Patent Application
20230220540
The invention relates to methods and devices for applying a layer to a body, and to a coated body. In particular, the invention relates to coatings that are generated by cathode sputtering.
It is known to provide bodies or parts of bodies with a surface coating in order to improve their mechanical or chemical properties. In particular for tools and components which are subject to wear, it is known to provide functional surfaces with coatings. In particular, hard substance layers are known as coatings.
To form thin coatings, in addition to CVD methods, particularly PVD coating methods are known, in particular the methods of cathode sputtering.
WO 2014/063676 A1 describes a component with a coating made of chromium, nitrogen, and carbon, which is applied in a PVD method with cathodic arc evaporation. In a vacuum chamber, a noble gas is introduced and ion etching initially is performed, using a bias voltage of −800 to −1200 V. The bias voltage is then set to a low value and a layer is applied. Argon can be used as the noble gas, or neon, which leads to lower internal stress than embedded argon.
WO 2013/045454 A2 describes a method and a device for coating substrates. Magnetron cathodes with sputtering targets are disposed in a vacuum chamber. Some of the cathodes are HIPIMS cathodes, i.e., they are operated with electrical power in the form of voltage pulses by means of an HIPIMS power supply. A bias voltage is applied to the substrates to be coated, which voltage has, in preferred embodiments, pulses which are synchronized with the voltage pulses at a cathode such that they are applied during at least a part of a period which is characterized by a high number of metal ions which are generated by the HIPIMS pulse at the cathode. Compared to pulses that are applied for longer or a continuous DC bias, lower amounts of the process gas, for example argon, are thus embedded in the layer.
US 2008/0135401 A1 describes a device for sputtering a target with a current density on a magnetron cathode between 0.1 and 10 A/cm2 in order to generate a coating on a substrate. The device comprises a power supply which is connected to the magnetron and a capacitor which is connected to the power supply. A first switch connects the power supply to the magnetron in order to charge the magnetron in coordination with a first pulse. A bias device is connected to the substrate to preset a substrate bias. A bias can be applied, for example, as RF power in a pulsed mode and synchronized with HIPIMS pulses. A synchronization device synchronizes a frequency and a temporal delay of the first pulse.
EP 3 457 428 A1 describes a method and a device for processing semiconductor substrates. A pulse synchronization controller is connected between a pulse RF bias generator and an HIPIMS generator. A first timing signal is sent from the pulse synchronization controller to the pulse RF bias generator and to the HIPIMS generator. A sputtering target and an RF electrode on a substrate carrier are energized based on the first timing signal and de-energized at the end of the timing signal. A second timing signal is sent from the pulse synchronization controller to the pulse RF bias generator and the electrode is energized and de-energized without the target being energized based on the second timing signal.
It can be regarded as an object to propose a method and a device for applying a layer to a body, and a coated body, with which particularly favorable layer properties can be achieved in a controlled way.
The object is solved by a method according to claim 1, a device according to claim 15, and a coated body according to claim 16. Dependent claims refer to advantageous embodiments of the invention.
The inventors started from the consideration that, when generating layers by means of cathode sputtering while applying pulsed voltages to the cathode, the layer composition can be predetermined differently by the temporal curve of the bias voltage. Depending on whether the bias voltage is applied as a DC voltage or pulsed voltage, and in the case of a pulsed voltage as a function of the temporal synchronization with the pulses at the cathode, the components prevailing in the plasma at different points in time can be selected in a controlled way and used to form the layer. In particular when the temporal curve of the gas ions present in the plasma differs from that of the metal ions, as in the HIPIMS method, the proportion of the gas ions relative to the metal ions can thus be set in a controlled way by the time course of the bias voltage.
In contrast to the known teaching of achieving a desired composition of the layer by a suitable time course of the bias voltage which stays the same over the coating duration, the inventors propose achieving different compositions of the layer over the layer thickness in a controlled way through variation of the time course of the bias voltage during the coating duration. This is because, contrary to the previous understanding that gas ions in the layer are generally undesired and must always be minimized, the inventors have recognized that—depending on the desired application of the body, the layer structure, the general layer properties, the type of substrate, etc. —a proportion of gas ions in certain regions of the layer, for example, depending on the present case on the layer surface, in the interface region, or in the middle regions of the layer, can in fact be advantageous, as long as the proportion varies over the layer thickness and can be set in a controlled way.
The gas ions under consideration are primarily ions of noble gases used as the process gas in the vacuum chamber, in particular argon.
Thus, it has been shown that at comparably high proportions of argon, layers can be achieved with very high hardness and high internal stress, i.e., hard and brittle layers, while layers without argon or with a lower proportion are rather ductile in comparison.
Surprisingly, it has been shown that for some applications, for example hard machining, layers that have high internal stress at least on the layer surface achieve particularly good results, for example high cutting performance. On the other hand, layer proportions that are rather ductile due to a lower proportion of argon have very favorable properties, for example in the interface region, e.g., for achieving good adhesion to the substrate or—depending on the intended use of the body, for example as a tool—also in the region of the layer surface, for example with regard to tribological properties or for run-in behav-ior.
To enable a controlled setting of the desired layer formation and the properties resulting from this, the method according to the invention for applying a layer to a body provides that the body is arranged in a vacuum chamber and, by supplying a process gas, for example a noble gas, preferably argon, a plasma is generated by operating one or more cathodes, and at least one target is sputtered. The cathodes are preferably magnetron cathodes, in particular unbalanced magnetrons, which are provided with targets made of a target material, preferably of one or more metals, which material is sputtered so that the plasma comprises gas ions and metal ions (magnetron sputtering).
According to the invention, at least one cathode is operated not with constant voltage, but by a pulsed cathode voltage which has temporally spaced cathode pulses. Preferably, one or more cathodes are operated according to the HIPIMS method (high power impulse magnetron sputtering), in which short cathode pulses with high voltage are applied and very high peak powers are achieved. The HIPIMS method is understood here to mean, in particular, operating within the parameter regions mentioned below as part of possible exemplary embodiments.
During at least a part of the coating duration, a bias voltage is applied to the body to be coated so that charge carriers of the plasma are accelerated into the direction of the body and attached to its surface as a layer. The method according to the invention is characterized in that the time course of the bias voltage varies during the coating duration.
The time course of the bias voltage can be—in the case of a DC voltage—at least in sections a constant time course or a variable time course, in particular a pulsed time course. Variation of the time course during the coating duration can be understood as any change, i.e., for example switching from DC voltage to a voltage with a temporally variable time course, in particular a pulsed voltage, or in the case of a continuously temporally varying, periodic time course, a change in frequency or phase position. In particular, a possible variation of the time course comprises a temporal synchronization with the cathode pulses that is different at various points in time or intervals during the coating duration. As explained, the composition of the layer can be influenced by the time course of the bias voltage: While, for example, at constant bias voltage (DC) all ions of the plasma are accelerated uniformly into the direction toward the body, by a pulsed bias voltage, the bias pulses of which are temporally synchronized with the cathode pulses, i.e., are applied with the same frequency and a fixed phase relationship, the species of ions present in the plasma at the selected point in time can each be selected and accelerated into the direction of the item by the duration and temporal position of the pulse.
Accordingly, a bias voltage with a time course that is variable during the coating duration can have a pulsed curve in sections or throughout, wherein the synchronization with the cathode pulses can vary over the coating duration. Likewise, the time course of the bias voltage can be a DC voltage curve in one or more temporal sections, while in other sections a pulsed time course can be applied.
Preferably, the time course of the bias voltage is pulsed at least during a part of the coating duration, i.e., the bias voltage comprises bias pulses which are synchronized with the cathode pulses, i.e., are applied with the same (or respectively, alternatively a multiple of the) frequency and a fixed phase relationship. The pulses are preferably DC voltage pulses, i.e., an at least basically constant bias voltage is preferably applied during the pulse duration. The time, relative to the cathode pulses, at which the bias pulses are effective can thus be characterized by the respective pulse duration and by the temporal position relative to the cathode pulses (i.e., the time difference of the respective beginning of the pulse before or respectively after the beginning of a cathode pulse, wherein the time difference can also potentially be zero). The variation according to the invention of the time course of the bias voltage during the coating duration can then comprise one or both of the following changes:
In each case, due to the variation of the time course of the bias voltage, different conditions for the layer growth result during different points in time or intervals during the coating duration so that, as the layer grown progresses, layers are obtained whose structure and/or composition varies over the layer thickness. It is thus possible to achieve specially suitable properties, for example good adhesion to the substrate, a hard or smooth surface, etc., in various regions of the layer.
The device according to the invention is suitable for carrying out the method according to the invention. It comprises a vacuum chamber with a carrier for the body, a process gas supply and a cathode with a target. The cathode is connected to a cathode power supply, and the body or respectively its carrier is connected to a controllable bias power supply. The cathode voltage with the cathode pulses is generated by means of the cathode power supply, preferably an HIPIMS power supply, and a bias voltage is generated by means of the bias power supply. A controller is provided here, with which the bias power supply can be controlled such that the time course of the bias voltage varies during the coating duration.
The controller can be in particular a programmable controller, with which, preferably in addition to the bias power supply, other functions of the coating device can also be controlled according to a coating program in a time-dependent manner, in particular electrical power supplies of various cathodes and the supply of process and/or reactive gases.
The coated body according to the invention can be produced, for example, by means of the method according to the invention and/or the device according to the invention. The body comprises a substrate which can be, for example, a base body made, for example, of steel, in particular HSS or CrMo steel, carbide, ceramic material or cBN (cubic boron nitride). The substrate can be, for example, a tool, in particular for machining, such as a drill, a milling cutter, an indexable insert, a punching or stamping tool, etc.
A layer made of a layer material applied by means of cathode sputtering is disposed on the surface of the substrate. The layer material according to the invention comprises at least one element from a first group comprising aluminum (Al), silicon (Si), yttrium (Y), and elements of groups 4-6 of the period table according to IUPAC (1988) and at least one element from a second group comprising nitrogen (N), oxygen (O), carbon (C), and boron (B). The selection of elements of the first and second group can be referred to as a material system. Preferred material systems comprise primarily nitrogen as well as one or more elements of the first group, in particular titanium (Ti), aluminum (Al), silicon (Si), and/or chromium (Cr). Material systems are shown here by naming the respective elements with hyphens, i.e., without indicating the chemical bonds. Particularly prefer-able layer systems are aluminum-titanium-nitride (Al—Ti—N), titanium-nitride (Ti—N), ti-tanium-aluminum-silicon-nitride (Ti—Al—Si—N), titanium-aluminum-chromium-silicon-nitride (Ti—Al—Cr—Si—N), titanium-boride (TiB2), titanium-carbonitride (Ti—C—N), titanium-aluminum-carbonitride (Al—Ti—C—N), chromium-nitride (Cr—N), zirconium-nitride (Zr—N), and titanium-carbide (Ti—C). It is preferred that the indicated elements of each material system are listed in the order of their relative atomic amounts.
The layer material also comprises proportions of a noble gas, preferably argon. Here, in the body according to the invention, the concentration of the noble gas in the layer varies over the layer thickness, i.e., different concentrations of the noble gas within the layer result at different locations of the layer, depending on the distance of each considered location of the layer from the layer surface or respectively the substrate.
The noble gas is the process gas used when applying the layer by means of cathode sputtering, preferably argon. As described above, controlling the proportion of the process gas in the layer is possible in particular through suitable selection of the time course of the bias voltage, so that the desired concentration profile can be set in a controlled way over the layer thickness.
Advantageous developments of the method according to the invention relate in particular to the type of variation of the time course of the bias voltage. Advantageously, as explained, it can be achieved by suitable application that the proportion of the process gas in the layer is dependent on the time course of the bias voltage. By variation of the time course during the coating duration, the desired proportion of process gas in the layer varying over the layer thickness can be achieved in this way.
As part of the method according to the invention, the device according to the invention, and the coated body according to the invention, various embodiments are possible. Thus, the bias voltage preferably has a pulse-shaped time course at least during a first time interval within the coating duration, i.e., it comprises voltage pulses which are referred to here as “bias pulses,”. The bias pulses are preferably synchronized with the cathode pulses, i.e., have the same frequency (or alternatively one of the frequencies is a multiple of the other frequency, which also represents a synchronization). While a synchronization is also possible in which bias pulses and cathode pulses always begin at the same time, and a lead-in time of the bias pulses is also possible, the bias pulses preferably occur delayed with respect to the cathode pulses by a delay time, i.e., their beginning is temporally after the beginning of the cathode pulses. The delay time can be, for example, in the range of 5-150 μs and is chosen according to the ions preferred in each case. The duration of the bias pulses is, for example in the range of 30-150 μs, preferably 50-100 μs.
During a further time interval, which can be temporally before or after the first time interval during the coating duration, possibly also with a temporal distance between them, the bias voltage then preferably has a time course deviating from the first time interval. This can be, for example, a pulse curve as in the first time interval, but with a deviating phase relationship, in particular a deviating delay time. Likewise, the deviating time course in the further time interval can also be a constant DC voltage (DC bias). By a DC bias voltage, all ions of the plasma are accelerated into the direction toward the substrate without exception and a coating with a relatively high proportion of process gas is formed, compared with a pulsed bias voltage in which, by suitable synchronization with the cathode pulses, a selective selection of ions is possible, so that, for example, a higher proportion of metal ions can be selected in a controlled way.
According to an advantageous embodiment, the time course of the bias voltage during the first time interval comprises bias pulses which are synchronized with the cathode pulses, and occur delayed with respect to the cathode pulses by a first delay time, and during a second time interval bias pulses which are also synchronized with the cathode pulses, but in this case occur delayed with respect to the cathode pulses by a second delay time deviating from the first. The second time interval here is preferably temporally after the first time interval and can either temporally directly follow it or a temporal distance between the time intervals can exist. The first time interval can be at the beginning of the coating duration.
The time intervals can be short, for example, a few minutes, or longer, up to multiple hours. For example, the duration of the first and/or the second time interval can be chosen so that, during it, the layer grows by a low amount of, for example, 0.1 μm, but embodiments are also possible in which the layer grows by up to 3 μm during the first and/or second time interval. To achieve individual layers in the layer with a layer thickness in the nano range, meaning, for example, 5-100 nm, preferably 5-50 nm, the time intervals can be chosen to be very short, for example 20-360, preferably 20-180 sec-onds. To achieve individual layers in the micro range, meaning, for example, from 0.5-10 μm, preferably 0.5-2 μm, the time intervals can be chosen, for example, in the range from 50-1200 minutes, preferably 50-360 minutes.
For example, one of the delay times can be in a range in which a relatively high proportion of metal ions and, relative to that, lower proportion of gas ions is present in the plasma, for example 30-80 μs, while the other delay time can be chosen so that a relatively high proportion of gas ions is present in the plasma, for example 0-20 its or more than 90 μs. For example, the delay time in the first time interval, which is temporally earlier within the coating duration, can be shorter so that a larger proportion of metal ions is used to form the layer, while the delay time in the second time interval, which is temporally later within the coating duration, is longer so that a higher proportion of gas ions is integrated into the layer.
Preferably, synchronized bias pulses with delay times with respect to the cathode pulses are thus generated during at least one time section or during the entire coating duration, wherein the delay times vary. The variation of the delay times can take place abruptly in steps or also (somewhat) continuously.
To form a transition layer with a gradual change of the layer properties, the variation of the delay times during a transition time interval, which can comprise a section or the entire coating duration, can take place, for example, in steps or continuously from a first value to a second value, wherein the first value is higher or lower than the first value. The course can be, for example, linear in the form of a ramp, but likewise, deviating courses are also possible. The duration of the transition time interval during which the change takes place can be chosen so that, during it, the layer grows by 0.5 μm-20 μm.
In other preferred embodiments, the variation can oscillate between two values in steps or continuously over one section or the entire coating duration, so that, for example, a multilayer structure is formed in the layer, preferably with more than 2 individual layers. Here, the delay time can assume a first value during a first switching subinterval and a second value deviating from it during a second switching subinterval. During a switching time interval, first and second switching subintervals can follow each other once or multiple times. In doing so, the duration of the first and/or of the second switching subinterval can each be chosen so that, during it, the layer grows by 5 nm-2 μm. Preferred examples are a thickness of each individual layer of, for example, 5-100, preferably 5-50 nm for a nanolayer structure and a thickness of each individual layer in the range of, for example, 0.1-2 μm, for example with 6-40 individual layers present in total in the layer, for a multilayer structure.
Further preferred embodiments relate to the device according to the invention. Thus, the device preferably comprises one or more HIPIMS cathodes, i.e., cathodes which are connected to an HIPIMS power supply. The HIPIMS power supply preferably comprises a capacitor for supplying the electrical power for HIPIMS pulses and a charging device for the capacitor. The power supply is preferably power-regulated. Multiple cathodes disposed in the vacuum chamber can be fitted with targets of different compositions. Thus, it is possible to deposit layers of various compositions on top of each other by switching on or off (or respectively increasing/reducing the power) of the associated power supplies in a continuous process without an interruption of the vacuum. This preferably takes place through the controller.
In the following, embodiments will be further described with reference to drawings. The drawings show:
A rotating substrate table 20 with planetarily rotating substrate carriers 22 is located within the vacuum chamber 12. Substrates 60 to be coated, i.e., base bodies, for example of tools (see
Magnetron cathodes 30, 34 and an anode 28 are also disposed within the vacuum chamber 10. Each of the magnetron cathodes 32, 34 comprises an unbalanced magnet system (not shown) and a plate-shaped sputtering target 32, 36.
The magnetron cathodes 30, 34, the substrate table 20, and the anode 28 are each connected from outside the vacuum chamber 12 to an outer electrical circuitry of the coating system 10 by means of an electrical feedthrough through the wall of the vacuum chamber 12.
In the example shown, the magnetron cathode 34 is wired as a DC cathode, i.e., connected to a DC power supply 44 which supplies a DC voltage to it with respect to the anode 28. The anode 28 is connected to an anode power supply 46 which supplies a DC voltage to it with respect to the conductive wall of the vacuum chamber 12. The magnetron cathode 30 is wired as an HIPIMS cathode, i.e., electrically connected to an HIPIMS power supply 40 which applies a pulsed voltage VP to it with respect to the chamber wall. The substrate table 20 is connected to a bias power supply 42 which supplies it with a bias voltage VB with respect to the anode 28.
The coating system 10 is equipped with a controller 48, by which the bias power supply 42 and the HIPIMS power supply 40 are controlled, as will be explained in detail below. In addition, the controller 48 controls the entire process, i.e., also the vacuum system, the rotary drive of the substrate table 20, the supply of process gas and reactive gas, and all other electrical power supplies 44, 46. The controller is programmable, i.e., it comprises a memory for coating programs, with which the procedures and method steps explained below are specified.
It should be noted that the electrical circuitry and the fitting of the coating system 10 with electrodes as shown is to be understood to be purely exemplary. In alternative embodiments, for example, the HIPIMS cathode 30 can be connected with respect to the anode 28, or, for example, the anode 28 can be dispensed with and the chamber wall can be wired as the anode for all cathodes and for the substrate table 20. Multiple or also no DC cathodes 34 can be provided. In addition to the HIPIMS cathode 30, additional HIPIMS cathodes can be provided in the vacuum chamber 12, each connected to its own HIPIMS power supply. The cathodes 30, 34 can be fitted with targets 32, 36 of the same or different compositions.
The HIPIMS power supply 40 supplies electrical power to the HIPIMS cathode 30 in accordance with the HIPIMS method, i.e., the supplied voltage VP, the current IP, and thus the instantaneous electrical power have a time course in the form of short, very high pulses.
As an example, a period duration T of such a periodic time course is shown in
By way of example, preferred parameters of the HIPIMS method are mentioned below. The voltage VP is applied periodically with a frequency of, for example, 100-10,000 Hz, preferably 500-4000 Hz, so that the period duration T is preferably in the range of 250-2000 μs. The pulse duration TP is preferably low, for example shorter than 200 μs, preferably 40-100 μs. Preferably, the duty cycle TP/T is in the range of 1% to 35%, preferably 10-30%, particularly preferably 20-28%. The operation of the HIPIMS cathode(s) 30 preferably takes place in a power-regulated manner, for example to a value of 3-20 kW per HIPIMS cathode, preferably 10-16 kW per cathode. The peak current resulting during a pulse, in relation to the front face of the target 32, is preferably 0.4-2 A/cm2, further preferably 0.5-0.8 A/cm2.
When the coating system 10 is operated for applying a coating 64 to the functional region 62 of a substrate 60, as shown by way of example in
As schematically shown, three time sections 54, 56, 58 can be defined, wherein in the first time section 54 (approx. 0-40 μs) gas ions prevail, in the following second time section 56 (from approx. 40-100 μs) the metal ions prevail, and in the following third time section 58 (from approx. 100 μs) the gas ions prevail considerably.
The positive gas and metal ions of the plasma are accelerated into the direction toward the surface of the substrate 60 by the negative bias voltage VB and thus become part of the coating 64 attaching itself there. In the case of a DC bias, i.e., a continuous DC voltage as the bias voltage VB, all ions are selected for the layer formation without exception. In
Alternatively to a DC bias, the bias voltage VB can be applied with a pulsed time course, synchronously to the time course of the voltage VP at the HIPIMS cathode 30. Such a pulsed time course of the bias voltage VB is shown by way of example in
By suitable selection of the temporal synchronization between the cathode pulses 50 and the bias pulses 52, i.e., in particular by suitable selection of the bias pulse duration TB and the delay time TD, a selection can be made among the gas and metal ions present in the plasma at various points in time.
For example, the effect of a presetting of a time course of the bias pulses 52 with a bias pulse duration TB of approx. 60 s and a delay time TD of approx. 40 μs is shown in
In experiments with an HIPIMS target 32 made of titanium, silicon, and aluminum and supplying nitrogen as the reactive gas for depositing a coating 64 made of a Ti—Al—Si—N material system, with the time course of the bias voltage VB illustrated in
In comparison to this, with an otherwise identical configuration and process control with the application of a DC bias (
As a further example of a possible time course of the bias voltage VB,
As another example,
Thus, by presetting the time course of the bias voltage VB, it is possible to influence the layer composition and in particular to set the proportion of argon in a controlled way to a value between a minimum proportion (
As a result, the layer properties are considerably influenced, in particular the internal stress in the coating 64 and its hardness.
By means of the coating system 10, coatings 64 are applied to each of the substrates 60. These coatings grow with the progressing coating duration D so that they each have a thickness S starting from the surface of the substrate 60. By means of the controller 48, both the HIPIMS power supply 40 and the bias power supply 42 are controlled during the coating duration D so that, in various time intervals during the coating duration D, time courses of the bias voltage VB that deviate from each other can be set. This results in a varying composition of the coating 64 over the layer thickness S, namely a different respective proportion of argon depending on the time course set in each case.
With bias pulses 52 synchronized with the cathode pulses 50 (
An exemplary embodiment is explained below with reference to
To apply the coating 66, initially the body 60 to be coated, made of substrate material 62, is positioned on the substrate carrier 22 within the vacuum chamber 12, for example a double-bladed ball end mill with a 6 mm diameter made of carbide (WC/Co) with a 6 at % cobalt content.
The coating system 10 is fitted with two four HIPIMS cathodes 30, which are disposed around the substrate table 20. Each two cathodes 30 disposed next to each other are fitted with targets 32 made of titanium aluminum material (for example, 60 at % Ti, 40 at % Al) and the two remaining are fitted with targets 32 made of titanium silicon material (for example, 80 at % Ti, 20 at % Si).
By operating the vacuum system 14, a vacuum is produced. The inside of the vacuum chamber 12 is heated up. The surface of the substrate 60 is cleaned by gas ion etching while the cathodes 30, 34 are operated. The targets 32, 36 are prepared by sputter cleaning.
At the beginning of the coating, initially a first layer Boa is deposited on the substrate 60 in a first time interval. For this purpose, the two cathodes 30 with Al—Ti targets are operated, each with 12 kW of cathode power, while the two remaining cathodes 30 with Ti—Si targets are initially not operated. The electrical power is supplied in the form of HIPIMS cathode pulses 50 with a frequency of 4000 Hz, pulse length 70 μs. A bias voltage VB is applied thereby to the substrate 60 via the substrate table 20 and the substrate carrier 22. The bias voltage VB is pulsed with bias pulses 52 of 60 V and a bias pulse duration TB of 40 μs, which are synchronous with the cathode pulses 60 but occur with a delay time TD of 40 μs.
The first layer Boa is deposited with a layer rate of approximately 1 μm/h so that it reaches a thickness of 1.5 μm after the duration of the first time interval of 1.5 h. Due to the pulsed bias voltage VB with a delay time TD of 40 μs, metal ions are selected in a controlled way to form the coating 64, while argon ions, which first increasingly occur in the later temporal curve of each pulse, are only present to a low degree (cf.
Subsequently, in a second time interval, a second layer Bob is deposited onto the 1.5 μm thick first layer 80a. For this purpose, in the further execution of the coating program, the controller 48 controlls the power supplies of the two cathodes 30 with Ti—Si targets such that they are each operated with 12 kW of cathode power, while the two remaining cathodes 30 with Al—Ti targets are not operated. The HIPIMS parameters of the electrical power supply in the second time interval are the same as in the first time interval, i.e., frequency of 4000 Hz, pulse length 70 μs.
However, in the transition from the first to the second time interval, a variation of the time course of the bias voltage VB is made such that it is not applied in the second time interval with a pulsed time course, but rather as a continuous DC voltage, so that argon ions are also contained in the coating 64 to a considerable extent.
The second layer Bob is deposited with a layer rate of approximately 1 μm/h so that it reaches a thickness of 1.5 μm after the duration of the second time interval of 1.5 h. Due to the non-pulsed bias voltage VB, the argon content of the coating 64 in the second layer Bob is at least 0.12 at %, such that internal stress of at least 5.3 GPa results.
As a result, the layer 64 is two-layered, wherein the first layer Boa achieves very good layer adhesion due to the low internal stress and higher ductility, while the outer, second layer Bob ensures a hard, smooth surface of the coated body 66. The ball end mill coated in this way is suitable for milling high-carbon steel of more than 60 HRC without emulsion.
In the following, further individual exemplary embodiments in which coatings 164, 264, 364, 464, 564, 664 are generated on the substrate 62 are shown, wherein the composition and the properties of the coatings are changed in each case by variation of the time course during the coating duration, in particular by changing the synchronization of the bias voltage VB. In the following representation, all further details of the coating procedure will not be mentioned, for example fitting the targets and the concrete parameters and time durations, since it is primarily about showing principal embodiments, which can be applied to various material systems and with various parameters.
When depositing the coating 164, the bias voltage VB is applied in each case with a pulsed time course with bias pulses 52 which are synchronized with the cathode pulses 50. However, as shown in
Such a coating 264 can be advantageous especially for coated bodies 260 which are provided for tribological applications. The first layer 280b serves as a hard base layer with internal stress. The second layer 280b serves as a top layer on top of it, which has good run-in properties due to the higher ductility. Possible applications can include thread-cutting taps, forming taps, drills, and punching and stamping tools.
In
The resulting coating 664 of the coated body 660 has as a result first layers 680a with a low argon content and second layers 680b with a higher argon content following alter-nately one after the other in the direction of the layer thickness S. The layer disposed directly on the substrate 62 in the interface region is a first layer 680a with low internal stress, which promotes adhesion. The outermost layer in the region of the surface is a second layer 680b of high hardness.
The thickness of the layers 680a, 680b is preset by the duration of the time intervals 670a, 670b at a constant layer rate. By selecting the time durations of the time intervals 670a, 670b and the number of switches accordingly, multilayer coatings 664, for example, with a thickness of the individual layers 680a, 680b of, for example, 0.1-2 μm can be generated. Likewise, a nanolayer coating 664 with a thickness of the individual layers 680a, 680b of, for example, 5-50 nm can be generated by switching the time intervals 670a, 670b more quickly.
The following table 1 shows other exemplary embodiments of coatings:
The coating according to example 1 can be applied, for example, to tools such as milling cutters, drills, indexable inserts, or similar made of steel, stainless steel, or CrMo steel as a substrate material. They are standard layers with little internal stress in the interface region and higher internal stress toward the surface.
In example 2, they are layers for special applications with little internal stress in the interface region and higher internal stress toward the surface (particularly smooth layers). These can be applied, for example, to tools such as milling cutters, drills, indexable m inserts for machining aluminum, titanium, or non-ferrous metals. Possible applications are demanding machining applications for special materials in which material buildup should be avoided, meaning smooth layers are required.
According to example 3, the content of argon is high at the beginning of the deposition and is reduced toward the surface. Such layers can be used, for example, for thread-cutting taps, forming taps, drills, or punching and stamping tools. Steel, stainless steel or CrMo steel, for example, can serve as the substrate material. The layers are characterized by a hard base layer with higher internal stress and a soft top layer with good run-in properties and low internal stress. Possible applications of tools with such layers are, in particular, tribological applications.
In example 4, a graded increase in the argon content toward the surface of the coating takes place, so that it is smooth and visually appealing. Such layers can be used for all types of machining tools and all types of substrate materials. Possible applications are, for example, of a decorative nature. A colored top layer can be applied in a separate process.
The layers according to examples 5, 6, and 7 provide, on the one hand, a modified composition of the layers following each other and, on the other hand, a modification of the argon content. This can be achieved, for example, in that various HIPIMS magnetron cathodes in the vacuum chamber are fitted with targets made of different materials and controlled separately from each other. By switching off the power supply of a first cathode which is fitted, for example, with an Al—Ti target and simultaneously switching on the power supply of a second cathode which is fitted with a Ti—C target, the change from the first to the second layer, for example, in example 5 can take place. The switching on and off of the correspondingly fitted cathodes can take place abruptly or gradually in the form of a short ramp.
In example 6, a first cathode is fitted with an Al—Ti target and a second cathode is fitted with a Ti—C target; switching between the cathodes takes place when the layers are changed.
In example 7, the second cathode is fitted with a Ti—C target and the supply of nitrogen as a reactive gas is switched off at the beginning of the deposition of the second layer.
In all three examples 5, 6, and 7, the argon content is reduced abruptly at the beginning of the second layer. The layers generated thus can be applied, for example, to tools such as thread-cutting taps, forming taps, drills, punching and stamping tools made of substrate materials such as steel, stainless steel, or CrMo steel. Applications are, for example, tribological applications, for which is it favorable that the generated layers have a hard base layer with internal stress and a softer top layer with good run-in properties and little internal stress.
The layer according to example 8 can be used for the same types of tools, substrate materials and applications as according to examples 5, 6 and 7. In contrast to the abrupt, stepped reduction in the argon content during the coating duration, according to example 8 the argon content is reduced gradually, i.e., in the form of a ramp.
The layers according to the examples 9, 10, and 11 also provide a modified composition of the layers, which is achieved by cathodes with different fitting of targets and correspondingly changed electrical control. The layers can be applied, for example, to tools such as end mills, ball end mills, drills, or indexable inserts made of substrate materials such as high-carbon steel, Ni-based alloys, titanium alloys, or stainless steel. Possible applications of the resulting layers, which are hard and smooth (property of the second layer as a functional layer with a high argon content) and have good adhesion (property of the first layer which, with a low argon content, serves as an adhesion agent), are in particular demanding machining applications.
Examples 12, 13, and 14 can serve for applications such as decorative layers on all types of functional layers or respectively layers for better wear detection. Such layers can thus be applied, for example, in a combined method to other layers as the top finish. All types of machining tools can be considered as substrates, made, for example, of steel, cast iron, CrMo steel, or stainless steel. The lower layer serves as a functional layer and the upper layer as a decorative color layer with, for example, a golden color, which enables good wear detection.
With a graded transition of the argon content, example 15 represents an alternative for the same applications and substrates as examples 12, 13, and 14. In the mentioned variant with a second layer of carbon (C), a gray top layer is generated, which enables simple visual wear detection.
In the multilayer layers according to example 16 and the nanolayer layers according to example 17, layers with a high argon content (i.e., high hardness, high internal stress) alternate with those with a low argon content. The constant alternation prevents crack formation and achieves low internal stress of the overall system. Such layers can be provided for all types of machining tools and for substrate materials such as steel, in particular stainless steel, high-carbon steel, CrMo, Ni-based alloys, titanium alloys.
In summary, the invention can be implemented by various coating methods, coating devices, and resulting coated bodies, wherein the individual embodiments each offer specific advantages for various applications. The embodiments mentioned in detail here each represent examples and are to be understood as illustrative and not restrictive. Various modifications and alternatives to the embodiments shown are possible. For example, the aforementioned embodiments can be implemented with a wide variety of layer materials, i.e., with deviating target fitting and with supplying various reactive gases or also without supplying a reactive gas. The advantage always remains that the resulting coatings can be optimized for the respective applications by controlled setting of properties in various layer regions.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10 2020 116 157.3 | Jun 2020 | DE | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2021/066499 | 6/17/2021 | WO |
