Surface Steps Research Articles

“Tension band wiring first” —an easy, fast and reproducible technique to reduce patellar fractures, a retrospective comparative study with traditional reduction technique

ObjectiveTo evaluate intraoperative and early postoperative clinical outcomes using the “tension band wiring first technique” to reduce C type patellar fractures.MethodsSixty-four patients with C type fractures were enrolled in this study. Thirty-four patients underwent open reduction and internal fixation (ORIF) surgeries using the traditional reduction technique by pointed clamps (TRT group). The other thirty patients received the patellar fracture reduction using the “Tension band wiring first technique” (TBWFT group). All patellar fractures were treated with a cable tension band and a cerclage cable. The duration of intraoperative procedure and X-ray exposure times were recorded. All patients were followed up at 1, 3, 6, and 12 months. Bone union time was recorded. The articular surface steps of the patellas were measured. After surgery, range of motion (ROM) of the knee, and complications were evaluated, and patellar function was evaluated using the Lysholm knee scores and Böstman scores.ResultsWhen compared to TRT group, the “Tension band wiring first technique” significantly reduced the intraoperative time and X-ray exposure times and tended to reduce the articular surface steps, though without statistical significance. In the two groups, there was no significant difference in bone union time, ROM, complications and patellar function.ConclusionThe utilization of “Tension band wiring first technique” proved to be a straightforward, expeditious, and reproducible technique for reducing patellar fracture in comparison to the conventional reduction technique utilizing pointed clamps. Further studies are required to ensure the generalizability of these findings to additional patient populations at other institutions.

Concentrated C2+ Alcohol Production Enabled by Post-Intermediate Modulation and Augmented CO Adsorption in CO Electrolysis.

The electrocatalytic synthesis of multicarbon products from CO2/CO feedstock represents a sustainable method for chemical production with a reduced carbon footprint. Traditional copper catalysts predominantly produce alkenes, but generating valuable and versatile C2+ alcohols, especially high-energy-density C3 alcohols, has been challenging due to issues with selectivity, activity, and stability. Here, we present the construction of Ru-doped Cu nanowires that enhance the selectivity of n-PrOH and C2+ alcohols. In situ Raman spectroscopy shows that our approach promotes both *CO binding and availability, particularly facilitating the formation of high-frequency-bound *CO (*COHFB) and maintaining multiple *CO adsorption modes on Ru-modified and bare low-coordinated Cu nanowires. Density-functional theory (DFT) simulations illustrate that introducing Ru species onto a low-coordinated Cu step surface simultaneously stabilizes CO and alcohol-related intermediates, shifting the dominant reaction pathway toward alcohols and facilitating CO-C2 coupling at the expense of ethylene selectivity. In an alkaline gas-diffusion electrolyzer, we attained a maximum Faradaic efficiency (FE) of 35.9% for n-PrOH and 62.4% for the total C2+ alcohols. Optimizing parameters in the membrane electrode assembly (MEA) system enabled the one-pot generation and separation of C2+ alcohols, achieving a record concentration of 18.8 wt % (4.2 wt % n-PrOH and 14.6 wt % EtOH) with nearly 100% purity at 200 mA/cm2 over 100 h. This work not only provides new insights and guidance for the development of future catalysts from the perspectives of surface science and mechanisms but also highlights the importance of coupling material engineering with reactor engineering to optimize the production process of high-value alcohol products.

Ultraflat Cu(111) foils by surface acoustic wave-assisted annealing

Ultraflat metal foils are essential for semiconductor nanoelectronics applications and nanomaterial epitaxial growth. Numerous efforts have been devoted to metal surface engineering studies in the past decades. However, various challenges persist, including size limitations, polishing non-uniformities, and undesired contaminants. Thus, further exploration of advanced metal surface treatment techniques is essential. Here, we report a physical strategy that utilizes surface acoustic wave assisted annealing to flatten metal foils by eliminating the surface steps, eventually transforming commercial rough metal foils into ultraflat substrates. Large-area, high-quality, smooth 2D materials, including graphene and hexagonal boron nitride (hBN), were successfully grown on the resulting flat metal substrates. Further investigation into the oxidation of 2D-material-coated metal foils, both rough and flat, revealed that the hBN-coated flat metal foil exhibits enhanced anti-corrosion properties. Molecular dynamics simulations and density functional theory validate our experimental observations.

Spiral‐Concave Prussian Blue Crystals with Rich Steps: Growth Mechanism and Coordination Regulation

AbstractInvestigating the formation and transformation mechanisms of spiral‐concave crystals holds significant potential for advancing innovative material design and comprehension. We examined the kinetics‐controlled nucleation and growth mechanisms of Prussian Blue crystals with spiral concave structures, and constructed a detailed crystal growth phase diagram. The spiral‐concave hexacyanoferrate (SC‐HCF) crystals, characterized by high‐density surface steps and a low stress‐strain architecture, exhibit enhanced activity due to their facile interaction with reactants. Notably, the coordination environment of SC‐HCF can be precisely modulated by the introduction of diverse metals. Utilizing X‐ray absorption fine structure spectroscopy and in situ ultraviolet‐visible spectroscopy, we elucidated the formation mechanism of SC‐HCF to Co‐HCF facilitated by oriented adsorption‐ion exchange (OA‐IE) process. Both experimental data, and density functional theory confirm that Co‐HCF possesses an optimized energy band structure, capable of adjusting the local electronic environment and enhancing the performance of the oxygen evolution reaction. This work not only elucidates the formation mechanism and coordination regulation for rich steps HCF, but also offers a novel perspective for constructing nanocrystals with intricate spiral‐concave structures.

Spiral-Concave Prussian Blue Crystals with Rich Steps: Growth Mechanism and Coordination Regulation.

Investigating the formation and transformation mechanisms of spiral-concave crystals holds significant potential for advancing innovative material design and comprehension. We examined the kinetics-controlled nucleation and growth mechanisms of Prussian Blue crystals with spiral concave structures, and constructed a detailed crystal growth phase diagram. The spiral-concave hexacyanoferrate (SC-HCF) crystals, characterized by high-density surface steps and a low stress-strain architecture, exhibit enhanced activity due to their facile interaction with reactants. Notably, the coordination environment of SC-HCF can be precisely modulated by the introduction of diverse metals. Utilizing X-ray absorption fine structure spectroscopy and in situ ultraviolet-visible spectroscopy, we elucidated the formation mechanism of SC-HCF to Co-HCF facilitated by oriented adsorption-ion exchange (OA-IE) process. Both experimental data, and density functional theory confirm that Co-HCF possesses an optimized energy band structure, capable of adjusting the local electronic environment and enhancing the performance of the oxygen evolution reaction. This work not only elucidates the formation mechanism and coordination regulation for rich steps HCF, but also offers a novel perspective for constructing nanocrystals with intricate spiral-concave structures.

Asymmetric Nanopore Sensor for Logic Detection of Dam and M.SssI Methyltransferases in Combination of DNA Walker and Autocatalytic Hybridization Reaction.

The detection of DNA methyltransferase (MTase) was crucial for understanding gene expression regulation, cancer mechanisms, and various biological processes, contributing significantly to disease diagnosis and drug development. Herein, a nanopore sensor based on cascaded signal amplification of DNA walker and autocatalytic hybridization reaction (AHR) was developed for the ultrasensitive determination of various MTases. In the presence of Dam MTase, the hairpin structure HD underwent methylation and cleavage by DpnI endonuclease, forming T-DNA fragments. These T-DNA fragments were used to activate the DNA walker, which moved across the surface of magnetic beads step by step, generating a large quantity of initiator I by cleaving the substrate. The initiator I subsequently activated the AHR. The AHR included a hybridization chain reaction (HCR) amplifier and a catalytic hairpin assembly (CHA) convertor. The HCR amplifier generated multiple novel CHA triggers, which activated the CHA convertor. This, in turn, stimulated the HCR amplifier, creating an AHR circuit that resulted in the formation of numerous DNA nanowires. These DNA nanowires were adsorbed onto the G4-PAMAM-modified nanopore surface under the influence of an electric field, thereby altering the surface charge of the nanopore and changing the ionic rectification curve. The detection limit of the Dam MTase nanopore sensor reached 0.0002 U/mL. By modification of the recognition sites of the probes, this nanopore system could also be used for the detection of M.SssI MTase. Moreover, a four-input parallel concatenated logic circuit (AND//INHIBIT-OR) had been constructed and applied for the multivariate detection of Dam MTase and M.SssI MTase, presenting a novel conceptual model for advancing the construction of nanopore logic gate systems and their applications in biosensing.

The Performance of Ethylene Partial Oxidation on Group IB Metal Stepped Surfaces

Group IB metal catalysts, particularly Ag, Au, and Cu, exhibit particular selectivity for ethylene oxide (EO) formation, while Ag demonstrating the highest performance so far. Previous studies have explored the EO formation mechanism on (100) and (111) surfaces of group IB metals, but the reaction mechanism on the (211) facet (analogous to the edge sites of a catalyst particle) remains poorly understood. Herein, we fill in the knowledge gap by analyzing ethylene partial oxidation to EO on the (211) surfaces of Ag, Au, and Cu through density functional theory (DFT) calculations, scaling relationship analysis, and microkinetic modeling. Our study demonstrates that the (211) surface decreases the energy barrier for the dissociation of oxygen molecules into oxygen atoms, while unfavorable for the production of EO. Therefore, we should preserve an appropriate concentration of (211) surface on the nanoparticles when designing catalysts for the ethylene epoxidation reaction.

Flapping dynamics of a flexible membrane attached to the leading edge of a forward-facing step

An experimental investigation of velocity fields over and wall pressure fluctuations on a forward-facing step (FFS) disturbed by a flexible membrane has been conducted. A two-dimensional flexible membrane of 40mm length and 0.15mm thickness attached to a FFS of 40mm height was tested with oncoming velocity in the range of 7.3 < U < 12.9 m/s, corresponding to Reynolds numbers of 20391 < ReH < 35312 based on the step height. A high-speed camera was used to reconstruct the configuration of the flapping membrane. The flow field velocity dataset in the horizontal-vertical plane and the pressure fluctuation on the step surface were measured by planar particle image velocimetry and pressure sensors, respectively. The flexible membrane displayed two distinct modes, viz. a bending mode or flapping mode. In the bending mode, the membrane elevates the shear layer, thereby delaying the reattachment of separation flow generated by a FFS. In the flapping mode, the membrane periodically generates flapping-induced vortices (FIVs) of different scales with varying Reynolds numbers. The pressure on the FFS also undergoes periodic fluctuations corresponding to these FIVs.

Observation of Zero-Energy Modes with Possible Time-Reversal Symmetry Breaking on Step Edge of CaKFe4As4

Abstract Topologically nontrivial Fe-based superconductors attract extensive attentions due to their ability of hosting Majorana zero modes (MZMs) which could be used for topological quantum computation. Topological defects such as vortex lines are required to generate MZMs. Here, we observe the robust edge states along the surface steps of CaKFe4As4. Remarkably, the tunneling spectra show a sharp zero-bias peak (ZBP) with multiple integer-quantized states at the step edge under zero magnetic field. We propose that the increasing hole doping around step edges may drive the local superconductivity into a state with possible spontaneous time-reversal symmetry breaking. Consequently, the ZBP can be interpreted as an MZM in an effective vortex in the superconducting topological surface state by proximity to the center of a tri-junction with different superconducting order parameters. Our results provide new insights into the interplay between topology and unconventional superconductivity, and pave a new path to generate MZMs without magnetic field.

Repetitive Rolling of Triptycene-Based Molecules on Cu Surfaces.

The metal surface-supported rotation of artificial molecular structures is technologically important for developing molecular-level devices. The key factors leading to the practical applications of these molecular machines on metal surfaces are the atomic-scale control of the rotation and the counterbalance of the temperature-driven instability of the molecules. In this work, we present a means by which triptycene-based molecular wheels can roll repetitively on a metal surface. Our results show that regularly stepped surfaces are the perfect candidate not only for stabilizing the molecule on the metal surface but also for providing the pivot points needed for repetitive vertical rotation of the molecule at higher temperatures. In addition to the geometrical compatibility of the substrate and the molecule, intermittent application of the external electric field is needed for rolling the molecule on a metal-stepped surface in a controllable manner.

Imaging of micro-steps on as-grown surface of sapphire with X-ray phase contrast technique

Basal-faceted sapphire ribbons grown using the Stepanov–LaBelle technology have a low density of surface steps. We present our results on a study of steps on the surface of a ribbon, misoriented relative to the singular face (0001) by several arc minutes. The ribbon has been characterized by means of in-line phase contrast imaging technique at Pohang Light Source, South Korea. It was shown for the first time that a step height of about 1 μm can be determined directly from an image. The step height obtained using the phase contrast method was confirmed by atomic force microscopy measurements. We have found that the experimental contrast matches the theoretical simulations only if the calculated intensity profile has been convolved with a Gaussian function. The full width at half maximum of the Gaussian was independently got from previous measurements. We have obtained an analytical solution in the case of theoretical fully coherent phase contrast image. The inverse problem is easy to solve, since there is a direct proportionality between the contrast and the step height.

Recrystallization of deformed metal nanoparticles

Despite great advances in the fabrication methods of metal nanoparticles with various sizes and shapes, the available tools for manipulating their microstructure and morphology still remain limited. In the present work we introduce the age-old metallurgical technique of recrystallization to the synthesis of metallic nanoparticles. We uniaxially compressed a large number of single crystalline and defect free Pt nanoparticles obtained by solid-state dewetting and annealed them at the temperature of 1000 °C. Our findings reveal that, while the as-dewetted particles exhibited similar shapes and crystallographic orientations, the plastic deformation and annealing led to a diverse range of shapes, microstructures, and orientations among the particles. We categorized the particles into four distinct types based on their appearance: slanted, terraced, “Danish pastry”, and broken particles. Finally, we propose a differentiation mechanism responsible for this diversification, which relies on a combination of recrystallization, surface step formation, and solid-state dewetting processes.

Water orientation on platinum surfaces controlled by step sites.

In this work, the adsorption structure of deuterated water on the stepped platinum surface is studied under an ultra-high vacuum by using heterodyne-detected sum-frequency generation spectroscopy. On a pristine Pt(553), D2O molecules adsorbed at the step sites act as hydrogen bond (H-bond) donors to the adjacent terrace sites. This ensures the net D-down orientation at the terrace sites away from the steps. In particular, the pre-adsorption of oxygen atoms at the step sites significantly alters the D-down configuration. The oxygen pre-adsorption leads to a spontaneous dissociation of the post-adsorbed water molecules at the step to form hydroxyl (OD) species. Since the hydroxyl at the step acts as a strong H-bond acceptor, D2O at the terrace no longer maintains the D-down configuration and adopts flat-lying configurations, significantly reducing the number of D-down molecules at the terrace. Density-functional theoretical calculations support these pictures. This work demonstrates the critical role of steps in controlling the net orientation of the interfacial water and provides an important reference for future considerations of the reactions at electrochemical interfaces.

A Study on Historical Big Data Analysis of Surface Ecological Damage in the Coal Mining Area of Lvliang City Based on Two Mining Modes

Coal mining inevitably causes damage to the surface ecological environment. In response to the characteristics of multiple factors, wide scope, and long time series of surface ecological environment damage in coal mining subsidence areas, how to integrate multiple data sources and monitoring methods to achieve monitoring and trend analysis of ecological damage throughout the entire mining cycle still needs to be studied. In addition, the 110 mining method provides an innovative method for underground coal mining to reduce its surface ecological damage, but the differences in surface damage between the two mining modes and the effectiveness of the 110 method in realizing surface ecological damage-reducing mining still need to be studied in depth. Therefore, this study takes the surface ecological damage in the mining area of Lvliang City, a typical resource city in Shanxi Province, China, as the object. It establishes a four-in-one “Satellite–UAV–Ground–Underground” information monitoring method, proposes a historical big data evolution analysis method, constructs three spatial scales of historical big databases, clarifies the current situation and development trend of damage in coal mining areas in Lvliang City and explores the differences in surface ecological environment damage characteristics in coal mining areas based on the 121 and 110 mining methods. The results show that: (1) The existing coal mining subsidence area in Lvliang City is as high as 92,191.47 hectares, and it is expected to continue to increase to 130,739.55 hectares in the future 2035, with a growth rate of 41.812%, which realizes the goals of mapping the current situation, retracing the history and predicting the future of the ecological damage of the surface in Lvliang City. (2) The surface NDVI of the 110 working face is restored to the average level of the mining area faster than that of the 121 working face. The surface crack width, step displacement, length, distribution density, and surface settlement height of the 110 working face are all smaller than those of the 121 working face. It has been verified that the unique top-cutting and swelling filling effect of the 110 methods can effectively reduce the ecological damage caused by coal mining subsidence. And its widespread application can effectively realize the ecological environmental protection of the coal mine area and contribute to the high-quality development of the coal industry in Lvliang City.

Exploring Older Adults' Perceptions of Stair Hazards and an m-health Fall Prevention App: A Focus Group Study

Older adults are disproportionately susceptible to hospitalizations and fatalities due to stair-related falls. While many intrinsic risk factors, such as mobility and vision, may increase the likelihood of falls on stairs, features of the stairs that increase the risk of falls are understudied. This study aimed to capture older adults’ perspectives of stair falls, as well as introduce the Safer Steps app and explore its feasibility in this population. This m-health technology was designed to gather data on stair-related falls and identify hazardous stair features (e.g., the absence of handrails, uneven steps). Capturing older adults’ perspectives of the role of the built environment in stair-related falls is crucial for fostering the adoption and use of the Safer Steps app in this demographic. Fifteen older adults (<em>M</em> = 73 years, SD = 5.29) participated in focus groups discussing falls, stair-related falls, technology use and the design concept of the Safer Steps app. Reflexive thematic analysis revealed that participants expressed fear of falling and cited intrinsic risk factors, such as age, medications, and footwear, alongside extrinsic risk factors related to the built environment, to be major causes of stair-related falls. They highlighted the significance of the built environment in fall prevention, particularly surface conditions, step dimensions, and handrails. Most participants were familiar with apps and endorsed the Safer Steps app design to mitigate stair-related fall risk. Findings indicate older adults' willingness to engage in strategies which reduce stair fall risk, such as modifying their behaviour by using handrails and changing footwear, viewing the Safer Steps app as a practical tool for identifying built environment hazards.

Selective Oxidation of Methanol to Methyl Formate on Gold: The Role of Low-Coordinated Sites Revealed by Isothermal Pulsed Molecular Beam Experiments and AIMD Simulations.

To elucidate the role of low-coordinated sites in the partial methanol oxidation to methyl formate (MeFo), the isothermal reactivity of flat Au(111) and stepped Au(332) in pulsed molecular beam experiments was compared for a broad range of reaction conditions. Low-coordinated step sites were found to enhance MeFo selectivity, especially at low coverage conditions, as found at higher temperatures. The analysis of the transient kinetics provides evidence for the essential role of Au x O y phases for MeFo formation and the complex interplay of different oxygen species for the observed selectivity. Ab initio molecular dynamic simulations yielded microscopic insights in the formation of Au x O y phases on flat and stepped gold surfaces emphasizing the role of low-coordinated sites in their formation. Moreover, associated surface restructuring provides atomic-scale insights which align with the experimentally observed transient kinetics in MeFo formation.

Growth of centimeter-scale single-crystal graphene on polycrystalline copper foil for ultrahigh sensitive sweat sensors

The low-cost growth of wafer-scale single-crystal (SC) shows great potential in its practical application. Epitaxial growth of large-area SC graphene on pre-produced SC metal foil with a specific index surface has been reported, which requires a high cost and complexity of operational processes. Here, we demonstrate an easy and low-cost approach for the growth of wafer-scale SC graphene on polycrystalline copper foil, the growth kinetics and the lattice orientation for graphene growth controlled by induced surface steps. Despite graphene domains grown across the Cu grain boundary, the domains have a common crystal orientation at the macroscale induced by the surface steps. This work demonstrates the polycrystalline Cu foil can also grow graphene domains with unidirectional alignment and seamless stitching on the large area. The wearable 2D graphene array sensors have also been developed for the detection of interleukin-6 (IL-6) in sweat, which can locate and detect infection or disease in a non-invasive way. Our growth method and novel application put up a new way of production and utilization of SC two-dimensional (2D) materials.

Near-Ambient Pressure Oxidation of Silver in the Presence of Steps: Electrophilic Oxygen and Sulfur Impurities.

The oxidation of Ag crystal surfaces has recently triggered strong controversies around the presence of sulfur impurities that may catalyze reactions, such as the alkene epoxidations, especially the ethylene epoxidation. A fundamental challenge to achieve a clear understanding is the variety of procedures and setups involved as well as the particular history of each sample. Especially, for the often-used X-ray photoemission technique, product detection, or photoemission peak position overlap are problematic. Here we investigate the oxidation of the Ag(111) surface and its vicinal crystal planes simultaneously, using a curved crystal sample and in situ X-ray photoelectron spectroscopy at 1 mbar O2 near-ambient pressure conditions to further investigate surface species. The curved geometry allows a straightforward comparative analysis of the surface oxidation kinetics at different crystal facets, so as to precisely correlate the evolution of different oxygen species, namely nucleophilic and electrophilic oxygen, and the buildup of sulfur as a function of the crystal orientation. We observed that emission from both surface and bulk oxide contributes to the characteristic nucleophilic oxygen core-level peak, which arises during oxygen dosing and rapidly saturates below temperatures of 180 °C. The electrophilic oxygen peak appears later, growing at a slower but constant rate, at the expenses of the surface oxide. Electrophilic oxygen and sulfur core-levels evolve in parallel in all crystal facets, although faster and stronger at vicinal surfaces featuring B-type steps with {111} microfacets. Our study confirms the intimate connection of the electrophilic species with the formation of adsorbed SO4, and points to a higher catalytic activity of B-type stepped silver surfaces for alkene epoxidation or methane to formaldehyde conversion.

Physical confinement versus adsorption driven reconstruction: The case of sulfate anion interaction with vicinal Cu(111) surfaces

Nano-electrochemistry, i.e., the research of the properties of nano-(structured) electrodes and their influence on electrochemical processes when immersed inside an electrolyte, represents a hot topic in view of applications in nano-electronics, electro-catalysis and energy storage devices. The role of physical confinement in the electrochemical fabrication and performances of the respective systems have been recently addressed in the context of metal-organic networks on surfaces, but rarely of nano-structured bare metal surfaces, for instance, regularly stepped (vicinal) surfaces. In this work we investigate the interplay between physical confinement and adsorbate induced restructuring by the electrochemical adsorption of sulfate anions on the flat and two distinctly different vicinal Cu(111) surfaces. Sulfate adsorption on the flat Cu(111) surface is known to create a long-range ordered Moiré-superstructure with lattice parameters in the 2–4 nm range due to an expansion of the topmost layer of copper atoms with respect to the underlying crystal planes. This restructuring is also observed on a vicinal Cu(111) surface whose original terrace width is considerably smaller than the lattice vectors of the sulfate induced Moiré-structure. The results clearly indicate not only that the Moiré formation lifts the physical confinement imposed by the initial terrace width, but also shine more light on the Moiré formation process itself. Such adsorbate induced restructuring, of course, depends on the respective adsorbate – electrode combination, but must, in principle, always be taken into account in order to understand electrochemical processes at nano-structured (and nano-sized) electrode surfaces.

Step feature line extraction from large-scale point clouds of open-pit mine based on structural characteristics

High-precision step feature lines play a crucial role in open-pit mine design, production scheduling, mining volume calculations, road network planning, and slope maintenance. Compared with the feature lines of the geometric model, step feature lines are more irregular, complex, higher in density, and richer in detail. In this study, a novel technique for extracting step feature line from large-scale point clouds of open-pit mine by leveraging structural attributes, that is, SFLE_OPM (Step Feature Line Extraction for Open-Pit Mine), is proposed. First, we adopt the k-dimensional tree (KD-tree) resampling method to reduce the point-cloud density while retaining point-cloud features and utilize bilateral filtering for denoising. Second, we use Point Cloud Properties Network (PCPNET) to estimate the normal, calculate the slope and aspect, and then filter them. We then apply morphological operations to the step surface and obtain more continuous and smoother slope lines. In addition, we construct an Open-Pit Mine Step Feature Line (OPMSFL) dataset and benchmarked SFLE_OPM, achieving an accuracy score of 89.31% and true positive rate score of 80.18%. The results demonstrate that our method yields a higher extraction accuracy and precision than most of the existing methods. Our dataset is available at https://github.com/OPMDataSets/OPMSFL.