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Measurements for the Optical Parameters of Linear Birefringence Materials by Using Thermal Light Polarization-Sensitive Optical Coherence Tomography * a,bYu-Lung Lo, aChia-Chi Liao, and bCheng-Yen Yeh a Department of Mechanical Engineering b Institute of Micro-Electro-Mechanical System Engineering National Cheng Kung University No.1, Ta-Hsueh Road, Tainan 701, Taiwan ROC * Corresponding Author: [email protected] Abstract The new integrated POSCT with OCT system employing the thermal light source for the higher axial resolution in improving capability of extracting the extraordinary and ordinary refractive indices and without using the highly precise scanning stage and stage controller can simultaneously measure the thickness, mean refractive index, apparent phase retardation and optical axis orientation of a linear birefringence sample. The extraordinary and ordinary refractive indices, therefore, also can be extracted from above parameters if the order and apparent phase retardation of the multi-order birefringent material is correctly chosen. The measured data are in good agreements with the theoretical ones. The more error could be found in 3.96% in apparent phase retardation due to the dispersion effects from the broadband source. As the authors’ knowledge, this is the first instrument that could extract all the optical parameters including the thickness, mean refractive index, apparent phase retardation, optical axis orientation, order, and extraordinary and ordinary indices from a linear birefringence material by using only one system. Introduction Developing the technology of OCT has decades, and it is suitable for in-depth cross-sectional images in scattering media based on optical coherence-domain reflectometry (OCDR) [1]. From then on, many reports in OCT have presented. The subjects of these research include improving the axial resolution with the thermal light source [2], combing OCT with confocal system [3], developing various modulation methods in Doppler OCT and wavelength-dependent OCT [4], and developing in full-field or three dimensional measurement [5]. The typical OCT has axial resolution of 10-20 µm corresponding to the coherence length of the light source and does not explain the polarization effect or birefringence in the material. A recent and important extension to OCT is the incorporation of polarized control into the system. Hee et al. [6] had proposed a polarization-sensitive OCDR system that adds the capabilities of controlling the polarization state of light incident upon the sample and measuring the reflectivity of the light returning in particular polarization states. Up to the present, many researches using PS-OCT to image the depth resolved optical birefringence of biological have been published. The feature of PS-OCT is able to provide new contrast mechanisms potentially. de Boer et al. [7] presented a PS-OCT to record 2D image of the change in the polarization of circularly polarized incoming light backscattered form a bovine tendon. Hitzenberger et al. [8] presented an improved method of PS-OCT that made the measurement in backscattered intensity, birefringence and optic axis orientation simultaneously with single A-scan. In this study, the goal is to integrate our previous OCT system [9, 10] with the PSOCT and adopt the thermal light source to achieve ultrahigh axial resolution. The new system with no high-precision scanning stage and stage controller would have the capabilities of simultaneously measuring the thickness, mean refractive index, apparent phase retardation and optical axis orientation of a single-layer multi-order birefringence sample. The extraordinary and ordinary refractive indices, therefore, also can be extracted from above parameters. if the order and apparent phase retardation of the multi-order birefringent material is correctly chosen. Measurements of the thickness and mean refractive index The new structure developed in this study is illustrated in Figure 1. The signal received by Detector (1) of the system is designed to measure the thickness and mean refractive index of a linear birefringent sample. The beam from the thermal light source is initially split by non-polarizing beam splitter (NPBS(1)) into two beams. One beam namely Beam (A) is defined as the reference beam and it is reflected by a reference mirror. The other beam can be treated as the light source of the right half part of the system, which is a conventional PS-OCT system, and then the beam is split into two beams by NPBS(2). Subsequently, one beam (Beam (C)) passes a quarter-waveplate (QWP1) and reflected by the mirror on the scanning stage for the path-length scanning. The other beam namely Beam (B) passes another quarter-waveplate (QWP2) and generates a circularly polarized light onto the birefringence sample. Figure 1. Schematic diagram of the new PS-OCT system Detector (1) is used to measure the thickness and mean refractive index of the sample that the two parameters are unconcerned with the polarization state of light. The locations of low-coherence interferometric signals are only considered while Beam (C) is scanning the optical path of the reflected light. Beside, the new PS-OCT using two cubic NPBSs in common path, the portion of path-matching signal that sample arm (Beam (B)) and reference arm (Beam (C)) recombined at NPBS(2) would also be delivered to Detector (1) by NPBS1. In other words, Detector (1) can observe the location of peaks of interferometric signals of the sample arm and reference arm sequentially. It can directly see the optical path difference by compared the location of peaks of interferometric signals of sample arm with and without a sample. Thus, the signals recorded only by Detector (1) can be used for calculating the thickness and mean refractive index of a single-layer sample. The first and second steps of the setting of the sample and reference planes are shown in Figure 2 for measuring the sample’s thickness and mean refractive index [10]. The reference plane of the sample stage is denoted as R0. The S and RS denote the front and rear surfaces of the sample, respectively. The reference plane of the fixed reference mirror by where Beam (A) reflected is denoted as A. R0 Tns RS S R0 RS ∆T Tst Ts Figure 2. Steps and the Signals in measuring the thickness and mean refractive index In the first step, the Beam (B) illuminates the sample stage, and the scanning stage is moved for scanning to record the location of peaks of the scanning interferometric signal. Two peaks denoted by A and R0 are recorded by Detector (1) and illustrated in Figure 2(A). In the second step, a sample is put on the sample stage, and the location of peaks of the scanning interferometric signal is recorded by moving the scanning stage. Three peaks denoted by A, S and RS, as shown in Figure 2(B) could be obtained. The location of Peak A is fixed for the reference point at each optical path scanning due to the immobile reference mirror and the locations of R0, S and RS are sequentially recorded by Detector (1). The time differences denoted Tns and Tst for the location of A to R0 and the location of A to S can represent the optical path difference with and without the sample. Furthermore, TS is the time difference for the location of S to RS, which is proportional to the optical path length in the sample. Therefore, the following equation could be used directly to obtain the thickness of the sample as d s = ∆T × V = (Tns − Tst ) × V (1) where V is the scanning velocity of the scanning stage. For the sample with birefringence, the measured refractive index would be the mean value of ne and no [11]. As a result, the mean refractive index of the sample could be determined by n= Ts × V ne + no = ds 2 (2) Measurements of the apparent phase retardation and optical axis orientation Assuming that the polarization state of the light reflected from the reference arm is linearly polarized with 45° angle with respect to the horizon perfectly, and the light has both equal amplitude and phase in two orthogonal polarization directions. As Beam (B) with circular polarization state illuminates the sample, due to birefringence of the sample, the reflected light from the sample is an elliptical polarization generally and will interfere with the same optical path from Beam (C). The PBS splits the interferometric signal into two orthogonal linear polarization states detected by Detectors (2) and (3). The interferometric signals in each polarization channel are given by [11] IH = I0 2 I IV = 0 2 ∆L 2 ln 2 Rs ( d ) sin ( β ) exp − lc 2 cos ( 2k ∆L + 2α ) 2 ∆L 2 ln 2 Rs ( d ) cos ( β ) exp − cos ( 2k ∆L ) lc (3) where d is the penetration depth, β is the phase retardation, ∆L = Lr - Ls is the path-length difference of two arms and the Ls is the path length in the sample arm which includes the optical path in the sample, Ls = Lt + nd , lc is the coherence length of the light source, and α is the optical axis orientation. Equation (3) indicates that amplitude implies the information of the phase retardation and the phase of the interference term with Doppler shift frequency implies the information of the optical axis orientation. The results are obvious that amplitude of signals is sensitive to phase retardation and independent of the axis orientation of the sample. The optical axis orientation just affects the phase of the carrier frequency. An algorithm, Hilbert transform, previously reported in the context of Doppler OCT [12] and differential phase contrast OCT [13] is used to determine the amplitude and phase of the oscillating term of each interferometric signal at any depth. Consequently, the apparent phase retardation and optical axis orientation can be determined from the processed value of two orthogonal signals by the following equations as [11] IH (d ) IV ( d ) β = kd ∆n = arctan α= ∆φ φH − φV = 2 2 (4) (5) Therefore, using Hilbert transform to solve the amplitude and apparent phase of the measured signals is a convenient and simple method to obtain the birefringence properties. However, it should be noticed in Equation (4) that it is restricted by the definition of the tangent function and a positive number in the amplitude of the Hilbert transform, which means the dynamic range of the apparent phase measurements is 0° ~ 90°. Measurements of the extraordinary and ordinary refractive indices The waveplates can be manufactured either as multi-order or zero-order plates. The phase retardation of a multi-order waveplate, therefore, can be expressed as β + 2mπ = 2π λ d ( ne − no ) (6) where β is the apparent phase retardation (0 to 2π), (ne-no) is the birefringence of optical materials at λ, m is the order of a multi-order waveplate, and d is the thickness of a waveplate. For the defined thickness, mean refractive index, apparent phase retardation, and the assumed order (i.e. m = 1~10), the birefringence is calculated by Equation (6), and, therefore, the extra ordinary and ordinary refractive indices calculated by Equation (7) could be obtained as λβ mλ + 4π d 2d λβ mλ no = n − − 4π d 2d ne = n + (7) Since the thickness, mean refractive index, and apparent phase retardation are all defined, the extra-ordinary and ordinary refractive indices of the linear birefringence sample can be calculated by Equation (7) if the order and the exactly apparent phase retardation are correctly chosen. It should be noticed that the dynamic range in measuring the apparent phase retardation is restricted in the range of 0~90°. Thus, the measured apparent phase retardation is needed to be verified and modified by the above reason and the further discussion is introduced in Section “Calculation of the extraordinary and ordinary refractive indices”. Axial resolution in the new PS-OCT The axial resolution is one of the important subjects in this study. The thermal light with center wavelength at 590 nm and spectral bandwidth ∆λ = 160 nm is used for improving the axial resolution, and the calculated coherence length is 0.96µm. After comparing with the experimental results, the actual coherence length of the thermal light is known about 1.5 µm. It is obvious that using thermal light truly improves the axial resolution. The dispersion effect has to be considered while using such a broadband light source like the halogen lamp. The group dispersion will increase the coherence length and decrease the amplitude of an interferometric signal [14]. It means that the dispersion will degrade the axial resolution and fringe visibility of the low coherence interferometry. In order to estimate the influence of the dispersion in the interferometric signal, the width and maximum amplitude of the interferometric signal are measured while inserting four different thicknesses of samples into the sample arm. The D263T glass plate is measured and the measured coherence envelopes of five different cases are shown in Figure 3. The experimental results show that the thicker sample results in the poorer axial resolution and the lower amplitude of the interferometric signals. This phenomenon can be compensated by inserting a dispersion compensating plate into the reference arm of the low coherence interferometer [15]. 1 No sample 150um 300um 450um 600um 0.9 Normalized amplitude 0.8 0.7 0.6 0.5 0.4 0.3 0.2 0.1 0 -20 -15 -10 -5 0 5 Optical path difference (um) 10 15 20 Figure 3. The measured coherence envelope with different thicknesses of D263T glass plate Measured results of the thickness and the mean refractive index There are two kinds of samples for demonstrating the capability of measuring the thickness and refractive index. One is the sample made up of D263T glass, and the other is a multi-order QWP (CVI, QWPM-633-10-4-R15). Before the measurement, the location of the fixed reference mirror A and reference plane R0 of the scanning interferometric signal have to be recorded. After that, D263T glass plate whose refractive index and thickness, 1.5116 (at 1550 nm wavelength) and 150 µm (supplied by the manufacturer), is put on the sample stage and the scanning stage is moved for matching the optical path length of the sample. Finally, three time differences, Tns, Tst and Ts can be calculated after the peak detection. Therefore, the thickness, ds, and refractive index, n, can be obtained by Equations (1) and (2), and the experimental results are illustrated in Table 1. It should be noted that due to the center wavelength of the thermal light source is around 590 nm, the refractive index which is the function of wavelength could not be the same as specification: 1.5116 (at 1550 nm wavelength). Therefore, the theoretical refractive index value at 590 nm is calculated by Sellmeier equation [16], and the theoretical refractive index of the glass plate at 590 nm is calculated about 1.5167. From the average value of the measured refractive index, the measured refractive index is very close to the theoretical value. From Table 1, the standard deviations of the refractive index and thickness of D263T glass plate are 0.00185 and 0.310 µm respectively. The measured refractive index compared with the theoretical value obtained from Sellmeier equation has an error of 0.23%, and the measured thickness compared with 150 µm has an error of 0.76%. The values express that the measured result of a 150µm glass plate is good, which also means the influence of dispersion on the thickness and refractive index is slight. Table 1. The results of the single-layer sample (D263T glass plate) New structure PSOCT n 1 2 3 4 5 6 7 8 9 10 AVG STD 1.51785 1.51623 1.51555 1.51974 1.51979 1.51661 1.51641 1.51963 1.51458 1.51764 1.51704 0.00185 ds (µm) 151.250 150.950 151.150 150.750 150.975 151.275 150.850 151.550 151.725 150.975 151.145 0.310 Next, the same procedure for measuring the multi-order QWP (CVI, QWPM-633-10-4-R15) at 633 nm wavelength is proceeded, and the experimental results are illustrated in Table 2. For the same reason mentioned above, the theoretical value of mean refractive index of the crystal quartz QWP can be obtained by averaging the ne and no, which can be calculated by a Laurent series formula [16]. The theoretical value of the mean refractive index of a multi-order QWP is 1.54877 at 590 nm obtained by averaging the theoretical values on ne = 1.55333 and no = 1.54421. In Table 2, the obtained thickness and mean refractive index are 582.555 µm and 1.5504 respectively. The theoretical value of thickness and mean refractive index of a multi-order QWP (CVI, QWPM-633-10-4-R15) are 575.917 µm and 1.54877 at 590 nm wavelength respectively, as illustrated later in Table 5, which is somewhat different from our measurement values. It is noticed that although the D263T is used to compensate for the dispersion effects, the dispersion of the sample could not be perfectly compensated. It is believed that the error of the mean refractive index and thickness of a birefringence sample mainly results from this imperfect dispersion compensation. The measured thickness and mean refractive index have error of 1.14 % and 0.11% respectively and it is believed that the experimental results are still acceptable. Table 2. The result of the single layer birefringent sample (QWPM-633-10-4-R14) New structure PS-OCT 1 2 3 4 5 6 7 8 9 10 AVG STD n ds (µm) 1.54849 1.54933 1.55216 1.55250 1.55039 1.54885 1.55159 1.54956 1.55103 1.55014 1.55040 0.00132 583.375 583.300 581.850 582.125 582.725 582.625 582.275 582.875 582.225 582.175 582.555 0.488 Measured results of the apparent phase retardation and optical axis orientation Before measuring the whole optical parameters of the birefringent sample with our new structure, the capability of the apparent phase retardation and optical axis orientation measurements needs to be demonstrated. Two different types of quarter-waveplate, zero-order QWP (CVI, QWP0-633-04-4-R10) and multi-order QWP (CVI, QWPM-633-10-4-R15), are used as the samples in our measurement system. The effect of the dispersion on measuring the optical path difference related to the thickness and mean refractive index is slighter than that on measuring the apparent phase retardation of a birefringent sample. It is because the dispersion easily affects the amplitude of signals and results in the more error in extracting the apparent phase retardation. Therefore, the dispersion has to be compensated well while measuring the apparent phase retardation. In this study, it is discovered that the D263T glass plate can still be used for compensation in experiments. According to the obtained amplitude and phase, the apparent phase retardation and optical axis orientation of the sample can be calculated by Equations (4) and (5). Figure 4 shows the experimental data in three different cases in examining the zero-order QWP for ten times. One of the three cases is without using the compensating plate, another is using a compensating plate, and the other is using a compensating plate and a 633 nm band-pass filter. The average apparent phase retardation of the measuring results without compensation is 81.9° and has a difference of 9 % as compared to 90°, and that with compensation is 86.31° and has a difference of 4.09 %. The quarter-waveplate provides 90° phase retardation only when the wavelength of light is 633 nm. As filtering the beam from the light source by a band-pass filter at 633 nm with 10 nm spectral bandwidth, the amplitude of the interferometric signal at the horizontal direction is too small to be observed. Thus, it could be said that the measured phase retardation extremely approach 90°. It indeed displays that the result with both dispersion compensation and band-pass filter at 633 nm is closest to 90° phase retardation since the incident light most fits the specification of the zero-order QWP (CVI, QWP0-633-04-4-R10). 92 Apparent phase retardation (deg) 90 88 86 84 82 80 78 76 Zero-order Zero-order-comp Zero-order-comp-filter 74 72 70 1 2 3 4 5 6 7 8 9 10 Measurements Figure 4. Apparent phase retardation measurements of zero-order QWP (CVI, QWP0-633-04-4-R10) Following the same experimental steps to measure the apparent phase retardation in the multi-order QWP, the experimental data in Figure 5 also show three different cases. The average apparent phase retardation of the multi-order QWP with and without 633 nm band-pass filter are 83.41° and 47.863° respectively, and the worst is the situation without neither the compensating plate nor the 633 nm band-pass filter. Obviously, the error of the phase retardation from the zero-order QWP is less than the multi-order one at the wide range of wavelength and it is attributed to the zero-order QWP offers substantially lower dependence on temperature and wavelength than multi-order waveplates [17]. Furthermore, because the dynamic range of the extracted apparent phase retardation is limited from 0° to 90°, a lot of difference between the cases with and without 633 nm band-pass filter is found. The further explanation in the modified apparent phase retardation could be explained in next Section by correctly defining the order of the multi-order sample. Apparent phase retardation (deg) 90 85 80 75 70 Multi-order 65 Multi-order-comp 60 Multi-order-comp-filter 55 50 45 40 35 30 1 2 3 4 5 6 7 8 9 10 Measurements Figure 5. Apparent phase retardation measurements of multi-order QWP (CVI, QWPM-633-10-4-R15) 100 90 80 70 60 50 40 30 20 10 0 -10 y = 1.0396x - 0.5634 Theoretical Measured 0 10 20 30 40 50 60 70 80 Set optical axis orientation (deg) 90 100 Measured optical axis orientation (deg) Measured optical axis orientation (deg) The measurement of the optical axis orientation is according to the phase difference between the two orthogonal polarization states of interferometric signals. The phase difference between two orthogonal interferometric signals can be obtained by Hilbert transform. The measurements are conducted for rotating the sample in the increment of 10° step by step, and each optical axis orientation is obtained from the average value of ten time measurements. Figure 6(A) shows the experimental results of the optical axis orientation in the zero-order QWP and the mean standard deviation is 2.9°. Figure 6(B) is the result of multi-order QWP and the mean standard deviation is 3.1°. It is observed that the measured results are not very good and the one possible reason for the worse measured result is that the vibration of a moving scanning stage will disturb the scanning interferometric signals of PS-OCT system. 100 90 y = 0.9812x - 0.2999 80 70 60 50 40 30 20 10 0 -10 0 Theoretical Measured 10 20 30 40 50 60 70 80 90 100 Set optical axis orientation (deg) (A) Zero-Order QWP (B) Multi-Order QWP Figure 6. The measured optical axis orientation Calculation of the extraordinary and ordinary refractive indices Up to the present, the thickness, mean refractive index, apparent phase retardation, and optical axis orientation of the sample have been obtained. It is also been discussed that the ne and no could be calculated by Equation (7) if the order of the sample is known correctly. For the measured thickness, mean refractive index, apparent phase retardation, and the assumed order (i.e. m = 1~10), the possible birefringence calculated by Equation (6) and the possible extra-ordinary and ordinary refractive indices calculated by Equation (7) are obtained and listed in Table 3. It is should be noticed that due to the limited dynamic range of the measuring apparent phase retardation in Equation (4), the possible apparent phase retardations in four quadrants are considered. In Table 3, the estimating values in the condition of m = 1~10 and the possible apparent phase retardations only in the first and fourth quadrants are listed. It could be observed that the estimating extraordinary refractive index is in the range of 1.55047~1.55591, and the ordinary one is in the range of 1.54490~1.55034. Table 3. The calculated birefringence for the assumed orders at 590 nm wavelength β = 47.863° (The First Quadrant) m 0 1 2 3 4 5 6 7 8 9 10 ∆n=ne-no 0.00013 0.00115 0.00216 0.00317 0.00419 0.00520 0.00621 0.00722 0.00824 0.00925 0.01026 ne 1.55047 1.55098 1.55148 1.55199 1.55250 1.55300 1.55351 1.55402 1.55452 1.55503 1.55554 β = 360°-47.863° = 312.137° (The Fourth Quadrant) no 1.55034 1.54983 1.54932 1.54882 1.54831 1.54780 1.54730 1.54679 1.54629 1.54578 1.54527 ∆n=ne-no 0.00088 0.00189 0.00290 0.00392 0.00493 0.00594 0.00695 0.00797 0.00898 0.00999 0.01101 ne 1.55084 1.55135 1.55186 1.55236 1.55287 1.55338 1.55388 1.55439 1.55489 1.55540 1.55591 no 1.54996 1.54946 1.54895 1.54845 1.54794 1.54743 1.54693 1.54642 1.54591 1.54541 1.54490 By comparing the possible birefringence with the common uniaxial birefringent crystals [18], the only material with the extra-ordinary and ordinary refractive indices corresponding to the estimating ones is quartz. Thus, the material of the sample (CVI, QWPM-633-10-4-R15) is confirmed as quartz. From the birefringence of quartz (∆n = 0.009), the possible order, 8 and 9, the corresponding apparent phase retardation, 312.137° and 47.863°, and the corresponding birefringence, 0.00898 and 0.00925, of a sample are chosen from Table 3 for the further confirmation. Based on the dispersion equation [17], the difference of birefringence between 590 and 633 nm wavelengths is only 0.00005. Therefore, for affirming which order of the sample is, the measured apparent phase retardation at 633nm wavelength with 633nm band-pass filter, as illustrated in Figure 5, could be reconsidered for confirmation. Again, substituting the measured thickness, the possible apparent phase retardation in four quadrants (83.412°, 96.858°, 263.412°, and 276.588° at 633 nm wavelength), and the assumed order, 1~10, into Equation (6), all the possible birefringence at 633 nm wavelength could be estimated. It is found that only the estimated birefringence at 633 nm wavelength, 0.00894, with the order 8 and the apparent phase retardation 83.412° is closest to the birefringence at 590 nm wavelength, 0.00898, with the order 8 and the apparent phase retardation 312.137°. Also, the difference of birefringence between 590 and 633 nm wavelengths is 0.00005, and it complies with the previous statement. In final, the order of a sample is confirmed to be 8 and therefore, the real measured apparent phase retardation is 312.137° at 590 nm wavelength. Since the measured thickness, the mean refractive index, the order, the birefringence, and the apparent phase retardation are all defined, the extra-ordinary and ordinary refractive indices of the linear birefringence sample also are able to be calculated by Equation (7). Therefore, the calculated ne and no are obtained as shown in Table 4. The calculated ne and no are 1.55489 and 1.54591 respectively on average, and the difference in refractive indices between ne and no could be calculated as 0.00898. They are in good agreements with the optical parameters in the crystal quartz at 590 nm wavelength. Times 1 2 3 4 5 6 7 8 9 10 AVG STD Table 4. The calculated ne and no of the multi-order QWP (QWPM-633-10-4-R14) Thickness (µm) Mean refractive index no ne 583.375 1.54849 1.55297 1.54401 583.300 1.54933 1.55382 1.54485 581.850 1.55216 1.55666 1.54767 582.125 1.55250 1.55700 1.54801 582.725 1.55039 1.55488 1.54590 582.625 1.54885 1.55334 1.54436 582.275 1.55159 1.55608 1.54709 582.875 1.54956 1.55405 1.54507 582.225 1.55103 1.55553 1.54654 582.175 1.55014 1.55463 1.54564 582.555 1.55040 1.554894 1.545914 0.513944 0.001386 0.001389 0.001383 ∆n 0.00897 0.00897 0.00899 0.00899 0.00898 0.00898 0.00899 0.00898 0.00899 0.00899 0.00898 7.92×10-6 The all measured parameters of the multi-order quarter waveplate (CVI, QWPM-633-10-4-R15) at 590 nm are all listed in Table 5. From the comparison between the measured values and the theoretical ones, the measurement in the thickness and mean refractive index are accurately enough and that in optical axis orientation is acceptable. However, the measured apparent phase retardation after modification has more error in 3.96 % because of the dispersion effects by using a broadband source in the new structure and also the imperfect dispersion compensation. Table 5. Measured results and theoretical value of multi-order QWP (QWPM-633-10-4-R14) at 590 nm wavelength Measured value Theoretical value Error Thickness 582.555 µm 575.917 µm 1.14 % Mean refractive index 1.55040 1.54877 0.11 % Apparent 360° - 47.863° 325.018° 3.96% Phase retardation (β) = 312.137° Birefringence (∆n) 0.00898 0.00912 1.54 % ne 1.55489 1.55333 0.1 % no 1.54591 1.54421 0.11 % Optical axis orientation (α) Figure. 6 NA. NA. Conclusions and Discussions The capability of a new PS-OCT without using the highly precise scanning stage and stage controller in measuring the thickness, mean refractive index, apparent phase retardation and optical axis orientation of a single-layer multi-order birefringence sample has been demonstrated successfully. Surprisingly, the extraordinary and ordinary refractive indices also could be precisely extracted. In general, the traditional PS-OCT has been applied many years in tissue sectioning, however only the case with the phase retardation in range from 0 to 900 with zero order is without further modification. Therefore, to develop a new PS-OCT that is suitable for the multiple-order linear birefringence materials with the full range of the phase retardation measurement is the future work. In summary, the measured data are in good agreements with the theoretical ones. As the authors’ knowledge, this is the first instrument that could extract all the optical parameters of a linear birefringence material including the thickness, mean refractive index, apparent phase retardation, optical axis orientation, order, and extraordinary and ordinary indices by using only a thermal-light PS-OCT system. 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