Introduction
Liquid crystal (LC) devices, well known by their consumer applications like TVs, monitors and smartphones, are showing in the last two decades a permanent increase in number and relevance of practical applications aside displays. These non-display liquid crystal devices (NDLCD) are extensively studied in many research centers since a remarkable number of new uses are being continuously found.
Regarding their structure, NDLCDs can be roughly classified into two broad groups: those having a large number of pixels (> 105) with constant shape, distributed in a regular matrix, usually driven by active matrix electronics, and those having a moderate number of pixels (say, < 103) with arbitrary shape, usually driven by external drivers on passive matrices.
The most common NDLCD with high pixel number is the Spatial Light Modulator (SLM). It has basically the structure of a display, usually employs multiplexed addressing like displays, and can work either in transmissive or reflective mode (
e.g., liquid crystal on silicon, LCoS) like them. SLMs can be addressed electrically or optically [
1] (EASLM and OASLM). While OASLMs are usually not pixelated, EASLMs can be assimilated, considering their size, to high-resolution projection displays (the terms are often interchanged). The main differences are the lack of polarizers and the maximum induced phase delay, that is usually above 2π in EASLMs and just π in displays.
SLMs have found plenty of applications [
2]. OASLMs can be used for real time object recognition by optical correlation [
3], whereas EASLMs are employed in a plethora of dissimilar systems. To name a few, optical switching [
4] and wavelength selective switches (WSS) [
5] are key in optical communications, while computer-generated holography [
6], adaptive optics [
7], optical Fourier neural systems [
8] or optical computing [
9] are applied to many fields, including hot topics like artificial intelligence [
10].
Nevertheless, SLMs also feature some drawbacks. They are expensive for many consumer photonics applications, have low light efficiency –mostly due to the active-matrix electronics shadowing the pixel area and reducing the fill factor– and may show diffraction and aliasing issues (
Figure 1) when dealing with high resolution patterns [
11]. It should be mentioned that the ring thickness of Fresnel lenses decreases as the distance from the center increases; this is the reason why the aliasing artifacts show up at the edges.
A second group of NDLCDs relies on a low number of pixels, perhaps tens or hundreds, whose shape is precisely designed for the application specs. Moreover, they are usually driven by external electronics, so that the active area is free from spurious shadowing components. Thus, the two main shortcomings of SLMs are avoided in one fell swoop: the fill factor is increased considerably, and aliasing is completely avoided.
These low-resolution passively addressed NDLCDs can be in turn divided into two families: those adapting a periodic linear shape and those having circular shape and often circular symmetry. The devices of the first group usually behave as diffraction gratings,
e.g., POLICRYPS [
12] or sawtooth gratings that can be used as beam steerers [
13]. Circular devices are perhaps the most important group of NDLCDs from the applications side. This group includes axicons [
14], optical vortex generators [
15] and the ample family of tunable lenses.
At present, LC lenses are finding applications in many dissimilar fields, such as vision –eyeglasses [
16], contact lenses [
17], intraocular [
18]–, adaptive optics for astronomy [
19], or wearable devices [
20], besides their traditional applications as tunable lenses for consumer photonics [
21,
22].
Although not included in liquid crystal lenses, it is worth mentioning the recent interest in liquid or optofluidic lenses controlled by magnets [
23] or piezoelectric devices [
24]. They are currently being offered as an alternative for tunable lenses in smartphone objectives [
25].
Low-resolution, passively addressable NDLCDs are also not without their drawbacks. The most relevant refers to the low power achieved by liquid crystals with moderate birefringence. The deviation angles of beam steerers are small, and the power of manufactured lenses and axicons is low.
As shown in the next section, possibly the best way to overcome this obstacle is to employ tunable structures (prisms, lenses) based on Fresnel geometries. Nevertheless, these structures create, in turn, additional problems mainly related to addressing.
In this work a global solution to the addressing problems derived from Fresnel geometries in circular structures such as axicons and lenses is described. The combination of structures with radial and azimuthal birefringence gradients produces devices with a significant increase in crucial characteristics such as diameter, fill factor or power, while maintaining simple addressing geometries. High power, large aperture lenses with nearly 100% fill factor are demonstrated.
The proposed structures are based on two key components: Fresnel structures and elements with variable azimuthal phase delay, which bestow orbital angular momentum (OAM) to the impinging light. OAM generates optical vortices that can be advantageous in certain structures, otherwise they can be removed at a later stage. In order to adequately describe the devices, therefore, it is advisable to previously review these structures and elements.
Polarization-independent devices: Blue Phases
All devices described above are usually based on nematics LCs, and are polarization-dependent, due to the uniaxial structure of the nematic. Polarization-independent devices would be far more useful in many applications; therefore, many designs have been proposed to create such devices: dual orthogonal cells, micropatterned Fresnel lenses or, more recently, birefringent materials index-matched to the LC [
68]. However, the most straightforward strategy to overcome the polarization dependence relies on Blue Phases.
The Blue Phases of cholesteric liquid crystals have recently become a coveted approach for their potential in photonic applications because of their peculiar properties and structure. Blue Phases (BP) appear in chiral LCs that induce a high twisting of the director [
69]. Contrary to other liquid crystal phases, BPs display a highly organized 3D structure with a lattice period in the hundreds of nanometers, which is achieved by the self-assembly of the LC molecules into periodic cubic structures that produce bright selective Bragg reflection in narrow bands.
BPs can be considered 3D photonic crystals as their sub-micrometer cubic structure is optically isotropic by symmetry. Unlike cholesteric liquid crystals, which only present Bragg reflection in one dimension, BPs are periodic in three dimensions, therefore they can produce multiple reflections in different directions [
70,
71]. Furthermore, their electrooptic behavior, with response times in the sub-millisecond range, additionally benefits their potential in photonics [
72].
At different temperature ranges, three BP phases may appear –BPIII, BPII and BPI from isotropic to cholesteric phases–. The photonic crystal structures are found in BPI and BPII, which are self-assembled in an intricate double twist cylinder structure that is organized in characteristic cubic lattices –body-centered (BCC) and simple cubic (SC) respectively [
67].
III.1. Orientation of BPs
Optical devices based on BP liquid crystals usually require, as in other structures, a tightly controlled orientation of the material in the LC cell. Examples of BP crystals observed by polarizing optical microscopy are shown in
Figure 14. Without any surface treatment a typical polycrystalline structure (platelet structure), made of tiny disorganized BP crystals, is obtained (
Figure 14, left). Platelet color is the result of the Bragg reflection from specific lattice planes.
Arranging the BP in the same lattice orientation with the same azimuthal angle is more involved than orienting nematics; still it can be achieved.
Figure 14 center and right images show two BPs; the homogeneous texture and single-colored reflection suggest a single lattice orientation. However, standard manufacturing protocols often yield platelet BPs. Platelets produce high scattering and their electrooptical response, (when compared to monocrystalline BPs) is poorer [
73].
Alignment control of BPs is an actual problem that needs to be successfully overcome to push the use of this advanced material in photonics. Their complex structure makes the lattice orientation control exceptionally challenging and producing large BP monocrystals has shown to be a particularly complex task.
III.1.1. Kossel patterns
Monocrystallinity can be confirmed by Kossel pattern analysis. Kossel patterns are equivalent to Bragg’s X-ray diffraction patterns except that the wavelength is orders of magnitude longer, in the 100’s nm region, corresponding to the lattice period of the cubic structures adopted by BPs (actually original Kossel is an X-ray divergent technique; the name has been kept for patterns in the visible range). Kossel patterns allow identifying the BP phase (I or II), confirming the lattice orientation, its azimuthal angle, and estimating the degree of monocrystallinity, (blurry Kossel patterns suggest there is loss of monocrystallinity in the bulk because the resulting diffracted patterns are an average of the collective lattice orientation changes) [
74].
Kossel patterns obtained for BP mono- and polycrystal are shown in
Figure 15. Note that the polycrystal structure produces a mix of numerous patterns overlapped with each other, while the monocrystals show a unique sharp pattern, confirming the single lattice orientation of the BP crystals – in this case these are BPI (110) and BPI (200) (center and right images respectively).
Controlling the growth of large BP crystals with a particular lattice plane orientation has just been started to be explored. BPs can be produced as monocrystals with a unique lattice orientation by different methods.
III.1.2. Conventional alignment
Conventional polyimide layers usually fail to produce aligned BP monocrystals, influenced by their strong anchoring energy, in the order of
. The alignment can become extremely complex when taking into account the 3D orientation. Besides, when BPI and BPII grow from different phases they can show hysteresis. This suggests that the phase the BP is grown from can also impact on the orientation [
75].
Weak anchoring layers, like Nylon (traditionally used for aligning for ferro- and antiferroelectric smectic liquid crystals), photoalignment, or soft-treated layers can easily decrease anchoring energy one or two orders of magnitude. Fixing a unique lattice orientation is, then, driven by the anchoring energy, where the interfacial free energy supports some lattice orientations and restricts others [
76].
Surface treatments employing Nylon-treated surfaces can produce BP monocrystals in large areas, and be stabilized in temperature, as well. By imposing precise confinement and anchoring, BPs of millimeter size with a uniform lattice orientation can be obtained.
III.1.3. Advanced alignments
Moreover, by adjusting different BP precursor mixture formulations, it is possible to tailor the resulting lattice orientation of a BP crystal as desired, when combined with smart surface treatments with weak anchoring energies. Having a control of both lattice plane orientation and azimuthal orientation results in a unique orientation (
Figure 16) of the 3D crystal. In addition, these methods allow resolving an unidentified lattice orientation of a given BP phase without the need of using Kossel analysis [
77].
Photoalignment treated surfaces are another excellent candidate with weak anchoring energies, with the additional advantage of being able to be patterned by light with precise micro- or submicrometer-sized designs. A predefined pattern, recorded on a photoalignment-treated substrate, can induce the BP crystals to follow the pattern by exploiting field-induced phase transitions [
78].
Large BP cells may show small localized crystalline defects not detected by Kossel analysis. In these cases, monocrystallinity can be demonstrated by direct observation of the bulk. This has been achieved in BPII by observing BP crystals by Transmission Electron Microscopy (TEM), and most recently in BPI (
Figure 16, right) [
79].
Other more sophisticated methods for orienting BPs rely in the design of nano-patterned surfaces. For instance, surfaces prepared by grafting polymer brushes or holography lithography create nanopatterned gratings with periodic homeotropic and planar anchoring regions which direct the lattice orientation of BPs [
80,
81].
III.2. Thermal stabilization
A characteristic drawback of BPs is the extremely short temperature range where a particular phase can be found. Most BP formulations produce BPs that are intrinsically stable over small temperature ranges (usually a few degrees) and, as a consequence, any reasonable application involving BPs will have the need of some sort of stabilization mechanism.
One of the most well-known methods of BP stabilization is polymer-stabilization. A polymer-stabilized BP crystal is a mixture of the LC bearing the BP phase and a small amount of monomer. The mixture is thus mainly composed by a liquid crystalline material. During the polymerization process, the monomers added to the BP mixture are pushed out to the topological disclination lines of the BP cubic structure. Essentially, monomers polymerizing within the disclination lines are functioning, in fact, as a scaffold supporting the whole structure [
82].
Other stabilization methods rely on using an assortment of different kind of doping materials, inserted into the disclination lines, which aid in expanding the temperature ranges where the BP phases are present: using properly functionalized gold nanoparticles, highly stable BPs with adjustable optical properties can be obtained [
83].
To name a few other examples, thermal stabilization is further improved by the inclusion of 0D fullerenes, 1D nanotubes and 2D graphene oxide sheets [
84]. On the other hand, the use of CoPt nanoparticles allows the stabilization of one particular BP phase over the other two [
85].
III.3. Applications of BPs
A quick look into previously reported research immediately reveals the wild variety of possible applications where Blue Phases might be involved, from color changing films to lasing devices. Most devices proposed here can be fabricated with BPs, with the advantage of avoiding polarization dependence of the system. Moreover, there are a number of applications that are specific to BPs.
By taking advantage of the everchanging Bragg reflection properties, it is possible to achieve stretchable BP gels [
86], with a flexible reflection peak or humidity-driven color-changing photonic polymer coatings [
87].
Non-stabilized BPs, while working in the proper temperature ranges, or softly-stabilized BP crystals can be addressed by electric fields, as well. In the electrooptics of BPs there is a relationship between the amplitude of the applied field and the field-induced birefringence. By addressing BPs with electric fields, crystal lattices may deform to orthorhombic or tetragonal crystals by electrostriction [
88,
89].
BPs electrooptic behavior can be described as in crystal optics, by two components: a purely electrooptic effect, with refractive index modulation and a secondary photoelastic effect, with shifting of the Bragg reflection wavelength –they are both the result of molecular reorientation under applied fields.
The refractive index change is influenced by local reorientations of the nematic LC, and with very short pitches, the switching times become extremely short at submillisecond response times. The reflection wavelength shift, though, is the result of the deformation of the BP lattice, to compensate for the increase of elastic energy with applied fields and is a much slower process.
In polymer-stabilized BP crystals, the lattice size is fixed and imposed by the polymeric network embed into the crystal disclination lines. As a result, under applied fields, the secondary Bragg shift effect is suppressed and there is only a fast refractive index modulation, which is ideal for phase modulation applications.
Different approaches to optical applications include polarization independent phase modulation [
71], where under applied voltage, well aligned monocrystalline BPs generate higher phase shifts than platelet BPs.
Several Fresnel lenses based on BP LCs have been proposed [
90]. Tunability can be controlled by adjusting the voltage applied to the edges of the Fresnel zones, while aperture can be enlarged increasing the number of zones of the lens.
In another interesting proposal, a Fresnel lens, made of a BP composite based on thermal-induced phase separation [
91] and a BP microlens array, using progressive masks to produce the gradient distribution of the electric field, has been demonstrated [
92].
By particular photo-patterning of BPII, a tunable polarization volume grating has been manufactured which produces wide angles when compared with cholesteric LC-based gratings, owing to the high symmetry of its cubic structure [
93].
Future BP devices for applications will probably be based on either polymer-stabilized (PS) or nanoparticle (NP)-doped BP LCs. Both show response times in the submillisecond range; the off-voltage state is isotropic, and manufacturing is relatively easy. However, the operating voltage is still high; PS BPs show noticeable hysteresis and optical performance is low, while NP BPs temperature range is still narrow. It has been suggested [
94] the use of nanoparticle-doped PS BPs. Within certain limits, these materials show a wide temperature range, no hysteresis, and no residual birefringence.
There has been an exceptional progress in new devices and applications for Blue Phase photonic crystals just in the last few years. However, there are still many unknowns, especially in the alignment mechanism and targeting of the resulting orientation of the BP crystals. Controlling and understanding the underlying processes of alignment will be crucial to allow the development of this photonic material on any novel application.
Figure 1.
Modelling of SLM aliasing. The SLM has been configured to generate Fresnel lenses of different powers (1x, 2x, 4x) approaching the SLM pixel resolution. White backlight is used, and a polarizer is set so that phase delays develop colors. Aliasing becomes slightly apparent in the second lens and quite noticeable in the third lens.
Figure 1.
Modelling of SLM aliasing. The SLM has been configured to generate Fresnel lenses of different powers (1x, 2x, 4x) approaching the SLM pixel resolution. White backlight is used, and a polarizer is set so that phase delays develop colors. Aliasing becomes slightly apparent in the second lens and quite noticeable in the third lens.
Figure 2.
A glass lens and a liquid crystal GRIN lens are optically equivalent. The LC molecules are partially switched, more tilted at the center and less tilted at the edges. This generates a refractive index gradient that modifies the optical path of the light impinging from the bottom plate. The sequence a, b, c, d shows lenses with increasing power, i.e., thicker glass lenses and more tilted LC lenses.
Figure 2.
A glass lens and a liquid crystal GRIN lens are optically equivalent. The LC molecules are partially switched, more tilted at the center and less tilted at the edges. This generates a refractive index gradient that modifies the optical path of the light impinging from the bottom plate. The sequence a, b, c, d shows lenses with increasing power, i.e., thicker glass lenses and more tilted LC lenses.
Figure 3.
Left, Fresnel lens with constant pitch and different amplitude on the sawtooth. Right, Fresnel lens with constant phase increment in every slice (same sawtooth amplitude) and different pitch. LC Fresnel lenses are usually based on the second model.
Figure 3.
Left, Fresnel lens with constant pitch and different amplitude on the sawtooth. Right, Fresnel lens with constant phase increment in every slice (same sawtooth amplitude) and different pitch. LC Fresnel lenses are usually based on the second model.
Figure 4.
Left, Fresnel lenses with different powers (1x, 2x, 3x) can be generated with the same electrode set, providing the number of electrodes is large enough. Electrodes induce delays in steps that mimic the analog Fresnel curve. Right, an example with 24 electrodes per ring. The yellow stepwise curve shows the position and width of the 24 electrodes on each ring. The brown curve is the Fresnel lens profile, and the blue curve is the actual lens profile without phase wrapping.
Figure 4.
Left, Fresnel lenses with different powers (1x, 2x, 3x) can be generated with the same electrode set, providing the number of electrodes is large enough. Electrodes induce delays in steps that mimic the analog Fresnel curve. Right, an example with 24 electrodes per ring. The yellow stepwise curve shows the position and width of the 24 electrodes on each ring. The brown curve is the Fresnel lens profile, and the blue curve is the actual lens profile without phase wrapping.
Figure 5.
Linear axicons are based on conical surfaces. The output beam focus on a segment rather than a point. The segment is called Depth of Focus. Beyond that, the beam adopts a Bessel ring shape.
Figure 5.
Linear axicons are based on conical surfaces. The output beam focus on a segment rather than a point. The segment is called Depth of Focus. Beyond that, the beam adopts a Bessel ring shape.
Figure 6.
Radial vs. azimuthal optical path gradient. In glass (lenses, mechanical vortex generators) the optical path gradient is achieved by modifying the glass thickness across the section. In LCs, the effective refractive index is modified.
Figure 6.
Radial vs. azimuthal optical path gradient. In glass (lenses, mechanical vortex generators) the optical path gradient is achieved by modifying the glass thickness across the section. In LCs, the effective refractive index is modified.
Figure 7.
Mechanical optical vortex generators (left) are usually continuous. The colors are used as an example of the induced phase shift. If a whole color gamut represents e.g., a 2π delay, the left vortex shown above would have 6π delay, i.e., an l=3 topological charge. Likewise the spiral phase plate (right) has different phase shifts expressed as colors. The phase shift in this case is not continuous, but provided by pixels shaped as pie slices. The higher the number of pie slices, the better, since more topological charges can be achieved.
Figure 7.
Mechanical optical vortex generators (left) are usually continuous. The colors are used as an example of the induced phase shift. If a whole color gamut represents e.g., a 2π delay, the left vortex shown above would have 6π delay, i.e., an l=3 topological charge. Likewise the spiral phase plate (right) has different phase shifts expressed as colors. The phase shift in this case is not continuous, but provided by pixels shaped as pie slices. The higher the number of pie slices, the better, since more topological charges can be achieved.
Figure 8.
A 24 pie slice SPP prototype driven by 24 independent signals. Left, scheme of the DLW maskless planning. Center and right, two configurations of the cell working between crossed polarizers so that different phase delays produce different colors. Center, distributed 2π delay; topological charge l=1. Right, binary configuration (0, π, 0, π …); topological charge l=12.
Figure 8.
A 24 pie slice SPP prototype driven by 24 independent signals. Left, scheme of the DLW maskless planning. Center and right, two configurations of the cell working between crossed polarizers so that different phase delays produce different colors. Center, distributed 2π delay; topological charge l=1. Right, binary configuration (0, π, 0, π …); topological charge l=12.
Figure 9.
Generation of Perfect Vortex Beams using liquid crystal devices. A polarized collimated laser beams impinges on a spiral phase plate (SPP) that produces an optical vortex with a certain topological charge. Then an axicon creates an nth-order Bessel-Gauss beam that can be focused with a standard lens to generate a PVB. This setup has been reproduced experimentally; the SPP, the axicon and the lens can be obtained out of liquid crystal cells. The sketch is not to scale.
Figure 9.
Generation of Perfect Vortex Beams using liquid crystal devices. A polarized collimated laser beams impinges on a spiral phase plate (SPP) that produces an optical vortex with a certain topological charge. Then an axicon creates an nth-order Bessel-Gauss beam that can be focused with a standard lens to generate a PVB. This setup has been reproduced experimentally; the SPP, the axicon and the lens can be obtained out of liquid crystal cells. The sketch is not to scale.
Figure 10.
Perfect Vortex Beams obtained with a 72 pie slice LC SPP and an LC Fresnel axicon using the scheme shown in the text. Topological charges from –10 to +10 are imposed. The PVBs have the same size, about 6 mm, and are substantially identical.
Figure 10.
Perfect Vortex Beams obtained with a 72 pie slice LC SPP and an LC Fresnel axicon using the scheme shown in the text. Topological charges from –10 to +10 are imposed. The PVBs have the same size, about 6 mm, and are substantially identical.
Figure 11.
Conversion from LCP to RCP by a waveplate oriented at 0º, 45º and 90º with respect to the instantaneous vertically polarized incident light. Upon passing the waveplate, the wavevector –hence the instant phase– is changed 0º, 90º and 180º respectively. For the shown exiting RCP beam, the light is phase accelerated. Had the incident light been RCP, the result would have been exiting LCP with phase delays changed 0º, 90º and 180º respectively.
Figure 11.
Conversion from LCP to RCP by a waveplate oriented at 0º, 45º and 90º with respect to the instantaneous vertically polarized incident light. Upon passing the waveplate, the wavevector –hence the instant phase– is changed 0º, 90º and 180º respectively. For the shown exiting RCP beam, the light is phase accelerated. Had the incident light been RCP, the result would have been exiting LCP with phase delays changed 0º, 90º and 180º respectively.
Figure 12.
2D and 3D sketches of the molecular orientation of an LC in a half order Q-plate configuration.
Figure 12.
2D and 3D sketches of the molecular orientation of an LC in a half order Q-plate configuration.
Figure 13.
Half order (top row) Q-plate introducing a topological charge of and first order (bottom row) Q-plate introducing a topological charge of . The left column shows the alignment patterns; the central column shows micrographs of the configurations between crossed polarizers, and the right column depicts the generated wavefronts with incident RCP light.
Figure 13.
Half order (top row) Q-plate introducing a topological charge of and first order (bottom row) Q-plate introducing a topological charge of . The left column shows the alignment patterns; the central column shows micrographs of the configurations between crossed polarizers, and the right column depicts the generated wavefronts with incident RCP light.
Figure 14.
Left, blue phase with random orientation (platelet structure). Center and right, two monocrystalline BP cells. Microscopic pictures between crossed polarizers.
Figure 14.
Left, blue phase with random orientation (platelet structure). Center and right, two monocrystalline BP cells. Microscopic pictures between crossed polarizers.
Figure 15.
Kossel patterns at λ = 450 nm for a polycrystalline BP sample (left) and two monocrystalline BP samples BPI (110) (center), and BPI (200) (right).
Figure 15.
Kossel patterns at λ = 450 nm for a polycrystalline BP sample (left) and two monocrystalline BP samples BPI (110) (center), and BPI (200) (right).
Figure 16.
Left, monocrystalline stabilized BP cell reflecting specific colors to the cell front plate. Light impinges at the cell edge from top. Right, TEM picture of a BPI (110). The cubic unit cells, with a lattice size of 280 nm, are clearly visible.
Figure 16.
Left, monocrystalline stabilized BP cell reflecting specific colors to the cell front plate. Light impinges at the cell edge from top. Right, TEM picture of a BPI (110). The cubic unit cells, with a lattice size of 280 nm, are clearly visible.
Figure 17.
Four interleaved spirals in Archimedean configuration (left) and Fermat configuration (right). In Archimedean spirals, the distance between turns is constant. In Fermat spirals, the area between consecutive turns is constant.
Figure 17.
Four interleaved spirals in Archimedean configuration (left) and Fermat configuration (right). In Archimedean spirals, the distance between turns is constant. In Fermat spirals, the area between consecutive turns is constant.
Figure 18.
A 24-pie slice spiral lens prototype driven by 24 independent signals. Left, scheme of the DLW maskless planning. Center and right, two configurations of the cell working between crossed polarizers so that different phase delays produce different colors. The lens at the center, with topological charge l=1, uses 24 steps for the Fresnel-like teeth. The lens at the right, with topological charge l=2, uses 12 steps per tooth, doubling the number of teeth and consequently the lens power. All electrical connections are external.
Figure 18.
A 24-pie slice spiral lens prototype driven by 24 independent signals. Left, scheme of the DLW maskless planning. Center and right, two configurations of the cell working between crossed polarizers so that different phase delays produce different colors. The lens at the center, with topological charge l=1, uses 24 steps for the Fresnel-like teeth. The lens at the right, with topological charge l=2, uses 12 steps per tooth, doubling the number of teeth and consequently the lens power. All electrical connections are external.
Figure 19.
Top, deployment of a simplified Fresnel lens. Bottom left, the three inner rings of the Fresnel lens with a possible set of electrical connections. Bottom center, spiral phase plate of 12 segments. This SPP can be transformed into the above Fresnel lens twisting the structure 5 turns. Bottom right is a simplified scheme of the lens (actually it is an axicon). Note that external electric contacts reach the center without further wiring.
Figure 19.
Top, deployment of a simplified Fresnel lens. Bottom left, the three inner rings of the Fresnel lens with a possible set of electrical connections. Bottom center, spiral phase plate of 12 segments. This SPP can be transformed into the above Fresnel lens twisting the structure 5 turns. Bottom right is a simplified scheme of the lens (actually it is an axicon). Note that external electric contacts reach the center without further wiring.
Figure 20.
Microphotographs between crossed polarizers of three axicons made of spirals. The axicons have topological charges l = 1, 8, 12, respectively.
Figure 20.
Microphotographs between crossed polarizers of three axicons made of spirals. The axicons have topological charges l = 1, 8, 12, respectively.
Figure 21.
Two examples of SDLs generated from the same structure. Each color is a different phase shift. The structure has a reasonable number of slices and turns (preferably numbers with many factors, e.g., 12, 48, or 72). The power 1, 2 is arbitrary. A lens with double topological charge and double power is obtained gathering the slices in two groups.
Figure 21.
Two examples of SDLs generated from the same structure. Each color is a different phase shift. The structure has a reasonable number of slices and turns (preferably numbers with many factors, e.g., 12, 48, or 72). The power 1, 2 is arbitrary. A lens with double topological charge and double power is obtained gathering the slices in two groups.
Figure 22.
Top row: four configurations of the same spiral having different powers. The power is increased increasing the topological charge. Bottom row: the spiral that generates this device, shown in black, gathers all configurations, encompassing one or several color scales depending on the topological charge.
Figure 22.
Top row: four configurations of the same spiral having different powers. The power is increased increasing the topological charge. Bottom row: the spiral that generates this device, shown in black, gathers all configurations, encompassing one or several color scales depending on the topological charge.
Figure 23.
Unwinding SDLs. In the upper row, the topological charge of an SDL is cancelled out with another identical SDL coupled back-to-back. The resulting power is twice the power of a single SDL. In the bottom row, the topological charge of an SDL is cancelled out with an SPP of opposite topological charge. The resulting power is the same as the SDL.
Figure 23.
Unwinding SDLs. In the upper row, the topological charge of an SDL is cancelled out with another identical SDL coupled back-to-back. The resulting power is twice the power of a single SDL. In the bottom row, the topological charge of an SDL is cancelled out with an SPP of opposite topological charge. The resulting power is the same as the SDL.
Figure 24.
Experimental microphotographs of spirals with different topological charges combined with compensating SPPs. Monochromatic green light is used. The upper left picture is a back-to-back pair of SDLs and the resulting experimental PFL (inset, calculated FPL). The remaining groups follow the same order as previous pictures: SPP+SDL=PFL.
Figure 24.
Experimental microphotographs of spirals with different topological charges combined with compensating SPPs. Monochromatic green light is used. The upper left picture is a back-to-back pair of SDLs and the resulting experimental PFL (inset, calculated FPL). The remaining groups follow the same order as previous pictures: SPP+SDL=PFL.