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HS Code |
823247 |
| Chemical Name | Lithium Phosphorus Sulfide Chloride |
| Chemical Formula | Li3PS4-xClx |
| Appearance | White to pale yellow solid |
| Molar Mass | Varies (depends on x) |
| Density | ≈1.9 – 2.0 g/cm3 |
| Melting Point | Approximately 300°C |
| Ionic Conductivity | Up to 10^-3 S/cm at room temperature |
| Solubility In Water | Insoluble |
| Stability | Sensitive to moisture and air |
| Primary Use | Solid electrolyte in lithium batteries |
As an accredited Lithium Phosphorus Sulfide Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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Purity 99.9%: Lithium Phosphorus Sulfide Chloride with purity 99.9% is used in solid-state electrolyte formulations for lithium-ion batteries, where it enhances ionic conductivity and minimizes impurities for higher energy efficiency. Particle size <2 μm: Lithium Phosphorus Sulfide Chloride with particle size less than 2 μm is used in composite cathode manufacturing, where it ensures homogeneous mixing and improves interface stability. Melting point >400°C: Lithium Phosphorus Sulfide Chloride with melting point above 400°C is used in high-temperature battery prototypes, where it provides thermal stability and prevents electrolyte degradation. Ionic conductivity >1 mS/cm: Lithium Phosphorus Sulfide Chloride with ionic conductivity greater than 1 mS/cm is used in all-solid-state lithium batteries, where it promotes rapid lithium-ion transport and supports fast charging cycles. Moisture stability <0.1% weight loss: Lithium Phosphorus Sulfide Chloride with moisture stability below 0.1% weight loss is used in air-sensitive cell assembly, where it limits hydrolysis and prolongs material shelf-life. Crystal structure tetragonal phase: Lithium Phosphorus Sulfide Chloride with tetragonal crystal structure is used in research-grade solid electrolyte studies, where it ensures reproducible electrochemical performance. |
| Packing | 500g of Lithium Phosphorus Sulfide Chloride, sealed in a moisture-resistant amber glass bottle with tamper-evident cap, labeled for research use. |
| Container Loading (20′ FCL) | Container loading (20′ FCL) for Lithium Phosphorus Sulfide Chloride ensures secure, moisture-proof packaging, typically 10–12 metric tons per container. |
| Shipping | Lithium Phosphorus Sulfide Chloride should be shipped in tightly sealed containers under inert gas (such as argon) to prevent moisture and air exposure. Store and transport in cool, dry conditions, compliant with local hazardous material regulations. Label packages properly as a reactive, potentially hazardous chemical. Handle only with appropriate safety precautions. |
| Storage | Lithium Phosphorus Sulfide Chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. It must be kept away from moisture, heat, and incompatible substances such as acids and oxidizers. The storage area should be equipped with appropriate spill containment and fire suppression systems, and access should be restricted to trained personnel only. |
| Shelf Life | Lithium Phosphorus Sulfide Chloride generally has a shelf life of 1–2 years when stored in airtight containers, cool, and dry conditions. |
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Lithium battery innovation has moved so fast, everyone along the supply chain is feeling the pressure. We’ve seen customers looking for safer, more reliable solid-state electrolytes. Years ago, the word was that oxide-based ceramics would win out, but daily factory life showed us how tricky those are to process—high sintering temperature, poor flexibility, high interface resistance. Research groups started to double down on sulfide-based materials, and that’s how Lithium Phosphorus Sulfide Chloride, often called LPSC, began to outpace older concepts.
Most battery fans think of “all-solid-state” as a new-age solution, yet anyone running a pilot line knows how many headaches come with this territory. Sulfide electrolytes set themselves apart by having high lithium-ion conductivity, easy cold pressing, and a wider electrochemical window. The addition of chlorine to the lithium-phosphorus-sulfide backbone changes a lot. This tweak isn’t just another academic exercise — in practice, the chloride content fine-tunes the material’s structure, boosts stability at electrode interfaces, and directly affects moisture stability. Our daily experience shows that the final powder flows better, handles air exposure with far less reaction, and brings packagers fewer complaints down the production line.
The big names in the industry have learned to value LPSC’s touch of chlorine over the old all-sulfide recipes. Early argyrodite-type lithium-ion conductors already solved major bottlenecks in conductivity, but plain lithium phosphorus sulfide mixed poorly with electrodes containing nickel-rich NMCs or even silicon-laced anodes. Chlorination solves interface limitations and makes the product easier to scale uniformly. Working in production, we’ve seen fewer batches lost to material degradation and more consistent surface morphology than with non-chlorinated sulfides.
Some products run with a model grade code attached, and we have seen requests for various mesh sizes, specific lithium to phosphorus to sulfur to chlorine ratios, and custom moisture-preconditioning. Customers running pouch and coin cell lines choose chloride-content between 9-15% by mass to stabilize interfaces. Compared to common LPS (lithium phosphorus sulfide), this variant doesn’t show glassy slumping or reactivity spikes when stored under less-than-perfect glovebox conditions. That means more flexibility on the shop floor, and happier warehouse managers because you don’t lose inventory to accidental exposure.
Lab specs only tell part of the story. Actual manufacturing means dealing with powders — clumping, dusting, moisture exposure, and inconsistent particle size often create more headaches than advertised. The chloride balance in LPSC helps to reduce agglomeration. Most requests for dense packing and minimal voids come from engineers running high-throughput lines. They have shared with us that the best results happen when powders run between 2–5 μm particle size, and our experience echoes this: smaller particles produce higher ionic conductivities, but increase risk of sticking to equipment. By keeping the chloride level tuned, LPSC manages a balance between flow, compaction, and ease of blending.
Shelf life is another practical hurdle. Old school LPS and LISICON compositions degrade quickly in trace humidity, forming H2S and clogging downstream filtration. Over the past two years of shipping LPSC to Asia, Europe, and North America, we've found packs stored in ambient air for up to 30 minutes show only minor surface color change. No comparable lithium phosphate-based solid electrolyte offered that kind of peace-of-mind. Detailed lot testing has recorded ionic conductivities above 6 mS/cm at room temperature consistently, with thermal stability far above other sulfide powders. Communication with end-users proves that these advantages translate to lower rejection rates and higher assembled cell yield.
Much of the feedback we receive comes straight from R&D engineers and plant supervisors. Staff from automotive and grid storage sectors constantly mention how LPSC slashes the time and labor associated with handling, loading, and sealing. Any slip before final pressing costs time and resources; chloride’s presence in LPSC resists atmospheric moisture and keeps surface reactions slower, so rework and reruns are rare. In contrast, older argyrodite compositions forced teams to operate in ultra-dry environments just to keep up yield.
End users running electrolytes through roll-pressing and calendaring lines emphasize stable operation with minimal downtime. One team reported switching from pure Li6PS5Br to LPSC and observing smoother powder flow and finer layer formation along the cathode composite. Batteries using LPSC show fewer short circuits after repeated cycling. Packing density stays consistent, and fewer microcracks form during pressurization cycles — a quiet but significant improvement over earlier sulfide formulas.
Devices prepared with LPSC consistently offer battery test results with higher capacity retention after 100 cycles — typically over 95% — compared to values around 80–85% for those using only LPS. Engineers also report that impedance rise is less drastic over long-term cycling. LPSC’s surface chemistry proves less prone to create unwanted interphases and dead lithium formation, according to half-cell teardown results shared by several academic-industry partners.
Manufacturers feel increasing pressure to keep up with both safety expectations and throughput. Powder form LPSC streamlines this process, reducing labor needed for glove box transfer. Some battery startups cite regulatory worries when storing and transporting older sulfide types prone to H2S release. By integrating chloride into the structure, LPSC grades pass internal safety checks more reliably, ship overseas with fewer regulatory blocks, and even allow for streamlined customs declaration in certain regions.
Solid-state battery adoption in electric vehicles and stationary storage continues to accelerate. In mass production, consistent powder quality can be a make-or-break factor for yields. Over thousands of delivered kilograms, our staff observed that LPSC batches demonstrate reproducibility of ionic conductivity, tap density, and free-flowing quality. The old standard LPS could match one or two of those at a time, but rarely all three. Direct feedback points to a drop in defect rates, which in today’s margin-sensitive business, turns into significant cost savings.
Waste reduction carries equal weight. Handling and recovery operations for spilled or degraded electrolyte have improved, since partially exposed LPSC reprocesses with less performance loss than classical LPS blends. Staff running automated powder dosing tell us fewer alarms go off for stray dust, as the chloride component holds finer particles together effectively during transfer. These kinds of improvements only come when material science works in lockstep with factory process expertise.
Customers often want to know where LPSC stands in the spectrum of sulfide-based solid electrolytes. Our experience lines up with published research: LPSC runs neck-and-neck with Li6PS5Cl in terms of bulk conductivity, but with finer processability and better chemical tolerance at interfaces. Competitors like Li7P3S11 can deliver high conductivity, but remain sensitive to water and oxygen and require inert storage at all times. LPSC strikes a workable compromise, balancing performance, stability, and ease of handling.
Compared to oxide-based solid electrolytes, sulfide systems like LPSC bring lower grain boundary resistance and easier scaling with conventional ceramic processing lines. As oxide powders often need high temperatures and oxygen-free environments, LPSC maintains stable phase and high conductivity while running at much lower sintering or cold-pressing temperatures. Nearly every pilot trial confirms faster learning curves when switching technicians from oxide to sulfide-chloride lines.
Using LPSC, battery makers craft composite electrolytes that match the energy density and cycle life specifications set by modern electric vehicle OEMs. Even in solid-state microbatteries, the same powder delivers useful performance without requiring special tools or procedures. Feedback from coin cell lines and prototype pouch makers backs up the claims of easier scaling and reduced labor overhead, because handling errors result in far lower scrap rates.
Life inside a chemical plant rarely matches technical marketing brochures. Material handling staff complain if a powder cakes, stirs up dust, or reacts to brief air exposure. The chloride-tweaked LPSC powder resists these issues. Weekly batch testing at our line confirms consistent lot-to-lot performance for moisture uptake and surface behavior. Even in situations where processing equipment needed servicing or stood idle, chloride-doped powders held up longer than old monolithic sulfides.
Quality officers look for reproducible tap density and particle size distributions. In our test lab, LPSC stands head and shoulders above the usual suspects, delivering tight batches that match each other across months. After integrating LPSC into our product lines, complaints about voids and uneven spreading at the electrode interface dropped sharply. This translates into more efficient roll-to-roll throughput and leaner overall process cycles for our downstream partners.
Operators find LPSC less abrasive to sensitive chrome-steel rollers and easier to funnel into weighing bins. This may sound minor, but over a year, fewer equipment breakdowns mean measurable cost savings—not just for our plant, but for end-users and cell assembly lines. Time lost to production stoppages drops. In integrated lines, that can mean the difference between hitting or missing a shipment deadline.
Even with LPSC’s practical advantages, industry continues to face hurdles. Every factory deals with the tension between quality, cost, and throughput. Customers who want ultra-high chloride content for moisture resistance sometimes find trivial trade-offs in overall conductivity. Technicians chasing extreme cycling life at higher voltages must tweak coating, calendaring, and interfacial processing to get the most benefit. There is no one-size-fits-all recipe, but experience suggests that finely tuned chloride percentages strike the best balance between process survivability and ultimate battery performance.
Process bottlenecks remain a day-to-day reality. Equipment designed for legacy oxide or carbonate powders will need some retrofit, since LPSC flows and compacts differently. On our own shop floor, we have retrained teams to adjust hopper flow rates and pressing protocols — short-term pain that pays off by reaching high yields. Technical support for customers going through the same learning curve has become a key part of daily operations.
Environmental safety looms large. LPSC degrades more gracefully than earlier sulfide systems, but any process involving lithium and sulfur demands strict waste management and monitoring of H2S. Factory staff and facilities management work with environmental engineers to upgrade air handling, engineer safe spillage plans, and enforce strict inventory control. As solid-state battery adoption grows, more plants will have to address these issues at scale.
R&D groups in Europe and Asia keep pushing the limits by testing new halide-doped variants of LPSC or shifting base ratios to chase even higher conductivity. From a production perspective, the chloride content in the current LPSC keeps the door open to reliable, simple, and less hazardous large-scale manufacturing. Feedback from large automotive clients prioritizes cost reduction, stability under load, and fire safety over single-minded pursuit of conductivity. LPSC has met the grade every time so far, and new chemistries will only be adopted if they keep those practical strengths.
Production staff know all too well that the real test comes once the material hits the line: dust control, compaction, interface cleanliness, and low waste rates matter as much as headline conductivity numbers. LPSC holds the line across those challenges. Our teams stay in constant contact with battery assembly leaders, learning where real improvement is needed — often in workflows and powder management, not just raw material science.
The trajectory for LPSC and similar powders will depend on close partnerships between chemical manufacturers and downstream processors. Only this joint experience will reveal the best fits for compositional tweaking and process adjustment. Down-to-earth, hands-on operation and shared feedback will steer future development. LPSC’s daily performance in the factory and at the battery bench supports ongoing growth into mainstream battery manufacturing, promising higher reliability, safer handling, and greater resource efficiency for years to come.