4.4 Article

Microlens array fabrication by enhanced thermal reflow process: Towards efficient collection of fluorescence light from microarrays

期刊

MICROELECTRONIC ENGINEERING
卷 86, 期 11, 页码 2255-2261

出版社

ELSEVIER
DOI: 10.1016/j.mee.2009.04.001

关键词

Microlens; Reflow method; Micro optics integration; Microarray fluorescent detection

资金

  1. Genome Quebec
  2. Genome Canada
  3. National Research Council of Canada

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This paper describes two enhanced resist reflow methods for the fabrication of microlens arrays and demonstrates their use for integrated biomolecular fluorescence detection on printed microarrays. A PDMS (polydimethylsiloxane) microlens array was fabricated by a double soft lithography approach using a photoresist microlens array as master mold. Additionally, by using both a careful control of the surface wettability and thermal treatments, we demonstrate the possibility to extend the resist reflow process in order to tune the diameters of microlens array over a large range by using a unique photomask pattern. We introduce an enhanced reflow on hydrophobic surfaces obtained by fluorosilane treatment and identify a threshold shrinkage temperature (T-shrinkage) of 140 degrees C, above which the diameter of microlenses can be then reduced down to 40% compared with the initial pattern on the photomask. Furthermore, on hydrophilic substrates, achieved by an accurate incomplete development of the photoresist, we demonstrate a nearly perfect linear dependency (1.4 mu m/degrees C) of microlens diameter spreading up to 70% the initial diameter inside a temperature reflow window of 110-140 degrees C. For both approaches, above a freezing temperature (T-freezing) of 170 degrees C, the microlens profile characteristics are temperature independent. By using high numerical aperture microlens array, we provide a proof of concept for the integration and enhanced light collection of the fluorescent signals collected form a microarray of fluorescent spots thus showing the potential of the concept for biophotonic integration. Crown Copyright (C) 2009 Published by Elsevier B.V. All rights reserved.

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