Adhesive-free bonding of dielectric materials, using nanojet microstructures
11598969 · 2023-03-07
Assignee
Inventors
- Artem Boriskin (Cesson-Sevigne, FR)
- Ray Keating (Camarillo, CA, US)
- Justin Cunningham (Camarillo, CA, US)
Cpc classification
B32B27/322
PERFORMING OPERATIONS; TRANSPORTING
G02B27/0927
PHYSICS
B32B1/00
PERFORMING OPERATIONS; TRANSPORTING
B82Y20/00
PERFORMING OPERATIONS; TRANSPORTING
B32B27/06
PERFORMING OPERATIONS; TRANSPORTING
B32B27/308
PERFORMING OPERATIONS; TRANSPORTING
B32B2457/206
PERFORMING OPERATIONS; TRANSPORTING
B82Y30/00
PERFORMING OPERATIONS; TRANSPORTING
B81C2203/037
PERFORMING OPERATIONS; TRANSPORTING
B32B2307/4026
PERFORMING OPERATIONS; TRANSPORTING
B32B27/20
PERFORMING OPERATIONS; TRANSPORTING
International classification
Abstract
A method of bonding layers of dielectric materials includes providing a surface one of the layers with microscale- and/or nanoscale-size bonding elements forming contact points of the layers and bringing a layer of the layers into a mutual position according to an intended use. The method also includes illuminating the layer whose surface is provided with bonding elements by an incident electromagnetic wave, the propagation direction of which is substantially orthogonal to the one of the layers, and whose wavelength is selected depending on an absorption spectrum of a material forming the one of the layers and generating condensed optical beams within said bonding elements or close to a tip of said bonding elements intended to be in contact with the other layer. The method further includes heating and melting the bonding elements by high-intensity focal spots formed by said generated optical beams and maintaining the layers into a mutual position until and bonding of the layers.
Claims
1. A method of bonding layers of dielectric materials, comprising: providing a surface of at least one of said layers with microscale size and/or nanoscale-size bonding elements forming contact points of said layers, the microscale-size and/or nanoscale-size bonding elements having a length in a direction perpendicular to the surface of less than 5000 nanometers; bringing said layers into a mutual position according to an intended use; illuminating a first layer of said layers whose surface is provided with bonding elements by an incident electromagnetic wave, the propagation direction of which forms an angle comprised between 70° and 110° with said first layer, and whose wavelength is selected depending on an absorption spectrum of at least one of materials forming said layers; generating, as a result of the illumination, condensed optical beams within said bonding elements or close to a tip of said bonding elements, the tip making contact with a second layer of said layers; heating and melting said bonding elements and/or said second layer by high-intensity focal spots formed by said generated optical beams; maintaining said layers in the mutual position until bonding of said layers.
2. The method of claim 1, wherein said bonding elements form a patterned microstructure on the surface of said first layer.
3. The method of claim 1, wherein said bonding elements have a form of pillars and/or ribs.
4. The method of claim 1, wherein a dimension of said bonding elements in the direction of said incident electromagnetic wave is targeted to be between half a wavelength of said incident electromagnetic wave and a few wavelengths of said incident electromagnetic wave.
5. The method of claim 1, wherein said layers are made of the same material.
6. The method of claim 1, wherein said layers are made of distinct materials.
7. The method of claim 1, wherein a material of said first layer which surface is provided with bonding elements belongs to the group comprising plastics and thermoplastics.
8. The method of claim 7, wherein a material of at least one of said layers comprises absorptive dyes or pigments.
9. The method of claim 1, wherein it also comprises providing a surface of at least one of said layers with engraved microfluidic channels.
10. The method of claim 1, wherein bringing said layers into a mutual position according to an intended use is performed after heating and melting (34) said bonding members.
11. The method of claim 1, wherein, when bringing said layers into a mutual position according to an intended use, said layers are placed into direct contact between two optically transparent plates.
12. The method of claim 1, wherein it also comprises cooling down a surface of said first layer opposite to said surface provided with said bonding elements.
13. The method of claim 1, wherein it also comprises pre-heating at least said surface provided with said bonding elements.
14. The method of claim 1, wherein providing a surface of at least one of said layers with microscale and/or nanoscale-size bonding elements is performed by molding or wet embossing said surface.
15. The method claim 1, wherein said bonding elements have a conical shape, wherein their dimensions are selected so that the condensed optical beams are generated close to but above the tip of said bonding elements intended to be in contact with the other layer, and wherein said layer whose surface is provided with bonding elements is made of a material which has lower losses and/or a higher melting temperature than a material of the other layer.
Description
4. BRIEF DESCRIPTION OF THE DRAWINGS
(1) The present disclosure can be better understood with reference to the following description and drawings, given by way of example and not limiting the scope of protection, and in which:
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(23) The components in the figures are not necessarily to scale, emphasis instead being placed upon illustrating the principles of the invention.
5. DETAILED DESCRIPTION
(24) The general principle of the present disclosure relies on the electromagnetic (EM) heating of dielectric materials, as well as on the so-called Nanojet (NJ) focusing phenomenon, which provides control over the EM field intensity distribution inside the materials. More specifically, the NJ phenomenon enables highly-localized heating and melting of microstructure elements distributed in a controlled manner along the bond line on the interface of two materials.
(25) Throughout the below text, the bonding elements are described as nanoscale-size bonding elements. It must be noted that this also encompasses microscale-size bonding elements, bearing in mind that, in some embodiments, a typical size of bonding elements is circa 1 to 5 microns (i.e. 1000 to 5000 nm).
5.1 First Embodiment and General Features
(26)
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(28) First, at step 21, a first layer 13.sub.1 of material is provided with nanoscale-size bonding elements, which may take the form of ribs 12 or pillars 11. In the embodiment of
(29) A second layer 13.sub.2 is also manufactured, which may be a thin layer of a material similar (or dissimilar) to the one used for layer 13.sub.1.
(30) This first layer 13.sub.1 and a second layer 13.sub.2 to which it must be bonded, are brought into a mutual position, according to an intended use, at step 22. For example, layers 13.sub.1 and 13.sub.2 are put in direct contact one to another and their outer lines are aligned.
(31) The two layers of material are joined under light pressure, for example between two optically-transparent plates (e.g. made of glass). At step 23, they are then exposed with a laser beam 14 from below, as illustrated on
(32) The formation of nanojet beams inside or at the tip of the pillars 11 causes heating and melting of the bonding elements 11, 12 at step 24. (It must be noted that, in the alternate embodiment described in Section 5.2, the formation of nanojet beams above the tip of the pillars 11 causes heating and melting of the second layer 13.sub.2 at step 24, rather than that of the bonding elements 11, 12).
(33) The structure is then left under pressure until it cools down (step 25).
(34) As will be apparent later on in this document,
(35)
(36) 5.1.1 Electromagnetic (EM) Model
(37) We now describe the electromagnetic model sustaining the method according to embodiments of the present disclosure, when no heat transfer effects are taken in to account.
(38) Let us assume that a light beam 14 with intensity I.sub.0 propagating in the positive z-direction is incident on a stack of two layers 13.sub.1 and 13.sub.2 of a material from below, as shown in
(39) Intensity of the light beam penetrating inside the plate at z=z.sub.1:
I.sub.e=I.sub.0(1−r) (1)
where I.sub.0 is the intensity of the incident light beam, r is the reflectivity of the plate bulk material, which can be derived from Fresnel's formula as a function of the material refractive index n:
(40)
(41) The intensity of the light beam at the upper surface of layer 13.sub.1 (z=z.sub.2) is defined as:
I.sub.d=I.sub.eexp(−αT) (3)
where T=z.sub.2−z.sub.1 is the thickness of layer 13.sub.1 and α is the absorption (or attenuation) coefficient defined as:
(42)
where k is the extinction coefficient being the imaginary part of the complex refractive index of the bulk material:
n*=n+ik (5)
(43) The rapid increase of the field intensity inside the pillar 11 is explained by the NJ focusing effect illustrated in
I.sub.m=M.Math.I.sub.d=M.Math.I.sub.eexp(αT) (6)
where M is the NJ lens intensity magnification number.
(44) Note that the light beam propagating inside the pillar 11 experiences the same exponential decay of the EM wave intensity as in layer 13.sub.1, which is compensated (and exceeded) by the field intensity increase due to the NJ lens focusing phenomenon (here we assume that bulk material is linear and thus its absorption coefficient does not depend on the field intensity). However, a part of the EM energy dissipates inside the pillar 11 (mostly near its focal spot region) and transforms into the thermal energy, resulting in a local heating and finally melting of the pillar 11 provided the incident beam intensity and exposure time are sufficient to heat the pillar up to the melting temperature.
(45) From the electromagnetic point of view, the feasibility conditions for the method according to embodiments of the present disclosure can be formulated as:
I.sub.e<I.sub.c≤I.sub.m (7)
where I.sub.c is the critical beam intensity, i.e. the minimum intensity required to melt the bulk material. This condition is to be read as (i) the incident beam intensity must be lower than critical in order to prevent melting of the bulk material at the bottom surface of layer 13.sub.1 at z=z.sub.1 and (ii) the NJ lens focusing ability must be high enough to enable melting of the material near the NJ lens focal spot area. Referring to Eqns. (1-6), the feasibility condition given by Eqn. (7) can be written as
M.Math.exp(αT)>1 (8)
which enables one to determine a critical thickness of layer 1:
(46)
where T.sub.c is the maximum allowed thickness of layer 1 corresponding to the condition I.sub.e=I.sub.c=I.sub.m. For fixed values of α and M, a thicker layer will result in premature melting of the material at the bottom surface of layer 13.sub.1. Reference data for T.sub.c=T.sub.c(M, α) is presented in
(47) As follows from Eqn. (9), the critical thickness is to be determined for each material and NJ lens focusing ability.
(48) The latter is represented using the NJ lens intensity magnification number M, which depends on the lens shape and dimensions. As explained in patent application PCT/EP17/057130 (not yet published at the time of filing the present application), its typical value is varied in between 5 and 50 (see Section 5.4 for more details).
(49) The material absorption coefficient α can be determined either (i) analytically using Eqn. 4, provided the extinction coefficient (or more generally complex refractive index) of the bulk material is known, or (ii) from the transmittance of the bulk material provided by the manufacturer or measured using a spectrophotometer, as described for example by B. Neuroth, in “The optical properties of optical glass”, Springer, 1995, pp 82-83. The latter definition is based on the ratio between the light intensity of the beam incident on the plate and that of the beam transmitted through the plate (in this definition, the plate has a form of a planar dielectric layer of a given thickness d):
(50)
(51) where τ is transmittance of a dielectric plate of a given thickness d, I.sub.0 and I.sub.t are intensities of the incident transmitted light beam, τ.sub.i=I.sub.d/I.sub.e is internal transmittance describing the propagation loss inside the plate, and P is the reflection factor describing reflection loss on both air/dielectric boundaries (including possible multiple internal reflections):
(52)
(53) Knowing material refractive index and transmittance of the bulk material (usually provided by manufacturer—e.g. see Ref. COVESTRO Deutschland AG, “Optical properties of Makrolon and Apec for non-imaging optics”, 2016), one can compute the absorption coefficient as:
(54)
(55) where d is the thickness of the dielectric slab (provided by manufacturer; typically varies between 1 and 4 mm).
(56)
(57) Finally,
(58) For optically transparent materials, like polycarbonate in the visible range, the transmittance τs close to 90%, which means that the loss is largely due to reflections rather than absorption. Thus, for the transmittance close to 90%, the absorption coefficient tends to zero. With a very low propagation loss inside the material even a small intensity magnification provided by the pillars 11 (e.g. M=5) enables one to satisfy the melting feasibility condition defined in Eqn. (7) even for a thick dielectric plate.
(59) In case of a nearly opaque material with transmittance τ≤5%, the feasibility condition (Eqn. 7) is reached already for a plate with a thickness of about 1 to 2 mm, which means that use of lossy materials may cause a problem with overheating of the bottom surface of the plate. This situation may occur, for instance, for a polycarbonate illuminated by a UV light with a wavelength λ<300 nm.
(60) Thus, optimal experimental conditions may be achieved for the transmittance of the bulk material varying in between about 20 to 70%. For polycarbonate, the required transmittance can be achieved either in the UV range (λ.sup.˜300-350 nm) or in the IR range (λ.sup.˜1650 nm). The transmission spectrum of a material can be changed using some additives.
(61) Note that higher propagation loss in the material (observed for lower transmittance) results in faster dissipation of the incident power and thus higher heating rates, achieved thanks to a more efficient transformation of the EM energy into the thermal one. The factors affecting efficiency of such a transformation are discussed in Section 5.4.
(62) 5.1.2 Heat Transfer Analysis
(63) In this section, we present some considerations about the processes related to the temperature increase in the structure presented in
(64) According to E. J. G. Peterman et al., in “Laser-induced heating in optical traps,” Biophysical J., vol. 84, pp. 1308-1316, 2003, the heat per volume, Q, generated per time by transmitting a plane wave of light with intensity, I, through a medium, in the z-direction is given by
(65)
(66) where α is the absorption coefficient defined as I (z)=I exp(−αz).
(67) The heat generated by the absorption will dissipate. The dissipating heat flow J({right arrow over (r)}) obeys the local differential equation
J({right arrow over (r)})=C.Math.∇(ΔT({right arrow over (r)})) (14)
(68) where C is the thermal conductivity and ΔT({right arrow over (r)}) is the temperature deviation from ambient temperature due to heating at position {right arrow over (r)}. In steady state the heat dissipated is equal to the heat generated:
(69)
(70) Using Eqs. (13) and (14), this becomes:
(71)
(72) The general equation (16) shows that the local temperature increase inside a medium is proportional to the intensity of the incident light and absorption coefficient of the medium, which suggests to use a material with a highest possible absorption coefficient, allowed for by the feasibility condition Eqn. (7).
(73) 5.1.3 Control Parameters of the Method According to Embodiments of the Present Disclosure
(74) In case of zero-heat-transfer (C=0), the steady state condition (Eqn. 15) is never reached, which means that the medium can be continuously heated to any temperature (this explains the exponential increase of T.sub.c in
(75) There are several parameters, which may control the method of bonding layers of materials according to embodiments of the present disclosure, among which: The material absorption coefficient, related to composition of the material and laser wavelength, Thickness of the layer, related to feasibility condition Eqn. (7) and heat flux conditions, Laser intensity and exposure time, related to melting and steady state temperatures, Heat transfer conditions, related to material thermal conductivity C and heat flux boundary conditions, NJ lens focusing ability, related to the shape and size of surface pattern features.
5.1.3.1 Absorption Coefficient
(76) The absorption coefficient depends on the composition of the material and, more specifically, on its atomic and chemical structure. Because of this, the absorption coefficient strongly depends on the wavelength of the incident wave. Matching known dispersion characteristics of polycarbonate (PC) (see for example COVESTRO Deutschland AG, “Optical properties of Makrolon and Apec for non-imaging optics,” 2016) with a list of existing lasers (see for example Weber, Marvin J. «Handbook of laser wavelengths», CRC Press, 1999), one can select the wavelength that will provide a desired transmittance of the bulk material in the range from less than 5% observed for DUV range and up to ˜90% observed for visible and NIR ranges. The transmittance/absorbance spectrum of PC can also be varied using some additives, which are typically used for coloring the bulk material.
(77) Moreover, the absorption coefficient may also vary as a function of the EM wave intensity (non-linear effect) and material temperature: α=α(I,T).
(78) The former non-linear effect α=α(I) is intrinsic to photochromic glass that changes color (i.e. becomes dark) when illuminated by a bright sun light. A photochromic-type additive to the bulk material may help further localize the heating process by increasing efficiency of the EM to thermal energy conversion directly in the focal spot of the NJ microlens.
(79) The latter effect α=α(T) is linked to change of the material physical properties when its temperature approaches that of the melting point.
(80) 5.1.3.2 Thickness of the Layer
(81) Thickness of the layer can be selected rather arbitrarily, provided the feasibility condition Eqn. (7) is satisfied.
(82) Additional considerations for selecting layer thickness may include assessment of the heat flux inside the structure, including its bottom surface and upper one with patterned microstructure. For a thick layer, it may be possible to cool down the bottom surface of layer 13.sub.1 to prevent its premature melting. This can be done either by air cooling (i.e. ventilation) or by a contact cooling. The latter option may be advantageous from a practical point of view. Table 1 provides typical, not specific values of the thermal conductivity and refractive index for some materials relevant to the present disclosure. As we can see, thermal conductivity of glass is about seven times higher than that of polycarbonate. Thus, one may expect to achieve a contact cooling effect for the bottom surface of Layer 13.sub.1 of the structure shown in
(83) The two additional advantages that can be gained using a glass substrate are the following: glass substrate can be used as a support and mechanical tool for pressing together the two layers of the structure in a certain phase of the heating process (e.g. after melting the top layer), the lower refractive index of glass will slightly reduce (.sup.˜2%) the reflection loss at the air/dielectric boundary (see
(84) TABLE-US-00001 TABLE 1 Typical, not specific values of C and n for some materials Thermal conductivity, C Material (W/(m .Math. K)) Refractive index, n Air 0.025 1 Polycarbonate 0.2 1.6 Glass 1.4 1.5
5.1.3.3 Laser Intensity & Exposure Time
(85) The optimal values of the laser intensity depend on many factors, including physical properties of the bulk material (i.e. refractive index, absorption and heat transfer coefficients as well as their variation as a function of wavelength, incident wave intensity, and temperature) and the focusing ability of the NJ microlenses, defined throughout the present disclosure in terms of intensity magnification number, M. These parameters define the heating rate and maximum heating temperature corresponding to steady state. The two extreme cases are: (i) intensity is too low and steady state is observed for T.sub.m<T.sub.melt and (ii) intensity is too high with entire layer melted down. The third unfavorable situation may occur for a thick layer of the material, namely melting of the bottom surface before melting microstructure elements in the contact area between the two layers 13.sub.1 and 13.sub.2.
(86) The optimal exposure time may be found empirically after determining a correct laser intensity, which guarantees the melting condition T.sub.m≥T.sub.melt.
(87) 5.1.3.4 Heat Transfer Conditions
(88) The heat transfer conditions can be controlled by varying composition of the material, thus changing its thermal conductivity, and/or changing the thermal flux boundary conditions. The former can be done using some additives, the latter via introducing a cooling mechanism at the bottom surface of layer 13.sub.1.
(89) 5.1.3.5 Parameters of the Microstructure
(90) Parameters of the microscopic features at the upper patterned surface of layer 13.sub.1 (i.e. shape, size and spacing between the pillars 11) will define the focusing ability of each nanoscale-size bonding element and heat transfer conditions. Note that the focal spot size is always proportional to the laser wavelength, whereas the peak intensity is a function of the feature size (e.g. radius of the pillar 11). A larger size pillar 11 will cause faster heating inside the pillar 11, however, the external surface will remain colder than that of a smaller pillar 11. Thus, an optimal size of the pillar 11 is to be found as a trade-off between the EM/thermal heating in the focal spot area and thermal flux from the hot area towards periphery. This is illustrated in
(91) The spacing between the pillars 11 may alter the thermal flux boundary condition for the pillars, thus affecting the heating rate, as well as the amount of the melted (adhesion) material available when pillars melt. The morphology and distance between the pillars can be selected in a way to provide a reliable sealing, strong enough not to break under mechanical deformations.
(92) 5.1.4 Characteristics of the Nanoscale Size Bonding Elements
(93) The basic theory of nanojet (NJ) microlenses has been reported in PCT patent applications PCT/EP17/057130 and PCT/EP17/057131 (yet to be published at the time of filing the present patent application). These two documents show:
(94) 1. How a field intensity pattern is created in the near zone of a dielectric particle (in a free space) or a cavity (in a dielectric host medium), from incident electromagnetic waves,
(95) 2. How a focused condensed optical beam, a so-called nanojet (NJ), is created as a result of diffraction of an EM wave by a step index discontinuity associated with edges of said dielectric particle or cavity, and
(96) 3. How a high-intensity NJ beam can be created by recombination of elementary NJ beams associated with different segments of the base edge line of a dielectric particle or a cavity inside a dielectric medium.
(97) The characteristics of NJ beams relevant to the heat-sealing method according to embodiments of the present disclosure are recalled below.
(98) According to patent application PCT/EP17/057130, the hot spot position (i.e. focal length) with respect to the base of the pillar 11 (the base is defined with respect to the incident wave arrival direction—see
F≈R/tan tan(θ.sub.B), (17)
(99) where R is the radius of a circular cylindrical pillar 11 and θ.sub.B is a nanojet radiation angle defined as:
(100)
(101) Here n.sub.1 and n.sub.3 (n.sub.3<n.sub.1) are refractive indexes of the material and host medium (e.g. air), respectively. For simplicity, we assume here that both layers 13.sub.1 and 13.sub.2 are made of the same material n.sub.1=n.sub.2). Notations are given in
(102) A reliable solution of the corresponding EM problem was obtained using a commercial software CST-v16, based on a 3D-FDTD full-wave EM solver. Two models were studied, namely (i) with circular cylindrical pillars and (ii) rectangular pillars, represented in
(103) The top and bottom substrates are infinitely thick and made of a uniform homogeneous dielectric material with refractive index similar to the one of polycarbonate, i.e. n.sub.1=n.sub.2=1.58. In this analysis, we assume that material is lossless, i.e. absorption coefficient α=0. Thus, our analysis are limited to the EM wave propagation and focusing phenomena, whereas no thermal effects are taken into account. Analysis is performed for three wavelength, namely λ=405 nm, λ=532 nm, λ=650 nm.
(104) The height of the pillar 11 is selected as H=2F, aiming at creating a hot spot in the middle of the pillar and thus providing a uniform heating for the entire pillar. In case of polycarbonate (n=1.58) it stands for H≈4.5R.
(105)
(106)
corresponding to the first field intensity maximum inside the pillar represented as a function of the pillar size, namely radius R in case of a circular pillar (
(107) The z-coordinate of the field intensity maxima is reported in
(108) Here, the reference solution shown by grey line corresponds to Eqn. (17). A good agreement between the reference solution and the data extracted from full-wave simulations is observed for R varying in between 300 and 600 nm (i.e. about 1 to 2 wavelength in free space) which corresponds to the range, in which the NJ phenomenon is dominant. For larger dimensions, the contribution from multiple internal reflections become strongly pronounced affecting the field distribution.
(109)
(110) Finally,
(111) As we can see, the NJ phenomenon leads to strong localization of the field in a focal spot located on z-axis close to z=F. Maximum bonding would occur when z.sup.˜F. A typical width of the spot is about 200 to 300 nm. Such a sub-wavelength focusing explains a high field intensity enhancement in the focal point.
(112)
(113) In one embodiment, both layers 13.sub.1 and 13.sub.2 can be made of the same dielectric material (e.g. plastic or polymer). For instance, it can be an optically-transparent plastic material, like polycarbonate, whose melting temperature is about 150° C. Polycarbonate is routinely used for CD and DVD fabrication. Polycarbonate can be easily processed via wet embossing method that allows one to create a layer of a polycarbonate material with an arbitrary surface microstructure that may comprise plurality of bonding elements having different sizes and shapes. In particular, such a microstructure may include microfluidic channels 10 as well as pillars 11 and ribs 12 acting as NJ microlenses, as shown on
(114) In another embodiment, the pillars 11 can be created on the surface of the second (top) layer 13.sub.2. They may cover either the entire surface (
(115) In another embodiment, illustrated by
(116) In yet another embodiment, a thin layer 13.sub.3 of a photopolymer or a thermoplastic can be deposited on a surface of layer 13.sub.2 made of an optically-transparent dielectric material (e.g. glass) and attached to layer 13.sub.1 made of another dielectric material (
(117) The proposed heat-sealing method according to embodiments of the present disclosure is not limited to optically transparent materials. It may actually be used at any other wavelength (e.g. THz or microwaves) and used to seal materials which may not be transparent in the optical range.
(118) As a consequence, there is also an embodiment when layer 13.sub.1 and layer 13.sub.2 are both made of a lossy (non-transparent) material. For instance, it may be polycarbonate at a wavelength below 300 nm. In such a case, the exposure method illustrated in
(119) As explained in Section 5.1.4, the shape of the pillars 11 can be selected rather arbitrarily. For instance, they may have a shape of a cylinder or prism with a circular or rectangular cross-section. Other shapes are also possible including a rib-type pillar that will act as a two-dimensional (2D) nanojet microlens. In case of a rib 12, its cross-section is to be defined following the same rules as for the 3D cylindrical or pyramidal pillars 11 presented below. However, the main advantage of 3D bonding elements is in their better ability to concentrate light that results in faster heating.
(120) The size of the bonding elements 11 must be selected with respect to the wavelength of the laser beam 14 and the desired position of the focal spot 15. In different embodiments, it may be advantageous to have a focal spot 15 inside the pillar (e.g. at half height of the pillar) or at the top tip of the pillar. The former choice results in a more uniform heating of the pillar, whereas the latter may enable simultaneous heating of a pillar 11 on bottom layer 13.sub.1 and its contact area of top layer 13.sub.2 thus potentially resulting in a better adhesion between the layers.
(121) This will be described in greater detail in relation with an alternate embodiment below.
5.2 Alternate Embodiment
(122) This alternate embodiment consists in choosing a particular shape of the microstructure elements (i.e. pillars) and peculiar material properties of the two layers sealed one to another. It differs from the first embodiment in that it is proposed to use the light focusing ability of the pillars to heat and locally melt the second layer, rather than the bonding elements themselves. The same pillars are used as ‘hot nails’ that penetrate the second layer and thus improve mechanical rigidity of the sealed structure.
(123) Specific aspects will be described in relation to
(124) Specific features of this alternate embodiment may be summarized as follows:
(125) 1. Shape of the microstructure elements (i.e. pillars) is chosen to be a cone, as illustrated in
(126) 2. Dimensions of the cone are to be selected so that the focal spot appears close to the tip of the conical pillar, preferable inside layer 13.sub.2 right above the tip, as illustrated in
(127) 3. Material of layer 13.sub.2 (characterized by a complex refractive index n*.sub.2=n.sub.2+ik.sub.2) must have higher losses than material of layer 13.sub.2 (characterized by a complex refractive index n*.sub.1=n.sub.1+ik.sub.i), namely k.sub.2>k.sub.1, where k.sub.1 and k.sub.2 are extinction coefficients of the material of layer 13.sub.1 and layer 13.sub.2, respectively.
(128)
(129) More precisely,
(130) 5.2.1 Design Guidelines
(131) Focal spot size of a nanojet microlens is about one half of the wavelength in the medium. Thus, it may be beneficial to create a cone 11 with a tip of the same radius, i.e.
(132)
This will guarantee uniform heating of the tip. It is known from the prior art that intensity of the NJ beam is proportional to the length of the base edge line, L=2πR.sub.1. Increasing the radius of the cone base may be used to enhance intensity of the NJ beam and, thus, provide a faster heating of the material in the vicinity of the NJ focal spot. Recommended value of the base radius is about one and a few wavelengths in the cone material. The focal length of a conical NJ microlens can be estimated as
(133)
where θ is the NJ deviation angle for a step having base angle α<90°.
(134) According to patent document PCT/EP17/057131, it can be derived as:
(135)
where θ.sub.TIR=sin.sup.−1(n.sub.3/n.sub.1) is the critical angle for a diopter with indices n.sub.1 and n.sub.3 (n.sub.1>n.sub.3), n.sub.3 being refractive index of the host medium. This empiric equation is valid at least for α=90°±30°.
(136) Recommended height of the conical pillar 11 is equal (or slightly smaller) than focal length:
H≈F (22)
Preferably, it should also be larger that at least one half of the wavelength in the cone material. The base angle can be selected rather arbitrarily (e.g. in the interval 45 to 90 degree).
(137) 5.2.2 Materials and Methods
(138) To enable the desired performance, layer 13.sub.1 and NJ microstructures on its surface should preferably be fabricated of a low-loss material (at the wavelength of the incident EM wave), whereas layer 13.sub.2 should have losses higher than that of layer 13.sub.1 (i.e. k.sub.2>k.sub.1, where k.sub.i is the extinction coefficient of the corresponding material).
(139) A higher loss in the material of layer 13.sub.2 will result in a stronger absorption of the EM radiation in layer 13.sub.2 that will be heated and melted right above the pillars 11 acting as light focusing elements. Note that, unlike in the first embodiment of Section 5.1, the pillars 11 themselves will not melt but instead will act as a kind of ‘hot nails’ that will finally penetrate into the melted material of layer 13.sub.2. Depending on the choice of materials for layers 13.sub.1 and 13.sub.2 (and especially depending on their melting temperature) the pillars can melt, at least partly, after penetration into the upper layer 13.sub.2.
(140) Like in the first embodiment, this alternate embodiment offers an adhesive-free heat sealing method that can be applied to join two similar or dissimilar materials under exposure of a non-ionizing electromagnetic (EM) radiation, e.g. a laser beam.
(141) Unlike other heat sealing methods, this method does not require any thermosoftening glue, resin, or another adhesive material to be added. Instead, it relies on a controlled highly-localized heating of a superficial layer of the bulk material. This offers a strong advantage in scenarios when materials that need to be sealed together already have some microscale surface patterns, which must be kept clean from any impurities, like in case of a microfluidic chip, as illustrated in
(142) 5.23 Operational Principle
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(144) When illuminated by an incident EM wave (e.g. laser beam) as shown in
(145) Under certain conditions, which may include adequate selection of materials of both layers, correct design of the NJ focusing elements, and certain exposure conditions, a highly-localized heating can be provided right above the tips of the pillars 11 resulting in melting (or softening) of layer 13.sub.2. A light pressure can be applied to press the layers one to another so that NJ elements of layer 13.sub.1 penetrate into the melted (softened) material of layer 13.sub.2. After cooling, a strong bond will be created along the contact line.
(146) The proposed method can be used for sealing various thermoplastic materials, such as ABS, PLA, PMMA, PTFE, Polycarbonate, COC, etc.
(147) In one embodiment, the loss in the material used for layer 13.sub.2 can be modified (i.e. increased) using a chemical additive (e.g. of a photochromic type, carbon black, absorptive dyes or pigments) added to the same bulk material, e.g. polycarbonate, like previously described in relation to the first embodiment.
(148) Note that some polymer materials, like PC, does not have a melting point in the true sense of this term. Instead, it has a glass transition temperature at which material transitions from glass to rubber. When reaching this glass transition temperature, the material becomes soft and flexible. For instance, in case of polycarbonate (PC), the glass transition temperature is about 147° C., whereas the temperature at which it can be used for injection molding is about 230 to 300° C. The sealing of the two layers of polycarbonate is possible at temperatures between 150° C. and 230° C. At higher temperatures, it will become liquid and may fill in and block microchannels.
(149) In one embodiment, main steps of the proposed method can be the following (note that they only slightly differ from the embodiment of
Note that Materials of the layers are to be selected so that k.sub.2>k.sub.1, where k.sub.1 and k.sub.2 are extinction coefficients of the material of layer 13.sub.1 and layer 13.sub.2, respectively. Preferably, k.sub.1 should be as small as possible (e.g. k.sub.1<10.sup.−5) so that most of the power loss occurs in layer 13.sub.2. In one embodiment, both layers can be fabricated from the same bulk material (e.g. PC) with some additives used for layer 13.sub.2. Wavelength of the laser is to be selected with respect to the absorption spectra of the materials in order to achieve desired values of the extinction coefficients for material of layer 13.sub.2 and 13.sub.2. Shape and size of the NJ focusing elements 11 are to be defined with respect to the wavelength of the incident EM wave and refractive index of the materials so that the focal spot appears above the tip of the pillar inside layer 13.sub.2.
(150) Note that unlike the first embodiment, thickness of the layers can be selected arbitrarily. This is because the loss (and thus heating) will largely occur in a superficial layer of layer 13.sub.2 in the vicinity of the focal spots created by NJ focusing elements 11.
(151) 5.2.4 Simulation Data
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(157) From
(158) In case when layer 13.sub.2 is made of a material with higher losses (
(159) Comparison of the temperature profiles reported in
(160) As shown in
(161) This alternate embodiment, as compared to the first one described in Section 5.1, is advantageous in that it is not as demanding as regards precise calibration for the laser power and exposure conditions. In the first embodiment, erroneous exposure conditions may result in premature melting of the entire layer (or its bottom surface) instead of the microstructure elements. Such a drawback is avoided thanks to the alternate embodiment of Section 5.2.
(162) As compared to the first embodiment, this alternate embodiment is simplified in the aspects related to (a) fabrication of the microstructure of bonding elements and (b) calibration of the exposure conditions. Moreover, the method is more versatile and more easily applicable for sealing of different materials. It also enhances mechanical rigidity of the sealed structure.
(163) 5.3 Comparison of the Focusing Ability of Cylindrical Shape Bonding Elements and Conical Shape Bonding Elements.
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(168) NJ laser welding method is based on local heating of the pillar and its surrounding. Thus, it is advantageous to have the maximum power density enhancement (PDE) inside the pillar compared to the power density of the EM wave propagating through the cover layer, whose thickness is large enough to be considered as unbounded medium. The power density enhancement in the pillar leads to premature heating of the pillar and faster temperature rise in its vicinity compared to the uniform medium. As one may see in
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(173) As one may see in
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