| Literature DB >> 31537802 |
Chao He1, Jintao Chang2,3, Qi Hu4, Jingyu Wang4, Jacopo Antonello4, Honghui He3, Shaoxiong Liu5, Jianyu Lin6, Ben Dai7, Daniel S Elson6, Peng Xi8, Hui Ma2,3, Martin J Booth9.
Abstract
Graded index (GRIN) lenses are commonly used for compact imaging systems. It is not widely appreciated that the ion-exchange process that creates the rotationally symmetric GRIN lens index profile also causes a symmetric birefringence variation. This property is usually considered a nuisance, such that manufacturing processes are optimized to keep it to a minimum. Here, rather than avoiding this birefringence, we understand and harness it by using GRIN lenses in cascade with other optical components to enable extra functionality in commonplace GRIN lens systems. We show how birefringence in the GRIN cascades can generate vector vortex beams and foci, and how it can be used advantageously to improve axial resolution. Through using the birefringence for analysis, we show that the GRIN cascades form the basis of a new single-shot Müller matrix polarimeter with potential for endoscopic label-free cancer diagnostics. The versatility of these cascades opens up new technological directions.Entities:
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Year: 2019 PMID: 31537802 PMCID: PMC6753074 DOI: 10.1038/s41467-019-12286-3
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919
Fig. 1GRIN lens properties and GRIN lens cascade. a Commercial GRIN lenses. b Schematic of the GRIN lens ray trace. c The birefringence and refractive index profile of a GRIN lens over its cross-section. d The fast axis/slow axis distribution of the local retardation across the GRIN lens. e The GRIN lens cascade. This cascade consists of the combination of one or more GRIN lenses along with various devices including interstitial components—such as P: polarizer; QWP: quarter waveplate; HWP: half waveplate; SHWP: spatially variant half waveplate; FQWP: four quadrant quarter waveplate array with four different fast axis orientations, and so on
Fig. 2VVBs generation through GRIN lens cascades. a (i) Schematic of a single GRIN lens cascade with (ii) right-hand circular input, output polarization fields for both simulation and experimental results (the red side of the colour scale indicates right-hand circular, whereas blue corresponds to left-hand circular). Note that before the GRIN lens cascade, there is a polarization state generator (PSG) to generate a chosen arbitrary polarization state; following the GRIN lens is a polarization state analyser (PSA) that enables Stokes vector measurement (see methods in Supplementary Note 3). Except in (iii) the PSG and PSA parts are omitted for clarity. (iii) An illustration for schematic in a with right-hand circular input and left hand circular analysis. The two spirals in the interferogram (iv) and the phase profile (v) indicated that the light beam contained two units of OAM. b–g show higher-order GRIN lens cascades and their generated light fields under specific inputs. In e–g the red-coloured GRIN lens indicate another GRIN type with a larger magnitude retardance profile almost equivalent to a sequence of three of the first (orange) type of lens (for details see Supplementary Note 4)
Fig. 3PSF modulation through GRIN lens cascade. a Schematic of a single GRIN lens cascade illuminated by right-hand circular polarized light, beam profile after the GRIN lens, and the corresponding axial PSF including the FWHM. b, c show the GRIN lens cascade including SHWP with horizontal and vertical linear polarized light input, beam profile after the GRIN lens, and the corresponding axial PSF to demonstrate the focus shift when using the radial/azimuthal polarization input light fields
Fig. 4Characterization of the GRIN lens-based MM polarimeter and measurement of tissue samples. a Simplified setup of the polarimeter. PSG: P1, polarizer; FQWP, four-quadrant quarter waveplate, with different fast axis orientations in each quadrant. PSA: P2, polarizer; HWP, half waveplate. b (i) and (ii) details of FQWP and the Poincaré sphere showing the SOPs generated by the PSG. c (i) The GRIN lens cascade in the PSA besides the P2. (ii) and (iii) Simulation and experimental results of retardance and the fast axis orientation of (i), derived by the MMPD method. d Demonstration of the samples H1 and C1 (unstained samples and their H–E-stained counterparts), sketches with corresponding random sampling points (see methods in Supplementary Note 10) and examples of retardance distributions measured by the MM microscope (as ground truth). Scale bar: 50 μm. e Statistic histogram (mean value and the standard deviation of the retardance) of the 10 points from each sample within the same region, measured by the GRIN lens cascade and a conventional MM microscope. Standard deviations are shown via the dashed lines. Numbers refer to Supplementary Table 1. Source data are provided as a Source Data file. f Overall data distribution (retardance value). The overall number of samples was 20 (half cancerous vs. half healthy, giving 10 testing points per sample). Note that blue (ball or histogram) represents healthy samples, while red represents cancerous samples