Morphology Of Deposits Research Articles

Controlling silver deposition morphology on aluminum surfaces: Surfactant modify anisotropy of aluminum surface energy

Faced with the challenge of uncontrollable Ag layer deposition morphology during the preparation of silver-coated aluminum particles (Al/Ag). A simple and nontoxic method involving the introduction of surfactants (PEG, PVP, and gelatin (GEL)) to alter the anisotropy of Al surface energy was proposed to achieve control over Ag deposition morphology. Theoretical calculations indicate that PEG undergoes physisorption to Al, while PVP and GEL can alter the surface energy of specific crystal planes by selectively binding to different crystal facets. This action alters the growth habit of Ag on the Al surface and modulates the Ag deposition behavior, these conclusions align with experimental results. Compared with PEG and PVP, the incorporation of GEL was beneficial for the formation of a conformal Ag layer. This can be attributed to GEL preferentially passivating the highest crystal plane Al (110) surface, forming a buffer layer at the solid-liquid interface, leveling out the Ag deposition rate on various crystal planes, and also effectively inhibiting side reactions, in addition to enhancing the wettability of reaction solution. The Al/Ag particle exhibits excellent electrical conductivity (1.03 × 10−6 Ω·cm) and electromagnetic absorption (−32.5 dB, 1.62 GHz), it is suitable for use as a highly conductive electromagnetic shielding material.

Combination of MSC Marc and SE-FIT to simulate the direct laser deposition of the multi-layer Ti–6Al–4V

Modeling the impact of a laser heat source on Ti6Al4V deposition is crucial for optimizing additive manufacturing, particularly in multi-layer contexts. This modeling provides insights into the material’s behavior during the Ti6Al4V manufacturing process. In this study, simulations using MSC Marc were conducted to model the impact of a laser heat source on the deposition of the multi-layer Ti–6Al–4V (abbreviated as Ti6Al4V) using the Ti–6Al–4V metal powder, followed by SE-FIT simulation to characterize their deposition morphology. MSC Marc was utilized to simulate the impact of a laser heat source on the Ti6Al4V, with a focus on identifying the melting area. Thermal conductivity was represented in the form of a chart as a function of temperature. Next, the morphology after deposition was defined using SE-FIT based on volume and boundaries. In the MSC Marc numerical model, a combined heat transfer coefficient of radiation and convection was applied to the convective coefficient. In the section depicting the multi-layered deposition morphology, a laser with 750[Formula: see text]W power was utilized at a speed of 3.3[Formula: see text]mm/s. After simulation, the resulting layer height and appearance were compared with the literature for a 25-layer composite. The practical implications of this research extend to the broader field of laser-induced heat deposition on Ti6Al4V deposition, which has applications beyond titanium alloys. The findings may contribute to advancements in the design and manufacturing of various metal components, impacting industries such as automotive, electronics and energy.

Development of potentiostatically deposited cerium conversion coating for Mg alloys

AbstractIn this work, cerium conversion coating (CeCC) was deposited on AZ91D Mg alloy using potentiostatic polarization method combined with phosphate pore‐sealing treatment. Initially, the optimum deposition parameters to obtain a crack‐free surface were found. The characterization of coating revealed the presence of a nodular morphology of cerium oxide deposits. Next, the electrochemical behavior of the coated surface was assessed using potentiodynamic polarization and electrochemical impedance spectroscopy in 3.5 wt% NaCl solution. Based on electrochemical characterization, the coating exhibited a fivefold increase in the charge transfer resistance and a corresponding 76% reduction in corrosion rate, when compared to the bare surface. Furthermore, the conversion coating exhibited improved corrosion resistance when evaluated using the immersion test. Therefore, these findings demonstrate the feasibility of the potentiostatic method for creating nearly crack‐free CeCC on Mg alloys, unlike conventional conversion coatings. Moreover, this approach holds great potential for effectively mitigating the corrosion issues in Mg alloys.

Alloying strategy to stabilize monocrystalline zinc anode under high utilization and working capacity

Zn(002) has been proven as a dendrite-free anode for Zn batteries. However, stable Zn plating/stripping behavior at an areal capacity exceeding 5 mAh cm−2 has remained unfulfilled so far. In this study, we show that the planar deposit on pure Zn (002) substrate is loosely stacked with high corrosion tendency by the aqueous electrolyte, the key obstacle to achieving considerable efficiency under high-capacity working conditions. To mitigate the side reactions, we introduce an alloying approach by combining monocrystalline Zn(002) with eutectic Al and Cu. The alloying strategy enhances the electrostatic interaction between deposits and substrate, favoring a dense-packed deposition morphology with improved corrosion resistant ability. Solid solution property of Al and Cu in Zn matrix also ensures the structure stability during repeated plating/stripping cycles. As a result, significant extension in cycle life of Zn alloy (002)-based symmetric cells even under 50 mA cm−2 and 25 mAh cm−2 and performance with high utilization also achieves a leading level without extra methods on surface protection. The modified Zn alloy (002) anode induces high anode utilization, paving the way for Zn batteries to meet the requirements of practical applications.

A low-cost all-iron hybrid redox flow batteries enabled by deep eutectic solvents

Redox flow batteries (RFBs) emerge as highly promising candidates for grid-scale energy storage, demonstrating exceptional scalability and effectively decoupling energy and power attributes. Nevertheless, the high cost of vanadium metal hinders the continued commercialization of vanadium redox flow batteries (VRFBs), prompting the exploration of low-cost all-iron RFBs as a viable alternative. In this context, we propose an innovative deep eutectic-based all-iron hybrid RFBs. By synthesizing a deep eutectic solvent through the mixture of choline chloride, ethylene glycol, and an appropriate amount of deionized water, the deficiencies in mass transport performance of the deep eutectic electrolyte have been successfully addressed, while enhancing its conductivity. The deep eutectic solvents facilitate the restructuring of the solvent shell surrounding the negative electrolyte Fe2+, effectively suppressing its hydrolysis. Additionally, the synergistic interaction between the restructured solvation structure and the chelating ring structure formed between Fe2+ and glycine improves the deposition morphology of iron. Simultaneously, utilizing a eutectic-based positive electrolyte improves the solubility of active substances while maintaining excellent cycling stability and mass transport performance. The entire battery system exhibits an average coulombic efficiency exceeding 98 % in a 360-hour charge–discharge cycle at 10 mA/cm2. In the first 66 cycles, the coulombic efficiency remains at 100 %, and the energy efficiency approaches 54 %. This indicates that the battery system developed using deep eutectic solvents demonstrates promising applications within the same category of eutectic-based batteries.

Effects of slope topography on rock avalanche mobility and deposition: A 2-D discrete element method investigation

The impact of rock avalanches is a major concern in mountain areas. However, fundamental understanding and reliable prediction of the depositional area of rock avalanches remains inadequate. Here, an idealized numerical study of granular materials flowing down a slope is carried out using two-dimensional (2-D) discrete element method simulations. The effects of the slope geometry on the mobility and deposit morphology of the granular flow are studied in detail. It is found that the granular flow mobility increases with the curvature radius of the circular ramp, leading to a longer runout distance, which is explained from the viewpoint of energy transfer and dissipation. The results are expected to enhance understanding of the travel and deposition mechanisms of rock avalanches and other related geophysical flows.

Mineralogy and Morphology of Iraqi Sea Salt and Sabkhas

A few studies have investigated the morphology and mineralogy of the salt deposits in Iraq. These deposits have amassed in substantial amounts as a result of the rise in temperature, specifically during the summer season. This study aims to analyze and characterize the mineral composition, morphology, and salt crystallization of the sabkhas and sea salt. The physicochemical tests (X-ray Diffraction, X-ray fluorescence, Field Emission Scanning Electron Microscopy, and energy dispersive spectroscopy) were used in this study. Samples were collected from sabkha salts in Diyala, Al-Emara, and the sea salt in Al-Basra. These locations exhibit an important and unique distribution of precipitated salt. The study showed that a semi-arid to arid climate in small pools located in specific locations led to the generation of Sabkhas and sea salt through saltwater evaporation. After processing the samples, the half-and-quarter method was used to obtain a 20-gram sample from the investigated bulk substance. According to the XRD analysis, halite is the main evaporite mineral present in the samples, with calcite, anhydrate, gypsum, and bischofite following it in decreasing order of abundance. The predominant trace elements include sulfur (S), magnesium (Mg), calcium (Ca), aluminum (Al), silicon (Si), iron (Fe), and molybdenum (Mo). Sea salt from the Al-Fao in Al-Basra exhibits exceptional mineral concentration and forms cubic-shaped crystals due to excellent evaporation of seawater. The most common crystallization patterns found in sabkhas and sea salt consist of hopper shapes, cubic crystals, rhombic crystals, cryptocrystals, and tabular shapes. Each of these forms of crystallization occurs at ambient temperatures.

Synthesis and growth mechanism of silicon-based nanostructures from polysiloxane via CVD process

The work is concerned with the deposition of ceramic layers of various morphologies, containing silicon and nitrogen, from a polysiloxane precursor in the chemical vapor deposition (CVD) process. The experiments involved the saturation of nitrogen as a gaseous carrier with polysiloxane molecules in the CVD reaction. Saturated nitrogen was supplied to the reaction zone and depending on the synthesis temperature (1000–1800 °C) and the concentration of resin in gas phase, various nanocrystalline and amorphous deposits were obtained on graphite foil, including polygranulated SiOC powders, fibrous layers composed of nanofibers (NFs) containing silicon and nitrogen, nanochains and composite fibrous components. The morphology, structure and chemical composition of the deposits formed in the CVD reaction changed with increasing temperature. Above 1300 °C, oxygen in the silicon oxycarbide deposits was gradually replaced by nitrogen, creating SiN bonds. The dominant phase in the deposits obtained in the temperature range of 1700–1800 °C were two-phase silicon oxynitride NFs. The core of these NFs consisted of a polycrystalline structure surrounded by an amorphous shell. These structures grew preferentially in the [111] direction through heterogeneous nucleation in the vapor-solid process (VS). The changes in deposits morphology were influenced by the CVD temperature and the resin content in the gas carrier. The activation energy of the crystallization process of silicon oxynitride nanofibers was approximately 96 kJ/mol.

Unveiling the effect law of carbon dots with polyfunctional groups on interface structure and ion migration in polymer electrolytes for solid lithium battery

Solid polymer electrolyte (SPE) has been considered as promising candidate electrolyte for solid-state lithium metal battery. However, the low ion conductivity and poor interface stability seriously hinder the development of SPE. Introducing the functional filler is a commonly used and effective approach to solving these issues. The poor compatibility and ambiguous mechanism of action are currently the main challenges. In this study, we design and synthesize carbon dots (NSFCDs) with quaternary functional groups, which are introduced into the SPE in the polymerization process of hybrid polymer electrolyte (HPE). The detailed effect law of polyfunctional groups on the polymer chain structure, interface structure of electrolyte/electrode and ion migration is systematically revealed. The dense polymer network endows HPE with enhanced mechanical properties. Through the regulation of polymer segments, the coordination environment of lithium ions is altered, promoting ion transport. The solid electrolyte interface (SEI) induced by NSFCDs and lithium salt anions effectively improves the morphology of lithium ion deposition and alleviates volume strain. As a result, the HPE based on polyethylene oxide (PEO) constructed by free radical polymerization of NSFCDs and polyethylene glycol diacrylate (PEGDA) exhibits excellent comprehensive performance, the assembled Li symmetric battery can cycle stably for 4000 h.

Analysis of Pressure Characteristics of Ultra-High Specific Energy Lithium Metal Battery for Flying Electric Vehicles

The lithium metal battery is likely to become the main power source for the future development of flying electric vehicles for its ultra-high theoretical specific capacity. In an attempt to study macroscopic battery performance and microscopic lithium deposition under different pressure conditions, we first conduct a pressure cycling test proving that amplifying the initial preload can delay the battery failure stage, and the scanning electron microscope (SEM) shows that the pressure is effective in improving the electrode’s surface structure. Secondly, we analyze how differing pressure conditions affect the topography of lithium deposits by coupling the nonlinear phase-field model with the force model. The results show that the gradual increase in the external pressure is accompanied by a drop in the length of the dendrite and the migration curvature in the diaphragm, and the deposition morphology is gradually geared towards smooth and thick development, which can significantly reduce the specific surface area of lithium dendrite. However, as cyclic charging and discharging continue, the decrease in the electrolyte diffusion coefficient results in higher internal stress inside the battery, and thus the external pressure must be increased so as to achieve marked inhibitory effects on the growth of the lithium dendrite.

Clean and efficient preparation of metallic bismuth from methane-sulfonate electrolyte in the membrane electrolysis cell

As a prevailing hydrometallurgical extraction system for bismuth sulfide concentrate, the acidic chloride solution has superior applicability to raw materials and high recovery ratio of metallic bismuth. Nevertheless, it has disadvantages of being easily volatile and strongly corrosive, as well as large energy consumption and poor deposition morphology during chloride electrolysis. Methane-sulfonic acid (MSA) solution is widely considered as the next generation of green hydrometallurgical system, due to its excellent physicochemical properties such as high metal salts solubility, low volatility, and biodegradability. In this study, membrane electrolysis technique was adopted based on the acidic bismuth methane-sulfonate leaching solution, and the influence of electrolyte composition, cathode current density (CCD), and temperature parameters on the bismuth conversion ratio (BCR) and deposition rate (BDR), techno-economic indicators and cathodic bismuth morphology were studied. The results show that the CCD affects the deposits morphology significantly, and the bismuth metal is partially dark and composed of loose ellipsoidal particles at high current density. Under the optimal conditions (70 g/L Bi3+ ions, 5 g/L Fe2+ ions, 110 g/L MSA, 35 °C, 180 A/m2), high-purity metallic bismuth (Bi 99.97 %) with silver-white luster is obtained. The BCR and BDR are 9.43 % and 0.46 kg/(h·m2), respectively. The cathodic current efficiency (CCE) reaches over 98 %, and specific energy consumption (SEC) is less than 715 kWh/t Bi. Compared with the traditional chloride system, the MSA-based membrane electrolysis medium has advantages of environmental friendliness, low occupational risks, low carbon and energy consumption, and can thus provide a sustainable green solution for bismuth hydrometallurgy.

Engineering a High-Strength and Superior-Electrolyte-Wettability Silk Fibroin-Based Gel Interface Achieving Dendrite-Free Zn Anode.

Zn metal anode is confronted with notorious Zn dendrite growth caused by inhomogeneous Zn2+ deposition, rampant dendrite growth, and serious interface side reactions, which significantly hinder their large-scale implication. Interface modification engineering is a powerful strategy to improve the Zn metal anode by regulating Zn2+ deposition behavior, suppressing dendrite formation, and protecting the anode from electrolyte corrosion. Herein, we have designed a high-strength and superior-electrolyte-wettability composite gel protective layer based on silk fibroin (SF) and ionic liquids (ILs) on the Zn anode surface by a straightforward spin-coating strategy. The Zn ion transport kinetics and mechanical properties were further improved by following the incubation process to construct a more well-ordered β-sheet structure. Consequently, the incubated composite gel coating serves as a command station, guiding the Zn ion's preferential growth along the (002) plane, resulting in a smooth and uniform deposition morphology. Driven by these improvements, the zinc anode modified with this composite gel exhibits a remarkably long-term cycling lifespan up to 2200 h at 2 mA cm-2, while also displaying superior rate capability. This study represents a landmark achievement in the realm of electrochemical science, delineating a clear pathway toward the realization of a highly reversible and enduring Zn anode.

Relating Chemo-Mechanical Hysteresis and Formation Protocols for Anode-Free Lithium Metal Batteries

Cell formation is an energy and time-intensive empirically-guided process crucial to manufacturing secondary lithium-ion batteries. As the rechargeable battery industry moves towards manufacturing lithium metal batteries—where a metallic lithium negative electrode is used instead of a porous graphite composite—the cell formation process may need reconsidering. The effects of formation rate and cycling protocol on lithium metal battery performance are poorly understood. In this work, we used operando acoustic transmission to measure physical changes during the formation cycles and the effect of formation cycling protocols on the long-term cycling of anode-free lithium metal pouch cells—where all the lithium inventory comes from the positive electrode and is deposited as metallic lithium on copper foil during initial charge. We show that a faster C/3 formation protocol results in comparable cycling performance and cell stiffness change to a slower C/10 formation step. Variations in acoustic metrics across different electrolytes tested are attributed to differences in gas formation, cell swelling, and lithium deposition morphology. NMC811 cathodes paired with a high-concentration ether electrolyte are shown to be particularly prone to gas formation, which is mitigated by using a localized high-concentration ether electrolyte and single-crystal NMC532. The results highlight differences in formation behavior between anode-free lithium metal cells and lithium-ion cells. These are important to consider when bringing new manufacturing plants online for lithium metal batteries.

A Versatile Deposition Model for Natural and Processed Surfaces

This paper introduces a robust deposition model designed for exploring the growth dynamics of deposits on surfaces under practical conditions. The study addresses the challenge of characterizing the intricate morphology of deposits, exhibiting significant visual variations. A generative approach is deployed to create diverse natural and engineered surface textures, governed by probabilistic principles. The model’s formulation addresses key questions related to deposition initiation, nucleation point behaviour, spatial scaling, deposit growth rates, spread dynamics, and surface mobility. A versatile algorithm, relying on six parameters and employing nested loops and Gaussian sampling, is developed. The algorithm’s efficacy is examined through extensive simulations, involving variations in nucleation scaling densities, aggregate scaling scenarios, spread factors, and diffusion rates. Surface statistics are computed for simulated deposits and analyzed using Fast Fourier Transform (FFT). The resulting database enables quantitative comparisons of surfaces generated with different parameters, where the database-derived parallel coordinates offer guidance for selecting optimal model parameters to achieve desired surface morphologies. The proposed approach is validated against urea-derived deposits, exhibiting statistical consistency and agreement with experimental observations. Overall, the model’s adaptable framework holds promise for understanding and predicting deposit growth on surfaces in diverse practical scenarios.

Deposition of high-quality, nanoscale SiO2 films and 3D structures

Silicon dioxide (SiO2) is ubiquitous in biomedical diagnostics and other applications as a capture medium for nucleic acids and proteins. Diagnostic devices have seen rapid miniaturisation in recent years, due to the increased demand for portable point-of-care diagnostics. However, there are increasing challenges with incorporating SiO2 nanostructures into diagnostic devices, due to the complexity of nanostructured SiO2 synthesis, often involving etching and chemical vapour deposition under high vacuum conditions.We report a novel and straightforward method for deposition of high-quality, nanoscale SiO2 films and 3D SiO2 structures using thermal decomposition of polydimethylsiloxane (PDMS), in a furnace at atmospheric pressure at 500 °C. This method allows individual nanometre controllability of conformal pinhole-free layers on a variety of materials and morphologies. The temperature ramp rate is a key factor in determining the SiO2 deposit morphology, with slower ramp rates leading to highly conformal 2D films and faster ones yielding 3D nanodentrite structures. For the 2D films, the film thickness, as determined by spectroscopic ellipsometry and confirmed by SEM data, is shown to correlate excellently with initial PDMS source material mass in the thickness range 0.8–18 nm. Fits to ellipsometry models confirm that the refractive index of the deposited film matches the expected value for SiO2, while electrical breakdown measurements confirm that the breakdown strength of the films is comparable to that of high-quality thermal oxides. Depositions on high aspect ratio ZnO nanostructures are shown to be highly conformal, leading to core-shell ZnO-SiO2 nanostructures whose shell thickness is in excellent agreement with the expected values from deposition on planar substrates. At faster ramp rates an abrupt morphological transition is seen to a deposit which displays a 3D nanodentrite morphology. The possibilities for applications of both morphologies (and core-shell combinations with other nanostructured materials) in biosensing and related areas are briefly discussed, and the DNA capture capabilities of each nanostructure are measured. The high aspect ratio nanodendrite structures allow for significant DNA capture within microfluidic devices in the presence of low DNA concentrations, with a maximum average capture efficiency of 43.4 % achieved in the presence of 10 ng/mL of DNA, which is an improvement by a factor of ∼ 3 over planar Si surfaces. Improvements by factors of >10 over planar surfaces were achieved at higher DNA concentrations of 100 and 1000 ng/mL.

Effects of deposited microstructure on wear behaviors of detonation sprayed Fe-based amorphous coatings

Fe-based amorphous coatings (AMCs) were deposited using the detonation spray at varying spraying distances. The study aimed to characterize the deposition morphologies and elemental composition of splats for single shots under different spraying distances. Additionally, the relationship between spraying distance, particle deposition behavior, spreading morphology, and wear behavior of the coatings was comprehensively discussed. The results indicate that modifying the spraying distance affects the melting state of spray particles, thereby influencing the morphology of deposition and determining the coating's microstructure. Larger spraying distances result in reduced deposition efficiency and lead to particles depositing in a manner similar to cold spraying, resulting in an uneven coating structure with higher porosity. Consequently, the coating becomes more susceptible to fatiguedelamination wear. Conversely, a moderate spraying distance leads to full melting and acceleration of powders, results in good spreading and the formation of a uniform and dense laminar structure.

On the Electrodeposition of Zinc in Low Magnetic Fields

Abstract While aqueous zinc-based batteries have garnered much research on account of their improved safety, lower cost, and easier fabrication over lithium-ion batteries, they remain held back by dendrite growth on the anode. While many different solutions have been proposed, these solutions often greatly complicate the synthesis or materials in the battery. The application of a magnetic field across the battery has been shown to inhibit dendrite formation without the need for any materials or interface engineering. Herein, we provide a study on the effects of low magnetic fields on the electrodeposition and cycling of zinc in various aqueous systems. We demonstrate that although stronger fields have more immediate impacts on the morphology of zinc deposits, low magnetic fields are still suitable for inhibiting dendrite growth over long periods of cycling. Magnetic field strengths as low as 29 mT were shown to decrease charge transfer resistance of zinc ion deposition by up to 54% and to stabilize the cycling of Zn/Zn symmetric cells. Furthermore, the versatility of magnetic field application was demonstrated by affecting the morphology of zinc deposits on both copper and single-walled carbon nanotubes, which are both compatible with anode-free configurations of aqueous zinc-ion batteries.

Polyphyllin B inhibited STAT3/NCOA4 pathway and restored gut microbiota to ameliorate lung tissue injury in cigarette smoke-induced mice

ObjectiveSmoking was a major risk factor for chronic obstructive pulmonary disease (COPD). This study plan to explore the mechanism of Polyphyllin B in lung injury induced by cigarette smoke (CSE) in COPD.MethodsNetwork pharmacology and molecular docking were applied to analyze the potential binding targets for Polyphyllin B and COPD. Commercial unfiltered CSE and LPS were used to construct BEAS-2B cell injury in vitro and COPD mouse models in vivo, respectively, which were treated with Polyphyllin B or fecal microbiota transplantation (FMT). CCK8, LDH and calcein-AM were used to detect the cell proliferation, LDH level and labile iron pool. Lung histopathology, Fe3+ deposition and mitochondrial morphology were observed by hematoxylin–eosin, Prussian blue staining and transmission electron microscope, respectively. ELISA was used to measure inflammation and oxidative stress levels in cells and lung tissues. Immunohistochemistry and immunofluorescence were applied to analyze the 4-HNE, LC3 and Ferritin expression. RT-qPCR was used to detect the expression of FcRn, pIgR, STAT3 and NCOA4. Western blot was used to detect the expression of Ferritin, p-STAT3/STAT3, NCOA4, GPX4, TLR2, TLR4 and P65 proteins. 16S rRNA gene sequencing was applied to detect the gut microbiota.ResultsPolyphyllin B had a good binding affinity with STAT3 protein, which as a target gene in COPD. Polyphyllin B inhibited CS-induced oxidative stress, inflammation, mitochondrial damage, and ferritinophagy in COPD mice. 16S rRNA sequencing and FMT confirmed that Akkermansia and Escherichia_Shigella might be the potential microbiota for Polyphyllin B and FMT to improve CSE and LPS-induced COPD, which were exhausted by the antibiotics in C + L and C + L + P mice. CSE and LPS induced the decrease of cell viability and the ferritin and LC3 expression, and the increase of NCOA4 and p-STAT3 expression in BEAS-2B cells, which were inhibited by Polyphyllin B. Polyphyllin B promoted ferritin and LC3II/I expression, and inhibited p-STAT3 and NCOA4 expression in CSE + LPS-induced BEAS-2B cells.ConclusionPolyphyllin B improved gut microbiota disorder and inhibited STAT3/NCOA4 pathway to ameliorate lung tissue injury in CSE and LPS-induced mice.

Increasing the Cycle Life of Zinc Metal Anodes and Nickel-Zinc Cells Using Flow-Through Alkaline Electrolytes

Alkaline electrolyte flow through porous Zn anodes and Ni(OH)2 cathodes can overcome diffusion limits, reduce dendrite growth, and improve cycle life. Zinc deposition morphology improves with low flow rates electrolyte in KOH/ZnO electrolytes at current densities near the diffusion-limit regime. Zinc dendrites present without flow are suppressed by micrometer-per-second flow at concentrations ranging from 0.2 to 0.6 M ZnO dissolved in 6 M and 10 M KOH solutions. Zn-Cu asymmetric cell tests reveal that flowing electrolyte increases the lifespan by more than 6 times in the diffusion-limit regime by suppressing gas evolution and dendrite formation. Ni-Zn cell tests show that a flow-assisted battery cycles 1500 times with over 95% Coulombic efficiency (CE) at 35 mA cm−2 current density and 7 mAh/cm2 charge capacity, increasing the battery lifespan by 17 times compared with a stagnant Ni-Zn cell. Flow-through electrolyte also stabilizes the Zn electrode in the over-limiting regime, achieving approximately 4 times increased lifespan and 297 cycles with over 90% CE at 52 mA cm−2.

Exploring debris flow deposit morphology in river valleys: Insights from physical modeling experiments

A comprehensive understanding of the deposit morphodynamics of debris flows in river valleys is crucial for disaster prevention and mitigation in mountainous areas. However, debris flows in river valleys are complex and variable, and the influence of the composition and terrain on deposit mechanisms and morphology remains unclear. In this study, a series of laboratory experiments were conducted to investigate the impact of the water content, slope, and grain size distribution on the deposit morphology of debris flows in river valleys. In the experiments, debris flows form narrow and elongated shuttle-shaped deposits upon entering river valleys. Increased water content and slope enhance the mobility of debris flows, resulting in wider deposit widths, gentler deposit slopes, and larger deposit areas. An increase in the gravel fraction partially facilitates the movement and deposition of debris flows. However, a large number of coarse particles may increase internal friction within the debris flow, hindering the spread of deposits and resulting in a relatively concentrated deposit with a steeper morphology. Furthermore, the debris flow regime shifts from friction to collision as the water content, slope, and gravel fraction increase. Debris flows dominated by collision forces exhibit higher mobility and a wider impact area, potentially leading to more severe disaster consequences. Compared with unconfined debris flows, the deposit area of debris flows in the river valley is smaller, and the deposit width to height ratio is larger. There is a power function relationship between deposition area and Savage number in river valleys. Additionally, particle sorting and flow regime transformation during the movement and deposition of debris flows can significantly impact the morphology and internal structure of the deposits in river valleys and then affect the development of debris flow dam breaching. In summary, this study utilized experiments to simulate natural debris flows, offering fresh insights into the depositional behavior of debris flows in river valleys.