Products

RCA Standard Clean Solution (SC-1, SC-2) Electronic/EL Grade

    • Product Name: RCA Standard Clean Solution (SC-1, SC-2) Electronic/EL Grade
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications
    HS Code 445027
    Product Name RCA Standard Clean Solution (SC-1, SC-2) Electronic/EL Grade
    Sc 1 Composition Ammonium hydroxide, hydrogen peroxide, deionized water
    Sc 2 Composition Hydrochloric acid, hydrogen peroxide, deionized water
    Typical Sc 1 Mixing Ratio 1:1:5 (NH4OH:H2O2:H2O) or 1:2:7
    Typical Sc 2 Mixing Ratio 1:1:6 (HCl:H2O2:H2O) or 1:2:8
    Grade Electronic/EL Grade, high-purity semiconductor processing
    Primary Function Of Sc 1 Removal of organic residues and particulate contaminants from silicon wafers
    Primary Function Of Sc 2 Removal of metallic contaminants including alkali and heavy metal ions
    Process Temperature Typically 70 to 80 degrees Celsius
    Ph At Operating Concentration SC-1 alkaline approximately pH 10-11; SC-2 acidic approximately pH 1-2
    Water Purity Basis Prepared with ultrapure deionized water, resistivity greater than 18 MOhm-cm
    Metallic Impurity Level Controlled to parts-per-billion or lower trace metal limits
    Physical Form Clear liquid solution supplied as liquid concentrates or ready-to-use mixtures
    Container Type Typically supplied in high-density polyethylene bottles or drums
    Storage Requirement Store in tightly sealed containers away from heat, light, and incompatible chemicals
    Safety Classification Corrosive and oxidizing; causes skin and eye damage, requires proper handling

    As an accredited RCA Standard Clean Solution (SC-1, SC-2) Electronic/EL Grade factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Each kit contains two 1-gallon HDPE bottles: SC-1 and SC-2 Electronic/EL Grade, with tamper-evident caps for safe handling.
    Container Loading (20′ FCL) 20′ FCL: Standard Clean Solution SC-1/SC-2 loaded in sealed drums/carboys, secured, labeled, documented for safe electronic-grade transport.
    Shipping Shipping this corrosive/oxidizing electronic-grade solution requires strict hazardous materials compliance. Packaged in UN-certified HDPE containers with corrosion labels and oxidizer placards. Transport by ground under DOT; air/sea subject to IATA/IMDG restrictions. Ship separately from acids, reducing agents, and organics. Proper documentation and trained personnel ensure safe delivery.
    Storage Store SC-1 and SC-2 separately in clean, clearly labeled high-purity HDPE or PFA containers. Keep tightly capped in cool, dry, ventilated cabinets away from incompatible acids, bases, and oxidizable materials. Protect from heat, sunlight, and contamination. Monitor expiry; hydrogen peroxide decomposes and releases gas, so vent periodically in approved conditions.
    Shelf Life Shelf life is typically six months from manufacture if stored unopened, tightly sealed, and refrigerated; use promptly after opening.
    Application of RCA Standard Clean Solution (SC-1, SC-2) Electronic/EL Grade

    RCA Standard Clean Solution (SC-1, SC-2) Electronic/EL Grade — Downstream Application Section

    RCA standard clean solutions are deployed as two-step oxidation and complexation sequences in semiconductor, display, photovoltaic, compound semiconductor, advanced packaging, and MEMS manufacturing. SC-1 (ammonium hydroxide, hydrogen peroxide, ultrapure water) removes organic films and particle-bound contamination by simultaneous oxidation and ammonia-mediated dissolution; SC-2 (hydrochloric acid, hydrogen peroxide, ultrapure water) removes alkali and transition metal ions by chloride complexation after the SC-1 step. Electronic/EL grade supply is specified against SEMI C27, SEMI C28, and SEMI C29 with trace metal analysis by ICP-MS, particle counting by laser light scattering, and anion exclusion by ion chromatography. The scenarios below are limited to downstream production routes in which published process records, contamination signatures, and final-product quality limits are documented; published data for this specific configuration is limited where noted.

    Electronic-grade reagentNormative specificationTrace metal control targets commonly reported on C of AApplicable analytical method
    Ammonium hydroxide 29%SEMI C2710 ppb for Fe, Cu, Ni, Zn; ≤5 ppb for Na, KICP-MS after pre-concentration
    Hydrogen peroxide 30–31%SEMI C291 ppb for Al, Ca, Fe, Na, CuICP-MS
    Hydrochloric acid 37%SEMI C285 ppb for Fe, Ni, Cr, Zn, NaICP-MS

    Silicon wafer surfaces immediately before gate dielectric growth are exposed to SC-1 chemistry at a bath composition of 1:1:5 NH4OH:H2O2:H2O by volume at 70–80°C for 600–900 s, followed by SC-2 at 1:1:6 at 70–80°C for 600 s in a quartz immersion wet bench with recirculation of 20–40 L/min through 0.05 μm point-of-use filters. The electronic/EL grade reagents are supplied with certificates of analysis against SEMI C27, SEMI C28, and SEMI C29, and the wet bench installation is maintained under ISO 14644-1:2015 Class 3 front-opening unified pod handling. SC-1 oxidizes surface-bound organic residues to water-soluble carboxylic acid species and undercuts particles by forming a hydrous oxide film, which is subsequently removed in dilute hydrofluoric acid. SC-2 removes alkali and transition metal ions that survive SC-1 by converting insoluble hydroxides into soluble chloride complexes. Bath temperature is maintained within ±2°C of setpoint because thermal oxide etch rate and NH3 volatilization respond exponentially to temperature; at 80°C the NH3 partial pressure above an open tank can shift bath pH downward by 0.2–0.5 units over 8 h, reducing particle removal efficiency and promoting re-deposition of Fe and Cu on silicon. Batch-to-batch variance in hydrogen peroxide stabilizer content influences foam formation in megasonic baths; electronic/EL grade H2O2 with stabilizer below 10 ppm is required to maintain stable cavitation and reduce organic re-deposition. In production-scale immersion tools equipped with megasonic transducers at 950 kHz–1 MHz and power density 10–20 W/cm² measured at the transducer face, the SC-1 bath is replenished by bleed-and-feed at 0.5–1.0 turnover per hour to hold ammonia concentration within 3% of nominal. Ratio control is a process-critical variable: moving from 1:1:5 to 1:2:7 at constant temperature increases silicon haze on Si(100), while moving to 1:1:50 in a single-wafer spray tool shortens contact time to 30–60 s and is used for backside and bevel contamination control. The downstream production process proceeds through ultrapure water rinse at 18.2 MΩ·cm resistivity, dilute HF, final rinse, and isopropyl alcohol vapor or Marangoni drying. Terminal finished product types include logic devices with gate oxide thickness below 10 nm, DRAM storage capacitors, and NAND flash memory dies. Operational boundaries include prohibition of SC-1 contact with exposed copper metallization because ammonia forms soluble [Cu(NH3)4]2+ complexes that elevate surface Cu concentration, and exclusion of stainless steel wetted parts because iron leaching at 50 ppb degrades gate oxide integrity.

    Why Does Indium Tin Oxide Adhesion Depend on SC-1 Residue Control?

    In TFT-LCD and OLED backplane manufacturing, indium tin oxide (ITO) adhesion loss on alkali borosilicate glass substrates is frequently traced to condensed organic films and alkali metal contamination remaining after detergent, brush, and carbon dioxide cleaning. The SC-1 step for display glass is operated at a lower temperature window of 45–60°C with a typical volumetric ratio of 1:1:10 NH4OH:H2O2:H2O because the glass surface leaches sodium and calcium at higher pH and temperature. SC-2 is applied at 1:1:10 HCl:H2O2:H2O at 45–60°C for 120–240 s to reduce Fe, Na, K, and Ca to levels required for sputtered ITO adhesion; residual alkali above 5×10¹² atoms/cm² measured by TOF-SIMS is a commonly reported threshold associated with mura and local work function shifts in finished panels. The chemical supply is governed by SEMI C27, SEMI C28, and SEMI C29 trace metal specifications; equipment safety compliance is audited under SEMI S2. The production process is a horizontal conveyorized multistage cleaner with brush scrub, megasonic immersion at 40–80 kHz, air knife drying, and cleanroom transfer under ISO 14644-1:2015 Class 5. Terminal finished product types include amorphous silicon TFT arrays, indium gallium zinc oxide backplanes for OLED, and low-temperature polysilicon frontplane glass. The process boundary is defined by glass surface damage: SC-1 temperature above 60°C or ammonia ratio above 1:2:10 increases surface haze beyond the photomask alignment threshold, and direct contact of SC-2 with aluminum gate electrodes before passivation will produce local pits.

    High-efficiency n-type monocrystalline photovoltaic lines insert RCA cleaning after alkaline texturing because metal-induced J0 degradation and transition metal catalysis make passivation layers sensitive to residual K, Na, Fe, and Ni. SC-1 at 1:1:5 to 1:1:10 at 65–70°C for 300–600 s is used after potassium hydroxide-isopropanol saw damage removal and texturing to dissolve organic additives and residues, while SC-2 at 1:1:6 at 65°C removes K, Na, Fe, and Ni that would otherwise incorporate into the subsequent boron and phosphorus diffusion layers. In batch immersion equipment with PVDF tanks and overflowing ultrapure water rinse, the solution is changed after 4–6 batches or at a conductivity rise of 10 μS/cm above baseline to prevent cross-contamination. Chemical purity for photovoltaic processing is not governed by a single PV-specific standard; the supply is specified to SEMI C27, SEMI C28, and SEMI C29 with additional REACH and RoHS declarations, and the process environment is controlled to ISO 14644-1:2015 Class 6. The downstream production process moves the cleaned wafers into low-pressure diffusion furnaces for boron or phosphorus doping, followed by passivation layer deposition by PECVD or ALD. Terminal finished product types are passivated emitter and rear contact (PERC), tunnel oxide passivated contact (TOPCon), and heterojunction (HJT) cells; cleaned surface condition is directly linked to carrier lifetime measured by quasi-steady-state photoconductance decay. Operational boundary: SC-1 at high ammonia concentration consumes 0.5–1.0 nm of textured silicon surface per cycle, so process engineers limit cleaning reworks to avoid reducing the pyramidal texture aspect ratio needed for light trapping. Published data for this specific configuration is limited where fabs have tuned proprietary ratios and dwell times.

    Thermal Desorption of Sulfur and Arsenic Cross-Contaminants from GaAs and GaN Templates

    For metalorganic chemical vapor deposition (MOCVD) of GaN on sapphire and for molecular beam epitaxy of GaAs-based HBT and pHEMT structures, substrate preparation requires removal of sulfur, arsenic, phosphorus, and metallic residues without leaving an oxygen-rich surface that modifies epilayer nucleation. SC-2 at 1:1:20 HCl:H2O2:H2O at 25–35°C for 60–120 s is applied first in some III-V substrate fabs to strip transition metal chlorides, followed by SC-1 at 1:1:20 NH4OH:H2O2:H2O at 25°C for 60 s to remove light organic contamination. Thermal desorption of sulfur and arsenic from contaminated templates is not a substitute for chloride complexation; SC-2 removes the alkali and transition metal fraction that thermal desorption leaves behind as nonvolatile sulfate residues, and SC-1 removes the organic overlayer that would otherwise carburize at pre-epitaxy temperatures. The ratios are more dilute than silicon front-end chemistries because concentrated SC-1 at elevated temperature etches GaAs at measurable rates and preferentially oxidizes arsenic to soluble arsenite species, changing surface stoichiometry from Ga-rich to As-deficient. Compliance requirements are driven by SEMI C27, SEMI C28, and SEMI C29 for trace metal levels, with additional documentation for REACH restrictions on arsenic-containing substrates and carrier transport. The downstream production process uses single-wafer spin cleaning tools with chemical nozzle delivery, ultrapure water rinse at 18.2 MΩ·cm, and nitrogen blow-off before loading into MOCVD reactors. Terminal finished product types include gallium nitride high-electron-mobility transistors, GaAs pHEMT power amplifiers, VCSELs for data communication, and LED chips. Process boundaries include incompatibility with silver-filled die attach surfaces and exclusion of phosphate-buffered cleaning agents; phosphate residues form insoluble phosphates with Group III cations and suppress nucleation density. Published data for this specific configuration is limited for narrow compound semiconductor substrate sizes, so equipment-specific dilution must be qualified by photoluminescence mapping and XPS surface stoichiometry checks.

    When the Hourly Bath Exchange Rate Falls Below 0.5, Ionic Copper Carryover Rewrites the Failure Signature

    When the bath exchange rate in an SC-1 immersion system for flip-chip and redistribution layer (RDL) wafers falls below 0.5 turnovers per hour, copper ions released from earlier process steps are not cleared fast enough to prevent galvanic deposition on exposed aluminum pads and on the backside of thinned wafers. SC-1 at 1:1:10 NH4OH:H2O2:H2O at 65°C for 300 s removes post-etch polymer residues from redistributed line patterns, while SC-2 at 1:1:10 HCl:H2O2:H2O at 65°C for 300 s removes sodium, potassium, and calcium ions before copper electroplating. The electronic-grade reagents are specified to SEMI C27, SEMI C28, and SEMI C29, and the wet bench tool set is validated under SEMI S2 for chemical handling interlocks. The downstream production process includes physical vapor deposition of Ti/Cu seed layers, electroplating of copper pillars at current densities of 3–8 A/dm², dry film resist stripping, solder bump reflow, and final wafer probe. Terminal finished product types are copper pillar bumped wafers, 2.5D through-silicon via interposers, and fan-out panel-level packages. The main operational limitation is copper ion complexation in SC-1: ammonia forms [Cu(NH3)4]2+, so combined waste streams from SC-1 and copper sulfate electroplating must be separated before neutralization to avoid re-precipitation of copper hydroxide in facility drains. Process control requires daily ICP-MS monitoring of the SC-1 bath for Cu at a detection limit of 0.1 ppb; if Cu exceeds 10 ppb, the bath is dumped and replenished.

    Anhydrous HF-Vapor Compatibility and SC-2 Last-Cleaning Sequences in MEMS Fabrication

    In surface-micromachined MEMS flows, the last aqueous cleaning sequence before alcohol-based or supercritical carbon dioxide drying determines release-related stiction yield and the final potassium ion concentration on movable polysilicon structures. SC-1 at 1:1:5 NH4OH:H2O2:H2O at 75°C for 300 s removes organic contamination and particle residues after deep reactive ion etching and sacrificial oxide release in vapor HF, but it is only compatible with polysilicon, silicon nitride, and silicon oxide surfaces. SC-2 at 1:1:8 HCl:H2O2:H2O at 75°C for 300 s then removes residual K, Na, Fe, and Ni from KOH and TMAH release steps and from dicing tape transfer. The chemicals are specified to SEMI C27, SEMI C28, and SEMI C29, and the cleaning process is performed in an ISO 14644-1:2015 Class 4 environment with point-of-use filtration at 0.02 μm. The downstream production process continues with isopropyl alcohol vapor drying or supercritical CO2 drying to avoid liquid-vapor surface tension collapse of high-aspect-ratio comb-drive gaps below 2 μm. Terminal finished product types include capacitive accelerometers, gyroscopes, pressure sensors, and RF MEMS resonators. The principal incompatibility is with exposed aluminum metallization: both SC-1 and SC-2 attack aluminum at this temperature, and aluminum bond pads must be protected by resist or deposited after the clean. A second operational boundary is that the ammonia concentration in SC-1 must be maintained within ±3% of the target; excess ammonia increases polysilicon surface roughness and reduces the effective gap dimension in resonant structures, while depleted ammonia leaves residue that increases stiction probability in release tests.

    Free Quote

    Competitive RCA Standard Clean Solution (SC-1, SC-2) Electronic/EL Grade prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8615365186327 or mail to admin@ascent-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615365186327

    Email: admin@ascent-chem.com

    Inquiry

    Get Free Quote of Ascent Petrochem Holdings Co., Limited

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    The RCA Standard Clean Solution (SC-1, SC-2) Electronic/EL Grade is supplied as a matched two-chemistry aqueous system for front-end silicon preprocessing. SC-1 is an alkaline oxidative mixture, conventionally prepared from 29% ammonium hydroxide, 30% hydrogen peroxide, and ultra-pure water in a 1:1:5 volume ratio. SC-2 is an acidic oxidative mixture prepared from 37% hydrochloric acid, 30% hydrogen peroxide, and ultra-pure water in a 1:1:6 volume ratio. The Electronic/EL Grade designation indicates that both components are handled, filled, and certified under control limits appropriate for semiconductor wet benches, not as generic technical chemicals. The process descends from the Kern and Puotinen RCA cleaning method reported in 1970, and the SC-1/SC-2 sequence remains a reference for pre-diffusion and pre-deposition cleaning of silicon surfaces where metallic contamination and particle loads must be reduced before high-temperature furnace operations.

    In a conventional batch immersion wet bench, SC-1 is heated in a quartz or high-purity PVDF tank and recirculated through 0.1 µm PTFE or PFA filters. Typical bath temperature is 70°C to 80°C, with immersion times of 5 min to 10 min. Megasonic transducers operating between 0.8 MHz and 1.2 MHz are often used during SC-1 processing to increase particle detachment efficiency; low-frequency sonic agitation below 0.4 MHz is generally avoided because of cavitation-induced surface damage on thermally sensitive gate oxide substrates. After the SC-1 step, the cassette passes through overflow rinses using 18 MΩ·cm water at 25°C, then enters SC-2 at the same temperature range for a second oxidative and ionic clean.

    Why Are SC-1 and SC-2 Not Combined into a Single Cleaning Bath?

    The two components are supplied separately because ammonia and hydrochloric acid neutralize to ammonium chloride with measurable heat release when combined. Premixing consumes oxidative equivalents without contributing to surface preparation, and chloride complexes formed in the mixed solution alter the metal-removal selectivity of SC-1. The sequential mode preserves the distinct functions: alkaline SC-1 oxidizes organic films and undercuts particle adhesion by forming a thin hydrous oxide layer on bare silicon, while acidic SC-2 exchanges alkali ions and removes residual metal contaminants through protonation and chloride complexation. Oxide growth after SC-1 is typically 0.7 nm to 1.0 nm on hydrogen-terminated silicon, as measured by single-wavelength ellipsometry; SC-2 does not require a separate chemical oxide step and serves as the final ionic clean before rinsing and drying.

    The SC-1 cleaning mechanism relies on simultaneous oxidation by hydrogen peroxide and etching by ammonium hydroxide. Organic films are oxidized to carboxylic and hydroxyl species that become more soluble in the alkaline medium; particle removal is assisted by the formation of a fresh chemical oxide that lifts adherent particles from the surface. In SC-2, the dilute hydrochloric acid matrix dissolves residual metal oxides and converts alkali ions to soluble chlorides. The key difference from a simple acid or base soak is the presence of hydrogen peroxide as an oxidizer that prevents re-adsorption of reduced metal species. This dual action is why SC-1 and SC-2 are described as clean rather than etch formulations: their objective is to remove contamination without substantially consuming the underlying film stack.

    Electronic/EL Grade raw materials are controlled at the component level to semiconductor supply-chain specifications. Ammonium hydroxide quality is commonly aligned to SEMI C28, hydrogen peroxide to SEMI C30, hydrochloric acid to SEMI C35, and dilution water to ASTM D5127 Type E-1.2 or equivalent. The blended product certificate routinely reports individual transition metal concentrations below 1 ppb to 10 ppb for Fe, Ni, Cu, Zn, Al, and Cr, with aggregate transition metal concentrations typically controlled below 50 ppb for critical front-end cleaning. Laser particle counters set at 0.2 µm sensitivity are used for lot qualification, and typical certificate limits remain below 100 particles/mL at ≥0.5 µm; however, the exact ceiling is defined by the receiving fab process specification rather than by a single universal value.

    For lot verification, inductively coupled plasma mass spectrometry is the reference technique for trace metal assays in both SC-1 and SC-2 because it provides detection limits below 1 ppt for elements such as Fe, Cu, Ni, and Al after matrix dilution. Anion analysis by ion chromatography is used to document chloride, nitrate, and sulfate levels; total organic carbon is measured by UV-persulfate oxidation. Particle content is inspected by optical particle counters, but the 0.2 µm channel may show baseline counts if the sample is not degassed before measurement, because hydrogen peroxide bubbles are counted as particles.

    Typical immersion wet-bench control ranges for SC-1 and SC-2
    ParameterSC-1SC-2
    Volumetric ratio1:1:5 NH4OH:H2O2:H2O1:1:6 HCl:H2O2:H2O
    Operating temperature70°C to 80°C70°C to 80°C
    Typical immersion time5 min to 10 min5 min to 10 min
    Point-of-use filtration0.1 µm PTFE or PFA0.1 µm PTFE or PFA
    Bath-life process controlH2O2 assay at or above 70% of make-up; pH 9.8 to 10.5H2O2 assay at or above 70% of make-up; pH 0.5 to 1.5
    Main residue targetParticles, organic films, some transition metalsAlkali ions, iron, magnesium, hydroxide residues

    Both baths are incompatible with exposed aluminum metallization. SC-1 attacks Al via alkaline ammonia etching and peroxide oxidation at the 70°C to 80°C operating range; SC-2 attacks Al via chloride-containing acid attack. Wetted components on recirculating lines should be limited to high-purity quartz, PFA, PTFE, and unpigmented PVDF. The use of stainless steel or conventional polymeric fittings with metallic fillers introduces Fe, Ni, and Cr contamination and accelerates hydrogen peroxide decomposition. Pump seals and valve diaphragms on production wet benches should be inspected for particulate shedding when the bath is held at temperature for extended periods; batch-to-batch variance in the peroxide assay is a more common cause of lot-to-lot cleaning drift than variation in raw ammonia or acid feed.

    Thermal Stability and Hydrogen Peroxide Decomposition in Heated Quartz Tanks

    Hydrogen peroxide decomposition dominates the useful life of both baths, but the rate is higher in SC-1 because alkaline pH accelerates decomposition. At 80°C, dissolved oxygen evolves at the tank walls and behind cassette supports; this produces microbubbles that can later release and disturb the meniscus of patterned wafers. A useful control window is to monitor the H2O2 assay and pH rather than relying only on elapsed time. SC-1 is typically replenished when the peroxide concentration falls below 70% of initial charge or when the pH shifts by more than 0.5 pH units. SC-2 has a longer bath life because the acidic matrix slows peroxide decomposition, but venting is still required to remove oxygen and HCl vapor. Ammonia loss from heated SC-1 also reduces pH; open baths can lose sufficient ammonia within 4 h to 8 h to shift the surface etch and particle removal balance.

    During production, bath temperature is monitored by platinum RTD sensors with calibration traceable to NIST or equivalent. Temperature overshoot beyond 85°C in SC-1 increases the decomposition rate of hydrogen peroxide and can produce erratic particle removal because the balance between oxidation and silicon etch shifts. Wet benches are equipped with pH and conductivity sensors downstream of the filter; a drop in conductivity may indicate drag-out dilution or exhaustion of the active bath. Some fabs operate with a bleed-and-feed scheme: for every 25-wafer lot processed, a set volume of fresh SC-1 or SC-2 is injected while an equal volume is sent to drain. This maintains stable cleaning rates at the expense of chemical consumption.

    The main usage points are pre-furnace clean before gate oxidation, pre-LPCVD silicon nitride or polysilicon deposition, post-CMP particle control, and pre-epitaxy surface preparation for silicon and some III-V substrates if compatibility is verified. SC-1/SC-2 is not recommended for wafers with exposed aluminum or copper because the alkaline and acidic oxidizer mixtures attack both metals. For copper damascene structures, a neutral or dilute organic acid clean is used instead. The RCA solution is also not a photoresist stripper for bulk resist; it can remove light organic contamination but is not intended to dissolve hardened resist after implant, where dry ashing or solvent-based stripping remains necessary.

    When HF or Piranha Is Substituted for RCA Cleaning on the Same Wet Bench

    Piranha solutions, usually sulfuric acid and hydrogen peroxide at 4:1 or 7:1, provide stronger organic oxidation and photoresist removal than SC-1, but they leave sulfur-bearing residues and have a larger mixing exotherm. Dilute HF at 0.5% to 2% removes chemical and native oxide faster than either RCA component but does not provide oxidative undercutting of particles. It also leaves the silicon surface hydrogen-terminated and can allow alkali-ion residues to remain unless an acid clean such as SC-2 or hydrochloric acid is used. Proprietary single-wafer cleaners based on citric acid, TMAH, or dilute ammonia peroxide mixtures can reduce chemical use but may not reproduce the same oxide-growth and metal-ion exchange behavior as SC-1 and SC-2 under identical immersion conditions. The Electronic/EL Grade product differs from technical-grade RCA-type blending in purity, lot documentation, and packaging; the chemistry itself is not uniquely proprietary, but the control of trace metal and particle burdens is the differentiating specification.

    Contrast with adjacent cleaning chemistries
    ChemistryTypical matrixMain functionKey limits
    SC-11:1:5 NH4OH/H2O2/H2OParticle undercut and organic oxidationNH3 loss, H2O2 decomposition, attacks Al
    SC-21:1:6 HCl/H2O2/H2OAlkali ion removal and metal chloride complexationHCl vapor, attacks Al
    Piranha4:1 to 7:1 H2SO4/H2O2Organic and photoresist stripHigh mixing exotherm, sulfur residue, high viscosity
    Dilute HF0.5% to 2% HFOxide etching and hydrogen terminationNo particle undercut, metal redeposition risk

    Technical-grade ammonium hydroxide and hydrochloric acid from general chemical supply chains may contain Fe, Cu, and Zn at levels 100 ppb to 1 ppm; this is sufficient to shift surface recombination velocity after cleaning. Electronic/EL Grade RCA components are purified by distillation, submicron filtration, and cleanroom packaging to reduce the total metal burden to roughly 1 ppb to 10 ppb. The term EL further implies that packaging extractables and particulate release have been characterized for cleanroom use. A field-bottled mixture using laboratory-grade chemicals and DI water from a non-validated tap will not meet the particle and cation budgets required for silicon oxide integrity; therefore, the product is not equivalent to an open-bench reagent kit unless the user performs the same analytical release testing.

    Incoming acceptance should verify the certificate of analysis for the exact lot, confirm that the SC-1 and SC-2 containers are segregated in storage, and reject any lot showing organic carbon or particle excursions above control limits. The two components must never be mixed in storage or waste lines; neutralization should occur in dedicated, continuously monitored waste treatment with separate acid and ammonia bleed lines. For high-volume fabs using central chemical distribution, the product is delivered through high-purity lines and spiked at point of use; for lower-volume lines, bottles or drums are dispensed into cleanroom-compatible cabinets under ISO 14644 Class 4 or better conditions. Published data for specific liner extractable profiles in 200 L high-purity drums is limited, and in-house extractable validation is recommended when the product is held for more than 12 months.

    Top