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The luminescence of InxGa1−xN nanowires (NWs) is frequently reported with large red-shifts as compared to the theoretical value expected from the average In content. Both compositional fluctuations and radial built-in fields were considered accountable for this effect, depending on the size, structure, composition, and surrounding medium of the NWs. In the present work, the emission properties of InGaN/GaN NWs grown by plasma-assisted molecular beam epitaxy are investigated in a comprehensive study combining ultraviolet-Raman and photoluminescence spectroscopy (PL) on vertical arrays, polarization-dependent PL on bundles of a few NWs, scanning transmission electron microscopy, energy-dispersive X-ray spectroscopy, and calculations of the band profiles. The roles of inhomogeneous In distribution and radial fields in the context of optical emission properties are addressed. The radial built-in fields are found to be modest, with a maximum surface band bending below 350 meV. On the other hand, variations in the local In content have been observed that give rise to potential fluctuations whose impact on the emission properties is shown to prevail over band-bending effects. Two luminescence bands with large positive and moderate negative polarization ratios of ≈+80% and ≤−60%, respectively, were observed. The red-shift in the luminescence is associated with In-rich inclusions in the NWs due to thermodynamic decomposition during growth. The negative polarization anisotropy is suggested to result from spontaneously formed superlattices in the In-rich regions of the NWs. The NWs show a preferred orthogonal absorption due to the dielectric boundary conditions and highlight the extreme sensitivity of these structures towards light polarization.

Культури клітин важливі для онкологічних і біологічних досліджень. Ми досліджуємо зростання в’язких клітин Hela на наноструктурованих, вертикально вирівняних, багатостінних каркасах із вуглецевих нанотрубок (VA-MWCNTs) порівняно з полірованими кремнієвими поверхнями за допомогою скануючої електронної мікроскопії (СЕМ). Каркаси VA-MWCNT були вирощені методом хімічного осадження з парової фази з посиленням плазми. Обидві поверхні стерилізували ультрафіолетовим випромінюванням і поміщали в чашку Петрі перед культивуванням клітин на 5 годин і 24 години відповідно. Після цього клітини були хімічно зафіксовані, щоб можна було охарактеризувати морфологію за допомогою СЕМ. Результати показали, що на поверхні каркасів VA-MWCNT зросла більша кількість клітин порівняно з полірованими кремнієвими пластинами. Ниткоподібні псевдоподії клітин Hela були виявлені на поверхні обох типів кремнієвих пластин. Клітини Hela демонстрували різні морфологічні характеристики на VA-MWCNTs у різний час культивування in vitro, що може бути пов’язано з циклом ділення клітин Hela. Схоже, що каркас VA-MWCNT впливає на цикл клітинного поділу, що може пояснити зміну морфології. На закінчення слід зазначити, що MWCNTs сприяли проліферації та росту клітин Hela, а також впливали на напрямок і морфологію росту клітин.

Considering the attractive optoelectronic properties of metal halide perovskites (MHPs), their introduction to the field of photocatalysis was only a matter of time. Thus far, MHPs have been explored for the photocatalytic generation of hydrogen, carbon dioxide reduction, organic synthesis, and pollutant degradation applications. Of growing research interest and possible applied significance are the currently emerging developments of MHP-based Z-scheme heterostructures, which can potentially enable efficient photocatalysis of highly energy-demanding redox processes. In this Perspective, we discuss the advantages and limitations of MHPs compared to traditional semiconductor materials for applications as photocatalysts and describe emerging examples in the construction of MHP-based Z-scheme systems. We discuss the principles and material properties that are required for the development of such Z-scheme heterostructure photocatalysts and consider the ongoing challenges and opportunities in this emerging field.

The development of high-efficiency oxygen electrocatalysts with earth-abundant transition metals rather than scarce noble metals has aroused growing interests due to their potential for energy storage and conversion applications. Herein, we developed a facile strategy to synthesize hollow tubular bimetallic Ni-Co oxide rooted with dense nanosheets for enhanced bifunctionality and facilitated redox reaction kinetics. Owing to the rational design of morphology and well-dispersed Ni and Co ions, the bimetallic samples exhibit admirable bifunctional electrocatalytic activities. This bimetallic Ni-Co oxide shows superior oxygen electrocatalytic performance in comparison with the monometallic Ni and Co oxides, according to the electrocatalytic synergistic effect from the bimetallic system. The optimized sample with the specific mass ratio of Ni and Co displays the oxygen reduction reaction (ORR) property comparable to commercial Pt/C and oxygen evolution reaction (OER) performance superior to commercial RuO2. The electrochemical tests and structural characterizations offer in-depth dissection on the electrocatalytic behaviors, especially the superb stability in both ORR and OER tests, as well as the outstanding resistance to methanol poisoning, representing a promising candidate in the renewable energy field.

New semiconducting metal oxides of various compositions are of great interest for efficient solar water oxidation. In this report, Mo-doped SnO2 (Mo:SnO2) thin films deposited by reactive magnetron co-sputtering in the Ar and O2 gas environment are studied. The Sn to Mo ratio in the films can be controlled by changing the O2 partial pressure and the deposition power of the Sn and Mo targets. Increasing the Mo concentration in the film leads to the increase in the oxygen vacancy density, which limits the maximum achievable photocurrent density. The thin films exhibit a direct band gap of 2.7 eV, the maximum achievable photocurrent density of 0.6 mA cm−2 at 0 VRHE and the onset potential of 0.14 VRHE. The incident photon to current transfer (IPCE) efficiency of 22% is shown at a 450 nm wavelength. The initial performance of the Mo:SnO2 thin films is evaluated for solar water oxidation.

The practical application of Li-S batteries demands low cell balance (Licapacity /Scapacity ), which involves uniform Li growth, restrained shuttle effect, and fast redox reaction kinetics of S species simultaneously. Herein, with the aid of W2 C nanocrystals, a freestanding 3D current collector is applied as both Li and S hosts owing to its lithiophilic and sulfilic property. On the one hand, the highly conductive W2 C can reduce Li nucleation overpotentials, thus guiding uniform Li nucleation and deposition to suppress Li dendrite growth. On the other hand, the polar W2 C with catalytic effect can enhance the chemisorption affinity to lithium polysulfides (LiPSs) and guarantee fast redox kinetics to restrain S species in cathode region and promote the utilization of S. Surprisingly, a full Li-S battery with ultralow cell balance of 1.5:1 and high sulfur loading of 6.06 mg cm-2 shows obvious redox plateaus of S and maintains high reversible specific capacity of 1020 mAh g-1 (6.2 mAh cm-2 ) after 200 cycles. This work may shed new sights on the facile design of full Li-S battery with low excessive Li supply.

Graphitic carbon nitride (CN) is considered as a promising photocatalyst for solar energy conversion. However, low specific surface area and fast electrons and holes recombination restrict the photocatalytic applications of CN material. Herein, a nitrogen defect-rich and highly porous CN nanostructure (CN-LT) was prepared by combining two strategies, i.e., LiOH treatment and heat etching. The as-prepared nitrogen defect-rich porous CN-LT not only has a larger specific surface area, as compared with pristine CN, but also the photogenerated electron-hole separation was boosted remarkably. Using Pt as a co-catalyst and lactic acid aqueous solutions as sacrificial reagent under visible light irradiation (λ > 400 nm), the hydrogen evolution reaction (HER) rate for CN-LT (1.54 mmol h−1 g−1) was 19.25 times higher than that for pristine CN (0.08 mmol h−1 g−1). While subjecting pristine CN to heat etching under the same experimental conditions, excepting the use of LiOH (CN-T), an increase in HER rate of 7.5 times was obtained. Our current study may shed more light on the enhancement of the photocatalytic activity of bulk CN materials by altering their microstructure.

Semiconducting ternary metal oxide thin films exhibit a promising application for solar energy conversion. However, the efficiency of the conversion is still limited by a band gap of a semiconductor, which determines an obtainable internal photovoltage for solar water splitting. In this report the tunability of the tin tungstate band gap by O2 partial pressure control in the magnetron co-sputtering process is shown. A deficiency in the Sn concentration increases the optical band gap of tin tungstate thin films. The optimum band gap of 1.7 eV for tin tungstate films is achieved for a Sn to W ratio at unity, which establishes the highest photoelectrochemical activity. In particular, a maximum photocurrent density of 0.375 mA cm−2 at 1.23 VRHE and the lowest reported onset potential of −0.24 VRHE for SnWO4 thin films without any co-catalyst are achieved. Finally, we demonstrate that a Ni protection layer on the SnWO4 thin film enhances the photoelectrochemical stability, which is of paramount importance for application.

Laser-induced periodic surface structures (LIPSSs) on various materials have been extensively investigated because of their wide applications. The combination of different materials allows for greater freedom in tailoring their functions and achieving responses not possible in a homogeneous material. By utilizing a femtosecond (fs) laser to irradiate the Fe-doped Polyvinyl Pyrrolidone (PVP) composite film, highly regular ultrafine nanogratings (U-nanogratings) with a period as small as 35.0 ($\pm$ 2.0) nm can be self-organized on the surface with extremely high efficiency. The period of the U-nanogratings can be controlled by varying the scanning speed of the laser beam (deposited energy) and the thickness of the composite film. Based on the experimental, theoretical, and simulation results, we propose a two-step formation mechanism: composite film excitation and two sequent grating-splitting. The high photosensitivity and low glass transition temperature of the composite film facilitate the fabrication of the ultrafine nanostructures. The proposed design method for the composite material and fabrication process could not only provide a strategy for obtaining highly regular U-nanogratings, but also offer a platform to explore the interaction physics between ultra-short pulses and matter under extreme conditions.

Colloidal assembly is a key strategy in nature and artificial device. Hereby, an electromicrofluidic assembly platform (eMAP) is proposed and validated to achieve 3D colloidal assembly and manipulation within water droplets. The water-in-oil emulsion droplets autoposition in the eMAP driven by dielectrophoresis, where the (di)electrowetting effect induces droplet deformation, facilitating quadratic growth of the electric field in water droplet to achieve "far-field" dielectrophoretic colloidal assembly. Reconfigurable 3D colloidal configurations are observed and dynamically programmed via applied electric fields, colloidal properties, and droplet size. Binary and ternary colloidal assemblies in one droplet allow designable chemical and physical anisotropies for functional materials and devices. Integration of eMAP in high throughput enables mass production of functional microcapsules, and programmable optoelectronic units for display devices. This eMAP is a valuable reference for expanding fundamental and practical exploration of colloidal systems.

Plasmonic metasurfaces have important applications in life science, optics, and catalysis. However, their industrial usage is limited by the challenges of high throughput nanofabrication. A promising solution is the transfer of a pattern into a substrate using block copolymers, nanostructured stamps or molds to create binary, three dimensional templates, which can then be decorated with plasmonically active metals. Here, we report on the optical properties of quasi-Babinet complementary arrays in the non-retarded regime investigated by finite-difference time-domain simulations. The structures consist of a nanopillar support, which is covered with metal disks on top of the pillars and a quasi-Babinet complementary hole array film at the base of the pillars. Strong vertical plasmonic coupling occurs for small separation distances of the plasmonic slabs. We present a comprehensive study of the near and far-field properties of such vertically coupled plasmonic arrays varying their critical geometric dimension and the employed metals with their intrinsic plasmonic material properties. In particular, we consider gold, silver, copper, aluminum, nickel, and palladium. Furthermore, the effect of the refractive index n of the nanopillar support between the range of n = 1.4 to n = 3.4 is investigated. The plasmonic slabs show tunable extraordinary transmission and large electric near-field enhancements, which are strongly dependent on the employed material and geometry. Further, we show that the templates are suitable for plasmonic heterostructures commonly used in plasmon-enhanced photocatalysis.

Until now, the growth of periodic vertically aligned multi-walled carbon nanotube (VA-MWCNT) arrays was dependent on at least one lithography step during fabrication. Here, we demonstrate a lithography-free fabrication method to grow hexagonal arrays of self-standing VA-MWCNTs with tunable pitch and MWCNT size. The MWCNTs are synthesized by plasma enhanced chemical vapor deposition (PECVD) from Ni catalyst particles. Template guided dewetting of a thin Ni film on a hexagonally close-packed silica particle monolayer provides periodically distributed Ni catalyst particles as seeds for the growth of the periodic MWCNT arrays. The diameter of the silica particles directly controls the pitch of the periodic VA-MWCNT arrays from 600 nm to as small as 160 nm. The diameter and length of the individual MWCNTs can also be readily adjusted and are a function of the Ni particle size and PECVD time. This unique method of lithography-free growth of periodic VA-MWCNT arrays can be utilized for the fabrication of large-scale biomimetic materials.

Melanin nanoparticles are known to be biologically benign to human cells for a wide range of concentrations in a high glucose culture nutrition. Here, we show cytotoxic behavior at high nanoparticle and low glucose concentrations, as well as at low nanoparticle concentration under exposure to (nonionizing) visible radiation. To study these effects in detail, we developed highly monodispersed melanin nanoparticles (both uncoated and glucose-coated). In order to study the effect of significant cellular uptake of these nanoparticles, we employed three cancer cell lines: VM-M3, A375 (derived from melanoma), and HeLa, all known to exhibit strong macrophagic character, i.e., strong nanoparticle uptake through phagocytic ingestion. Our main observations are: (i) metastatic VM-M3 cancer cells massively ingest melanin nanoparticles (mNPs), (ii) the observed ingestion is enhanced by coating mNPs with glucose, (iii) after a certain level of mNP ingestion, the metastatic cancer cells studied here are observed to die—glucose coating appears to slow that process, (iv) cells that accumulate mNPs are much more susceptible to killing by laser illumination than cells that do not accumulate mNPs, and (v) non-metastatic VM-NM1 cancer cells also studied in this work do not ingest the mNPs, and remain unaffected after receiving identical optical energy levels and doses. Results of this study could lead to the development of a therapy for control of metastatic stages of cancer.

Colloidal synthesis of photocatalysts with potential to overcome the drawback of low photocatalytic efficiency brought by charge recombination and narrow photo-response has been a challenge. Herein, a general and facile colloidal approach to synthesize orthorhombic phase Bi2S3 particles with rod and flower-like morphology is reported. We elucidate the formation and growth process mechanisms of these synthesized nanocrystals in detail and cooperate these Bi2S3 particles with metallic gold nanoparticles (AuNPs) to construct heterostructured photocatalysts. The unique properties of AuNPs featuring tunable surface plasmon resonance and large field enhancement are used to sensitize the photocatalytic activity of the Bi2S3 semiconductor particles. The morphology, structure, elemental composition, and light absorption ability of the prepared catalysts are characterized by (high-resolution) transmission electron microscopy, scanning electron microscopy, X-ray diffraction spectroscopy, X-ray photoelectron spectroscopy, and UV–vis absorption spectroscopy. The catalysts exhibit high and stable photocatalytic activity for the degradation of organic pollutants demonstrated using rhodamine B and methyl orange dyes under solar light irradiation. We show that the incorporation of the AuNPs with the Bi2S3 particles increases the photocatalytic activity 1.2 to 3-fold. Radical trapping analysis indicates that the production of hydroxyl and superoxide radicals are the dominant active species responsible for the photodegradation activity. The photocatalysts exhibit good stability and recyclability.

The development of high-efficiency oxygen electrocatalysts with earth-abundant transition metals rather than scarce noble metals has aroused growing interests due to their potential for energy storage and conversion applications. Herein, we developed a facile strategy to synthesize hollow tubular bimetallic Ni-Co oxide rooted with dense nanosheets for enhanced bifunctionality and facilitated redox reaction kinetics. Owing to the rational design of morphology and well-dispersed Ni and Co ions, the bimetallic samples exhibit admirable bifunctional electrocatalytic activities. This bimetallic Ni-Co oxide shows superior oxygen electrocatalytic performance in comparison with the monometallic Ni and Co oxides, according to the electrocatalytic synergistic effect from the bimetallic system. The optimized sample with the specific mass ratio of Ni and Co displays the oxygen reduction reaction (ORR) property comparable to commercial Pt/C and oxygen evolution reaction (OER) performance superior to commercial RuO

Transparent conductive films (TCFs) are irreplaceable components in most optoelectronic applications such as solar cells, organic light-emitting diodes, sensors, smart windows, and bioelectronics. The shortcomings of existing traditional transparent conductors demand the development of new material systems that are both transparent and electrically conductive, with variable functionality to meet the requirements of new generation optoelectronic devices. In this respect, TCFs with periodic or irregular nanomesh structures have recently emerged as promising candidates, which possess superior mechanical properties in comparison with conventional metal oxide TCFs. Among the methods for nanomesh TCFs fabrication, nanosphere lithography (NSL) has proven to be a versatile platform, with which a wide range of morphologically distinct nanomesh TCFs have been demonstrated. These materials are not only functionally diverse, but also have advantages in terms of device compatibility. This review provides a comprehensive description of the NSL process and its most relevant derivatives to fabricate nanomesh TCFs. The structure-property relationships of these materials are elaborated and an overview of their application in different technologies across disciplines related to optoelectronics is given. It is concluded with a perspective on current shortcomings and future directions to further advance the field.

Lithium–sulfur batteries (LSBs) have shown great potential as a rival for next generation batteries, for its relatively high theoretical capacity and eco‐friendly properties. Nevertheless, blocked by the shuttle effect of lithium polysulfides (LPSs, Li2S4‐Li2S8) and insulation of sulfur, LSBs show rapid capacity loss and cannot achieve the practical application. Herein, a composite of carbon nanofibers coated by Co3S4 nanosheets (denoted as CNF@Co3S4) is successfully synthesized as freestanding sulfur host to optimize the interaction with sulfur species. The combination of the two materials can lead extraordinary cycling and rate performance by alleviating the shuttle of LPSs effectively. N‐doped carbon nanofibers serve as long‐range conductive networks and Co3S4 nanosheets can accelerate the conversion of LPSs through its electrocatalytic and chemical adsorption ability. Benefiting from the unique structure, the transporting rate of Li+ can be enhanced. Distribution of Li+ is uniform for enough exposed negative active sites. As a result, the cell with CNF@Co3S4 as sulfur host is able to stabilize at 710 mA h g−1 at 1 C after 200 cycles with average coulombic efficiency of 97.8% in a sulfur loading of 1.7 mg cm−2 and deliver 4.1 mA h cm−2 at 0.1 C even in 6.8 mg cm−2 for 100 cycles.

Lithium–sulfur batteries (LSBs) have shown great potential as a rival for next generation batteries, for its relatively high theoretical capacity and eco‐friendly properties. Nevertheless, blocked by the shuttle effect of lithium polysulfides (LPSs, Li2S4‐Li2S8) and insulation of sulfur, LSBs show rapid capacity loss and cannot achieve the practical application. Herein, a composite of carbon nanofibers coated by Co3S4 nanosheets (denoted as CNF@Co3S4) is successfully synthesized as freestanding sulfur host to optimize the interaction with sulfur species. The combination of the two materials can lead extraordinary cycling and rate performance by alleviating the shuttle of LPSs effectively. N‐doped carbon nanofibers serve as long‐range conductive networks and Co3S4 nanosheets can accelerate the conversion of LPSs through its electrocatalytic and chemical adsorption ability. Benefiting from the unique structure, the transporting rate of Li+ can be enhanced. Distribution of Li+ is uniform for enough exposed negative active sites. As a result, the cell with CNF@Co3S4 as sulfur host is able to stabilize at 710 mA h g−1 at 1 C after 200 cycles with average coulombic efficiency of 97.8% in a sulfur loading of 1.7 mg cm−2 and deliver 4.1 mA h cm−2 at 0.1 C even in 6.8 mg cm−2 for 100 cycles., CNF@Co3S4 as a freestanding sulfur host optimizes the interaction between sulfur species and the host material by the polarity and catalytical effect of Co3S4 nanosheets. The electronegative property of Co3S4 can further alleviate the growth of Li‐dendrites through realizing the uniform Li+ flux and deposition. These advantages guarantee extraordinary cycling and rate performance of corresponding Li–S batteries.

In this work, we report a quick and controllable method for fabricating Ag nanoparticles (NPs) and nano-assemblies (NAs) on silicon (Si) surface via a galvanic reaction assisted by surfactant hexadecyltrimethylammonium bromide (CTAB). Obtained Si substrates with high density Ag NAs serve as surface-enhanced Raman scattering (SERS) substrates for unlabelled molecular sensing. The addition of CTAB enables not only the electromagnetic enhancement by controllable producing Ag NAs “hotspots”, but also the signal enhancement by enriching probe molecules via hydrophobic interaction. Two concentration regimes of 1.0 × 10−8–1.0 × 10−11 M and 1.0 × 10−12–1.0 × 10−16 M have been obtained for quantitative and qualitative detection of Rhodamine 6G (R6G) in aqueous solution, respectively. As a result, for determination of R6G, the quantitative and qualitative detection limits of 1.0 × 10−11 and 1.0 × 10−16 M have been obtained, respectively, with high reproducibility showing the relative standard deviation (RSD) of ∼7.3%. Simulation has been carried out using finite-difference time-domain (FDTD) to evaluate the dependence of electric field on the size and inter-gap of Ag NPs, showing good agreement with experimental results. The high sensitivity also enables SERS characterization of non-resonant and low Raman cross-section biomolecules, for example, amino acids. Such a fabrication process is simple, fast, cheap and reproducible; and therefore, it would be helpful to produce high sensitive SERS substrates to broaden their applications in chemical and biological fields for molecular diagnostics to single-/multiple-molecule detection.

Cu2Se with high theoretical capacity and good electronic conductivity have attracted particular attention as anode materials for sodium ion batteries (SIBs). However, during electrochemical reactions, the large volume change of Cu2Se results in poor rate performance and cycling stability. To solve this issue, nanosized-Cu2Se is encapsulated in 1D nitrogen-doped carbon nanofibers (Cu2Se-NC) so that the unique structure of 1D carbon fiber network ensures a high contact area between the electrolyte and Cu2Se with a short Na+ diffusion path and provides a protective matrix to accommodate the volume variation. The kinetic analysis and DNa+ calculation indicates that the dominant contribution to the capacity is surface pseudocapacitance with fast Na+ migration, which guarantees the favorable rate performance of Cu2Se-NC for SIBs.

Fabrication of large-area devices with patternable nanostructures is important for practical applications in optical or electrical devices. In this work, we describe an easy and environment-friendly method for preparing large-area nano-dot (ND) arrays via the electrolytic reaction of a metal oxide film. NDs with various size and morphology can be obtained by adjusting the applied voltage, electrolysis time, and the film thickness of the indium tin oxide (ITO) layer. High-density NDs with size of 50–60 nm can be obtained by electrolysis of a 25-nm-thick ITO film at 150 V for 1.5 min under a water droplet medium, which have been applied for surface-enhanced Raman spectroscopy (SERS) after depositing a thin layer of silver. The SERS substrate with optimized ND structure exhibits sensitive detection of Rhodamine 6G (R6G) with detection limit down to 5 × 10-12 M. The enhancement factors (EFs) of 1.12 × 106 and 6.79 × 105 have been achieved for characterization of 4-methylbenzenethiol (4-MBT) and R6G, respectively. With an additional photolithographic step, multiple areas of ND arrays can be created on one substrate, enabling simultaneous detection of various samples containing different molecules at once experiment. Such a method is quick, easy, patternable, and environment-friendly, being suitable for on-site quick and synchronous determination of various molecules for applications in point-of-care, environmental monitoring, and airport security fields.

Topography is a key factor that governs important properties of surfaces, such as adhesion and wettability, and materials with switchable surface topographies will have switchable surface properties. We demonstrate a principle to generate electrically switchable surface topographies on the surface of a thin nematic liquid crystal elastomer film which is sandwiched between a continuous electrode and a random metal network. Voltage-controlled displacement of the metal network toward the continuous electrode is achieved, resulting in unprecedented topographical modulations in the range of 0-2.5 μm. We show that this depth variation is significantly larger than the expected deformation because of electrostatic attraction between the network and the continuous electrode. This effect is explained by deformation due to the rotation of the liquid crystal side groups along the electric field lines.

Nanonail shaped ZnS-CuS-Bi three component nanoparticles are synthesized via a simple one-pot colloidal synthesis route by thermal decomposition of metal-thiolate precursors. A thiol serves as the sulfur source and a phase directing capping agent promotes selective anisotropic growth of the nanocrystals in a noncoordinating solvent. After the nucleation and growth of a CuS rod, reactive Cu ions serve as catalytic seeds for the nucleation and growth of ZnS and Bi at the CuS nanorod tips. Thereby the obtained ZnS-CuS-Bi nanocrystals form a chain of two semiconductors of decreasing band gap and a metallic Bi nanoparticle. The three components absorb light in different spectral regions enabling efficient light harvesting. Furthermore, the band edge alignment of ZnS and CuS promote photogenerated electron funneling towards the Bi catalyst particle, which promotes charge carrier separation, effectively channeling the catalytic activity. The photocatalytic performance is assessed at the example of the photodegradation of the organic dye Rhodamine B, and shows excellent performance rendering these nanonails as inexpensive, non-toxic and efficient photocatalyst to remedy environmental pollution.

The construction of definitive correlation between structure and catalytic properties for electrochemical artificial N2 fixation is still challenging yet significative. Herein, we have explored the coordinative unsaturation (Fe-N2) in isolated Fe atoms with nitrogen vacancies (VN, which are located at the opposite coordination sites of the Fe atom) on interconnected carbon for electrocatalytic ammonia synthesis. Benefiting from dual active centers (Fe-N2 and VN) and the spin density on both of them, the novel catalyst exhibits a synergistic improvement of catalytic activity, selectivity, and stability. This work guides the design of the catalyst theoretically and synergistically and combines the advantages of Fe-N2 with VN structure creation, defect and spin-state engineering introduction toward the concurrent fulfillment of effective N2 adsorption and activation. We believe our strategy will incite more investigation into designing high-performance catalysts with well-defined coordinative unsaturation single-atom active sites for ambient ammonia synthesis and other energy conversion system.

The aim of the current study was to determine whether the MWCNT-based scaffold has a suitable structure for cell growth and provides a biocompatible environment for human MDA-MB-231 cell lines. MWCNT-based nanostructured scaffolds were produced by plasma-enhanced chemical vapor deposition (PECVD) technique. MDA-MB-231 cells were seeded on MWCNTs-textured silicon scaffolds and on pristine silicon surfaces. After 1 week of culturing, the scaffolds were prepared for SEM analysis and immunocytochemical staining was performed for the two groups (MWCNT scaffold and pristine silicon surface), using MMP-2, MMP-9, PI3K, AKT and NF-κB primary antibodies. SEM analyses showed that the MDA-MB-231 cells better adhered to the MWCNT-based nanostructured scaffold than the pristine silicon surface. Immunohistochemical activity of the MDA-MB-231 cells on both materials has similar staining with anti-AKT MMP-2, MMP-9 and NF-κB primary antibodies. Therefore, the results of the present study suggest that the MWCNT-based scaffolds enhanced cell adhesion to the scaffold and exhibited more biomimetic properties and physiological adaptation with the potential to be used for in vitro metastasis studies of BrCa cell lines.

Bacterial biofilms cause a considerable amount of prosthetic joint infections every year, resulting in morbidity and expensive revision surgery. To address this problem, surface modifications of implant materials such as carbon nanotube (CNT) coatings have been investigated in the past years. CNTs are biologically compatible and can be utilized as drug delivery systems. In this study, multi-walled carbon nanotube (MWCNT) coated TiAl6V4 titanium alloy discs were fabricated and impregnated with Rifampicin, and tested for their ability to prevent biofilm formation over a period of ten days. Agar plate-based assays were employed to assess the antimicrobial activity of these surfaces against Staphylococcus epidermidis. It was shown that vertically aligned MWCNTs were more stable against attrition on rough surfaces than on polished TiAl6V4 surfaces. Discs with coated surfaces caused a significant inhibition of biofilm formation for up to five days. Therefore, MWCNT-modified surfaces may be effective against pathogenic biofilm formation on endoprostheses.

A plasmonic structure with transmission highly tunable in the mid-infrared spectral range is developed. This structure consists of a hexagonal array of metallic discs located on top of silicon pillars protruding through holes in a metallic Babinet complementary film. We reveal with FDTD simulations that changing the hole diameter tunes the main plasmonic resonance frequency of this structure throughout the infrared range. Due to the underlying Babinet physics of these coupled arrays, the spectral width of these plasmonic resonances is strongly reduced, and the higher harmonics are suppressed. Furthermore, we demonstrate that this structure can be easily produced by a combination of the nanosphere lithography and the metal-assisted chemical etching technique.

To achieve an ultrasensitive biosensor, the modified nanomaterials with high specific surface area, proper chemical and electrical/optical properties are highly required. In the present work, we designed a rapid and ultrasensitive label-free electrochemical immunosensor for interleukin-6 (IL-6) detection based on nanoporous mesoporous-carbon (NMC) composite decorated with gold nanoparticles (NMC@AuNPs). The NMC served as the transducer matrix, which is modified on the surface of glassy carbon electrode (GCE), to deposit the gold nanoparticles (AuNPs). NMC is synthesized via a wrinkled SiO2-nanoparticle (wSiO2NP) assisted sacrificing strategy, which displays an interconnected 3D structure to achieve high specific surface area and abundant porous for rapid sample enrichment; meanwhile, the composited hierarchical porous structure promotes the deposition and entanglement of AuNPs to form stable NMC@AuNPs and achieve enhanced electrical conductivity. Specific antibody against IL-6 protein is immobilized onto the surface of AuNPs, based on the antibody-antigen recognition strategy, the constructed immunosensors demonstrate high sensitivity and selectivity for assay of IL-6 with a linear dynamic range of 0.5–1200 pg mL−1 and the ultralow limit of detection (LOD) of 0.14 pg mL−1. Toward the detection of IL-6 in human serum samples, this label-free biosensor with a short detection period (within 60 min, including sample processing and electrochemical measurement). Moreover, the label-free biosensor exhibited an excellent sensitivity and specificity, suggesting it possesses the potential for other biomarkers in point-of-care biosensing application.

We propose a simple and inexpensive SiO2 submicron particle synthesis method based on a PTFE helical capillary microreactor. The device is based on Dean flow mediated, ultrafast mixing of two liquid phases in a microfluidic spiral pipe. Excellent control of particle size between 100 nm and 600 nm and narrow polydispersity can be achieved by controlling the device and process parameters. Numerical simulations are performed to determine the optimal device dimensions. In the mother liquor the silica particles exhibit zeta potentials

Transparent conductors (TCs) are materials, which are characterized by high transmission of light and simultaneously very high electrical DC conductivity. These materials play a crucial role, and made possible numerous applications in the fields of electro-optics, plasmonics, biosensing, medicine, and “green energy”. Modern applications, for example in the field of touchscreen and flexible displays, require that TCs are also mechanically strong and flexible. TC can be broadly classified into two categories: uniform and non-uniform TC. The uniform TC can be viewed as conventional metals (or electron plasmas) with plasma frequency located in the infrared frequency range (e.g. transparent conducting oxides), or ultra-thin metals with large plasma frequency (e.g. graphen). The physics of the nonuniform TC is much more complex, and could involve transmission enhancement due to refraction (including plasmonic), and exotic effects of electron transport, including percolation and fractal effects. This review ties...

An ideal network window electrode for photovoltaic applications should provide an optimal surface coverage, a uniform current density into and/or from a substrate, and a minimum of the overall resistance for a given shading ratio. Here we show that metallic networks with quasi-fractal structure provides a near-perfect practical realization of such an ideal electrode. We find that a leaf venation network, which possesses key characteristics of the optimal structure, indeed outperforms other networks. We further show that elements of hierarchal topology, rather than details of the branching geometry, are of primary importance in optimizing the networks, and demonstrate this experimentally on five model artificial hierarchical networks of varied levels of complexity. In addition to these structural effects, networks containing nanowires are shown to acquire transparency exceeding the geometric constraint due to the plasmonic refraction., In photovoltaics window electrodes must display uniform current transport, as well as high light transmission from the substrate. Here, Han et al. show that quasi-fractal metallic networks provide a practical realization of an electrode structure with an optimal surface coverage and a uniform current density.