The present disclosure relates generally to imaging apparatus, and in particular to bijective illumination collection ellipsometry (BICE) apparatus and method for high-resolution imaging and polarimetry.
Lenses have been widely used in fields of imaging. Generally, a converging lens is associated with a focal point defined along an optical axis of the lens, which determines the position of a light sensor or light detector (denoted “focused sensor position”, which defines an image plane) for capturing a focused or clear image of an object at a certain distance (denoted “focused object position” hereinafter). Examples of light sensors may be eyes, photosensitive materials such as camera films, photoelectrical sensors, and the like.
The captured image would be blurred if the light sensor is offset from the focused sensor position or the object is offset from the focused object position. In prior art, the depth-of-focus (DOF) of a lens refers to a range about the focused sensor position (which may be characterized by a corresponding range about the focal point) within which the captured image may be blurred (when the light sensor is offset from the focused sensor position) but within an acceptable extent and still providing an acceptable sharpness (for example, blurred but perceptually clear). An extended depth-of-focus (EDOF) allows the object to be positioned within an extended object range about the focused object position while still obtaining an acceptable image.
High-resolution microscopic imaging of tissue microstructures is instrumental to biology and enables numerous clinical applications. Microscopic imaging in three dimensions enables numerous biological and clinical applications. However, high-resolution optical imaging preserved in a relatively large depth range is hampered by the rapid spread of tightly confined light due to diffraction. As known in the art, optical microscopy using tightly focused light cannot be maintained in a relatively large depth range due to rapid spread of light dictated by diffraction. Imaging modalities such as confocal (see Reference 1) and two-photon (see Reference 2) microscopies achieve high-resolution imaging only from a narrow region around a focal point. Thus, additional scanning mechanisms are necessary to axially translate the focal point with respect to the target for depth-resolved imaging (see Reference 3). This impedes rapid imaging and the imaging depth, often limited to a few hundred microns (see Reference 4), is inadequate for many applications.
Using coherence gating, optical coherence tomography (OCT) captures real-time depth-resolved images of structures millimeters deep into the scattering tissue (see References 5-9). Though addressing axial resolution, OCT is still challenged by the competing lateral resolution and depth-of-focus due to diffraction that impedes high-resolution imaging in three-dimensions in a large depth range (see References 10-12).
The central question is how light intensity should be distributed to obtain high-resolution imaging in three-dimensions within a large depth range. Focusing light on a single depth point, widely used in the existing imaging systems, yields arbitrary primacy to that point which is inconsistent with the goal of depth imaging. Alternatively, more equitable distribution of the optical intensity along the axial direction inevitably compromises lateral resolution due to diffraction.
Ellipsometry is the measurement of optical polarization-altering properties of a substance or a system (see Reference 60). An optically linear substance or system may be characterized by a 4×4 Mueller matrix (M) which transforms incident light with a Stokes vector Sin to (reflected, transmitted, or scattered) light with a Stokes vector Sout (Sout=M×Sin). If the substance or system does not depolarize light, a 2×2 Jones matrix (J) may provide a complete description of the polarization-altering properties of the substance or the system. Determination of M and J requires at least four and three measurements, respectively.
Traditionally, ellipsometry has been conducted by recording multiple measurements and post-processing of the measured values. However, this method is slow due to sequential nature of the measurements. Real-time imaging of biological substance or tissue in vivo calls for a fast method for ellipsometry. Rotating-compensator ellipsometry (see Reference 61) has been reported for fast ellipsometry, however, in principle, it still is a sequential method and involves moving parts which complicates the design.
According to one aspect of this disclosure, there is provided a lens comprising: an optical center and an optical axis passing through the optical center; and one or more lens portions; the one or more lens portions comprise at least a first lens portion for refracting light rays of a predefined polarization state impinging at right angle thereto from a first side towards the optical axis on a second side at a constant bending angle thereby defining a focal line on the second side along the optical axis.
In some embodiments, the at least first lens portion is positioned at a distance away from the optical center.
In some embodiments, the at least first lens portion comprises the first lens portion and a second lens portion; centers of the first and second lens portions are on diagonally opposite sides of the optical center; and the first and second lens portions are configured for passing therethrough the light rays of orthogonal polarization states.
In some embodiments, the one or more lens portions further comprise: at least a third lens portion for refracting light rays impinging at the constant bending angle thereto from the focal line on the second side to the first side at a direction parallel to the optical axis.
In some embodiments, the at least a third lens portion comprises the third lens portion and a fourth lens portion; centers of the third and fourth lens portions are on diagonally opposite sides of the optical center; and the third and fourth lens portions are configured for passing therethrough the light rays of orthogonal polarization states.
In some embodiments, for a two-dimensional (2D) coordinate system defined on the lens with the origin thereof at the optical center, each of the one or more lens portions is positioned in a respective quadrant of the 2D coordinate system.
In some embodiments, centers of each circumferentially neighboring pair of the one or more lens portions are at right angle with respect to the optical center.
In some embodiments, the bending angle is 21°.
In some embodiments, each of the one or more lens portions has a circular shape.
In some embodiments, each of the one or more lens portions has a diameter of 1.1 millimeters (mm).
In some embodiments, each of the one or more lens portions comprises a metasurface coupled to a substrate.
In some embodiments, each metasurface comprises a plurality of nano-pillars in a pattern of arcs, said arcs being portions of a plurality of concentric circles centered at the optical center. In some embodiments, the plurality of nano-pillars have cubical shapes with square cross-sections; and the plurality of nano-pillars have a same height and varying widths.
In some embodiments, the widths of the plurality of nano-pillars are between 80 nanometers (nm) and 300 nm.
In some embodiments, the height of the plurality of nano-pillars is 750 nm.
In some embodiments, the neighboring pair of plurality of nano-pillars have a center-to-center distance of 370 nm.
In some embodiments, the lens further comprises an axicon with the vertex thereof being the optical center; and the one or more lens portions are defined on the axicon.
In some embodiments, the lens is opaque except at the one or more lens portions.
According to one aspect of this disclosure, there is provided an imaging apparatus comprising: a polarizing beam splitter for splitting a light ray into a first polarized light ray and a second polarized light ray of orthogonal polarization states; a beam conditioning module for receiving the first and second polarized light rays and outputting the first and second polarized light rays to the lens of any one of claims 1 to 17; and an adjustment module for introducing time delay to and/or for adjusting frequency of at least one of the first and second polarized light rays before the first and second polarized light rays are input into the beam conditioning module.
In some embodiments, the lens is the above-described lens; the beam conditioning module comprises: a main knife-edge prism, a first knife-edge prism for direction the first polarized light ray towards the main knife-edge prism, and a second knife-edge prism for direction the second polarized light ray towards the main knife-edge prism; and the main knife-edge prism is configured for: outputting the first and second polarized light rays towards a lens, receiving a third light ray and a fourth light ray from the lens, directing the third light ray towards the first knife-edge prism, and directing the fourth light ray towards the second knife-edge prism.
According to one aspect of this disclosure, there is provided a method of fabricating the above-described lens, the method comprising: depositing an amorphous silicon (a-Si) layer is on the substrate using a plasma-enhanced chemical vapor deposition; coating a layer of negative tone photoresist on the a-Si layer; using electron beam lithography (EBL) to create an etching pattern on the layer of negative tone photoresist; and using deep reactive ion etching to generate a-Si nano-pillars for forming the metasurfaces of the one or more lens portions.
In some embodiments, the etching pattern corresponds to the pattern of arcs.
In some embodiments, the etching pattern corresponds to the plurality of concentric circles. In some embodiments, the method further comprises: masking the one or more unusable areas to opaque.
According to one aspect of this disclosure, there is provided a method of using the lens of claim 5 or any one of claims 6 to 17, the method comprising at least one of: aiming a first light beam to the first lens portion; and collecting a third light beam and a fourth light beam from the third lens portion and the fourth lens portion, respectively; the first light beam has a cross-sectional size matching a size of the first lens portion.
According to one aspect of this disclosure, there is provided a lens comprising: an optical center and an optical axis passing through the optical center; and a plurality of lens portions comprising a first lens portion and a second lens portion on diagonally opposite first and second quadrants of a plane perpendicular to the optical axis for refracting light rays from a first side to a second side, and a third lens portion on a third quadrant of the plane for refracting light rays from the second side to the first side; the first and second lens portions are configured for refracting light rays impinging at right angle thereto from the first side towards the optical axis on the second side at a constant bending angle thereby defining a focal line on the second side along the optical axis, and the third lens portion is configured for refracting light rays impinging from the focal line on the second side at the constant bending angle thereto to the first side parallel to the optical axis; or the third lens portion is configured for refracting light rays impinging at right angle thereto from the second side towards the optical axis on the first side at the constant bending angle thereby defining the focal line on the first side along the optical axis, and the first and second lens portions are configured for refracting light rays impinging from the focal line on the first side at the constant bending angle thereto to the second side parallel to the optical axis.
In some embodiments, the plurality of lens portions are away from the optical center.
In some embodiments, centers of the first and third lens portions or the centers of the second and third lens portions are at right angle with respect to the optical center.
In some embodiments, the plurality of lens portions further comprises: a fourth lens portion on a fourth quadrant of the plane for refracting light rays impinging from the focal line on the second side at the constant bending angle thereto to the first side parallel to the optical axis; or for refracting light rays impinging at right angle thereto from the second side towards the optical axis on the first side at the constant bending angle thereby towards the focal line on the first side.
In some embodiments, the bending angle is 21°.
In some embodiments, each of the one or more lens portions has a circular shape.
In some embodiments, each of the one or more lens portions has a diameter of 1.1 mm.
In some embodiments, each of the one or more lens portions comprises a metasurface coupled to a substrate.
In some embodiments, each metasurface comprises a plurality of nano-pillars in a pattern of arcs, said arcs being portions of a plurality of concentric circles centered at the optical center.
In some embodiments, the plurality of nano-pillars have cubical shapes with square cross-sections; and the plurality of nano-pillars have a same height and varying widths.
In some embodiments, the widths of the plurality of nano-pillars are between 80 nm and 300 nm.
In some embodiments, the height of the plurality of nano-pillars is 750 nm.
In some embodiments, the neighboring pair of plurality of nano-pillars have a center-to-center distance of 370 nm.
In some embodiments, the lens comprises an axicon with the vertex thereof being the optical center; and the one or more lens portions are defined on the axicon.
In some embodiments, the lens is opaque except at the one or more lens portions.
Embodiments disclosed herein relate to a bijective illumination collection imaging (BICI) apparatus and method for high-resolution imaging in three dimensions within a relatively large depth range.
According to one aspect of this disclosure, there is provided a lens having a focal line defined along an optical axis of the lens. Light rays impinging various positions of the lens at an angle parallel to the optical axis are converged by the lens to various positions within the focal line. Therefore, such a lens with a focal line provides an improved depth-of-focus (DOF) such that a light sensor positioned anywhere within the improved DOF thereof may capture clear images (that is, images of high resolution). In comparison, images captured using conventional extended depth-of-focus (EDOF) technologies may still be blurred or with reduced resolution.
According to one aspect of this disclosure, high-resolution imaging is achieved through a particular disposition of illumination and collection paths that allows a one-to-one spatial correspondence (bijection) between the illumination and collection light defined along a focal line, thereby liberating optical imaging from the restrictions imposed by diffraction. The impact on imaging is demonstrated by applying BICI to overcome the limitations in high-resolution optical coherence tomography (OCT).
The boundaries of lateral resolution and depth-of-focus are coupled by diffraction. There exists a class of so-called diffraction-free (see References 18-23) solutions to the Helmholtz equation. However, these modes in their exact mathematical forms have spatially unbounded profiles (plane waves are a trivial example) and give rise to side-lobes that carry a significant portion of the optical power (even in their physical realizations limited by a finite aperture). When used for imaging, the out-of-focus scattering from the side-lobes compromises imaging resolution and sensitivity.
Revisiting lateral resolution and depth-of-focus in the context of imaging point spread function (PSF) provides opportunities to evade the restrictions imposed by diffraction. The PSF at any point is the product of the probabilities of photons illuminating (Pin) and collected from (Pcoll) that point: PSF=Pill×Pcoll (see References 24-25). Based on this notion, it is possible to decouple lateral resolution from depth-of-focus using uniquely crafted illumination and collection paths. Herein, the illumination path refers to the path of light rays impinging on an object from a light emitting source, and the collection path refers to the path of light rays scattered from or otherwise originated from the object.
In some embodiments, metasurfaces (see References 13-17) with the ability to impart tailored phases are used to realize the illumination and collection paths required for the implementation of BICI. In some embodiments, a lateral resolution of about 3.2 micrometers (μm) is maintained nearly intact over 1.25 mm imaging depth with no additional acquisition or computation burden, giving rise to about 12-fold larger imaging depth-of-focus compared to that obtained using an ideal Gaussian beam with the same lateral resolution. Imaging swine tracheobronchial tissue specimens indicates the BICI's prospect for high-resolution imaging preserved within a large depth range. The method disclosed herein may be adapted across various existing imaging modalities.
Turning now to
As shown in
Each of the illumination and collection lens portions 102 and 104 are positioned at a distance away from the optical axis. More specifically, for the two-dimensional (2D) x-y coordinate system, the illumination and collection lens portions 102 and 104 are positioned in neighboring quadrants of the x-y plane and symmetric about one of the axes such as the x-axis on the BICI lens 100, such that the center 112 of each of the illumination or collection lens portions 102 and 104 with respect to the optical center 108 is at φ=45° to the x-axis. In other words, the centers 112 of the illumination and collection lens portions 102 and 104 are at 900 with respect to the optical center 108. For the purpose of noise reduction, it is preferable that, except the illumination and collection lens portions 102 and 104, the other area of the BICI lens 100 (denoted in
In these embodiments, each lens portion 102, 104 comprises a metasurface formed by arrays of nanoscale, subwavelength-spaced optical elements (denoted “nano-pillars”) as shown in
As shown in
The light-ray-bending angle β is constant with respect to r and θ. Therefore, as shown in
As the collection metasurface 104 has a flip profile of the illumination metasurface 102 with respect to the x-axis, the illumination metasurface 102 has similar optical characteristics as the illumination metasurface 102. As shown in
Although light beams 132 and 142 with any suitable cross-sectional sizes may be used, the light beams 132 and 142 preferably have the same size as that of the illumination and collection lens portions 102 and 104 for best optical efficiency. Therefore, the size of the illumination or collection lens portion 102 or 104 is also denoted as the beam size hereinafter.
As an example,
Remarkably, the BICI lens 100 yields invariant lateral resolution (determined by P) along the focal line 134. The lateral resolution is dictated solely by the bending angle β (regardless of the beam size) based on wave analyses using a Fresnel-Kirchhoff integral (see Reference 26). Depth-of-focus or the focal line 134, however, depends on both the bending angle β and the beam size according to the simple geometry shown in
Thus, the desired depth-of-focus and the bending angle β (set from the desired resolution) yield the beam size such as the radius R thereof. In some embodiments, the calculation shown in
The BICI lens 100 establishes a one-to-one correspondence or a bijective relationship defined exclusively on the focal line 134 between the points illuminated and points from which light is collected, eliminating out-of-focus signals and back-reflection signals. The separated illumination path 132-132′ and collection path 142-142′ ensure that the illumination beam for illuminating points on the focal line 134 and the collection beam collected from the illuminated points on the focal line 134 do not overlap.
As described above, the illumination and collection lens portions 102 and 104 may comprise metasurfaces. The distribution and geometry of pillars on metasurfaces are engineered to realize the illumination and collection beams in BICI. Based on the generalized Snell's law (see Reference 13), the phase Φ required to bend ray sheets (as defined in
where, in some embodiments, λd=1300 nm is the design wavelength, for example, corresponding to the center wavelength of an OCT source. Referring to
For example, in some embodiments, the a-Si nano-pillars have the same height of H=750 nm. The a-Si nano-pillars may have square cross-sections with the widths S (which determines the base sizes thereof) between 80 nm and 300 nm which may provide a full phase range [0-2π] with high transmittance (greater than 78%) at the wavelength of 1300 nm. The a-Si nano-pillars are distributed in a lattice pattern of P=370 nm unit cells 166 (that is, the center-to-center distance between neighboring a-Si nano-pillars is P=370 nm).
Also shown in
Nano-pillars of varying base sizes across the lattice impart the required local phase. Owing to its high refractive index and low absorption in the near infrared range (see References 29-31), a-Si is a suitable material to achieve efficient metasurfaces (greater than 70% of the incident power concentrated on the focal line 134) for this application. Metasurfaces may be fabricated on a glass substrate using electron beam lithography.
In particular, the metasurfaces of the illumination and collection lens portions 102 and 104 may be fabricated using a top-down lithography technique (see References 30 and 32). An a-Si layer (for example, a 750 nm thick a-Si layer) is deposited on a glass substrate using the plasma-enhanced chemical vapor deposition. Negative tone photoresist (Micro resist technology, ma-N 2403) is then coated on the a-Si layer and Electron beam lithography (EBL) is used to create the intended pattern, such as the pattern of the illumination and collection lens portions 102 and 104 shown in
Indispensable to high-resolution imaging, the BICI lens 100 rejects out-of-focus signals using the uniquely crafted illumination and collection paths 132-132′ and 142-142′ without compromising the depth range. Thus, the BICI lens 100 provides high lateral resolution within a large depth range. Moreover, the BICI lens 100 may capture the image of the entire depth range due to the focal line 134 created by the illumination and detection beams.
On the other hand, in the existing high-resolution imaging systems, the effect of out-of-focus signals is typically lessened using tightly focused light to comparatively increase the signal from the focal point (using a confocal geometry or nonlinear effects at the focal point). This approach inevitably limits the depth range due to severe diffraction of tightly focused light.
Unless rectified using special techniques (see References 33 to 37), metasurfaces often exhibit strong chromatic dispersion. Application of BICI to OCT operating at a broad wavelength range (1240 nm to 1350 nm) entails resolution of issues associated with chromatic dispersion. The bending angle β imparted to the ray paths (see
To demonstrate the impact on imaging, a BICI lens 100 is used in a Fourier-domain OCT system in the near infrared range. The illumination/collection beam has a wavelength λ=1300 nanometers (nm)±50 nm with a Gaussian distribution (350 μm 1/e2 intensity fall-off radius). The illumination and collection lens portions 102 and 104 are centered at (x, y)=(550 μm, 550 μm) and (x, y)=(550 μm, +550 μm), respectively, according to the coordinates defined in
Wave analyses using a Fresnel-Kirchhoff integral (see Reference 26) were performed to engineer the imaging PSF needed for the intended resolution and depth-of-focus. Design parameters are selected to achieve microscopic resolution imaging in a relatively large depth range (greater than one (1) mm) beyond which scattering becomes the dominant limitation. Given the design parameters (collimated beam size about 1.1 mm; 1=21°), wave analyses yield a sharp PSF of 3.2 μm full-width at half maximum (FWHM) and a relatively large axial range of 1.25 mm depth-of-focus (defined as 1/e2 PSF intensity fall-off in the axial direction) with negligible contributions from out-of-focus signals, as shown in
In particular,
A target 216 such as a sample is axially positioned to overlap the focal line 134 which reflects the illumination beam 132′. The reflected light forms the collection beam 142′ towards the collection lens portion 104 of the BICI lens 100. The collection lens portion 104 refracts the collection beam 142′, and the refracted collection beam 142 is injected to the receiving lens assembly 218. The receiving lens assembly 218 passes the received light through a receiving light path 222 and combined with the first-path light 206. The combined light 224 is injected into the light detector 212.
The intensity profiles of the illumination and collection beams 132 and 142 were measured. The measured illumination (see
The BICI lens 100 was characterized in terms of lateral resolution and depth-of-focus through imaging a resolution target made of a subwavelength gold line (200 nm width and 50 nm height) fabricated on a glass substrate. The BICI lens 100 was coupled to an in-house Fourier-domain OCT system. As illustrated in
There are also techniques in which mathematically optimized phase profiles are imparted using freeform metasurfaces to obtain maximum depth-of-focus (see References 40 to 43). Although these techniques can somewhat alleviate the issue through a modest increase in depth-of-focus (about 1.5 time to 2 times), they cannot be considered as a strategy to radically overhaul the limitations in the maintenance of high-resolution imaging across a relatively large depth range.
The BICI lens 100 entails no additional processing (see Reference 44) or acquisition (see Reference 10) burden and may be implemented across various wavelength ranges as its working principles remain unaltered with a wavelength change. For instance, the BICI lens 100 may be implemented in broadband OCT systems operating at shorter wavelengths with improved axial resolution. The wavelength range described herein is chosen to avoid increased scattering at shorter wavelengths that predominantly limits the imaging depth (see References 10, 45, and 46).
Various configurations of illumination and collection beams were previously reported in OCT (for speckle-reduction (see References 47 and 48) and deep tissue imaging (see Reference 49)), in two-photon microscopy (for enhanced signal-to-background ratio (see References 50 to 52)), in theta confocal (see References 25 and 53), 4pi (see Reference 54), and light sheet (see Reference 55) microscopy (for improved resolution), and dark-field microscopy (see Reference 56) (for enhanced sensitivity). These systems are designed to capture signals from a region neighboring a single focal point. Aa a result, imaging within a modest depth range entails either using very small (see References 47 to 49) (compromising lateral resolution) or physical translation of the target with respect to the imaging system (see Reference 25, and 50 to 56) (compromising imaging speed).
Sensibly, the optical arrangement for depth imaging with preserved lateral resolution should 1) focus light equitably along the depth range (on a focal line), and 2) reject out-of-focus signals originating from the points outside the focal line. Unlike the previous works, the optical arrangement of the BICI lens 100 meets both criteria, enabling imaging relatively large depth range along which the lateral resolution is maintained.
OCT, being a coherence imaging technique, comprises of speckles which are carriers of information and, at the same time, a source of noise (see Reference 57). The signal-degrading speckles are due mainly to the effects of multiple backscatters, while the signal-carrying speckles are the result of the single back-scattered component whose spatial frequency content extends to the diffraction limit of the imaging optics (see Reference 57). Scaling up proportionally to the spot size, the signal-carrying speckles originate from the focal zone and the signal-degrading speckle is created by out-of-focus light scattered multiple times. BICI lens 100 suffers considerably less from the effects of speckles due to: 1) its higher lateral resolution maintained along the depth range, resulting in notably smaller speckle sizes, 2) the ability to eliminate out-of-focus signal and, in turn, the effects of multiple scattering, and 3) the ability to reject back-reflection from imaging optics.
Pathological changes at early stages of diseases like cancers are often very subtle and can be easily overlooked. In vivo high-resolution imaging maintained in a large depth range has the potential to enable early and accurate detection and diagnosis. Being implemented using metasurfaces, the BICI lens 100 may be feasibly miniaturized into endoscopic devices (see References 58 and 59) for in vivo high-resolution imaging of internal organs.
The advent of high-resolution optical imaging techniques has impacted fundamental medical research as well as clinical applications. Expanding the scope of applications, however, necessitates overcoming major limitations in the current techniques. The diffraction-imposed trade-off between lateral resolution and depth-of-focus is circumvented through bijective illumination collection imaging, enabling high-resolution imaging in three dimensions. While the BICI metasurface lens 100 is applied to OCT in this disclosure, the underlying concept is general and the BICI metasurface lens 100 may be adapted across various imaging modalities such as confocal and two-photon microscopy.
Those skilled in the art will appreciate that various alternative embodiments are readily available. For example, although the metasurfaces in above embodiments comprise square nano-pillars 162, in various embodiments, the metasurfaces may comprise other suitable nano-structures such as nano-pillars with circular or elliptical cross-section.
In above embodiments, the arcs 110 or circles 114 are concentric (see
Although the illumination and collection lens portions 102 and 104 in above embodiments have circular shapes of a same size. In alternative embodiments, the illumination and collection lens portions 102 and 104 may have any suitable shapes and sizes.
In some embodiments, the area 106 of the BICI lens 100 may be transparent or semi-transparent, but are prohibited or otherwise disallowed for use.
In above embodiments, the centers 112 of the illumination and collection lens portions 102 and 104 are at φ=90° with respect to the optical center 108. In some embodiments as shown in
In above embodiments, the illumination and collection lens portions 102 and 104 are in adjacent quadrants with respect to the optical center 108, thereby allowing the illumination and collection paths to extending to the diagonally opposite quadrants, respectively, and ensuring that the illumination and collection paths do not overlap except on the focal line 134.
In some alternative embodiments as shown in
In some embodiments wherein the BICI lens 100 comprises three lens portions (similar to those shown in
In some embodiments wherein the BICI lens 100 comprises three lens portions (similar to those shown in
The arrangement of the illumination and collection beams in BICI necessitates using a higher bending angle (β) to achieve resolution equivalent to that obtained by imaging a focal point with an ideal diffraction-limited lens (with an NA matching the bending angle β). However, this can be rectified in some embodiments using a BICI lens 100 having two illumination and two collection lens portions 102 and 104. As shown in
In these embodiments, the two illumination paths overlap outside the focal line 134, and the two collection paths also overlap outside the focal line 134. However, the collection paths do not overlap with the illumination paths.
The BICI lens 100 in these embodiments maintains the required bijective relationship with improved resolution.
In some embodiments wherein the BICI lens 100 comprises four lens portions (similar to that shown in
In some embodiments, the BICI lens 100 may be manufactured by fabricating a lens 100′ having a metasurface with a pattern of a plurality of concentric circles 114 centered at the optical center 108, as shown in
In some embodiments, the illumination and collection lens portions 102 and 104 may be first fabricated and then embedded or otherwise coupled to the BICI lens 100.
As shown in
In some embodiments, some of the illumination and collection lens portions 102 and 104 may not be symmetric.
In above embodiments, the BICI lens 100 is shown as having a circular shape. In some embodiments, the BICI lens 100 may have any suitable shape such as a square shape as shown in
In above embodiments, the optical center 108 of the BICI lens 100 is also the centroid thereof. In some embodiments such as the embodiment shown in
In above embodiments as shown in
Those skilled in the art will appreciate that the illumination and/or collection lens portions 102 and 104 may be implemented using other suitable optical structures. For example, in some embodiments, the illumination and/or collection lens portions 102 and 104 and the linear phase profile in Equation (1) may be implemented using an axicon which is a lens having a conical surface.
As shown in
The BICI lens implemented using axicon may not provide the same advantage as the BICI lens using metasurface. For example, the BICI lens using axicon may have shorter depth-of-focus than the BICI lens using metasurface for the same lateral resolution. As the resolution achieved by the BICI lens is predominantly determined by the bending angle β, given the desired resolution, one may exactly realize the required bending angle using metasurfaces. On the other hand, it may be more difficult to design a BICI lens using axicon to achieve the same bending angle β and subsequently the same resolution. Moreover, the BICI lens using axicon may be more difficult to accomplish a wide range of performances and achieve miniaturization for endoscopic applications.
In above embodiments, the BICI lens 100 comprises one or more illumination lens portions 102 and one or more collection lens portions 104 offset from the optical axis, wherein the illumination and collection lens portions 102 and 104 form a focal line 134 along the optical axis. In some embodiments, the illumination and collection lens portions 102 and 104 may be conventional lenses which, although not forming the focal line 134, have sufficient depth-of-focus (while the lateral resolution thereof may be degraded compared to the illumination and collection lens portions 102 and 104 described above). With the space-separated illumination and collection paths, the BICI lens in these embodiments may still provide superior performance than conventional lens.
In above embodiments, the BICI lens 100 comprises one or more illumination lens portions 102 and one or more collection lens portions 104 offset from the optical axis. In some embodiments, the BICI lens 100 may only comprise one or more illumination lens portion 102 offset from the optical axis. In these embodiments, light collection and imaging of the samples or target objects may be conducted using other suitable means.
In some embodiments, the BICI lens 100 may only comprise one or more collection lens portion 104 offset from the optical axis. In these embodiments, illumination of samples or target objects may be conducted using other suitable means.
In some embodiments as shown in
In these embodiments, focal points such as the focal points 402 to 412 along the focal line 134 are mapped into the arcs 422 to 432 and subsequently mapped into various pixels 442 to 452 of a light detector 462 such as a camera with a line light-sensor (that is, a light sensor having a plurality of light-detection pixels arrange in a line). This is achieved when the phase of the collection lens portion 104 is engineered to map the focal line 134 onto the pixels of the light detector 462. Such a BICI lens 100 may resolve the depth information independent of OCT.
In above embodiments, the illumination and collection lens portions 102 and 104 are the usable areas for illuminating and imaging purposes and the other area of the BICI lens 100 (for example the area 106 shown in
Each of the illumination and collection lens portions 102 and 104 are positioned at a distance away from the optical axis. The two illumination lens portions 102 are located in two diagonally opposite quadrants (or the two diagonally opposite sides of the optical center 108) and symmetric with respect to the optical center 108. The two collection lens portions 104 are located in the other two diagonally opposite quadrants (or the other two diagonally opposite sides of the optical center 108) and symmetric with respect to the optical center 108. The illumination and collection lens portions 102 and 104 are symmetric about respective axes.
The illumination and collection lens portions 102 and 104 are generally the same as those described above (also see Reference 62). More specifically, the illumination and collection lens portions 102 and 104 are generally focused within a continuous focal line 134 along the optical axis (that is, the z-axis), thereby ensuring high-resolution imaging along the entire depth range. As described above, this requires all incident rays whose projections on the lens 102 or 104 have the same distance to the optical axis to be bent with the same angle towards the optical axis.
In these embodiments, the meta-surfaces of the two illumination lens portions 102 are used for illuminating the substance with light rays of two orthogonal polarization states, and the meta-surfaces of the two collection lens portions 104 are used for collecting light rays of the two orthogonal polarization states from the substance.
Each of the illumination and collection lens portions 102 and 104 comprises a metasurface for allowing light rays of a respective polarization state to pass therethrough. In the embodiments shown in
The collection lens portions 104 are designed to collect light rays of LCP and RCP from the substance within the focal line 134, wherein the collected light rays correspond to the excitations or illuminations of the light rays incident from the illumination lens portions 102A and 102B, respectively. For example, as shown in
In some embodiments, the illumination light rays 502 and 504 may be separated or otherwise isolated by time-multiplexing and/or frequency-multiplexing. For example, in one example, the isolation of the illumination light rays 502 and 504 is accomplished by using interferometry when light rays 504 incident on the illumination lens 102B is time-delayed with respect to the light rays 502 incident on the illumination lens 102A. In another example, the incident light rays 502 and 504 on the illumination lens 102A and 102B are modulated at various frequencies as to be isolated from each other, and are demodulated accordingly at the receiving side.
In the example shown in
In the example shown in
In above embodiments, RCP and LCP polarization states are used. The use of RCP and LCP is suitable for ellipsometry of linear birefringent substances.
In other embodiments, other suitable two orthogonal polarization states such may be used. For example, in some embodiments, linear polarization states may be used, for example, for substances with significant optical activities (such as circular birefringence).
In the examples shown in
In the ellipsometry system 600 shown in
The light ray 610 is further split by a polarizing beam splitter 614 into two polarized light rays 616 and 618 of different polarization states. Each of the two polarized light rays 616 and 618 are passed through a respective quarter wave plate (QWP) 620 for obtaining respectively phase-shifted, polarized light rays 622 and 632, respectively. One of the phase-shifted, polarized light rays, such as the phase-shifted, polarized light ray 632, is then guided by, for example, a plurality of reflectors 634 and 636, through an additional propagation path to introducing a time delay. In these embodiments, the introduced additional propagation path may be adjustable for adjusting the introduced time delay of the the phase-shifted, polarized light ray 632.
Then, the phase-shifted, polarized light rays 622 and 632 (wherein light ray 632 is also time-delayed) are guided into a beam conditioning module 624, which outputs the illumination light rays 502 and 504 incident into the BICE lens 100 for illuminating the substance within the focal line 134 thereof. The BICE lens 100 collects light reflected and/or refracted from the substance and outputs the collected polarized light rays 512 and 514 as described above, which are guided into the beam conditioning module 624.
The beam conditioning module 624 outputs the polarized light rays 628 and 638 are passed through a respective QWP 646 for phase-shifting. The phase-shifted, polarized light rays 652 and 654 outputted from the QWPs 646 are then guided into polarized beam combiners 656 and 658, respectively.
The light ray 612 outputted from the beam splitter 608 is further split by a polarizing beam splitter 704 into two polarized light rays 706 and 708 of different polarization states. Each of the two polarized light rays 706 and 708 is guided by, for example, a plurality of reflectors 714 and 716 for polarized light ray 706, and a plurality of reflectors 724 and 726 for polarized light ray 708, through a respective additional propagation path to introducing a respective time delay. In these embodiments, the additional propagation paths of the polarized light rays 706 and 708 may be adjustable for adjusting the introduced time delays thereof. Moreover, the time delays introduced into the polarized light rays 632, 706, and 708 may be different.
The time-delayed, polarized light rays 706 and 708 are then guided into the polarized beam combiners 656 and 658, respectively.
The polarized beam combiner 656 combines the light rays 652 and 706, which have the same polarization state, and outputs a combined light ray 802 which is then guided into a light detector 806 (denoted “Detector X” in
The polarized beam combiner 658 combines the light rays 654 and 708, which have the same polarization state (orthogonal to the polarization state of the light rays 652 and 706), and outputs a combined light ray 812 which is then guided into a light detector 816 (denoted “Detector Y” in
As indicated by the arrows 840, the polarized light ray 622 is guided to a reflector 842 such as a mirror which reflects the polarized light ray 622 to a knife-edge prism 844. The knife-edge prism 844 directs the polarized light ray 622 to a main knife-edge prism 846, which outputs the polarized light ray 622 as the illumination light ray 502 for incident to the BICE lens 100.
Similarly, as indicated by the arrows 860, the polarized light ray 632 is guided to a reflector 852 such as a mirror which reflects the polarized light ray 632 to a knife-edge prism 854. The knife-edge prism 854 directs the polarized light ray 632 to the main knife-edge prism 846, which outputs the polarized light ray 632 as the illumination light ray 504 for incident to the BICE lens 100.
As described above, the BICE lens 100 collects light rays from the focal line 134. As indicated by the arrows 880, the collection light ray 512 is guided to the main knife-edge prism 846 of the beam conditioning module 624, which directs the collection light ray 512 (renumbered as 628) to the knife-edge prism 844. The knife-edge prism 844 then directs the collection light ray 628 to the reflector 856, which outputs the collection light ray 628 from the beam conditioning module 624.
Similarly, as indicated by the arrows 890, the collection light ray 514 is guided to the main knife-edge prism 846 of the beam conditioning module 624, which directs the collection light ray 514 (renumbered as 638) to the knife-edge prism 854. The knife-edge prism 854 then directs the collection light ray 638 to the reflector 858, which outputs the collection light ray 638 from the beam conditioning module 624.
The the BICE lens 100 disclosed herein combines the principles of ellipsometry with that of the BICI lens to provide rapid high-resolution ellipsometry in a relatively large depth range.
In some embodiments, the BICE lens 100 may be readily implemented in the endoscopic setting using fiber optic components and gradient-index (GRIN) lenses to collimate the light towards the BICE lens 100 located at the distal end of an endoscope.
Although embodiments have been described above with reference to the accompanying drawings, those of skill in the art will appreciate that variations and modifications may be made without departing from the scope thereof as defined by the appended claims.
The references cited in this disclosure are listed below, the content of each of which is incorporated herein by reference in its entirety.
Observation of parabolic nondiffracting optical fields. Opt. Express 13, 2364-2369 (2005).
This application claims priority to and benefit of U.S. Patent Application No. 63/320,589 filed on Mar. 16, 2022, which is hereby incorporated by reference in its entirety.
Filing Document | Filing Date | Country | Kind |
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PCT/CA2023/050343 | 3/16/2023 | WO |
Number | Date | Country | |
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63320589 | Mar 2022 | US |