Corrosion: The Primary Threat to Battery Pack Longevity
This article is contributed by Luke Workman and Electric Goddess
- Corrosion is the primary cause of failure in vehicle battery packs during their long service periods.
- If batteries are not adequately protected from corrosion, they will be vulnerable to failure, including catastrophic thermal events. Corrosion risk can be greatly reduced by adhering to design principles that mitigate vapor ingress (e.g., road salt spray, humidity) into the battery pack.
- A long-term, environmentally rugged solution for battery pack design is to use potting material to encapsulate all corrosion-sensitive surfaces of the pack. Corrosion mitigation requires solutions to protect circuit boards, connectors, and power bussing.
- Current industry standards for safety testing do not always represent the operational and environmental conditions that battery packs experience in the field. Safety standards need to be updated to address corrosion-related pack failure.
Corrosion in Battery Packs
Understanding the cyclic corrosion processes that occur within a lithium-ion cell plays a critical role in the design of a battery pack. While the redox reactions of the lithium and electrolyte with the anode and cathode during cycling are fundamentally important to cell operation, they are not a threat to long-term reliability and safety. Further, production cells are quality tested and screened such that their specification and performance are well understood. Provided the quality control methods are effective, there is a low probability of finding serious cell defects in end-use products. The leading threat to battery packs, however, is the corrosion that can occur on the external surfaces of components and the interconnect bussing of cells.
Corrosion refers to the slow electrochemical reaction of components with oxidants such as chlorides, sulfates, carbonates, oxygen, and hydroxides. A well-known example of electrochemical corrosion is rusting, or the formation of iron oxides. The rusting of iron produces various oxide states and salts which show distinctive coloration from red-orange to black. When corrosion occurs in materials other than metals, such as ceramics or polymers, the term “degradation” is more commonly used.
Corrosion degrades the useful properties of materials and structures including strength, appearance and permeability to liquids and gases.
When humidity condenses as liquid droplets onto internal surfaces in a battery pack, condensate pathways are formed. Driven by capillary action, these droplets then wick into interfaces between conductive surfaces. Corrosion is then caused by voltage gradients across these aqueous condensate pathways in cells, cell interconnects, thermal management interfaces, connectors, bussing, etc. The droplets travel a distance along the interface that is proportional to the surface energy along the interface, and form connecting capillary pathway networks between metal-metal, polymer-metal, and polymer-polymer surface interfaces. Even if the condensate droplets are originally formed with low ion content, exposure to atmospheric CO₂ (410 ppm) results in the formation of carbonic acid (H₂CO₃). This acid functions as an electrolyte that, when combined with a voltage difference, rapidly corrodes nickel, copper, aluminum, iron, tin, and other materials.
Even gold, platinum or tantalum plating of conductive elements in the battery assembly cannot protect against dissociation potentials over ~6 Vᴅᴄ The corrosion of these platings then exposes the base metals to high electrolysis potentials from the EV battery. Since the corrosion process is slow, the liquid water may evaporate before the metal has progressed to failure. Still, the dissolved salts are left behind as salt residues, which offer favorable pathways for wicking condensed water, reinforcing the corrosive pathway with each subsequent exposure.
If the salt residue-hydrate conversion cycle reaches the correct hydrate state, a molten ionic liquid can be created at room-temperature, which conducts electricity very effectively.
Vulnerable locations in batteries include circuit boards, connectors, flex circuits, sense tap, temperature sense harnessing, and any interfaces that offer both a voltage difference and the opportunity for condensates to wick across. During a battery’s use, it can be exposed to water vapor, tire spray from salted winter roads, ocean mist, powerwashing, cleaning detergents and solvents.
The following design characteristics of a battery pack can influence gas exchange and the rate of corrosion:
- Temperature fluctuation from the cells’ operation and day/night weather cycles
- Atmospheric pressure changes between high and low altitude that expand and contract air volumes
- Large voltage gradients across the thinnest voltage regions of the pack, such as the dielectric layer maintaining isolation between cells and the “cold plate” or cooling manifold. This is due to dielectric decay from ionic migration driven by the electric field.
Corrosion is a gradual process that steadily removes material from the anode side and deposits corrosion byproducts on the cathode side. Since the voltages present in batteries greatly exceed the galvanic series, the influence of the metal composition is insignificant compared to actual voltages imposed directly across the ionic pathway.
Battery systems that are insufficiently protected from corrosion can show the effects of failure in weeks, months, or even years after a product enters service. The onset of failure depends on several factors such as temperature, humidity, free gas volume, voltage gradient strength and available surface metal ions. Monitoring the chassis-to-cell string isolation resistance by the BMS is often the first available warning sign that a corrosion process has been taking place. In these situations, actions must be taken to prevent the risks of a fire hazard. It is much easier to discover evidence of corrosion-driven failures in the early stages. After corrosion has progressed to molten salt-bridging and fire, identifying root causes may be challenging.
Clear evidence of corrosion-induced failure can sometimes still be apparent post-event, but requires more tedious forensics, so it is always ideal to analyze isolation faults that may have appeared prior to a severe thermal event.
One method to conclusively determine if a chassis isolation fault is related to a corrosion path is to perform bi-polar cyclic voltammetry sweeps over a long time interval. For example, it might take 5 minutes to sweep up, and another 5 minutes to sweep down voltage between the chassis and each end of the battery string assembly. Non-linearities in the sweeps are the signature of an electrolysis pathway. High resistance (>1 kΩ) isolation faults in EV packs are often induced by condensate paths and may cause the chassis to take on the voltage of the interconnect string along that path. These condensate pathways tend to become more conductive over time.
One common factor accelerating corrosion is the cooling of gas inside the battery assembly in the presence of high humidity or corrosive vapors. Testing at high temperatures in humidity or salt spray does not validate vapor ingress resistance, as the contraction of internal air volume in the pack enhances the mechanics of ingress due to the favorable pressure differential.
While the isolation fault remains a single-point failure, the battery can still be safely decommissioned. When the liquid path bridges between the chassis and any secondary voltage potential in the EV assembly, highly accelerated corrosion occurs, driven by the high pack voltages in EVs. These voltages can split the surface species into radical ion forms and/or re-bond radicals into new electrically-formed species. Even very reactive, short-lived species and compounds can be evolved steadily through sustained electrolysis.
Mitigating Corrosion in Battery Packs
Safe, reliable battery design solutions that mitigate against corrosion are critical to the electrification of transportation. A battery system that does not survive in the wild will ultimately be more expensive than a battery that can be used over its full intended lifetime. Designing to mitigate corrosion not only prevents recalls and safety hazards, but also decreases waste across the industry. Second-life battery applications, which are of increasing interest to promote sustainability, are not practical or possible without batteries surviving their first life.
While there are many battery safety test standards in use today, they fall short of replicating real-world battery operation and do not test in multi-metal ion salt fog blends while the pack undergoes temperature swings. For instance, the published “Salt Fog Test” standards from UL, SAE, ASTM all use 99.9% NaCl blended with distilled water in the test specification. The advantage of this is a repeatable test anywhere in the world. The downside, however, is that this test is passed too easily, leading to a false sense of product integrity. When the product is exposed to the compositions of road salt mist that are actually sprayed onto the vehicle during use, thermal runaway can be induced by the many ions other than Na⁺ and Cl⁻ that are more prone to forming molten salt bridges at low melting temperatures.
Safety standards and test conditions need to be updated to include the multi-ion salt mixes present in real road salt and marine sprays. These include Na⁺, Ca²⁺, K⁺, Mg²⁺, Al³⁺, paired with Cl⁻, CO₃²⁻, and SO₄²⁻ ions. Endemic sources of metal ions in the battery assembly or BMS may include Fe²⁺, Sn²⁺, and Cu²⁺.
All of these salt compounds dissociate in molten form to free radical ions between 1.5 and 4.5 V. While these compounds have negligible conductivity in their crystalline state, they become impressive conductors in their molten ionic state and are capable of rapidly discharging at 10’s or 100’s of kW from the battery assembly, causing localized heating that can lead to runaway.
These are several methods to mitigate the risk of corrosion in battery pack design:
- Minimization of voltage gradients (Volts/meter) in the layout
- Encapsulation of all vulnerable areas of the assembly, including cells and interconnects
- Dam-and-fill encapsulation of circuit boards for protection
- Anti-capillary wires to prevent water filling in connector cavities
- Dielectric gel in connector cavities
- Repeatable processes during manufacturing, especially that of interconnect process between cells to eliminate electrolyte weepage from cells
Voltage Design Considerations
The voltage gradient creates dielectric stress in the materials, which can lead to electromigration and dielectric decay. To improve heat transfer, packs are designed with minimal distance, often 200 μm or less between the cells and a common heat transfer system. In a 400 Vᴅᴄ system, this creates a dielectric stress of 2 MV/m. While this is not enough to instantly break down many dielectrics, it is sufficient to drive ionic migration and decomposition in many materials over time. Furthermore, when materials are saturated with humidity, effects induced by ionic migration occur much more rapidly. Polymers in the nylon family exhibit these effects quickly; materials like carbonates, epoxides, and poly-amides tend to be slower to fail, and arc tracking plasma heating and fire is the typical failure mode. Polypropylene, urethanes, HDPE, polyureas, and fluoropolymers tend to exhibit excellent long-term resilience to dielectric stress, but individual stack-up material compatibility testing should be performed with the representative interface materials and increasing voltage stress, including stress-to-failure testing. It is important to understand that a hi-pot test, or any voltage stress testing that is completed in less than a day cannot measure dielectric decay; rather, these procedures test resistance to instantaneous dielectric breakdown, which is largely unrelated to its dielectric decay and the mechanics of ionic migration.
Electromigration occurs when metal atoms are transported along the paths of peak electrostatic field gradients induced by a voltage differential. Similarly, in a dielectric material, dielectric decay occurs when ions move through the material due to a voltage gradient caused by an electric field. Both of these processes exacerbate corrosion: electromigration forms pits that preferentially corrode whereas dielectric decay degrades formerly protective polymers and coatings. Migrated ions in the polymer tend to improve ionic conductivity, enabling additional ions to be ripped from the metallic surface and reinforcing the corrosion pathway.
Use Potting in Battery Packs
Potting is composed of a polymer material, which is injected into the battery pack between cells or used to protect electronics. Since weight is a strong consideration for pack design in vehicles, utilizing a potting material in the battery pack and electronics can seem counterintuitive as it adds weight and decreases the gravimetric energy density. Despite this drawback, potting is often the best option for ensuring pack reliability with the lowest size and weight penalties, and decreases the risk of corrosive failure, fire losses and/or recalls.
Potting materials that are endothermic fillers undergo a one-time thermo-chemical decomposition, which limits cell-to-cell heat transfer, enabling very tight cell spacing while maintaining outstanding resistance to thermal runaway propagation and limiting the penalties on pack energy density.
Conformal coatings designed specifically to protect circuit boards sometimes yield similar failure modes during corrosion testing, albeit with marginally longer time intervals when compared to a bare assembly. The ‘dam-and-fill’ method for protecting PCBAs is a repeatable method of ensuring defect-free encapsulation and yields excellent results when exposed to mixed salt sprays.
Not all potting materials are created equal. Some oxamine-cure silicone-based materials are not recommended as ionic migration can occur under prolonged DC voltage stress, whereas platinum cure silicones generally do not exhibit this effect. In applications dedicated to optimizing battery safety and weight such as aircraft, multi-layered potting can be used, with different layers carefully selected for mechanical strength, cell failure protection, and corrosion prevention.
The activation of current interrupt devices (CIDs) in cylindrical cells is often a concern in potted battery packs. Based on many internal tests of CID activation in assemblies with and without potting, however, there is no statistically significant difference in the activation pressure. This is because internal activation pressures of the CID diaphragm are about 350–500 psi, significantly greater than the resistance offered by 500µm of displacement in the soft durometer potting compounds.
Since pouch cells expand as they age (6–12% for Gr/NCM), it is critical to account for this space in the pack at the beginning of life. Pouch cells must also have low-density displacing materials for each pouch that can displace the local potting material to accommodate gas headspace. For most pouches, this is the area where the tab is encapsulated in the pouch. This is the only meaningful gas volume inside the pack envelope where gas presence does not impact the cell’s electrochemical performance.
Without potting, the battery is exposed to air, humidity, and other environmental contaminants that can initiate and exacerbate corrosion. A common misconception is that using a robust seal is good enough to keep water and contaminants out of the pack. In reality, not only are the particles of water vapor smaller than droplets of liquid water, but water itself is a smaller and lighter molecule than the N₂ and O₂ composing the bulk of our atmosphere.
The higher the voltage gradient, or higher the battery voltage, the higher the force of these corrosive processes.
Low voltage batteries mitigate these issues by decreasing the voltage gradients and, thus, the risk of electromigration and dielectric decay failure. More information on low voltage battery design and other benefits is available here.
In industry, the reasons publicly stated for recalls are seldom related to the actual causes of the recall. Corrosion-induced failure modes and forensics are unfortunately often misdiagnosed by industry experts even today. Industry standards for safety testing must seek to assess susceptibility to corrosion-induced failures and develop test methods that can reliably recreate long-term failure modes, including sprays of several road salt blends. Such tests must be accelerated to enable multiple iterations between corrosion resistance design and testing validation. High-voltage architectures show increased corrosive driving forces, dielectric decay and ionic migration risks; these have limited awareness in the industry today.
While cell scientists in the industry take efforts to tame cyclic corrosion occurring inside a cell, the effects of corrosion outside of the cell are the leading reason for EV battery replacement today. Battery designs that consider and address each corrosion risk area, from the cells to the connectors, as well as robust safety testing that mimics real-world environmental conditions are crucial for reducing recalls and fires.
Luke “LiveForPhysics” Workman began his battery career working for Microsoft data centers. He then served as the lead battery designer for Zero Motorcycles where a collaboration with Farasis Energy led to a robust industry standard in pouch cell battery design topology. During his time freelance consulting, he became an industry leader in powersports and electric aviation. His passion for physics, racing, and mindful design considerations and the lessons learned along the way have paved his way to success. Luke is also known for his YouTube videos torturing batteries, for having the fastest electric bicycle on the planet, DeathBike, and for hotrodding EVs to push the limits of performance. He is the Chief Scientist at Electric Goddess, a battery consultancy firm with an analytical test lab that thrives in solving the industry’s toughest challenges.
Special thanks to Erika Guerrero and Jill Pestana for their contributions to this article.
Electric Goddess contributed this article to bring more awareness to the challenge of corrosion-induced failures in the industry. For more information on corrosion mitigation, contact Electric Goddess here.
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