lithiation. Meanwhile, the rigid chains can provide sufficient mechanical strength to maintain the integrity of silicon anode during de-lithiation. Moreover, the presence of TBA-VTLES can improve the adhesive strength between the copper collector and the binder. This novel type of siloxane-based copolymer binder with hardness and softness provides a feasible way to improve the silicon anode performance of Li-ion batteries.
Graphical abstractThe synthesized cross-linked copolymer binder can improve the interfacial interaction and electrochemical performance of Si anode-- present in Graphical abstract figure-- need or not.
相似文献Nanotechnologies known as a developing applied science have significant global socioeconomic values and many advantages obtained from nanoscale materials. Its applications can have significant effects on the performance of organizations. The advance of two-dimensional (2D) MXene-derived QDs (MQDs) is currently in the initial stages. Scholars have shown distinguished optical, electronic, thermal and mechanical attributes by surface chemistry and versatile transition metal. In this field of study, many applications are introduced like energy electromagnetic interference shielding, storage, sensors, transparent electrodes, photothermal therapy, catalysis and so on. The vast range of optical absorption attributes of MQDs along with high electronic conductivity has been detected to be key attributes because of their achievement in the mentioned usages. Currently, relatively little materials are highly known because of their basic electronic and optical properties, which can limit their full potentials. From a theoretical and experimental point of view, in this work, electronic and optical properties of MQDs along with applications corresponding to those properties were evaluated.
Graphical abstractProton conductivity, morphology, phase composition and mechanical properties of (1-x)CsH2PO4-xp(VDF/HFP) (x?=?0.05–0.25, weight ratio) polymer electrolytes were investigated for the first time. The chemical interaction of the organic matrix and acid salt was not observed and crystal structure of CsH2PO4 was preserved. A method for the synthesis of thin membranes with uniform distribution of the components was proposed. Thin flexible membranes with uniform distribution of sub-micrometer CsH2PO4 particles in the polymer membranes and improved hydrolytic stability were obtained firstly by using a bead mill. The mechanical strength of the hybrid polymer compounds was determined using the Vickers microhardness measurements. Proton conductivity in the (1-x)CsH2PO4-xp(VDF/HFP) electrolytes decreases monotonically with x increase due to the «conductor–insulator» percolation. Nevertheless, the values of proton conductivity remain sufficiently high, and along with small thickness, flexibility, improved mechanical and hydrophobic properties, it makes polymer electrolytes based on CsH2PO4 promising for membranes of medium-temperature fuel cells.
Graphical abstractThe caloric effects under combined applications of magnetic field and hydrostatic pressure to a MnCoSi meta-magnet were investigated. Under a magnetic field change of 0–5 T, the maximum magnetic entropy change was enhanced by 35.7% when a 3.2kbar hydrostatic pressure was applied, and the cooling temperature span was extended by 60 K when a hydrostatic pressure of 9.7 kbar was applied. The coupled caloric entropy change, which originates from the coupling between the magnetism and volume, was calculated and accounted for the enhanced entropy change of MnCoSi. The present work facilitates the use of MnCoSi as a solid-state refrigerant and also enriches the investigation of the multicaloric effect under multiple external fields.
Graphical abstractHybrid organic–inorganic nanocomposites are great candidates for display and illumination systems due to improved optoelectronic properties and photostability. This work endeavours towards the scientific study of the influence of defect-induced zinc oxide nanoparticles (ZnO) on the optical characteristics of poly[2-methoxy-5-(2′-ethylhexyloxy)-1,4-phenylenevinylene] (MEH-PPV). ZnO nanoparticles consist of many vacancies which facilitate light emission across the visible region. The green defective emission occurring due to the presence of oxygen vacancies in ZnO was used to re-excite MEH-PPV and hence, improve the luminescence quantum efficiency. The photostability of the nanocomposite was enhanced through charge transfer (prevents the formation of superoxides) and energy transfer (reduces the non-radiative decay) mechanisms.
Graphical abstractWe review the literature describing the use of interleaves to increase interlaminar fracture toughness in fibre-reinforced polymer composites and hence to improve damage tolerance. From an analysis of data provided in the literature from the use of microfibre and nanofibre interleaves, we show that the performance of these widely researched systems is clearly differentiated when plotted against the mean coverage of the interleaf. Using a simple analysis, we suggest that this can be attributed to the influence of their porous architectures on the infusion of resin. We show also that the superior toughening performance of microfibre interleaves is only weakly influenced by the choice of fibre. We find also that the inclusion of carbon nanotubes within interleaves to deliver multifunctional composites can be optimised by using a hybrid system with microfibres.
Graphical abstractPolyimide aerogels are promising for diverse applications owing to their nanoporous structure and superior performance in thermal insulation, dielectric protection, etc. However, the severe shrinkage they usually suffer has long been a threat, and can pose great challenges to their shape-stable preparation and reliable applications. It is very important to clarify the effects of various factors on the shrinkage of PI aerogels and the effective strategies available for shrinkage reduction. These are also the focuses of the present review, to provide guidance for preparing PI aerogels with greatly reduced shrinkage, and thereby improved shape stability and use reliability. Since the shrinkage of PI aerogels is quite a complex issue, further studies on PI aerogels against shrinkage deserve continuous attention.
Graphical abstractPlanar perovskite solar cells (PSCs) have excellent photoelectric properties and show great commercialization potential. However, there are a lot of crystal defects in the perovskite films prepared by solution method, which reduces the development process of solar cells. In this work, alizarin red s (ARS) was doped into MAPbI3 films to passivate the defect. It was shown that the addition of ARS increased the quality of perovskite film and doped perovskite film exhibited improved light absorption. In addition, it was found that there was a strong interaction between ARS and perovskite, which reduced the density of defect states. The results showed that the passivated perovskite device had improved PL intensity, increased carrier lifetimes and reduced charge recombination. After passivation, the device obtained a higher open-circuit voltage (VOC) of 1.103 V where the control device was 1.055 V, and the best power conversion efficiency (PCE) of the doped device was 18.82%, which is 11.36% higher than that of the control device of 16.90%.
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