Reconfigurable Anisotropic Coatings via Magnetic Field‐Directed Assembly and Translocation of Locking Magnetic Chains

A method for the generation of remotely reconfigurable anisotropic coatings is developed. To form these coatings, locking magnetic nanoparticles (LMNPs) made of a superparamagnetic core and a two‐component polymer shell are employed. Two different polymers form phase‐separated coaxial shells. The outer shell provides repulsive interactions between the LMNPs while the inner shell exerts attractive forces between the particles. Applying a non‐uniform magnetic field, one gathers the particles together, pushing them to come in contact when the internal shells could effectively hold the particles together. When the magnetic field is turned off, the particles remain locked due to these strong interactions between internal shells. The shells are thus made stimuli‐responsive, so this locking can be made reversible and the chains can be disintegrated on demand. In a non‐uniform magnetic field, the assembled chains translocate, bind to the solid substrate and form anisotropic coatings with a “locked” anisotropic structure. The coatings can be constructed, aligned, realigned, degraded, and generated again on demand by changing the magnetic field and particle environment. The mechanism of the coating formation is explained using experimental observations and a theoretical model.     

Electrosprayed Enzyme Coatings as Bioinspired Alternatives to Bioceramic Coatings for Orthopedic and Oral Implants

The biological performance of orthopedic and oral implants can be significantly improved by functionalizing the non‐physiological metallic implant surface through the application of biologically active coatings. In this paper, a cost‐effective alternative to traditional biomedical coatings for bone substitution through exploitation of the specific advantages of the electrospray deposition technique for the immobilization of the enzyme alkaline phosphatase (ALP) onto the implant surface is presented. Since ALP increases the local inorganic phosphate concentration required for physiological mineralization of hard tissues, ALP coatings will enable enzyme‐mediated mineralization onto titanium surfaces. To evaluate the bone‐bioactive capacity of the ALP‐coated titanium surface, soaking experiments are performed. Although the purely inorganic so‐called simulated body fluid is the standard in vitro procedure for predictive studies on potential bone bonding in vivo, an alternative testing solution is proposed that also contains organic phosphates (cell culture medium supplemented with the organic β‐b;‐glycerophosphate (β‐b;‐GP) and serum proteins), thereby resembling the in vivo conditions more closely. Under these physiological conditions, the electrosprayed ALP coatings accelerated mineralization onto the titanium surface as compared to noncoated implant material by means of enzymatic pathways. Therefore, this novel approach toward implant fixation holds significant promise.     

Hydrophilic and Antimicrobial Zeolite Coatings for Gravity‐Independent Water Separation

Condensing heat exchangers onboard manned spacecraft require hydrophilic fin surfaces to facilitate wetting and wicking of condensate to achieve gravity‐independent water separation in the zero‐ or micro‐gravity environment of space. In order to prevent the proliferation of microbes, the coating must also be biocidal. Here we show for the first time that zeolite A and ZSM‐5 coatings deposited via in‐situ crystallization on stainless steel and aluminum alloys have excellent hydrophilicity, biocidal properties, and adhesion. Water contact angles below 5° were obtained on most substrates tested. When silver‐ion exchange is carried out on the zeolite A coating, it becomes highly antibacterial. This biocidal capability of zeolite A is regenerative by repeated ion exchange. All coatings exhibit the highest rating of 5B as determined by adhesion test ASTM D‐3359‐02 (American Society for Testing and Materials). These properties, in addition to zeolite coating's low‐temperature crystallization process and demonstrated corrosion resistance, make zeolite coatings advantageous over the current sol–gel coatings and well suited for use in condensing heat exchangers onboard manned spacecraft.     

VEGF‐Functionalized Polyelectrolyte Multilayers as Proangiogenic Prosthetic Coatings

Stimulation of transprosthetic vascularization represents an interesting strategy in implantology to allow rapid tissue integration and finally to avoid prosthetic rejection. To achieve this goal, we modified the surface of porous titanium implants with polyelectrolyte multilayer (PEM) films functionalized with vascular endothelial growth factor (VEGF). Among the two PEM systems investigated, poly(L‐lysine)/poly(L‐glutamic acid) (PLL/PGA) and poly(allylamine hydrochloride)/poly(sodium 4‐styrenesulfonate) (PAH/PSS), the (PAH/PSS)₄ architecture was selected to functionalize porous titanium, both for its high efficiency to adsorb VEGF and for its biocompatibility toward endothelial cells. In an original way, we unambiguously demonstrated that VEGF adsorbed on (PAH/PSS)₄ maintains its bioactivity in vitro and stimulates endothelial cells proliferation. This effect was correlated with specific activation of intracellular signaling pathways induced by successive phosphorylation of the endothelial VEGF receptor VEGFR2 and mitogen‐activated protein kinases (MAPK) ERK1/2. By clearly demonstrating the proangiogenic activity of the VEGF‐PEM coating in vitro, the present study constitutes a first step toward in vivo application.     

Magnetic Tilting in Nematic Liquid Crystals Driven by Self-Assembly

Self-assembly is one of the crucial mechanisms allowing the design multifunctional materials. Soft hybrid materials contain components of different natures and exhibit competitive interactions which drive self-organization into structures of a particular function. Here a novel type of a magnetic hybrid material where the molecular tilt can be manipulated through a delicate balance between the topologically-assisted colloidal self-assembly of magnetic nanoparticles and the anisotropic molecular interactions in a liquid crystal matrix is demonstrated.     

Copper‐Free Clickable Coatings

The copper‐catalyzed azide–alkyne 1,3‐dipolar cycloaddition (CuAAC) is extensively used for the functionalization of well‐defined polymeric materials. However, the necessity for copper, which is inherently toxic, limits the potential applications of these materials in the area of biology and biomedicine. Therefore, the first entirely copper‐free procedure for the synthesis of clickable coatings for the immobilization of functional molecules is reported. In the first step, azide‐functional coatings are prepared by thermal crosslinking of side‐chain azide‐functional polymers and dialkyne linkers. In a second step, three copper‐free click reactions (i.e., the Staudinger ligation, the dibenzocyclooctyne‐based strain‐promoted azide–alkyne [3+2] cycloaddition, and the methyl‐oxanorbornadiene‐based tandem cycloaddition?retro‐Diels?Alder (crDA) reaction) are used to functionalize the azide‐containing surfaces with fluorescent probes, allowing qualitative comparison with the traditional CuAAC.     

Smart Materials by Nanoscale Magnetic Assembly

Magnetic assembly at the nanoscale level holds great potential for producing smart materials with high functional and structural diversity. Generally, the chemical, physical, and mechanical properties of the resulting materials can be engineered or dynamically tuned by controlling external magnetic fields. This Review analyzes the recent research progress on nanoscale magnetic assembly approaches toward the development of smart materials. The magnetic interactions between nanoparticles (both magnetic and nonmagnetic) and the interactions between nanoparticles and external magnetic fields are fully expatiated based on numerical simulations. In particular, the advancements of nanoscale magnetic assembly in responsive optical nanostructures, shape‐morphing systems, and advanced materials with tunable surface properties are introduced in three subsections. The key roles of magnetic interactions in nanoscale assembly toward customizable physical and chemical properties are highlighted, with focus on how to enable direct manipulation of the positional and orientational orders of the building blocks and orientational control of soft matrices through the incorporation of anisotropic magnetic structures.     

Magnetic Multi‐Functional Nano Composites for Environmental Applications

A novel concept is proposed to synthesize a new class of composites featuring magnetic, molecular sieve and metallic nanoparticle properties. These multi‐functional materials have potential applications as recyclable catalysts, disinfectants and sorbents. The magnetic property enables effective separation of the spent composites from complex multiphase systems for regeneration and recycle, safe disposal of the waste and/or recovery of loaded valuable species. The zeolite molecular sieve provides a matrix which supports a remarkably new, simple, efficient and economical method to make stable, supported silver nanoparticles by silver ion exchange and controlled thermal reduction. The silver nanoparticles generated in this way have excellent properties such as high reactivity and good thermal stability without aggregation, which act as nano reactors for desired functionality in a wide range of applications. Magnetic component (Fe₃O₄), molecular sieve matrix (zeolite) and silver nanoparticles generated by ion exchange followed by controlled reduction, together form this unique novel composite with designed functions. It represents a practically operational, economical, sustainable and environmentally friendly new advanced functional material. This paper focuses on the novel synthesis and characterization of the composite, with an example of applications as sorbents for the removal of vapor‐phase mercury from the flue gas of coal‐fired power plants.     

Quantum Dots Decorated with Magnetic Bionanoparticles

A new class of water‐soluble, fluorescent, magnetic quantum dots––magnetoferritin bioconjugate––is prepared. The nanostructures are patterned mainly as dimer particles as characterized by high‐angle annular dark‐field scanning transmission electron microscopy and electron energy loss spectroscopy. Magnetic (high spontaneous magnetization values, superparamagnetism) and fluorescent (narrow emission peaks, uniform brightness) properties of both nanoblocks are maintained in the final nanostructure.     

FeSiAl微波衰减涂层电磁特性分析

采用矢量网络分析仪对FeSiAl微波衰减涂层的电磁参数进行了测试，通过利用电磁波衰减理论进行分析，搞清了FeSiAl微波衰减涂层的衰减类型以及FeSiAl涂层具有优异衰减特性的实质。     

激光熔覆制备非晶复合涂层的研究进展

非晶态合金是一种极有发展潜力的新型金属材料。激光熔覆非晶复合涂层不仅能有效提高材料表面性能,还是将非晶态合金推向应用的有效方法。综述了激光熔覆非晶复合涂层的研究现状,包括激光熔覆非晶涂层的材料体系、组织结构和性能特点等,并指出了激光熔覆非晶涂层目前存在的主要问题与发展方向。     

Sub‐20 nm Magnetic Dots with Perpendicular Magnetic Anisotropy

A new and simple method for the preparation of magnetic dot arrays is introduced. Diblock copolymer micelles with a silica core are used as template for the generation of nanostructure arrays. The silica cores are utilized as mask for ion milling preparation. The morphology and size of the silica and magnetic dot arrays are discussed. The magnetic dots are made from Co/Pt multilayer films. Ferromagnetic dots with a diameter well below 20 nm and perpendicular easy axis of magnetization are created. The switching behavior changes from domain wall motion, dominant in the film, to single domain particle switching in the dots. The magneto‐optic saturation signals and the evolution of magnetic anisotropy are discussed.     

Recent Developments and Practical Feasibility of Polymer‐Based Antifouling Coatings

While nature has optimized its antifouling strategies over millions of years, synthetic antifouling coatings have not yet reached technological maturity. For an antifouling coating to become technically feasible, it should fulfill many requirements: high effectiveness, long‐term stability, durability, ecofriendliness, large‐scale applicability, and more. It is therefore not surprising that the search for the perfect antifouling coating has been going on for decades. With the discovery of metal‐based antifouling paints in the 1970s, fouling was thought to be a problem of the past, yet its untargeted toxicity led to serious ecological concern, and its use became prohibited. As a response, research shifted focus toward a biocompatible alternative: polymer‐based antifouling coatings. This has resulted in numerous advanced and innovative antifouling strategies, including fouling‐resistant, fouling‐release, and fouling‐degrading coatings. Here, these novel and exciting discoveries are highlighted while simultaneously assessing their antifouling performance and practical feasibility.     

纳秒激光诱导氧化钛片及涂层的润湿性研究

采用纳秒激光在纯钛片表面制备微织构,并辅助化学处理的方法,获得了类似"荷叶效应"且润湿稳定的超疏水表面。通过调整激光加工工艺参数,获得了具有不同润湿性的微纳米结构;在此基础上,采用全氟癸基三甲氧基硅烷和乙醇溶液的混合溶液在微结构表面制备涂层。采用扫描电子显微镜和能谱分析后可知钛板在激光作用下产生了多尺度的氧化钛多孔微结构;通过接触角测量表征进一步分析了钛片表面的亲水性与微纳米结构表面变化规律的关系,以及涂层对表面润湿性的影响,为生物医学药物输送方面的研究提供了参考。     

Magnetic Field‐Induced Phase Transformation in NiMnCoIn Magnetic Shape‐Memory Alloys—A New Actuation Mechanism with Large Work Output

Magnetic shape memory alloys (MSMAs) have recently been developed into a new class of functional materials that are capable of magnetic‐field‐induced actuation, mechanical sensing, magnetic refrigeration, and energy harvesting. In the present work, the magnetic &!hyphen;field‐induced martensitic phase transformation (FIPT) in Ni₄₅Mn_36.5Co₅In_13.5 MSMA single crystals is characterized as a new actuation mechanism with potential to result in ultra‐high actuation work outputs. The effects of the applied magnetic field on the transformation temperatures, magnetization, and superelastic response are investigated. The magnetic work output of NiMnCoIn alloys is determined to be more than 1 MJ m^?3 per Tesla, which is one order of magnitude higher than that of the most well‐known MSMAs, i.e., NiMnGa alloys. In addition, the work output of NiMnCoIn alloys is orientation independent, potentially surpassing the need for single crystals, and not limited by a saturation magnetic field, as opposed to NiMnGa MSMAs. Experimental and theoretical transformation strains and magnetostress levels are determined as a function of crystal orientation. It is found that [111]‐oriented crystals can demonstrate a magnetostress level of 140 MPa T^?1 with 1.2% axial strain under compression. These field‐induced stress and strain levels are significantly higher than those from existing piezoelectric and magnetostrictive actuators. A thermodynamical framework is introduced to comprehend the magnetic energy contributions during FIPT. The present work reveals that the magnetic FIPT mechanism is promising for magnetic actuation applications and provides new opportunities for applications requiring high actuation work‐outputs with relatively large actuation frequencies. One potential issue is the requirement for relatively high critical magnetic fields and field intervals (1.5–3 T) for the onset of FIPT and for reversible FIPT, respectively.     

Hybrids of Magnetic Nanoparticles with Double‐Hydrophilic Core/Shell Cylindrical Polymer Brushes and Their Alignment in a Magnetic Field

The synthesis of double‐hydrophilic core/shell cylindrical polymer brushes (CPBs), their hybrids with magnetite nanoparticles, and the directed alignment of these magnetic hybrid cylinders by a magnetic field are demonstrated. Consecutive grafting from a polyinitiator poly(2‐(2‐bromoisobutyryloxy)ethyl methacrylate) (PBIEM) of tert‐butyl methacrylate (tBMA) and oligo(ethylene glycol) methacrylate (OEGMA) using atom‐transfer radical polymerization (ATRP) and further de‐protection yields core/shell CPBs with poly(methacrylic acid) (PMAA) as the core and POEGMA as the shell, which is evidenced by ¹H NMR, gel permeation chromatography (GPC), and dynamic and static light scattering (DLS and SLS). The resulting core/shell brush is well soluble in water and shows a pH responsiveness because of its weak polyelectrolyte core. Pearl‐necklace structures are observed by cryogenic transmission electron microscopy (cryo‐TEM) at pH 4, while at pH 7, these structures disappear owing to the ionization of the core. A similar morphology is also found for the polychelate of the core/shell CPBs with Fe³⁺ ions. Superparamagnetic magnetite nanoparticles have also been prepared and introduced into the core of the brushes. The hybrid material retains the superparamagnetic property of the magnetite nanoparticles, which is verified by superconducting quantum interference device (SQUID) magnetization measurements. Large‐scale alignment of the hybrid cylinders in relatively low magnetic fields (40–300 mT) can easily be performed when deposited on a surface. which is clearly revealed by the atomic force microscopy (AFM) and TEM measurements.     

Versatile Nanocomposite Coatings with Tunable Cell Adhesion and Bactericidity

TiO₂‐Ag nanocomposites are known for their bactericidal effect during exposure to appropriate UV radiation. While involving hazardous radiation, and limited to accessible areas, the bactericidity of these coatings is not persistent in the absence of UV light, which impedes their commercial application. Herein it is shown that TiO₂‐Ag nanocomposites can be made highly bactericidal without the need of irradiation. Beyond this, bactericidity can even be mitigated in the presence of pre‐irradiated coatings. Biocompatibility and cell adhesion are also negligibly small for the as‐processed, non‐irradiated coatings, and become fairly high when the coatings are irradiated prior to testing. This opens the possibility to pattern the coatings into areas with high and low cell adhesion properties. Indeed by irradiating the coating through a mechanical mask it is shown that fibroblast cell adherence is sharply confined to the irradiated area. These properties are achieved using TiO₂‐Ag thin films with high silver loadings of 50 wt%. The films are processed on stainless steel substrates using solution deposition. Microstructural characterization by means of X‐ray diffraction, Raman, and X‐ray photoelectron spectroscopy, high‐resolution scanning electron microscopy, and atomic force microscopy show a highly amorphous TiO₂‐Ag_xO nanocomposite matrix with scattered silver nanoparticles. UV irradiation of the films results in the precipitation of a high density of silver nanoparticles at the film surface. Bactericidal properties of the films are tested on α‐haemolyzing streptococci and in‐vitro biocompatibility is assessed on primary human fibroblast cultures. The results mentioned above as to the tunable bactericidity and biocompatibility of the TiO₂‐Ag coatings developed herein, are amenable to silver ion release, to catalytic effects of silver nanoparticles, and to specific wettabilities of the surfaces.     

Ultra-Thin Protective Coatings for Sustained Photoelectrochemical Water Oxidation with Mo:BiVO4

As global warming caused by the greenhouse effect is becoming one of the major issues of the 21st century, hydrogen as an alternative to fossil-based fuels and other energy carriers has gained importance in current research. One promising approach to produce hydrogen is photoelectrochemical water splitting, which uses solar energy combined with suitable semiconducting photoabsorber electrodes to generate hydrogen and oxygen from water. However, most water splitting applications reported to date suffer from degradation of the photoabsorber, resulting in a loss of activity after just a few seconds or minutes. Here, a new approach using conformal ultra-thin and oxidation-stable protective layers is presented on Mo:BiVO₄ thin films combined with a thin Fe_0.1Ni_0.9O water oxidation co-catalyst, applied by electrochemical deposition, to achieve unprecedented photocurrent densities of up to 5.6 mA cm⁻² under simulated AM1.5G illumination and a neutral pH while providing more stable electrodes for water oxidation.     

磁性涂层碳纤维在吸波材料领域的应用

通过电沉积技术在碳纤维表面制备了四氧化三铁磁性涂层。测试结果表明：通过电沉积法制备的磁性涂层均匀致密;磁性纤维具有优异的吸波性能,理论计算结果显示,当匹配厚度大于1．7mm时,其最大损耗均低于-20dB。这种磁性纤维有望实现复合材料的结构增强和吸波功能一体化。     

宽频段太赫兹辐射计高吸收率涂层的特性

为了对宽频段高吸收率太赫兹辐射计的特性进行表征,研究了吸收涂层材料的特性;对常见的吸波材料在太赫兹波段的吸收率进行仿真,探寻在太赫兹波段具有高吸收率的材料;将碳化硅与3M黑漆进行混合,以进一步提高涂层的吸收率,并通过仿真调整涂层内碳化硅颗粒的尺寸;根据仿真结果制备混合涂层,利用太赫兹时域光谱仪对混合涂层样品进行测量。结果表明:该混合涂层样品的光谱吸收率大于0.99,与仿真结果基本吻合。