Browse Topic: Electrolytes

Items (433)
Additive manufacturing (AM) processes facilitate the production of components with high geometrical complexity, presenting substantial opportunities for innovation in demanding sectors such as aerospace and biomedical engineering. A significant challenge impeding their broader application is the characteristic surface roughness of as-fabricated parts, which results from the layer-wise construction and the presence of partially melted powder particles. While electrochemical polishing (EP) represents a viable post-processing technique for achieving a smooth surface finish, a comprehensive understanding of how the non-equilibrium microstructures characteristic of AM materials interact with the EP process remains incomplete. This investigation centers on the electrochemical polishing behavior of Ti-6Al-4V alloy fabricated by direct energy deposition (DED), utilizing a sodium chloride-ethylene glycol electrolyte. The findings reveal that the material's distinct engenders anisotropic anodic dissolution. This behavior is attributed to the differential electrochemical potentials among the constituent phases and their crystallographic orientations, which consequently narrows the operational process window for effective, uniform polishing. This preferential dissolution of certain phases results in the formation of a subtle, micro-scale topographical variation that mirrors the orientation of the original columnar grain structure. Notwithstanding this microstructural influence, the EP treatment proved highly successful in refining the surface finish, substantially decreasing the average surface roughness from 0.350 μm to 0.042 μm. Concurrently, the treatment led to a significant enhancement in the alloy's corrosion resistance, attributed to an oxide layer. These findings underscore the critical necessity of accounting for microstructural characteristics when developing optimized electrochemical polishing protocols for additively manufactured components.
He, HongxiWu, ChenxiLi, YongjunKang, Chengwei
As global demand for sustainable energy solutions increases, there is a push to develop alternatives to lithium-ion batteries, which face limitations in cost, resource availability, and safety. In particular, multivalent-ion batteries based on magnesium, calcium, zinc, and aluminum have emerged as promising candidates due to their ability to transfer multiple electrons per ion, offering higher volumetric energy density and greater material abundance. This review examines recent advances in electrode and electrolyte development for these systems, highlighting cathode innovations such as cobalt sulfides for magnesium, NASICON-type and redox-coupled materials for calcium, molybdenum trioxide frameworks for zinc, and organic and composite electrodes for aluminum. Electrolyte research has produced improved ionic transport and stability through solvation tuning, hybrid and polymer systems, and deep eutectic solvents. Interfacial engineering is identified as a key enabler for enhancing reversibility, dendrite suppression, and long-term cycling stability. A comparative analysis of the different chemistries found that zinc-ion systems are closest to commercial deployment, aluminum-ion batteries are advancing for grid and flexible devices, and magnesium and calcium-ion batteries hold long-term potential for high-energy applications. The study concludes with future research directions emphasizing solvation control, sustainable materials, and intelligent diagnostics to achieve scalable multivalent battery technologies.
Mittal, VikramShah, RajeshLi, Ivy
Currently, electric propulsion is playing an increasingly important role in marine propulsion systems.Lithium metal batteries are new-generation high-performance energy storage system with development prospect. Traditional flammable and volatile organic liquid electrolytes pose a risk of thermal runaway, while solid-state lithium metal batteries using solid electrolytes have significant advantages in energy density and safety, and are considered the most promising mobile power sources. Among numerous solid electrolyte systems, polymer solid electrolytes have excellent flexibility, good interface compatibility, and good processing characteristics, which have attracted the attention of researchers. Polyurethane (PU) is a common polymer with high mechanical strength and a flexible and adjustable molecular structure, making it one of the best choices for polymer electrolyte matrices. Based on the structural design of polyurethane polymers, this paper explores polycaprolactone type polyurethane electrolyte and the effect of high dielectric constant polycaprolactone on the dissolution and dissociation of lithium salts was studied. We found that polycaprolactone, as the soft segment, exhibits greater electronegativity and provides more oxygen atoms for coordination with lithium ions, which is crucial for enhancing lithium ion transport and improving ionic conductivity.The prepared PU-based solid polymer electrolyte has a conductivity of up to 2.4 × 10-4S/cm, lithium ion migration number 0.78, electrochemical stability window 4.74V. The tensile strengths of PU-based solid polymer electrolyte can reach 2.36 MPa, that balance ionic conductivity and mechanical strength.Besides, it also possesses excellent thermal stability.The symmetrical battery assembled based on the prepared PU-based solid polymer electrolyte exhibits excellent cycling stability (400 hours). The assembled solid-state lithium metal battery based on LiFePO4 can stably cycle for 200 cycles at a current density of 1C, with a Coulombic efficiency of over 99% and a capacity retention rate of up to 99.4%, demonstrating exceptional reliability.
Yuan, MengTang, QingYu, Gongye
All-solid-state batteries (ASSBs) based on sulfide electrolytes hold great promise for next-generation energy storage, yet their performance is critically constrained by unstable cathode–electrolyte interfaces. Here, we report a dual-modification strategy utilizing ionic liquids (ILs) in combination with lithium salts to simultaneously improve interfacial wettability, ionic transport, and electrochemical stability in NCM811 composite cathodes. Three ILs (EMIMTFSI, Pyr₁₄FSI, and PP₁₃FSI) and three lithium salts (LiTFSI, LiDFOB, and LiBOB) were systematically evaluated and screened. While neat ILs improved initial capacities by reducing solid–solid contact resistance, they also triggered parasitic reactions with sulfides, resulting in capacity fading. Among the lithium salts, LiBOB was identified as the most chemically compatible additive, forming thin and uniform hybrid interphases enriched with B–O species. This interphase effectively suppressed high-voltage side reactions and reduced electrode polarization. Strikingly, the synergistic combination of PP₁₃FSI and 1 wt% LiBOB transformed discontinuous point contacts into continuous ionic pathways, yielding a discharge capacity of 165.9 mAh g-1 and maintaining excellent stability over 100 cycles at 0.1C. This work highlights a rational IL–Li salt pairing strategy that not only overcomes intrinsic limitations of sulfide-based composite cathodes but also provides a generalizable route to interfacial design in ASSBs. By integrating molecular-level ion transport regulation with interphase stabilization, our approach offers practical guidance toward realizing high-energy-density, long-cycle-life solid-state batteries.
Gu, Yu-YangTian, Shi-YuQi, JiYang, Li-PengZhan, Wen-WeiYang, Xiao-GuangYi, Yong
Sodium-ion batteries (SIBs) are becoming a strong candidate for large-scale energy storage applications due to their cost-effectiveness and abundant sodium resource reserves. Ether solvents have advantages such as excellent low-temperature performance and good reduction stability. However, poor oxidation stability limits the use of ether-based electrolytes, which need to be addressed urgently. In this study, 1 M sodium tetrafluoroborate (NaBF4) and 0.05 M sodium difluoro(oxalato)borate (NaDFOB) were added in tetraethylene glycol dimethyl ether (G4), which is named “BDG4”. BDG4 electrolyte can promote the formation of cathode electrolyte interface (CEI) layers containing NaF and B─O/B─Na inorganic components on the surface of the cathode. The dense CEI layers can prevent the solvent from undergoing oxidation reactions. Therefore, thanks to the lower highest occupied molecular orbital (HOMO) energy level of G4 and its close coordination structure with Na+, the electrolyte has a high-voltage stability exceeding 4.5 V versus Na+/Na. Therefore, BDG4 electrolyte can be stably cycled on Na3(VO)2(PO4)2F (NVOPF) and NaNi1/3Fe1/3Mn1/3O2 (NFM) cathode for over 250 cycles at room temperature, exhibiting a high Coulombic Efficiency (CE) exceeding 99.8%. Furthermore, BDG4 demonstrated excellent rate performance of NFM cathode, maintaining 75% capacity retention even at 4 C. Due to the stable solid electrolyte interface (SEI) layers formed by the mixture of inorganic and organic components, BDG4 electrolyte can also cycle stably on the Hard Carbon (HC) anode. Therefore, the commercial NFM||HC pouch full cell can cycle stably with 88.3% capacity retention after 80 cycles. This work reveals the role of NaDFOB and provides a feasible approach for the design of high-voltage ether electrolytes of SIBs.
Bai, ZhengMai, XinyuDou, XinChen, ZixinSong, ZhenChen, LongLi, Chunzhong
Aluminum foils have gained traction with EV battery manufacturers for their pouch cell format. Over the years, it has evolved as a material of choice, but it is still plagued by the issues of stress concentration and swelling due to lower strength and lower stiffness of base aluminum layer. Preliminary investigation revealed that laminates using steel foil material (thickness < 0.1mm) could be a potential candidate for EV pouch cell casing. Thus, steel-based laminate was developed meeting key functional requirements (e.g., barrier performance, insulation resistance, peel strength, electrolyte resistance, formable without cracking at edges, and heat sealing compliant). This innovative patented steel-based laminate [1] was further used to manufacture pouch cell prototypes (up to a maximum capacity of 2.8Ah) for key performance evaluation (e.g., cell cycling and nail penetration). The study paves the way for a low cost, sustainable and flexible yet strong steel-based laminate packaging material solution for lithium-ion pouch cells.
Singh, Pundan KumarRaj, AbhishekKumar, AnkitChatterjee, SourabhVerma, Rahul KumarSamantaray, BikashGautam, VikasPandey, Ashwani
In the recent years, the urgency to decarbonize the mobility sector has highlighted the importance of the electrochemical hydrogen use in fuel cells to complement the battery-based electrification. Hydrogen is the greenest energy carrier, and low-temperature Polymer Electrolyte Membrane Fuel Cells (PEMFCs) are part of an ever-evolving scenario, with particularly promising use in high energy demand sectors. Hydrogen is the main player in decarbonisation scenarios, but there are many issues, including its production and storage. There are many categories of hydrogen; in these applications, the finest category of hydrogen, called green hydrogen, is required. To achieve completely green vehicle mobility, enormous technological advances are necessary. This paper presents a 3D-CFD study to analyse the behaviour of PEMFCs by examining the role of humidification, covering fully humidified (anode and cathode), anode-only, cathode-only, and fully dry operations. This is simulated for several membrane thicknesses, reproducing a wide matrix of operating conditions and separator choices, and examining their respective effect on the cell’s resistance. The obtained results confirm that the fully dry operation results in a significant increase in cell’s internal resistance, as well as the opposite is verified for fully humidified operation. However, maintaining an external anode-only humidification and relying on the internal self-humidification can be a highly effective strategy, allowing to reduce the complexity of the balance of plant by simplifying the humidifiers sub-system. This is analysed in conjunction with the effect of the electrolyte thickness, which opens to the possibility to enhance or even suppress self-humidification and water transport. Conclusions provide an overview of the design and operating choices to minimize the cell’s resistance at a minimum system complexity cost.
Scialpi, LeonardoD'Adamo, AlessandroMarra, Carmine
Lithium-ion batteries used in electric vehicles (EVs) are facing issues owing to internal short-circuit (ISC), leading to thermal runaway. In this study, a pseudo-two-dimensional (P2D) model is employed to numerically investigate the effects of charging rate (C-rate) and separator electrical conductivity on the ISC behavior of a lithium-ion cell. The results reveal that as C-rate increases, both the voltage and capacity decrease more rapidly marked by higher solid potential gradient indicating increased internal resistance. These effects further intensified at higher separator conductivity, which facilitates greater ISC current and accelerates cell degradation. Also, the variations in current density and solid-phase lithium concentration become more pronounced at higher C-rates, particularly near the anode–separator interface, indicating increased non-uniformity during ISC conditions. Furthermore, the electrolyte voltage drop intensifies with rising C-rate, contributing to additional polarization. Further, it is observed that the separator conductivity has a significant influence on ISC current, although it shows a minimal effect on the terminal voltage. The value of the ISC current is found to increase with the increase in the value of the conductivity of the separator. Finally, it can be inferred that the lower electrical conductivity of the separator is desirable to prevent ISC of the Li-ion cell. The study highlights that a lower separator conductivity is beneficial in mitigating the severity of ISC events. These findings provide valuable insights for the design of safer lithium-ion cells considering the separator conductivity and operational C-rates.
Ch, Narendra BabuParamane, AshishRandive, Pitambar
Electric double-layer capacitors (EDLCs) store charge by adsorbing ions at the electrode–electrolyte interface, offering fast charge–discharge rates, high power density, minimal heat generation, and long cycle life. These characteristics make EDLCs ideal for memory backup in electronic devices and power assistance in electric and hybrid vehicles, where rapid energy response and high-power delivery are critical. However, their energy density remains lower than that of batteries, requiring improvements in capacitance and operating voltage. Activated carbon with high surface area is commonly used as the electrode material, but its microporous structure limits ion transport at high rates, reducing power performance. This limitation is especially critical in automotive motor drive systems. Recent research has shifted toward mesoporous carbon materials, which improve ion diffusion and accessibility. In this study, resorcinol–formaldehyde carbon cryogels (RFCCs) with controlled mesoporous architectures were synthesized and applied as EDLC electrode materials, in combination with organic electrolytes that provide a wider electrochemical window. A CO2-activated RFCC (RFCC-CO2) demonstrated the most balanced electrochemical performance, combining high surface area and interconnected mesoporous networks. Characterization using scanning electron microscopy (SEM) and Brunauer–Emmett–Teller (BET) surface area analysis confirmed the hierarchical porous structure. Electrochemical evaluations through cyclic voltammetry (CV) and constant current charge–discharge measurements demonstrated that RFCC-CO2 achieved high specific capacitance and excellent rate capability. These results point to the importance of mesopore engineering in addressing ion transport limitations in conventional carbon materials and highlight RFCC-CO2 as a promising electrode candidate for EDLCs in regenerative braking and other fast-response electric mobility applications.
Cheng, ZairanOkamura, TsubasaOhnishi, YutoNakagawa, Kiyoharu
Scientists are racing against time to try and create revolutionary, sustainable energy sources (such as solid-state batteries) to combat climate change. However, this race is more like a marathon, as conventional approaches are trial-and-error in nature, typically focusing on testing individual materials and setting pathways one by one. To get us to the finish line faster, researchers at Tohoku University developed a data-driven AI framework that points out potential solid-state electrolyte (SSE) candidates that could be “the one” to create the ideal sustainable energy solution.
This study presents a novel biomimetic flow-field concept that integrates a triply periodic minimal surface (TPMS) porous architectures with a hierarchical leaf-vein-inspired distribution zone, fabricated through 3D printing. By mimicking natural transport systems, the proposed design enhances oxygen delivery and water removal in proton exchange membrane fuel cells (PEMFCs). The results showed that I-FF and G-FF significantly improved mass transport and water management compared to conventional CPFF. The integrated design I-FF-LDZ achieves up to 32% improvement in power density at 1.85 A/cm2@0.4 V and delays the onset of mass transport losses. The study also reveals that optimizing the volume fraction Vf significantly affects gas penetration, with lower Vf (30%) improving performance in the mass-limited region. These findings underscore the promise of nature-inspired, 3D-printed flow-field architectures in overcoming key transport limitations and advancing the scalability of next-generation PEMFC systems.
Ho-Van, PhucLim, Ocktaeck
Researchers developed wearable skin sensors that can detect what’s in a person’s sweat. Using the sensors, monitoring perspiration could bypass the need for more invasive procedures like blood draws and provide real-time updates on health problems such as dehydration or fatigue. The sensor design can be rapidly manufactured using a roll-to-roll processing technique that essentially prints the sensors onto a sheet of plastic.
Southwest Research Institute is working to expand software normally used to model electrolytes and predict corrosion and turn it into a tool that can help determine whether ice-covered worlds have the right conditions for microbial life. The project is supported by NASA’s Habitable Worlds program, which seeks to use knowledge of the history of the Earth and the life upon it as a guide for determining the processes and conditions that create and maintain habitable environments.
Technological advances have led to the widespread use of electric devices and vehicles. These innovations are not only convenient but also environmentally friendly, offering an alternative to polluting fuel-driven machines. Lithium-ion batteries (LIBs) are widely used in electrical appliances and vehicles. Commercial LIBs comprise an organic electrolyte solution, which is considered indispensable to make them energy efficient. However, ensuring safety becomes a concern and may be difficult to achieve with the rising market demand.
Researchers have developed a pacifier designed to monitor a baby’s electrolyte levels in real time, potentially eliminating the need for repeated invasive blood draws. The team constructed a tiny tunnel, or microfluidic channel, into the body of the pacifier.
The interplay of electrochemistry, two-phase flow, and heat transfer generates complex transport phenomena within the porous materials of fuel cells that are not yet fully understood. This lack of comprehensive understanding complicates the modeling of liquid water transport, which is critical because the hydration of the polymer electrolyte membrane significantly impacts the cell performance. The liquid water transport mechanisms in porous media can be explained by capillary force, hydraulic permeation and gravity effects, as well as water condensation and evaporation. In general, the liquid water transport is mainly driven by the capillary force, while body forces, such as gravity, do not significantly affect its momentum. Due to limited experimental data on capillary pressure and saturation in gas diffusion media, the Leverett approach has been widely used for modeling liquid water transport in PEMFCs. The Leverett approach is a polynomial fitting of capillary pressure data for water imbibition in unconsolidated sand packs. Due to its nature, this approach may not accurately predict capillary pressure in gas diffusion media. Fuel cell GDM materials, naturally hydrophilic, are typically coated with a nonwetting polymer like polytetrafluoroethylene to create hydrophobic surfaces and pores. The resulting nature of GDM materials, with intermediate wettability due to the coexistence of hydrophilic and hydrophobic pore spaces, complicates transport phenomena. Consequently, the applicability of the traditional Leverett approach is questionable. This work focuses on capillary transport within PEMFCs, highlighting key experimental and modeling approaches for predicting the capillary pressure-saturation relationship. Starting from the Leverett function, improved models have been proposed and are here implemented in a 3D-CFD model. This research provides an overview of key experimental and theoretical developments in understanding capillarity in PEMFCs. Furthermore, it implements selected capillary pressure correlations in a 3D-CFD model to evaluate their performance in simulating water transport within the porous media, providing guidelines for their use in large-scale models.
Marra, CarmineCroci, FedericoFontanesi, StefanoBerni, FabioD'Adamo, Alessandro
The intention of this exploration is to evolve an optimization method for the Electrochemical Machining (ECM) process on Haste alloy material, taking into account various performance characteristics. The optimization relies on the amalgamation of the Taguchi method with an Adaptive Neuro-Fuzzy Inference System (ANFIS). Haste alloy is extensively utilized in the aerospace, nuclear, marine, and car sectors, specifically in situations that are prone to corrosion. The experimental trials are organized based on Taguchi's principles and involve three machining variables: feed rate, electrolyte flow rate, and electrolyte concentration. This examination examines performance indicators, including the pace at which material is removed and the roughness of the surface. It also includes geometric factors such as overcut, shape, and tolerance for orientation. The results suggest that the rate at which the feed is supplied is the most influential element affecting the necessary performance standards. For improving the accuracy of predictions, numerous regression models are created and performance metrics are constructed. A validation test was performed to authenticate the findings acquired through the ANFIS methodology. The test outcomes show that the suggested strategy is considerably more efficient than earlier approaches.
Pasupuleti, ThejasreeNatarajan, ManikandanRamesh Naik, MudeSomsole, Lakshmi NarayanaSilambarasan, R
The aspiration of this exploration is to evolve an optimization technique for the Electrochemical Drilling process on Haste alloy material, considering various performance factors. The Taguchi approach, along with Grey Relational Analysis (GRA), forms the basis for optimization. Haste alloy has a wider range of uses in industries such as aerospace, nuclear, and marine, especially in harsh environments. The experimental trials conducted in accordance with Taguchi's approach have utilized three machining variables: feed rate, electrolyte flow rate, and electrolyte concentration. When doing this examination, we analyze not only the rate at which material is removed and the roughness of the surface, but also other characteristics that indicate performance, such as overcut, shape, and orientation tolerance. The analytical findings indicate that the feed rate is the primary factor that directly impacts the required performance standards. Regression models are constructed to make predictions, and performance measures are established to assess their effectiveness. The test results unequivocally showed that the new procedure is markedly superior to the prior one.
Natarajan, ManikandanPasupuleti, ThejasreeSagaya Raj, GnanaSilambarasan, RSomsole, Lakshmi Narayana
The aim of this study is to create an Adaptive Neuro-Fuzzy Inference System (ANFIS) model for the Electrochemical Machining (ECM) process using Nimonic Alloy material, with a specific focus on several performance aspects. The optimization strategy utilizes the combination of the Taguchi method and ANFIS integration. Nimonic Alloy is widely employed in the aerospace, nuclear, marine, and car sectors, especially in situations that are susceptible to corrosion. The experimental trials are designed according to Taguchi's method and involve three machining variables: feed rate, electrolyte flow rate, and electrolyte concentration. This study investigates performance indicators, such as the rate at which material is removed, the roughness of the surface, and geometric characteristics, including overcut, shape, and tolerance for orientation. Based on the analysis, it has been determined that the feed rate is the main component that influences the intended performance criteria. In order to improve the precision of forecasts, numerous regression models are created and performance indicators are formulated. A validation test was performed to affirm the results achieved through the use of the ANFIS methodology. The test findings indicate that the proposed strategy surpasses previous methodologies to a significant degree.
Natarajan, ManikandanPasupuleti, ThejasreeC, NavyaKiruthika, JothiSilambarasan, R
The objective of this research is to develop an optimization strategy for the Electrochemical Drilling process on Nimonic alloy material, taking into account various performance factors. The optimization strategy relies on the integration of the Taguchi method with Grey Relational Analysis (GRA). Nimonic is extensively utilized in aerospace, nuclear, and marine industries, specifically in situations that are prone to corrosion. The experimental trials are structured based on Taguchi's principle and encompass three machining variables: feed rate, electrolyte flow rate, and electrolyte concentration. This inquiry examines performance indicators like the rate of material removal, surface roughness, as well as geometric parameters such as overcut, shape, and orientation tolerance. Based on the investigation, it is determined that the feed rate is the primary factor that directly affects the intended performance criteria. In order to enhance the accuracy of predictions, multiple regression models are created and performance metrics are constructed. A validation test was performed to corroborate the findings acquired using the GRA approach. The test results demonstrate that the proposed strategy is markedly superior to earlier approaches.
Pasupuleti, ThejasreeNatarajan, ManikandanD, PalanisamySilambarasan, RKrishnamachary, PC
Existing commercial battery technologies, which use liquid electrolytes and carbonaceous anodes, have certain drawbacks such as safety concerns, limited lifespan, and inadequate power density particularly at high temperatures. This has prompted researchers to search for solid electrolytes that are safe and compatible with lithium metal anodes, which are known for their high theoretical specific power capacity.
Anode-free sodium metal batteries (AFSMBs) with initial zero sodium anodes are promising energy-storage devices to achieve high energy density and low cost. The morphology and reversibility of sodium controls the cycling lifespan of the AFSMBs, which is directly affected by the separator. Here, we compared the sodium deposition and corresponding electrochemical behaviors under the influence of three commercial separators, which were Celgard 2500, Al2O3-coated PP separator and glass fiber (denoting as 2500, C-PP and GF). Firstly, the reversibility of sodium plating/stripping was tested using half-cells, where coulombic efficiencies were stable at ~99.89% for C-PP and GF compare to 99.65% for 2500, indicating more dead sodium were formed for 2500. Then, the morphologies of deposited sodium were compared using optical microscopy. Compared to inhomogeneous sodium growth under 2500, C-PP obtained more flatter sodium layer with less height difference, attributing to the high mechanical strength of Al2O3 layer. Differently, we discovered that sodium was grown into pores in GF to form sodium particles with large active surface, which contacts with sufficient electrolytes and could be reversibly stripped. The reversibility of the sodium in GF were further verified using in situ X-ray diffraction tests. Accordingly, cycling performance of AFSMBs were improved using C-PP and GF, where capacity retention after 120 cycles were 56.9%, 61.6% and 69.2% for 2500, C-PP and GF, respectively. Moreover, the AFSMB using 2 mAh cm-2 Na[Ni1/3Fe1/3Mn1/3]O2 as cathode with GF exhibiting excellent capacity of 117.61 mAh g-1 under high current density of 1 C. Subsequently, in situ EIS tests after/during charging/discharging process were further conducted to illustrate the enhancement of rate and cycling performance. This work demonstrates the effect of separators on the sodium deposition for higher irreversibility and stability, which could also offer insights for developing advanced separators to achieve high performance AFSMBs.
Qin, NanJin, LimingZheng, Jim P.
To gain high efficiencies and long lifetimes, polymer electrolyte membrane fuel cell systems require precise control of the relative humidity of the cathode supply air. This is usually achieved by the use of membrane humidifiers. These are passive components that transfer the product water of the cathode exhaust air to humidify the supply air. Due to the passive design, controllability is achieved via a bypass. It is possible to use map-based control strategies to avoid the use of humidity sensors. Such map-based control requires deep insights into the humidifier behavior in all possible thermodynamic operating states, including various water loads. This paper focuses on typical operating conditions of heavy-duty application at high load, specifically on the occurrence of liquid water in the cathode exhaust gas, which has not been sufficiently investigated in the literature yet. In order to simulate these conditions, we built a test rig with an optically accessible single-channel set-up of a humidifier. We used a perfluorosulfonic acid membrane without a gas diffusion layer. It was shown that condensed liquid fractions, even isolated droplets, at the cathode outlet significantly enhance the water transfer. The influence of water mass flow rate, pressure level, temperature, and gas flow rate on humidifier’s water transfer rate was investigated. Static and dynamic measurements were obtained, with the presence of droplets also leading to characteristic enhancements in mass transfer during dynamic operation. The analyzed data show that if liquid water is not taken into account: a) the risks of flooding, which lead to irreversible ageing processes and thus to permanent performance loss of the fuel cell are not identified and b) opportunities to improve the membrane humidifier in terms of design, operating strategies and model-based control strategies in heavy-duty applications remain unused.
Mull, SophieWeiss, LukasWensing, Michael
Dr. Park Jun-woo of the Korea Electrotechnology Research Institute (KERI) Next-Generation Battery Research Center and Sung Junghwan, student researcher at the UST KERI Campus, have successfully engineered a technology focused on the “size-controlled wet-chemical synthesis of solid-state electrolytes (sulfide superionic conductors).” It not only cuts the processing time and cost by over fifty percent but also doubles the resultant quality.
With the rapid development of electric vehicles, the demands for lithium-ion batteries and advanced battery technologies are growing. Today, lithium-ion batteries mainly use liquid electrolytes, containing organic compounds such as dimethyl carbonate and ethylene carbonate as solvents for the lithium salts. However, when thermal runaway occurs, the electrolyte decomposes, venting combustible gases that could readily be ignited when mixed with air and leading to pronounced heat release from the combustion of the mixture. So far, the chemical behavior of electrolytes during thermal runaway in lithium-ion batteries is not comprehensively understood. Well-validated compact chemical kinetic mechanisms of the electrolyte components are required to describe this process in CFD simulations. In this work, submechanisms of dimethyl carbonate and ethylene carbonate were developed and adopted in the Ansys Model Fuel Library (MFL). Further improvements were made to enhance the kinetic consistency between these submechanisms and the base mechanism of the MFL. These mechanisms were validated using recently published experimental datasets over a wide range of conditions and show satisfactory performance. Analysis of the simulated results has revealed the important reaction pathways in the decomposition of dimethyl carbonate and ethylene carbonate. The species involved in the most critical pathways were selected as key species in the subsequent mechanism reduction using Ansys Reaction Workbench. Multiple mechanism reduction approaches were applied in combination to reduce the mechanism described here to 38 species and 177 reactions. This mechanism is ready to be used in CFD simulation.
Zhang, KuiwenPuduppakkam, KarthikShelburn, Anthony
Super duplex stainless steel (SDSS) is a type of stainless steel made of chromium (Cr), nickel (Ni), and iron (Fe). In the present work, a 1.6 mm wide thin sheet of SDSS is joined using gas tungsten arc welding (GTAW). The ideal parameter for a bead-on-plate trial is found, and 0.216 kJ/mm of heat input is used for welding. As an outcome of the welding heating cycle and subsequent cooling, a microstructural study revealed coarse microstructure in the heat-affected zone and weld zone. The corrosion rate for welded joints is 9.3% higher than the base metal rate. Following the corrosion test, scanning electron microscope (SEM) analysis revealed that the welded joint’s oxide development generated a larger corrosive attack on the weld surface than the base metal surface. The percentages of chromium (12.5%) and molybdenum (24%) in the welded joints are less than those in the base metal of SDSS, as per energy dispersive X-ray (EDX) analysis. Corrosion modeling is done using the COMSOL Multiphysics software. Electrochemical corrosion modeling is used to determine the electrolyte potential (i.e., 0.09 V) and current density (i.e., 0.2 A/m2 to 1.8 A/m2). An entire mesh model contains 6240 elements. The largest and smallest element sizes are 4 mm and 0.1 mm, respectively. The maximum element rate of growth is 1.2.
Kumar, SujeetKumar, YogeshE. K., Vimal K.
A team from Lawrence Berkeley National Laboratory (Berkeley Lab) and Florida State University has designed a new blueprint for solid-state batteries that are less dependent on specific chemical elements, particularly critical metals that are challenging to source due to supply chain issues. Their work could advance solid-state batteries that are efficient and affordable.
Polymer Electrolyte Membrane Fuel Cells (PEMFCs) are undergoing a rapid development, due to the ever-growing interest towards their use to decarbonize power generation applications. In the transportation sector, a key technological challenge is their thermal management, i.e. the ability to preserve the membrane at the optimal thermal state to maximize the generated power. This corresponds to a narrow temperature range of 75-80°C, possibly uniformly distributed over the entire active surface. The achievement of such a requirement is complicated by the generation of thermal power, the limited exchange area for radiators, and the poor heat transfer performance of conventional coolants (e.g., ethylene glycol). The interconnection of thermal/fluid/electrochemical processes in PEMFCs renders heat rejection as a potential performance limiter, suggesting its maximization for power density increase. To this aim, suspensions of coolants and nanoparticles (nanofluids) have been proposed for PEMFCs cooling, although their characterization has often been limited to the superior thermal conductivity, overlooking a comprehensive understanding, and leaving a relevant research gap. In this paper, nanofluids cooling is simulated using 3D-CFD in a small laboratory scale (25 cm2) model of a hydrogen-air PEMFC with a liquid cooling circuit. The variation of the coolant fluid is studied considering flow uniformity, heat rejection, pressure losses, and power generation, ultimately leading to a high-level analysis on the trade-off between heat transfer/storage, relevant for coolant channels in PEMFCs. The study elucidates the membrane conditions and the compositional requirements for ethylene glycol and water based nanofluids to lead to a net gain in the generated power density, modelled in the range of +5/10% for high particle loading (10%) and envisaged to reach +15% for hypothesized ideal compositions. The study clarifies the role of nanofluids for PEMFC cooling and redefines their enabler contribution in the development of high power density PEMFCs, indicating guidelines for their application-designed formulation.
D'Adamo, AlessandroCorda, GiuseppeBerni, FabioDiana, MartinoFontanesi, Stefano
ABSTRACT Cornerstone Research Group (CRG) developed a lithium metal (Li-metal) battery cell for military applications. Utilizing a Li-metal anode, high energy density cathode, and an advanced low-temperature fluorinated electrolyte, the cell was designed and developed to provide high-power and low temperature capabilities. The 1.5 Ah Li-metal pouch cell had a specific energy of 247 Wh/kg and was able to discharge at ultra-low temperatures (-57 °C). Moreover, the Li-metal cell demonstrated extremely high-power by fully discharging at 10 C while maintaining over 70% its initial capacity. To demonstrate the Li-metal cell’s utility for military vehicle use, CRG modeled the cell into the 6T battery platform. A novel module housing was designed to evenly apply compression to the Li-metal cells to improve cell performance. Based on these projections, the Li-metal 6T battery could have a capacity of 163 Ah with a specific energy of 179 Wh/kg. Citation: J. Hondred, F. Zalar, P. Nikolaev, B. Henslee, “High Power Li-Metal Battery Cell for Military Applications,” In Proceedings of the Ground Vehicle Systems Engineering and Technology Symposium (GVSETS), NDIA, Novi, MI, Aug. 15-17, 2023.
Hondred, JohnZalar, FrankNikolaev, PashaHenslee, Brian
Development of all-solid-state batteries is crucial to achieve carbon neutrality. However, their high surface resistance causes these batteries to have low output, limiting their applications. To this end, researchers have employed a novel technique to investigate and modulate electric double layer dynamics at the solid/solid electrolyte interface. The researchers demonstrate unprecedented control of response speed by over two orders of magnitude, a major steppingstone towards realization of commercial all-solid-state batteries.
By the end of 2023 there will be 10 Chinese electric passenger vehicles using advanced semi-solid-state batteries (ASSB) - an industry-first application for EVs and a milestone for vehicle electrification, according to Paul Haelterman, North American VP at Autodatas, a vehicle benchmarking and research firm. It's “a huge step for the industry's production pursuit of all-solid-state batteries,” Haelterman told SAE Media ahead of his presentation on China's EV market at SAE's WCX 2023 conference in Detroit. A semi-solid-state battery can be one in which one electrode does not contain a liquid electrolyte and the other electrode does. Or it can be a battery in which the mass or volume of the solid electrolyte in the monomer accounts for half of the total mass or volume of the electrolyte in the monomer. Some battery experts view semi-solid-state as a compromise technology, offering a faster route to scale, but is heavy and requires more volume.
Buchholz, Kami
Researchers have devised a tiny, nano-sized sensor capable of detecting protein biomarkers in a sample at single-molecule precision. Coined as hook and bait, a tiny protein binder fuses to a small hole created in the membrane of a cell — known as a nanopore — which allows ionic solution to flow through it.
Start-up battery developer Factorial Energy's workforce of engineers, chemists and other technology specialists has topped 100 with recent hirings in the Asia-Pacific region. A pilot manufacturing plant for the firm's solid-state lithium-metal batteries is slated to launch later this year. And, Hyundai Motor Co., Stellantis and Mercedes-Benz have invested in the Woburn, Massachusetts-based company and its proprietary Factorial Electrolyte System Technology, trademarked FEST. CEO Siyu Huang recently spoke with SAE Media's Kami Buchholz. Condensed highlights of the interview:
Solid-state lithium-ion batteries that use a solid electrolyte may potentially operate at wide temperatures and provide satisfactory safety. Moreover, the use of a solid electrolyte, which blocks the formation of lithium dendrites, allows batteries to use metallic lithium for the anode, enabling the batteries gain an energy density significantly higher than that of traditional lithium-ion batteries. Solid electrolytes play a role of conducting lithium ions and are the core of solid-state lithium-ion batteries. However, the development of solid lithium electrolytes towards a high lithium ionic conductivity, good chemical and electrochemical stability and scalable manufacturing method has been challenging. We report a new material composed of nitrogen-doped lithium metaphosphate, denoted as NLiPO3. The material delivers a lithium ionic conductivity on the order of 10-4 S/cm at room temperature, which is about two orders of magnitude higher than that of conventional LiPON – the electrolyte currently used in solid-state thin-film lithium-ion batteries, and is comparable or generally higher than that of most of the existing solid electrolytes. The high lithium ionic conductivity was attributed to the formation of P−N
Zhang, QifengDing, Yi
Lithium-ion batteries have a well-documented failure tendency under abuse conditions with a significant release of gases and heat. This failure originated from the decomposition reactions within the battery’s electrochemical components, resulting in gas generation and increased internal pressure. To optimize battery safety, it is crucial to understand their behaviors when subjected to abuse conditions. The 18650 format cell incorporates a vent mechanism within a crimped cap to relieve pressure and mitigate the risk of rupture. However, cell venting introduces additional safety concerns associated with flammable gases and liquid electrolyte that flow into the environment. Experiments were performed with two venting caps with well-known geometries to quantify key parameters in describing the external dynamic flow of battery venting and to validate a CFD model. Thus, the jet of pure CO2 was measured on a dedicated experimental bench using Schlieren’s optical technique and the jet shape and penetration were calculated. The CFD model was validated by comparing the experimental results with those obtained from the CFD model. Furthermore, emissions data from two different cathode chemistries, LFP and NCA, for three distinct SOC´s were collected from the literature [1,2] and simulated using the two venting caps to obtain insights on the spatial and temporal species (CO, CH4, H2) distribution. Considering results, species distribution was more dependent on the design of the venting cap, but also on the SOC of the battery.
Garcia, AntonioGil, AntonioGolke, DiegoMicó, Carlos
This work elaborates the transferability of electrode diffusion coefficients gained from fitting procedures in frequency domain to an electrochemical battery model run in time domain. An electrochemical battery model of an NMC622 half-cell electrode is simulated with sinusoidal current excitations at different frequencies. The current and voltage signals are analyzed in frequency domain via Nyquist and Bode plots. The frequency domain analysis of time domain simulations is applied to assess the numerical convergence of the simulation and the sensitivity on particle diameter, electrode and electrolyte diffusion coefficients. The simulated frequency spectra are used to fit the electrode diffusion coefficient by means of different electrical equivalent circuit models and the electrochemical battery model itself. The fitted diffusion coefficients from the different electrical equivalent circuit models deviate by one order of magnitude from the a priori known reference data. The fitting results from the electrochemical battery model show a perfect match and the corresponding simulation times underline the feasibility of this fitting approach. The impact of different electrode diffusion coefficients is further assessed by constant current discharge and pulse discharge simulations at different C-rates. The voltage responses deviate in the range of 20 mV for the 2C discharge pulse.
Wurzenberger, Johann C.Lechner, ChristophChen, ChaoKolmbauer, MichaelMele, IgorKatrasnik, Tomaz
A large increase in GHG emissions has led to a substantial increase in EV adoption. Due to its complexity, predicting the states of LIB remains to be a roadblock for mass adoption. Furthermore, the ability to predict the performance of an EV through its lifetime continues to be a difficult task. The following work provides how a detailed electro-thermal P2D battery model, GT-AutoLion1D, can be implemented along with a 1D vehicle model to predict how the system will age over 40 weeks of operation. The battery is calibrated using experimental data and is capable of predicting performance and aging. It considers aging mechanisms like solid electrolyte interphase (SEI) layer growth, active material isolation (AMI), and SEI cracking. It is also coupled with a lumped thermal model. The 1D vehicle model considers aerodynamic, rolling resistance, driveline inefficiency, motor-inverter losses, battery resistive losses and auxiliaries. The results showed that simulation is over 30000 times faster than real time and the capacity decreased over 7% assuming a recurrent weekly routine and charging pattern.
Chopra, UjjwalBiju, Nikhil
Battery Electric Vehicles (BEVs) are becoming more competitive day by day to achieve maximum peak power and energy requirement. This poses challenges to the design of Thermal Interface Material (TIM) which maintains the cell temperature and ensure retention of cell and prevent electrolyte leak under different crash loads. TIM can be in the form of adhesives, gels, gap fillers. In this paper, TIM is considered as structural, and requires design balance with respect to thermal and mechanical requirements. Improving structural strength of TIM will have negative impact on its thermal conductivity; hence due care needs to be taken to determine optimal strength that meets both structural and thermal performance. During various crash conditions, due to large inertial force of cell and module assembly, TIM is undertaking significant loads on tensile and shear directions. LS-DYNA® is used as simulation solver for performing crash loading conditions and evaluate structural integrity of TIM. Prior literature discuss usage of MAT138 (Cohesive mixed mode), MAT169 (Arup adhesive) for modeling TIM adhesive failure. To generate such material models, there is extensive coupon level testing needs to be performed. In early development of battery module design, such sophisticated failure models are not feasible to implement. To overcome this challenge, TIE BREAK contacts in LS-DYNA® are leveraged to define interface failure for quick turnaround. TIE BREAK is penalty-based contact definition which allows to model both tensile and compressive forces until failure on adhesive/glue. Variation studies could be performed in short time for designing the required TIM strength before generating detailed material models. Various techniques available in TIE BREAK contacts such as failure initiation (force based/stress based), shell offset and critical parameters are iterated to arrive at more appropriate modeling considerations. In this paper, contact-based failure is compared with various material-based failure models to gain confidence and simplify design iterations for selection of appropriate TIM.
Seshadri, Srirambhavsar, TejasR, NarayanaGH, Shivaprakash
Accelerating demand for renewable energy and electric vehicles is sparking a high demand for the batteries that store generated energy and power engines. But the batteries behind these sustainability solutions aren’t always sustainable themselves. In a paper published in the journal Matter, scientists created a zinc battery with a biodegradable electrolyte from an unexpected source — crab shells.
Lithium-ion (Li-ion) batteries are one of the most used batteries that support modern ITC society, including smartphones and EVs. These batteries are repeatedly charged and discharged by Li-ions passing back and forth between the positive and negative electrodes, with the Li-ion electrolyte acting as a passageway for the ions.
Redox flow batteries are stationary batteries in which the energy is located in the electrolyte, outside of the cell itself, as in a fuel cell. They are often marketed with the prefix “eco” since they open the possibility of storing excess energy from, for example, the Sun and wind. It appears that they can be recharged an unlimited number of times; however, redox flow batteries often contain vanadium, a scarce and expensive metal. The electrolyte in which energy is stored in a redox flow battery can be water-based, which makes the battery safe to use but results in a lower energy density.
Researchers at NASA’s Jet Propulsion Laboratory (JPL) are developing a novel microthruster that could provide easy-to-control propulsion during spaceflight. Using solid silver as the fuel source, this innovative microthruster provides thrust via electrospray without heating the fuel reservoir or transporting liquid metals. Instead of transporting a molten metal, this design transports metal ions via a solid electrolyte film.
Engineers at the University of California San Diego have developed lithium-ion batteries that perform well at freezing cold and scorching hot temperatures, while packing a lot of energy. The researchers accomplished this feat by developing an electrolyte that is not only versatile and robust throughout a wide temperature range, but also compatible with a high energy anode and cathode.
Open Circuit Potential (OCP) is the potential established between the working electrode (the metallic surface to be studied) and the environment, with respect to a reference electrode, which will be placed in the electrolyte close to the working electrode. It is very important to measure the electric potentials of various metallic materials in order to know their corrosion behavior in various environments. But perhaps if there is brazing joint involved, as in the case of aluminium heat exchanger components, there are some challenges involved in knowing the potential of the fillet part which includes the selective masking of the areas within the same sample for testing. Firstly, getting reliable & accurate data due to masking process is one concern. Secondly, about the aluminium heat exchanger sample, the variation in OCP values within a single sample are possible due to various factors i.e. presence of cladding on the surface of the materials, presence of sacrificial Zn coating on the microtubes, variation in brazing parameters etc. In this study analytical correlation is made to OCP values of individual postbrazed child part samples w.r.t the entire brazed joint sample. This is being done in order to calculate & estimate the electric potential of the brazing fillet part. The individual currents at various areas within the sample w.r.t total specimen area are calculated & evaluated in order to arrive at a correlation between the observed potential vs. the sample area. From the obtained results it was found that the predicted theoretical fillet potential was in close agreement with the measured value. However, there is a scope of improvement in refining the simulation methods used in this study, in order to obtain more repeatable & accurate measurement OCP values.
Shandily, Prem MohanGuruprasanna, PraveenKumar, RajSoni, Sunil
A team of researchers led by chemists at the U.S. Department of Energy’s (DOE) Brookhaven National Laboratory has learned that an electrolyte additive allows stable high-voltage cycling of nickel-rich layered cathodes. Their work could lead to improvements in the energy density of lithium batteries that power electric vehicles.
Engineers at the University of California San Diego have developed lithium-ion batteries that perform well at freezing cold and scorching hot temperatures, while packing a lot of energy. The researchers accomplished this feat by developing an electrolyte that is not only versatile and robust throughout a wide temperature range, but also compatible with a high energy anode and cathode.
The element niobium (Nb), a transition metal, stands ready to improve the performance of one of the lithium-ion (Li-ion) battery’s confusing array of possible electrode chemistries — the LTO (lithium titanium oxide) anode, which after graphite is the second most-produced. During battery charging, lithium ions leave the positive cathode and move through the battery’s electrolyte to take up positions of higher energy in the anode. During discharge, this process reverses and drives electrons through an external circuit to power the load.
Researchers have developed new polymer electrolytes for redox flow batteries that are flexible, efficient, and environmentally friendly.
Currently the preferred technology to power electric vehicles, lithium-ion (Li-ion) batteries, has become too expensive for long-duration grid-scale energy storage systems — not to mention that lithium itself is becoming more and more elusive.
Items per page:
1 – 50 of 433