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Low-temperature Sintering Silver Paste Electronic/EL Grade

    • Product Name: Low-temperature Sintering Silver Paste Electronic/EL Grade
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications
    HS Code 852455
    Product Name Low-temperature Sintering Silver Paste Electronic/EL Grade
    Appearance Silver gray viscous paste
    Silver Content 80-90 wt%
    Viscosity 50000-150000 mPa·s at 25°C
    Average Particle Size 0.5-5 μm
    Sintering Temperature 120-250°C
    Sheet Resistivity ≤1×10⁻⁴ Ω·cm
    Adhesion Strength ≥10 N/mm²
    Solids Content 85-95 wt%
    Binder Type Low-temperature curable organic resin system
    Solvent Type Ether alcohol or terpineol based slow-drying solvent
    Application Method Screen printing, stencil printing, or dispensing
    Shelf Life 6 months at recommended storage conditions
    Storage Condition Sealed, 2-10°C, protected from light and humidity

    As an accredited Low-temperature Sintering Silver Paste Electronic/EL Grade factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed 100 g HDPE bottle, light-resistant and moisture-proof, ensuring safe storage of low-temperature sintering silver paste for electronic/EL applications.
    Container Loading (20′ FCL) 20′ FCL: 20-foot full container load, palletized, secured drums/cartons of low-temperature sintering silver paste, with proper segregation and ventilation.
    Shipping Shipping of Low-temperature Sintering Silver Paste requires sealed, anti-static containers to prevent contamination and oxidation. Transport in temperature-controlled vehicles, avoiding extreme heat or cold. Ensure compliance with hazardous material regulations, upright handling, and shockproof cushioning. Use expedited services to minimize transit time and preserve paste integrity for optimal electronic-grade performance.
    Storage Store in original tightly sealed container in a cool, dry, well-ventilated area, ideally refrigerated at 2–8°C. Protect from direct sunlight, heat, moisture, and freezing. Keep away from ignition sources and incompatible materials. Thoroughly mix before use and allow to reach room temperature while sealed to prevent solvent condensation. Follow manufacturer’s shelf-life recommendations.
    Shelf Life Shelf life is 6 months from manufacture date when stored sealed at 2–8°C, away from light and moisture.
    Application of Low-temperature Sintering Silver Paste Electronic/EL Grade

    On heat-stabilized polyethylene terephthalate film, low-temperature sintering silver paste is used for double-sided polymer thick-film circuits where plated through-holes are not cost-viable. The paste is formulated with 65–72 wt% silver flake, 8–14 wt% thermoplastic polyester or acrylic binder, 12–20 wt% glycol ether/dibasic ester solvent, and 0.5–2 wt% rheology modifiers. D90 particle size is maintained below 12 µm to reduce mesh plugging. Viscosity at 25 °C is commonly 25–45 Pa·s at 1 rpm on a Brookfield RVT with a CP-52 spindle. The wet film is printed through 250–325 mesh stainless-steel screens with 15–20 µm emulsion and 65–75 Shore A squeegee at 60–70° attack angle and 80–160 mm/s squeegee speed. Wet thickness is 18–25 µm. Cure in forced-air convection at 130–150 °C for 12–30 min yields a dry film with sheet resistance of 15–35 mΩ/sq/25 µm. Heat-stabilized PET of 125 µm thickness is preferred because unstabilized film distorts above 120 °C. Adhesion to corona-treated PET at surface energy above 42 dyn/cm is rated 4B–5B under ASTM D3359-17. RoHS compliance is evaluated against 2011/65/EU Annex II and Delegated Directive 2015/863. Halogen-free binder versions are screened against IEC 61249-2-21:2003 limits of 900 ppm chlorine, 900 ppm bromine, and 1500 ppm total halogens. Terminal products include wearable sensor interconnects, flexible printed tails for membrane keypads, and low-cost medical cable replacement circuits. The main production bottleneck is screen blocking during long runs when ambient relative humidity falls below 30%; slow-evaporating solvent packages are used to delay ink drying in open mesh.

    What Limits Rear Electrode Cure Below 130°C in EL Lamps?

    The rear electrode layer in AC electroluminescent lamps is printed directly over the dielectric layer and must deliver low sheet resistance without damaging the phosphor stack. Electronic/EL grade low-temperature silver paste is generally formulated with 68–75 wt% silver flake, 10–14 wt% acrylic or fluoropolymer binder, and 10–18 wt% slow-evaporating ester solvent to maintain screen open time. The paste is printed with 180–230 mesh polyester screens, often in two consecutive passes, to achieve a dry film thickness of 20–30 µm. Curing is performed in forced-air ovens at 115–130 °C for 6–15 min. Surface temperature above 135 °C is generally avoided because the underlying dielectric layer in many EL stack constructions is rated only for short excursions above 130 °C. Sheet resistance after cure is typically 12–25 mΩ/sq/25 µm. Voltage drop across the rear electrode is a limiting factor: for a 100 mm lamp width, sheet resistance above 25 mΩ/sq begins to produce visible non-uniformity at 100 V/400 Hz. Compliance for this segment is governed by RoHS 2011/65/EU Annex II and customer-specific flammability requirements for the completed EL module under UL 94 VTM-0; the silver paste itself is not flame-rated until incorporated into the laminate. Terminal products include automotive instrument cluster backlights, keypad backlighting, safety signage, and architectural thin-lamp elements. The primary manufacturing failure mode is pinhole formation in the silver layer, which creates local field concentrations and dark spots. This is controlled by maintaining screen tension above 25 N/cm and squeegee pressure below 0.35 MPa. High-humidity storage of uncured paste must be avoided because absorbed water in the binder can form micro-bubbles during rapid cure.

    Application/substrateDry film or cured line thicknessCure profileSheet resistance or conductivityAdhesion/reliability test
    PTF circuits on stabilized PET15–25 µm130–150 °C, 12–30 min15–35 mΩ/sq/25 µmASTM D3359-17
    EL lamp rear electrode20–30 µm115–130 °C, 6–15 min12–25 mΩ/sq/25 µmUL 94 VTM-0 module; ASTM F1996-14
    RFID antenna on coated paper/PET4–8 µm110–150 °C, 3–8 s NIR25–80 mΩ/sqASTM D3359-17 tape
    Disposable ECG electrode12–18 µm wet105–120 °C, 20 minElectrode impedance under ANSI/AAMI EC12ISO 10993-5:2009
    Printed heater bus bar20–35 µm130–160 °C, 15–30 min10–30 mΩ/sq/25 µm85 °C/85% RH; ASTM D3359-17
    HJT front metallization15–35 µm finger height190–220 °C, 15–25 min3–6 µΩ·cmIEC 61215-1:2021

    In roll-to-roll smart label production, low-temperature silver paste is deposited as UHF and HF RFID antenna patterns on 50–80 µm coated paper or 38–50 µm PET. Antenna-grade paste is adjusted to lower viscosity than polymer thick-film circuits, commonly 10–20 Pa·s at 25 °C. Formulation ratios are typically 60–68 wt% silver flake, 6–10 wt% binder, and 20–28 wt% solvent. Rotary screen printing uses 300–400 mesh screens and web speeds of 25–40 m/min. Near-infrared tunnel drying achieves surface cure at 110–150 °C for 3–8 s, leaving a dry film of 4–8 µm. Sheet resistance after cure is 25–80 mΩ/sq, depending on substrate roughness and silver laydown. Printed antennas are die-cut and chip-attached using anisotropic conductive adhesive or conventional isotropic conductive adhesive. Compliance for smart labels includes RoHS 2011/65/EU, REACH EC 1907/2006 SVHC absence, and volatile organic compound limits set by packaging converters. In food-contact smart packaging, the silver trace is separated from food by a barrier film. Extractables data are generated under EU Regulation 1935/2004 migration screening when such packaging enters the converter workflow. Terminal products include retail apparel tags, pharmaceutical anti-counterfeit labels, logistics box labels, and airline baggage tags. The major process conflict is substrate moisture. Above 8% moisture in uncoated paper, steam generation during NIR cure creates voids and raises line resistance unpredictably. Published data for printed UHF antenna read-range retention after repeated flexing on coated paper is limited; converters generally run internal bend-cycle protocols rather than relying on a universal standard.

    When Silver Paste Replaces Conductive Carbon in Disposable ECG Electrodes

    Disposable resting ECG electrodes use a printed silver layer as the low-impedance current collector beneath an Ag/AgCl transducer pad or carbon top-coat. This low-temperature silver paste contains 58–66 wt% silver flake, 12–18 wt% polyurethane or polyester binder, and 15–25 wt% high-boiling solvent. Chloride is not incorporated into the silver paste; the chloride function is printed separately as an Ag/AgCl ink to stabilize half-cell potential. Screen printing is performed with 200–250 mesh screens on 0.125 mm PET or TPU film, at a wet thickness of 12–18 µm. Curing is limited to 105–120 °C for 20 min because the substrate and adjacent pressure-sensitive adhesive cannot withstand higher temperature. The cured silver trace is then overprinted with a carbon or dielectric passivation layer. Electrical impedance of finished electrodes is verified under ANSI/AAMI EC12:2000/(R)2015. The silver paste contributes below 5 Ω to the overall electrode impedance at 10 Hz after curing, but final impedance depends heavily on the gel and Ag/AgCl interface. Biological evaluation of the cured film follows ISO 10993-5:2009 for cytotoxicity and ISO 10993-10:2010 for skin sensitization when the device is submitted for regulatory clearance. Residual solvent content in the cured film is controlled by headspace GC-MS at an internal limit commonly below 100 µg/g for extended skin contact. Terminal products include diagnostic ECG electrodes, TENS electrodes, and integrated wearable cardiac monitoring patches. The primary processing bottleneck is insufficient cure at low-temperature settings causing solvent entrapment and adhesive breakdown after ethylene oxide sterilization. Medical converters avoid adding amine-based adhesion promoters because these can react with polyester binder during storage and shift the formulation toward premature chain scission.

    Thermally, printed heater bus bars require a cure window that avoids substrate distortion while maximizing silver particle coalescence. For PET and TPU heater circuits, the paste is formulated with 70–78 wt% silver flake, 8–12 wt% heat-resistant polyester or polyimide binder, and 8–15 wt% solvent. Screen printing uses 200–230 mesh screens and a dry film thickness of 20–35 µm. A second bus bar layer is often printed over the heater trace ends to reduce current crowding. Curing is performed at 130–160 °C for 15–30 min in forced-air ovens. Sheet resistance after cure is typically 10–30 mΩ/sq/25 µm, and the silver conductor has a temperature coefficient of resistance near 0.0038 /°C. Heater power density is normally designed in the 0.2–0.8 W/cm² range. The main reliability tests are damp heat exposure at 85 °C/85% RH for 1000 h and thermal cycling from -40 °C to 105 °C for 1000 cycles. After aging, adhesion is re-checked under ASTM D3359-17 and must remain at 4B or above. Automotive interior heater applications may be qualified to OEM-specific profiles based on ISO 16750-4:2010. RoHS compliance is required under 2011/65/EU, and halogen-free variants are screened to IEC 61249-2-21:2003. Terminal products include wearable heated garments, automotive camera lens defoggers, battery pack preconditioning heaters, and medical fluid warmers. The main production failure mode is hot-spot formation at the junction between printed silver and copper ribbon connectors. Resistance at those interfaces is kept below 0.1 Ω by increasing bus bar width to 2–5 mm and printing a silver over-layer after connector placement.

    Membrane Switch Conductor Deposition, Crease Testing, and Silver Migration Limits

    Membrane switch circuits represent a mature deposition regime. The paste is printed on 0.125 mm PET through 250 mesh screens at a dry film of 8–12 µm, then cured at 120–130 °C for 10 min. Silver flake content is 62–68 wt% and viscosity is 20–30 Pa·s. Crease resistance is assessed by ASTM F1683-16, and silver migration under DC bias in humid environments is evaluated by ASTM F1996-14. The upper operational limit is defined by dielectric overcoat integrity. Trace spacing below 0.5 mm under 5 V DC and 85 °C/85% RH is vulnerable to dendritic silver growth unless a UV-curable dielectric coverlay is applied. Terminal products include industrial keypads, appliance control panels, and test-instrument front-panel switches. Compliance is governed by RoHS 2011/65/EU and customer-specific total halogen limits.

    Low-Temperature Front-Side Metallization for Silicon Heterojunction Cells

    For silicon heterojunction cells, low-temperature silver paste replaces fire-through paste because the amorphous silicon passivation layer degrades above 250 °C. The paste contains 88–92 wt% silver powder, a minimal binder-frit package of 1–4 wt%, and a solvent system designed for screen printing at 150–300 Pa·s viscosity. Fine-line screens with 360–430 mesh, 15–25 µm emulsion, and finger openings of 30–50 µm are used to achieve high aspect ratio. Printing speed is 150–300 mm/s. The paste is dried and cured in a belt furnace with peak wafer temperature of 190–220 °C for 15–25 min. Bulk line resistivity after cure is typically 3–6 µΩ·cm, and contact resistivity on indium-tin-oxide or aluminum-doped zinc oxide layers is specified below 5 mΩ·cm² by cell manufacturers. Cure below 180 °C often leaves residual organics and increases contact resistivity by 20–50%. Cure above 240 °C can increase passivation stack defect density and reduce open-circuit voltage. Published data for low-temperature paste interactions with non-standard transparent conductive oxide compositions is limited. Evaluation is therefore required when changing TCO supplier. Batch-to-batch paste viscosity is controlled in production to ±8% at 25 °C to maintain finger width. Module qualification follows IEC 61215-1:2021 and IEC 61730-1:2016. RoHS compliance to 2011/65/EU applies at module level. Terminal products are utility, commercial, and rooftop photovoltaic modules. The dominant production failure mode is screen clogging in fine-line screens, which appears as discontinuous fingers and is controlled by controlled-polymer shear thinning and filtered paste with D90 below 10 µm.

    SegmentMaterial-level complianceProcess or device standard
    PTF circuitRoHS 2011/65/EU Annex II; IEC 61249-2-21:2003ASTM D3359-17; ASTM F1896-16
    EL lamp rear electrodeRoHS 2011/65/EU; REACH EC 1907/2006UL 94 VTM-0 module; ASTM F1996-14
    RFID smart labelREACH SVHC; EU Regulation 1935/2004 if barrier-separatedISO/IEC 18000-63:2015 read-range verification
    ECG electrodeISO 10993-5:2009; ISO 10993-10:2010ANSI/AAMI EC12:2000/(R)2015
    Membrane switchRoHS 2011/65/EUASTM F1683-16; ASTM F1996-14
    HJT solar cellRoHS 2011/65/EUIEC 61215-1:2021; IEC 61730-1:2016

    Printed strain gauge arrays on 25 µm polyimide require a low-temperature silver conductor that can survive repeated flexing without cracking. The strain gauge paste is formulated with 60–66 wt% silver flake, 12–18 wt% polyimide or phenoxy binder, 15–25 wt% solvent, and 1–3 wt% flexibilizer. Line widths are 150–200 µm, dry thickness is 10–15 µm, and curing is 140–160 °C for 20–30 min. Resistance change under bending is evaluated by repeated flex to 2 mm bend radius for 100,000 cycles. Drift beyond 5% is considered a failure in most sensor builds. The silver conductor has a gauge factor near 2, which is low relative to constantan foil. Strain-gauge designs therefore use half-bridge or full-bridge configurations to compensate temperature coefficient of resistance. Compliance follows RoHS 2011/65/EU and REACH EC 1907/2006 SVHC screening. Terminal products include robotic gripper haptic arrays, patient position monitoring mats, smart seating pressure sensors, and instrument force plates. The key production conflict is maintaining stable resistance during high-temperature lamination of the coverlay. If cure is incomplete, resistance drifts upward by 8–15% during subsequent 150 °C lamination. Vacuum lamination is therefore preferred over hot-roll lamination for this application.

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    Certification & Compliance
    More Introduction

    Designated LTS-EL-4250, the low-temperature sintering silver paste is formulated for screen-printed conductor deposition on ITO-coated polyethylene terephthalate, polycarbonate, and soda-lime glass. The product is classified as an electronic/electroluminescent grade material because its cure envelope remains below 150 °C, allowing reflow-free interconnections on heat-stabilized polymer films. Silver content is specified as 77.0–79.0 wt% by thermogravimetric analysis per ASTM E1131-20. The metallic fraction consists of a bimodal distribution of sub-micrometer flakes and spherical particles; laser diffraction per ISO 13320:2020 reports d50 of 0.9 µm and d90 of 2.3 µm. Brookfield viscosity at 25 °C is 22,000 mPa·s at 10 rpm with a CP52 spindle, and the thixotropic index measured between 1 rpm and 10 rpm is 4.8. The material cures to a conductive silver network after 20 min at 130 °C in forced-air convection, yielding volume resistivity of 9.5 × 10⁻⁶ Ω·cm under ASTM D257-14. Cross-hatch adhesion to ITO-PET is rated 5B under ASTM D3359-17. The cured layer contains less than 0.5 wt% residual organic residue by headspace thermogravimetry, which correlates with stable contact resistance in high-humidity aging.

    Specification profile for LTS-EL-4250
    PropertySpecified rangeReference method
    Silver content77.0–79.0 wt%ASTM E1131-20
    Viscosity18,000–26,000 mPa·s at 25 °C, 10 rpm, CP52ASTM D2196-20
    Thixotropic index4.2–5.5ASTM D2196-20
    Particle size d500.7–1.1 µmISO 13320:2020
    Particle size d902.0–2.6 µmISO 13320:2020
    Volume resistivity after 130 °C/20 min8.5 × 10⁻⁶–1.2 × 10⁻⁵ Ω·cmASTM D257-14
    Cross-hatch adhesion on ITO-PET5BASTM D3359-17
    Halogen content<900 ppm total Br/ClEN 14582
    Sintering window120–150 °CForced-air convection, product qualification
    Storage life, unopened6 months at −20 ± 5 °CInternal stability protocol

    Screen printing is the primary deposition route. The paste is designed for 200–325 mesh stainless-steel screens with a 10–20 µm emulsion over mesh. When processed on a semi-automatic flatbed printer with a 70–75 Shore A polyurethane squeegee, snap-off of 0.5–1.0 mm, and squeegee speed of 60–120 mm/s, the printed wet film stabilizes at 10–25 µm after leveling. Minimum line/space capability is 150 µm / 150 µm on 325-mesh screens, provided edge definition is maintained by a screen tension of 25–30 N/cm. The paste should be conditioned at 23 ± 2 °C for 4 h before opening. If moisture condensation is observed on the paste surface or substrate, printing should stop; at relative humidity above 60%, pre-drying at 60 °C for 10 min is required.

    What distinguishes this material from conventional high-temperature silver paste?

    Conventional silver conductor pastes require peak firing at 500 °C to 850 °C and cannot be processed on polyester films. LTS-EL-4250 undergoes metallic sintering through a transient liquid-phase boundary at particle contacts within 120–150 °C; the sintered structure is not a percolated carbon-filled polymer matrix but a densified silver network. In cross-sectional scanning electron microscopy at 15,000×, the cured layer shows continuous silver necks, and residual porosity is typically below 8% when sintering above 130 °C; published data for this specific formulation is limited. The consequence appears in humidity aging: after 85 °C / 85% RH for 250 h, conductor resistance drift is specified at ≤ 10%. High-temperature silver maintains lower absolute resistivity, generally 2–5 × 10⁻⁶ Ω·cm on ceramic substrates, but the substrate compatibility boundary makes it unsuitable for ITO-PET and electroluminescent lamp construction. Compared with nano-silver inkjet inks, LTS-EL-4250 has higher viscosity and higher metal loading, making it unsuitable for piezoelectric jetting below 20 mPa·s; it is instead optimized for thick-film screen deposition with a wet thickness above 10 µm to achieve low trace resistance.

    Comparative conductor properties after optimal processing
    ParameterLTS-EL-4250High-temperature silver pasteNano-silver inkjet inkSilver-coated copper paste
    Processing temperature120–150 °C500–850 °C100–200 °C150–220 °C
    Volume resistivity8.5 × 10⁻⁶–1.2 × 10⁻⁵ Ω·cm2–5 × 10⁻⁶ Ω·cm5–10 × 10⁻⁵ Ω·cm1–3 × 10⁻⁵ Ω·cm
    Compatible substratesITO-PET, PC, glassAl₂O₃, Si, glassPET, PI, paperPI, PET, glass
    Primary deposition methodScreen/stencil printingScreen printingInkjet/aerosolScreen printing
    Adhesion to ITO-PET5BNot processable4B–5B with primer4B with primer
    Resistance stability at 85 °C/85% RH, 250 h≤ 10% driftNot applicable≤ 20% drift published≤ 15% drift published

    When oven residence time conflicts with roll-to-roll throughput

    In continuous reel-to-reel processing, the static cure condition of 130 °C for 20 min must be converted to a temperature-time integral that matches the solvent evolution and sintering kinetics of the vehicle. A forced-air tunnel with heated length of 6 m and zone temperatures 90 °C / 135 °C / 120 °C at belt speed 0.8 m/min provides a reference cure profile. If the belt speed is raised to 1.2 m/min without increasing mid-zone temperature, incomplete organic removal leaves residual solvent above 0.5 wt% and produces volume resistivity that shifts upward by 25–40% after 85 °C / 85% RH aging for 250 h. Infrared-assisted profiles reduce total residence time but create a skin-over risk at high radiant flux: the surface densifies before solvent vapor escapes, producing blisters in films thicker than 25 µm. The processing boundary is defined by a maximum substrate surface temperature of 150 °C and a minimum cure integral of 130 °C for 15 min; below this integral, cross-hatch adhesion may still pass but high-humidity drift increases. Production qualification should include inline four-wire resistance measurements after cure and witness coupons tested to ASTM D257-14 and ASTM D3359-17.

    Viscosity recovery after screen printing and paste thixotropy

    The paste exhibits shear thinning under ASTM D2196-20: apparent viscosity drops from 22,000 mPa·s at 10 rpm to 6,500 mPa·s at 100 rpm. After shear removal, recovery follows a two-stage profile. Within 10 s, 85% of low-shear viscosity is recovered; within 60 s, the material reaches 95% recovery. This prevents line bleed-out beyond 25 µm on treated ITO-PET and preserves 150 µm-pitch pattern integrity. On production lines, paste pots should not be opened immediately from frozen storage; tempering at 23 ± 2 °C for 4 h prevents condensation-induced rheology drift. If viscosity after tempering falls outside 18,000–26,000 mPa·s or thixotropic index falls below 4.2, the paste is outside specification and should not be reduced by solvent blending without qualification, because uncontrolled dilution alters sintering kinetics and void content.

    Production-scale experience indicates that the most common failure modes are screen drying during line stoppages, paste freezing in squeegee reservoirs, and moisture condensation after transfers between temperature zones. Screen drying during stoppages longer than 3 min raises viscosity above 30,000 mPa·s; the screen should be flooded between prints. On automated lines with dual squeegees, batch-to-batch viscosity variance of ±1,500 mPa·s is accommodated by blade-pressure adjustment between 0.2–0.4 MPa, but larger changes require requalification because wet film thickness shifts by 2–4 µm. Paste recovered from a flooded screen after 8 h exposure at 23 °C and 50% RH exhibited a 12% increase in d90 by ISO 13320:2020 due to agglomeration; recovered material should not be blended back into fresh paste.

    In electroluminescent lamp backplanes, the paste is printed as the rear electrode on ITO-PET and cured at 130 °C for 20 min. Qualification under IPC-TM-650 2.4.3 for flexural endurance specifies resistance change not exceeding 10% after 1,000 cycles at 25 °C, and production-scale testing of laminates is recommended because adhesion to phosphor-dielectric layers can differ from adhesion to raw ITO-PET. In membrane touch switches, the material replaces subtractive copper etching and removes undercut variations below 100 µm trace pitch. In radio-frequency identification antenna straps, the lower volume resistivity relative to graphite polymer thick-film conductors—approximately 2 orders of magnitude—reduces series loss, although conductivity remains below etched copper foil, which is typically 1.7 × 10⁻⁶ Ω·cm.

    The product differs from silver-coated copper paste in that no cuprous oxide diffusion layer forms at silver-copper particle boundaries during low-temperature cure, because the silver fraction is not subject to galvanic displacement at the low process temperatures. Silver-coated copper paste can exhibit oxidation-driven drift if the cladding is incomplete; LTS-EL-4250 avoids this by using a single-metal conductive phase. The trade-off is raw material cost and paste density; silver content at 77–79 wt% gives a cured film density of approximately 5.1–5.6 g/cm³ compared to 4.0–4.5 g/cm³ for silver-coated copper pastes. This density difference affects paste coverage calculations but not printed thickness.

    Electroluminescent/EL grade designation imposes additional requirements beyond general electronic grade: cured paste must not release volatile residues that condense on phosphor-dielectric layers during subsequent UV lamination or encapsulation. Specification limits total mass loss to <0.5 wt% at 150 °C for 1 h by thermogravimetric analysis. Residue above this level can shift the dielectric constant of the adjacent phosphor layer and produce visible dark spots under 115 V / 400 Hz AC drive. The paste is not recommended for direct contact with amine-based encapsulants because amine migration can raise contact resistance at silver-polymer interfaces; compatibility testing under 85 °C / 85% RH for 500 h is required for any overcoat system. The cured conductor is designed to comply with the restrictions of 2011/65/EU as amended by (EU) 2015/863, and halogen content is controlled to <900 ppm total bromine and chlorine by EN 14582. The paste is not intended for high-current power applications above 0.5 A/mm² because current crowding at sintered contacts can accelerate electromigration in humid conditions; for such service, plated or etched copper is appropriate. Cleanroom class ISO 14644-1 Class 8 or better is recommended for printing to limit particulate defects below 50 µm.

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