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Gaining Micropattern Fidelity in an NOA81 Microsieve Laser Ablation Process.
Rahman Sabahi-Kaviani1, Regina Luttge1
1Neuro-Nanoscale Engineering, Mechanical Engineering Department and Institute of Complex Molecular Systems, Eindhoven University of Technology (TU/e), 5600MB Eindhoven, The Netherlands.
Micromachines
|December 30, 2020
Summary
Researchers optimized laser micromachining for creating 3D micropores in Norland Optical Adhesive 81 (NOA81) microsieves. This process ensures high micropore quality and reproducibility for cell capture applications.
Area of Science:
- Materials Science
- Biotechnology
- Microfabrication
Background:
- Microsieves fabricated using soft-lithography and laser micromachining are crucial for cell capture via passive pumping.
- Achieving high reproducibility in micropore geometry is essential for consistent cell capture yield and survival.
Purpose of the Study:
- To investigate and optimize the micropattern fidelity of Norland Optical Adhesive 81 (NOA81) microsieves.
- To determine the key fabrication parameters controlling the formation of three-dimensional (3D) micropores.
Main Methods:
- Soft-lithography and laser micromachining were employed to fabricate NOA81 microsieves.
- Systematic investigation of NOA81 film thickness, laser pulse repetition rate, number of pulses, and beam focusing distance.
- Characterization using scanning electron microscopy (SEM) and focused ion beam (FIB) for cross-sectional analysis.
Main Results:
- The number of laser pulses was identified as the dominant factor controlling pore aperture formation for NOA81 films.
- Laser pulse repetition rates between 50 and 200 Hz showed no significant influence on micropore quality.
- Optimized laser ablation conditions resulted in smooth micropore surfaces with minimal debris.
Conclusions:
- The combined soft-lithography and laser micromachining process enables the creation of high-quality, reproducible 3D micropores in NOA81.
- The established process window is sufficiently large for reliable biological applications, including cell capture.

