Abstract
Polarised light imaging microscopy, with the addition of a liquid crystal (LC) phase retarder, was used to determine the birefringence of silk fibres with high (∼1 μm) spatial resolution. The measurement was carried out with the silk fibres (the optical slow axis) and the slow axis of the LC-retarder set at parallel angles. The direct fit of the transmission data allowed for high fidelity determination of the birefringence Δn ≈ 1.63 × 10−2 (with ∼2% uncertainty) of the brown silk fibre, (Antheraea pernyi) averaged over the wavelength range λ = (425–625) nm. By measuring retardance at four separate wavelengths, it was possible to determine the true value of the birefringence of a thicker sample when an optical path may include a large number of wavelengths. The numerical procedures and required hardware are described for the do-it-yourself assembly of the imaging polariscope at a fractional budget compared to commercial units.
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Introduction
Optical imaging of metasurfaces for defining the engineered birefringence and its orientational pattern is gaining rapid interest due to the ability to directly evaluate the fabrication quality and phase retardance of flat optical elements using transmission polariscopy1. This method was previously demonstrated to be able to determine the slow axis orientation and retardance of any arbitrary sample2 and was commercially implemented as a side-port addition onto a microscope (Abrio). A wider use of this technique, however, was hampered by its comparatively high price and production of the unit was consequently discontinued. Nevertheless, there is a need for the in situ monitoring of birefringence in complex micro-fluidic flow cells3 and cell division microscopy where optical detection of cell division can be monitored in real time4 using such simple instrumentation. Measurements of birefringence are highly necessary in microscopy and material science fields, however, expensive dedicated microscopes or bulky add-on microscopy units must be used which generally only operate at fixed wavelengths2. Birefringence can be inferred from Stokes polarimetry which is realised by different principles of phase delay or polarisation rotation e.g. based on photoelasticity5 or the use of LC retarders6,7. When waveplates are used together with rotating elements and lock-in amplifiers, setups of high sensitivity and resolution can be created. A crossed polariser-analyser setup with a rotating quarter-waveplate compensator was recently used for determination of 3D orientation maps of birefringent fibre structures in brain tissue8. These custom set-ups, however, can become bulky, complex and, frequently, wavelength specific.
Simplification of the optical retardance measurement over a broader spectral range remains a requirement for flat optical elements and bio-materials which display high orientational anisotropy and domain structure. For example, the birefringence of silk is usually measured by shear interferometry9,10,11, which is not capable of high resolution imaging. The emerging optical applications which utilise transparent wood12 also require better understanding of the optical properties of the micro-tubular wood structure. Stress-induced birefringence in crystals/glasses/polymers13,14,15, volume phase transitions16, and complex topological structures for volumetric stress control17, or patterning of absorbance in transparent materials18 all produce complex optical anisotropy which demands high resolution ∼λ imaging. A set-up consisting of a crossed polariser and analyser can be used to reveal the birefringence Δn of a sample placed between them using optical imaging at a selected wavelength, λ. The retardance Δnd is defined by the thickness of the sample d and birefringence Δn. The transmittance T through the birefringent medium of thickness d, when reflectance and absorbance are negligible for the crossed polariser and analyser, is given by (Fig. 1(a)):
where Iθ and I0 are the transmitted and incident intensities, respectively, θ is the angle between the transmission axis of the analyser and the horizontal x-direction of the field of view where it is also positive for the anti-clockwise rotation (looking into the beam), θR is the slow (or fast) axis direction with the slow axis19 usually aligned to the main molecular chain or along the polymer stretch or, in this study, aligned along the length of the silk fibre. Equation 1 represents the Maltese cross pattern shown in Fig. 1(a).
In this study, we used a simple LC-cell (Fig. 1(a)), which has an electrically controlled birefringence (Fig. 1(b)), as a compensator for the determination of the birefringence of a single silk fibre. The silk sample was placed directly on the LC-cell window and aligned with the slow axis of the LC-retarder. Transmission vanished at the regions with zero birefringence (Eqn. 1). Data acquisition and analyses were fully automated using Labview and Matlab scripts. By using standard microscopy imaging at a freely chosen wavelength, the birefringence of a single strand of silk was determined with high fidelity, achieving a resolution which is comparable to the wavelength λ at tight focusing. Therefore, this method can potentially be used to measure the birefringence of any transparent material over the visible 400–800 nm spectral range which is determined by the transparency of the LC-cell. Due to the virtue of multi-wavelength measurement capability, the method used in this study allows to determine the birefringence of a material even when the retardance possesses wavelength changes.
Method and Samples
Polarisation change due to birefringence
The setup used in this study was based on illumination of the sample using linearly polarised light (Fig. 1(a)). Simple Jones matrix calculus20,21 (as compared to the more general Mueller calculus) was applied to determine the evolution of the electric field of light as outlined next. The x-polarised (horizontally) incident light can be defined by the E-field Jones vector (Fig. 1):
The analyser is crossed and can only transmit y-polarised (vertical) light. The corresponding Jones matrix is given by:
A generic Jones matrix of the retarder with the phase delay ϕ = kΔnd, wavevector k = 2π/λ, and with the slow axis at angle θ with respect to the x-axis is given by:
During the measurements, the LC-retarder was inserted with the silk fibre oriented parallel to the slow axis of the LC-retarder (Fig. 1). Eqn. 4 was used for the LC-retarder JLC(ϕ, θ). The setup and calibration curves for the retardance vs. voltage is shown in Fig. 1. The silk fibre contribution to the phase retardance is given as Js(ϕs, θs), where θs is calculated from the x-axis (θs = 0). The overall transmission through the setup (Fig. 1(a)) can therefore be determined by the following equation:
The analytical expressions for the coefficients of A = a1 + ia2 and B = b1 + ib2 are given by:
The intensity of the transmission image detected by the CCD camera (Fig. 1(a)) is thereby given as I = AA*, where A* is the complex conjugate. Further simplification of the trigonometric expressions A,B occurs at θLC = θs = π/4 and allows for the simple calculation of the intensity at each [x, y] pixel I(x, y). By matching I(x, y) with the experimentally measured retardance \(Re{t}_{exp}\equiv \arcsin \sqrt{{T}_{\theta }}\mathrm{/2}\pi \) (Eqn. 1), the retardance Δn × d can be determined. Furthermore, when the thickness of the birefringent region d is known (measured independently), the birefringence Δn at each pixel can be calculated.
Samples and measurements
A Nikon Optophot-POL microscope with an Olympus LMP PlanFLN objective lens with 20× magnification and numerical aperture NA = 0.4 was used for all measurements in this study. The optical images with VGA resolution 480 × 640 pixels were captured with a CCD camera BU030C Toshiba teli for analyses at N = 718 number of points (voltage values of the LC-retarder cell). The LC-retarder (LCC1223T-A, Thorlabs) was used in conjunction with the LCC25 controller and a temperature stabilizer TC200. The temperature stabilizer was used for the quantitative determination of the retardance. Factory calibration of retardance vs. applied voltage at selected wavelengths was provided by the vendor (Fig. 1(a)), however, we applied a different calibration procedure suitable for each wavelength selected by the bandpass filter. Image acquisition at different LC-retardance (number of points N = 718) was computer controlled and a Matlab code was used for the final image analysis using the protocol described in Sec. 2.1.
Two types of silk, white Bombyx mori and brown Antheraea pernyi, were used in this study. Prior to the experiment, both silk fibres were degummed, i.e. the sericin cladding was dissolved as described previously22 and single strands were used for imaging. Both types of silk have similar composition and structure, therefore, they should possess similar birefringence22. Brown silk strands have, on average, a slightly larger diameter. Image acquisition was carried out at standard room temperature and pressure.
Calibration of retardance of LC-cell
Factory calibration of the retardance vs. applied voltage was provided by the vendor, however, the LC-retarder is sensitive to temperature and wavelength. Therefore, precise calibration is required for each measurement. The light intensity at “Air” ROI was utilized for the calibration.
The retardance of LC-cell RetLC is the function of applied voltage V. When the slow axis of LC-retarder is set to π/4 radian between the polariser and analyser of the microscope, the light intensity IAir at the “Air” ROI (out of sample) is given by:
where \({I}_{Air}^{max}\) and \({I}_{Air}^{min}\) are the maximum and minimum light intensity Iair. Retardance change by the applied voltage V is continuous as shown in Fig. 1(b). Using Eqn. 6, the retardation can be obtained from the intensity by the following equation:
where Vmax and Vmin are the applied voltage when light intensity IAir is equal to \({I}_{Air}^{max}\) or \({I}_{Air}^{min}\). We can calculate RetLC from IAir by Eqn. 7. As a result, calibration of RetLC was carried out by measuring light intensity IAir when applied voltage V changes using Eqn. 7.
Results and Discussion
First, we show a qualitative method of retardance imaging using silk fibres. Then, a quantitative method is demonstrated using a simple LC-retarder cell without employing waveplates (Sec. 2.1).
Qualitative imaging of retardance
Phase retardance is used in polarisation microscopy to create colour contrast under a white light (condenser) illumination. This is useful for the qualitative distinction of regions with different birefringence (phase thickness) in the image. Figure 2 shows images of a single white silk Bombyx mori fibre after degumming taken at different LC-retarder voltages. The slow axis of the LC-retarder was aligned perpendicularly to the silk fibre in order to counteract the birefringence by decreasing the retardance at larger voltages (Fig. 1(a)). When the birefringence Δn was corrected the polar plot of the mean intensity formed a pattern similar to the Maltese cross (Fig. 1(a)). The darkest region in each image was observed to change when capturing images at larger voltages (Fig. 2). It is presumed that the triangular or trapezoidal shape of the cross section of the silk fibre was contributing to the non uniform colour appearance over the entirety of the fibre. Nevertheless, only a qualitative estimate of the birefringence can be made using this method, even when imaging is carried out at one wavelength or at a spectrally narrow bandwidth.
Quantitative imaging of retardance
In this section, we describe the determination of the birefringence with good reproducibility, using CCD camera imaging at different LC-retarder voltages (number of points N = 718) at different ϕLC values and by application of the formulas in Eqns 2–5. We used a ∼10 nm bandwidth filter to select a narrow spectral window from the white light condenser illumination. The silk fibre was set at an angle of π/4 radian between the polariser and analyser (Fig. 3). Additionally, the fibre was set parallel to the slow axis of the LC-retarder (θ − θR) = π/4. A region of interest (ROI) “Air” was selected outside the silk fibre (Fig. 3(a)) where only the reference retardance of the LC-cell was present in the optical path. The N = 718 number of measurement points of transmittance were selected in equidistant steps of retardance over the entire range of LC-retarder voltages as shown in (Fig. 3(b)). To establish the relationship between the average intensity on the CCD camera image (b), which is proportional to the measured transmittance Texp = IAir/I0, and to calculate the retardance using Eqn. 1, the intensity, IAir, at the “Air” ROI (out of sample) was measured. The incident light intensity I0 was controlled by electrical current in order to prevent saturation over a single LC-retarder cycle. The minimum intensity corresponded to the 0-wavelengths (or 1) while the maximum corresponded to 0.5-wavelengths (Fig. 4(a)). Since \({sin}^{2}\mathrm{2(}\theta -{\theta }_{R}\mathrm{)=1}\) by the selection of LC-retarder orientation (θR = ±π/4), the reference retardance of the LC-cell can be determined by \({T}_{exp}={sin}^{2}(\pi \Delta {n}_{LC}{d}_{LC}/\lambda )\) (Eqn. 1, where nLC, dLC are the birefringence and thickness of the LC-cell, respectively (Fig. 3(c)).
The measured intensity was averaged over the ROI 2 × 2 pixels (see Fig. 4 inset). Regions on the LC-retarder and silk fibre are plotted in Fig. 4(a,b), respectively. It was necessary to select smaller ROIs due to a non-uniform thickness of the fibre, as described earlier, and to test the smallest integration area; potentially the noisiest signal. Since the “Air” region outside the silk fibre was used for reference retardance measurements, the transmittance follows Eqn. 1: \({T}_{\theta }={sin}^{2}(\pi \Delta nd/\lambda )\). Importantly, for the retardance corresponding to the half-wavelength Δnd/λ = 0.5 the transmittance has a maximum (see arrow in Fig. 3(b)) and for the full wavelength Δnd/λ = 1 it has a minimum (see arrow in Fig. 3(b)). This was expected and shows the validity of the employed calibration method. It was repeated for the different set of bandpass filters defining different wavelengths.
Figure 4(b) shows experimentally measured transmittance integrated over the 2 × 2 pixels ROI area on the silk fibre (rectangular box in the inset in (a)) vs. retardance of the LC-cell using the same procedure as used for the calibration of LC-retarder shown in (a). Even for a small number of the averaged pixels 2 × 2, a high confidence fit by \(fit(x)=a{sin}^{2}(\pi [x\pm b])+o\) was obtained with a,o defining the amplitude and offset, x = ΔnLCdLC/λ is the retardance of LC-cell, and b = Δnd/λ ± m where m = 0, 1, 2..., is determined by silk with the sign conventions: “+” for the LC-cell orientation as shown in the inset of (a) and “−” for the one perpendicular to that. The phase of the sin-wave was solely determined by the cumulative retardance through the LC-cell (“air”) and silk fibre Δnd. However, when the retardance of the sample is exceeding one wavelength, it has an uncertainty of ±m. The best fit for the silk orientation shown in Fig. 4(b) was obtained with the “+” sign fit(x) = 110sin2(π(x + 0.35)) + 55 and corresponds to Δnd/λ ± m = 0.35. The shaded region in Fig. 4(b) shows the ±5% change in Δn around the best fit value. This qualitatively shows that a birefringence with ±2% difference can be distinguished. It is important to note that thickness and a change in birefringence equally affect the measured retardance. In this study, the thickness and orientation of the slow axis of the fibre did not affect the vertical offset of the sinusoidal curve in Fig. 4(b). The variation in d is the variation in retardance, therefore it changes the horizontal shift of the curve. Since the orientation of the slow axis is the first sinusoidal part of the Eqn. 1, it affects only the amplitude of the curve in Fig. 4(b). One possible explanation for the vertical offset is the depolarisation of the light due to the scattering at the surface of the silk fibre sample.
Retardance averaged over 2 × 2 pixels was determined for the entire image using the fitting method shown in Fig. 4(b). It is presented in Fig. 5 for the four different wavelengths selected by interference filters with 10 nm bandwidth. To obtain the exact Δn value, retardance was measured at four wavelengths and Δnd/λ vs. 1/λ was plotted, as shown in Fig. 6. A good linear fit was obtained for the retardance averaged over the ROI (Fig. 5) plotted in Fig. 6. Since the uncertainty of ±m affects only the vertical shift on the Δnd/λ vs. 1/λ plot, the exact Δn value can therefore be obtained. For the central part of the fibre, the birefringence Δn ≈ (1.63 ± 0.05) × 10−2 was determined when d ≈ 30 μm (for simplicity the silk fibre was assumed to be a cylinder).
To obtain the map of the averaged retardance Δnd [nm] over the spectral range from 425 nm to 625 nm, the same procedure as for Fig. 6 was carried out for each 2 × 2 pixels of the image at four wavelengths. From the slope of the linear fit, Δn was calculated (as in Fig. 6) and is plotted in Fig. 7. Edges of the silk fibre scattered light stronger which resulted in a higher detected light intensity Tθ (Eqn. 1) and a corresponding two-fold increase in effective retardance.
Conclusions and Outlook
In summary, the addition of a simple LC-retarder to a common polarisation microscopy set-up provides a highly sensitive method to image birefringence, as demonstrated for silk fibres. The proposed method relies on a large data set (sampling) of images obtained at different LC-retarder voltages (phase delays) used for the best fit. Here, it was shown that the birefringence of silk Δn ≈ 1.6 × 10−2 could be determined with an uncertainty of just ∼±2% measured from an area of merely 2 × 2 pixels. Integration over larger ROI areas can be flexibly applied to achieve a better spatial resolution or an average birefringence, respectively. Measurements at several wavelengths were made to establish the absolute phase retardance. This is one advantage of our method over the commercial microscopy-based techniques for measuring birefringence which are carried out at merely one wavelength. The multi-wavelength measurement allows for extension of the retardance range beyond just one wavelength.
The technique for measuring birefringence established in this work, is simple and requires a fractional budget of ∼$2 k compared to the commerically established birefringence measurement tools. When the slow axis of the sample is unknown, or it is changing orientation over the image area, the axial alignment can be made by an additional measurement at four points (the minimum number required for the fit) of the angular orientation of the sample. Additionally, absorption anisotropy (diattenuation) can be measured using transmission with adequately high resolution ∼λ using this simple technique for analysis of molecular alignment23.
The proposed technique could also find application in the bio-medical field for cell monitoring and optical detection of cell division exploiting a new dimension, the birefringence, in addition to the usual set of the big-data dimensions of the lateral xy-position of the cell, time, intensity and shape of the object.
References
Khorasaninejad, M. & Capasso, F. Metalenses: Versatile multifunctional photonic components. Science 358, eaam8100 (2017).
Shribak, M. & Oldenbourg, R. Techniques for fast and sensitive measurements of two dimensional birefringence distributions. Appl. Optics 42, 3009–3010 (2003).
Sun, C.-L. & Huang, H.-Y. Measurements of flow-induced birefringence in microfluidics. Biomicrofluidics 10, 011903 (2016).
Charnley, M. & Russell, S. Imaging Asymmetric T Cell Division, vol. 1584, 383–398 (Humana Press, New York, NY, 2017).
Kemp, J. C., Henson, G. D., Steiner, C. T. & Powell, E. R. The optical polarization of the sun measured at a sensitivity of parts in ten million. Nature 326, 270–273 (1987).
Shribak, M. Complete polarization state generator with one variable retarder and its application for fast and sensitive measuring of two-dimensional birefringence distribution. J. Opt. Soc. Am. A 28, 410–419 (2011).
Oldenbourg, R. Polarization microscopy with the LC-PolScope, 205–237 (Cold Spring Harbor Laboratory Press, NY, 2005).
Axer, M. et al. A novel approach to the human connectome: ultra-high resolution mapping of fiber tracts in the brain. Neuroimage 54, 1091–1101 (2011).
Fouda, I. M. & El-Tonsy, M. M. Birefringence behaviour of annealed silk fibres. J. Mat. Sci 25, 4752–4757 (1990).
Cronin-Golomb, M., Murphy, A. R., Mondia, J. P., Kaplan, D. L. & Omenetto, F. G. Optically induced birefringence and holography in silk. J Polym. Sci.: B Polym. Pphys 50, 257–262 (2012).
Holland, C., O’Neil, K., Vollrath, F. & Dicko, C. Distinct structural and optical regimes in natural silk spinning. Biopolymers 97, 368–373 (2012).
Li, Y., Vasileva, E., Sychugov, I., Popov, S. & Berglund, L. Optically transparent wood: Recent progress, opportunities, and challenges. Adv. Optical Mater. 1800059 (2018).
Beresna, M., Brambilla, G., Juodkazis, S., Wang, X. & Rumpf, R. Geometric phase via stress induced birefringence. 2pp (CLEO-Pacific Rim, Singapore. 31 Jul–04 Aug, 2017 (2017).
Morikawa, J., Orie, A., Hashimoto, T. & Juodkazis, S. Thermal and optical properties of the femtosecond-laser-structured and stress-induced birefringent regions of sapphire. Opt. Express 18, 8300–8310 (2010).
Morikawa, J., Orie, A., Hikima, Y., Hashimoto, T. & Juodkazis, S. Influence of ordering change on the optical and thermal properties of inflation polyethylene films. Appl. Surf. Sci. 257, 5439–5442 (2011).
Juodkazis, S., Mukai, N., Wakaki, R., Yamaguchi, A. & Misawa, H. Reversible phase transitions in polymer gels induced by radiation forces. Nature 408, 178–181 (2000).
Gemmer, J. & Venkataramania, S. C. Shape transitions in hyperbolic non-Euclidean plates. Soft Matter 9, 8151 (2013).
Wang, X. W., Buividas, R., Funabiki, F., Stoddart, P. R. & Hosono, H. Analysis of defects patterned by femtosecond pulses inside KBr and SiO2 glass. Appl. Phys. A 122, 194–200 (2016).
Born, M. & Wolf, E. Principle of Optics (Pergamon Press Ltd., 1959).
Jones, R. C. A New Calculus for the Treatment of Optical SystemsI. Description and Discussion of the Calculus. J. Opt. Soc. Am. 31, 488–493 (1941).
Shurcliff, W. A. Polarized Light (Harvard University Press, 1962).
Balčytis, A. et al. Silk: Optical properties over 12.6 octaves THz-IR-Visible-UV range. Materials 10, 356 (2017).
Cruz, D. H., Rousseau, M.-E., West, M. M., Pezolet, M. & Hitchcock, A. P. Quantitative mapping of the orientation of fibroin α-sheets in B. mori cocoon fibers by scanning transmission x-ray microscopy. Biomacromolecules 7, 836–843 (2006).
Acknowledgements
JM acknowledges partial support by a JSPS Kahenki Grant No. 16K06768, and No. 18H04506. A part of this work was carried out under the Cooperative Research Project Program of the Research Institute of Electronics, Shizuoka University. SJ is grateful for sabbatical stay supported by the Tokyo Institute of Technology and Shizuoka University. This method of birefringence measurement was developed in conjunction with the proposal M13416 of the Australian synchrotron.
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J.M. and S.J. come up with the idea of experiments, R.H. developed numerical analysis, wrote the program for image acquisition, and carried out experiments together with M.R.; J.L.L. and V.M. made birefringent samples for testing. All the authors participated in discussion and analysis of the results and contributed to editing of the manuscript.
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Honda, R., Ryu, M., Li, JL. et al. Simple multi-wavelength imaging of birefringence:case study of silk. Sci Rep 8, 17652 (2018). https://doi.org/10.1038/s41598-018-36114-8
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DOI: https://doi.org/10.1038/s41598-018-36114-8
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