Formation Of Arrays Research Articles

Two-dimensional optical binding based on graphene surface plasmon excitation.

In this work, we present a detailed analysis of the optical binding force resulting from the near field scattering between dielectric nanoparticles and a graphene substrate. We pay special attention to the two-dimensional array formation for which the stability is raised owing to the multiple surface plasmon (SP) scattering. Because of the small values of the SP wavelength on graphene in comparison with those of the photon, the size of these particle arrangements falls below the diffraction limit. By using a rigorous formalism based on the electromagnetic Green theory, we calculate the binding energy potential whose depth quantifies the stability of such configurations. We find multiple configurations for a given number of nanoparticles, from which only a subset of them remains stable under thermal fluctuations. Our contribution can be valuable for understanding the formation of new optically reconfigurable polaritonic materials.

Formation of vanadium dioxide nanocrystal arrays via post-growth annealing for stable and energy-efficient switches

The abrupt and reversible semiconductor-metal phase transition in vanadium dioxide nanocrystals has attracted considerable attention for potential applications in oxide electronics, including neuromorphic systems. This study presents a systematic investigation of post-growth annealing conditions for the formation of single VO2 M-phase nanocrystals arrays from VOx films synthesized by atomic layer deposition. The composition of the initial VOx films and the annealing parameters were found to significantly affect the morphology, phase composition and electrical properties of the obtained single nanocrystal arrays. Our results demonstrate that the formation of VO2 M-phase nanocrystal arrays occurs at annealing temperatures of 650 °C and above, irrespective of the initial film composition. More homogeneous in size nanocrystals are formed from initial VOx films with higher V+4 content. The structures with the initial V+4 content of 60 % annealed at 650 °C for 2 h demonstrates the resistive switching with an energy less than 150 fJ, and a total number of stable switching cycles more than 101⁰. Our results pave the way for the novel energy-efficient nanoelectronic and nanophotonic devices based on VO₂ nanoparticles.

Effect of Chemical Polishing on the Formation of TiO2 Nanotube Arrays Using Ti Mesh as a Raw Material

As a unique form of TiO2, TiO2 nanotube arrays (TiO2NTAs) have been widely used. TiO2NTAs are usually prepared by Ti foil, with little research reporting its preparation by Ti mesh. In this paper, TiO2NTAs are prepared on a Ti mesh surface via an anodic oxidation method in the F-containing electrolyte. The optimal parameters for the synthesis of TiO2NTAs are as follows: the solvent is ethylene glycol and water; the electrolyte is NH4F (0.175 mol/L); the voltage is 20 V; and the anodic oxidation time is 40 min without chemical polishing. However, there is a strange phenomenon where the nanotube arrays grow only at the intersection of Ti wires, which may be caused by chemical polishing, and the other areas, where TiO2NTAs cannot be observed on the surface of Ti mesh, are covered by a dense TiO2 film. New impurities (the hydrate of TiO2 or other products) introduced by chemical polishing and attaching to the surface of the Ti mesh reduce the current of anodic oxidation and further inhibit the growth of TiO2 nanotubes. Hence, under laboratory conditions, for commercially well-preserved Ti mesh, there is no necessity for chemical polishing. The formation of TiO2NTAs includes growth and crystallization processes. For the growth process, F− ions corrode the dense TiO2 film on the surface of Ti mesh to form soluble complexes ([TiF6]2−), and the tiny pores remain on the surface of Ti mesh. Given the basic photoelectrochemical measurements, TiO2NTAs without chemical polishing have better properties.

Controlled Formation of Porous Cross-Bar Arrays Using Nano-Transfer Printing.

Nano-transfer printing (nTP) has emerged as an effective method for fabricating three-dimensional (3D) nanopatterns on both flat and non-planar substrates. However, most transfer-printed 3D patterns tend to exhibit non-discrete and/or non-porous structures, limiting their application in high-precision nanofabrication. In this study, we introduce a simple and versatile approach to produce highly ordered, porous 3D cross-bar arrays through precise control of the nTP process parameters. By selectively adjusting the polymer solution concentration and spin-coating conditions, we successfully generated discrete, periodic line patterns, which were then stacked at a 90-degree angle to form a porous 3D cross-bar structure. This technique enabled the direct transfer printing of PMMA line patterns with well-defined, square-arrayed holes, without requiring additional deposition of functional materials. This method was applied across diverse substrates, including planar Si wafers, flexible PET, metallic copper foil, and transparent glass, demonstrating its adaptability. These well-defined 3D cross-bar patterns enhance the versatility of nTP and are anticipated to find broad applicability in various nano-to-microscale electronic devices, offering high surface area and structural precision to support enhanced functionality and performance.

Self-Reconstructed Amorphous CoOx/NiCoB Heterostructure Catalysts for Enhanced HER Performance.

Amorphous electrocatalysts exhibit potentials as precursors for triggering the in situ reconstruction to generate the real catalytic active species toward electrochemical processes. In this work, a new kind of amorphous Ni-Co-B alloy pre-catalysts for hydrogen evolution reaction (HER) is reported, which is obtained via a facile electroless plating strategy on the nickel foam (NF). Interestingly, X-ray photoelectron spectroscopy, X-ray absorption spectroscopy and morphological characterizations identify the in situ reconstruction process during HER accompanied by the preferential leaching of surface B species and the formation of amorphous CoOx nanosheet arrays as the real active sites. Benefiting from the synergistic effect between the surface CoOx layer and the inner unaltered NiCoB phase, the resultant CoOx/NiCoB heterostructure catalyst achieves a low overpotential of 209mV at the elevated current density of 500mA cm-2 and maintains stability for 300h without significant attenuation. Theoretical calculation reveals the electron reconfiguration at the interfaces between the newly formed CoOx and inner NiCoB phases, which is favorable for the stabilization of reconstructed active oxide layers at the reductive potentials for catalyzing HER. Moreover, the CoOx/NiCoB heterostructure optimizes hydrogen adsorption free energies, thereby enhancing HER catalytic activity.

Diffusive ex situ galvanic growth of metal nanocrystals on transmission electron microscopy grid

The uniform modification of commercial and standardized objects features considerable potential, as in the case of dip-pen lithography, biosensor kits, and disposable electrodes. In this study, we devised a dense nanoparticle array formation using the metallic mesh of a transmission electron microscopy (TEM) grid, which was formerly solely employed as a sampling stage. Incompletely oxidized cationic species generated from the galvanic replacement reaction of the metallic support mesh at the opposite side of the carbon layer diffused to the exposed top side and led to ex situ nanostar formation. A uniform nanoparticle array was obtained by immersion in an aqueous solution of replacing metal cations without reducing agents or surface energy-controlling compounds. Moreover, the array density was exclusively regulated by the incubation time. The straightforward nanoparticle array formation was successfully extended to various metal mesh TEM grids and different transition metal cations capable of spontaneous redox reactions. Cu mesh TEM grid and Mo grids could be utilized as sacrificial templates, and the growth of Au, Pd, Pt, Ag, and Rh nanostructures was confirmed.

Evaluation of Cross-Linked Actin Networks (CLANs) in Human Trabecular Meshwork Cells and Tissues.

Elevated intraocular pressure (IOP) is a major risk factor for the development and progression of glaucoma, the leading cause of irreversible vision loss and blindness. An overall increase in resistance to aqueous humor outflow causes sustained elevation in IOP. Glaucomatous insults in the aqueous humor outflow pathway, including the trabecular meshwork (TM), precede such chronic physiological changes in IOP. These insults include ultrastructural changes with excessive extracellular matrix deposition and actin cytoskeletal reorganization that leads to pathological stiffening of the ocular tissues. One of the most common cytoskeletal changes associated with TM tissue stiffness in glaucoma is the increased prevalence of cross-linked actin networks (CLANs) in cells of the trabecular meshwork (TM) and lamina cribrosa (LC). In glaucomatous cells, rearrangement of linear actin stress fibers leads to formation of polygonal arrays within the cytoplasm, resembling a geodesic dome-like structure, that we identified as CLANs. In addition to increased amounts of CLANs in POAG TM cells and tissues, we also discovered that glucocorticoid (GC) and TGFβ2 signaling pathways associated with the development of ocular hypertension (OHT) and glaucoma also induced CLANs in the TM. Despite a clear association, we are yet to completely understand the mechanisms involved in CLAN formation and their direct relevance to disease pathology. In this chapter, we will describe methods to identify and characterize CLANs using fluorescent microscopy in primary TM cell cultures, ex vivo perfusion cultured human anterior segments, and in situ in human donor eyes.

Microfluidic Exploitation of Liquid Crystal Properties of Boron Nitride Nanotubes and Enhancing Neutron Shielding with Aligned Structure

Boron nitride nanotubes (BNNTs) are cylindrical nanostructures characterized by alternating boron and nitrogen atoms. Unlike carbon nanotubes (CNT), BNNTs are electrically insulating and exhibit high thermal stability and neutron shielding capabilities. Their unique tubular structure enables the formation of 1D arrays, which can achieve a nematic liquid crystal phase, ideal for fabricating high‐density structures. However, the widespread application of BNNTs has been hindered by challenges in purifying and dispersing high‐purity BNNTs. This study aims to exploit the liquid crystal properties of BNNTs by generating high‐purity BNNT dispersions through a series of dispersion and purification processes. Furthermore, this study utilizes microfluidics technology to encapsulate the BNNT dispersions. Using this approach, the transition of liquid crystal phases in relation to BNNT concentration is efficiently examined. This process results in the production of high‐density BNNT films characterized by pronounced anisotropy, which in turn provides significant thermal neutron shielding effects.

Comparative analysis of microlens array formation in fused silica glass by laser: Femtosecond versus picosecond pulses

The growing demand for flexible, high-quality fabrication of free-form micro-optics drives the development of laser-based fabrication techniques for both the shape formation and surface polishing of optical elements. In this paper, we performed a thorough and systematic study on fused silica glass ablation using 10 ps and 320 fs duration pulses. Ablation processes for both pulse durations were optimized based on the measurements of the removed material layer thickness and surface roughness, and by analyzing the topographies of ablated cavities to remove material layers as thin as possible with minimum surface damage. Our findings demonstrate higher process resolution and surface quality for femtosecond pulses. Ablation of pre-roughened glass reduced the minimal removable glass layer thickness well below the 1 μm mark for both pulse durations, improving the process resolution. The minimal removable glass layer thickness was 14 times smaller for the femtosecond pulses, with up to 4.5 times lower surface roughness compared to samples processed with picosecond pulses. On the other hand, results revealed faster glass removal rates with picosecond pulses. In the end, arrays of microlenses were fabricated with both pulse durations and subsequently polished with a CO2 laser. Results revealed higher performance of microlenses fabricated with femtosecond pulses, providing better focusing capabilities and lesser beam scattering. Finally, this study demonstrated the successful fabrication of free-form optical elements with femtosecond and picosecond pulses, demonstrating the versatility and the potential of laser-based techniques.

Fabrication with magnetic-spin coating: Influence of magnetic-inertia energy ratio on gold-pickering ferrofluid droplet assembly morphology

Magnetic self-assembly of nanoparticles is a well-known technique for creating thin-film array-patterned functional microstructures. However, an uncontrollable hierarchical assembly formation of magnetically stimulated particles has hindered the desired formation of free-standing two-dimensional (2D) array patterns in thin-film layers. In this study, we proposed a fluidic shearing effect from spin coating to reduce the magnetically stimulated particles’ disarrayed and complex chain formations. This would thus promote linear array formations, even as the film becomes thinner. A series of tests were conducted on a gold-pickering ferrofluid emulsion (GPFE) dispersed in 15.2 mPas aqueous polyvinyl alcohol (PVAh) under varying spin speeds and magnetic setups such as single (SI), compound (CC), and concentric (CR). These setups were chosen to observe the influence of magnetic field strength and distribution on the generated pattern profile from microscopic binary images of the resulting thin films. The aim was to quantify the formed chain thickness (ChT), chain gaps (ChG), and chain lengths (ChL) to capture the morphology and geometrical features of the formed patterns. Our results showed that the quantified values of these profiles and their dimensionless relationships were significantly influenced by the ratio between the applied magnetic packing energy and the centrifugally controlled fluidic energy, QPD. This investigation showed that ChT/ChG for a corresponding QPD value is 98.6% the same for all configurations, and CR was the best setup going forward, as it yielded the lowest array quality defectivity of 14%. Therefore, we assert that this fabrication method offers flexibility, cost-effectiveness, and expandability in generating linear array patterns that contain graduating variability in grating order dimensions within a single cast that can serve efficiently as a substrate for biomolecules under enhanced Raman and Infrared spectroscopies.

Controlled Fabrication of Distinct Nanostructures from Discrete Oligourethanes via Thermal Annealing.

The self-assembly of sequence-defined polymers (SDPs) enables the formation of a diverse array of nanostructures; however, the construction of complex hierarchical structures via thermal annealing from SDPs remains relatively unexplored. In this study, two series of oligourethanes, 2Cit-pBn-OH and 2Cit-mBn-OH, were synthesized to investigate their thermal annealing behaviors. Nanorod clusters were generated from 2Cit-pB6-OH in a mixture of 1,4-dioxane and toluene, whereas 2Cit-pB8-OH formed nanosheets after thermal annealing. Upon modifying the structure of the repeating units, 2Cit-mB6-OH self-assembled into ultrathin nanosheets, transitioning from nanospheres after thermal annealing in a mixture of isopropanol and cyclohexane, while "flower" micelles were produced from 2Cit-mB8-OH. Interestingly, when isopropanol was replaced with a mixture of isopropanol and tetrahydrofuran (THF), uniform nanotubes were generated by 2Cit-mB6-OH under the same thermal annealing conditions. Additionally, a discrete amphiphile (2Cit-mB4-(S)DPEG) was synthesized, leading to the formation of uniform nanosheets in aqueous solution after thermal annealing. This work highlights the significant effects of sequence and repeating unit structure of SDPs on their self-assembly behaviors and presents a novel strategy for the controlled fabrication of unique nanostructures from SDPs.

Solution State-Like Reactivity of a Flexible Crystalline Werner-Type Metal Complex.

Flexible crystalline solids exhibit unique properties in response to external stimuli like heat and light. However, challenges exist in developing crystalline solids that have similar degrees of flexibility as in solution. Herein, we report the preparation of the new flexible crystalline metal complex [Cd(CF3SO3)2(4-spy)4] (4-spy=4-styrylpyridine), which contains photoreactive 4-spy ligand. Unlike traditional solids, this metal complex displays solution state-like [2+2] photocycloaddition reactivity. Specifically, UV irradiation of the crystalline material leads to formation of the same diverse array of dimers and cis isomer that are generated by photoreaction in the solution state. In addition, the photoresponsive flexibility of the solid leads to a photosalient effect and photo-induced formation of pores. The origin of the solution state-like photoreactivity of the solid is related to properties of the Cd(II) cation and fluorinated CF3SO3 anion, and the multi-orientational arrangement of the 4-spy ligands.

Rectangular Microstrip With Co‐Planar Corner Loading: Advanced Antenna and Array Design for High Cross‐Polar Isolation Across All Radiation Planes

AbstractA newly conceived microstrip element, that features adequately suppressed cross‐polar discrimination (XPD) over both the orthogonal (H‐) and diagonal (D‐) planes, has been explored here. The proposed patch is of rectangular shape with a pair of loading at its corner region. A standalone patch as well as its linear and square array formation has been investigated. Their design and characterization along with a partial experimental verification are presented. They promise considerable improvement in D‐plane XPD, around 6 dB for single element, 10 dB for four‐element linear and 5 dB for four‐element square sub‐arrays. The XPD performance over H‐plane is equally promising, 8 dB for single element (10–18) dB for both planar and square arrays. The overall 3D‐XP scenario thus gets improved by about (8–10) dB on average which is quite significant in the case of arrays.

Scalable Atomic Arrays for Spin-Based Quantum Computers in Silicon.

Semiconductor spin qubits combine excellent quantum performance with the prospect of manufacturing quantum devices using industry-standard metal-oxide-semiconductor (MOS) processes. This applies also to ion-implanted donor spins, which further afford exceptional coherence times and large Hilbert space dimension in their nuclear spin. Here multiple strategies are demonstrated and integrated to manufacture scale-up donor-based quantum computers. 31PF2 molecule implants are used to triple the placement certainty compared to 31P ions, while attaining 99.99% confidence in detecting the implant. Similar confidence is retained by implanting heavier atoms such as 123Sb and 209Bi, which represent high-dimensional qudits for quantum information processing, while Sb2 molecules enable deterministic formation of closely-spaced qudits. The deterministic formation of regular arrays of donor atoms with 300nm spacing is demonstrated, using step-and-repeat implantation through a nano aperture. These methods cover the full gamut of technological requirements for the construction of donor-based quantum computers in silicon.

Room-Temperature Superconductivity in 1D

We review the theoretical model underpinning the recently reported room-temperature, ambient-pressure superconductivity along line defects on the surface of highly oriented pyrolytic graphite. The main ingredients for this 1D room-temperature superconductivity are pairing by effective strain gauge fields, the formation of an effective Josephson junction array in its Bose metal state on the surface and the suppression of phase slips by dimensional embedding in an extremely well-conducting 3D bulk structure.

Epigenetics in the formation of pathological aggregates in amyotrophic lateral sclerosis.

The progressive degeneration of motor neurons in amyotrophic lateral sclerosis (ALS) is accompanied by the formation of a broad array of cytoplasmic and nuclear neuronal inclusions (protein aggregates) largely containing RNA-binding proteins such as TAR DNA-binding protein 43 (TDP-43) or fused in sarcoma/translocated in liposarcoma (FUS/TLS). This process is driven by a liquid-to-solid phase separation generally from proteins in membrane-less organelles giving rise to pathological biomolecular condensates. The formation of these protein aggregates suggests a fundamental alteration in the mRNA expression or the levels of the proteins involved. Considering the role of the epigenome in gene expression, alterations in DNA methylation, histone modifications, chromatin remodeling, non-coding RNAs, and RNA modifications become highly relevant to understanding how this pathological process takes effect. In this review, we explore the evidence that links epigenetic mechanisms with the formation of protein aggregates in ALS. We propose that a greater understanding of the role of the epigenome and how this inter-relates with the formation of pathological LLPS in ALS will provide an attractive therapeutic target.

Structure and dynamics of cholesterol-mediated aquaporin-0 arrays and implications for lipid rafts

Aquaporin-0 (AQP0) tetramers form square arrays in lens membranes through a yet unknown mechanism, but lens membranes are enriched in sphingomyelin and cholesterol. Here, we determined electron crystallographic structures of AQP0 in sphingomyelin/cholesterol membranes and performed molecular dynamics (MD) simulations to establish that the observed cholesterol positions represent those seen around an isolated AQP0 tetramer and that the AQP0 tetramer largely defines the location and orientation of most of its associated cholesterol molecules. At a high concentration, cholesterol increases the hydrophobic thickness of the annular lipid shell around AQP0 tetramers, which may thus cluster to mitigate the resulting hydrophobic mismatch. Moreover, neighboring AQP0 tetramers sandwich a cholesterol deep in the center of the membrane. MD simulations show that the association of two AQP0 tetramers is necessary to maintain the deep cholesterol in its position and that the deep cholesterol increases the force required to laterally detach two AQP0 tetramers, not only due to protein–protein contacts but also due to increased lipid–protein complementarity. Since each tetramer interacts with four such ‘glue’ cholesterols, avidity effects may stabilize larger arrays. The principles proposed to drive AQP0 array formation could also underlie protein clustering in lipid rafts.

Structure and dynamics of cholesterol-mediated aquaporin-0 arrays and implications for lipid rafts.

Aquaporin-0 (AQP0) tetramers form square arrays in lens membranes through a yet unknown mechanism, but lens membranes are enriched in sphingomyelin and cholesterol. Here, we determined electron crystallographic structures of AQP0 in sphingomyelin/cholesterol membranes and performed molecular dynamics (MD) simulations to establish that the observed cholesterol positions represent those seen around an isolated AQP0 tetramer and that the AQP0 tetramer largely defines the location and orientation of most of its associated cholesterol molecules. At a high concentration, cholesterol increases the hydrophobic thickness of the annular lipid shell around AQP0 tetramers, which may thus cluster to mitigate the resulting hydrophobic mismatch. Moreover, neighboring AQP0 tetramers sandwich a cholesterol deep in the center of the membrane. MD simulations show that the association of two AQP0 tetramers is necessary to maintain the deep cholesterol in its position and that the deep cholesterol increases the force required to laterally detach two AQP0 tetramers, not only due to protein-protein contacts but also due to increased lipid-protein complementarity. Since each tetramer interacts with four such 'glue' cholesterols, avidity effects may stabilize larger arrays. The principles proposed to drive AQP0 array formation could also underlie protein clustering in lipid rafts.

Formation of linear arrays of holes in self-assembled collagen films

Collagen is one of the main constituents of mammalian extracellular matrix and is used extensively as a coating for tissue culture dishes and medical implants to promote cell growth and proliferation. By modulating the topography of the collagen coating at the nanometer to micrometer length scales, it is possible to achieve spatial control over cell growth and morphology. In this work, we are exploring the self-assembly of a thin collagen film on a glass substrate as a way to create new nanoscale surface features. By controlling the collagen concentration and adding an oscillatory flow, we are able to enrich the collagen film surface with a localized pattern of ripples oriented perpendicular to the flow direction. We propose that these ripples are the result of dewetting of the collagen film that leads to the formation of adjacent holes. We observe that individual holes form with an anisotropic rim due to the microstructure of the deposited collagen fibril network. This intrinsic anisotropy and the oscillatory flow yield new holes being formed in the film next to existing rims. As holes keep growing deeper, the rims extend along the flow direction, and the holes appear rectangular in shape, which gives the linear array of holes the apparent morphology of a ripple. Overall, we are able to create localized ripples at the surface of collagen films that would be difficult to produce via standard nanofabrication techniques.

Forming mechanism of a novel shape-surface integrated incremental sheet forming process for fabricating parts with enhanced surface functionality

Metallic components with surface microfeatures are increasingly used in aerospace, automotive and other applications due to their drag-reducing properties. In this situation, we proposed a novel shape-surface integrated incremental sheet forming (S2-ISF) process to achieve the simultaneous fabrication of both surface microfeatures and desired geometric shape. It was found that an increase in the forming angle was most effective in improving the formation of microgroove array, followed by the step size, the spindle speed and the feed rate. Moreover, when the forming angle is constant, the step size and microgroove pitch increase linearly. Compared to the as-received sheet, the yield strength is increased by more than 20% after the S2-ISF process. Moreover, we observed that the increase of forming angle in the S2-ISF process has promoted grain deformation and grain fragmentation, which is favorable for the formed part to obtain more uniform and finer grains. The grain size distribution along the thickness direction shows the characteristics of ‘coarse in the middle and fine at both ends’. Finally, we found that the formed parts with different microgroove pitch from the S2-ISF process have the significant enhancement on the hydrophobicity and anti-friction property. When microgroove pitch is 155.5 μm, the surface contact angle of formed part improved from 70.65° to 101.39°, and the wear volume of formed part decreases from 4.89 × 10−3 mm3 to 3.65 × 10−3 mm3. This work provides a solution for the efficient and economical fabrication of three-dimensional thin-walled parts with microgroove array to enhance surface functionality.