METHOD FOR LABELING PRODUCTS WITH A TRANSPARENT PHOTOLUMINESCENT LABEL, AND TRANSPARENT PHOTOLUMINESCENT LABEL

Abstract

A method for marking a product (1) with a photoluminescent mark, said mark comprising a photoluminescent portion (10) which is transparent under normal light conditions and revealed by photoluminescence under UV illumination, said mark further comprising a non photoluminescent portion (9) which is transparent under normal light conditions as well as under UV illumination, said method comprising: deposing on said product a stack, said stack comprising alternatively layers (2, 4), such as AlN, with a thickness of less than 1 micron and layers (3) of a second material, such as GaN, with a thickness of less than 10 nm; raising the transparency of said non photoluminescent portion (10) with a deposition of transparent material (6) or incorporation of ions into said non photoluminescent portions.

Claims

1. A method for labeling a product with a photoluminescent label, said label comprising a photoluminescent portion which is transparent under normal light conditions and revealed by photoluminescence under UV illumination, said label further comprising a non photoluminescent portion which is transparent under normal light conditions as well as under UV illumination, wherein said method comprises: deposing on said product a stack, said stack comprising successive alternate layers of a first material with a thickness of less than 1 micron and a second material with a thickness less than 10 nm, resulting in quantum nano-structures at the interface between the two materials, incorporating ions or deposing a transparent material into said non photoluminescent. portions.

2. The method of claim Therein said stack comprising successive layers a number less than or equal to 100 stackings.

3. The method of claim 1, wherein said layers being grown by one of the methods among sputtering, Atomic Layer deposition, Molecular Beam Epitaxy or Metal Organic Chemical Vapor Deposition.

4. The method of claim 1, wherein said layers of second material comprising GaN alloys with less than 50% of Indium, Aluminum, Arsenic and/or Phosphor.

5. The method of claim 1, wherein said layers of second material comprising presence of rare-earth elements with contents of less than or equal 10%.

6. The method of claim 1, wherein said quantum nano-structures being created in said layers second material and comprising quantum dots.

7. The method of claim 6, wherein said quantum dots being integrated in layers of second material by roughning the grown stack.

8. The method of claim 1, wherein said layers of first material comprising less than 20% of Magnesium, Silicon, Lithium, Berilium, Cadmium and/or Zinc as dopant elements.

9. The method of claim 1, wherein said ions including Oxygen, Nitrogen, Hydrogen, Helium, Neon, Argon, Magnesion, Lithium, Beryllium, Bore, Phosphor, Aluminum, Zinc, Arsenic, Galium, Silicon, Cadmium and/or any kind of element capable degrading the photoluminescent stack and creating non-radiative recombination center defects into the stack.

10. The method of claim 1, wherein said ions being incorporated withih the stack by diffusion or implantation techniques.

11. The method of claim 1, wherein said ions being incorporated through a mask so as to create a pattern.

12. The method of claim 1, wherein said transparent material being deposited in replacement to selectively removed photoluminescent portions.

13. The method of claim 12, wherein said transparent material having a refractive index substantially equal to the refractive index of said stack.

14. The method of claim 1, wherein the method comprises use of a one-time mask for creating a unique pattern for each product.

15. The method of claim 1, wherein the photoluminescent portions remitted light color depends on the intensity of incoming UV light.

16. (canceled)

17. The method of claim 1, wherein said UV illumination and/or UV light comprises UV wavelengths of less than or equal 400 nm.

18. A product comprising a photoluminescent pattern, wherein said pattern comprises: a photoluminescent portion which is transparent under normal light conditions and revealed by photoluminescence under UV illumination, said photoluminescent portion comprising a stack with alternatively layers of a first material with a thickness of less than or equal to 1 micron and layers of a second material with a thickness of less than or equal 10 nm, including quantum nano-structures at the interface between the two materials; a non photoluminescent portion which is transparent under normal light conditions as well as under UV illumination, said non photoluminescent portion comprising an additional transparent material or ions for raising the transparency.

19. The product of claim 17, wherein said ions including Oxygen, Nitrogen, Hydrogen, Helium, Neon, Argon, Magnesion, Lithium, Beryllium, Bore, Phosphor, Aluminum, Zinc, Arsenic, Galium, Silicon, Cadmium an/or any kind of element capable degrading the photoluminescent stack and creating non-radiative recombination center defects into the stack.

20. The product of claim 17, wherein said transparent material having a refractive index substantially equalto the refractive index of said stack.

21. The product of claim 17, wherein said product being transparent.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0040] The invention will be better understood with the aid of the description of an embodiment given by way of example and illustrated by the figures, in which:

[0041] FIG. 1 shows an example of product to be marked.

[0042] FIGS. 2, 3 and 4 show the successive deposition of layers onto said product, so as to create a stack of photoluminescent material.

[0043] FIG. 5 shows the engraving of selected portions of the created stack, so as to delimitate photoluminescent portions of label with a process according to a first embodiment of the invention.

[0044] FIG. 6 shows the filling of the engraved portions with transparent material, so as to create non photoluminescent portions of label.

[0045] FIG. 7 shows the ion incorporation into the stack, so as to deactivate the photoluminescent ability of selected portions of the stack and to create non photoluminescent portions of the label with a process according to a second embodiment of the invention.

[0046] FIG. 8 shows an example of label.

DETAILED DESCRIPTION OF POSSIBLE EMBODIMENTS OF THE INVENTION

[0047] A first embodiment of the process for labeling a product 1 with a label 10 will now be described in relation with FIGS. 1 to 6. The product 1 may be a transparent product, such as a watch glass, a glass for a display, a transparent label, etc. It might for example be a sapphire glass.

[0048] On FIG. 2, a relatively thick initial layer 2 of a first material, such as AlN is deposited onto the product 1, for example on the inner side of a watch glass. This initial layer is optional; it improves the adhesion of the following layers onto the substrate. The thickness of the initial layer 2 may be between 20 and 1000 nm.

[0049] On FIG. 3, a stacking with an additional layer 3 of the second material, such as GaN, and a layer 4 of a first material, such as AlN, is deposited onto the initial layer 2.

[0050] The layer 3 of second material, such as GaN, may have a thickness of less than 20 nm, for example between 2 and 8 nm.

[0051] A layer 4 of first material, such as AlN, is then deposited onto the first layer 3. The layer 4 may have a thickness of less than 50 nm, for example between 5 and 15 nm. The layer 4 of first material is thus thinner than the layer 2 of first material.

[0052] Lattice parameter mismatches between the GaN layer 3 and the AlN layer 4 create a local strain at the interface between AlN layer 4 and GaN layer 3, resulting in GaN/AlN quantum nano-structures. Such quantum nano-structures trap free current carriers (i.e. electrons and holes in a semiconductor), hence improving their radiative recombination rates. In particular, the quantum nano-structures absorb UV light and reemit visible light.

[0053] The layers 4 of first material, such as Aluminum Nitride, AlN, may comprise less than or equal 20% of Magnesium, Silicon, Lithium, Berilium, Cadmium and/or Zinc as dopant elements.

[0054] Rare-earth elements with contents of less than or equal 10% may be included into some or all layers of the second material, for increasing the amount of light emitted and/or for controlling its color.

[0055] The second material may be a GaN alloy with less than or equal 50% of Indium, Aluminum, Arsenic and/or Phosphor, for increasing the amount of light emitted and/or for controlling its color.

[0056] Various type of quantum nano-structures may be used within the invention, including quantum wires, quantum wells, and/or quantum dots. 3D nano-structures, such as quantum dots, might be less transparent due to their higher roughness degree, when compared to 2D nano-structures, such as quantum wells. On another hand, 3D nano-structures exhibit higher light emission performances when comparing to 2D nano-structures.

[0057] Therefore, an adequate combination of 3D and 2D nano-structures may present an acceptable trade-off between transparency and light emission performance.

[0058] In one embodiment, the product includes a suitable combination of 2D nano-structures, such as quantum well, and 3D nano-structures, such as quantum dots, for increasing the amount of reemitted light without prejudicing the transparency when no light is reemitted.

[0059] The quantum nano-structures may grow by various methods, such as sputtering, molecular beam epitaxy, atomic layer deposition or metal organic chemical vapour deposition. These processes enable a growth control of the monolayer precision, allowing a precise control of the quantum nano-structure size, and thus a control of the quantum nano-structure emission color, as will be discussed hereafter.

[0060] The method may comprise a step of roughing at least one layer of second material for creating said quantum dots in layers 3 of second material.

[0061] By repeating this process N times, a stack is then created as shown on FIG. 4. The number N of stackings in the stack may be for example between 4 and 100 stackings, each stacking comprising one layer of the first material 4 and one layer of the second material 3. This results in an increased luminosity of the final label 11.

[0062] This stack is transparent under invisible light, but is revealed by photoluminescence under UV illumination.

[0063] We will now describe with FIGS. 5-6 a first embodiment of a process for producing nearly invisible, non reemitting regions.

[0064] In this first embodiment, the layers 2,3,4 of the stack are engraved in order to create a pattern or a logo 11 as shown in FIG. 8. In such a case, difference in the refraction index between the photoluminescent portions 10 and the ambient air creates a partial refraction of the light at the interface, so that the motive would be visible even under normal light conditions.

[0065] In order to reduce this problem, the portions 9 of the mark 12 on which the photoluminescent stack is engraved are filled with a non photoluminescent material 6, as shown on FIG. 6. This material 6 is selected to have a refractive index similar to the one of the stack; similar means here that the refractive index is close to the refractive index of the stack, and in any case much closer than the refractive index of ambient air to the stack.

[0066] The non photoluminescent material 6 may be deposited over the complete surface of the mark 12. In one embodiment, it may cover the photoluminescent portions 10 as well.

[0067] We will now describe with FIGS. 7-8 a second embodiment of a process for producing nearly invisible, non reemitting regions.

[0068] In this second embodiment, as illustrated on FIG. 7, a stack of first and second layers 3,4 is deposited over the whole surface of the mark 12; in this embodiment, the mask 8 could be omitted, although it could be used to define the boundaries of the mark 12, or some pattern within the mark.

[0069] Non photoluminescent portions 9 are then created in this stack by incorporating into the layers ions 7, such as Oxygen, Nitrogen, Hydrogen, Helium, Neon, Argon, Magnesion, Lithium, Beryllium, Bore, Phosphor, Aluminum, Zinc, Arsenic, Galium, Silicon, Cadmium ions, and/or any kind of element capable of degrading the photoluminescent stack. The ions create non-rediative defects into the exposed portions 9, and thus deactivate their photoluminescent ability.

[0070] By carefully selecting the portions 9 of the stack in which the ions are incorporated, it is possible to create a mark 12 with a photoluminescent pattern 11 and non photoluminescent portions 9. The ions may be incorporated through a mask 8.

[0071] Since only a limited number of ions need to be incorporated for this purpose, they don't modify much the refractive index of the exposed portions 9. The boundary between the photoluminescent portions 10 and the non photoluminescent portions 9 is thus entirely invisible.

[0072] The mask 8 may be one-time masks. They may be personalized. Therefore, the pattern 11 may be unique for each product.

[0073] The color, or wavelength, of the light emitted by the GaN/AlN quantum nano-structure depends on several factors in addition to the energy bandgaps of bulk GaN or AlN. First, the energy quantization in such a low-dimensional quantum nano-structure yields an energy transition depending on the quantum nano-structure size, as the smaller the structure the larger the fundamental state energy level. Second, the large polarization mismatch between GaN and AlN results in a huge electric field in GaN/AlN quantum nano-structures, which is about 5 MV/cm. This electric field reduces the effective transition energy in such structures. This is known as the quantum confined Stark effect (QCSE). The strong QCSE induced by the large polarization electrical field results in UV absorbtion by the quantum nano-structure, while visible light is emitted from the ground state of such structure.

[0074] By controlling carefully the quantum nano-structure size, the energy transition, and thus the emitted light, can be tuned over a broad range of colors.

[0075] As previously discussed, another parameter can be used in order to tune the emission color. Indeed, large carrier densities inside the quantum nano-structures may screen the QCSE, which yields a blue-shift emission. This happens under large pump power. Indeed, when varying the UV illumination intensity from low to high, emitted light from the quantum nano-structure shifts to shorter wavelengths, such as from yellow to green or green to blue. This feature is due to the QCSE and is thus a unique property of GaN/AlN quantum nano-structures and, which cannot be replicated using alternate technologies, for example phosphors or rare earth elements, such as, Thulium, Erbium, Europieum or Praseodynium, as the emission color of such materials is set by their intrinsic characteristics.

[0076] Therefore, in one embodiment, a mark 12 is created with quantum nano-structures whose reemitted light color depends on the intensity of UV light, resulting in photoluminescent portions of a variable color which are even more difficult to reproduce.