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G-line Photoresist TOK TSMR-8900

    • Product Name: G-line Photoresist TOK TSMR-8900
    • 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 903035
    Product Name TOK TSMR-8900
    Product Type G-line positive photoresist
    Chemistry Novolak resin and diazonaphthoquinone photoactive compound
    Exposure Wavelength 436 nm
    Viscosity 3 to 10 mPa·s typ., depending on grade
    Solid Content 18–25 wt%
    Density approximately 1.0 g/cm³
    Flash Point 44–46 °C
    Photosensitivity approximately 100 mJ/cm²
    Resolution submicron lines and spaces typ.
    Film Thickness Range 0.8–10 µm
    Contrast gamma > 3
    Developer aqueous alkaline developer such as TMAH
    Etching Resistance good
    Storage Temperature 5–25 °C
    Shelf Life 6 months from date of manufacture in original sealed container

    As an accredited G-line Photoresist TOK TSMR-8900 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing G-line photoresist TOK TSMR-8900 is supplied in a sealed brown glass bottle, quantity 1 liter, for cleanroom use.
    Container Loading (20′ FCL) One 20′ FCL of G-line Photoresist TOK TSMR-8900, securely packed, labeled hazardous, and loaded for safe transport.
    Shipping Ship as **UN1263, Photoresist solution (G-line Photoresist TOK TSMR-8900), Class 3 Flammable Liquid, Packing Group II/III**. Use grounded, sealed containers, upright and cushioned. Avoid heat, ignition sources, moisture, and oxidizers. Label as hazardous material and include shipping papers, emergency response information, and compatible segregation.
    Storage Store G-line Photoresist TOK TSMR-8900 in its original, tightly sealed container in a cool, dry, well-ventilated area away from direct sunlight and heat/ignition sources. Maintain stable temperatures between 5–30°C. Avoid exposure to moisture, dust, and incompatible materials. Handle with clean, dry tools to prevent contamination, and follow manufacturer shelf-life guidance.
    Shelf Life Shelf life is typically 6 months when stored tightly sealed at 5–25°C, away from light and heat.
    Application of G-line Photoresist TOK TSMR-8900

    On a 200 mm silicon wafer line running 0.5 µm g-line lithography for aluminium-copper interconnect layers, TOK TSMR-8900 is dispensed through 0.2 µm point-of-use filtration at a static volume of 3.0 mL to 4.0 mL per wafer, then spin-coated to a nominal film thickness of 0.95 µm to 1.10 µm at 3000 rpm depending on exhaust backpressure and wafer bow. The softbake is performed on a hotplate at 90 °C for 60 s, a thermal budget that drives off residual PGMEA without causing thermal crosslinking of the novolak resin. Exposure is carried out at 436 nm with a dose of 80–120 mJ/cm² on a g-line stepper or aligned scanner; post-exposure bake at 110 °C for 60 s suppresses standing-wave ripples on reflective aluminium-grain surfaces. Development in 2.38% tetramethylammonium hydroxide with a single-puddle process for 60 s produces 0.5 µm line/space resolution in 1.0 µm film. The patterned resist is then used as an etch mask in a BCl3/Cl2 plasma at 13.56 MHz; photoresist-to-AlCu selectivity is 1.5:1 to 2.0:1, requiring a hardbake at 120 °C for 60 s to reduce top loss. The terminal wafer surface contains analog/mixed-signal CMOS devices, power management controllers, or discrete high-side switches. Mask adhesion is monitored with a scribe-tape test consistent with ASTM D3359-17, linewidth uniformity is measured by top-down CD-SEM with ±5% three-sigma control, and resist thickness is checked by spectroscopic ellipsometry against a 1.0 µm reference. Chemical safety and equipment interaction are documented under SEMI S2-0718; PGMEA waste is handled under 40 CFR 261 hazardous waste classifications.

    What Changes When TSMR-8900 Is Used as an Electroplating Mold for Copper RDL in Wafer-Level Packaging?

    The electroplating mold configuration changes the substrate from silicon oxide to sputtered copper seed, and the photoresist film is no longer a sacrificial etch mask but a negative cavity former. After wafer-level dielectric coating and Ti/Cu seed deposition, the wafer is dehydrated at 150 °C for 60 s and treated with HMDS vapor at 120 °C for 5 min; however, excessive amine-containing adhesion promoters on copper seed must be controlled because they can retard TMAH dissolution at the base of the resist feature. TSMR-8900 is coated at 2500 rpm to a thickness of 1.2 µm, softbaked at 85 °C for 60 s, exposed at 436 nm with 100–140 mJ/cm², and developed in 2.38% TMAH using a spray-puddle sequence for 90 s to clear high-aspect-ratio redistribution layer vias. A post-develop descum at 50 W in argon for 30 s removes resist residue without oxidizing the Cu seed; oxygen descum is avoided because CuOx forms at the seed surface and causes plating voids. Copper electroplating is then performed in an acid copper bath containing CuSO4·5H2O at 160 g/L, H2SO4 at 60 g/L, and chloride ion at 50 ppm, with a brightener concentration maintained by cyclic voltammetry stripping; line/space RDL features are plated to 5–8 µm thickness at 2.0 A/dm² current density. Resist stripping in NMP-based solvent at 80 °C is followed by seed etch and polyimide cure. The finished wafer-level chip-scale package contains fan-in copper redistribution lines and under-bump metallization pads; thermal cycling of the packaged device is qualified according to JEDEC JESD22-A104, and the resist supplier’s lot-to-lot viscosity variation is held within ±0.2 cP to keep RDL CD variation below ±0.15 µm on a total thickness variation of ±0.03 µm across a 200 mm wafer.

    Application configurationFilm thickness and spin speedSoftbakeDeveloper immersion/puddleCritical limitation
    AlCu front-end etch mask0.95–1.10 µm at 3000 rpm90 °C / 60 s2.38% TMAH / 60 s single puddlePlasma erosion of resist
    Cu RDL plating mold1.2 µm at 2500 rpm85 °C / 60 s2.38% TMAH / 90 s spray-puddleCu seed oxidation
    GaAs gate lift-off1.0 µm at 3000 rpm90 °C / 60 s2.38% TMAH / 30 s immersion after chlorobenzene soakUndercut control without PEB
    SAW IDT wet etch mask0.9 µm at 4000 rpm85 °C / 60 s proximity bake2.38% TMAH / 45 s immersionPyroelectric discharge from LiTaO3

    When a Chlorobenzene Soak Is Required for GaAs pHEMT Gate Lift-Off

    When TSMR-8900 is used as a lift-off mask for T-gate or rectangular-gate metallization on gallium arsenide, the native positive-tone sidewall must be converted into a controlled undercut. After HMDS priming at 110 °C for 5 min, the resist is coated at 3000 rpm to 1.0 µm and softbaked at 90 °C for 60 s; exposure at 436 nm with 90–120 mJ/cm² is followed by a room-temperature chlorobenzene soak for 10–20 min to selectively harden the resist surface and retard vertical dissolution. The wafer is developed in 2.38% TMAH for 30 s with no post-exposure bake, because a PEB at 110 °C would promote the normal positive-tone diffusion path and eliminate the undercut. Cross-sectional SEM is used to confirm an undercut of 0.1–0.3 µm per edge; variations beyond this window produce either metal stringer formation or collapse of narrow gate structures. Electron-beam evaporation of Ti/Pt/Au is performed with the wafer mounted on a planetary fixture; deposited metal thickness is 0.5 µm for the gate foot and 1.0–1.5 µm for the cap, with deposition pressure below 5 × 10⁻⁷ Torr to minimize sidewall coating. Lift-off in NMP at 80 °C with 40 kHz ultrasonic agitation removes the mask, leaving gate metal with a defined foot and wide cap. The terminal products are depletion-mode GaAs pHEMTs for low-noise amplifiers operating from 6 GHz to 40 GHz. Chlorobenzene handling demands a dedicated coater cup, exhaust face velocity above 0.3 m/s, and compliance with OSHA 1910.1000 Table Z-1 for chlorobenzene exposure below 10 ppm 8-hour TWA; REACH Regulation (EC) No 1907/2006 annex-based SDS disclosure is required, and chlorobenzene-laden waste must be segregated from PGMEA developer waste under 40 CFR 261 to avoid hazardous solvent mixtures.

    SAW Filter Interdigital Transducer Patterning on 36° Y-X Lithium Tantalate

    On 36° Y-X lithium tantalate or 128° Y-X lithium niobate piezoelectric wafers, TSMR-8900 is applied directly over sputtered aluminium of 0.2–0.4 µm thickness to define interdigital transducer fingers. Because lithium tantalate is pyroelectric, the hotplate softbake must use a proximity bake at 85 °C for 60 s or a ramp rate below 5 °C/min to avoid pyroelectric discharge that punctures the aluminium film. Exposure at 436 nm on a g-line stepper with 80–130 mJ/cm² creates risk of standing-wave interference from the high-refractive-index substrate; a dyed or bottom antireflective layer is often not used because resist thickness is fixed at 0.9 µm by the IDT etch selectivity. Development in 2.38% TMAH for 45 s clears 0.4 µm IDT lines and spaces, and the resist is hardbaked at 110 °C for 60 s before wet etching the aluminium in a phosphoric acid/nitric acid/acetic acid mixture at 35–40 °C; the etch rate is 0.8–1.2 µm/min, and resist-to-aluminium etch selectivity is approximately 10:1. After etching, the resist is stripped in NMP at 70 °C; residual scum is not tolerated because it shifts the acoustic aperture and alters resonator frequency. The terminal products are RF SAW filters and resonators operating from 800 MHz to 2.5 GHz, used in mobile front-end modules. Final electrode adhesion is verified by ASTM D3359-17 cross-cut tape test; device reliability is assessed under IEC 60068-2-58 high-temperature storage and JEDEC JESD22-A101 steady-state temperature-humidity bias. RoHS compliance for the finished SAW component is evaluated under 2011/65/EU for lead-free soldered terminations.

    Application scenarioApplicable safety/equipment standardAdhesion or performance testRestriction / boundary
    Silicon front-end AlCu etchSEMI S2-0718ASTM D3359-17 scribe-tapeHardbake required before BCl3/Cl2 etch
    Cu RDL plating moldSEMI S2-0718, JEDEC JESD22-A104CD-SEM and plating void inspectionAvoid oxygen descum on Cu seed
    GaAs gate lift-offOSHA 1910.1000, REACH 1907/2006Cross-sectional SEM undercutNo PEB after chlorobenzene soak
    SAW IDT wet etchIEC 60068-2-58, ASTM D3359-17Electrode adhesion cross-cutProximity bake below 5 °C/min
    MEMS sacrificial oxide wet etchSEMI S2-0718, 40 CFR 261Cross-cut adhesion before/after hardbakeIncompatible with exposed aluminium pads
    Photodiode nitride etchSEMI S2-0718, JEDEC J-STD-020EOptical CD and IEC 60747-5 performanceSeparate TMAH and CHF3/O2 exhaust streams

    For a MEMS silicon oxide sacrificial layer definition on 150 mm silicon-on-insulator wafers, TSMR-8900 is applied as a wet-etch mask in buffered hydrofluoric acid-based etchants. The wafer receives a dehydration bake at 200 °C for 120 s on a contact hotplate, followed by HMDS vapor priming at 120 °C for 5 min; this sequence raises adhesion from 2B to 5B when assessed by ASTM D3359-17 cross-cut, a necessary condition for immersion in HF-based etch baths. TSMR-8900 is coated at 4000 rpm to 0.9 µm, softbaked at 90 °C for 60 s, exposed at 436 nm with 70–110 mJ/cm², and developed in 2.38% TMAH for 45 s. After a hardbake at 120 °C for 90 s, the patterned resist protects selected regions during room-temperature etching in buffered HF at 6:1 ratio; etch time for 1.0 µm of thermal oxide is 8–12 min, during which resist adhesion loss or pinhole formation results in oxide pitting. The process is not compatible with exposed aluminium bond pads, which are rapidly attacked by the HF bath; when aluminium pads are present, a double-layer masking sequence or an alternative dry-etch path is required. After etch completion, the resist is stripped in oxygen plasma at 150 °C for 30 min or with 80 °C NMP. The terminal devices are MEMS gyroscopes, accelerometers, or pressure-sensor membranes in which the sacrificial oxide layer defines the released microstructure; critical dimension loss during wet etch is held below 0.1 µm per edge by overbake densification and adhesion monitoring. Process safety is governed by SEMI S2-0718 for the HF wet bench, and the waste stream is categorized under 40 CFR 261 as corrosive hazardous waste, with pH neutralization before discharge.

    Photodiode Front-Side Contact Patterning on Plasma-Deposited Silicon Nitride

    When a front-side illuminated photodiode wafer requires contact window opening in a 0.3 µm PECVD silicon nitride passivation layer, TSMR-8900 is used as a dry-etch mask for CHF3/O2 plasma. The nitride film is first cleaned in 100:1 diluted hydrofluoric acid for 30 s to remove native oxide, dehydration-baked at 180 °C for 60 s, and HMDS-primed at 120 °C for 5 min. The resist is spin-coated at 3000 rpm to 1.0 µm, softbaked at 90 °C for 60 s, exposed at 436 nm with 90–130 mJ/cm², and developed in 2.38% TMAH for 60 s. A post-develop oxygen descum at 40 W for 20 s removes scum before nitride etch; the presence of caustic developer residues on the nitride surface can cause uneven etch initiation and is minimized by a 30 s deionized water rinse at 20 °C. Reactive-ion etching is performed with CHF3/O2 at 50 mTorr and 150 W RF power, giving nitride etch rates of 30–40 nm/min and photoresist etch rates of 25–35 nm/min, so the 1.0 µm resist mask can safely clear 0.3 µm of nitride without excessive faceting. After etch, the resist is stripped in oxygen plasma at 120 °C for 20 min; remaining nitride defines the photodiode active area and contact windows. The terminal components are front-side illuminated silicon photodiodes for optical sensors, automotive light detection, or medical pulse oximetry; final photodiode performance is tested according to IEC 60747-5 semiconductor photodetector specifications, and the packaged device is assessed for lead-free soldering under JEDEC J-STD-020E moisture sensitivity classification. Solvent and stripper handling on the line is covered by SEMI S2-0718, and PGMEA-containing waste is segregated under 40 CFR 261; the combination of TMAH developer and CHF3/O2 plasma requires separate exhaust streams to prevent fluoride-amine salt formation in ductwork.

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    Certification & Compliance
    More Introduction

    G-line Photoresist TOK TSMR-8900 is a positive-working photoresist supplied by Tokyo Ohka Kogyo Co., Ltd. for contact, proximity, and stepper lithography at 436 nm. The formulation belongs to the diazonaphthoquinone–novolac class; exposure initiates Wolff rearrangement of the diazonaphthoquinone sulfonate ester to indene carboxylic acid, rendering exposed regions soluble in aqueous tetramethylammonium hydroxide developer. The product is supplied as a filtered, electronic-grade liquid and is used in semiconductor packaging, MEMS, compound semiconductor, and research and development applications requiring single-coat film thicknesses from approximately 0.8 µm to 5.0 µm, depending on dispense and spin parameters. Unlike chemically amplified deep-ultraviolet resists, TSMR-8900 does not require post-exposure bake to form the solubility differential and is not subject to post-coat delay instability caused by airborne amine contamination. The principal engineering trade-offs are g-line diffraction-limited resolution, thermal flow onset in the 120–130 °C range, and sensitivity to humidity during extended post-exposure delay.

    Manufacturer lot data for TSMR-8900 is distributed through controlled technical datasheets rather than open secondary sources; process windows cited in this document are class-typical for g-line diazonaphthoquinone–novolac systems and must be verified against the lot-specific certificate of analysis before production release.

    What Distinguishes TSMR-8900 from I-Line and Broadband DNQ/Novolac Resists?

    The spectral sensitization is the primary distinction. Formulating a diazonaphthoquinone–novolac resist for 436 nm rather than 365 nm shifts the photolysis rate deeper into the film; this permits more uniform sidewall angle in thicker films and reduces standing-wave amplitude on reflective substrates when used with bottom antireflective coatings or dyed resists. In comparison with broadband resists that absorb across 350–450 nm, TSMR-8900 suppresses unwanted i-line response where a g-line-only aligner or stepper is specified, reducing exposure in nominally unexposed regions during out-of-band illumination. In i-line resists, diazonaphthoquinone concentration and novolac dissolution inhibition are optimized for higher resolution at 0.35 µm geometries, but the same formulations often show excessive dark erosion in 4–5 µm films because of longer development times. TSMR-8900 is formulated instead to preserve class-typical dark erosion below 10 nm during 60 s immersion development in 2.38 wt% tetramethylammonium hydroxide at 23 °C.

    Comparative classification matrix for TSMR-8900 versus adjacent photoresist classes
    Parameter TSMR-8900 g-line DNQ/novolac Typical i-line DNQ/novolac Typical deep-ultraviolet chemically amplified
    Actinic wavelength 436 nm 365 nm 248 nm
    Post-exposure bake requirement Not required for image formation Not required for image formation Required for acid-catalyzed deprotection
    Airborne amine sensitivity Low Low High; post-coat delay shifts critical dimension
    Typical film thickness range 0.8–5.0 µm 0.5–3.0 µm 0.1–0.5 µm
    Resolution at k1 = 0.5, NA 0.45 0.48 µm 0.41 µm 0.28 µm
    Dark erosion in 2.38 wt% TMAH, 60 s <10 nm <10 nm Not applicable

    Values in the matrix are compiled from standard optical lithography scaling equations and supplier technical bulletins for resist classes; lot-specific values for TSMR-8900 appear on the certificate of analysis.

    On a contact or proximity aligner, coating thickness control begins with substrate dehydration and hexamethyldisilazane vapor priming. A 60 s hotplate dehydration bake at 150 °C followed by hexamethyldisilazane vapor prime in a YES-310 or equivalent vapor-prime oven improves adhesion on thermal silicon dioxide and silicon nitride. The photoresist is dispensed through a 0.1 µm point-of-use filter onto a static or low-speed wafer; spin speed is selected from the lot-specific spin curve to achieve the target film thickness. Typical g-line novolac resists produce 1.0 µm films at 4,000 rpm, 1.5 µm at 2,500 rpm, and 3.0 µm at 1,200 rpm on 150 mm silicon wafers, but TSMR-8900 requires its own spin curve because solids content and solvent evaporation affect final thickness. Film-thickness metrology is performed by reflectometry or spectroscopic ellipsometry after softbake.

    Softbake, Post-Exposure Delay, and Development Latitude in Thick-Film G-Line Patterning

    For 1.0–2.0 µm films, hotplate softbake at 100 °C for 90 s is typical; for 4–5 µm films, a two-step softbake of 90 °C for 90 s followed by 110 °C for 60 s may be used to drive residual solvent below 2% by weight. Excessive softbake above 120 °C can convert diazonaphthoquinone to a less photosensitive ester and introduce development scum at the resist-substrate interface. Insufficient softbake leaves residual propylene glycol monomethyl ether acetate, which causes bubbles and inconsistent development. A low-temperature hotplate with ±1 °C wafer-to-wafer uniformity and an exhaust balance not exceeding 0.3 m/s across the plate suppresses edge-bead solvent accumulation. Published data for TSMR-8900-specific residual solvent thresholds is limited; the above values are common for g-line novolac systems.

    Development is performed in 2.38 wt% tetramethylammonium hydroxide, pH 13.2 to 13.5, at 23 °C ± 0.5 °C, with immersion, spray, or puddle equipment. Development time is determined by contrast curve and dark erosion; 60 s in a puddle process is common for 1.0–1.5 µm films. Thick films may require 120–180 s to clear exposed features without excessive dark erosion. Endpoint monitoring by laser reflectometry or a development-rate monitor on a Tokyo Electron ACT-8 track reduces variability caused by developer temperature drift. Rinse in deionized water with 18 MΩ·cm resistivity and spin-dry at 2,000 rpm for 30 s completes the develop step. Hardbake is typically 120 °C for 30 min in a convection oven or 110 °C for 60 s on a hotplate, depending on subsequent etch selectivity. Thermal flow onset is class-typical at 120–130 °C; hardbake above 130 °C can round submicron contact profiles and reduce linewidth.

    Metals control is a primary reason for selecting electronic-grade resists over general-purpose photoresists. The product is supplied with total alkali metal specifications typically below 50 ppb sodium and potassium, with total trace metals below 200 ppb, as measured by inductively coupled plasma mass spectrometry after acid digestion. This is relevant for gate oxide integrity in metal-oxide-semiconductor devices; mobile ion contamination above 1×10¹¹ cm⁻² during photoresist processing can shift threshold voltage. The lot certificate should be reviewed for aluminium, chromium, copper, iron, lead, and zinc. Particle specifications are typically fewer than 10 particles/mL at a 0.5 µm detection threshold in as-packaged liquid. Published data for TSMR-8900-specific particle and metals limits is limited; the values shown are common for semiconductor-grade g-line novolac resists and must not replace the supplier lot-specific certificate of analysis.

    Characterization and compliance matrix for TSMR-8900 process introduction
    Parameter Method or Standard Typical control range or limit
    Viscosity at 25 °C ASTM D2196-20 20–60 mPa·s, series-dependent
    Flash point ASTM D93-20 Reported on safety data sheet; PGMEA typically 42–45 °C
    Water content Karl Fischer titration <0.1% by weight
    Total trace metals ICP-MS after digestion <200 ppb
    Alkali metals ICP-MS <50 ppb each
    Particle count at 0.5 µm Laser particle counter <10 particles/mL
    Environmental compliance REACH (EC) No 1907/2006, RoHS 2011/65/EU Restricted substances per applicable Directives

    When Post-Exposure Delay Exceeds Four Hours at Relative Humidity Above 60%

    The dissolution-inhibition contrast of diazonaphthoquinone–novolac resists is not chemically amplified, but it is still sensitive to water uptake and surface inhibition. Post-exposure delay between exposure and development can produce a surface inhibition layer in which partially exposed resist surfaces lose development rate due to water adsorption at the novolac surface. In production environments with relative humidity above 60% and delay beyond 4 h, a distinct T-topping profile can appear in 0.8–1.2 µm features. The mechanism is a reduction in indene carboxylic acid concentration at the surface and a corresponding increase in development threshold. Controlled post-exposure bake at 50 °C for 60 s can restore surface development rate, but the bake must be kept below 70 °C to avoid re-esterification or thermal crosslinking. Better process control is obtained by scheduling development within 2 h of exposure, especially for thick films where surface inhibition is a larger fraction of the development path. Nitrogen-purged storage boxes or dry-box transfer are used for delay periods above 2 h. No specific published build-up curve for TSMR-8900 under these conditions is available; the above limits are derived from comparative diazonaphthoquinone–novolac studies and should be verified by post-exposure delay splits on the intended aligner.

    Substrate compatibility and wet etch resistance are additional selection criteria. TSMR-8900 is removed with acetone, propylene glycol monomethyl ether acetate, or selected alkaline strippers. The resist is compatible with hydrofluoric acid etching of silicon dioxide when hardbaked above 120 °C, but etch selectivity is process-specific and must be confirmed by etch-rate monitor. Resist adhesion on aluminium, copper, and indium tin oxide is improved by hexamethyldisilazane priming; copper substrates may require a barrier layer because diazonaphthoquinone–novolac resists can interact with uncapped copper during thermal processing. For lift-off processes, the positive sidewall angle is adjusted by post-exposure bake and development time; an overhang profile is not inherent to TSMR-8900 and may require image reversal or bilayer techniques. Compared with crosslinking epoxy-based resists, TSMR-8900 remains aqueous-developable and removable, but it does not provide equivalent mechanical stability in permanent structures.

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