DIC100 Series differential interference contrast microscope system

Product Introduction

The Differential Interference Contrast (DIC) microscope operates on birefringent double-beam polarisation interference:
1. Linearly polarised light from the polariser passes through a birefringent Nomarski prism, splitting into two orthogonally polarised beams with a defined phase difference.
2. When the incoherent beams illuminate the specimen, micro-relief or refractive-index variations introduce an optical path difference; after reflection, the beams recombine upon re-entering the Nomarski prism.
3. The analyser aligns the vibration directions of the recombined beams to produce interference.
4. Interference modulates beam amplitude, enhancing contrast and delivering a pseudo-three-dimensional relief appearance.
The Nomarski prism can be translated horizontally as a phase compensator, adjusting brightness and interference colours between specimen and background to achieve the desired observation. Figure 1 illustrates the DIC100 differential interference contrast system.

Product Features

  • Standard and long working distance objectives available
  • Imaging path: 1X (tube lens focal length 180 mm) with optional reducers
  • Image circle: 25 mm
  • Spectral range: visible light
  • Camera interfaces: C / M42 / M52 (optional)
  • Illumination: critical illumination or Köhler illumination (optional)
  • Light source: 10 W white LED / blue LED (optional)

System Configuration and Parameters

Professional differential interference contrast microscopy system providing excellent imaging solutions for transparent samples

System working principle

The Differential Interference Contrast (DIC) system uses birefringent double-beam polarisation interference to achieve high-contrast imaging.

Step 1
Beam separation

Linearly polarised light passes through the Nomarski prism, splitting into two orthogonally polarised beams with a defined phase difference.

Step 2
Sample interaction

Two incoherent beams illuminate the specimen; surface relief or refractive-index variations create an optical path difference.

Step 3
Beam recombination interference

After reflecting from the specimen, the two beams pass through the Nomarski prism again and recombine; the analyser aligns their vibration directions to produce interference.

Step 4
Enhanced contrast

Interference-induced amplitude changes render sample details with enhanced contrast and a three-dimensional relief appearance.

Objective Series Parameters

Standard working-distance objective series (60 mm parfocal distance with a 200 mm tube lens )
Model Magnification NA Working Distance Focal Length Resolution Object Field Image Field
DIC2.5XA 2.5X 0.075 6.2mm 80 mm 4.46µm 10 mm 25 mm
DIC5XA 5X 0.15 23.5mm 39mm 2.2µm 5mm 25 mm
DIC10XA 10X 0.3 22.8mm 20 mm 1.1µm 2.5mm 25 mm
DIC20XA 20X 0.4 19.2mm 10 mm 0.8µm 1.1mm 25 mm
DIC50XA 50X 0.55 11mm 4 mm 0.6µm 0.44mm 25 mm
Long working-distance objective series (95 mm parfocal distance with a 200 mm tube lens )
Model Magnification NA Working Distance Focal Length Resolution Object Field Image Field
DICL2XA 2X 0.055 33.7mm 95 mm 6.1µm 12.5mm 25 mm
DICL5XA 5X 0.14 33.6mm 40 mm 2.2µm 5mm 25 mm
DICL10XA 10X 0.28 33.4mm 20 mm 1.2µm 2.5mm 25 mm
DICL20XA 20X 0.34 29.5mm 10 mm 0.8µm 1.25mm 25 mm
DICL50XA 50X 0.5 18.9mm 4 mm 0.7µm 0.5mm 25 mm

System Technical Specifications

Optical System
Imaging Path
1X (tube lens focal length 180 mm), custom reduction optics available
Image Size
25 mm
Spectral Range
Visible light
Tube Lens Focal
200 mm
Illumination System
Illumination
Selectable critical or Köhler illumination
Light Source
10W LED
Mechanical System
Camera Interface
Selectable interfaces: C / M42 / M52
Objective Thread
M26×0.705
Prism Adjustment
Precision lateral adjustment

Typical Application Cases

Successful applications of DIC100 system in various fields

Conductive particle inspection for LCD/OLED products

The number of conductive particles in LCD circuit paths determines conductivity: too few reduce performance and may cause display faults, while too many waste material. The DIC100 system clearly reveals particle outlines, enabling accurate counting and distribution analysis while avoiding errors caused by agglomeration.

  • Conductive particle outlines are clearly visible
  • Accurately identify and count agglomerated particles
  • Improves measurement accuracy
  • Blue LED illumination with a monochrome camera yields optimal contrast.
  • White LED illumination paired with a colour camera delivers natural colour reproduction.

Detection of surface cracks and defects

As a powerful method for modern metallographic analysis, DIC requires relatively simple specimen preparation and produces pronounced relief under the microscope. It readily reveals fine structures or defects that are invisible or barely visible in brightfield metallographic microscopes.

  • Observe particle, pore, crack, and surface relief details within specimens
  • Low specimen preparation requirements
  • Provides a pronounced three-dimensional relief effect
  • Makes materials analysis more reliable

More Application Fields

Microbial cell inspection

The DIC100 series enables non-destructive imaging of live cells. By tuning interference colours according to staining response and adjusting focus, it captures sharp images at multiple depths, revealing internal cell structures with high resolution.

  • Non-destructive observation of live cells
  • Sharp imaging across multiple focal planes
  • Internal cellular contours are clearly visible

Comparison with other microscopy techniques

Comparison Technology DIC Technology Advantages
Conventional metallographic microscope DIC reveals fine structures and defects that are invisible or barely visible under brightfield metallographic microscopes.
Biological microscope DIC provides superior contrast and three-dimensional relief, allowing transparent specimens to be observed without staining.
Phase-contrast microscope DIC has no halo artefacts, delivering higher resolution and sharper images.
Fluorescence microscopy DIC requires no staining, enabling live-sample observation while avoiding phototoxicity and photobleaching.

System Configuration and Accessories

Standard Configuration
  • DIC100 main system
  • Nomarski prism module
  • Polariser
  • Analyser
  • Coaxial polarised illumination module
  • Precision focusing stage
Optional Accessories
  • Standard and long working distance objective sets
  • Rotating specimen stage
  • Automated stage control
  • Image acquisition and analysis software
  • Custom-wavelength LED sources
  • Anti-vibration platform

The DIC100 Series features modular design, allowing flexible configuration based on specific application requirements

DIC100 System Advantages

Professional differential interference contrast technology providing excellent imaging effects

Superior Contrast Enhancement

Through dual-beam interference technology, phase differences are converted to amplitude differences, making minute details of transparent samples clearly visible.

Three-Dimensional Imaging

Unique relief effect presents sample surface morphology with three-dimensional appearance, facilitating observation and analysis of minute structures.

Flexible System Configuration

Standard/long working distance objectives optional, adapting to different samples and application requirements, meeting diverse inspection needs.

Precision Adjustment System

Nomarski prism horizontal precision adjustment achieves optimal interference effects and image quality.

Non-Invasive Living Cell Observation

Observe living cells without staining, avoiding phototoxicity and photobleaching, preserving sample viability.

High-Resolution Imaging

No halo effect, resolution superior to phase contrast microscopy, providing clearer image details.