The 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 abstractCarbon nanomaterials have shown great potential as electric heating elements in electrothermal applications. However, carbon-based heating elements with high flexibility, ultrafast electrothermal response, low driving voltage, high heating temperature, and stretchability are still lacking. Here, continuous electrospun carbon nanofiber films (CNFFs) and corresponding composite films additionally containing silicone (CSCFs) as electric heating elements are proposed. CNFFs were prepared by electrospinning and subsequent heat treatment, and CSCFs were prepared by composing CNFFs with silicone via hot-pressing procedure. Both of them have shown excellent performance as electrothermal films, such as ultrafast electrothermal response, high resistance adjustability, high flexibility, high operation stability, and high infrared emissivity. In particular, a temperature as high as 200 °C can be reached within 2 s at 8 V. Suitable robustness and flexibility allow CSCFs to bear various deformations, such as bending, twisting, folding, and even stretching by a factor of 1.3, without worsening electrothermal performance. Also, excellent water resistance has been confirmed. The superior electrothermal performance is mainly attributed to the high electrical conductivity, continuous fiber structure, high specific surface area, and adjustability of nanofiber stacking density and thickness of CNFFs.
Graphical abstractHere, we report a multiferroic relaxor material 0.41Bi(Ni1/2Zr1/2)O3–0.59PbTiO3, which exhibits a large piezoelectric coefficient (d33, 391 pC/N), high remnant polarization (Pr, 52.3 μC/cm2) and a high electrical freezing temperature (Tf, 498 K). The electric-field-induced transition from a cubic-like phase to a tetragonal phase was confirmed by the XRD patterns and first-cycle bipolar electrostrain loop. The magnetization and magnetic field relationship changes from nonlinear to linear when cooled from 300 to 2 K. The unusual trend in magnetic behavior could be interpreted as the transitions between the super short-range orderings. Furthermore, the maximum value of magnetization shows a 14% decrease at 300 K after electrical poling.
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 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 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 abstractIn view of the disadvantages of concentration polarization and trade-off effects in the application of membrane in desalination field, oxide-nano graphene oxide/polyamide (O-NGO/PA) loose intermediate layer and PA ultra-thin dense layer were introduced to fabricate PA/O-NGO/polyphenylene sulfide composite membrane with sandwich structure via multi-step interfacial polymerization (MS-IP) method. The selective permeation mechanism of ultrathin layer produced by different aqueous monomers (PIP and MPD) was studied, the effect of its physicochemical structure on the relief of concentration polarization phenomenon and the breakthrough of trade-off effect was analyzed. The ultra-thin and dense PA layer mainly played the role of interception and shortened the water molecular penetration path. In the retention test of metal salt solution, compared with the rough surface, it was found that the smooth surface was more conducive to the diffusion of intercepted metal ions into the feed solution, thus alleviating the concentration polarization phenomenon.
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 abstractElectric vehicles must be widely accepted because of environmental concerns and carbon restrictions. Previous research has looked at consumer policy preferences and their influence on electric vehicle adoption. However, none have investigated the impact of policies linked to battery recycling on electric vehicle adoption. This study used a discrete choice model (the panel-data mixed logit model) to evaluate 552 actual consumer choice data from Southwest China collected via an online questionnaire. Our results indicate that (1) 75% of respondents feel that electric vehicles enhance the environment and are eager to embrace them. However, the lack of strong recycling policies may hinder their adoption of electric vehicles. Specifically, the four battery recycling policies significantly impact electric vehicle adoption. (2) Consumers appreciate producer-oriented incentives more than consumer-oriented incentives to a lesser extent, such as mandated battery recycling policies and electric vehicle battery flow tracing policies. (3) Consumers place a larger willingness to pay on charging station density than vehicle attributes. (4) Regarding consumer heterogeneity, the usual young group in higher-rated cities prefers electric vehicles, while customers who own a car are more inclined to buy electric vehicles. Finally, more management insights and policy recommendations are provided based on these findings to help government and producer policymakers.
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%.
Graphical abstractA novel bilirubin adsorbent with high hydrophilicity was facilely synthesized via one-step hydrothermal carbonization reaction by using glucose and [3-(methacryloylamino)propyl]trimethylammonium chloride (MAPTAC) as precursors, in which sustainable carbohydrate could be converted into functionalized carbonaceous materials enriched with quaternary ammonium groups using an environmentally mild process. The properties of synthesized adsorbents were characterized by helium ion microscopy, static water contact angle measurement, FT-IR, elemental analysis and nitrogen adsorption/desorption measurement. The contact angle results indicated that these materials possessed very good hydrophilicity along with the lowest contact angle at 16.2°. Moreover, the hydrophilic adsorbent prepared by only one-step demonstrated good adsorption capacity toward bilirubin (141 mg/g) than commercialized activated carbon (70 mg/g) and low non-specific adsorption toward albumin (0.21%), which had great potential to be used in hemoperfusion. In addition, kinetic adsorption behaviors were conducted using pseudo-first-order and pseudo-second-order models. The regression results showed that the kinetic adsorption data were more accurately represented by pseudo-second-order model. The equilibrium adsorption data were analyzed using two widely applied isotherm models: Langmuir and Freundlich. The results revealed that Langmuir isotherm matched the experimental results well.
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 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 abstractIn this work, we systematically investigated the effects of single-step and two-step sintering methods on the structural, dielectric and energy storage properties of pure AgNbO3 lead-free antiferroelectric ceramics. Compared with the single-step sintered ceramic, the ceramic prepared by two-step sintering method has smaller grain size, dense and homogeneous microstructure. In addition, the results of dielectric temperature spectra reveal that the two-step sintering method hardly changes the phase transition temperature of AgNbO3 ceramics but greatly decreases the dielectric loss value. Most importantly, the ceramic prepared by the two-step sintering method displays high breakdown electric field strength (22 kV/mm), larger recoverable energy storage density-Wrec (2.59 J/cm3) and higher energy storage efficiency-η (45%) as well as excellent temperature stability than those of the ceramic by single-step sintering method. Furthermore, it also exhibited high power density (PD?=?25.7 MW/cm3) and extremely fast charge–discharge speed (25 ns). Our results provide a simple and novel way to design high-performance AgNbO3-based energy storage lead-free ceramics.
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 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 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 abstractThe electrical conductivity and piezoresistivity of multiwall carbon nanotube (MWCNT)/polypropylene (PP) composites obtained by extrusion are investigated, with particular attention to the possible directional effects generated during the extrusion process. This is accomplished by investigating the electrical and electromechanical responses of the nanocomposites at three MWCNT weight concentrations (3, 4 and 5 wt%) in three directions, viz. the extrusion direction, transverse to extrusion (in-plane) and through thickness. Higher electrical conductivity in the extrusion direction was more evident for the lowest MWCNT content. However, the piezoresistive sensitivity was similar in all directions. Films with 4 wt% showed the highest piezoresistive sensitivity, reaching gage factors of?~?4.5 for strains between 0 and 0.8%, and?~?10.2 for strains between 1 and 3%. After an initial drop in the electrical resistance, concomitant with stress relaxation, the changes in electrical resistance showed large reproducibility. Digital image correlation conducted during cyclic piezoresistive testing at 0.8% strain indicates small accumulation of local plasticity as the number of cycles increases, especially in zones near the electrodes. These irreversible changes in the material are expected to trigger the permanent changes in the electrical resistance measured.
Graphical abstractThe greigite (Fe3S4)/reduced graphene oxide (RGO) hierarchical structural composites (F–R) with the Fe3S4 nanoparticles attached to the RGO layers were successfully prepared via a simple one-pot solvothermal method. The microwave absorption properties were evaluated by calculating the reflection loss (RL) values. The results show that the RGO content and the filler loading of composites in paraffin mixture are very critical to the microwave absorption properties because they can improve the electromagnetic parameters. Sample F–R-3 presents the best microwave absorption capacity, in which an optimum RL value of ??62.3 dB and an effective absorption bandwidth (EAB, RL value?<???10 dB) of 3.04 GHz (14.96–18 GHz) can be obtained when the matching thickness is only 1.29 mm. Meanwhile, the widest EAB reaches 4.08 GHz (13.92–18 GHz) at the matching thickness of only 1.37 mm. Impressively, when the matching thickness is in the range of 1.2–5.5 mm, all RL peaks are below ??20 dB, and the EAB can be 14.98 GHz (3.02–18 GHz), covering the whole C, X and Ku bands. The distinguished absorption property is mainly ascribed to the combined effect of strong loss ability and good impedance matching. Apparently, the F–R composite with strong absorption ability, thin thickness and wide EAB is suitable for the efficient microwave absorber.
Graphical abstract