Browse Topic: Lithium-ion batteries
Current lithium-ion batteries should generally only be charged above 0 °C, as charging below this temperature can promote lithium plating and irreversible degradation. However, conventional pack-level heating elements increase system mass and design complexity. In addition, heat is transferred from outside into the cell, causing the temperature inside the cell to rise slowly. This study evaluates internal Joule heating of cylindrical Li-ion cells using a zero-mean square-wave current excitation and quantifies the associated aging impact. LG INR21700-M50L cells were tested at 0 °C, −10 °C, and −20 °C with three excitation frequencies (50 Hz, 1 Hz, 10 mHz) at 5 A amplitude. Each cycle consisted of 30 min heating followed by 60 min cooling; reference capacity-based state of health (SOH) was assessed every 50 cycles up to 400 cycles. A maximum surface temperature rise of 14.3 K was achieved, with larger temperature rise at lower ambient temperature and lower excitation frequency. Capacity fade remained below approximately 1% for most conditions; however, at −20 °C and 10 mHz a pronounced SOH decrease to 87% was observed, indicating a critical operating regime. The results provide practical guidance for pulse-heating parameter selection and highlight the need for safeguards and further diagnostics in extreme low-frequency excitation at very low temperatures. This heating approach is particularly suitable for simpler battery-electric applications without thermal management, such as e-bikes or power tools. However, it may also be relevant for applications with existing thermal management systems, as it simplifies battery pack design.
Researchers at Columbia Engineering have developed a new gel electrolyte that both improves the lifetime and safety of anode-free lithium batteries, an emerging battery architecture that could dramatically boost energy density while simplifying manufacturing. Although such design promises higher energy density and lower cost, the approach has long been plagued by short battery life and safety concerns caused by unstable lithium plating and parasitic reactions at the electrode-electrolyte interface.
As the electric vehicle era enters full scale, demand is increasing for batteries that can travel farther and last longer. Lithium-metal batteries have been attracting attention as a next-generation technology capable of surpassing the capacity limits of existing lithium-ion batteries. However, during the charging process, needle-shaped crystals called “dendrites” grow, shortening battery life and increasing the risk of fire, which has been identified as the biggest obstacle to commercialization. A Korean research team has developed a key technology that can solve this challenge.
Electric vertical takeoff and landing aircraft impose significantly higher electrochemical and thermal demands on Li-ion batteries than conventional electric vehicles, yet publicly available aging datasets for this application remain limited in applicability, cell technology, and statistical robustness. This study experimentally characterizes the degradation behavior of state-of-the-art Molicel P45B 21700 cells under realistic Urban Air Mobility operating conditions involving high power demand, rapid turnaround, and repeated cycling. Eight cells are subjected to over 3,000 cycles using a fast constant-current charging protocol and a multi-segment constant-power discharge profile. The discharge profile is derived from a representative 7000-lb winged eVTOL with a 20-mile range, requiring normalized power rates of 6.4E during takeoff and landing and 1.6E during cruise. Periodic Reference Performance Tests are conducted to track capacity fade, internal resistance evolution, and energy efficiency. The cells retained over 90% of their initial capacity after 3,270 cycles, while total energy efficiency remained stable at 91%, comprising impedance and hysteresis-driven components of approximately 94% and 97%, respectively. Direct current internal resistance exhibited an initial decrease before stabilizing, yet total discharged capacity increased from 1.81 Ah to 1.84 Ah, indicating aging-driven polarization effects not captured by DCIR. A zero-order equivalent circuit model underpredicts discharged capacity by approximately 4% for fresh cells, increasing to nearly 6% at cycle 3,270 due to unmodeled time-dependent polarization effects. These results demonstrate that while modern Li-ion cells exhibit strong durability under repetitive high-power usage, the accuracy of battery performance prediction is strongly dependent on dynamic impedance effects beyond conventional DCIR-based models.
From material selection to system-level performance Transportation's shift toward electric power - whether cars, planes, or big trucks - has made battery engineering a pretty wild, multidisciplinary puzzle. It's not just about coming up with a prototype anymore. To hit the right mix of energy density, power, safety, cost, and longevity, teams need to rethink how they design these systems. Enter simulation and modeling tools. Engineers now use these digital tools to blend electrochemistry, thermal management, materials science, and whole-system design. Instead of jumping straight to building, they try out battery ideas in the virtual world first, speeding up how long it takes to figure out what works and what doesn't and boosting the reliability of those batteries in the real world. Today, battery simulation spans multiple scales from the behavior of active materials within electrodes to the thermal dynamics of the entire battery pack as integrated into a vehicle.
Battery thermal management is crucial for ensuring the safety, efficiency, and longevity of lithium-ion battery packs, particularly in electric vehicles (EVs). The primary purpose of a lithium-ion battery in an electric vehicle is to store and provide electrical energy for vehicle propulsion while maintaining safety under different operating conditions. This work proposes a thermal correlation between 1D CFD simulation and experimental test data under passive environmental heat exchange conditions without active coolant flow of a battery pack comprising four modules. An environmental exchange test was conducted using a 50% state of charge (SOC) battery pack, which is stabilized at 25°C to assess passive heat dissipation, thermal soak behavior, temperature distribution, and potential thermal runaway risks. The simulation predictions correlate well within a 1.5°C range compared to test results using ambient temperature and flow inputs, which confirms the reliability of the modeling approach. The simulation work was carried out using the GT-SUITE software. This study improves battery thermal management strategies by enhancing predictive accuracy and optimizing simulation frameworks for real-world applications. It minimizes overheating risks in practical scenarios, such as prolonged exposure to high ambient temperatures.
As the utilization of lithium-ion batteries in electric vehicles expands, monitoring the usable cell capacity (UCC) is essential for ensuring accurate state-of-health (SOH) estimation. Battery performance degradation is influenced by temperature and constraints. Capacity tests in laboratory settings are typically conducted at low C-rates to approximate equilibrium conditions, whereas in real vehicle applications, charging currents are often much higher. This discrepancy in rates frequently results in deviations between laboratory characterization and on-board Battery Management Systems (BMS) capacity estimation. To investigate how C-rate of diagnostic Reference Performance Test (RPT) modulates aging effects under temperature and mechanical loading, we conducted long-term cycling tests on lithium iron phosphate/graphite pouch cells at 25°C and 45°C under different constrained conditions. The cycling protocol is a tiered multi-rate protocol. Cells were aged at Block1 under 1C, and UCC evolution was quantified after each block. The result shows battery aging can be divided into three stages: a decelerated, steady, and accelerated aging stage. The degradation of LFP cells is dominated by loss of lithium inventory (LLI), and elevated temperature accelerates the degradation. By combining differential voltage analysis (DVA), direct current internal resistance, electrochemical impedance spectroscopy, and ultrasonic testing, we found that under 45°C free condition, accelerated aging is consistent with intensified SEI growth and electrolyte decomposition, accompanied by increased LLI, gas-generation, and increased resistance. These signals emerge earlier than the apparent capacity divergence and may serve as early indicators for predicting the onset of rapid degradation. Appropriate constrain mitigates aging, and its influence becomes more pronounced when using higher-rate RPTs. At 25°C, high-rate RPTs exhibit an apparent capacity recovery. DVA analyses indicate the recovery originates from gradual activation of lithium. Overall, these findings illustrate and explain the degradation characteristics and capacity recovery phenomenon, providing a reference for connecting laboratory standard tests with on-board BMS capacity estimation.
This research demonstrates a new way to make carbon-based battery materials much safer, longer lasting, and more powerful by fundamentally redesigning how fullerene molecules are connected. Today’s lithium-ion batteries rely mainly on graphite, which limits fastcharging speed and poses safety risks due to lithium plating. These research findings mean progress toward safer electric vehicles, longer-lasting consumer electronics, and more reliable renewable-energy storage.
A joint research team led by Professor Soojin Park and Dr. Dong-Yeob Han of the Department of Chemistry at POSTECH, together with Professor Nam-Soon Choi and Dr. Saehun Kim of KAIST, and Professor Tae Kyung Lee and researcher Junsu Son of Gyeongsang National University, has successfully achieved a volumetric energy density of 1270 Wh/L in an anode-free lithium metal battery. This value is nearly twice that of lithium-ion batteries currently used in electric vehicles, which typically deliver around 650 Wh/L. The achievement was published in Advanced Materials.
Asolid, rather than liquid, electrolyte between the opposite electrodes of a battery should, in theory, enable a rechargeable lithium metal battery that is safer, packs much more energy, and charges considerably faster than the lithium-ion batteries commercially available today. For decades, scientists and engineers have explored several paths to realize the great promise of lithium metal batteries. A major problem with the solid, crystalline electrolytes under study has been the formation of microscopic cracks that grow during use until the battery fails.
Researchers at McGill University have made a major breakthrough in advancing all-solid-state lithium batteries, a promising next-generation technology for electric vehicle (EV) batteries.
Multimodal sensors, capable of simultaneously acquiring multiple physical or chemical signals, have shown broad application potential in fields such as health monitoring, soft robotics, and energy systems. However, current multimodal sensors often suffer from complex fabrication processes and signal decoupling challenges, which limit their practical deployment. To address these issues, this work presents a thin-film temperature–strain multimodal sensor (FTSMS) fabricated via laser processing. The temperature-sensing unit, based on the Seebeck effect, achieves a sensitivity of 9.08 μV/°C, while the strain-sensing unit, utilizing BaTiO₃/AlN@PDMS as the sensitive layer, exhibits a gauge factor (GF) of 43.2. By integrating distinct sensing mechanisms (thermovoltage for temperature and capacitance change for strain), the FTSMS enables self-decoupled measurements over 20–90 °C. Applied in LIB monitoring, it successfully captures real-time temperature and strain variations during charge-discharge cycles and provides multidimensional information throughout thermal runaway (TR) processes, enabling early TR warning and supporting safety-oriented battery design.
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