Carbon Dots as Fillers Inducing Healing/Self‐Healing and Anticorrosion Properties in Polymers

Self‐healing is the way by which nature repairs damage and prolongs the life of bio entities. A variety of practical applications require self‐healing materials in general and self‐healing polymers in particular. Different (complex) methods provide the rebonding of broken bonds, suppressing crack, or local damage propagation. Here, a simple, versatile, and cost‐effective methodology is reported for initiating healing in bulk polymers and self‐healing and anticorrosion properties in polymer coatings: introduction of carbon dots (CDs), 5 nm sized carbon nanocrystallites, into the polymer matrix forming a composite. The CDs are blended into polymethacrylate, polyurethane, and other common polymers. The healing/self‐healing process is initiated by interfacial bonding (covalent, hydrogen, and van der Waals bonding) between the CDs and the polymer matrix and can be optimized by modifying the functional groups which terminate the CDs. The healing properties of the bulk polymer–CD composites are evaluated by comparing the tensile strength of pristine (bulk and coatings) composites to those of fractured composites that are healed and by following the self‐healing of scratches intentionally introduced to polymer–CD composite coatings. The composite coatings not only possess self‐healing properties but also have superior anticorrosion properties compared to those of the pure polymer coatings.     

Solid‐State Carbon Dots with Red Fluorescence and Efficient Construction of Dual‐Fluorescence Morphologies

Stable solid‐state red fluorescence from organosilane‐functionalized carbon dots (CDs) with sizes around 3 nm is reported for the first time. Meanwhile, a novel method is also first reported for the efficient construction of dual‐fluorescence morphologies. The quantum yield of these solid‐state CDs and their aqueous solution is 9.60 and 50.7%, respectively. The fluorescence lifetime is 4.82 ns for solid‐state CDs, and 15.57 ns for their aqueous solution. These CDs are detailedly studied how they can exhibit obvious photoluminescence overcoming the self‐quenching in solid state. Luminescent materials are constructed with dual fluorescence based on as‐prepared single emissive CDs (red emission) and nonfluorescence media (starch, Al₂O₃, and RnOCH₃COONa), with the characteristic peaks located at nearly 440 and 600 nm. Tunable photoluminescence can be successfully achieved by tuning the mass ratio of CDs to solid matrix (such as starch). These constructed dual‐fluorescence CDs/starch composites can also be applied in white light‐emitting diodes with UV chips (395 nm), and oxygen sensing.     

Far‐Red to Near‐Infrared Carbon Dots: Preparation and Applications in Biotechnology

As novel fluorescent nanomaterials, carbon dots (CDs) exhibit excellent photostability, good biocompatibility, and high quantum yield (QY). Their superior properties make them promising candidates for biomedical assays and therapy. Among them, the red‐emission (>600 nm) CDs have attracted increasing attention in the past years due to their little damage to the biological matrix, deep tissue penetration, and minimum autofluorescence background of biosamples. This Review, summarizes the recent progress of far‐red to near‐infrared (NIR) CDs from the preparation and their biological applications. The challenges in designing far‐red and NIR CDs and their further applications in biomedical fields are also discussed.     

Photo‐Stimulated Polychromatic Room Temperature Phosphorescence of Carbon Dots

Single‐component multicolor luminescence, particularly phosphorescence materials are highly attractive both in numerous applications and in‐depth understanding the light‐emission processes, but formidable challenges still exist for preparing such materials. Herein, a very facile approach is reported to synthesize carbon dots (CDs) (named MP‐CDs) that exhibit multicolor fluorescence (FL), and more remarkably, multicolor long‐lived room temperature phosphorescence (RTP) under ambient conditions. The FL and RTP colors of the CDs powder are observed to change from blue to green and cyan to yellow, respectively, with the excitation wavelength shifting from 254 to 420 nm. Further studies demonstrate that the multicolor emissions can be attributed to the existence of multiple emitting centers in the CDs and the relatively higher reaction temperature plays a critical role for achieving RTP. Given the unique optical properties, a preliminary application of MP‐CDs in advanced anti‐counterfeiting is presented. This study not only proposes a strategy to prepare photo‐stimulated multicolor RTP materials, but also reveals great potentials of CDs in exploiting novel optical materials with unique properties.     

One‐Step Synthesis of Silica‐Coated Carbon Dots with Controllable Solid‐State Fluorescence for White Light‐Emitting Diodes

Carbon dots (CDots)‐based solid‐state luminescent materials have important applications in light‐emitting devices owing to their outstanding optical properties. However, it still remains a challenge to develop multiple‐color‐emissive solid‐state CDots, due to the serious self‐quenching of the CDots in the aggregation or solid state. Herein, a one‐step synthesis of multiple‐color‐emissive solid‐state silica‐coated CDots (silica/CDots) composites by controlling CDots loading fraction and composite morphology to realize the adjustment of emitting color is reported. The emission of resultant silica/CDots composites shifts from blue to orange with the photoluminescence quantum yields of 57.9%, 34.3%, and 32.7% for blue, yellow, and orange emitting, respectively. Furthermore, the yellow emitting silica/CDots composites exhibit an excellent fluorescence thermal stability, and further have been applied to fabricate white‐light‐emitting devices with a high color rendering index of above 80.     

Recent Advances of Carbon Dots with Afterglow Emission

Carbon dots (CDs) have gradually become a new generation of nano-luminescent materials, which have received extensive attention due to excellent optical properties, wide source of raw materials, low toxicity, and good biocompatibility. In recent years, there are many reports on the luminescent phenomenon of CDs, and great progress has been achieved. However,there are rarely systematic summaries on CDs with persistent luminescence. Here, a summary of the recent progress on persistent luminescent CDs, including luminous mechanism, synthetic strategies, property regulation, and potential applications, is given. First, a brief introduction is given to the development of CDs luminescent materials. Then, the luminous mechanism of afterglow CDs from room temperature phosphorescence (RTP), delayed fluorescence (DF), and long persistent luminescence (LPL) is discussed. Next, the constructed methods of luminescent CDs materials are summarized from two aspects, including matrix-free self-protected and matrix-protected CDs. Moreover, the regulation of afterglow properties from color, lifetime, and efficiency is presented. Afterwards, the potential applications of CDs, such as anti-counterfeiting, information encryption, sensing, bio-imaging, multicolor display, LED devices, etc., are reviewed. Finally, an outlook on the development of CDs materials and applications is proposed.     

Microstructural and Nano‐Mechanical Characterisation of Multicomponent Composites Nanocrystalline Matrix

Multicomponent, Ti‐based, in situ formed composites with a nanocrystalline matrix are a promising new type of material for structural applications. The materials exhibit an excellent combination of mechanical properties resulting from the composite microstructure. This paper contains a detailed introduction to such materials and a review of the most recent developments in the specific areas of microstructural and nano‐mechanical characterization.     

Nature‐Inspired Nacre‐Like Composites Combining Human Tooth‐Matching Elasticity and Hardness with Exceptional Damage Tolerance

Making replacements for the human body similar to natural tissue offers significant advantages but remains a key challenge. This is pertinent for synthetic dental materials, which rarely reproduce the actual properties of human teeth and generally demonstrate relatively poor damage tolerance. Here new bioinspired ceramic–polymer composites with nacre‐mimetic lamellar and brick‐and‐mortar architectures are reported, which resemble, respectively, human dentin and enamel in hardness, stiffness, and strength and exhibit exceptional fracture toughness. These composites are additionally distinguished by outstanding machinability, energy‐dissipating capability under cyclic loading, and diminished abrasion to antagonist teeth. The underlying design principles and toughening mechanisms of these materials are elucidated in terms of their distinct architectures. It is demonstrated that these composites are promising candidates for dental applications, such as new‐generation tooth replacements. Finally, it is believed that this notion of bioinspired design of new materials with unprecedented biologically comparable properties can be extended to a wide range of material systems for improved mechanical performance.     

Novel Nanoparticle‐Reinforced Metal Matrix Composites with Enhanced Mechanical Properties

This paper summarizes and reviews the state‐of‐the‐art processing methods, structures and mechanical properties of the metal matrix composites reinforced with ceramic nanoparticles. The metal matrices of nanocomposites involved include aluminum and magnesium. The processing approaches for nanocomposites can be classified into ex‐situ and in‐situ synthesis routes. The ex‐situ ceramic nanoparticles are prone to cluster during composite processing and the properties of materials are lower than the theoretical values. Despite the fact of clustering, ex‐situ nanocomposites reinforced with very low loading levels of nanoparticles exhibit higher yield strength and creep resistance than their microcomposite counterparts filled with much higher particulate content. Better dispersion of ceramic nanoparticles in metal matrix can be achieved by using appropriate processing techniques. Consequently, improvements in both the mechanical strength and ductility can be obtained readily in aluminum or magnesium by adding ceramic nanoparticles. Similar beneficial enhancements in mechanical properties are observed for the nanocomposites reinforced with in‐situ nanoparticles.     

Highly Ordered N‐Doped Carbon Dots Photosensitizer on Metal–Organic Framework‐Decorated ZnO Nanotubes for Improved Photoelectrochemical Water Splitting

In spite of having several advantages such as low cost, high chemical stability, and environmentally safe and benign synthetic as well as operational procedures, the full potential of carbon dots (CDs) is yet to be explored as photosensitizers due to the challenges associated with the fabrication of well‐arrayed CDs with many other photocatalytic heterostructures. In the present study, a unique combination of metal–organic framework (MOF)‐decorated zinc oxide (ZnO) 1D nanostructures as host and CDs as guest species are explored on account of their potential application in photoelectrochemical (PEC) water splitting performance. The synthetic strategy to incorporate well‐defined nitrogen‐doped carbon dots (N‐CDs) arrays onto a zeolitic imidazolate framework‐8 (ZIF‐8) anchored on ZnO 1D nanostructures allows a facile unification of different components which subsequently plays a decisive role in improving the material's PEC water splitting performance. Simple extension of such strategies is expected to offer significant advantages for the preparation of CD‐based heterostructures for photo(electro)catalytics and other related applications.     

Determination of Dynamic Modulus of Syntactic and Particulate Foams by a Non‐Destructive Approach

Abstract: Developments in aviation posed requirement of lightweight, high strength and highly damage‐tolerant materials. Sandwich‐structured composites fulfilling these requirements have become the first choice for many aerospace applications as well as structural components for ground transport and marine vessels. Sandwich composites are a special class of composite materials which are widely used because of their high specific strength and high bending stiffness. Syntactic foams, which are hollow particle‐filled core materials used in sandwich composites, have recently emerged as attractive material for applications requiring low weight, low moisture absorption and high insulation properties. Quasi‐static and dynamic properties of these syntactic foams are commonly determined though various destructive techniques such as quasi‐static compression and split Hopkinson pressure bar testing. However, there is a need for characterising these materials non‐destructively in the field. The present study focuses on the prediction of dynamic Young's modulus using ultrasonic testing in various types of hollow particle‐reinforced syntactic foam and solid particulate composites. Hollow particle‐filled syntactic foams and solid particulate composites are fabricated with three different volume fractions of 10%, 30% and 60%. Longitudinal and shear wave velocities are used for calculating the dynamic modulus. Effect of longitudinal attenuation behaviour along with longitudinal and shear wave velocities on the varying density and volume fraction of syntactic foams is also discussed.     

Critical factors on manufacturing processes of natural fibre composites

Elevated environmental awareness of the general public in reducing carbon footprints and the use non-naturally decomposed solid wastes has resulted in an increasing use of natural materials, biodegradable and recyclable polymers and their composites for a wide range of engineering applications. The properties of natural fibre reinforced polymer composites are generally governed by the pre-treated process of fibre and the manufacturing process of the composites. These properties can be tailored for various types of applications by properly selecting suitable fibres, matrices, additives and production methods. Besides, due to the complexity of fibre structures, different mechanical performances of the composites are obtained even with the use of the same fibre types with different matrices. Some critical issues like poor wettability, poor bonding and degradation at the fibre/matrix interface (a hydrophilic and hydrophobic effect) and damage of the fibre during the manufacturing process are the main causes of the reduction of the composites’ strength. In this paper, different manufacturing processes and their suitability for natural fibre composites, based on the materials, mechanical and thermal properties of the fibres and matrices are discussed in detail.     

Critical factors on manufacturing processes of natural fibre composites

Elevated environmental awareness of the general public in reducing carbon footprints and the use non-naturally decomposed solid wastes has resulted in an increasing use of natural materials, biodegradable and recyclable polymers and their composites for a wide range of engineering applications. The properties of natural fibre reinforced polymer composites are generally governed by the pre-treated process of fibre and the manufacturing process of the composites. These properties can be tailored for various types of applications by properly selecting suitable fibres, matrices, additives and production methods. Besides, due to the complexity of fibre structures, different mechanical performances of the composites are obtained even with the use of the same fibre types with different matrices. Some critical issues like poor wettability, poor bonding and degradation at the fibre/matrix interface (a hydrophilic and hydrophobic effect) and damage of the fibre during the manufacturing process are the main causes of the reduction of the composites’ strength. In this paper, different manufacturing processes and their suitability for natural fibre composites, based on the materials, mechanical and thermal properties of the fibres and matrices are discussed in detail.     

Carbon‐Nanotube‐Based Thermoelectric Materials and Devices

Conversion of waste heat to voltage has the potential to significantly reduce the carbon footprint of a number of critical energy sectors, such as the transportation and electricity‐generation sectors, and manufacturing processes. Thermal energy is also an abundant low‐flux source that can be harnessed to power portable/wearable electronic devices and critical components in remote off‐grid locations. As such, a number of different inorganic and organic materials are being explored for their potential in thermoelectric‐energy‐harvesting devices. Carbon‐based thermoelectric materials are particularly attractive due to their use of nontoxic, abundant source‐materials, their amenability to high‐throughput solution‐phase fabrication routes, and the high specific energy (i.e., W g^?1) enabled by their low mass. Single‐walled carbon nanotubes (SWCNTs) represent a unique 1D carbon allotrope with structural, electrical, and thermal properties that enable efficient thermoelectric‐energy conversion. Here, the progress made toward understanding the fundamental thermoelectric properties of SWCNTs, nanotube‐based composites, and thermoelectric devices prepared from these materials is reviewed in detail. This progress illuminates the tremendous potential that carbon‐nanotube‐based materials and composites have for producing high‐performance next‐generation devices for thermoelectric‐energy harvesting.     

Creating Stiff,Tough, and Functional Hydrogel Composites with Low‐Melting‐Point Alloys

Reinforcing hydrogels with a rigid scaffold is a promising method to greatly expand the mechanical and physical properties of hydrogels. One of the challenges of creating hydrogel composites is the significant stress that occurs due to swelling mismatch between the water‐swollen hydrogel matrix and the rigid skeleton in aqueous media. This stress can cause physical deformation (wrinkling, buckling, or fracture), preventing the fabrication of robust composites. Here, a simple yet versatile method is introduced to create “macroscale” hydrogel composites, by utilizing a rigid reinforcing phase that can relieve stress‐induced deformation. A low‐melting‐point alloy that can transform from a load‐bearing solid state to a free‐deformable liquid state at relatively low temperature is used as a reinforcing skeleton, which enables the release of any swelling mismatch, regardless of the matrix swelling degree in liquid media. This design can generally provide hydrogels with hybridized functions, including excellent mechanical properties, shape memory, and thermal healing, which are often difficult or impossible to achieve with single‐component hydrogel systems. Furthermore, this technique enables controlled electrochemical reactions and channel‐structure templating in hydrogel matrices. This work may play an important role in the future design of soft robots, wearable electronics, and biocompatible functional materials.     

Rational Design of Covalent Bond Engineered Encapsulation Structure toward Efficient,Long-Lived Multicolored Phosphorescent Carbon Dots (Small 31/2023)

Multicolored phosphorescent materials based on carbon dots (CDs) constructed using the same or similar precursors with long lifetimes are conducive to their wide range of practical applications due to the developed compatibility. Herein, a universal method is developed to prepare long-lived multicolored phosphorescent CD-based composites for which heavy-metal doping is not required. The multicolored CDs are encapsulated in silica via silane hydrolysis, which forms many covalent Si O C and Si C bonds; hence, the vibrations and rotations of the luminescent centers on the CD surfaces are hindered. The transformation of Si O C to a more rigid Si C moiety occurs during high-temperature calcination. Furthermore, during calcination, the silica collapses, resulting in more tightly encapsulated CDs. The synergistic effect of these two calcination phenomena produces blue, green, yellow, and red phosphorescence, at wavelengths spanning 465 to 680 nm and with lifetimes of up to 2.11 s. Taking advantage of their superior phosphorescence performances, the CD-based composites are successfully applied to 3D multichannel information storage and encryption.     

Progress in Piezo‐Phototronic‐Effect‐Enhanced Light‐Emitting Diodes and Pressure Imaging

Wurtzite materials exhibit both semiconductor and piezoelectric properties under strains due to the non‐central symmetric crystal structures. The three‐way coupling of semiconductor properties, piezoelectric polarization and optical excitation in ZnO, GaN, CdS and other piezoelectric semiconductors leads to the emerging field of piezo‐phototronics. This effect can efficiently manipulate the emission intensity of light‐emitting diodes (LEDs) by utilizing the piezo‐polarization charges created at the junction upon straining to modulate the energy band diagrams and the optoelectronic processes, such as generation, separation, recombination and/or transport of charge carriers. Starting from fundamental physics principles, recent progress in piezo‐phototronic‐effect‐enhanced LEDs is reviewed; following their development from single‐nanowire pressure‐sensitive devices to high‐resolution array matrices for pressure‐distribution mapping applications. The piezo‐phototronic effect provides a promising method to enhance the light emission of LEDs based on piezoelectric semiconductors through applying static strains, and may find perspective applications in various optoelectronic devices and integrated systems.     

Lanthanide‐Doped Photoluminescence Hollow Structures: Recent Advances and Applications

Lanthanide‐doped nanomaterials have attracted significant attention for their preeminent properties and widespread applications. Due to the unique characteristic, the lanthanide‐doped photoluminescence materials with hollow structures may provide advantages including enhanced light harvesting, intensified electric field density, improved luminescent property, and larger drug loading capacity. Herein, the synthesis, properties, and applications of lanthanide‐doped photoluminescence hollow structures (LPHSs) are comprehensively reviewed. First, different strategies for the engineered synthesis of LPHSs are described in detail, which contain hard, soft, self‐templating methods and other techniques. Thereafter, the relationship between their structure features and photoluminescence properties is discussed. Then, niche applications including biomedicines, bioimaging, therapy, and energy storage/conversion are focused on and superiorities of LPHSs for these applications are particularly highlighted. Finally, keen insights into the challenges and personal prospects for the future development of the LPHSs are provided.     

Prospects of Supercritical Fluids in Realizing Graphene‐Based Functional Materials

Supercritical‐fluids science and technology predate all the approaches that are currently established for graphene production by several decades in advanced materials design. However, it has only recently been proposed as a plausible approach for graphene processing. Since then, supercritical fluids have emerged into contention as an alternative to existing technologies because of their scalability and versatility in processing graphene materials, which include composites, aerogels, and foams. Here, an overview is presented of such materials prepared through supercritical fluids from an advanced materials science standpoint, with a discussion on their fundamental properties and technological applications. The benefits of supercritical‐fluid processing over conventional liquid‐phase processing are presented. The benefits include not only better performances for advanced applications but also environmental issues associated with the synthesis process. Nevertheless, the limitations of supercritical‐fluid processing are also stressed, along with challenges that are still faced toward the achievement of the great expectations from graphene materials.     

Reinforcement in Al Matrix Composites: A Review of Strengthening Behavior of Nano‐Sized Particles

Aluminum matrix composites (AMCs) reinforced with the nano‐sized particles are very important materials for the applications in industrial fields. These aluminum matrix composites consist of an aluminum matrix and nano‐sized particles, which own very different physical and mechanical properties from those of the matrix. Nano‐sized particles show a more obvious strengthening effect on the matrix than the micro‐sized particles do, because of the high specific surface area which is positive for the pinning effect during the deformation process. Thus, the nano‐sized particle‐reinforced AMCs usually exhibit a good ductility. The main issues of the fabrication methods are the low wettability between the nano‐sized particles and the molten aluminum alloys, which is fatal to the conventional casting methods, and the agglomeration of nano‐sized particles which happened easier than the larger particles. Several alternative processes have been presented in literature for the production of the nano‐sized particle‐reinforced aluminum composites. This paper is aimed at reviewing the feasible manufacturing techniques used for the fabrication of nano‐sized particle‐reinforced aluminum composites. More importantly, the strengthening mechanisms and models which are responsible for the improvement of mechanical properties of the nano‐sized particle‐reinforced aluminum composites have been reviewed.