High performance hard carbon coatings (diamond‐like coatings)

Different dLc coating types are applied at an industrial scale by sulzer Metco thin Film. The coatings are generated with different coating architecture. Deposition methods are: magnetron sputtering, electron beam evaporation and PA‐cVd. Reactive magnetron sputtering is used to deposit metal containing a‐c:h coatings (a‐c:h:Me), e.g. MAXit W‐ch. Pure a‐c:h coatings as functional top coatings are used for cavidur®, MAXit® AhdLc and special versions of dylyn® coatings. In addition to the pure a‐c:h coatings, doped a‐c:h coatings are also used. The dylyn® family of coatings is comprised of at least one layer a‐c:h:si:O. The dylyn® coatings may be doped with metal (a‐c:h:ti:si:O) to adapt selected properties like electrical conductivity.     

Performance Improvements in Conjugated Polymer Devices by Removal of Water‐Induced Traps

The exploration of a wide range of molecular structures has led to the development of high‐performance conjugated polymer semiconductors for flexible electronic applications including displays, sensors, and logic circuits. Nevertheless, many conjugated polymer field‐effect transistors (OFETs) exhibit nonideal device characteristics and device instabilities rendering them unfit for industrial applications. These often do not originate in the material's intrinsic molecular structure, but rather in external trap states caused by chemical impurities or environmental species such as water. Here, a highly efficient mechanism is demonstrated for the removal of water‐induced traps that are omnipresent in conjugated polymer devices even when processed in inert environments; the underlying mechanism is shown, by which small‐molecular additives with water‐binding nitrile groups or alternatively water–solvent azeotropes are capable of removing water‐induced traps leading to a significant improvement in OFET performance. It is also shown how certain polymer structures containing strong hydrogen accepting groups will suffer from poor performances due to their high susceptibility to interact with water molecules; this allows the design guidelines for a next generation of stable, high‐performing conjugated polymers to be set forth.     

Underwater Mechanically Robust Oil‐Repellent Materials: Combining Conflicting Properties Using a Heterostructure

The development of underwater mechanically robust oil‐repellent materials is important due to the high demand for these materials with the increase in underwater activities. Based on the previous study, a new strategy is demonstrated to prepare underwater mechanically robust oil‐repellent materials by combining conflicting properties using a heterostructure, which has a layered hydrophobic interior structure with a columnar hierarchical micro/nanostructure on the surface and a hydrophilic outer structure. The surface hydrophilic layer imparts underwater superoleophobicity and low oil adhesion to the material, which has oil contact angle of larger than 150° and adhesion of lower than 2.8 µN. The stability of the mechanical properties stemming from the interior hydrophobic‐layered structure enables the material to withstand high weight loads underwater. The tensile stress and the hardness of such a heterostructure film after 1 month immersion in seawater and pH solution are in the range from 83.92 ± 8.22 to 86.73 ± 7.8 MPa and from 83.88 ± 6.8 to 86.82 ± 5.64 MPa, respectively, which are superior to any underwater oil‐repellent material currently reported.     

Spinel Structural Disorder Influences Solar‐Water‐Splitting Performance of ZnFe2O4 Nanorod Photoanodes

Zinc spinel ferrite, ZnFe₂O₄ (ZFO), is an emerging photoanode material for photoelectrochemical (PEC) solar fuel production. However, a lack of fundamental insight into the factors limiting the photocurrent has prevented substantial advance in its performance. Herein, it is found that ZFO nanorod array photoelectrodes with varying crystallinity exhibit vastly different PEC properties. Using a sacrificial hole scavenger (H₂O₂), spatially defined carrier generation, and electrochemical impedance spectroscopy, it is shown that ZFO with a relatively poor crystallinity but a higher spinel inversion degree (due to cation disorder) exhibits superior photogenerated charge separation efficiency and improved majority charge carrier transport compared to ZFO with higher crystallinity and a lower inversion degree. Conversely, the latter condition leads to better charge injection efficiency. Optimization of these factors, and the addition of a nickel–iron oxide cocatalyst overlayer, leads to a new benchmark solar photocurrent for ZFO of 1.0 mA cm^?2 at 1.23 V versus reversible hydrogen electrode (RHE) and 1.7 mA cm^?2 at 1.6 V versus RHE. Importantly, the observed correlation between the cation disorder and the PEC performance represents a new insight into the factors important to the PEC performance of the spinel ferrites and suggests a path to further improvement.     

Water‐Rich Biomimetic Composites with Abiotic Self‐Organizing Nanofiber Network

Load‐bearing soft tissues, e.g., cartilage, ligaments, and blood vessels, are made predominantly from water (65–90%) which is essential for nutrient transport to cells. Yet, they display amazing stiffness, toughness, strength, and deformability attributed to the reconfigurable 3D network from stiff collagen nanofibers and flexible proteoglycans. Existing hydrogels and composites partially achieve some of the mechanical properties of natural soft tissues, but at the expense of water content. Concurrently, water‐rich biomedical polymers are elastic but weak. Here, biomimetic composites from aramid nanofibers interlaced with poly(vinyl alcohol), with water contents of as high as 70–92%, are reported. With tensile moduli of ≈9.1 MPa, ultimate tensile strains of ≈325%, compressive strengths of ≈26 MPa, and fracture toughness of as high as ≈9200 J m^?2, their mechanical properties match or exceed those of prototype tissues, e.g., cartilage. Furthermore, with reconfigurable, noncovalent interactions at nanomaterial interfaces, the composite nanofiber network can adapt itself under stress, enabling abiotic soft tissue with multiscale self‐organization for effective load bearing and energy dissipation.     

Design of Domain Structure and Realization of Ultralow Thermal Conductivity for Record‐High Thermoelectric Performance in Chalcopyrite

Chalcopyrite compound CuGaTe₂ is the focus of much research interest due to its high power factor. However, its high intrinsic lattice thermal conductivity seriously impedes the promotion of its thermoelectric performance. Here, it is shown that through alloying of isoelectronic elements In and Ag in CuGaTe₂, a quinary alloy compound system Cu_1?xAg_xGa_0.4In_0.6Te₂ (0 ≤ x ≤ 0.4) with complex nanosized strain domain structure is prepared. Due to strong phonon scattering mainly by this domain structure, thermal conductivity (at 300 K) drops from 6.1 W m^?1 K^?1 for the host compound to 1.5 W m^?1 K^?1 for the sample with x = 0.4. As a result, the optimized chalcopyrite sample Cu_0.7Ag_0.3Ga_0.4In_0.6Te₂ presents an outstanding performance, with record‐high figure of merit (ZT) reaching 1.64 (at 873 K) and average ZT reaching 0.73 (between ≈300 and 873 K), which are ≈37 and ≈35% larger than the corresponding values for pristine CuGaTe₂, respectively, demonstrating that such domain structure arising from isoelectronic multielement alloying in chalcopyrite compound can effectively suppress its thermal conductivity and elevate its thermoelectric performance remarkably.     

High Performance of N‐Doped Graphene with Bubble‐like Textures for Supercapacitors

Nitrogen‐doped graphene (NG) with wrinkled and bubble‐like texture is fabricated by a thermal treatment. Especially, a novel sonication‐assisted pretreatment with nitric acid is used to further oxidize graphene oxide and its binding with melamine molecules. There are many bubble‐like nanoflakes with a dimension of about 10 nm appeared on the undulated graphene nanosheets. The bubble‐like texture provides more active sites for effective ion transport and reversible capacitive behavior. The specific surface area of NG (5.03 at% N) can reach up to 438.7 m² g^?1, and the NG electrode demonstrates high specific capacitance (481 F g^?1 at 1 A g^?1, four times higher than reduced graphene oxide electrode (127.5 F g^?1)), superior cycle stability (the capacitance retention of 98.9% in 2 m KOH and 99.2% in 1 m H₂SO₄ after 8000 cycles), and excellent energy density (42.8 Wh kg^?1 at power density of 500 W kg^?1 in 2 m KOH aqueous electrolyte). The results indicate the potential use of NG as graphene‐based electrode material for energy storage devices.     

Properties of nisin‐incorporated polymer coatings as antimicrobial packaging materials

Nisin was incorporated into binder solutions of acrylic polymer and vinyl acetate‐ethylene co‐polymer, and then coated on to paper. Diffusive migration of incorporated nisin and the antimicrobial activity of the polymer coatings were investigated in order to understand the way of controlling nisin migration and the extent of microbial suppression by the coated paper. Vinyl acetate–ethylene co‐polymer exhibited a faster rate and higher degree of migration into aqueous food simulant solutions compared to acrylic polymer, and also exhibited a higher degree of suppression against Micrococcus flavus ATCC 10240 inoculated into the microbial medium. Addition of NaCl, sugar and citric acid to water significantly reduced the rate of diffusion of nisin in the case of acrylic polymer, while only slight change was observed due to the additive for vinyl acetate‐ethylene co‐polymer. The simulant type slightly affected the equilibrated migration level of nisin. When the nisin‐incorporated coatings were in contact with pasteurized milk and orange juice at 10°C, significant suppression of total aerobic bacteria and yeasts was observed without any noticeable difference between the two types of coatings. Copyright © 2002 John Wiley & Sons, Ltd.     

All‐Carbon Pressure Sensors with High Performance and Excellent Chemical Resistance

An all‐carbon pressure sensor is designed and fabricated based on reduced graphene oxide (rGO) nanomaterials. By sandwiching one layer of superelastic rGO aerogel between two freestanding high‐conductive rGO thin papers, the sensor works based on the contact resistance at the aerogel–paper interfaces, getting rid of the alien materials such as polymers and metals adopted in traditional sensors. Without the limitation of alien materials, the all‐carbon sensors demonstrate an ultrawide detecting range (0.72 Pa–130 kPa), low energy consumption (≈0.58 µW), ultrahigh sensitivity (349–253 kPa^?1) at low‐pressure regime (<1.4 Pa), fast response time (8 ms at 1 kPa), high stability (10 000 unloading–loading cycles between 0 and 1 kPa), light weight (<10 mg), easily scalable fabrication process, and excellent chemical stability. These merits enable them to detect real‐time human physiological signals and monitor the weights of various droplets of not only water but also hazardous chemical reagents including strong acid, strong alkali, and organic solvents. This shows their great potential applications in real‐time health monitoring, sport performance detecting, harsh environment‐related robotics and industry, and so forth.