On copper-seed redistribution layers for
150 mm and
200 mm wafer bumping, OFPR-800 is processed as a positive-tone novolak-diazonaphthoquinone resist after vapor-phase HMDS priming, which controls adhesion on sputtered copper and TiW seed layers. A dehydration bake at
150 °C for
60 s on a vacuum hotplate precedes coating, and the resist is dispensed with a spin coater programmed from
500 rpm spread to
4,000 rpm final spin, yielding a nominal film thickness of
1.8 µm to
2.4 µm. Softbake is maintained at
95 °C to
110 °C for
90 s to
120 s on a contact hotplate; insufficient softbake leaves residual solvent that causes lifting during acid copper sulfate electroplating. Exposure on a g-line projection aligner uses the
436 nm mercury arc line at
120 mJ/cm² to
180 mJ/cm², with the dose adjusted for copper reflectivity and topography. Development in aqueous
2.38% tetramethylammonium hydroxide is run in double puddle or spray mode to suppress scumming at the resist-substrate interface on high-topography redistribution layers. A post-develop hardbake of
110 °C to
130 °C for
60 s to
120 s densifies the novolak matrix and improves resistance to acid copper sulfate baths operating below pH
1.0. Plating compatibility is checked by immersion in a vertical cup-plate tool at
25 °C to
28 °C; resist thickness loss should remain below
5% after
1 h when measured by stylus profilometry. After copper pillar or solder bump deposition, the resist template is stripped with N-methyl-2-pyrrolidone at
80 °C to
100 °C, followed by oxygen plasma ash at
200 W to
400 W to remove organic residue before seed-layer etch. Adhesion is verified by tape test according to
ASTM D3359-17 on TiW and copper seed layers, with a target classification of
5B after HMDS priming. Production failure modes include edge lifting after electroplating when softbake falls below
95 °C and plating solution penetration when dehydration is incomplete.
What Keeps OFPR-800 in Thin-Film Transistor Array Patterning for Flat-Panel Display Factories?
Flat-panel display fabs retain g-line resists for non-critical gate and data-metal layers because older Gen
4.5 and Gen
5 exposure equipment operates at
436 nm without requiring i-line conversion. OFPR-800 is coated on glass substrates with a roller coater or slit coater after cleaning and dehydration; target film thickness is normally
1.2 µm to
1.8 µm for wet etching of aluminum/molybdenum bilayers. Softbake at
90 °C to
105 °C for
120 s on a hotplate removes solvent while limiting thermal stress on
0.5 mm to
0.7 mm glass. Exposure through a proximity mask aligner uses a near-contact gap of
30 µm to
50 µm and a dose of
90 mJ/cm² to
150 mJ/cm²; the practical resolution limit under these conditions is approximately
3 µm line/space. Development with aqueous
2.38% TMAH is configured as shower spray with developer-drainage endpoint detection; double spray development prevents active-matrix via residue. For aluminum wet etching in phosphoric-nitric-acetic acid mixtures at
35 °C to
45 °C, the resist must remain adherent without lifting for
2 min to
4 min immersion. Hardbake is not always used for TFT wet etching because excessive crosslinking complicates stripping, but a low-temperature postbake at
105 °C for
60 s can reduce swelling. Stripping uses amine-based solvents at
60 °C to
70 °C followed by ultrasonic cleaning. The terminal output is the gate or source/drain electrode array in thin-film transistor backplanes for LCD televisions and monitors. Defect density after etching is monitored by automated optical inspection under
50× magnification, and the process specification commonly requires fewer than
0.1 particles per square centimeter larger than
1 µm in a cleanroom maintained to
ISO 14644-1 Class 5. Non-uniform developer puddle has been observed to generate mura on large glass panels, which is a key reason for spray development on Gen
4.5 lines.In silicon microelectromechanical systems fabrication, OFPR-800 functions as a mask for deep reactive-ion etching when the silicon etch depth does not exceed
50 µm and the resist thickness can be confined to
2.0 µm to
4.0 µm. Coating follows vapor HMDS priming on the smooth or lightly roughened silicon surface, and edge bead removal with propylene glycol monomethyl ether acetate prevents contact with electrostatic chuck surfaces in the etcher. Softbake proceeds at
100 °C to
110 °C for
90 s to
150 s, followed by exposure on a contact aligner with a
436 nm mercury arc output and a dose of
150 mJ/cm² to
220 mJ/cm² to preserve vertical sidewall angles. Development in
2.38% TMAH is extended for
45 s to
70 s in puddle mode, and a hardbake at
120 °C to
140 °C for
180 s improves resistance to the Bosch process alternating SF₆ and C₄F₈ plasmas. Selectivity to silicon in DRIE is typically in the range of
40:1 to
80:1, depending on chamber passivation and silicon loading; resist erosion is monitored by stylus profilometry before and after etching. The hardbaked resist is stripped after deep etching with oxygen plasma ashing at
300 W to
600 W followed by wet treatment in N-methyl-2-pyrrolidone at
80 °C to
100 °C to remove fluorinated residues. The terminal outputs include silicon resonators, inertial sensor proof masses, and microfluidic master molds. Sidewall angle and critical dimension are verified by cross-sectional scanning electron microscopy; a post-etch critical dimension bias of less than
0.2 µm is considered acceptable for bonded-silicon inertial sensors. Residual resist micromasking during DRIE has been observed to generate black silicon on unprotected areas, so the strip sequence must include both ashing and solvent cleaning.
| Downstream configuration | Nominal film thickness | G-line exposure dose | Softbake | Hardbake | Developer mode |
|---|
| Wafer bumping RDL | 1.8–2.4 µm | 120–180 mJ/cm² | 95–110 °C, 90–120 s | 110–130 °C, 60–120 s | 2.38% TMAH double puddle |
| TFT array | 1.2–1.8 µm | 90–150 mJ/cm² | 90–105 °C, 120 s | 105 °C, 60 s optional | 2.38% TMAH double spray |
| MEMS DRIE | 2.0–4.0 µm | 150–220 mJ/cm² | 100–110 °C, 90–150 s | 120–140 °C, 180 s | 2.38% TMAH puddle 45–70 s |
| SAW filter | 0.8–1.2 µm | 100–140 mJ/cm² | ramp 60–95 °C, hold 90 s | not used | 2.38% TMAH spray/puddle |
Metal Lift-Off Undercut Profiles on GaAs Heterojunction Bipolar Transistor Wafers
Metal lift-off on gallium arsenide heterojunction bipolar transistor wafers requires an overhang profile that prevents continuous metal film coverage along the resist sidewall. OFPR-800 can be used in a chlorobenzene soak process because the solvent penetrates the upper resist surface and reduces development rate at the surface, producing a reverse-tapered profile. The wafers are coated to
1.5 µm to
2.5 µm after HMDS vapor priming and softbaked at
90 °C to
100 °C for
90 s. After exposure with a g-line contact aligner at
130 mJ/cm² to
190 mJ/cm², the wafers are immersed in chlorobenzene for
10 min to
20 min, then developed in
2.38% TMAH with gentle agitation to preserve the overhang. The metal stack, typically Ti/Pt/Au or Ni/Ge/Au ohmic contacts, is deposited by electron-beam evaporation to a thickness not exceeding
0.5 to
0.7 times the resist thickness, maintaining a clean discontinuity at the overhang. Lift-off is performed in N-methyl-2-pyrrolidone at
70 °C to
90 °C with ultrasonic assistance, and residual metal flags are inspected by scanning electron microscopy. Adhesion of the resist to GaAs and silicon nitride passivation is evaluated by tape test following
ASTM D3359-17; a typical target classification is
4B or better. The terminal products are emitter, base, and collector metal electrodes in gallium arsenide heterojunction bipolar transistors used for radio-frequency power amplifiers. Because chlorobenzene handling requires closed-loop solvent recovery and compliance with volatile organic compound emission limits, the process is confined to fabs with solvent hoods and appropriate fire suppression. Published data comparing OFPR-800 to dedicated bilayer lift-off resists on GaAs is limited, so each lot is qualified with a monitor wafer measuring undercut by scanning electron microscopy before device wafers are processed. Lifted-metal flaps are a known failure mode when exposure dose exceeds
190 mJ/cm² and the overhang becomes too shallow.
When AlGaInP LED Mesa Etching Requires a G-Line Resist With Tighter Thermal Stability
AlGaInP light-emitting diode mesa fabrication involves inductively coupled plasma etching in BCl₃/Cl₂ chemistry, where the resist is subjected to thermal and ion bombardment stress. When the fab’s aligner inventory is restricted to g-line steppers or contact aligners, OFPR-800 is evaluated for mesa masking instead of switching to i-line resists. Film thickness is typically
2.0 µm to
3.0 µm by double coating or low spin speed, and the softbake condition is set at
100 °C to
110 °C for
120 s. Exposure on a g-line stepper at
436 nm uses a dose of
160 mJ/cm² to
240 mJ/cm² to ensure complete development through the thick film. After development in
2.38% TMAH, a deep-UV flood exposure or a hardbake at
120 °C to
135 °C for
240 s stabilizes the resist for plasma etch. The mesa etch is run in an ICP-RIE tool with Cl₂/BCl₃ gas ratio between
1:1 and
1:4, substrate temperature from
20 °C to
60 °C, and RF bias power that determines resist erosion rate. Published quantitative selectivity data for OFPR-800 in AlGaInP mesa etching is limited; process qualification therefore measures resist remaining after etch by stylus profilometry and requires a residual thickness of at least
0.5 µm to protect the underlying semiconductor. Endpoint detection by optical emission spectroscopy is used to terminate the main etch at the AlInP layer, preventing over-etching. The terminal product is the red-orange LED die with defined p-GaP and n-AlInP sidewalls. Post-etch residue is removed with oxygen plasma ashing and wet strip in N-methyl-2-pyrrolidone at
80 °C to
100 °C. Plasma erosion at the mesa edge has been observed to cause sidewall roughening when residual resist falls below
0.5 µm, so etch time and resist thickness are monitored together.In discrete power device manufacturing, OFPR-800 is applied to delineate silicon nitride or polyimide passivation openings over anode and cathode regions. The wafers are processed through passivation deposition, then coated with the resist after an oxygen plasma descum to improve wetting. Because the surface has steps from field plates, a lower spin speed or spray coating is used to achieve a conformal film of
1.5 µm to
2.0 µm over edge topography. Softbake is performed at
95 °C to
105 °C for
100 s to
140 s. Exposure through a proximity aligner at
436 nm includes deliberate overexposure of
10% to
20% to compensate for reflective notching over metal pads. Development in
2.38% TMAH is completed in spray mode with endpoint detection, followed by a hardbake at
115 °C to
135 °C for
180 s to stabilize the mask against buffered oxide etch or reactive ion etch of silicon nitride. The dry etch step uses CF₄/O₂ plasma; resist thickness loss should remain below
0.3 µm for the required nitride etch depth. After etching, the resist is removed by oxygen plasma ashing and NMP wet solvent. The terminal outputs are p-n junction termination and contact openings in discrete power rectifiers, thyristors, and transient voltage suppression diodes. Residual resist after strip is inspected by scanning electron microscopy and quantified by energy-dispersive X-ray spectroscopy for carbon content below
1 atomic percent on the etched surface. The process window is limited by substrate reflectivity variation; on metal pad areas, a slightly thicker resist is often required to avoid scumming and incomplete development.
Lithium Niobate Pyroelectricity Complicates Interdigital Transducer Patterning
Lithium niobate surface acoustic wave filter fabrication uses OFPR-800 for aluminum interdigital transducer definition by wet etching or lift-off. LiNbO₃ is pyroelectric and requires careful bake temperature ramping to avoid crystal fracture; hotplate softbake is ramped from
60 °C to
95 °C over
60 s and held for
90 s. The resist is coated to
0.8 µm to
1.2 µm, because transducer finger widths of
1.5 µm to
3.0 µm require thinner films for resolution. Exposure is performed with a g-line stepper at
436 nm and a dose of
100 mJ/cm² to
140 mJ/cm²; reflective notching is controlled by reducing exposure dose on high-reflectivity aluminum or by using a dyed resist process. Development in
2.38% TMAH produces vertical sidewalls, and no hardbake is used prior to aluminum wet etching to avoid undercut changes. The aluminum wet etch in phosphoric-nitric-acetic acid at
30 °C to
40 °C is timed to achieve a finger width bias of less than
0.1 µm. After etching, resist is stripped with solvent and oxygen plasma; the interdigital transducer electrode pitch is measured by scanning electron microscopy or atomic force microscopy. The terminal product is a surface acoustic wave filter chip for mobile communication bands between
700 MHz and
2.7 GHz. Adhesion to LiNbO₃ is verified by tape test according to
ASTM D3359-17, with
5B classification expected after HMDS priming. Published data for OFPR-800 on lithium niobate is limited; qualification monitors are used to check pyroelectric cracking and finger edge roughness before production lots are released.
In semiconductor and microelectromechanical-systems lithography, the positive-tone photoresist supplied by Tokyo Ohka Kogyo under the designation OFPR-800 is a novolak resin solution containing a diazonaphthoquinone photoactive compound. The product is specified for g-line exposure with primary sensitivity at
436 nm. The liquid resist is dispensed from amber glass or high-density polyethylene containers using production-scale track equipment such as a Headway PWM 32 spin coater or SUSS MicroTec Gamma cluster. The principal solvent is propylene glycol monomethyl ether acetate; this solvent requires local exhaust ventilation and excludes contact with oxidizers. Unlike chemically amplified resists, OFPR-800 does not depend on catalytic deprotection and does not require a post-exposure bake in standard contact aligner processing. Development is performed in aqueous alkaline developer, commonly
2.38 wt% tetramethylammonium hydroxide, which places it in the same process infrastructure as many g-line and i-line novolak resists. The resist is applied on silicon, thermal silicon dioxide, low-pressure chemical vapour deposited silicon nitride, borosilicate glass, and selected III/V substrates where moderate thickness wet etching, lift-off, or plasma etching is required. Its operational boundary is tied to the novolak/DNQ dissolution inhibition mechanism: exposed areas convert to a soluble indene carboxylic acid, while unexposed areas remain insoluble until the development rate overwhelms the dark erosion threshold.
What Determines the Spin-Coated Thickness and Exposure Dose for OFPR-800?
On a vacuum-contact aligner such as a SUSS MicroTec MA/BA6 or Karl Suss MJB3, the delivered dose for a given film thickness is set by a focus-exposure matrix. Public process sheets for g-line novolak resists of this class frequently report useful doses in the low-hundreds of millijoules per square centimetre, but the installed lamp power, mask transmission, and optical path influence the value. Contact aligner resolution is further controlled by mask contact mode and substrate flatness rather than solely by resist contrast. A nominal development time of 30 s to 60 s in 2.38 wt% tetramethylammonium hydroxide is representative for films in the 1–3 µm range; thicker films may require puddle development or intermittent agitation to clear exposed features without excessive dark erosion. Soft-bake conditions are normally 90–110 °C on a hotplate with vacuum contact. Convection ovens are generally avoided for soft bake of thin films because slower heat transfer changes residual solvent distribution and can widen critical dimension variation across the wafer.
Film thickness is controlled by selecting the viscosity grade and final spin speed. Documented cleanroom recipes list multiple grades, including 10 cP, 20 cP, and 50 cP. A 20 cP grade is frequently used for single-layer masking in the 1–2 µm thickness range, while a 50 cP grade is selected for thicker films up to approximately 5–10 µm. Spin curves should be generated on the specific coater because exhaust balance, ambient solvent vapour, dispense volume, and acceleration rate can shift final thickness by more than 100 nm. A two-step spin recipe of 500 rpm spread followed by 2000–3000 rpm final spin is representative in published process documentation. After spinning, edge bead removal is performed using solvent swabbing or optical edge-bead exposure; the selected method is matched to the downstream etch or lift-off process.
Representative OFPR-800 processing envelope from published cleanroom process sheets
| Process step | OFPR-800 20 cP | OFPR-800 50 cP |
| Adhesion promotion | HMDS vapour prime, 120–150 °C, 60 s | HMDS vapour prime, 120–150 °C, 60 s |
| Dispense and spread | static dispense, 500 rpm for 5 s | static dispense, 500 rpm for 5 s |
| Final spin | 3000 rpm for 30 s | 2000–3000 rpm for 30 s |
| Soft bake | hotplate 90–110 °C, 60–90 s | hotplate 90–110 °C, 90–120 s |
| Exposure | g-line 436 nm, dose determined by focus-exposure matrix | g-line 436 nm, dose determined by focus-exposure matrix |
| Development | 2.38 wt% TMAH immersion or spray, 30–60 s | 2.38 wt% TMAH immersion or puddle, time increased with thickness |
| Hard bake | 120–140 °C, 30 min convection oven | 120–140 °C, 45–60 min convection oven |
Before exposure, the coated wafer is inspected under filtered amber or yellow light for striations, comets, voids, and edge-bead contamination. On a 100 mm silicon wafer a static dispense volume of 2–4 mL is typical, but the actual volume is set by substrate size, resist viscosity, and coater bowl clearance. A Cee Model 100CB hotplate or equivalent is used for soft bake; hotplate surface temperature is verified with a process wafer and thermocouple at established intervals. If soft bake is below the recommended range, the film retains greater solvent content and may show increased dark erosion during development. If soft bake is excessive, adhesion may degrade on hydrated oxide surfaces. For silicon dioxide and silicon nitride substrates, HMDS vapour priming at 120–150 °C for 60 s is used before coating. The resulting adhesion is verified after development by inspection of cleared feature edges or by cross-sectional scanning electron microscopy of patterned structures. Coating and handling are performed in a cleanroom classified to ISO 14644-1 Class 5 or better for critical processes; point-of-use filtration at 0.1–0.2 µm is common for particle-sensitive applications. A delay of more than a few hours between dehydration bake and HMDS priming can permit rehydration of the substrate surface, producing loss of adhesion during spray development or agitated wet etching. Storage of the resist at manufacturer-defined temperatures, typically 5–25 °C, in tightly closed bottles is required; containers removed from cold storage are brought to room temperature before opening to prevent water condensation. Mixing with alkaline additives or incompatible solvents is avoided because amine contamination can reduce shelf life and shift dissolution inhibition.
When Aqueous Alkaline Developability and Wet-Etch Compatibility Are Required
In wet-etch patterning of thermal silicon dioxide, OFPR-800 is processed to a hard-baked mask before immersion in 6:1 buffered oxide etch at 25 °C. The hard bake step at 120–140 °C in a convection oven improves adhesion and reduces film loss at the feature edge, but it also densifies the resist and makes rework more difficult. Because the resist is thermally densified during hard bake, subsequent removal in acetone or N-methyl-2-pyrrolidone may require extended immersion, heated solvent, or oxygen plasma ashing after the substrate has been patterned. In lift-off applications, the hard bake is omitted or reduced; the resist sidewall is intentionally kept more easily solvent-swollen so that metal lift-off proceeds cleanly. Published data for OFPR-800 in image-reversal mode is limited; a dedicated image-reversal resist is generally selected if a controlled overhang profile is required. For conventional lift-off, metal evaporation is carried out as a discontinuous film over the resist, and the resist is dissolved in heated N-methyl-2-pyrrolidone or a proprietary stripper. Compatibility with oxide etchants is acceptable for the novolak matrix, but strongly oxidising acid mixtures can attack the resist and should be tested before use. Sulfuric acid/peroxide stripping is used only after solvent clean and when the tooling is compatible with the exothermic mixture.
For plasma etching of silicon nitride and silicon dioxide with CHF₃/CF₄ chemistries, OFPR-800 shows moderate selectivity. Selectivity is measured on the installed reactive ion etching system because it shifts with substrate temperature, bias power, and polymerizing gas ratio. The resist is not recommended for prolonged deep reactive-ion etching of thick silicon without an inorganic hardmask. In contact aligner processing on substrates with surface topography exceeding a few micrometres, OFPR-800 is applied at higher viscosity grades; coverage is quantified by contact profilometry across a dummy step. The conformal coverage is governed by the spin speed, solvent evaporation rate, and feature density, and it should be established for each mask set.
Comparative Chemistry of DNQ/Novolac, i-Line, and Chemically Amplified DUV Resists
The primary difference between OFPR-800 and an i-line novolak resist is the spectral sensitization of the diazonaphthoquinone photoactive component. OFPR-800 is exposed at 436 nm, whereas i-line resists are optimized for 365 nm. Both classes use aqueous alkaline development and are compatible with 2.38 wt% tetramethylammonium hydroxide. In contrast, chemically amplified deep-ultraviolet resists operate through photogenerated acid and require a post-exposure bake, which introduces sensitivity to substrate contamination, delay time, and airborne amine concentration. The table below summarizes structural differences relevant to process selection.
Comparison of OFPR-800 with other resist classes
| Attribute | OFPR-800 | i-Line DNQ/novolak | Chemically amplified DUV | SU-8 negative tone |
| Primary exposure wavelength | 436 nm | 365 nm | 248 nm or 193 nm | 365 nm |
| Post-exposure bake | not required | not required | required | required |
| Development | 2.38 wt% TMAH | 2.38 wt% TMAH | 0.26 N TMAH, process-dependent | solvent development |
| Film thickness range | approximately 0.5–10 µm by viscosity grade | approximately 0.5–4 µm | approximately 0.1–0.5 µm | approximately 1–500 µm |
| Dose verification | focus-exposure matrix on installed aligner; published data for specific configurations is limited | same verification method | dose and post-exposure bake latitude verified jointly | dose and bake latitude verified jointly |
| Dry-etch selectivity | moderate for oxide/nitride plasma processes | similar novolak matrix behaviour | lower in thick-film applications | high in crosslinked regions |
| Process complexity | low; no diffusion-sensitive latent image | low | high due to airborne base contamination | high due to crosslinking and bake control |
Compared with SU-8 negative-tone resist, OFPR-800 requires a much lower film thickness at similar spin speed and is removed more readily in standard organic solvents before hard bake. SU-8 is solvent-developed and crosslinks via cationic polymerization, yielding a permanent high-crosslink film after hard bake; OFPR-800 remains thermoplastic in the soft-baked state and does not form the same crosslink density. This difference makes OFPR-800 more suitable for temporary masking, wet etching, and liftoff, whereas SU-8 is used for permanent microstructures. For g-line contact lithography, the resolution limit of OFPR-800 is usually dominated by contact aligner optics, mask contact mode, and substrate reflectivity rather than by the resist contrast alone. Published performance data for a specific aligner configuration is limited; resolution, sidewall angle, and linewidth uniformity must be established on the intended tool. For regulatory documentation, the material safety data sheet for the dispensed formulation should be consulted for classification under REACH 1907/2006/EC and RoHS 2011/65/EU. The presence of propylene glycol monomethyl ether acetate makes the resist subject to local volatile organic compound emission rules; all dispense and bake tools are vented through exhaust stacks with solvent monitoring where required.