Polyimide 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 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 abstractPolyimide (PI) possesses high heat resistance and low dielectric loss, but exhibits low dielectric constant (k) and energy storage density, which constrains its further application in the field of high-temperature energy storage dielectric. The compounding of high-k filler and PI can greatly improve the dielectric constant of polymer-based dielectric composites, but it is often accompanied by the increase of dielectric loss and deterioration of breakdown strength. This issue can be effectively solved by the fabrication of dielectric filler with core–shell structure and construction of a layered structure. Therefore, in this research, a new SiC@polydopamine (PDA)@Ag nanoparticles (AgNPs)/PI flexible composite film with a sandwich structure (SSP) was prepared by a step-by-step casting method, in which the insulating layer (pristine PI) was intercalated between two polarization layers (SiC@PDA@Ag/PI composites). Pristine PI in the middle layer effectively hinders the transmission of carriers in the middle layer of the composite multilayer film. The SSP shows the highest energy storage density (1.35 J cm?3 under 273.4 kV mm?1), and the tanδ is as low as 0.0057. Additionally, SSP also shows excellent thermal stability and moisture resistance.
Graphical abstractOrganic/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 abstractThe room temperature aerosol deposition method is especially promising for the rapid deposition of ceramic thick films, making it interesting for functional components in energy, mobility, and telecommunications applications. Despite this, a number of challenges remain, such as an enhanced electrical conductivity and internal residual stresses in as-deposited films. In this work, a novel technique that integrates a sacrificial water-soluble buffer layer was used to fabricate freestanding ceramic thick films, which allows for direct observation of the film without influence of the substrate or prior thermal treatment. Here, the temperature-dependent chemical and structural relaxation phenomena in freestanding BaTiO3 films were directly investigated by characterizing the thermal expansion properties and temperature-dependent crystal structure as a function of oxygen partial pressure, where a clear nonlinear, hysteretic contraction was observed during heating, which is understood to be influenced by lattice defects. As such, aliovalent doping and atmosphere-dependent annealing experiments were used to demonstrate the influence of local chemical redistribution and oxygen vacancies on the thermal expansion, leading to insight into the origin of the high room temperature conductivity of as-deposited films as well as greater insight into the influence of the induced chemical, structural, and microstructural changes in room temperature deposited functional ceramic thick films.
Graphical abstractShort hemp fibers, an agricultural waste, were used for producing biochar by pyrolysis at 1000 °C. The so-obtained hemp-derived carbon fibers (HFB) were used as filler for improving the properties of an epoxy resin using a simple casting and curing process. The addition of HFB in the epoxy matrix increases the storage modulus while damping factor is lowered. Also, the incorporation of HFB induces a remarkable increment of electrical conductivity reaching up to 6 mS/m with 10 wt% of loading. A similar trend is also observed during high-frequency measurements. Furthermore, for the first time wear of these composites has been studied. The use of HFB is an efficient method for reducing the wear rate resistance and the friction coefficient (COF) of the epoxy resin. Excellent results are obtained for the composite containing 2.5 wt% of HFB, for which COF and wear rate decrease by 21% and 80%, respectively, as compared with those of the unfilled epoxy resin. The overall results prove how a common waste carbon source can significantly wide epoxy resin applications by a proper modulation of its electrical and wear properties.
Graphical abstractLicorice residue, a considerable amount of biomass waste discarded during the excellent extraction process of traditional Chinese medicine every year, is a potential low-cost and green material for the synthesis of porous carbon material. In this work, spinel phase NiCo2O4 nanosheets were produced on the licorice residue-derived nitrogen-doped carbon aerogel (LNCA) using simple hydrothermal and calcination methods. LNCA was first prepared from the carbonation of freeze-dried licorice residue aerogel, which was subsequently utilized to prepare an LNCA/NiCo2O4 composite employing hydrothermal reaction and annealing treatment. As a consequence of its properties, the as-prepared hybrid electrode exhibited ultrahigh capacitance specific capacity (956 F g?1 at 1 A g?1) and long-term stability. This work provides some new insights on the preparation of biomass-derived porous carbon for application in supercapacitors, as well as multifaced considerations.
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 AbstractThe effect of thermal pretreatment on the porous structure and adsorption properties of asphalt-based carbons activated with potassium hydroxide was investigated by FTIR, Raman spectroscopy, TEM, N2 and CO2 adsorption. Two series of the activated carbons were prepared by a one-stage method using KOH as the activating agent and a two-stage method including pretreatment of asphalt at 450 °C. A cross-effect of the KOH/asphalt ratio and pretreatment conditions on the characteristics of the porous structure of the activated carbons was revealed. The pretreatment of asphalt before activation is demonstrated to be a necessary stage for the effective control of the carbon porous structure by variation the KOH/asphalt ratio from 2 to 4. The porous carbon derived from petroleum asphalt exhibited the high CO2 adsorption capacity of 3.8 mmol/g at 25 °C and 1 atm and good selectivity for CO2 over N2, indicating possible applications in CO2 capture technology.
Graphical abstractModifications of the binder phase (γ) of cemented carbides have the potential to increase the hardness and wear resistance of the whole material. Partially, coherent precipitations with L12 structure (γ’) promise these improved properties without sacrificing tensile strength or toughness. γ’ is a metastable phase in the Al–Co–W ternary system in the form of Co3(Al,W) which is stabilized by the substitution of cobalt with nickel. Superalloys of the composition Co–(30Ni)–9Al–7 W with different carbon contents were prepared by inductive melting, and the resulting microstructures were analysed using SEM–EDS, XRD and Vickers hardness. Cemented carbides with γ/γ’ binder microstructure were prepared via DTA, and the phase equilibria in the composite material were investigated experimentally and in silico. It was shown that nickel stabilizes the γ’ phase in superalloys as well as in cemented carbides. Carbon leads to the formation of an additional phase with E21 structure (κ). DTA measurements of cemented carbides with different aluminium–cobalt–nickel mixtures as binder gave an overview of the compositional influence. Enthalpies of formation for compounds with L12 and E21 structure were calculated using ab initio methods and compared to experimental results.
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 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 abstractHydroxyapatite (HA) is a bioceramic material that shares similar crystal and chemical structures with inorganic components of the bone. However, HA lacks osteoinductive activity and has a brittle nature, making it challenging to apply for direct load-bearing bone applications. In this study, we used a wet chemical method to synthesize zinc-doped hydroxyapatite powders with different Zn/(Zn+Ca) molar ratios of 0, 0.025, 0.05, and 0.1. The corresponding Zn-HA was designated as HA, Zn2.5-HA, Zn5-HA, and Zn10-HA. The Zn-HA powders at 30 wt% were used to fabricate poly(propylene fumarate) (PPF)-based nanocomposite scaffolds (HA/PPF, Zn2.5-HA/PPF, Zn5-HA/PPF, and Zn10-HA/PPF). The physical properties of obtained scaffolds were examined by scanning electron microscopy, energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), and atomic force microscopy (AFM). Live/dead cell viability assay showed that these scaffolds were biocompatible and supported excellent adhesion of MC3T3-E1 preosteoblast cells. Additionally, the proliferation of cells was detected at 1, 4, and 7 days on these scaffolds. Alkaline phosphatase (ALP) activity measurement and alizarin red staining showed good osteogenic differentiation and matrix mineralization for MC3T3-E1 cells growing on these scaffolds. Taken together, the results here indicate that Zn5-HA/PPF nanocomposite scaffolds are promising scaffold material for bone tissue engineering.
Graphical abstractThe development of hydrogen production via environment-friendly and efficient electrochemical water splitting technology leans heavily on the exploitation of highly active and durable oxygen evolution reaction (OER) electrocatalysts. Herein, nanocoral-like cerium-activated cobalt selenide (Ce-CoSe2) nanocomposites to enhance the OER catalytic activity have been successfully prepared by one-pot hydrothermal route via simply altering the cerium content. Owing to the ingenious introduction of cerium, as-prepared Ce-CoSe2 electrode displays remarkable OER performance in comparison with CoSe2. The nanocoral-like Ce-CoSe2 catalyst prepared under optimal condition just needs low overpotential of 276 and 398 mV at 10 and 50 mA cm?2, respectively. Additionally, it attains the current density of 255 mA cm?2 at the potential of 2.0 V vs. RHE, and shows long-term stability during OER. This work offers a simple and feasible pathway for the design and construct of metal dichalcogenides for green and renewable hydrogen production by electrocatalytic water splitting.
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 surface of titanium oxide nanotubes (TiNTs) was chemically modified after synthesis to determine their influence on the non-isothermal crystallization of polypropylene nanocomposites compared to pristine titanium oxide nanotube-reinforced systems. Pimelic acid (PA) was used to carry out the chemical functionalization (TiNT-PA). The FTIR spectrum revealed that PA successfully bound to the TiNT surface due to the appearance of new vibrational bands at 29834, 2868, 1578, and 1407 cm?1. After the functionalization process, the morphology of TiNT remained unchanged according to TEM images. In addition, the new filler showed high thermal stability when subjected to TGA (between 320 and 450 °C). DSC studies were carried out to investigate the influence of this chemical functionalization on the crystallization behavior of the nanocomposites. The nanocomposites with the modified TiNTs showed more significant shifts of the crystallization temperature peaks with large heterogeneous nucleation. According to Jeziorny's analysis, the effect of fillers was only observed for the functionalized nanotubes with the lowest crystallization times, while the systems with pristine TiNT practically remained the same. This behavior is attributable to the fact that the acid's presence reduced agglomeration and improved the efficiency of the nucleation activity. Mo's model results confirmed that the heat flux requirements of the crystallization process were lower for the nanocomposites reinforced with TiNT-PA as they act better as heterogeneous nuclei. Then, they provide the surface area to serve as a nucleation center and help crystallize the polypropylene due to the aliphatic chain of the organic molecule.
Graphical abstractNovel thermal nanoparticles [hollow mesoporous silica nanospheres (HMSNs)–poly (N-isopropyl acrylamide-acrylic acid) PNIPAM-AA] were developed with Ag nanoparticles (AgNps) as the core, mesoporous silica nanoparticles as the layer, and thermally responsive polymers PNIPAM-AA as the shell. The AgNps had good photothermal effects, PNIPAM-AA was responsive to temperature, the combination of AgNps and PNIPAM-AA could be used as a photothermal-responsive switch for drug release, and HMSNs greatly increased the drug loading of the carrier. The samples were characterized by means of scanning electron microscopy, transmission electron microscopy, N2 adsorption–desorption, thermogravimetric analysis, Fourier transform infrared spectroscopy, and UV–Vis absorption spectra. The results showed that Ag@HMSN nanoparticles possessed a uniform diameter (330 nm), high specific surface area (822.45 m2/g), and mesoporous pore size (2.75 nm). Using ibuprofen (IBU) as a model drug, the release process was monitored under in vitro conditions to investigate its release characteristics at different temperatures. The results showed that the nanoparticles had a significant regulatory effect on IBU release.
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To strengthen the economic pillar in sustainability assessment, the indicator ‘domestic value added’ is introduced. It aims at comparing established and less developed technologies regarding their prospective value added in a country. This is done by classifying a technology’s value added to the developed categories: domestic, potential domestic and non-domestic. Within this paper, two methods for assessing this indicator are introduced focussing on their applicability in a sustainability assessment context. Both methods are tested on a case study comparing two alternative drivetrain technologies for the passenger car sector (battery and fuel cell electric vehicle) to the conventionally used internal combustion engine. The first method is life cycle cost-based whereas the second is based on Input Output analysis. If a life cycle cost assessment is already available for the technology under assessment, the easier to implement life cycle cost-based approach is recommended, as the results are similar to the more complex Input Output-based approach. From the ‘domestic value added’ perspective, the battery electric vehicle is already more advantageous than the conventional internal combustion engine over the lifecycle. Fuel cell electric vehicles have the highest potential to increase their ‘domestic value added’ share in the future. This paper broadens the economic pillar in sustainability assessment by introducing a new indicator ‘domestic value added’ and giving practical information on how to prospectively assess it for existing and less developed technologies or innovations.
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