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Design and Optimization of Microring Resonators in Biochemical Sensing
Design and Optimization of Microring Resonators in Biochemical Sensing
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Abstract—Microring resonators can be exploited for biochem- tration or minute amount of analytes, a long interaction length
ical sensing applications. To gain a better understanding of the (i.e., large device size, typically in the range of centimeters for
design and optimization of microring sensors, the authors an- straight-waveguide sensors) is often required to accumulate a
alytically derive the detection limit and the sensitivity. Other
important parameters, including the ON–OFF contrast ratio and detectable phase shift and obtain a reliable signal-to-noise ratio
the signal-to-noise ratio (SNR), are also considered. In this paper, (SNR). It also means that a significant amount of analytes is
the combination of two sensing mechanisms and two sensing needed, which might not be available in many applications.
schemes are analyzed. These calculations provide a guideline for This issue can be addressed using microresonator sensors.
determining the microring geometry to satisfy the desired sensing Recently, microresonators have been proposed for sensing
requirements. In addition, the results can provide insights on how
to enhance the sensitivity and lower the detection limit. applications [10]–[12]. These devices offer a unique advantage
of reducing the device size by orders of magnitude without
Index Terms—Biochemical sensors, biosensors, integrated sacrificing the interaction length by virtue of their high quality-
optics, microcavity, microresonator, microring, microring res-
onator, optical waveguides, ridge waveguides, sensors, waveguide. factor (Q) resonance. The resonance effect provides an equiva-
lently long interaction length to achieve a sufficient phase shift.
I. I NTRODUCTION Such a property can dramatically reduce the device size and
the amount of analytes needed for detection. For example, the
(cladding index nc in homogeneous sensing and adsorbed film −1 neff (A − 1)−2 2A n2cl
thickness t in surface sensing). According to the definition, (Sw )s,TE = × − 2 2 · γc − 2 kx B
n2f − n2cl k0 neff nco
the sensitivity S for four different combinations is listed in
Table I. From the mathematical expression, it can be seen that 1 W ncl
2
ncl
2
+ (A − 1) × + (1 + B ) + 2
2
B (8)
the sensitivity can be further divided into two parts, which we γc 2n2co nco kx
call device sensitivity and waveguide sensitivity, respectively.
and
The device sensitivity is defined as the ratio of the change in
neff
the measured optical parameter to the effective-index change, (Sw )−1
s,TM =
while the waveguide sensitivity is the ratio of the effective- n2f − n2cl
index change to the change in the waveguide parameter
1 1 kx W W kx W
affected by analytes. The device sensitivity only depends on × + tan + sec2 (9)
γc kx 2 2 2
the device property, and the waveguide sensitivity is relevant
to a waveguide structure regardless of the type of devices. for TE and TM polarizations, respectively. The definition of all
These two parts can be enhanced separately to achieve a higher parameters used and the details of the derivation can be found
overall sensitivity. in Appendix II.
The device sensitivity is related to the measured optical
parameter, which implies that it depends on sensing schemes.
For a resonant-wavelength-shift scheme, the device sensitivity C. Detection Limit
can be derived from (2) as In most biological and chemical sensors, the detection limit
is a very important parameter to evaluate the sensing capa-
∂λc λc L bility of a device. The detection limit is typically defined as
(Sd )RWS ≡ = = (4)
∂neff neff m the smallest detectable change of the waveguide parameters
1398 JOURNAL OF LIGHTWAVE TECHNOLOGY, VOL. 24, NO. 3, MARCH 2006
caused by analytes, which is directly related to the smallest In addition to the aforementioned requirements, a large
analyte amount that a sensor can detect. The detection limit detection range is pursued, which can be achieved by tracking
is proportional to the smallest detectable index change of the the resonance [8]. However, if the acquisition time is slower
top cladding δnc for the case of microring sensors utilizing than the reaction time, the detection range is limited by an adja-
resonant-wavelength-shift monitoring as the sensing scheme cent resonance. In this situation, it is desirable to have a wider
and to the smallest detectable thickness change of the adsorbed free spectrum range (FSR), which is defined as the difference
analyte film δt for the case in surface sensing. According to the between two adjacent resonant wavelengths. From (1) and (3),
definitions of sensitivity, the detection limit is then proportional the FSR for each propagation mode can be calculated as
to δλc /S, where δλc is the distinguishable wavelength shift.
Theoretically, δλc is independent of the resonance shape or λ2c λ2c
the resonant bandwidth and should be determined merely by FSR =
= (10)
L · neff − λc ∂n eff L · ng
the instrument resolution. However, in reality, a noise can ∂λc
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