Slow Deposition Research Articles

Enhancing Li Deposition Behavior through Valence Gradient-Assisted Iron Layer.

Uncontrolled lithium (Li) dendrite formation presents major safety risks and challenges in the Li host design. A novel approach is introduced, using a valence gradient in iron nanoparticles (Fe0, Fe2+, Fe3+) to stabilize the anodes. An Fe0 component, with fast Li diffusion, ensures a steady supply of Li to Fe2+ and Fe3+ components, which have slower Li diffusion. This coordinated interplay between fast and slow diffusion uniformizes Li deposition near the substrate, effectively reducing the rate of dendrite growth. The as-prepared framework demonstrates uniform Li plating with a minimal hysteresis voltage after extensive cycling for 1200 h in symmetric cells. Integrated into a full cell with LiFePO4, it demonstrates outstanding cycling stability for almost 950 cycles with a capacity of 92.2 mA h g-1 at 1C with an ultralow N/P ratio of 1.19. This valence gradient design strategy broadens the design potential for transition-metal compounds in regulating Li deposition by mitigating interfacial Li+ behavior.

Cyclohexanol Proportion Influence on Catalyst Paste Rheological Properties and Screen-Printed Hydrogen PEMFC Electrochemical Performance

Nowadays environmental deterioration and global warming are among the principal concerns for humankind. One of the upstanding technologies to settle them is proton exchange membrane fuel cells (PEMFCs), where through an electrochemical reaction, oxygen and fuel (as hydrogen) are transformed into electric energy, water and heat, usually using carbon supported platinum (Pt/C) as catalyst and Nafion as proton conductive ionomer. PEMFC production at the laboratory scale is mainly done by spray method, having some counterbacks such as catalyst wasting and slow deposition rate. Recently, the screen print method has caught attention worldwide for industrial-scale production of PEMFC since it was successfully employed in a variety of applications, such as solar cells, microelectronics, etc. This method consists of preparing a catalyst paste dispersing the catalyst with ionomer and solvents, once homogenized the paste is passed through a mesh and then deposited on a substrate in a single quick step avoiding material waste. For an effective screen print process, a stable and workable catalyst paste is needed, being rheological properties and drying time the most important features to fit those needs. Despite water and low molecular weight alcohols being the typical solvents used for catalyst paste fabrication and the rheological properties of resulting pastes using these solvents are already reported [1], they do not fit the requirements for screen print industrial production. On the other hand, cyclohexanol has a high viscosity and long drying time, being a promising alternative to obtain a paste suitable for the industry's needs, however, the rheological properties of a catalyst paste containing cyclohexanol remain unclear. In addition, it has been reported that this solvent has positive effects on the catalyst and ionomer interactions, enhancing the catalyst activity and improving mass transport [2]. In this research, several screen print catalyst pastes having the same final volume and different solvent proportions of water, 1 propanol, and cyclohexanol (W:1PA:CHN) were prepared. The same proportion of water and 1 propanol was kept but the proportion of cyclohexanol was gradually increased for each sample: (1:1:0), (1:1:0.5), (1:1:1), (1:1:2) and (1:1:3). Additionally, a sample containing only cyclohexanol was prepared (0,0,1) to discern the isolated effect of this solvent. From the resulting pastes, PEMFC were produced by the screen print method. The relation between cyclohexanol content and catalyst paste rheological properties was investigated using a cone/plate rheometer, while the screen printed PEMFC electrochemical characteristics by the polarization curve, cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS), especially for evaluating proton conductivity.

Record-Low thermal boundary resistance at bonded GaN/diamond interface by controlling ultrathin heterogeneous amorphous layer

Thermal boundary resistance (TBR) in semiconductor-on-diamond structure bottlenecks efficient heat dissipation in electronic devices. In this study, to reduce the TBR between GaN and diamond, surface-activated bonding with a hybrid SiOx-Ar ion source was initially applied to achieve an ultrathin interfacial layer. The simultaneous surface activation and slow deposition of the SiOx binder layer enabled precise control over layer thickness (2.5–5.3 nm) and formation of an amorphous heterogeneous nanostructure comprising a SiOx region between two inter-diffusion regions. Crucially, the 2.5-nm-thick interfacial layer achieved a TBR of 8.3 m2⋅K/GW, a record low for direct-bonded GaN/diamond interface. A remarkable feature is that the TBR is extremely sensitive to the interfacial thickness; Varying from 8.3 m2⋅K/GW to 34 m2⋅K/GW with thickness difference of only 2.8 nm. Theoretical analysis revealed the origin of this phenomena: a diamond/SiOx inter-diffusion layer extend the vibrational frequency, far exceeding that of crystalline diamond, which increases the lattice vibrational mismatch and suppresses phonon transmission.

Soft carbon filled in expanded graphite layer pores for superior fast-charging lithium-ion batteries

The slow kinetics and lithium deposition of graphite anode are considered the key limitations of fast-charging lithium-ion batteries. Expanded graphite has shown tremendous potential for the improvement of rate performance due to its massive active sites released and lifted lithium storage platform. However, the risk of structural collapse caused by fast charging will reduce the cycling life of the expanded graphite anode. Herein, this study designed a stable structure of expanded graphite by filling its layer pores with pitch-derived soft carbon (EGC). The honeycomb-like EGC is a great fast-charging candidate material with rich active sites, enlarged ion transport channels, and efficient ion transport interfaces. As the experimental and simulation results, the EGC electrode demonstrated significantly fast lithium-ions storage kinetics and durable long cycle life, compared to commercial fast-charging graphite anode. Notably, the EGC//LiNi0.8Co0.1Mn0.1O2 full cell delivered a superior fast-charging and stability performance (near 20 min charging for 80 % State of Charge). The simple multifunctional modification strategy for graphite anode in this work provides a new approach for superior fast-charging lithium-ion batteries.

Powder bed fusion factory productivity increases using discrete event simulation and genetic algorithm

Powder bed fusion is importance is growing with uses across industries in both polymer and metallic components, particularly in mass individualization. However, due to the relatively slow mass deposition speed compared to conventional methods, scheduling and production planning play a crucial role in scaling up additive manufacturing productivity to higher volumes. This paper introduces a framework combining discrete event simulation and a genetic algorithm showing makespan improvement opportunities for multiple powder bed fusion factories varying workers, jobs and available equipment. The results show that bottlenecks move among workstations based on worker and capital equipment availability, which depend on the size of the facility indicating a resource-driven constraint for makespan. A makespan reduction of 78% is achieved in the simulation. This shows the trade-off of worker and capital equipment to achieve makespan improvements. The addition of personnel or equipment increases production with further gains achieved by scheduling optimization. Two levels of job demands are analyzed showing productivity gains of 45% makespan improvement when adding the first worker and additional savings with scheduling optimization using a genetic algorithm up to 11%. Most research on additive manufacturing production has focused on the quality of produced parts and printing technology rather than factory level management. This is the first application of this methodology to varying sizes of these potential factories. The method developed here will help decision-makers to determine the appropriate number of resources to meet their customer demand on time, additionally, finding the optimal route for jobs before starting the production process.

Investigation of Sub-Bandgap Emission and Unexpected n-Type Behavior in Undoped Polycrystalline CdSexTe1-x.

Se alloying has enabled significantly higher carrier lifetimes and photocurrents in CdTe solar cells, but these benefits can be highly dependent on CdSexTe1-x processing. This work evaluates the optoelectronic, chemical, and electronic properties of thick (3µm) undoped CdSexTe1-x of uniform composition and varied processing conditions (CdSexTe1-x evaporation rate, CdCl2 anneal, Se content) chosen to reflect various standard device processing conditions. Sub-bandgap defect emission is observed, which increased as Se content increased and with "GrV-optimized CdCl2" (i.e., CdCl2 anneal conditions used for group-V-doped devices). Low carrier lifetime is found for GrV-optimized CdCl2, slow CdSexTe1-x deposition, and low-Se films. Interestingly, all films (including CdTe control) exhibited n-type behavior, where electron density increased with Se up to an estimated ≈1017cm-3. This behavior appears to originate during the CdCl2 anneal, possibly from Se diffusion leading to anion vacancy (e.g., VSe, VTe) and ClTe generation.

Two stages of subsidence and its formation mechanisms in Mid-Late Triassic Ordos Basin, NW China

Based on a large number of newly added deep well data in recent years, the subsidence of the Ordos Basin in the Mid-Late Triassic is systematically studied, and it is proposed that the Ordos Basin experienced two important subsidence events during this depositional period. Through contrastive analysis of the two stages of tectonic subsidence, including stratigraphic characteristics, lithology combination, location of catchment area and sedimentary evolution, it is proposed that both of them are responses to the Indosinian Qinling tectonic activity on the edge of the craton basin. The early subsidence occurred in the Chang 10 Member was featured by high amplitude, large debris supply and fast deposition rate, with coarse debris filling and rapid subsidence accompanied by rapid accumulation, resulting in strata thickness increasing from northeast to southwest in wedge-shape. The subsidence center was located in Huanxian–Zhenyuan–Qingyang–Zhengning areas of southwestern basin with the strata thickness of 800–1 300 m. The subsidence center deviating from the depocenter developed multiple catchment areas, until then, unified lake basin has not been formed yet. Under the combined action of subsidence and Carnian heavy rainfall event during the deposition period of Chang 7 Member, a large deep-water depression was formed with slow deposition rate, and the subsidence center coincided with the depocenter basically in the Mahuangshan–Huachi–Huangling areas. The deep-water sediments were 120–320 m thick in the subsidence center, characterized by fine grain. There are differences in the mechanism between the two stages of subsidence. The early one was the response to the northward subduction of the MianLüe Ocean and intense depression under compression in Qinling during Mid-Triassic. The later subsidence is controlled by the weak extensional tectonic environment of the post-collision stage during Late Triassic.

Mathematical modelling of impurity deposition during evaporation of dirty liquid in a porous material

When a contaminated liquid evaporates from within a porous material, the impurities or dirt accumulate and deposit within the pore space. This occurs during the cleaning of filters and fouling of textiles, and is related to the ‘coffee-ring’ problem. To investigate how and where dirt is deposited in the pore space, we present a model for the motion of an evaporation front through a porous material, and the related accumulation, transport, and deposition of dirt, assuming that the liquid remains stationary. For physically relevant parameters, vapour transport out of the porous material is quasi-steady and we derive a single ordinary differential equation describing the motion of the evaporation front in time. Model solutions exhibit spatially non-uniform profiles of the deposited dirt-layer thickness through the porous material. The dirt accumulation and evaporation problems are coupled: deposited dirt hinders vapour transport through the porous material, slowing the evaporation. We identify two scenarios in which the porous material becomes clogged with dirt. Accumulation of suspended dirt at the evaporating interface along with slow dirt diffusion results in the deposited dirt layers clogging the pores at the evaporating interface, halting the drying and trapping liquid in the porous material. Alternatively, slow dirt deposition results in the suspended dirt being pushed far into the porous material by the evaporation, eventually leaving only dirt (with no liquid) in the pore space. We investigate the dynamics of both clogging scenarios, characterising the parameter regimes for which each occurs. Both clogging scenarios must be avoided in practice since they may be detrimental to future filter efficacy or textile breathability.

Chronology by luminescence and radiocarbon on core sediments from the northeastern pearl river plain and implications for delta process

Accurate dating is the basis for deciphering eustatic and climatic changes on deltaic sedimentary processes. In the Pearl River Delta (PRD) plain of south China, scarce robust chronology hinders the detailed interpretation of sedimentary history. In this study, quartz optically stimulated luminescence (OSL) (21 samples), feldspar post-IR IRSL (pIRIR) (4 samples) and radiocarbon (14C) (2 samples) dating were applied to obtain detailed chronological framework of core SXG06 (23-m long to bedrock) from the northeastern PRD. SXG06 consists an upper marine unit (M1) and a lower marine unit (M2), separated by a terrestrial unit (mottled clay, T1). For M1, quartz OSL and 14C samples yielded ages from 5.2 ± 0.3 to 0.32 ± 0.02 ka. The sample on top of T1 produced a quartz OSL age of 35 ± 2 ka. For other 12 samples in T1 and M2, quartz OSL signals reached saturation and generated minimum ages (>51 ka). For these the saturated quartz OSL samples, feldspar pIR50IR250 provides an age range of 123 ± 7–105 ± 7 ka. The compilation of all the above ages and previous sedimentology data reveals that: (1) M2 was formed during marine transgression of Marine Isotope Stage (MIS) 5; (2) A hiatus with an age gap of between ∼35 ka and ∼5 ka was observed, which might be due to the low sea level and resultant weathering scouring; (3) Initial M1 deposits from the northeastern PRD postdated the central and southern PRD by ∼3 ka, indicating delayed delta development in the northeastern PRD during the Holocene. (4) SXG06 experienced slow deposition 0.3 m/ka in ∼5–3 ka because of the coevally decreased sediment supply, followed by accelerated deposition rate of 3 m/ka after ∼3 ka associated with strengthen human activity.

Dust storms from the Taklamakan Desert significantly darken snow surface on surrounding mountains

Abstract. The Taklamakan Desert (TD) is a major source of mineral dust emissions into the atmosphere. These dust particles have the ability to darken the surface of snow on the surrounding high mountains after deposition, significantly impacting the regional radiation balance. However, previous field measurements have been unable to capture the effects of severe dust storms accurately, and their representation on regional scales has been inadequate. In this study, we propose a modified remote-sensing approach that combines data from the Moderate Resolution Imaging Spectroradiometer (MODIS) satellite and simulations from the Snow, Ice, and Aerosol Radiative (SNICAR) model. This approach allows us to detect and analyze the substantial snow darkening resulting from dust storm deposition. We focus on three typical dust events originating from the Taklamakan Desert and observe significant snow darkening over an area of ∼ 2160, ∼ 610, and ∼ 640 km2 in the Tien Shan, Kunlun, and Qilian mountains, respectively. Our findings reveal that the impact of dust storms extends beyond the local high mountains, reaching mountains located approximately 1000 km away from the source. Furthermore, we observe that dust storms not only darken the snowpack during the spring but also in the summer and autumn seasons, leading to increased absorption of solar radiation. Specifically, the snow albedo reduction (radiative forcing) triggered by severe dust deposition is up to 0.028–0.079 (11–31.5 W m−2), 0.088–0.136 (31–49 W m−2), and 0.092–0.153 (22–38 W m−2) across the Tien Shan, Kunlun, and Qilian mountains, respectively. This further contributes to the aging of the snow, as evidenced by the growth of snow grain size. Comparatively, the impact of persistent but relatively slow dust deposition over several months during non-event periods is significantly lower than that of individual dust events. This highlights the necessity of giving more attention to the influence of extreme events on the regional radiation balance. This study provides a deeper understanding of how a single dust event can affect the extensive snowpack and demonstrates the potential of employing satellite remote sensing to monitor large-scale snow darkening.

Dual-Function Electrolyte Additive Design for Long Life Alkaline Zinc Flow Batteries.

Alkaline zinc-based flow batteries (AZFBs) have emerged as a promising electrochemical energy storage technology owing to Zn abundance, high safety, and low cost. However, zinc dendrite growth and the formation of dead zinc greatly impede the development of AZFBs. Herein, a dual-function electrolyte additive strategy is proposed to regulate zinc nucleation and mitigate the hydroxide corrosion of zinc depositions for stable AZFBs. This strategy, as exemplified by urea, introduces an electrolyte additive to coordinate with Zn2+/Zn with proper strength, slowing zinc deposition kinetics to induce uniform nucleation and protecting the deposited zinc surface from attack by hydroxide ions through preferable adsorption. The zincate complexes with urea are identified to be Zn(OH)2(urea)(H2O)2 and Zn2(OH)4(H2O)4(urea), which exhibit slow zinc deposition kinetics, allowing instantaneous nucleation. Calculation results reveal an additional energy barrier of 1.29eV for the subsequent adsorption of an OH- group when a urea molecule absorbs on the zinc cluster, significantly mitigating the formation of dead zinc. Consequently, prolonged cell cycling of the prototype alkaline zinc-iron flow battery demonstrates stable operation for over 130 h and an average coulombic efficiency of 98.5%. It is anticipated that this electrolyte additive strategy will pave the way for developing highly stable AZFBs.

Short-Time Infrequent Metadynamics for Improved Kinetics Inference.

Infrequent Metadynamics is a popular method to obtain the rates of long time-scale processes from accelerated simulations. The inference procedure is based on rescaling the first-passage times of the Metadynamics trajectories using a bias-dependent acceleration factor. While useful in many cases, it is limited to Poisson kinetics, and a reliable estimation of the unbiased rate requires slow bias deposition and prior knowledge of efficient collective variables. Here, we propose an improved inference scheme, which is based on two key observations: (1) the time-independent rate of Poisson processes can be estimated using short trajectories only. (2) Short trajectories experience minimal bias, and their rescaled first-passage times follow the unbiased distribution even for relatively high deposition rates and suboptimal collective variables. Therefore, by basing the inference procedure on short time scales, we obtain an improved trade-off between speedup and accuracy at no additional computational cost, especially when employing suboptimal collective variables. We demonstrate the improved inference scheme for a model system and two molecular systems.

Superhydrophilic conformal polydopamine coating on nanostructured surface formed by capillary-induced solution infusion

As a material-independent adhesive coating agent with excellent functionality on interfaces of materials, polydopamine (PDA) has been widely applicable in bioengineering, environment, and energy fields. Conventional coating methods using dopamine (DA) solutions suffer from slow deposition rates, hindering the attainment of adequate thickness and durability. This work introduces a technique involving rapid capillary-induced solution infusion and in-air polymerization to overcome these limitations. By immersing nanostructured surfaces for just 10 s into the solution, the DA solution is uniformly infused onto the surface, and distributed evenly over the nanostructured surfaces. Polymerization is facilitated by oxygen diffusion from the air, resulting in the formation of a conformal coating up to a micrometer thick. These PDA coatings exhibit persistent superhydrophilicity with water contact angle below 10° and maintain resistance to abrasion, sonication, and oil fouling. Additionally, when applied to microfiber textiles, the PDA coating leads to excellent underwater oil repellency. Our method holds promise for compatibility with various wet-based coating techniques such as drop casting, spraying, spin coating, or ink-jet printing, opening avenues for versatile applications in diverse fields.

In Development: 3D printed large Format composite tooling using a Robot-Mounted pellet extruder

Large Format Additive Manufacturing (LFAM) addresses the limitations of traditional 3D printing, including slow deposition rates, limited scalability, lengthy prints, and high tooling costs for large structures. Current LFAM relies on quasi-planar, 2.5D printing strategies. This fails to reap the advantages of multi-axis printing, such as reduced support material use and the ability to create complex curved surfaces. A pellet-fed, multi-axis, large-format 3D printer was developed, featuring a KUKA robot and linear rail to enable multi-axis capabilities. LFAM’s potential is demonstrated by designing and simulating the printing process for a mold of a composite wing with a winglet.

Dispersion and Dosimetric Challenges of Hydrophobic Carbon-Based Nanoparticles in In Vitro Cellular Studies.

Methodologies across the dispersion preparation, characterization, and cellular dosimetry of hydrophilic nanoparticles (NPs) have been developed and used extensively in the field of nanotoxicology. However, hydrophobic NPs pose a challenge for dispersion in aqueous culture media using conventional methods that include sonication followed by mixing in the culture medium of interest and cellular dosimetry. In this study, a robust methodology for the preparation of stable dispersions of hydrophobic NPs for cellular studies is developed by introducing continuous energy over time via stirring in the culture medium followed by dispersion characterization and cellular dosimetry. The stirring energy and the presence of proteins in the culture medium result in the formation of a protein corona around the NPs, stabilizing their dispersion, which can be used for in vitro cellular studies. The identification of the optimal stirring time is crucial for achieving dispersion and stability. This is assessed through a comprehensive stability testing protocol employing dynamic light scattering to evaluate the particle size distribution stability and polydispersity. Additionally, the effective density of the NPs is obtained for the stable NP dispersions using the volumetric centrifugation method, while cellular dosimetry calculations are done using available cellular computational modeling, mirroring approaches used for hydrophilic NPs. The robustness of the proposed dispersion approach is showcased using a highly hydrophobic NP model (black carbon NPs) and two culture media, RPMI medium and SABM, that are widely used in cellular studies. The proposed approach for the dispersion of hydrophobic NPs results in stable dispersions in both culture media used here. The NP effective density of 1.03-1.07 g/cm3 measured here for black carbon NPs is close to the culture media density, resulting in slow deposition on the cells over time. So, the present methodology for dispersion and dosimetry of hydrophobic NPs is essential for the design of dose-response studies and overcoming the challenges imposed by slow particle deposition.

High-density stable glasses formed on soft substrates.

Enabled by surface-mediated equilibration, physical vapour deposition can create high-density stable glasses comparable with liquid-quenched glasses aged for millions of years. Deposition is often performed at various rates and temperatures on rigid substrates to control the glass properties. Here we demonstrate that on soft, rubbery substrates, surface-mediated equilibration is enhanced up to 170 nm away from the interface, forming stable glasses with densities up to 2.5% higher than liquid-quenched glasses within 2.5 h of deposition. Gaining similar properties on rigid substrates would require 10 million times slower deposition, taking ~3,000 years. Controlling the modulus of the rubbery substrate provides control over the glass structure and density at constant deposition conditions. These results underscore the significance of substrate elasticity in manipulating the properties of the mobile surface layer and thus the glass structure and properties, allowing access to deeper states of the energy landscape without prohibitively slow deposition rates.

Macromolecular Crowding Enhances Matrix Protein Deposition in Tissue-Engineered Vascular Grafts.

Successful in vitro culture of small-diameter tissue-engineered vascular grafts (TEVGs) requires rapid deposition of biomacromolecules secreted by vascular smooth muscle cells in a polyglycolic acid mesh scaffold's three-dimensional (3D) porous environment. However, common media have lower crowding conditions than in vivo tissue fluids. In addition, during the early stages of construction, most of the biomolecules secreted by the cells into the medium are lost, which negatively affects the TEVG culture process. In this study, we propose the use of macromolecular crowding (MMC) to enhance medium crowding to improve the deposition and self-assembly efficiency of major biomolecules in the early stages of TEVG culture. The addition of carrageenan significantly increased the degree of MMC in the culture medium without affecting cell viability, proliferation, and metabolic activity. Protein analysis demonstrated that the deposition of collagen types I and III and fibronectin increased significantly in the cell layers of two-dimensional and 3D smooth muscle cell cultures after the addition of a MMC agent. Collagen type I in the culture medium decreased significantly compared with that in the medium without a MMC agent. Scanning electron microscopy demonstrated that MMC agents considerably enhanced the formation of matrix protein structures during the early stages of 3D culture. Hence, MMC modifies the crowding degree of the culture medium, resulting in the rapid formation of numerous matrix proteins and fiber structures. Impact Statement Small-diameter tissue-engineered vascular grafts (TEVGs) are one of the most promising means of treating cardiovascular diseases; however, the in vitro construction of TEVGs has some limitations, such as slow deposition of extracellular matrix (ECM), long culture period, and poor mechanical properties. We hypothesized that macromolecular crowding can increase the crowding of the culture medium to construct a more bionic microenvironment, which enhances ECM deposition in the medium to the cell layer and reduces collagen loss, accelerating and enhancing TEVG culture and construction in vitro.

Tunable growth of a single high-density ZIF nanoshell on a gold nanoparticle isolated in an optical trap.

Here, we demonstrate an all-optical method using an optical tweezer to controllably grow high quality zeolitic imidazolate framework (ZIF) nanoshells on the surface of gold nanoparticles (AuNPs) and monitor the growth via darkfield spectroscopy. Our single particle approach allows us to localize an individual NP within a microscope slide chamber containing ZIF precursors at the focus of an optical microscope and initiate growth through localized heating without affecting the bulk system. Darkfield spectroscopy is used to characterize changes to the localized surface plasmon resonance (LSPR) of the AuNP resulting from refractive index changes as the ZIF crystal grows on the surface. We show that the procedure can be generalized to grow various types of ZIF crystals, such as ZIF-8, ZIF-11, and a previously undocumented ZIF variety. Utilizing both computational models and experimental methods, we identify the thickness of ZIF layers to be self-limiting to ∼50 nm or less, depending on the trapping laser power. Critically, the refractive index of the shells here was found to be above 1.6, indicating the formation of high-density crystals, previously accessible only through slow atomic layer deposition and not through a bulk heating process. The single particle method developed here opens the door for bottom-up controllable growth of custom nanostructures with tunable optical properties.

Solution-Processed Non-Crystalline Solid Electrolytes for Advanced Energy Storage

Advanced batteries containing a Li metal anode (LMA) are needed to enable the clean economy and meet ambitious climate targets. Currently, LMA batteries are limited by dendrite propagation due to the non-uniform plating and stripping of Li, which is detrimental to cell performance. The non-crystalline solid electrolyte (SE), lithium phosphorus oxynitride (LiPON) is unique in demonstrating stable Li plating/stripping at appreciable rates, but its synthesis requires costly and slow vacuum deposition methods. We use aqueous precursor solutions which are rapidly condensed during spin coating and gently annealed to produce dense, flat, Li metal oxide films without long-range order. However, such solution-processed SEs typically exhibit ionic conductivities (σ ion ) too low for energy storage applications (~10-8 S cm-1) and far lower than vacuum-deposited LiPON (~10-6 S cm-1).We will discuss various approaches to increase the σion of these materials, including compositional engineering and controlled processing conditions. Structure-property relationships have been elucidated using modelling of the local structure and interphase formation against Li evaluated by time-dependent electrochemical impedance spectroscopy and in situ X-ray photoelectron spectroscopy. Electrochemical testing of these films deposited onto a current collector in an anode-free cell will be used to evaluate their ability to facilitate stable deposition and stripping of Li.Initial exploration of processing parameters have yielded σion values > 10-7 S cm-1 [1] and the presence of medium-range order (nanocrystalline domains) in some cases. Beyond Li, new non-crystalline SEs for other ions will be discussed. As only limited chemical compositions and processing conditions of these materials have been reported, with no corresponding structural studies, our work provides insight to enable the optimisation and discovery of scalable non-crystalline SEs for advanced batteries.1. P. Vadhva, T. Gill, J. H. Cruddos, S. Said, M. Siniscalchi, S. Narayanan, M. Pasta, T.S. Miller, A.J.E. Rettie. Engineering solution-processed non-crystalline solid electrolytes for Li metal batteries. Chemistry of Materials, 2022, 35, 3, 1168–1176.

Sedimentological and ichnological variations in fluvio‐tidal translating point bars, McMurray Formation, Alberta, Canada

ABSTRACTSedimentological and ichnological descriptions of fluvio‐tidal translating point bars are rare, and complex physico‐chemical processes make highly detailed but concise facies descriptions challenging. Herein, mesofacies are defined to describe and interpret three ancient translating point bars from the Lower Cretaceous McMurray Formation, Alberta, Canada. Twenty‐three mesofacies are defined, based on their recurring sedimentological and ichnological characteristics. These mesofacies form the building blocks of beds and bedsets that make up three depositional facies. Facies 1 reflects sand dune migration at the channel base, which grades into inclined heterolithic stratification of Facies 2 and 3. Facies 2 occurs in the centre and seaward portions of the translating point bars and records tide‐dominated deposition of sand and muddy sand during periods of reduced river discharge. Ichnological suites and bioturbation intensities in these beds reflect persistent but variable brackish‐water conditions, fluctuating deposition rates and the deposition of mud. Mud beds are derived from flows with high suspended‐sediment concentrations. Tidally derived mud beds are typically bioturbated with trace fossil suites indicative of slow deposition rates and brackish‐water conditions. Mud deposited during elevated river discharge is burrowed after the dewatering of the bed. Facies 3 occurs at the landward apex of the translating point bar and is marked by sand‐rich and mud‐rich dune deposits with abundant soft‐sediment deformation, indicative of elevated flow velocities and deposition rates. Bioturbation is rare and sporadically distributed owing to unstable substrates. The distribution of the facies reflect the hydrodynamic variations that occurred vertically and laterally across the bar in response to temporal variations in fluvial and tidal flow interaction, as recorded by their mesofacies. The detailed facies analysis strongly suggests that deposition of the three McMurray Formation translating point bars occurred in proximity to the turbidity maximum zone of a fluvio‐tidal channel system.