BACKGROUND OF THE INVENTION
1. Field of the invention
[0001] The present invention relates to a security document, particularly a banknote comprising
an electrochromic element as an electronic security means.
2. Description of the Related Art
[0002] The identification and authentication of security documents, and in particular banknotes
is a long-standing problem. In order to solve this goal, security means for security
documents have been developed and are being developed to allow users and/or machines
to distinguish between genuine and forged security documents and/or to discriminate
among different kind of security documents.
[0004] Although these traditional security means have been derived from sophisticated technological
developments, it must be realised that they are becoming dated and more vulnerable
to technological advances. Therefore, new security means have to be developed.
[0005] For example,
EP-A-1 431 062 discloses a banknote comprising on-board electrical power supply means for driving
a new class of electronic security means utilizing on-board power supply. The electronic
security means are means comprising a microchip, electroluminescent materials, electro-active
polymers/materials, light-emitting diodes and polymeric electronic displays.
[0006] A very similar approach is disclosed in
WO 00/07151.
[0007] The security means as disclosed in
EP-A-1 431 062 and
WO 00/07151 have some very important disadvantages. First of all, it should be noted that the
electrical power supply means and the microchips are widespread. Therefore, such elements
are easily available. On the other hand, if very special chips are produced, these
elements will cause enormous costs. Furthermore, the lifetime of the electric power
supply means, the security means and the security document, especially the banknotes
comprising these elements are limited, respectively.
[0008] The publication
P. M. S. Monk et al. Electrochromic paper: utility of electrochromes incorporated
in paper Electrochimica Acta 46 (2001) 2195 - 2202 teaches that the electrochemistry of electrochromic paper is similar to that of electrochromes
without the paper. An electrochromic paper can be obtained by dispersing an organic
or inorganic electrochrome in a paper. An image is generated when a stylus electrode
touches it, generating an electrochromic image. Possible applications of the electrochromic
paper comprise viable paper products having security implications, such as tickets,
vouchers and banknotes, wherein the electrochromic paper product is merely placed
between two electrodes and a voltage applied. Visual inspection for the formation
of colour confirms (or otherwise disproves) the genuineness of the product.
[0009] However, major drawbacks of an electrochromic paper of that kind comprise the low
contrast achievable; the limited long-term stability of the electrochromic paper because
the electrochrome is directly exposed to the environment and because of the high voltages,
which are needed to operate the electrochromic paper, the comparatively simple structure
making it easy to counterfeit the paper, and the comparatively long time needed for
carrying out a testing cycle, i. e. colouring and bleaching of the electrochromic
image.
SUMMARY OF THE INVENTION
[0010] It is an object of the present invention to provide a security document, particularly
a banknote with a new class of electronic security means for allowing users and/or
machines to distinguish between genuine and counterfeited security documents solving
the problems of the prior art. In particular, it is an object of the present invention
to provide a security feature, which is difficult to counterfeit, which can be applied
on flexible substrates, preferably banknotes, and which can be tested by means of
a simple power supply machine together with an human operator. The security feature
should be thin, preferably thinner than 100 µm, more preferably below 50 µm, and allow
a short testing cycle, preferably shorter than thirty seconds, more preferably shorter
than 10 seconds, especially shorter than 5 seconds. In addition, the security feature
should have high long-term stability and its production should be possible in a simple
and cost efficient way.
[0011] These problems are solved with the features of claim 1. Preferred embodiments of
the invention are described in the dependent claims. The other claims describe particularly
favourable ways of producing and using the security document of the present invention.
[0012] The present invention provides a security document with a new kind of a reversible
security feature
➢ which allows users and/or machines to distinguish between genuine and counterfeited
security documents in a very simple way;
➢ which is very difficult to counterfeit;
➢ which is particularly suitable for security documents requiring a thin and highly
bendable security feature, such as a banknote;
➢ which allows for very short test cycles;
➢ which has a comparatively high contrast;
➢ which makes the use of low voltages possible, so that degradation processes due
to high voltages can be avoided;
➢ which has a very high long-term stability; and
➢ which can be prepared in a comparatively simple and cost efficient way once the
special and sophisticated equipment is on hand.
DETAILED DESCRIPTION OF THE INVENTION
[0013] The following is a detailed description of the present invention. It provides a security
document comprising an electrochromic element and at least two power supply points.
[0014] The term "security document", as used herein, refers to all kind of documents that
contain at least one feature that can be used to prevent counterfeiting by providing
authentication, identification, verification and/or classification of the document.
In particular, they include banknotes, passports, chequebooks, identity cards, credit
cards and/or debit cards, wherein banknotes are especially preferred.
[0015] According to the present invention, the security document comprises an electrochromic
element. Elements of that kind are known in the art and usually contain at least one
electrochromic material. The electrochromic material changes its colour upon oxidation
or reduction reversibly. Preferred classes of electrochromic materials comprise a
pair of redox substances, which form coloured, positively or negatively charged, chemically
reactive free radicals after reduction or oxidation. The pair of redox substances
preferably used is in each case a reducable and oxidizable substance. Both are preferably
colourless or have only a slight colour. Under the action of an electric potential,
one substance is reduced and the other is oxidized, at least one becoming coloured.
For some preferred classes of electrochromic materials in parallel to the electron
injection and extraction, which causes the reversible colour change, an injection
and extraction of positive ions, like protons or Li
+ takes place. Depending on the detailed materials, after switching off the potential,
the two original redox substances can be reformed with their coloration or lightening
of colour occurring.
[0016] Electrochromic substances particularly suitable for the purposes of the present invention
are tungsten oxide, niobium oxide, titanium oxide, iridium oxide, nickel oxide, molybdenum
oxide, antimon-tin oxide, prussian blue, polyaniline, polythiophene, viologene, polypyrrole,
iodide or mixtures of two or more of these materials. Preferred polythiophene compounds
are 3,4 polyethylene dioxythiophene (PEDOT) and poly(3,4-ethylenedioxythiophene-didodecycloxybenzene)
(PEB).
[0017] Furthermore, as mentioned above, the electrochromic element may comprise a second
redox couple, which can be considered as an ion-storage component or as a redox couple
in form of ions, which are comprised in an electrolyte as mentioned above. This second
redox couple may be electrochromic by itself. Therefore, the materials described above
as electrochromic substances may be used. Particularly useful components for a redox
couple in form of ions dissolved in a solvent are iodide/triodide, bromide/tribromide
or fluoride/trifluoride.
[0018] The electrochromic element of the present invention comprises at least two electrodes,
at least one electrolyte and at least one electrochromic material. The electrode is
the area, which conducts the electrons parallel to the substrate from the power supply
points to the different locations of the electrochromic material. In general, it may
be formed of transparent conducting materials, as will be described below, or of non-transparent
materials, like metals. A high conductivity is desired to allow short switching times.
Therefore, the sheet resistance of a square geometry is preferably below 1 kΩ, more
preferably below 100 Ω.
[0019] The term "electrolyte" refers to a substance containing free ions, which behaves
as an electrically conductive medium. It is not limited to ionic solutions, i. e.
ions in solutions, but also comprises ionic liquids (molten electrolytes) and solid
electrolytes. The specific conductivity of the electrolyte at 20°C is preferably greater
than 0.1 mS/cm. The vapour pressure of the electrolyte at 20°C is preferably lower
than 0.1 Pa. In a preferred embodiment, the electrolyte comprises a redox salt, like
lithium iodide, optional together with additional iodide and/or iodine. The solubility
of this redox salt in the electrolyte is preferably at least 0.01 mol/l, more preferably
at least 0.1 mol/l at 25°C.
[0020] Particularly suitable ionic liquids are present in the form of a liquid at 20°C and
preferably have a dynamic viscosity, measured at 20°C at 1 Hz, of 1000 mPas or less.
[0021] In the present invention, the electrodes enclose the electrochromic material and
the electrolyte and protect them from the environment. At least one of the electrodes
preferably has a light transmittance allowing to see through. Its transparency at
550 nm is preferably at least 25 %, more preferably at least 50 % and most preferably
at least 75 %. The transparent electrodes preferably comprise a chemically inert support
material, such as glass or a polymer substrate, which preferably has a thickness not
exceeding 50 µm, more preferably not exceeding 30 µm. The use of polymer foils, such
as PET foils, is particularly preferred in that context.
[0022] Furthermore the electrodes preferably comprise a transparent electronically conducting
layer. Such layers are known in the art. These layers preferably comprise highly doped
metal oxides, such as SnO
2:F, SnO
2:Sb, In
2O
3:Sn (ITO), Cd
2SnO
4, ZnO:Al and ZnO:In.
[0023] In a first particular preferred embodiment of the present invention, the electrochromic
material is dissolved in the electrolyte. A particular suitable example of that kind
is an electrochromic element having the so-called "solution setup", i. e. an electrochromic
element comprising the following layers in the following order:
electrode / electrochromic electrolyte solution / electrode.
[0024] The electrochromic material undergoes an electron-transfer reaction on the surface
of the first electrode, and changes its colour. On the counter electrode, a similar
or different reaction takes place. A preferred example comprises methyl viologen in
water as electrochromic electrolyte solution.
[0025] In a second particular preferred embodiment of the present invention, the electrochromic
element comprises a first electrochromic layer between the first electrode and an
electrolyte layer. A particular suitable example of that kind is an electrochromic
element having the so-called "solution-to-solid setup", i. e. an electrochromic element
comprising the following layers in the following order:
electrode / electrochromic layer / electrolyte / electrode.
[0026] Here, an electrochromic layer is formed during the colouring or bleaching cycle as
a consequence of a redox reaction on the electrolyte-electrode surface (example: heptyl
viologen), or it may be a fixed electrochromic layer, like WO
3, which changes its colour upon electron and ion (e. g. H
+ or Li
+) uptake from the electrolyte. On the counter electrode, a second redox reaction takes
place, which is favourably catalysed by a thin Pt layer.
[0027] In a third particular preferred embodiment of the present invention, the electrochromic
element comprises a first electrochromic layer between the first electrode and an
electrolyte layer and a second electrochromic layer between the electrolyte and the
second electrode. A particular suitable example of that kind is an electrochromic
element having the so-called "battery setup", i. e. an electrochromic element comprising
the following layers in the following order:
electrode / first electrochromic layer / electrolyte / second electrochromic layer
/electrode
[0028] Here, ions (e. g. H
+ and Li
+) are shifted from the first electrochromic layer to the second electrochromic layer
and vice versa, similar to the charging and decharging of a battery.
[0029] The electrochromic layers are again formed during the colouring or bleaching cycle
as a consequence of a redox reaction on the electrolyte-electrode surface, or may
be fixed electrochromic layers, which changes its colour upon electron and ion (e.
g. H
+ or Li
+) uptake from the electrolyte.
[0030] For the purposes of the present invention, the use of the "solution-to-solid setup"
with just one electrochromic layer has proven of particular advantage, since the problem
of precharging the electrochromic device can be avoided. A "battery setup" needs a
method to create a first charge in the device before it can be shifted between the
electrodes. The "solution-to-solid setup" solves this problem, as the charge is present
from the beginning in the electrolyte.
[0031] This problem of precharging is important especially for the application of security
features like banknotes, as here typically there is a long time between two colour
cycles (typically several days up to months). This is in contrast to other applications,
like windows or displays. During such a long time of not being cycled, a charge having
been incorporated before can get lost easily. This is intensified by the special usage
of thin foils as substrates, as these typically show a limited but non avoidable permeability
to water and/or oxygen, which accelerates the self-discharging.
[0032] According to a particularly preferred embodiment of the present invention, the security
document comprises an electrochromic element, in which one electrode is at least partially
coated with an electrochromic material and the other electrode is at least partially
coated with a catalytic layer, and wherein the electrolyte comprises at least one
redox salt. Especially suitable the electrolyte comprises an iodide, bromide or fluoride
and positive ions of the first group of the periodic table of elements, in particular
H
+ or Li
+.
[0033] In the present invention, the outer surface of the electrochromic element is preferably
at least partially covered with a support material. Preferably at least 50 % of the
total outer surface, more preferably at least 75 % of the total outer surface, and
most preferably the entire outer surface are/is covered with a support material. The
support material is not particular restricted and, in principle, can be chosen freely
from papers, polymer foils, e. g. polyethylene terephthalate foils, and similar materials.
However, it has proven of particular advantage to use materials with a low water and
oxygen permeability to increase the long-term stability of the electrochromic element.
The best results are achieved by the use of thin polymer foils having a thickness
of less than 50 µm, preferably less than 25 µm, and comprising a barrier coating on
one side, such as SiO
2 or Al
2O
3 and an additional barrier coating on the other side, which simultaneously acts as
an transparent electrode of the electrochromic cell, such as ITO. Advantageously,
this layer is deposited by sputtering or evaporation, as this leads to good barrier
properties.
[0034] Preferably, the electrochromic element comprises a reflector layer, more preferably
a reflecting electrode, reflecting substrate, a reflecting support or a reflecting
electrolyte. Preferred reflector layers have a white colour and do essentially not
attack the organic substances contacting the reflector layer or disturb the ionic
or electronic conductivity. Particular useful materials are ZnO and TiO
2. These may be printed onto the substrates or dispersed in the electrolyte in form
of small particles with typical sizes of 10 µm down to 10 nm, preferably 1 µm down
to 100 nm. Surprisingly, by using a reflector layer the visibility of the colour change
of the electrochromic element can be further improved.
[0035] For a security feature it is important to make the device as difficult as possible
for counterfeiting. For this aim the following setup is especially advantageous:
Reflecting substrate (e. g. paper) with printed symbols / additional substrate (e.
g. foil) / preferably transparent electrode / first electrochromic layer / electrolyte
with redox agent / catalytic layer / transparent electrode /substrate (e. g. foil)
[0036] The printed symbols may be any symbol, which shows a high resolution, which is difficult
to incorporate in the electrochromic device, e. g. by applying a reflecting electrolyte
or a reflecting electrode.
[0037] In a very preferred embodiment of the present invention, the electrochromic material
and/or the catalytic material is designed as a symbol, for example by using masks
during the deposition process, or by etching processes or by a printing process. This
also makes it more difficult to counterfeit the device.
[0038] Therefore, anybody, who tries to counterfeit the device, has to use a similar setup
as the original, which makes it more difficult.
[0039] According to a very preferred embodiment of the present invention, the electrochromic
element is flexible. Flexibility means that the electrochromic element can be bend
with a radius of curvature of 5 cm, more preferably 1 cm, most preferably 0.5 cm.
The radius is measured according to the "simple support ends" method, top part of
fig. 5, in "
A mechanical assessment of flexible optoelectronic devices", Zhong Chen, Braina Cotterell,
Wei Wang, Ewald Guenther, Soo-Jin Chua, Thin Solid Films vol. 394, pages 202-206 of
the year 2001.
[0040] In addition, the electrochromic element preferably comprises a bend protection. Bend
protection means that the security document, especially a banknote can be bended without
destroying the electrochromic element. A bend protection can be achieved by a stable
metal frame surrounding the electrochromic element or a metal sheet below the element.
Furthermore, the bend protection may be achieved by producing a electrochromic element
having a small dimension. Preferably, the maximum dimension of the electrochromic
element does not exceed 3 cm.
[0041] The switching time of the coloration of the electrochromic element, i. e. the time
needed to switch the electrochromic element from the bleached state to the coloured
state is preferably short. The switching time of the electrochromic element is preferably
below thirty seconds, more preferably below 10 seconds and most preferably below 5
seconds. The switching time is defined as follows: For the colouring process, the
security document is connected to a power source with voltages below 3V, wherein the
use of 1.5V is particularly preferred. Then the change in the visual reflectance is
measured. The "switching time" is defined here to be the time, in which 63% of the
total change of the visual reflectance is reached.
[0042] In the present invention, the switching time of the electrochromic element can be
further improved by using an assembly, wherein in a top view at least one of the electrodes,
and more preferably both electrodes, has (have) a greater surface than the electrochromic
layer. This special geometry reduces the effective resistance and in consequence,
the switching time. One should note that for electrochromic layers, the charge and
in consequence for a determined switching time the current is proportional to the
area of the electrochromic layer. As the current defines the ohmic voltage losses,
and the voltage is limited for keeping the device stable, a small area of the electrochromic
layer is helpful for a limitation of the voltage. This may be achieved by a simple
circle of the electrochromic layer, surrounded by a larger area of the electrode,
or by structuring the electrochromic area in form of a symbol, which reduces the effective
area, but which keeps the symbol large in its diameter and therefore keeps it clearly
visible for a human observer.
Preferably, the surface of at least one electrode, more preferably of both electrodes
is at least 25% greater than, more preferably at least 50% greater than, even more
preferably at least 100% greater than and most preferably at least 200% greater than
the surface of the electrochromic layer in the top view. Thereby a ratio of electrode
surface : electrochromic layer surface in the range of 2:1 to 20:1 has proven of particular
advantage.
[0043] The quality of the security document can be further improved by using two or even
more electrochromic elements. Thereby the electrochromic elements preferably have
different switching times to make counterfeiting even more difficult.
[0044] The bleaching time of the electrochromic element, i. e. the time needed to switch
the electrochromic element from the coloured state to the bleached state is preferably
short. The bleaching time of the electrochromic element is preferably below thirty
seconds, more preferably below 10 seconds and most preferably below 5 seconds. The
switching time for the bleaching process is defined as the time, in which 63% of the
total change of the visual reflectance is reached after switching of the illumination.
[0045] The bleaching and/or the coloration time can be adjusted by the use of catalysts
accelerating the reaction kinetics. Useful catalysts are Pt, Pd, Ni, Au, Os, Re, Ir,
Ru, and Rh. The catalyst can be arranged as a separate layer, for example, onto a
layer, which comprises an electrochromic material, or onto a transparent electronically
conducting layer. If these layers are made in such a way, that they are porous, the
catalyst can also be arranged below these layers. Furthermore, the catalyst can be
arranged as an additive in the electrolyte.
[0047] According to the present invention, the security document comprises at least two
power supply points each electronically connected to the electrochromic element, but
electronically isolated from each other. The present invention distinguishes between
two kinds of charge transport: charge transport by electrons and by ions. The first
shall be referred as "electronical" and the second as "ionical". The term "electronical
connection" refers to a connection via a material preferably having a resistivity
ρ of less than 10
-1 Ω · cm, very preferably of less than 5*10
-3 Ω · cm, when measured at 25°C. By the way of contrast, two articles will be "electronically
isolated one from another" if there is no electronical connection between the articles,
in particular via a material having a resistivity ρ of less than 10
2 Ω · cm, when measured at 25°C.
[0048] In principle, there are no particular restrictions on the material of the power supply
points used in the present invention. However, they preferably comprise an electrically
conductive material preferably having a resistivity ρ of less than 10
-1 Ω · cm, very preferably of less than 10
-3 Ω · cm, when measured at 25°C.
[0049] Particular suitable materials are metals, such as silver, gold, aluminium, messing,
iron, chromium, and stainless steel.
[0050] The surfaces of the power supply points are preferably left exposed to the environment.
In such circumstances, it will be apparent to those skilled in the art that materials
will be preferably chosen that suffer minimal tarnishing or corrosion during everyday
use of the secure document.
[0051] The power supply points are each electronically connected to the electrochromic element,
preferably via one or more electronically conducting tracks. Thereby the electronically
conducting tracks can be made of any electronically conducting material, but preferably
have a resistivity ρ of less than 10
-1 Ω · cm, very preferably of less than 5* 10
-3 Ω · cm, when measured at 25°C.
[0052] For preferred embodiments, a sealing is added, which encloses an inner area, which
comprises electrolyte, electrochromic material, and not wholly the electrodes. In
these embodiments, the power supply points are preferably outside of this inner area,
and the electrodes electronically connect the power supply points optionally via additional
electronically conducting tracks with the inner area. In particularly preferred cases,
the sealing is applied by a thermal step, like welding of the supporting material
or application of a hot melt, which does not destroy the conductivity of the electrodes,
especially the electronical contact from the inner area to outside of the inner area.
[0053] The security document of the present invention is preferably adapted for checking
its authenticity by electronically connecting the power supply points to a power source
and observing a status change of the electrochromic element, preferably a change in
the optical status.
[0054] The positions of the power supply points and of the electrochromic element on the
security document can principally be chosen freely. It is merely important that the
power supply points are electronically isolated from each other and that they are
electronically connected to the electrochromic element so that a reversible status
change of the electrochromic can be induced by connecting the power supply points
to a power source.
[0055] However, the electrochromic element is preferably located nearby a color reference
to ease the visibility of a correct color change of the electrochromic element. Such
color reference may comprise different tints, which the electrochromic element passes
through.
[0056] The kind of the substrate means used in the present invention is not critical. However
the use of substrate means comprising paper, plastic, polymer, elemental metallic
foils, metallic alloy foils and/or synthetic paper is preferred.
[0057] The security document of the present invention is comparatively thin and its thickness
is preferably smaller than 100 µm. In one especially preferred embodiment, the overall
thickness of the power supply points, not including the substrate thickness, is between
approximately 10 to 50 µm. The thickness of the interconnects between the power source
and the electrochromic element is preferably within the range from approximately 1
to 30 µm. The thickness of the electrochromic element, not including the substrate
means is preferably in the range from 10 to 100 µm.
[0058] Preferred methods for the production of a security document of the present invention
are described in the following sections. The substrate means is preferably provided
with the power supply points and the electrochromic element, wherein the power supply
points and the interconnects are preferably printed onto the substrate and the complete
electrochromic element is preferably subsequently attached to the substrate. In this
case, electronical connection will be made by ensuring that exposed printed power
supply points on the substrate align with power supply points on the electrochromic
element. Alternatively, the power supply points, optionally the interconnects, and
the electrochromic element is preferably arranged together in one element, which is
then attached to the substrate means.
[0059] In a specific embodiment of the present invention, the conducting tracks and/or the
power supply points are deposited onto the substrate using an electroless deposition
technique. In this technique, specially formulated catalytic ink is printed onto the
substrate in a desired pattern. The substrate is then immersed in a chemical solution
containing ions of the metal to be deposited. Over time, electroless deposition of
the metal onto the substrate areas printed with catalytic ink occurs. This technique
is advantageous compared to other methods for producing the desired electrically conducting
tracks and the power supply points, such as printing of metal-loaded inks, since the
technique produces deposited material with a density that is very close to that of
the bulk material. Furthermore, this technique is advantageous over standard printing
of loaded inks in that the adhesion of the deposited material to the substrate is
superior. The aforementioned electroless deposition technique is described in detail
in Patent Application
WO 02/099163 and is suitable for a range of substrates (such as polyester, polypropylene, synthetic
paper, fine-weave cloths and polycarbonate) and a range of deposited metals (including
copper, nickel, cobalt, iron, tin and a variety of magnetic and non-magnetic alloys).
However, the present invention does not preclude other methods of depositing electrically
conducting materials. Other methods include printing (such as screen printing and
gravure printing) of particle-loaded inks, electroplating methods, chemical vapour
deposition, sputtering, evaporation and etch-resist methods, all of which are known
to those skilled in the art.
[0060] The manufacture of the electrochromic element can be achieved in a conventional manner.
The electrochromic layer, the preferably transparent conducting layer, the metallic
conducting layers, and/or the catalytic layer are preferably prepared by deposition
techniques, more preferably by physical vapour deposition (PVD), which includes magnetron
sputtering and evaporation. Here, masks can be used to allow the preparation of specific
shapes, area ratios and symbols.
[0061] At the end, the space between the electrodes is preferably filled with the electrolyte
and the electrochromic element is sealed to avoid leakage, evaporation or impurification
of the components. Said sealing is preferably achieved by encapsulating the electrolyte,
the electrochromic material and part of the electrodes in a suitable support material,
such as a polymeric film or a flexible glass foil, wherein the support material preferably
has high oxygen and/or water barrier properties. The sealing is preferably achieved
by a heating step, preferably by welding the electrodes together, wherein the electronically
conducting layer is preferably not destroyed.
[0062] In a particularly preferred embodiment of the present invention, at least two electrodes
each comprising a support layer, preferably a PET foil, and an electronically conducting
layer, preferably an ITO-layer, are placed in front of each other in a way, that the
electronically conducting layers look at each other. At least one of these electronically
conducting layers is provided with an electrochromic layer. Thereafter, an electrolyte,
preferably comprising a redox couple, is applied onto one of the electronically conducting
layers, for example by printing or means of a microdispenser. Then, the other electrode
is applied onto this, followed by an application of a sealing, for example by using
a hot melt or melting the substrates together.
[0063] Surprisingly, it was found, that the conductivity of the electronically conducting
layer is not destroyed by heating up the support during the sealing process. Both
approaches, to seal the device with a hotmelt or by melting the foils, require a heating
step of the foil. As the device has to be contacted from outside of the sealing, an
electrode has to be lead through the sealing. It was found that a too long time of
heating up the foil during the sealing process or a too high temperature destroy the
conductivity of the electronically conducting, especially the ITO-layer, whereas a
too short time or a too low temperature does not lead to a tight sealing. Preferred
values for the temperature were in the range of 200°C up to 300°C and preferred times
in the range of 1sec up to 10 sec.
[0064] On the other hand it was found, that by melting two support foils coated with an
electronically conducting layer together, a electronically conducting connection can
be produced from the one electronically conducting layer on the first support foil
to the other electronically conducting layer on the second support foil.
[0065] For checking authenticity of the security document of the present invention, the
power supply points are electrically connected to a power source and a status change
of the electrochromic element is observed. Thereby a voltage below 3V, more preferably
below 1.5V, is preferably used. The quality of verification can be further increased
by simultaneously measuring optical and electrical properties of the electrochromic
element and/or by measuring changes of optical and/or electrical properties of the
electrochromic element with time.
[0066] The accompanying drawings show particularly preferred embodiments of the present
invention for the purpose of further illustrating the present invention; it being
understood that the invention is not limited to the precise arrangements shown.
[0067] FIG. 1 shows a schematic top view of a first particularly preferred electrochromic
element, which has been opened in the middle. The element comprises a first and a
second electrode comprising a first and a second support layer (1, 3), e. g. a PET
foil, on top of which a first and a second electronically conducting layer (5, 7),
e. g. ITO, are located. Each of the electrodes also comprises a power supply point
(11, 13).
[0068] The electrodes are mechanically connected to each other by a sealing (19). Said sealing
(19) can be achieved by the use of a suitable sealing material, such as an inert polymer
material, or by welding together the different layers of the electrochromic element.
[0069] The sealing (19) encloses an inner area (21) which is preferably filled with an electrolyte.
This electrolyte preferably contains a redox couple, e.g. iodide and triodide. The
inner area of the first electrode comprises an image made of electrochromic material
(9), e.g. tungsten oxide, which is placed on top of the first electronically conducting
layer (5) and only covers a small area of the first electrically conducting layer
(5) in order to ensure a comparatively short switching time. The inner area of the
second electrode, i. e. the area of the second electrode, which is enclosed by the
sealing (19), partially comprises the second electronically conducting layer, which
is at least partially covered with a catalytic layer (17), such as Pt.
[0070] In a closed state, both electronically conducting layers (5, 7) extend to opposite
directions and merely overlap in the middle, i. e. the inner area of the second electrode.
The design avoids carefully that there are locations, where first and second electrode
and sealing fall together, as this should lead to short circuits. Both power supply
points (11, 13) are easily accessible, since they are not covered neither by the opposite
electrode (7, 5) nor by the opposite substrate layer (3, 1). In addition, the second
electrode (7) and the second substrate layer (3) comprise a hole (15) at the location
of the second power supply point (13), so that the second power supply point (13)
is also easily accessible from the same side as the first power supply point (11).
[0071] FIG. 2 shows a schematic top view of a second particularly preferred electrochromic
element, which has been opened in the middle. The element comprises a first and a
second electrode comprising a first and a second support layer (101, 103), e. g. a
PET foil, on top of which a first and a second electronically conducting layer (105,
107), e. g. ITO, are located. In addition, the first substrate layer (101) comprises
an extension of the second electrode (106), which is electronically connected to the
second electrode (107) via a welding (120) and which is electronically isolated from
the first electrode (105).
[0072] The first electrode and the extension of the second electrode (106) each comprise
a power supply point (111, 113). The electrodes are mechanically connected to each
other by a sealing (119). Said sealing (119) can be achieved by the use of a suitable
sealing material, such as an inert polymer material, or by welding together the different
layers of the electrochromic element.
[0073] The sealing (119) encloses an inner area (121), which is preferably filled with an
electrolyte. This electrolyte preferably contains a redox couple, e.g. iodide and
triodide. The inner area of the first electrode comprises an image made of electrochromic
material (109), e.g. tungsten oxide, which is placed on top of the first electronically
conducting layer (105) and only covers a small area of the first electronically conducting
layer (105) in order to ensure a comparatively short switching time. The inner area
of the second electrode, i. e. the area of the second electrode, which is enclosed
by the sealing (119), partially comprises the second electronically conducting layer
(107), which is at least partially covered with a catalytic layer (117), such as Pt.
[0074] In a closed state, both electronically conducting layers (105, 107) extend to opposite
directions and merely overlap in the middle, i. e. the inner area of the second electrode.
Again, the design avoids carefully that there are locations, where first (105) and
second electronically conducting layer (107) and sealing (119) fall together, as this
should lead to short circuits. The second power supply point (113) is connected to
the second electrode (107) via an additional melting step, for example by melting
the two substrate layers together in form of a ring (120). Here, the same technology
can be applied as for the sealing ring (119). Both power supply points (111, 113)
are easily accessible from the top, since they are not covered neither by the opposite
electrode (107) nor by the second substrate layer (103).
1. Security document comprising substrate means, an electrochromic element and at least
two power supply points each electronically connected to the electrochromic element,
but electronically isolated from each other, characterized in that the electrochromic element comprises at least two electrodes, at least one electrolyte
and at least one electrochromic material, wherein the electrolyte and the electrochromic
material are enclosed by the electrodes.
2. Security document according to claim 1, wherein the security document is a banknote.
3. Security document according to claim 1 or 2, wherein the electrochromic material comprises
tungsten oxide, niobium oxide, titanium oxide, iridium oxide, nickel oxide, molybdenum
oxide, antimon-tin oxide, prussian blue, polyaniline, polythiophene, viologene, polypyrrole,
iodide or mixtures of two or more of these materials.
4. Security document at least one of the preceding claims, wherein the electrochromic
material is dissolved in the electrolyte.
5. Security document at least one of the preceding claims, wherein the electrochromic
element comprises a first electrochromic layer between the first electrode and an
electrolyte layer.
6. Security document according to claim 5, wherein the electrochromic element additionally
comprises a second electrochromic layer between the electrolyte layer and the second
electrode.
7. Security document according to at least one of the preceding claims, wherein at least
one of the electrodes is transparent.
8. Security document according to claim 7, wherein one electrode is transparent and the
other electrode is reflecting.
9. Security document according to at least one of the preceding claims, wherein the electrolyte
comprises an ionic liquid.
10. Security document at least one of the preceding claims, wherein the electrolyte has
a specific conductivity of greater than 0.1 mS/cm at 20°C.
11. Security document according to at least one of the preceding claims, wherein the vapour
pressure of the electrolyte at 20°C is lower than 0.1 Pa.
12. Security document according to at least one of the preceding claims, wherein the electrolyte
comprises a reflecting material.
13. Security document according to at least one of the preceding claims, wherein the electrochromic
element has a solution-to-solid-setup.
14. Security document according to at least one of the preceding claims, wherein one electrode
is at least partially coated with an electrochromic material and the other electrode
is at least partially coated with a catalytic layer, and wherein the electrolyte comprises
at least one redox salt.
15. Security document according to claim 14, wherein the electrolyte comprises an iodide,
bromide or fluoride and positive ions of the first group of the periodic table of
elements.
16. Security document according to claim 15, wherein the positive ions comprise H+ or Li+.
17. Security document according to at least one of the preceding claims, wherein the outer
surface of the electrochromic element is at least partially covered with a water and/or
oxygen barrier coating.
18. Security document according to at least one of the preceding claims, wherein the switching
time of the electrochromic element is below 30 seconds.
19. Security document according to at least one of the preceding claims, wherein the electrochromic
element comprises at least one electrochromic layer and wherein in a top view at least
one of the electrodes has an at least 25% greater surface than the electrochromic
layer.
20. Security document according to claim 19, wherein in a top view both electrodes have
an at least 25% greater surface than the electrochromic layer.
21. Security document according to at least one of the preceding claims, wherein the electrodes
are not electronically connected to each other.
22. Security document according to at least one of the preceding claims, wherein the security
document comprises at least two electrochromic elements.
23. Security document according to claim 22, wherein the electrochromic elements have
different switching times and/or colours.
24. Security document according to at least one of the preceding claims, wherein the electrochromic
element is flexible.
25. Security document according to at least one of the preceding claims, wherein the electrochromic
element comprises a bend protection.
26. Security document according to at least one of the preceding claims, wherein the maximum
length of the electrochromic element does not exceed 3 cm.
27. Security document according to at least one of the preceding claims, wherein the power
supply points comprise an electronically conductive material.
28. Security document according to claim 27, wherein the electronically conductive material
is selected from the group consisting of electronically conductive metals, electronically
conductive metal alloys and electronically conductive polymers.
29. Security document according to at least one of the preceding claims, wherein the power
supply points exhibit resistance to oxidation and/or tarnishing from exposure to the
atmospheric environment.
30. Security document according to at least one of the preceding claims, wherein the substrate
means comprises paper, plastic, polymer, elemental metallic foils, metallic alloy
foils and/or synthetic paper.
31. Security document according to at least one of the preceding claims, wherein its thickness
is smaller than 100 µm.
32. Security document according to at least one of the preceding claims, wherein, the
electrochromic element comprises a sealing, which encloses the electrochromic material,
the electrolyte and partially, but not fully each of the electrodes.
33. Security document according to at least one of the preceding claims, wherein the security
document is adapted for checking its authenticity by electrically connecting the power
supply points to a power source and observing a status change of the electrochromic
element.
34. Method for the production of a security document according to at least one of the
preceding claims, wherein the power supply points and the electrochromic element are
provided on the substrate means.
35. Method according to claim 34, wherein the power supply points are printed onto the
substrate means.
36. Method according to claim 34 or 35, wherein the power supply points are deposited
onto the substrate means by using electroless deposition, sputtering and/or vacuum
deposition.
37. Method according to at least one of the claims 34 to 36, wherein the electrochromic
element is provided before or after the provision of the power supply points.
38. Method according to at least one of the claims 34 to 37, wherein a sealing is applied,
which encloses the electrochromic material, the electrolyte and partially, but not
fully each of the electrodes, wherein the electronically conducting layer of the electrodes
are not destroyed.
39. Use of a security document according to at least one of the claims 1 to 33 for checking
its authenticity, wherein the power supply points are electrically connected to a
power source and a status change of the electrochromic element is observed.
40. Use according to claim 38, characterized in that optical and electrical properties of the electrochromic element are measured simultaneously.
41. Use according to claim 37, characterized in that changes of optical and/or electrical properties of the electrochromic element are
measured with time.