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DO 2012
Summary
Introduction
Transparent polymers have emerged as new materials in diffractive optics over the
last decade1. Polymer optical devices have advantages over inorganic devices, for
example, organic materials are more flexible, less brittle, require lower processing
temperatures. Processing inorganic materials typically required sophisticated etching
techniques while polymer structures can be fabricated, for example, by simply
replicating a master stamp at relatively low temperature. The thermal expansion
coefficients of polymers are an order of magnitude larger than those of optical
inorganic glasses. Thermal expansion and thermo-optic coefficient values of
polycarbonate used in our calculations are 6.55 x 10-5 and -1.07 x 10-4 °C-1. 2,3
Discussion
The spectral position of the resonance peak is observed to change towards longer
and shorter wavelength regions depending on the thermal expansion and thermo-
optic coefficients of the polycarbonate and TiO2 materials. Figure 1a shows the
central resonance peak at 855 nm, calculated at room temperature with full width at
half maximum FWHM 10.7 nm. Figure 1b shows thermal spectral shifts based on the
thermal expansion TEC and thermo-optic TOC coefficients at 100 °C. In Fig. 1b,
spectral curve 1 shifts to longer-wavelength region which is because of the TEC of
TE-Mode resonance wavelength of binary grating at 25 °C TE-Mode resonance wavelength of binary grating at 100 oC
1 1
X: 852, Y: 1 1-TEC
0.9 X: 855, Y: 1 0.9 2-TOC
X: 856, Y: 1
3-TEC+TOC
0.8 0.8 X: 859, Y: 1
0.7 0.7
Reflectance
0.6
Reflectance
0.4 0.4
0.3 0.3
0.2 0.2
0.1 0.1
0 0
800 810 820 830 840 850 860 870 880 890 900 800 810 820 830 840 850 860 870 880 890 900
Wavelength [nm] Wavelength (nm)
(a) (b)
Fig. 1 Spectral reflectance of binary grating structure at resonance wavelength (a) calculated central resonance wavelength at room
temperature (b) calculated central resonance wavelength at 100 °C due to TEC (1), TOC (2) and combined effect.
Conclusion
Nearly athermalized optical waveguide filters are designed and fabricated by
considering large thermal expansion materials (polymers). Combination of thermal
expansion and thermo-optic effects is responsible to keep the resonance peak close
to its original position over a range of tens of degrees above room temperature: the
spectral shift is small in comparison to the resonance line width at the central
wavelength. The experimentally measured results are in good agreement with the
calculated results. The replicated structures in polymers are economic in large-scale
production of nearly athermalized devices.
1
. H. P. Herzig, “Replication”, in Micro-optics: Elements, Systems and Applications (Taylor & Francis, London,
1997).
2
. G. P. Behrmann and J. P. Bowen, Appl. Opt. 14, 2483 (1993).
3
. H. S. Nalwa, Polymer Optical Fibers (American Scientific publisher, Valencia, CA, 2004).
4
. S. F. Pellicori, and H. Hettich, Appl. Opt. 27, 3061 (1988).