Magnetic Hyperporous Elastic Material with Excellent Fatigue Resistance and Oil Retention for Oil-Water Separation.

Oily wastewater has caused serious threats to the environment; thus, high-performance absorbing materials for effective oil-water separation technology have attracted increasing attention. Herein, we develop a magnetic, hydrophobic, and lipophilic hyperporous elastic material (HEM) templated by high internal phase emulsions (HIPE), in which free-radical polymerization of butyl acrylate (BA) and divinylbenzene (DVB) is employed in the presence of poly(dimethylsiloxane) (PDMS), lecithin surfactant, and modified Fe3O4 nanoparticles. The adoption of the emulsion template with nanoparticles as both stabilizers and cross-linkers endows the HEM with biomimetic hierarchical open-cell micropores and elastic cross-linked networks, generating an oil absorbent with outstanding mechanical stability. Compressive fatigue resistance of the HEM is demonstrated to endure 2000 mechanical cycles without plastic deformation or strength degradation. By exploiting the synergistic effect of hierarchical structures and low-surface-energy components, the resulting HEM also possesses excellent and robust hydrophobicity (water contact angle of 164°) and good oil absorption capacity, in which Fe3O4 nanoparticles lead to convenient magnetically controlled oil recyclability as well. Notably, the unique biomimetic microporous structure demonstrates superior oil retention capacity (>95% at 1000 rpm and >60% at 10,000 rpm) over the state-of-the-art porous materials for a diverse variety of oils to reduce the risk of secondary oil leakage, along with good recoverability by squeezing owing to the excellent compression resilience. These excellent performances of our HEM provide broad prospects for practical applications in oil-water separation, energy conversion, and smart soft robotics.

Dual functionalized copper nanoparticles for thermoplastics with improved processing and mechanical properties and superior antibacterial performance.

The utilization of metal nanoparticles for antibacterial thermoplastic composites has the potential to enhance the safety of human and animal life by mitigating the spread and transmission of foodborne pathogenic bacteria. The dispersion, antioxidant and antimicrobial activities of metal nanoparticles directly affect the application performance of the composites. This study focused on achieving amine-carboxyl co-modified copper nanoparticles (Cu-AC) with excellent antioxidant properties and monodispersity through in situ grafting of amine and carboxyl groups onto the surface of copper nanoparticles via ligand interaction. Polyacrylic acid's extended carbon chain structure was utilized to improve its dispersion and antioxidant properties, and its antibacterial properties were synergistically enhanced using secondary amines. It was found that Cu-AC possesses high antibacterial properties, with a minimum inhibition concentration of 0.156 mg mL-1. Antibacterial masterbatches and their composites (polypropylene/Cu) manufactured by melt blending of polypropylene and Cu-AC exhibited excellent antibacterial rates of up to 90% and 99% at 300 ppm and 700 ppm Cu-AC, respectively. Additionally, Cu-AC bolstered the thermal degradation, processing and mechanical properties of polypropylene. The successful implementation of this product substantiates the potential applications of polypropylene/Cu composite materials across diverse industries.

Roll to roll in situ preparation of recyclable, washable, antibacterial Ag loaded nonwoven fabric.

Functional fabrics with antibacterial performance are more welcome nowadays. However, the fabrication of functional fabrics with durable, steady performance via a cost-effective way remains a challenge. Polypropylene (denoted as PP) nonwoven fabric was modified by polyvinyl alcohol (denoted as PVA), followed by the in-situ deposition of silver nanoparticles (denoted as Ag NPs) to afford PVA-modified and Ag NPs-loaded PP (denoted as Ag/PVA/PP) fabric. The encapsulation of PP fiber by PVA coating contributes to greatly enhancing the adhesion of the loaded Ag NPs to the PP fiber, and the Ag/PVA/PP nonwoven fabrics exhibit significantly improved mechanical properties as well as excellent antibacterial activity against Escherichia coli (coded as E. coli). Typically, the Ag/PVA/PP nonwoven fabric obtained at a silver ammonia concentration of 30 mM has the best mechanical properties and the antibacterial rate reaches 99.99% against E. coli. The fabric retains excellent antibacterial activity even after washing for 40 cycles, showing prospects in reuse. Moreover, the Ag/PVA/PP nonwoven fabric could find promising application in industry, thanks to its desired air-permeability and moisture-permeability. In addition, we developed a roll-to-roll production process and conducted preliminary exploration to verify the feasibility of this method.

Silver Nanoparticle-Decorated Silica Nanospheres and Arrays as Potential Substrates for Surface-Enhanced Raman Scattering.

Poly(vinylpyrrolidone) (PVP) was used as both a modifier and reductant to in situ deposit silver nanoparticles (denoted Ag NPs) on the surface of silica nanospheres (nanosilica or nano-SiO2), affording Ag-decorated nanosilica (denoted SiO2@Ag). The as-obtained SiO2@Ag composite can form silver nanoparticle-decorated silica nanosphere arrays (denoted SiO2@Ag arrays) via evaporation-induced self-assembly. The as-prepared SiO2@Ag composite and SiO2@Ag array were used as the SERS substrates to measure the Raman signals of the dilute solutions of rhodamine 6G (denoted R6G), an organic dye that is a potential pollutant to the environment. The findings indicate that the as-prepared SiO2@Ag composite and SiO2@Ag array as potential SERS substrates simultaneously exhibit a high degree of metal coverage and small size of Ag NPs as well as good stability and abundant "hot spots", which contributes to their desired Raman enhancement capacities. For the detection of trace R6G, they provide a limit of detection of as low as 10-9-10-11 M as well as good reproducibility, showing promising potential for monitoring chemical and biological molecules.

Thiol-functionalized nano-silica for in-situ remediation of Pb, Cd, Cu contaminated soils and improving soil environment.

Heavy metal contamination has been threatening the health of human beings. To decrease the bio-toxicity of heavy metals, a thiol-functionalized nano-silica (SiO2-SH) was adopted to remediate the soil contaminated by lead (Pb), cadmium (Cd) and copper (Cu). The remediation effect of SiO2-SH on contaminated soils was investigated by the uptake of the heavy metals into lettuce and pakchoi in pot experiment. The bio-toxicity of the SiO2-SH was evaluated, and its immobilization mechanisms were proposed by the fraction distribution of Cd, Pb and Cu. It was found that the SiO2-SH can significantly reduce the uptake of Cd, Pb, Cu into pakchoi by 92.02%, 68.03%, 76.34% and into lettuce by 89.81%, 43.41%, 5.76%, respectively. The chemical species analyses of Cd, Pb, Cu indicate SiO2-SH can transform the heavy metal in acid soluble states into reducible fraction and oxidizable fraction, thereby inhibiting the extraction of heavy metals into soil solution. The concentrations of microbial biomass carbon, organic matter, and cation exchange capacity of the soil increased while the soil bulk density decreased after remediation. Those changes demonstrate that SiO2-SH not only has no bio-toxic impact on the soil environment but also improves the soil environment, which proves the prepared SiO2-SH is environmental-friendly. The SiO2-SH could be a promising amendment for heavy metal contaminated soils.

Mercapto propyltrimethoxysilane- and ferrous sulfate-modified nano-silica for immobilization of lead and cadmium as well as arsenic in heavy metal-contaminated soil.

Nano-silica as an important part of soil is an ideal carrier of passivator material. In this paper, nano-silica was modified by silane coupling agent containing mercapto group and iron (II) salt to afford an organic-inorganic hybrid containing -S-Fe-S functional group (coded as RNS-SFe) on the surface of nano-silica. Results demonstrate that the RNS-SFe nanoparticle has network-like spheroidal shape and a primary particle size is about 18.0 nm. The RNS-SFe hybrid as a potential immobilization agent for heavy metal in soil shows excellent performance for the remediation of the contaminated soil. Specifically, with a dosage of 3.0% (mass ratio) in the soil, it can immobilize bioavailable Pb, Cd, and As by 97.1%, 85.0%, and 80.1%, respectively. Namely, the RNS-SFe hybrid can transform the bioavailable Pb, Cd, and As into insoluble mercapto metal compounds (-S-Pb-S- and -S-Cd-S-) and less soluble iron arsenate (Fe3(AsO4)2, FeAsO4) precipitate on the surface of nano-silica particle, thereby reducing the toxicity and mobility of the toxic contaminant fractions. In the meantime, the immobilized products of the Pb, Cd and As fractions have good resistance against acid leaching. These results are contributive to the application of RNS-SFe for the remediation of multi-heavy metal-contaminated soils in field.

Functional Janus-SiO2 Nanoparticles Prepared by a Novel "Cut the Gordian Knot" Method and Their Potential Application for Enhanced Oil Recovery.

Currently available methods (e.g., interfacial protection and phase separation) for preparing Janus nanoparticles are often complex and expensive. Furthermore, the preparation of Janus nanoparticles with a particle size below 10 nm is challenging. In this work, we combine an in situ surface-modification route with a chemical etching route to establish a novel "cut the Gordian knot" method for the preparation of functional Janus-SiO2 nanoparticles. Hydrophobic SiO2 nanoparticles with a three-dimensional network structure prepared via an in situ surface-modification route were dispersed in NaOH solution containing surfactant or ethanol to enable corrosion close to the modifier-nanoparticle interface with a relatively low content of surface modifiers. Thus, amphipathic Janus-SiO2 nanoparticles with a hydrophilic surface containing Si-OH species and a hydrophobic surface containing -CH3 fragments were generated. The as-prepared Janus-SiO2 nanoparticles with a size of 4-9 nm and a specific surface area of up to 612.9 m2/g can be easily dispersed in water, and they also can transfer from the water phase to the oil phase by tuning the surface polarity. Moreover, they can be tuned to achieve bidirectional regulation of surface wettability plus a reduction of the oil/water interface tension. Hence, a significant reduction (by 33∼50%) of water injection pressure and an enhanced oil recovery (EOR) (by 21.1% ∼ 26.6%) can be achieved. Apart from that, Janus-SiO2 nanoparticles are able to increase the viscosity of partially hydrolyzed polyacrylamide by 282.9% and significantly decrease its viscosity loss ratio in brine, causing an EOR of about 36.6%. With simple, low-cost, and scalable procedures, the following approach could be well applicable to fabricating Janus-SiO2 nanoparticles with a high potential for augmented water injection as well as EOR of low-permeability reservoirs.

Hydrophobic Silica with Potential for Water-Injection Augmentation of a Low-Permeability Reservoir: Drag Reduction and Self-Cleaning Ability in Relation to Interfacial Interactions.

An aqueous nanofluid containing superhydrophobic silica nanoparticles with a high surface activity and an average size of 7 nm was used to enhance the water injection of a low-permeability well. The mechanism for the aqueous nanofluid to enhance water injection was discussed. Findings indicate that the silica aqueous nanofluid can greatly increase the effective water permeability even after injecting water for 2100 pore volumes. This is because the hydrophobic silica nanoparticles can be well adsorbed onto the surface of the porous channels to cause hydrophilic to hydrophobic transformation. Both the hydrophobic capillary force and adhesion work contribute to increasing water injection; and in particular, there is a critical point in the pressure-permeability curves for the rock cores with different wettabilities. Only above the critical point, the hydrophobic rock core exhibits a higher effective water permeability than that of the hydrophilic one, which is imperative for drag reduction. Moreover, the hydrophobic rock core surface has a remarkable self-cleaning ability and can reduce the expansion ratio of clay and inhibit the formation of scale in association with the increase of effective porosity via decreasing the hydration film amount. This approach, highlighting the important role of wettability alteration in increasing water injection, could potentially promote the application of a silica aqueous nanofluid in enhanced oil recovery.

Waterproof, Ultrahigh Areal-Capacitance, Wearable Supercapacitor Fabrics.

High-performance supercapacitors (SCs) are promising energy storage devices to meet the pressing demand for future wearable applications. Because the surface area of a human body is limited to 2 m2 , the key challenge in this field is how to realize a high areal capacitance for SCs, while achieving rapid charging, good capacitive retention, flexibility, and waterproofing. To address this challenge, low-cost materials are used including multiwall carbon nanotube (MWCNT), reduced graphene oxide (RGO), and metallic textiles to fabricate composite fabric electrodes, in which MWCNT and RGO are alternatively vacuum-filtrated directly onto Ni-coated cotton fabrics. The composite fabric electrodes display typical electrical double layer capacitor behavior, and reach an ultrahigh areal capacitance up to 6.2 F cm-2 at a high areal current density of 20 mA cm-2 . All-solid-state fabric-type SC devices made with the composite fabric electrodes and water-repellent treatment can reach record-breaking performance of 2.7 F cm-2 at 20 mA cm-2 at the first charge-discharge cycle, 3.2 F cm-2 after 10 000 charge-discharge cycles, zero capacitive decay after 10 000 bending tests, and 10 h continuous underwater operation. The SC devices are easy to assemble into tandem structures and integrate into garments by simple sewing.

Production of Two-Dimensional Nanomaterials via Liquid-Based Direct Exfoliation.

Tremendous efforts have been devoted to the synthesis and application of two-dimensional (2D) nanomaterials due to their extraordinary and unique properties in electronics, photonics, catalysis, etc., upon exfoliation from their bulk counterparts. One of the greatest challenges that scientists are confronted with is how to produce large quantities of 2D nanomaterials of high quality in a commercially viable way. This review summarizes the state-of-the-art of the production of 2D nanomaterials using liquid-based direct exfoliation (LBE), a very promising and highly scalable wet approach for synthesizing high quality 2D nanomaterials in mild conditions. LBE is a collection of methods that directly exfoliates bulk layered materials into thin flakes of 2D nanomaterials in liquid media without any, or with a minimum degree of, chemical reactions, so as to maintain the high crystallinity of 2D nanomaterials. Different synthetic methods are categorized in the following, in which material characteristics including dispersion concentration, flake thickness, flake size and some applications are discussed in detail. At the end, we provide an overview of the advantages and disadvantages of such synthetic methods of LBE and propose future perspectives.

Charging Guidance of Electric Taxis Based on Adaptive Particle Swarm Optimization.

Electric taxis are playing an important role in the application of electric vehicles. The actual operational data of electric taxis in Shenzhen, China, is analyzed, and, in allusion to the unbalanced time availability of the charging station equipment, the electric taxis charging guidance system is proposed basing on the charging station information and vehicle information. An electric taxis charging guidance model is established and guides the charging based on the positions of taxis and charging stations with adaptive mutation particle swarm optimization. The simulation is based on the actual data of Shenzhen charging stations, and the results show that electric taxis can be evenly distributed to the appropriate charging stations according to the charging pile numbers in charging stations after the charging guidance. The even distribution among the charging stations in the area will be achieved and the utilization of charging equipment will be improved, so the proposed charging guidance method is verified to be feasible. The improved utilization of charging equipment can save public charging infrastructure resources greatly.

Biomimicking Topographic Elastomeric Petals (E-Petals) for Omnidirectional Stretchable and Printable Electronics.

Elastomeric petals directly replicated from natural rose petal are new versatile substrates for stretchable and printable electronics. Compared with conventional flat polydimethylsiloxane substrates, elastomeric petals have biomimicking topographic surfaces that can effectively inhibit the propagation of microcracks formed in the conducting layer, which is deposited on top, regardless of the type of conductive materials and the deposition methods.

Full-solution processed flexible organic solar cells using low-cost printable copper electrodes.

Full-solution-processed flexible organic solar cells (OSCs) are fabricated using low-cost and high-quality printable Cu electrodes, which achieve a power conversion efficiency as high as 2.77% and show remarkable stability upon 1000 bending cycles. This device performance is thought to be the best among all full-solution-processed OSCs reported in the literature using the same active materials. This printed Cu electrode is promising for application in roll-to-roll fabrication of flexible OSCs.

Photosensitive graphene transistors.

High performance photodetectors play important roles in the development of innovative technologies in many fields, including medicine, display and imaging, military, optical communication, environment monitoring, security check, scientific research and industrial processing control. Graphene, the most fascinating two-dimensional material, has demonstrated promising applications in various types of photodetectors from terahertz to ultraviolet, due to its ultrahigh carrier mobility and light absorption in broad wavelength range. Graphene field effect transistors are recognized as a type of excellent transducers for photodetection thanks to the inherent amplification function of the transistors, the feasibility of miniaturization and the unique properties of graphene. In this review, we will introduce the applications of graphene transistors as photodetectors in different wavelength ranges including terahertz, infrared, visible, and ultraviolet, focusing on the device design, physics and photosensitive performance. Since the device properties are closely related to the quality of graphene, the devices based on graphene prepared with different methods will be addressed separately with a view to demonstrating more clearly their advantages and shortcomings in practical applications. It is expected that highly sensitive photodetectors based on graphene transistors will find important applications in many emerging areas especially flexible, wearable, printable or transparent electronics and high frequency communications.

Organic electrochemical transistors with graphene-modified gate electrodes for highly sensitive and selective dopamine sensors.

Organic electrochemical transistors (OECTs) are successfully used as highly sensitive and selective dopamine sensors. The selectivity of the OECT-based dopamine sensors is significantly improved by coating biocompatible polymer Nafion or chitosan on the surface of the gate electrodes. The interference induced by uric acid and ascorbic acid is effectively eliminated especially after the modification of Nafion. The sensitivity of the devices is improved by graphene flakes co-modified on the gate electrodes. The detection limit of the devices to dopamine is down to 5 nM, which is much lower than that of conventional electrochemical approaches. Because the OECT-based dopamine sensors are solution processable, they are suitable for low-cost and disposable sensing application.

Salt-assisted direct exfoliation of graphite into high-quality, large-size, few-layer graphene sheets.

We report a facile and low-cost method to directly exfoliate graphite powders into large-size, high-quality, and solution-dispersible few-layer graphene sheets. In this method, aqueous mixtures of graphite and inorganic salts such as NaCl and CuCl2 are stirred, and subsequently dried by evaporation. Finally, the mixture powders are dispersed into an orthogonal organic solvent solution of the salt by low-power and short-time ultrasonication, which exfoliates graphite into few-layer graphene sheets. We find that the as-made graphene sheets contain little oxygen, and 86% of them are 1-5 layers with lateral sizes as large as 210 µm(2). Importantly, the as-made graphene can be readily dispersed into aqueous solution in the presence of surfactant and thus is compatible with various solution-processing techniques towards graphene-based thin film devices.

Highly selective and sensitive glucose sensors based on organic electrochemical transistors with graphene-modified gate electrodes.

The sensitivity of glucose sensors based on organic electrochemical transistors (OECT) is increased by co-modifying graphene or reduced graphene oxide (rGO) and enzyme (glucose oxidase) on the gate electrodes for the first time. The optimized device shows linear responses to glucose in a broad concentration region from 10 nM to 1 µM and with a detection limit down to 10 nM, which is two orders of magnitude better than that for the device without the graphene modification. The selectivity of the device is systematically studied for the first time. The device selectivity is dramatically improved when the gate electrode is modified with biocompatible polymers (chitosan or Nafion). The interfering effect caused by uric acid and l-ascorbic acid is almost negligible for practical applications. Therefore, highly sensitive and selective OECT-based glucose sensors can be realized by functionalizing the gate electrodes. In addition, the devices are solution processable and low-cost, and are thus suitable for disposable sensing applications.