| HS Code | 878215 |
| Product | Silicon Etch for Backside Thinning Electronic/EL Grade |
| Grade | Electronic/EL Grade |
| Chemical Components | Hydrofluoric acid (HF), nitric acid (HNO3), and acetic acid (CH3COOH) |
| Target Material | Silicon (Si) wafers |
| Process Use | Backside thinning |
| Mechanism | HNO3 oxidizes silicon while HF dissolves the silicon oxide layer |
| Physical Form | Liquid |
| Appearance | Clear, colorless liquid |
| Operating Temperature C | 20 to 25 |
| Etch Rate Um Per Min | 0.5 to 3 depending on formulation, temperature, and agitation |
| Surface Quality | Smooth, uniform, and damage-free after thinning |
| Purity | High purity with controlled low metallic impurity content |
| Density G Per Cm3 | Approximately 1.10 to 1.20 depending on exact formulation |
| Safety Information | Highly corrosive; use acid-resistant handling and ventilation |
| Product Name | Silicon Etch for Backside Thinning Electronic/EL Grade |
| Product Type | Wet chemical etchant |
| Grade | Electronic / EL Grade |
| Chemical System | Hydrofluoric acid, nitric acid, and acetic acid mixture |
| Appearance | Clear colorless to slightly yellowish liquid |
| Specific Gravity | 1.15 - 1.25 at 20°C |
| Ph Value | < 1 |
| Boiling Point | Approximately 100 - 120°C |
| Silicon Etch Rate | Typical 1 - 5 micrometers per minute depending on temperature and agitation |
| Operating Temperature | Recommended 20 - 30°C |
| Storage Temperature | Store at 5 - 35°C in a tightly sealed HF-resistant container |
| Shelf Life | 6 months from date of manufacture |
| Metal Impurities | EL-grade trace metals in parts per billion range |
| Solubility | Fully miscible with water and organic solvents |
| Primary Application | Backside thinning of silicon wafers in semiconductor fabrication |
As an accredited Silicon Etch for backside thinning Electronic/EL Grade factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Silicon Etch for backside thinning Electronic/EL Grade is packaged in 4-liter HDPE bottles with secure seals and clear hazard labeling. |
| Container Loading (20′ FCL) | 20ft FCL: Electronic/EL Grade Silicon Etch for backside thinning, packed in sealed containers on pallets, ready for safe transport. |
| Shipping | Ship as hazardous chemical in UN-approved containers, with proper labeling and SDS documentation. Use ground transport only, avoiding air freight. Ensure leak-proof seals, upright orientation, and segregation from incompatible materials. Include absorbent spill kit and emergency contact details. Verify compliance with local and international dangerous goods regulations before dispatch. |
| Storage | Store in a cool, dry, well-ventilated area in the original, tightly sealed container. Keep away from sunlight, moisture, heat, alkalis, and reactive metals. Use corrosion-resistant secondary containment. Maintain stable temperatures (15–25°C), inspect regularly for leakage, and follow all hazard labels and handling protocols. |
| Shelf Life | Shelf life is typically 12 months from manufacture if unopened and stored correctly in original sealed container. |
In backside via reveal for 300 mm wafer-level packaging, the silicon etch is introduced after mechanical backgrinding to remove sub-surface damage and expose copper via plugs with controlled silicon loss. A typical process sequence begins with temporary bonding of the device wafer to a glass carrier using a UV-release adhesive, followed by coarse grinding on a dual-spindle grinder equipped with 6000-grit diamond wheels to leave 80–120 µm of remaining silicon. The electronic/EL grade blend is then dispensed through a single-wafer spin processor having a PTFE-wetted bowl and Bernoulli chuck at 800–1,200 rpm. A volumetric ratio of 49 wt% hydrofluoric acid, 70 wt% nitric acid, and glacial acetic acid at 1:3:2 is mixed in-line at 20–22 °C and delivered at 0.8–1.5 L/min to remove 5–12 µm of damaged silicon at an etch rate of 8–12 µm/min. Laser reflectance interferometry at 670 nm tracks residual silicon thickness and terminates the dispense step at a within-wafer total thickness variation of ≤1.0%. The wafer is rinsed with 18 MΩ·cm deionized water within 5 s after chemical shutoff to prevent localized etching in the spin-off film. Because exposed copper TSV structures are sensitive to nitric acid, dispense timing is programmed to stop before full via reveal; final 2–3 µm of silicon is removed by low-pressure chemical mechanical polishing. Trace metal impurities are controlled by ICP-MS per ASTM D5673 to ≤10 ppb total, preventing copper diffusion into low-k interlayer dielectrics, while particles larger than 0.5 µm are maintained below 50 particles/mL per SEMI C35. Thinned wafers enter 2.5D and 3D package assemblies that include high-bandwidth memory interposers, silicon bridges, and fan-out wafer-level packages.
| Wafer configuration | HF:HNO3:CH3COOH volumetric blend | Process temperature (°C) | Measured etch rate (µm/min) | Post-grind silicon removed (µm) |
|---|---|---|---|---|
| TSV reveal, 300 mm | 1:3:2 | 20–22 | 8–12 | 5–12 |
| IGBT/MOSFET thinning | 1:1:4 | 15–18 | 3–5 | 3–8 |
| SOI interposer handle removal | 1:2:5 | 16–18 | 2–4 | 5–10 above buried oxide |
| BSI image sensor stress relief | 1:4:2 | 10–14 | 4–6 | 3–7 |
For power semiconductor wafers, backside thinning is a trade-off between conduction losses and mechanical integrity. The acid blend removes the amorphous silicon layer left by mechanical grinding after the wafer has been thinned to 70–90 µm; the final target before backside implant and metallization is commonly 40–70 µm. A formulation with a higher acetic acid fraction, HF:HNO3:CH3COOH = 1:1:4, is used at 15–18 °C to reduce the etch exotherm and maintain removal at 3–5 µm/min on a single-wafer spin tool. When final thickness drops below 60 µm, unsupported 300 mm wafer bow can exceed the vacuum chuck flatness envelope, causing seal loss at the wafer edge and process interruption. The etch tool is therefore configured with a soft-contact carrier ring and backside cooling water at 14 °C to stabilize wafer temperature. In-line spectral reflectance measurements after the rinse step confirm removal of the 3–8 µm damage layer. Sodium and potassium are specified at ≤1 ppb in the electronic/EL grade because residual mobile ions increase reverse-bias leakage in trench gate oxides. Backside metallization then uses sputtered Al/Ti/Ni/Ag stacks or evaporated Ti/Ni/Ag layers, and thinned dies enter discrete IGBT and MOSFET packages, including TO-247, TO-264, and power modules with direct-bonded copper substrates. If the etch proceeds below 40 µm, die fracture during pick-and-place and wire bonding rises sharply, so the process window is guarded by both thickness monitoring and die shear testing per MIL-STD-883 Method 2019.
Piezoresistive pressure sensor wafers for automotive manifold absolute pressure applications are thinned on the backside before diaphragm formation. The silicon etch is applied in an immersion tank rather than spin processing when wafer diameters are 150 mm or 200 mm and the required removal is uniform to ±1.5%. The bath is constructed from perfluoroalkoxy polymer and fitted with a 0.1 µm PTFE recirculation filter and an external fluoropolymer heat exchanger to hold the liquid at 18–20 °C. A volumetric ratio of HF:HNO3:CH3COOH = 1:4:5 removes silicon at 5–7 µm/min after backgrinding has brought the wafer from 400 µm to 200 µm. The target backside removal is 20–30 µm to eliminate grinding-induced microcracks before the diaphragm is patterned by anisotropic etching. Bath loading per liter is limited to one 150 mm wafer to keep dissolved silicon concentration below 2 g/L, beyond which etch rate drops by more than 15% in production logs. Wafers are rinsed in a cascade overflow tank with 18 MΩ·cm deionized water and transferred to a spin dry module. Terminal products are capacitive and piezoresistive pressure sensors packaged in ceramic or metal cans for engine intake and fuel rail pressure measurement.
For RF SOI interposer wafers, the acid etch step is timed to terminate before the buried oxide layer because the HNA system does not provide infinite selectivity to silicon dioxide. Mechanical backgrinding stops at 5–10 µm above the buried oxide, leaving a residual silicon film that is then removed with a low-rate formulation of HF:HNO3:CH3COOH = 1:2:5 at 16–18 °C. The etch rate under these conditions is 2–4 µm/min, and endpoint is detected by a reflectance shift when the buried oxide is approached; over-etch is controlled by ellipsometric measurement of oxide loss after each maintenance cycle. A multi-zone dispense arm maps the blend across the wafer surface from center to edge to compensate for slower edge removal, and the chemical delivery line is purged with nitrogen between batches to prevent nitric acid decomposition. The electronic/EL grade product is filtered at point of use through a 20 nm rated chemical filter to reduce metallic residue on the buried oxide surface. Residual silicon not removed by the wet step is cleared in a downstream selective dry etch, preserving the buried oxide for subsequent via opening. Terminal products include RF switches, antenna tuners, and silicon interposers with through-buried-oxide vias for high-frequency front-end modules.
Backside-illuminated CMOS image sensor wafers require final silicon thickness in the 5–10 µm range without sub-surface damage because crystal defects within the depletion region increase dark current. The etchant is used as a stress-relief operation after grinding on a 300 mm backgrind tool with 2000-grit diamond wheels. The acid mixture is dispensed at 10–14 °C in a single-wafer non-contact spin processor to remove 3–7 µm of damaged silicon at 4–6 µm/min. A higher nitric acid fraction of HF:HNO3:CH3COOH = 1:4:2 favors oxide formation on the silicon surface prior to oxide removal by hydrofluoric acid, producing a smoother post-etch surface with lower haze. After spin rinse, the wafer is transferred to a chemical mechanical polishing step that brings the final silicon to 5 µm with ±0.5 µm total thickness variation. Dark current is characterized at 60 °C according to EMVA 1288 test methods, and wafers with residual acid damage show elevated leakage across the pixel array. The electronic/EL grade is controlled for transition metals below 1 ppb per element to avoid trap states in the photodiode region. Terminal image sensors are assembled in chip-scale packages for mobile phone cameras and automotive advanced driver assistance systems.
Active-matrix electroluminescent microdisplays use single-crystal silicon backplanes that are thinned to 70–90 µm before module assembly. The product grade is selected because mobile ion contamination at the thin-film transistor gate dielectric shifts threshold voltage and causes pixel non-uniformity under constant-current driving. The etchant is applied after backgrind to remove 3–5 µm of silicon damage at a low etch rate of 3–5 µm/min using a chilled HF:HNO3:CH3COOH = 1:2:3 mixture at 14–16 °C. Single-wafer processing avoids batch-to-batch cross-contamination, and the chemical delivery system includes point-of-use 20 nm rated filtration. Sodium and potassium are controlled at ≤1 ppb each by ICP-MS, while chloride is maintained below 50 ppb per SEMI C35. Backside thinning lowers thermal resistance between the emissive layer and the silicon driver backplane, enabling stable operation below 85 °C junction temperature. Published direct application data for acid-thinned electroluminescent backplanes at final thickness below 50 µm is limited; qualification relies on wafer-level acceptance tests including film stress, gate oxide integrity, and die shear. The thinned backplane receives a backside bonding layer and is flip-chip mounted to a driver flex circuit. Terminal products are silicon-based electroluminescent microdisplays used in head-mounted display viewfinders and wearable augmented reality optical modules.
| Parameter | Reference method | Electronic/EL grade control limit |
|---|---|---|
| Total trace metals | ASTM D5673 | ≤10 ppb |
| Sodium | ICP-MS | ≤1 ppb |
| Potassium | ICP-MS | ≤1 ppb |
| Particles ≥0.2 µm | SEMI C35 | ≤50 particles/mL |
| Chloride | SEMI C35 | ≤50 ppb |
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Silicon Etch for backside thinning Electronic/EL Grade is a filtered acidic wet-etch product supplied for silicon removal after mechanical backgrinding or lapping in power-device, integrated-circuit, and MEMS wafer thinning operations. The grade designation Electronic/EL appears on the certificate of analysis and denotes extra-low metal and particulate control for backside processing in which the thinned silicon remains within 50 µm of active frontside devices. The product is a ternary hydrofluoric/nitric/acetic acid mixture built from semiconductor-grade component acids: hydrofluoric acid conforming to SEMI C12, nitric acid conforming to SEMI C7, and acetic acid conforming to SEMI C18 where applicable. Nominal active-component concentrations are 49.0 ± 0.5 wt% HF, 70.0 ± 0.5 wt% HNO₃, and a balance of acetic acid. The blended product is packaged in 20 L fluoropolymer drums and 200 L high-density polyethylene containers after point-of-dispense filtration through 0.1 µm or 0.2 µm membrane filters.
At 20°C, the formulation exhibits a density of 1.18 g/cm³ to 1.24 g/cm³ and viscosity between 2.0 mPa·s and 3.5 mPa·s. The solution freezes below -20°C; storage in unheated chemical cabinets below that temperature is unsuitable. Trace metal release is performed by inductively coupled plasma mass spectrometry for chromium, copper, iron, nickel, and zinc. In the etch mechanism, nitric acid oxidises silicon to silicon dioxide, hydrofluoric acid dissolves the oxide, and acetic acid buffers the reaction while lowering surface tension to improve wetting on lapped or patterned backside surfaces.
The primary distinction is the trace metal and particle specification. Electronic/EL Grade controls individual transition metals to < 1 ppb and total trace metals to < 5 ppb, while technical-grade mixed acid etchants commonly report 20 ppb to 500 ppb of iron, copper, and zinc. This difference is operationally significant in backside thinning. At final wafer thicknesses of 50 µm or less, a contaminated backside etch can deposit mobile ions within the etched layer, and subsequent thermal processing can drive those species toward frontside junctions, causing threshold-voltage drift or gate-oxide degradation. Particle control follows a similar boundary: Electronic/EL Grade is specified at < 100 particles/mL for particles at 0.2 µm and < 20 particles/mL at 0.5 µm, whereas technical-grade etchants may exceed 1000 particles/mL at the same size channels.
| Parameter | Specification | Analytical basis |
|---|---|---|
| Hydrogen fluoride | 49.0 ± 0.5 wt% | acid-base titration |
| Nitric acid | 70.0 ± 0.5 wt% | acid-base titration |
| Acetic acid | balance, water difference < 0.2 wt% | gas chromatography or titration |
| Individual transition metals | < 1 ppb each | ICP-MS |
| Total trace metals | < 5 ppb | ICP-MS |
| Chloride | < 1 ppm | ion chromatography |
| Sulfate | < 1 ppm | ion chromatography |
| Particle count at 0.2 µm | < 100 particles/mL | light-scatter liquid particle counter |
| Particle count at 0.5 µm | < 20 particles/mL | light-scatter liquid particle counter |
For single-wafer backside thinning, the etchant is dispensed through a polytetrafluoroethylene nozzle onto the backside of a wafer held on an edge-grip or porous chuck. The frontside is protected by temporary bonding adhesive, sacrificial tape, or a carrier. Process recipes typically maintain etchant flow between 50 mL/min and 250 mL/min, wafer rotation between 300 rpm and 900 rpm, and chuck temperature between 20°C and 30°C. A nitrogen curtain or centrifugal edge rinse prevents chemical wrap-around to the frontside bevel. Endpoint control is provided by infrared interferometry or white-light reflectance thickness measurement; tool suppliers specify final thickness repeatability of ±2 µm for wafers above 30 µm and ±1 µm for wafers below 20 µm.
Batch immersion is used for lower-cost production of power devices and discrete components. Wafers are loaded in fluoropolymer cassettes and immersed in an agitated bath fitted with continuous filtration through 0.2 µm polytetrafluoroethylene membrane cartridges and external heat exchange. Bath turnover is maintained at 5–10 bath volumes per hour. Temperature is held within ±1°C of setpoint to avoid local etch acceleration at the heating jacket. For a removal depth of 10–30 µm at 25°C, immersion times between 2 min and 15 min are typical depending on dopant type, crystal orientation, and agitation. Batch endpoint is established by timed etch calibrated against monitor wafers because in-bath thickness measurement is not practical.
Mechanical grinding reduces wafer thickness from 725 µm to 100–250 µm and leaves subsurface damage at a depth of 5–20 µm, depending on wheel grit and feed force. The acid etch removes this damaged layer rather than serving as the sole bulk removal step. For final thickness below 100 µm, residual microcracks above 5 µm can increase die fracture during subsequent pick-and-place, wafer sawing, and wire bonding. A post-grind stress-relief etch removes between 10 µm and 30 µm of silicon and can reduce roughness from several micrometres RMS to below 1 nm RMS on monitor wafers as measured by atomic force microscopy under optimized rotation and flow conditions; published data for patterned production wafers with this specific grade is limited, and qualification on device wafers is required.
Etch rate is strongly dependent on the nitric-to-hydrofluoric ratio. At high nitric acid fraction the reaction is diffusion-limited and produces a smoother surface but consumes the oxidiser rapidly; at low nitric acid fraction the reaction becomes surface-limited and can increase roughness. Backside-thinning formulations commonly select a volumetric HF:HNO₃:CH₃COOH ratio in the range 1:3:5 to 1:5:8, giving an etch rate between 2 µm/min and 10 µm/min at 25°C. Composition drift in production is held below 2% of the target acid ratio because a shift toward higher nitric acid content raises exothermic heating, while a shift toward higher HF content accelerates undercutting of exposed oxide or nitride passivation.
Dilution with deionized water is not recommended for lot-to-lot composition control because the ternary etch rate is nonlinear with water content. Small water additions can either accelerate or decelerate the reaction depending on the starting nitric acid fraction. Replenishment of production baths is performed with certified stock acid or blended replenisher rather than water-only additions, and the bath is discarded when dissolved silicon exceeds the specified concentration, typically between 5 g/L and 20 g/L.
The replacement of potassium hydroxide or tetramethylammonium hydroxide with an electronic-grade acid etchant is driven by metal contamination, etch isotropy, and process temperature. The following comparison summarises operational differences for backside thinning of 100 mm to 200 mm wafers.
| Property | Electronic/EL acid mixture | Technical-grade mixed acid | KOH or TMAH alkaline etch |
|---|---|---|---|
| Etch character | Isotropic | Isotropic, less controlled | Anisotropic, orientation-dependent |
| Typical process temperature | 20°C–30°C | 20°C–30°C | 70°C–90°C |
| Silicon etch rate | 2–10 µm/min | 2–10 µm/min but lot-variable | 0.5–2.0 µm/min depending on concentration |
| Transition metal control | < 1 ppb individual, < 5 ppb total | 20–500 ppb total typical | KOH: potassium residues; TMAH: lower metal but higher cost |
| Ionic contamination risk | Low | Moderate | KOH: high potassium; TMAH: moderate ammonium |
| Dielectric and metal compatibility | Dissolves SiO₂; attacks Al and Cu | Same attack but metallic impurities may plate | KOH: etches SiO₂ slowly; can stop on boron-doped layers |
| Waste treatment | Fluoride precipitation and nitrate control | Fluoride precipitation | Neutralization and ammonia/amine control |
Compared with plasma etching, the wet acid route offers higher throughput for blanket silicon removal but cannot achieve the lateral profile control of deep reactive ion etching. The acid mixture is therefore used where backside silicon removal is unpatterned and aggressive frontside topography is absent. Plasma thinning is reserved for device structures with pre-existing cavities or thick metal redistribution layers that would be chemically attacked.
The product is not suitable for wafers with exposed aluminum or copper metallization unless the metal features are fully masked by silicon nitride or a chemically resistant polymer. Hydrofluoric acid reacts with aluminum to form solid aluminum fluoride residues, and the nitric/hydrofluoric chemistry dissolves copper at rates above 0.5 µm/min at 25°C. Temporary bonding adhesives must be screened for acetic acid compatibility; some epoxy and acrylate adhesives swell and delaminate during spin processing. After etching, wafers are rinsed with ultrapure water conforming to ASTM D5127-13 and dried by Marangoni or low-speed spin drying. Fluoride-containing waste is treated by calcium precipitation, and nitrate discharge limits are confirmed before production release. Handling is performed in cleanrooms meeting ISO 14644-1 Class 5 with dedicated acid exhaust, calcium gluconate gel first-aid stations, and polypropylene- or fluoropolymer-compatible bench surfaces. Regulatory classification under EC 1907/2006 (REACH) and Directive 2011/65/EU (RoHS) is documented in the extended safety data sheet; engineering controls must maintain airborne hydrogen fluoride and nitric acid below applicable national occupational exposure limits.