Electrically Responsive Materials and Devices Directly Driven by the High Voltage of Triboelectric Nanogenerators

Smart materials with electrically responsive characteristics and devices relying on different electrostatic effects can be directly driven by triboelectric nanogenerators (TENGs). The open circuit voltage from a TENG can easily reach thousands of volts with a separation distance of a few millimeters and this high output voltage can be used to effectively drive or control some devices with high internal resistance. This kind of combination is the most straightforward way for achieving a self‐powered smart system. Hence, a detailed survey of electrically responsive materials and devices that can be successfully combined with TENG is summarized, including dielectric elastomers, piezoelectric materials, ferroelectric materials, electrostatic manipulators, electrostatic air cleaners, and field emission and mass spectrometers. Moreover, key factors in determining suitable materials or devices to work with TENG are clarified and an in‐depth discussion of the current challenges related to these combined systems is provided. With the cost‐effectiveness and simple manufacturing process, these TENG‐based composite systems have great application prospects in the field of smart mechanics, human–machine interaction systems, intelligent storage systems, self‐powered microfluidic chips, portable mass spectrometers, and so on.     

Stimuli‐Responsive Bioinspired Materials for Controllable Liquid Manipulation: Principles,Fabrication, and Applications

Many emerging interfacial technologies, such as self‐cleaning surfaces, oil/water separation, water collection, and microfluidics, are essentially liquid manipulation processes. In this regard, micro‐nanostructures of the living organisms are highly preferable, by virtue of the evolutionary pressure and the adaptation to the specific environments, to inspire the optimization of man‐made interfaces. With the increasing demands of modern life, research, and industry, intelligent materials with stimuli‐responsive liquid manipulation functions have gained substantial attention from interfacial scientists. This review introduces the recent progress in the development of stimuli‐responsive liquid‐manipulating materials with bioinspired structures and surface chemistry according to two classified manipulation modes: (i) smart manipulation of liquid wetting behaviors, including lyophobic/lyophilic and superlyophobic/superlyophilic, and (ii) smart manipulation of liquid motion behaviors, including coalescence, transportation, rolling/adhesion, and sliding/pinning. At the beginning of the presentation of each classification, the theoretical basis and the sources of inspiration are introduced comprehensively to ensure a better understanding. This review mainly focuses on the mechanisms, fabrication, and applications of the state‐of‐the‐art works related to smart and biomimetic liquid‐manipulating materials. Finally, conclusions and future prospects are provided, and the remaining problems and promising breakthroughs in fabricating large‐scale, cost‐effective, and efficient smart liquid‐manipulating materials are outlined.     

Whirling‐Folded Triboelectric Nanogenerator with High Average Power for Water Wave Energy Harvesting

Ocean wave energy, as one of the most abundant resources on the earth, is a promising energy source for large‐scale applications. Triboelectric nanogenerators (TENGs) provide a new strategy for water wave energy harvesting; however, its average performance in realistic water wave conditions is still not high. In this work, a whirling‐folded TENG (WF‐TENG) with maximized space utilization and minimized electrostatic shielding is constructed by 3D printing and printed circuit board technologies. The flexible vortex structure responds easily to multiform wave excitation with improved oscillation frequency. A standard water wave tank is established to generate controllable water waves to characterize the device performance. It is found to be determined by wave conditions and internal structure, which is also revealed by a theoretical dynamical analysis. The WF‐TENG can produce a maximum peak power of 6.5 mW and average power of 0.28 mW, which can power a digital thermometer to operate constantly and realize self‐powered monitoring on the TENG network to prevent possible damage in severe environments. Moreover, a self‐charge‐supplement WF‐TENG network is proposed to improve the output performance and stability. This study provides an effective strategy for improving the average power and characterizing the performance of spherical TENG towards large‐scale blue energy.     

Theoretical Model and Outstanding Performance from Constructive Piezoelectric and Triboelectric Mechanism in Electrospun PVDF Fiber Film

Flexible materials with high electromechanical coupling performance are highly demanded for wide applications for electromechanical sensors and transducers, including mechanical energy harvesters. Here, outstanding electromechanical performance is obtained in electrospun‐aligned polyvinylidene fluoride (PVDF) fiber film. A theoretical model is developed from systematic theoretical analyses to clarify the underlying constructive piezoelectric‐triboelectric mechanism in the polarized PVDF fiber films that explains the experimental observations well. The electrospinning process induces polarization alignment and thus tunes the electron affinity for PVDF fibers with different polarization terminals, which results in the constructive piezoelectric and triboelectric responses in the obtained PVDF fiber films. Extremely large effective piezoelectric performance properties are achieved in the direct piezoelectric measurements, reaching the maximum effective piezoelectric strain and voltage coefficients of ?1065 pm V^?1 and ?9178 V mm N^?1, respectively, at 100 Hz. In the converse piezoelectric measurements without a significant contribution from reversible triboelectric effect, the maximum effective piezoelectric strain and voltage coefficients are ?166 pm V^?1 and ?1499 V mm N^?1, respectively. The theoretical analyses and experimental results show the great potential of the electrospun aligned polar PVDF fiber material for various electromechanical device applications, particularly for mechanical energy harvesting.     

3D Printed Supercapacitor: Techniques,Materials, Designs,and Applications

Supercapacitors (SCs) offer broad possibilities in the rising domain of military and civilian owing to their intrinsic properties of superior power density, long lifetime, and safety features. Despite of low-cost, facile manufacture, and time-saving, 3D printing technology unleashes the potential of SCs in terms of achieving desirable capacitance with high mass loading, fabrication of well-designed complicated structures, and direct construction of on-chip integration systems. In this review, first, the representative printing technologies for SCs and advanced printable materials are scrutinized for SCs and advanced printable materials. Then the structure design principles of electrodes and devices are respectively highlighted and reported cases are systematically summarized. Next, configurations of the SCs and their applications in various areas are described in detail. Finally, the promising research directions for the future are discussed. The perspectives reviewed here are expected to provide a comprehensive understanding of 3D-printed SCs and guidance in realizing their promise in various applications.     

Bio‐Inspired Photonic Materials: Prototypes and Structural Effect Designs for Applications in Solar Energy Manipulation

Natural creatures have evolved elaborate photonic nanostructures on multiple scales and dimensions in a hierarchical, organized way to realize controllable absorption, reflection, or transmitting the desired wavelength of the solar spectrum. A bio‐inspired strategy is a powerful and promising way for solar energy manipulation. This feature article presents the state‐of‐the‐art progress on bio‐inspired photonic materials on this particular application. The article first briefly recalls the physical origins of natural photonic effects and catalogues the typical natural photonic prototypes including light harvesting, broadband reflection, selective reflection, and UV/IR response. Next, typical applications are categorized into two primary areas: solar energy utilization and reflection. Recent advances including solar‐to‐electricity, solar‐to‐fuels, solar‐thermal (e.g., photothermal converters, infrared detectors, thermoelectric materials, smart windows, and solar steam generation) are highlighted in the first part. Meanwhile, solar energy reflection involving infrared stealth, radiative cooling, and micromirrors are also addressed. In particular, this article focuses on bioinspired design principles, structural effects on functions, and future trends. Finally, the main challenges and prospects for the next generation of bioinspired photonic materials are discussed, including new design concepts, emerging ideas, and possible strategies.     

Meta‐Stable Molecular Configuration Enables Thermally Stable and Solution Processable Organic Charge Transporting Materials

The construction of state‐of‐the‐art charge transporting materials (CTMs) is challenging in modulating molecular configurations for simultaneously achieving high thermal stability and appreciable solution processability. Herein, N,N′‐bis(1‐indanyl)naphthalene‐1,4,5,8‐tetracarboxylic diimide (NDI‐ID) is served as a theoretical model to investigate the influence of molecular structure on the tradeoff between thermal stability and solubility. Compared with the alkyl substituted analog, the thermal stability of NDI‐ID is enhanced by the intramolecular and intermolecular short contacts, indicating the conformational rigidity dictates the morphological stability of the film phase. On the other hand, the dynamic topological transformation of material molecules occurs during the solvation process and, where the intramolecular hydrogen bonds are attenuated by the interactions with the surrounding solvent, leads to the increased solubility. The meta‐stable molecular configuration endows NDI‐ID a favorable union of superior solution processability and higher thermal stability, and this insight is also perfectly exemplified by the newly designed CTMs. Therefore, these results reveal the significant role of structural dynamics on material properties, which can provide a new train of thought to develop CTMs for highly efficient and stable perovskite solar cells.     

Fe3O4 Nanoparticles Confined in Mesocellular Carbon Foam for High Performance Anode Materials for Lithium‐Ion Batteries

Fe₃O₄ nanocrystals confined in mesocellular carbon foam (MSU‐F‐C) are synthesized by a “ host–guest ” approach and tested as an anode material for lithium‐ion batteries (LIBs). Briefly, an iron oxide precursor, Fe(NO₃)₃·9H₂O, is impregnated in MSU‐F‐C having uniform cellular pores ～30 nm in dia­meter, followed by heat‐treatment at 400 °C for 4 h under Ar. Magnetite Fe₃O₄ nanocrystals with sizes between 13–27 nm are then successfully fabricated inside the pores of the MSU‐F‐C, as confirmed by transmission electron microscopy (TEM), dark‐field scanning transmission electron microscopy (STEM), energy dispersive X‐ray spectroscopy (EDS), X‐ray diffraction (XRD), and nitrogen sorption isotherms. The presence of the carbon most likely allows for reduction of some of the Fe³⁺ ions to Fe²⁺ ions via a carbothermoreduction process. A Fe₃O₄/MSU‐F‐C nanocomposite with 45 wt% Fe₃O₄ exhibited a first charge capacity of 1007 mA h g^?1 (Li⁺ extraction) at 0.1 A g^?1 (～0.1 C rate) with 111% capacity retention at the 150^th cycle, and retained 37% capacity at 7 A g^?1 (～7 C rate). Because the three dimensionally interconnected open pores are larger than the average nanosized Fe₃O₄ particles, the large volume expansion of Fe₃O₄ upon Li‐insertion is easily accommodated inside the pores, resulting in excellent electrochemical performance as a LIB anode. Furthermore, when an ultrathin Al₂O₃ layer (<4 Å) was deposited on the composite anode using atomic layer deposition (ALD), the durability, rate capability and undesirable side reactions are significantly improved.     

An Alternative Approach to Constructing Solution Processable Multifunctional Materials: Their Structure,Properties, and Application in High‐Performance Organic Light‐Emitting Diodes

A new series of full hydrocarbons, namely 4,4′‐(9,9′‐(1,3‐phenylene)bis(9H‐fluorene‐9,9‐diyl))bis(N,N‐diphenylaniline) (DTPAFB), N,N′‐(4,4′‐(9,9′‐(1,3‐phenylene)bis(9H‐fluorene‐9,9‐diyl))bis(4,1‐phenylene))bis(N‐phenylnaphthalen‐1‐amine) (DNPAFB), 1,3‐bis(9‐(4‐(9H‐carbazol‐9‐yl)phenyl)‐9H‐fluoren‐9‐yl)benzene, and 1,3‐bis(9‐(4‐(3,6‐di‐tert‐butyl‐9H‐carbazol‐9‐yl)phenyl)‐9H‐fluoren‐9‐yl)benzene, featuring a highly twisted tetrahedral conformation, are designed and synthesized. Organic light‐emitting diodes (OLEDs) comprising DNPAFB and DTPAFB as hole transporting layers and tris(quinolin‐8‐yloxy)aluminum as an emitter are made either by vacuum deposition or by solution processing, and show much higher maximum efficiencies than the commonly used N,N′‐di(naphthalen‐1‐yl)‐N,N′‐diphenylbiphenyl‐4,4′‐diamine device (3.6 cd A^?1) of 7.0 cd A^?1 and 6.9 cd A^?1, respectively. In addition, the solution processed blue phosphorescent OLEDs employing the synthesized materials as hosts and iridium (III) bis[(4,6‐di‐fluorophenyl)‐pyridinato‐N, C²] picolinate (FIrpic) phosphor as an emitter present exciting results. For example, the DTPAFB device exhibits a brightness of 47 902 cd m^?2, a maximum luminescent efficiency of 24.3 cd A^?1, and a power efficiency of 13.0 lm W^?1. These results show that the devices are among the best solution processable blue phosphorescent OLEDs based on small molecules. Moreover, a new approach to constructing solution processable small molecules is proposed based on rigid and bulky fluorene and carbazole moieties combined in a highly twisted configuration, resulting in excellent solubility as well as chemical miscibility, without the need to introduce any solubilizing group such as an alkyl or alkoxy chain.     

Recent Progress in MXene‐Based Materials: Potential High‐Performance Electrocatalysts

The family of transition metal carbides, nitrides, and carbonitrides (collectively called MXenes) has been a thriving field since the first invention of Ti₃C₂T_x (MXene) in 2011. MXene is a new type of nanometer 2D sheet material, which exhibits great application potentials in various fields due to its multiple advantages such as high specific surface area, good electrical conductivity, and high mechanical strength. Electrocatalysis is regarded as the core of future clean energy conversion technologies, and MXene‐based materials provide inspiration for the design and preparation of electrocatalysts with high activity, high selectivity, and long loading life time. The applications of MXene‐based materials in electrocatalysis, including hydrogen evolution reaction, nitrogen reduction reaction, oxygen evolution reaction, oxygen reduction reaction, carbon dioxide reduction reaction, and methanol oxidation reaction are summarized in this review. As a crucial session regarding experiments, the current safer and more environmentally friendly preparation methods of MXene are also discussed. Focusing on the materials design and enhancement methods, the key challenges and opportunities for MXene‐based materials as a next‐generation platform in both fundamental research and practical electrocatalysis applications are presented. This account serves to promote future efforts toward the development of MXenes and related materials in the electrocatalysis applications.     

Toward the Effective Exploitation of Topological Phases of Matter in Catalysis: Chemical Reactions at the Surfaces of NbAs and TaAs Weyl Semimetals

By means of density functional theory and experiments, surface chemical reactivity of single crystals of NbAs and TaAs Weyl semimetals is studied. Weyl semimetals exhibit outstanding reactivity toward simple molecules (oxygen, carbon monoxide, and water), with several active sites available for surface chemical reactions (adsorption, decomposition, formation of reaction products, recombination of decomposition fragments). When different chemical species are adsorbed on Weyl semimetals, strong lateral interactions between coadsorbed species occur, evidenced by CO‐promoted water decomposition at room temperature. The resulting ? OH groups react with CO to form HCOO, which is an intermediate species in water–gas shift reaction. These findings unambiguously demonstrate that Weyl semimetals could be effectively used in catalysis, whereas their employment in nanoelectronics or plasmonics is complicated by the poor ambient stability, due to the rapid surface oxidation, inevitably occurring unless protective capping layers are used.     

Developments and Challenges in Self‐Healing Antifouling Materials

Self‐healing antifouling materials have gained rapidly increasing interest over the past decade and have been studied and used in a rapidly increasing range of applications. Recent developments and challenges in self‐healing antifouling materials are summarized in four sections: first, the different mechanisms for both antifouling and self‐healing are briefly discussed. Second, three main categories of self‐healing antifouling materials based on surface replenishing and dynamic covalent and noncovalent interactions are discussed, with a focus on the preparation, characterization, and central characteristics of different self‐healing antifouling materials. Third, different types of potential applications of self‐healing antifouling materials are summarized, such as injectable hydrogels and oil/water separations. Finally, a summary of future development of the field is provided, and a number of critical limitations that are still outstanding are highlighted.     

Heterogeneous Nanosized Metal (Metallic Compound)@Metal-Organic Framework Composites: Recent Advances in the Preparation and Applications

Metal-organic framework (MOF) composites based on MOFs-wrapped metals or metallic compounds (denoted as M/MC@MOFs) are an important class of materials that integrate M/MCs and MOFs. MOFs can fix and confine M/MCs to regulate their size, prevent uncontrollable aggregation, and enhance the exposure and ordered arrangement of active sites. In turn, M/MCs support the MOFs to enhance their stability and realize more targeted properties. In this review, the features and application scope of different M/MC@MOF synthesis methods are explored, considering the influential factors and regulation modes of the M/MC–MOFs integration. Additionally, the performances of the M/MC@MOF composites are comprehensively discussed, and the underlying mechanisms are clarified. The performance of M/MC@MOFs is dependent on the orderly synergy between the MOFs and M/MCs. MOFs can sieve and transfer specific molecules to the M/MC surface, whereas the robust interface provides new charge/energy-transfer pathways, which enhance the activity and selectivity of the composites for diverse molecules. Furthermore, the challenges facing this field are analyzed, and the recommendations for advancing the development of M/MC@MOF composites are presented.     

Multifunctional Fluorene‐Based Oligomers with Novel Spiro‐Annulated Triarylamine: Efficient,Stable Deep‐Blue Electroluminescence,Good Hole Injection,and Transporting Materials with Very High Tg

A series of fluorene‐based oligomers with novel spiro‐annulated triarylamine structures, namely DFSTPA, TFSTPA, and TFSDTC, are synthesized by a Suzuki cross‐coupling reaction. The spiro‐configuration molecular structures lead to very high glass transition temperatures (197–253 °C) and weak intermolecular interactions, and consequently the structures retain good morphological stability and high fluorescence quantum efficiencies(0.69–0.98). This molecular design simultaneously solves the spectral stability problems and hole‐injection and transport issues for fluorene‐based blue‐light‐emitting materials. Simple double‐layer electroluminescence (EL) devices with a configuration of ITO/TFSTPA (device A) or TFSDTC (device B)/ TPBI/LiF/Al, where TFSTPA and TFSDTC serve as hole‐transporting blue‐light‐emitting materials, show a deep‐blue emission with a peak around 432 nm, and CIE coordinates of (0.17, 0.12) for TFSTPA and (0.16, 0.07) for TFSDTC, respectively, which are very close to the National Television System Committee (NTSC) standard for blue (0.15, 0.07). The maximum current efficiency/external quantum efficiencies are 1.63 cd A^?1/1.6% for device A and 1.91 cd A^?1/2.7% for device B, respectively. In addition, a device with the structure ITO/DFSTPA/Alq₃/LiF/Al, where DFSTPA acts as both the hole‐injection and ‐transporting material, is shown to achieve a good performance, with a maximum luminance of 14 047 cd m^?2, and a maximum current efficiency of 5.56 cd A^?1. These values are significantly higher than those of devices based on commonly usedN,N′‐di(1‐naphthyl)‐N,N′‐diphenyl‐[1,1′‐biphenyl]‐4,4′‐diamine (NPB) as the hole‐transporting layer (11 738 cd m^?2 and 3.97 cd A^?1) under identical device conditions.     

高频PCB基材介电常数与介电损耗的特性与改性进展

随着高频化PCB技术与产品占有越来越重要的地位,高频电路基板材料的发展也出现了高速化,其中比较重要的一方面就是低介电常数和低介质损耗因数的材料的选择,这是PCB基板材料实现高速化,高频化的重要性能项目。文章针对基板材料的介电常数与介电损耗的关系加以论述,并对它们与外部环境的关系做出相应的阐述,使得在PCB的制造中对各种基板材料进行合理正确的评估和使用。     

Modeling Diffusion in Functional Materials: From Density Functional Theory to Artificial Intelligence

Diffusion describes the stochastic motion of particles and is often a key factor in determining the functionality of materials. Modeling diffusion of atoms can be very challenging for heterogeneous systems with high energy barriers. In this report, popular computational methodologies are covered to study diffusion mechanisms that are widely used in the community and both their strengths and weaknesses are presented. In static approaches, such as electronic structure theory, diffusion mechanisms are usually analyzed within the nudged elastic band (NEB) framework on the ground electronic surface usually obtained from a density functional theory (DFT) calculation. Another common approach to study diffusion mechanisms is based on molecular dynamics (MD) where the equations of motion are solved for every time step for all the atoms in the system. Unfortunately, both the static and dynamic approaches have inherent limitations that restrict the classes of diffusive systems that can be efficiently treated. Such limitations could be remedied by exploiting recent advances in artificial intelligence and machine learning techniques. Here, the most promising approaches in this emerging field for modeling diffusion are reported. It is believed that these knowledge‐intensive methods have a bright future ahead for the study of diffusion mechanisms in advanced functional materials.     

Creating Directionality in Nanoporous Carbon Materials: Adjustable Combinations of Structural and Chemical Gradients

The properties of porous materials benefit from hierarchical porosity. A less noted element of hierarchy is the occurrence of directionality in functional gradient materials. A sharp boundary is replaced by a transition from one feature to the next. The number of cases known for porous materials with either structural or chemical gradients is small. A method capable of generating combinations of structural and chemical gradients in one material does not exist. Such a method is presented with a focus on silver and nitrogen containing carbon materials because of the potential of this system for electrocatalytic CO₂ reduction. A structural gradient results from controlled separation using ultracentrifugation of a binary mixture of template particles in a resorcinol–formaldehyde (RF) sol as carbon precursor. A new level of complexity can be reached, if the surfaces of the template particles are chemically modified. Although the template is removed during carbonization, the modification (Ag, N) becomes integrated into the material. Understanding how modified and unmodified large and small particles sediment in the RF sol enables almost infinite variability of combinations: chemically graded but structurally homogeneous materials and vice versa. Ultimately, a material containing one structural gradient and two chemical gradients with opposing directions is introduced.