Electrolyte Wetting and Electrolyte Additive Selection for Lithium-Ion Batteries: Optimization of Electrolyte Filling and Wetting on the Separator and Positive Electrode in Battery Production
Electrolyte filling and wetting is one of the slowest steps in battery production, and a cell that is not fully wet before formation can plate lithium. Measure electrolyte surface tension and contact angle on separators and electrodes to rank each electrolyte additive, separator and electrode treatment before you build cells.
Who this is for: Battery R&D teams, electrolyte and separator suppliers, and cell production engineers working on lithium-ion batteries.
Where it fits: Electrolyte design and additive screening, separator and electrode lot release, and filling process development.
What it does not do: It does not measure ionic conductivity, SEI quality or cell performance, and it does not replace cell builds.
Droplet Lab Team
Droplet Lab builds precision instruments and software for surface science measurement, specialising in contact angle analysis and surface tension characterisation. Used by researchers across materials science, pharmaceuticals, coatings, and advanced manufacturing, Droplet Lab's Dropometer has contributed to studies published in peer-reviewed journals including Advanced Functional Materials (Impact Factor 19). The team combines instrument engineering with deep domain knowledge in wettability science with a focus on practical accuracy.
Why electrolyte wetting matters in battery manufacturing
1.5 h vs under 40%
electrolyte reached every surface in 1.5 hours with optimised filling settings; with poor settings under 40% of the area was wet in the same time.
Günter et al., Journal of Power Sources 517:230668 (2022)
46.2° to 15.2°
contact angle of a LiPF6 carbonate electrolyte on an uncoated PE separator versus an Al2O3 coated one, measured by sessile drop.
Hofmann et al., International Journal of Molecular Sciences 16:20258 (2015)
Sources: D. L. Wood III, J. Li, C. Daniel, Prospects for reducing the processing cost of lithium ion batteries, Journal of Power Sources 275:234 to 242, 2015; F. J. Günter et al., Influence of pressure and temperature on the electrolyte filling of lithium-ion cells, Journal of Power Sources 517:230668, 2022; A. Hofmann et al., Interaction of high flash point electrolytes and PE based separators for Li-ion batteries, International Journal of Molecular Sciences 16:20258 to 20276, 2015. Figures come from these sources, not from Droplet Lab measurements.
What this electrolyte wetting check does and what it does not
A quick reference for battery teams checking fit before reading further.
Evidence Box
Slow or incomplete electrolyte wetting of separators and electrodes, and choosing additives and materials that wet faster.
There is no battery specific wetting standard we know of. Contact angle follows the general sessile drop method, and surface tension the pendant drop method.
The Dropometer drop shape method was validated against a KRUSS DSA100E in two peer reviewed papers, in Review of Scientific Instruments and Colloids and Surfaces A.
A North American battery materials R&D team uses the Dropometer to see how ionic liquid and aqueous electrolytes wet treated cathode and anode materials.
Hofmann et al. measured electrolyte surface tension by pendant drop and separator wetting by sessile drop, the same two methods the Dropometer runs.
Wetting readings rank materials. Conductivity, SEI and cell performance still need electrochemical tests and cell builds.
What electrolyte wetting question are you trying to answer?
Pick the card closest to your role. Each one points to the part of this page that answers it.
Electrolyte R&D
You are choosing additive quantities and solvent ratios. Surface tension and contact angle on your separator and electrodes show the effect of additives on wetting before you commit to cell builds and formation.
Separator or electrode supplier
Customers report slow filling with some lots. A contact angle and absorption check on each lot catches finish, coating or calendering changes before material ships.
Cell production engineer
Wetting time sets how long cells wait before formation. Knowing which materials wet fastest helps you set filling and wetting process windows and avoid lithium plating from incomplete wetting.
Is this the right test for your electrolyte wetting problem?
It helps when the question is how well a liquid electrolyte wets a material. It helps less for in cell distribution and electrochemistry.
Good fit if
Less relevant if
How to optimise electrolyte wetting and additive selection
The answer in under a minute.
Measure the battery electrolyte's surface tension by pendant drop, then its contact angle and absorption time on your separator and electrodes. Lower surface tension and lower contact angle usually mean faster wetting. Use the readings to choose additive quantities and materials, then confirm wetting time in cells before formation.
The Dropometer contact angle and surface tension kit runs both checks with disposable plastic needles; our contact angle measurement guide and surface tension measurement guide explain the methods. A North American battery materials R&D team uses it on ionic liquid and aqueous electrolytes. Our wettability glossary entry and transportation guide cover the wider context.
Expert perspective on additive screening
Surface tension versus concentration is one of the few measurements that lets you watch a surfactant reorganise an interface in real time; read the curve, not just the endpoint.
Why filling liquid electrolytes in lithium-ion batteries is slow
In battery manufacturing, the liquid electrolyte must fill every pore of the separator and the positive and negative electrodes before formation, especially in lithium-ion batteries using a carbonate-based electrolyte. The wetting process is slow: Wood and colleagues at ORNL describe a standard 10 to 14 day wetting and formation process. How fast it goes depends on the electrolyte composition, electrolyte viscosity and surface tension, and on how the electrode material and separator surfaces wet. Process settings matter too: in one neutron imaging study, a visualization of the electrolyte filling, optimised pressure and temperature wet a large cell in 1.5 hours while a poor process wet under 40% of the area in the same time. Incomplete wetting has a cost. Hagemeister and colleagues found strong lithium plating in pouch cells charged before they were fully wet, and concluded that about 98% wetting is needed before formation. Each electrolyte additive, separator coating or calendering change shifts this behavior. Contact angle and surface tension measurements show the shift before you build cells.
Why electrolyte wetting is slow and what to check
Why:
- Polyolefin separators have low surface energy, so carbonate electrolytes sit at a high contact angle and enter the pores slowly.
How to detect:
- High contact angle and long absorption time on the separator against a coated or treated reference.
Corrective action:
Compare ceramic coated or surface treated separators, or a wetting additive, to improve the wetting. Our guide to reproducible contact angle measurement covers fair comparisons.Why:
- Higher lithium salt concentration and some electrolyte solvent choices raise viscosity and slow wetting; the stability of the electrolyte limits how far you can change it.
How to detect:
- Surface tension changes with composition, and absorption is slower even when contact angle is similar.
Corrective action:
- Screen solvent ratios and salt levels on the same samples, and record viscosity alongside surface tension.
Why:
- Film-forming additives such as VC are chosen for the solid electrolyte interphase, not for wetting; some barely change surface tension.
How to detect:
- Surface tension and contact angle stay close to the base electrolyte at the planned concentration.
Corrective action:
- Measure the effect of additives at several concentrations, and pair a film-forming additive with a wetting aid if needed.
Why:
- Heavy calendering, binder at the surface or a dense coating slow electrolyte infiltration into the battery electrode. Graphite anodes for lithium-ion batteries usually wet much faster than NMC cathodes (Davoodabadi et al., 2019), so a slow graphite electrode is a warning sign.
How to detect:
Long absorption time on the electrode surface after a calendering change. Our contact angle reference values give a sense check for common materials.Corrective action:
- Compare calendering settings and check porosity; track absorption time by electrode batch.
Why:
- Reactions between the electrolyte and water turn LiPF6 into HF and change the electrolyte components, and residues on separators change wetting.
How to detect:
- Readings drift through the day or differ between storage conditions.
Corrective action:
- Measure in a controlled atmosphere, keep vials sealed, and use a fresh needle for each liquid.
Why:
- Viscosity rises at low temperature, so wetting slows.
How to detect:
- Absorption time rises when samples and electrolyte are measured cooler.
Corrective action:
- Set filling temperature from your own wetting data; published work shows wetting is fastest at elevated temperature.
Not sure what is slowing your wetting?
Send a separator or electrode lot that wets well and one that does not, and we will compare them on a call.
What an electrolyte wetting record contains
Each test produces a record you can file with the electrolyte, separator or electrode lot. These records can feed into your existing quality records under IATF 16949, ISO 9001 or your battery technology development process.
Materials
Electrolyte and electrode materials: electrolyte, additive and concentration, separator type and lot, electrode type and batch.
Conditions
Atmosphere and moisture level, temperature, and sample storage before the test.
Method settings
Needle type, drop age, drop volume, contact angle read time and spots per sample.
Readings
Surface tension, contact angle at the read time, and absorption time.
Decision
Release, shortlist, retest or hold, with the operator and date.
Drop images
Automatic edge and baseline detection gives the same reading from the same image, so a reviewer can recheck any result.
What to measure for electrolyte wetting
Electrolyte surface tension by pendant drop
Why it matters: Lower surface tension helps the electrolyte spread and enter small pores.
How to interpret: Compare additives and solvent ratios with the base electrolyte. Hofmann et al. measured 29.4 mN/m for LiPF6 in EC/DMC.
When it is not enough: It says nothing about the solid; measure contact angle too.
Contact angle at a fixed read time
Why it matters: It shows the wetting behavior of the electrolyte on the separator before it soaks in.
How to interpret: Read at the same time after the drop lands for every sample. Set gates from your own reference lot.
When it is not enough: On very porous samples the drop soaks in too fast for a stable angle.
Absorption time into separator or electrode
Why it matters: Porous electrodes absorb drops, so the wetting rate is a better measure than angle.
How to interpret: Shorter is faster wetting; compare at the same drop volume and use one criterion for the end point.
When it is not enough: It is a surface test, not the full electrode and electrolyte system in a cell.
Surface tension against additive concentration
Why it matters: It shows where more additive stops helping.
How to interpret: Measure several concentrations of the additives and use the curve for the selection of electrolyte additive quantities, not a single point.
When it is not enough: It does not show the additive's effect on SEI or gas.
Validated measurement approach for electrolyte wetting
How the Dropometer itself has been validated, and where customers have used it.
Peer reviewed method
The Dropometer drop shape method is published in Review of Scientific Instruments and Colloids and Surfaces A. Contact angle was validated against a KRUSS DSA100E, with a published accuracy of 0.35°.
See the validation papersCustomer evidence in battery R&D
A North American battery materials R&D team needed to see how ionic liquid and aqueous electrolytes wet cathode and anode materials after surface treatment. Some of its electrolytes attack metal, so Droplet Lab set up an automatic dropper with disposable plastic needles for contact angle, surface tension and surface energy.
Read the case studyHow to screen electrolyte additives and separators by wetting
Six steps for one electrolyte system and cell design. Repeat when a material or additive changes.
Plan safe handling
Decide where the electrolyte can be handled: a glovebox, a dry room, or a fume hood for less sensitive electrolytes. Keep vials sealed.
Lock the method
Fix needle type, drop age, drop volume, contact angle read time and spots per sample, with a fresh needle for each liquid.
Baseline the base electrolyte
Measure its surface tension, and its contact angle and absorption time on reference separator, positive electrode and negative electrode samples.
Screen additives and materials
Measure various electrolyte formulations and each additive at several concentrations, and each separator or electrode option, on the same day.
Confirm in cells
Turn the lab ranking into a recommendation, build test cells with the best options and compare wetting time and formation results with the lab readings.
Release lots and trend
Set gates from that comparison, release separator and electrode lots against them, and trend by supplier.
We completed our gage R&R study on the unit and it performed very well.
Brandon Barbee
Corporate Quality Engineer, Zeus Industries, Polymer Manufacturing
Download the electrolyte wetting and additive screening SOP
A two page SOP you can adapt for your electrolyte, separators and electrodes, with the method lock, gate setting, safety notes, a troubleshooting table and a record sheet.
Contact angle measurement with the Dropometer
Example electrolyte additive and separator screening log
Example data only. Your values and gates will differ and must come from your own references.
Example gates: contact angle at 10 s at or below 35° and absorption at or below 60 s on the separator. Additive A lowered surface tension and wetting time, so it is shortlisted. Additive B made no difference. A new PE lot wet worse than the reference, so it is held.
Example electrolyte additive and separator screening log
| Electrolyte | Separator | Surface tension (mN/m) | Contact angle at 10 s (°) | Absorption (s) | Result |
|---|---|---|---|---|---|
| Base electrolyte | PE, reference lot | 29.5 | 46 | 120 | Reference |
| Base + additive A 0.5 wt% | PE, reference lot | 26.8 | 31 | 45 | Shortlist |
| Base + additive B 1 wt% | PE, reference lot | 29.2 | 45 | 115 | No gain |
| Base electrolyte | Al2O3 coated PE | 29.5 | 16 | 20 | Shortlist |
| Base electrolyte | PE, new lot | 29.5 | 58 | 210 | Hold |
Example data, not customer data. LiPF6 carbonate base electrolyte, measured in a dry atmosphere at 25 °C; ranges are in line with Hofmann et al. (2015).
The order to check signals when wetting slows
Check these in order. Each one rules out a cause before you look at the next.
Electrolyte surface tension
Shows whether the liquid itself changed.
Separator contact angle
Shows whether the separator lot or coating changed.
Electrode absorption time
Shows whether calendering or binder changed the electrode surface.
Atmosphere and storage
Moisture and storage time for liquids and samples.
Filling process settings
Dosing pressure, wetting pressure, temperature and rest time in the cell.
Common questions about electrolyte wetting and additives
Questions battery R&D and production teams ask before adding contact angle and surface tension.
Why does electrolyte wetting take so long?
The electrolyte has to fill fine pores in the separator and both electrodes, and carbonate electrolytes wet polyolefin separators poorly. Wetting speed depends on surface tension, viscosity, pore structure and process settings. Studies on the wetting of cells show it is slow: Wood and colleagues describe a standard 10 to 14 day wetting and formation process.
How do electrolyte additives for lithium-ion batteries affect wetting?
The use of electrolyte additives for wetting is simple in principle: wetting additives and surfactants lower surface tension and contact angle, a wetting enhancement that speeds infiltration without hurting the performance of the electrolyte if chosen well. Adding VC to the electrolyte, a film-forming additive, is done for the SEI and may change wetting little. Measure surface tension and contact angle at several concentrations to see the effect of additives before cell builds.
What happens if cells are not fully wet before formation?
Dry areas are not used, and current concentrates where the electrode is wet. Hagemeister and colleagues found strong lithium plating in pouch cells charged before complete wetting, and set about 98% wetting as the threshold to begin formation.
Can contact angle be measured on porous electrodes?
Only briefly. Porous electrodes in lithium-ion batteries soak up the drop, so a static angle is not meaningful for long. Read the angle at a fixed short time and record absorption time; the rate is the more useful number for electrodes.
Do we need a glovebox?
LiPF6 carbonate electrolytes react with moisture and form HF, so most teams working on lithium batteries handle them in a glovebox or dry room. Plan where the instrument will sit before you buy. Ionic liquid and aqueous electrolytes, as in our case study, are easier to handle.
Which standards apply?
We know of no battery specific wetting standard. Contact angle follows the general sessile drop method and surface tension the pendant drop method. Our guide to the best contact angle goniometer for industrial QA compares instruments for lot release.
What changes when you screen electrolyte wetting before cell builds
Typical changes in how teams work. Benchmarks are given only where a published source exists.
Before and with wetting screening
| Metric | Before Dropometer | With Dropometer | Indicative Benchmark |
|---|---|---|---|
| Additive screening | Cell builds for each candidate | Surface tension and contact angle first | No published benchmark; track on your own candidates |
| Wetting and formation time | Fixed long rest | Materials chosen for faster wetting | 10 to 14 day wetting and formation baseline (Wood et al., 2015) |
| Process window | Trial and error | Lab wetting data plus cell checks | 1.5 h full wetting vs under 40% with poor settings (Günter et al., 2022) |
| Separator lot release | Supplier certificate only | Contact angle and absorption gate | No published benchmark; track on your own lots |
See the check on your own materials
Send a separator or electrode that wets well and one that does not. We will show the difference on a call.
Estimate saved development trials
Enter your own numbers. The result is an estimate, not a Droplet Lab claim.
Battery electrolyte R&D cost estimate
Estimate saved development trials and lab cost.
Result
Monthly savings = materials saved + technician time saved from reduced iterations.
What wetting readings cannot tell you about a battery
Honest limits, so you know when to reach for another test.
Surface tension and contact angle rank electrolytes and materials by wetting. Ion transport, SEI, gas, electrolyte distribution in the cell, the performance of lithium-ion batteries and overall battery performance still need electrochemical tests and cell builds.
Evidence and related battery wetting workflows
These pages cover the customer evidence, the methods and the other battery and electrode wetting problems behind this check.
Case study
Battery materials R&D team
Ionic liquid and aqueous electrolytes on treated electrodes.
Instrument
Dropometer
Pendant drop surface tension and contact angle in one kit.
Guide
Contact angle measurement
How sessile drop contact angle works.
Guide
Surface tension measurement
How pendant drop surface tension works.
Related use case
Battery wetting and electrolyte spreading
All battery wetting use cases in one place.
Related use case
Corrosive liquids
Contact angle and surface tension of acids and other corrosive liquids.
Related use case
LIG electrode QC
Wetting checks on laser induced graphene electrodes.
How this page was created
Editorial and technical transparency notes for this page.
Drafting assistance
Drafted with Claude Opus 5.5 (Anthropic) using web search for sources, then edited by the Droplet Lab team.
Technical review
Reviewed and edited for technical accuracy by the Droplet Lab Team.
Verification steps
Standard identifiers, units, thresholds and key procedural claims are checked against cited sources before publication.
Updates
Reviewed every 12 months or when the underlying method changes.
Report a correction
Spotted an issue in this summary? Send a correction request and our team will review it.
Correction Request
We work hard to keep this page accurate and up to date. If you spot an error (wrong revision/year, missing requirement, incorrect interpretation, or broken link), tell us and we'll review it.
Contact us to report a correctionReferences
Lux, S. F. et al. The mechanism of HF formation in LiPF6 based organic carbonate electrolytes. Electrochemistry Communications 14:47 to 50, 2012.
https://doi.org/10.1016/j.elecom.2011.10.026Chen, X. et al. Contact angle measurement with a smartphone. Review of Scientific Instruments 89(3):035117, 2018.
https://pubs.aip.org/aip/rsi/article-abstract/89/3/035117/368179/Contact-angle-measurement-with-a-smartphoneSurface tension measurement with a smartphone using a pendant drop. Colloids and Surfaces A: Physicochemical and Engineering Aspects.
https://www.sciencedirect.com/science/article/abs/pii/S0927775717307744