Oil sorbents play a very important part in the remediation processes of oil spills. To enhance the oil‐sorption properties and simplify the oil‐recovery process, various advanced oil sorbents and ...oil‐collecting devices based on them have been proposed recently. Here, we firstly discuss the design considerations for the fabrication of oil sorbents and describe recently developed oil sorbents based on modification strategy. Then, recent advances regarding oil sorbents mainly based on carbon materials and swellable oleophilic polymers are also presented. Subsequently, some additional properties are emphasized, which are required by oil sorbents to cope with oil spills under extreme conditions or to facilitate the oil‐collection processes. Furthermore, some oil‐collection devices based on oil sorbents that have been developed recently are shown. Finally, an outlook and challenges for the next generation of oil‐spill‐remediation technology based on oil‐sorbents materials are given.
Hydrophobic and oleophilic sorbent materials are demonstrated as promising candidates for the cleanup of oil spills. An overview of the latest developments and advances in the fabrication of oil sorbents through modification strategy, carbon‐based oil sorbents, and polymer‐based oil sorbents, as well as some smart oil sorbents and oil‐collecting devices based on oil‐sorbent materials are presented.
SiOx is proposed as one of the most promising anodes for Li‐ion batteries (LIBs) for its advantageous capacity and stable Li uptake/release electrochemistry, yet its practical application is still a ...big challenge. Here encapsulation of SiOx nanoparticles into conductive graphene bubble film via a facile and scalable self‐assembly in solution is shown. The SiOx nanoparticles are closely wrapped in multilayered graphene to reconstruct a flake‐graphite‐like macrostructure, which promises uniform and agglomeration‐free distribution of SiOx in the carbon while ensures a high mechanical strength and a high tap density of the composite. The composites present unprecedented cycling stability and excellent rate capabilities upon Li storage, rendering an opportunity for its anode use in the next‐generation high‐energy LIBs.
SiOx nanoparticles are closely wrapped in multilayered graphene to reconstruct a macrostructure resembling flake graphite, which promises agglomeration‐free distribution of SiOx in the bulk while ensuring a high mechanical strength and a high tap density of the bubble film. By taking the advantages of the graphene network, the composites present unprecedented cycling stability and excellent rate capabilities upon Li storage.
A
bstract
We show that the cosmological abundance of string axions is much smaller than naive estimates if the Hubble scale of inflation,
H
inf
, is sufficiently low (but can still be much higher ...than the axion masses) and if the inflation lasts sufficiently long. The reason is that the initial misalignment angles of the string axions follow the Bunch-Davies distribution peaked at the potential minima. As a result, the cosmological moduli problem induced by the string axions can be significantly relaxed by low-scale inflation, and astrophysical and cosmological bounds are satisfied over a wide range of the mass without any fine-tuning of the initial misalignment angles. Specifically, the axion with its decay constant
f
ϕ
= 10
16
GeV satisfies the bounds over 10
−18
eV ≲
m
ϕ
≲ 10 TeV for
H
inf
≲ 10 keV-10
6
GeV. We also discuss cases with multiple axions and the QCD axion.
Single‐atom catalysts (SACs) are of great interest because of their ultrahigh activity and selectivity. However, it is difficult to construct model SACs according to a general synthetic method, and ...therefore, discerning differences in activity of diverse single‐atom catalysts is not straightforward. Herein, a general strategy for synthesis of single‐atom metals implanted in N‐doped carbon (M1‐N‐C; M=Fe, Co, Ni and Cu) has been developed starting from multivariate metal–organic frameworks (MOFs). The M1‐N‐C catalysts, featuring identical chemical environments and supports, provided an ideal platform for differentiating the activity of single‐atom metal species. When employed in electrocatalytic CO2 reduction, Ni1‐N‐C exhibited a very high CO Faradaic efficiency (FE) up to 96.8 % that far surpassed Fe1‐, Co1‐ and Cu1‐N‐C. Remarkably, the best‐performer, Ni1‐N‐C, even demonstrated excellent CO FE at low CO2 pressures, thereby representing a promising opportunity for the direct use of dilute CO2 feedstock.
A series of porphyrinic multivariate metal–organic frameworks (MTV‐MOFs) were pyrolyzed to generate a range of single‐atom metals implanted in N‐doped carbon (M1‐N‐C; M=Fe, Co, Ni and Cu). The M1‐N‐C model catalysts, with an almost identical carbon support environment, demonstrated different activities toward CO2 electroreduction. The best performer, Ni1‐N‐C, achieved highly selective reduction of CO2 even at low pressures.
Inspired by smart biological tissues, artificial muscle-like actuators offer fascinating prospects due to their distinctive shape transformation and self-healing function under external stimuli. ...However, further practical application is hindered by the lack of simple and general routes to fabricate ingenious soft materials with anisotropic responsiveness. Here, we describe a general in situ polymerization strategy for the fabrication of anisotropic hydrogels composed of highly-ordered lamellar network crosslinked by the metal nanostructure assemblies, accompanied with remarkably anisotropic performances on mechanical, optical, de-swelling and swelling behaviors. Owing to the dynamic thiolate-metal coordination as healing motifs, the composites exhibit rapid and efficient multi-responsive self-healing performance under NIR irradiation and low pH condition. Dependent on well-defined anisotropic structures, the hydrogel presents controllable solvent-responsive mechanical actuating performance. Impressively, the integrated device through a healing-induced assembly way can deliver more complicated, elaborate forms of actuation, demonstrating its great potentials as superior soft actuators like smart robots.
Superelastic carbon aerogels have been widely explored by graphitic carbons and soft carbons. These soft aerogels usually have delicate microstructures with good fatigue resistance but ultralow ...strength. Hard carbon aerogels show great advantages in mechanical strength and structural stability due to the sp3‐C‐induced turbostratic “house‐of‐cards” structure. However, it is still a challenge to fabricate superelastic hard carbon‐based aerogels. Through rational nanofibrous structural design, the traditional rigid phenolic resin can be converted into superelastic hard carbon aerogels. The hard carbon nanofibers and abundant welded junctions endow the hard carbon aerogels with robust and stable mechanical performance, including superelasticity, high strength, extremely fast recovery speed (860 mm s−1), low energy‐loss coefficient (<0.16), long cycle lifespan, and heat/cold‐endurance. These emerging hard carbon nanofiber aerogels hold a great promise in the application of piezoresistive stress sensors with high stability and wide detection range (50 kPa), as well as stretchable or bendable conductors.
A family of hard carbon aerogels with nanofibrous structure templated by various nanofibers is fabricated, displaying robust and stable mechanical performances, including high strength, extremely fast recovery speed (860 mm s−1), and ultralow energy loss coefficient (<0.16). After being compressed for 104 cycles (50% strain), they show only ≈2% plastic deformation and retain ≈93% stress.
Self-healability is essential for supercapacitors to improve their reliability and lifespan when powering the electronics. However, the lack of a universal healing mechanism leads to low capacitive ...performance and unsatisfactory intelligence. Here, we demonstrate a multi-responsive healable supercapacitor with integrated configuration assembled from magnetic Fe
O
@Au/polyacrylamide (MFP) hydrogel-based electrodes and electrolyte and Ag nanowire films as current collectors. Beside a high mechanical strength, MFP hydrogel exhibits fast optical and magnetic healing properties arising from distinct photothermal and magneto-thermal triggered interfacial reconstructions. By growing electroactive polypyrrole nanoparticles into MFP framework as electrodes, the assembled supercapacitor exhibits triply-responsive healing performance under optical, electrical and magnetic stimuli. Notably, the device delivers a highest areal capacitance of 1264 mF cm
among the reported healable supercapacitors and restores ~ 90% of initial capacitances over ten healing cycles. These prominent performance advantages along with the facile device-assembly method make this emerging supercapacitor highly potential in the next-generation electronics.
Energy efficient buildings require materials with a low thermal conductivity and a high fire resistance. Traditional organic insulation materials are limited by their poor fire resistance and ...inorganic insulation materials are either brittle or display a high thermal conductivity. Herein we report a mechanically resilient organic/inorganic composite aerogel with a thermal conductivity significantly lower than expanded polystyrene and excellent fire resistance. Co‐polymerization and nanoscale phase separation of the phenol‐formaldehyde‐resin (PFR) and silica generate a binary network with domain sizes below 20 nm. The PFR/SiO2 aerogel can resist a high‐temperature flame without disintegration and prevents the temperature on the non‐exposed side from increasing above the temperature critical for the collapse of reinforced concrete structures.
Fire not starter: Taking advantage of a co‐polymerization strategy an organic–inorganic binary network hybrid aerogel with a nanoscale homogeneity can be prepared. The phenol‐formaldehyde‐resin/SiO2 aerogel is mechanically resilient and has a thermal conductivity significantly lower than expanded polystyrene and excellent fire resistance.
The past decade has witnessed great progress in the synthesis and electrocatalytic applications of 1D hollow alloy nanotubes with controllable compositions and fine structures. Hollow nanotubes have ...been explored as promising electrocatalysts in the fuel cell reactions due to their well‐controlled surface structure, size, porosity, and compositions. In addition, owing to the self‐supporting ability of 1D structure, hollow nanotubes are capable of avoiding catalyst aggregation and carbon corrosion during the catalytic process, which are two other issues for the widely investigated carbon‐supported nanoparticle catalysts. It is currently a great challenge to achieve high activity and stability at a relatively low cost to realize commercialization of these catalysts. An overview of the structural and compositional properties of 1D hollow alloy nanotubes, which provide a large number of accessible active sites, void spaces for electrolytes/reactants impregnation, and structural stability for suppressing aggregation, is presented. The latest advances on several strategies such as hard template and self‐templating methods for controllable synthesis of hollow alloyed nanotubes with controllable structures and compositions are then summarized. Benefiting from the advantages of the unique properties and facile synthesis approaches, the capability of 1D hollow nanotubes is then highlighted by discussing examples of their applications in fuel‐cell‐related electrocatalysis. Finally, the remaining challenges and potential solutions in the field are summarized to provide some useful clues for the future development of 1D hollow alloy nanotube materials.
One‐dimensional hollow alloyed nanotubes with desired composition and controlled fine structures are emerging as a unique type of electrocatalysts, which hold vast potential and broad development space in fuel‐cell reactions. The potential and challenges of hollow alloyed nanotubes in electrocatalytic application are reviewed, providing a perspective on the further development of these nanotubes.
The general synthesis and control of the coordination environment of single‐atom catalysts (SACs) remains a great challenge. Herein, a general host–guest cooperative protection strategy has been ...developed to construct SACs by introducing polypyrrole (PPy) into a bimetallic metal–organic framework. As an example, the introduction of Mg2+ in MgNi‐MOF‐74 extends the distance between adjacent Ni atoms; the PPy guests serve as N source to stabilize the isolated Ni atoms during pyrolysis. As a result, a series of single‐atom Ni catalysts (named NiSA‐Nx‐C) with different N coordination numbers have been fabricated by controlling the pyrolysis temperature. Significantly, the NiSA‐N2‐C catalyst, with the lowest N coordination number, achieves high CO Faradaic efficiency (98 %) and turnover frequency (1622 h−1), far superior to those of NiSA‐N3‐C and NiSA‐N4‐C, in electrocatalytic CO2 reduction. Theoretical calculations reveal that the low N coordination number of single‐atom Ni sites in NiSA‐N2‐C is favorable to the formation of COOH* intermediate and thus accounts for its superior activity.
A host–guest cooperative protection strategy has been developed for constructing single‐atom catalysts (SACs), extending the range of available precursors from nitrogenous to non‐nitrogenous MOFs. The obtained Ni‐SACs (NiSA‐Nx‐C; x=2, 3, 4) at different pyrolysis temperatures feature varying nitrogen coordination numbers. The best of these catalysts, NiSA‐N2‐C, shows superior activity and selectivity in CO2 electroreduction.
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