Back to Home

A visual field guide

From digital pattern
to physical structure.

DMD maskless photolithography. How it works, what Polygon makes easier, and what changes when you move from one photon to two.

21 min exploration2 simulation labs15 technical sources
An original technical illustration of a digital mirror mask, projection lens and a patterned structure on a substrate
Microscope projection · conceptual optical geometry

01 / The principle

The mask is a file.
The chemistry makes the structure.

A digital micromirror device replaces a physical photomask with an array of tilting mirrors. On mirrors send light into the projection optics; off mirrors send it away. Change the file and the next exposure can have a new shape.

01

Draw

Create a bitmap, line pattern or region of interest. Its pixels define where light is requested.

02

Project

Image the DMD onto the work plane through a calibrated relay and objective.

03

React

A matched photoinitiator or photosensitive group changes the material where exposure is sufficient.

04

Reveal

Develop a resist, wash away uncured precursor, or read out a patterned surface reaction.

Maskless exposure removes mask fabrication from the iteration loop. Coating, alignment, exposure calibration and material processing still determine the result. Polygon application context: [2][3]

02 / Choose the physical process

One photon patterns a film. Two photons can write inside a volume.

reaction follows illuminated regions

1P / linear absorption

Project an entire layer

One absorbed photon can initiate the chemistry. UV or visible light exposes a resist, hydrogel or functional surface. Optical focus alone does not provide intrinsic depth confinement.

D = I × t · source matched to absorption
local reactionshort, intense pulses

2P / nonlinear absorption

Localise the reaction in 3D

Two photons contribute to one excitation through a nonlinear process. Reaction depends on intensity squared; a tightly focused, ultrashort pulse can confine polymerisation around a focal region.

R₂ ∝ I² · femtosecond laser + 2P chemistry
Practical differences between single-photon projection and two-photon lithography
Design questionSingle-photon projectionTwo-photon lithography
What is written?A surface pattern or exposed film; stacked layers with added z control.Voxels, multiple foci, or a temporally focused patterned layer.
What sets the dimensions?Projected sampling, optical contrast and material processing.Focus geometry, pulse conditions, nonlinear threshold and chemistry.
Where is it useful?Fast design iterations, hydrogel patterns, resist masters, surface chemistry.3D scaffolds, micro-optics and structures requiring internal depth control.
How does Polygon fit?A packaged pattern projector and microscope integration route.A standard Polygon is not documented as a turnkey two-photon writer.

The 2P excitation spectrum must be measured or supplied for the initiator; doubling a one-photon wavelength does not establish a useful two-photon cross-section. The 3D mechanisms are demonstrated in [6][7][8]

Follow the optical path
365 / 405 nm sourcematched to chemistry01Polygon DMDsoftware-defined mask02Relay + adaptermicroscope infinity path03Objectiveimage the mask on film04resist on substrateMICROSCOPE PROJECTION / SINGLE PHOTONCameracalibrationseparate source / pattern timing signals
Conceptual microscope configuration. Fit the source, relay, objective and filters to the selected wavelength; measure exposure at the substrate.

03 / Single-photon exposure lab

A sharp bitmap is only the start.
See what reaches the material.

Change the feature width, optics and exposure. Watch the same pattern pass from binary mirrors to delivered light to retained resist. Try a long exposure with residual light to see why dark regions matter.

Interactive / mask → light → material

Test pattern
Objective magnification
Exposure wavelength

Projected pixel

0.38 µm

Full field

495 × 310

µm · Nikon G, standard relay

Rayleigh reference

0.56 µm

0.61 λ / NA

On-field dose

100.0 mJ/cm²

01DMD mask
lines mask sampled on projected DMD pixels

Bright = mirror on

02Delivered light
Intensity after Gaussian optical blur and uniform residual light

Bright = higher irradiance

03Retained material
Threshold model of retained negative resist after development

Gold = remains; slate = removed

Same 36.5 × 24.3 µm crop in all three views. The crop uses 96 × 64 DMD pixels.

Development response
Dose profile through the centre row
reaction threshold036.5 µm

The intended regions cross threshold. Change dose to watch the edges move.

Model, equations & limitations

D = I × t, using mW/cm² and seconds to give mJ/cm². The threshold is an arbitrary user input, with the same ideal step response used for positive and negative tone.

The Nikon Polygon1000-G standard-relay values are 9.9 × 6.2 mm and 7.6 µm per pixel at 1×, divided by objective magnification. Other microscope relays and Polygon models need their own calibration. Magnification and NA are independently adjustable here.

The binary mask is sampled at DMD-pixel centres, expanded 3× for calculation, and convolved with a Gaussian intensity PSF, σ = 0.21 λ / NA. A uniform residual-light fraction is then added. This approximates incoherent projection; the Rayleigh distance is a point-separation reference, not a printed linewidth guarantee.

This is a thin-film, in-focus model. It omits coherent speckle, defocus, distortion, absorption, standing waves, bake chemistry, diffusion, oxygen inhibition, shrinkage and development kinetics. Residual-light settings are illustrative and are not Polygon contrast specifications.

Sampling

A projected DMD pixel is a placement increment. A single-pixel line is not automatically a reliable printed line.

Optical transfer

NA, wavelength, focus and aberrations determine contrast. Coherent laser illumination can add speckle and diffraction artefacts.

Material response

Exposure, film thickness, bake and development shift the final edge. Verify linewidth and gap clearing on a test coupon.

04 / Build with Polygon

Easier to change the pattern.
Fewer projector parts to engineer.

Polygon packages the DMD, projection module and microscope coupling. PolyScan provides pattern design, sequences and calibration tools. This makes single-photon prototyping more approachable; the exposure process still needs development for your material. [1][4]

A microscope route

Choose a supported infinity-path adapter and objective instead of building a DMD relay from scratch.

Microscope adapters

A software mask

Create or import patterns, map image coordinates to projected coordinates, then run an exposure sequence.

PolyScan software

A source route

Select lightguide or laser-fibre coupling and verify delivered power, uniformity and wavelength transmission.

Light sources
Choose the input before choosing the exposure wavelength [1][10]
Polygon modelOptical input / stated rangeLithography planning
Polygon1000-G3 mm liquid lightguide · 350–1000 nmCandidate for 365 nm exposure with a suitable source and UV-transmitting downstream optics.
Polygon1000-DLSMA laser fibre · 400–1000 nmCandidate for 405 nm chemistry; 365 nm is outside its stated range. Circular projected field.
Polygon1000-DILightguide: 350–1000 nm; fibre: 400–1000 nmFor 365 nm, assess the lightguide path. Confirm each input separately.
Polygon UHCSMA laser fibre · 400–700 nmCandidate for background-sensitive visible-light chemistry. 365 nm is outside its stated range.

Example: a 365 nm negative-resist master

An SU-8 process is one possible starting point: the cited SU-8 2000 data recommends 365 nm and includes a post-exposure bake. Evaluate a G or DI lightguide configuration, UV optics, a calibration target and a dose matrix. Choose the exact formulation and process from its current supplier data. [5]

Example: a 405 nm hydrogel pattern

Use a precursor and initiator validated at 405 nm. Screen formulation, oxygen inhibition, substrate adhesion and wash conditions. Start with islands and line/gap coupons before a device layout; verify cell compatibility separately when relevant. Polygon microfluidic applications include hydrogel fabrication and curing. [3]

Timing, grayscale and contrast: what the headline values mean

The brochure specifies up to 6,600 frames/s at 1-bit depth. A pattern refresh rate does not determine the time needed to expose a resist. Confirm grayscale timing, minimum stable source pulse and trigger behaviour for the chosen configuration. PolyScan camera support depends on the model and licence. [1][4]

For 1P exposure, temporal duty q gives D ≈ q × Ion × t when the source and material behave linearly over that timing range. For 2P excitation, pulsing the same peak illumination on for fraction q gives ⟨I²⟩ ∝ q × Ion²; it is not equivalent to reducing continuous intensity to q × Ion. Grayscale requires calibration.

UHC’s stated 10,000,000:1 ratio compares all-on and all-off images. It does not establish local dark-region contrast beside bright features in a resist. Measure background and edge leakage with the actual mask and exposure duration. [10]

05 / Applications

Four jobs that suit patterned light.

Polygon is worth evaluating when the experiment needs selected surface regions, changing illumination masks or a spatial exposure map. These examples show useful workflows; the advantages described here are engineering interpretations of the cited demonstrations.

digital maskpatterned film

Prototype thin-film layouts

Change the layout in software; illuminate multiple regions together.

Mightex reports patterned exposure of an acrylate film using Polygon and a 400 nm LED.

Before relying on it: Measure linewidth, film thickness and exposure uniformity.

Manufacturer-reported demonstration [2]

selectand opentarget selected membranes

Open selected microwells

Select which membranes receive the intended exposure in a registered field.

A published Polygon400 study used photodegradable hydrogel membranes to retrieve bacteria from selected microwells.

Before relying on it: Validate registration, background exposure and retrieval in your preparation.

Published study · historical Polygon400 setup [12]

dark / bindlight / releasedark / rebind

Switch protein binding locally

Revisit a field with different illumination masks during observation.

Mightex reports light-driven protein dissociation on a coverslip, followed by rebinding in the dark.

Before relying on it: Verify chemistry-specific reversibility and imaging compatibility.

Manufacturer-hosted laboratory demonstration [2]

exposure mapsurface attachment

Pattern surface-chemistry gradients

Encode spatial differences in surface attachment through an exposure map.

A Polygon1000 application report describes 365 nm functionalisation of glass, with local exposure time used to vary attached dye density.

Before relying on it: Calibrate the dose-to-attachment response for the actual surface chemistry.

Researcher application report · manufacturer-hosted [13]

Original conceptual drawings; no measured response, exposure time or fabricated dimensions are represented.

How does this relate to a Nanoscribe system?

A microscope-based Polygon workflow may suit surface photochemistry or selected-region exposure in an existing experiment. A dedicated two-photon fabrication system addresses additional requirements such as freeform 3D geometry and controlled writing in depth. Nanoscribe documents these capabilities for Quantum X shape. [14]

Hydrogels and custom materials are also supported by Nanoscribe Quantum X bio. Material flexibility alone does not establish a Polygon advantage. [15]

The sources above do not establish a head-to-head ranking. Compare the same target geometry and material for total processing time, reliable feature size, surface quality, alignment and yield before making a speed, cost or accuracy claim.

06 / Two-photon lithography

Yes, a DMD can write in 3D.
The optical architecture changes.

Published systems use a DMD for either holographic multi-focus writing or patterned-plane projection with temporal focusing. Both need ultrafast pulse delivery and suitable two-photon chemistry. They are distinct research architectures. [6][7][8]

Route A / multiple foci

Write several voxels at once

A binary hologram redistributes the wavefront to selected foci. The hologram is not a direct image of the printed shape. Geng et al. demonstrated parallel, independently controlled writing with a custom DMD scanner. [7]

Route B / patterned plane

Write a thin layer in parallel

Spatial and temporal focusing bring the shortest pulse to the build plane. Saha et al. demonstrated patterned-layer fabrication with a DMD. Pulse recombination supplies depth selectivity that ordinary wide-field projection lacks. [6][8]

Can a standard Polygon become that two-photon system?

The cited Polygon documents establish patterned illumination, not a qualified femtosecond lithography path. A nominal 800 nm transmission range does not establish pulse preservation, dispersion compensation, diffraction-order collection or pulse-damage tolerance. Common 1030 nm sources also sit outside the G/DL/DI stated upper wavelength limit. A 2P design requires a dedicated optical review and manufacturer confirmation. [1][9]

Try splitting the same laser power across more foci.

This lab uses a point-focus model to show intensity-squared scaling. Double the number of foci at fixed total power and the drive per focus falls fourfold. Stretch the pulse and the nonlinear drive falls too.

Interactive / why peak intensity matters

Compare trends at fixed exposure and focus size. These settings are not a hardware operating envelope.

Two-photon drive / focus

1.000×

relative to 10 mW, 80 MHz, 100 fs

Pulse energy / focus

0.125 nJ

Peak-power scale / focus

1250 W

Ep / τ; pulse-shape factor omitted

Squared Gaussian-focus intensity along z · fixed Rayleigh range, 2 µm
−8 µmfocus · z = 0+8 µmdashed: arbitrary reaction threshold (0.25)Vertical axis rescales with drive; shaded region crosses threshold.

The illustrative above-threshold depth is 4.00 µm. Raising the drive also broadens the reacting region.

Model, equations & limitations

For identical pulse shapes and fixed wavelength, R₂ ∝ ⟨I²⟩ ∝ Pavg² / (f × τ × A²). With N equally powered, identical foci, each receives Pavg / N, so per-focus drive falls as 1/N². Total drive summed over foci falls as 1/N at fixed total power. The temporal on/off duty cycle of a DMD is a separate quantity.

Depth uses R₂(z) = R₂(0) / [1 + (z/zR)²]², with zR = 2 µm and threshold = 0.25 relative units. This describes an ideal Gaussian point focus. The projection-TPL temporal-focusing architecture has a different axial response and requires measured pulse and field profiles.

The graph predicts relative excitation trends, not conversion or fabricated dimensions. It omits saturation, radical kinetics, pulse dispersion, material cross-sections, thermal accumulation and damage. Lowering repetition rate increases pulse energy at constant average power; practical limits require a separate assessment.

07 / From a coupon to a usable process

Calibrate once. Test the material. Then scale the pattern.

  1. 01

    Prepare

    Clean and coat. Set film thickness and any soft bake using the chosen material’s process.

  2. 02

    Register

    Calibrate mirror-to-substrate coordinates. Check scale, orientation, focus and fiducials at the field edges.

  3. 03

    Expose

    Measure irradiance at the substrate. Run a dose matrix with lines, gaps and isolated islands.

  4. 04

    Process

    Apply required bake and development or washing. The drawing shows negative tone; positive tone reverses retention.

  5. measure

    05

    Measure

    Check linewidth, open gaps, height, adhesion and alignment. Save the mask and process conditions.

Beyond one field

Stitching adds a positioning and dose problem.

Use an XY stage for tiles and z control for focus or layers. In an overlap, exposures add. Match edge dose with calibrated masks or exposure weighting, verify stage repeatability and distortion, and test seams. Higher magnification reduces the field, so more tiles may be required.

Total job time includes all exposures, pattern loading, stage motion, settling, focusing and processing. The DMD frame rate alone does not predict throughput.

tile Atile Boverlap: Dtotal = DA + DB

Bridged gaps or swollen edges

Reduce exposure first; check focus, residual light, film thickness and material diffusion. Inspect an isolated line beside a dense array.

Islands disappear after development

Check dose, wavelength response, adhesion and development. For a 2P system, measure pulse duration and per-focus power at the sample.

Centre works, corners fail

Measure field uniformity, tilt, aberrations and distortion. Flat-field exposure correction requires a measured intensity map.

Height varies or tiles show seams

Check coating / resin thickness, z calibration, overlap dose, stage registration and shrinkage. Grayscale dose is not automatically a grayscale height map.

Why resin depth needs its own calibration

A simple 1P photopolymer working curve is Cd = Dp ln(D/Dc) for D > Dc, where Dp is an effective penetration depth and Dc is a critical exposure. These are measured for the actual resin, wavelength and geometry. Absorption and thresholding can provide layer control; they do not give one-photon projection intrinsic optical sectioning. Resist bake chemistry, bleaching and thick films can depart from this simple model. [11]

For 2P, measure the 3D writing window versus power, dwell, depth and pulse conditions. Two-photon absorption is an excitation mechanism; fabricated feature size also depends on reaction kinetics, diffusion and development.

Turn a pattern into a setup

Start with the chemistry, feature size and field.

Bring the material, wavelength, film thickness, microscope and a test mask. We can help assess a Polygon configuration and identify what needs experimental validation.

Sources & further reading

Manufacturer data and original experiments.

Reviewed 17 October 2026. Product specifications, published demonstrations and illustrative models are identified separately throughout the guide.

  1. 01
    Polygon1000 technical brochure

    Model-specific inputs, wavelengths, relay geometry and binary timing.

  2. 02
    Mightex: photopatterning applications

    Surface patterning and light-controlled material examples.

  3. 03
    Mightex: patterned illumination for microfluidics

    Hydrogels, UV curing and programmable microfabrication.

  4. 04
    PolyScan software and supported hardware

    Pattern design, hardware integration and licence tiers.

  5. 05
    Kayaku: SU-8 2000 processing data

    365 nm recommendation, film processing and post-exposure bake.

  6. 06
    Saha et al. · Science (2019)

    Scalable submicrometer additive manufacturing: DMD projection with spatial and temporal focusing.

  7. 07
    Geng et al. · Nature Communications (2019)

    Binary holography for independently controlled two-photon writing foci.

  8. 08
    Somers et al. · Light: Science & Applications (2021)

    Rapid, continuous projection multi-photon 3D printing using spatiotemporal focusing.

  9. 09
    Texas Instruments · DMD thermal and pulsed-source considerations

    Device thermal limits and additional constraints with pulsed illumination.

  10. 10
    Polygon UHC technical brochure

    400–700 nm laser input and the manufacturer’s all-on/all-off contrast definition.

  11. 11
    NIST · Working-curve interlaboratory study (2024)

    Jacobs-model parameters, measured cure depth and the importance of calibrated exposure.

  12. 12
    van der Vlies et al. · ACS Applied Bio Materials (2019)

    Selected bacterial retrieval through photodegradable microwell membranes; supporting information documents a Polygon400 setup.

  13. 13
    Mitmoen · Polygon1000 surface-functionalisation application report (2021)

    Manufacturer-hosted researcher report: 365 nm surface attachment and exposure-controlled dye density.

  14. 14
    Nanoscribe · Quantum X shape

    Manufacturer description of a dedicated two-photon 3D microfabrication system; application context rather than a comparative benchmark.

  15. 15
    Nanoscribe · Quantum X bio

    Manufacturer documents hydrogel bioresins, third-party and custom materials, and high-resolution 3D bioprinting.

Illustrations are original conceptual drawings. Simulator outputs are educational calculations, not microscope images, fabricated samples or manufacturer performance data.