This invention relates to the joining of bodies of material over bonding regions of large dimension using reactive composite materials such as reactive multilayer foils.
Reactive composite joining, such as shown in U.S. Pat. No. 6,534,194 B2 to Weihs et al and in U.S. Pat. No. 6,736,942 to Weihs et al. is a particularly advantageous process for soldering, welding, or brazing materials at room temperature. The process involves sandwiching a reactive composite material (RCM) between two layers of a fusible material. The RCM and the fusible material are then disposed between the two components to be joined, and the RCM is ignited. A self-propagating reaction is initiated within the RCM which results in a rapid rise in temperature within the RCM. The heat released by the reaction melts the adjacent fusible material layers, and upon cooling, the fusible material bonds the two components together.
Alternatively, depending upon the composition of the two components, the layers of fusible material are not used, and the reactive composite material is placed directly between the two components. Thermal energy released by ignition of the RCM melts material from the adjacent component surfaces and consequently joins the components.
Turning to
The process of joining the two components 10A and 10B occurs more rapidly with a reactive composite joining process than with conventional joining techniques such as those which utilize furnaces or torches. Thus, significant gains in productivity can be achieved. In addition, with the very localized heating associated with the reactive composite joining process, temperature sensitive components, as well as dissimilar materials such as metals and ceramics, can be soldered or brazed without thermal damage. Fine-grained metals can be soldered or brazed together using a reactive composite joining process without grain growth, and bulk amorphous materials can be welded together with only a local excursion from room temperature, producing a high strength bond while minimizing crystallization.
The reactive composite materials 12 used in reactive composite joining process are typically nanostructured materials such as described in U.S. Pat. No. 6,534,194 B2 Weihs et al. The reactive composite materials 12 are typically fabricated by vapor depositing hundreds of nano-scale layers which alternate between elements having large, negative heats of mixing, such as nickel and aluminum. Recent developments have shown that it is possible to carefully control both the heat of the reaction as well as the reaction velocity by varying the thicknesses of the alternating layers. It has also been shown that the heats of reaction can be controlled by modifying the foil composition, or by low-temperature annealing of the reactive multi-layers after their fabrication. It is further known that alternative methods for fabricating nanostructured reactive multilayers include mechanical processing.
Two key advantages achieved by the use of reactive composite materials for joining components are speed and the localization of heat to the joint area. The increased speed and localization are advantageous over conventional soldering or brazing methods, particularly for applications involving temperature-sensitive components or components with a large difference in coefficient of thermal expansion, such as occur in metal/ceramic bonding. In conventional welding or brazing, temperature-sensitive components can be destroyed or damaged during the process. Residual thermal stress in the components may necessitate costly and time-consuming operations, such as subsequent anneals or heat treatments. In contrast, joining with reactive composites subjects the components to little heat and produces only a very local rise in temperature. Generally, only the adjacent fusible layers and the adjoining surfaces of the components are heated substantially. Thus, the risk of thermal damage to the components is minimized. In addition, reactive composite joining is fast and results in cost-effective, strong, and thermally conductive joints.
In one aspect, the invention relates to the joining of large area assemblies especially the joining of temperature sensitive materials. While conventional reactive composite joining works well in joining components over lengths less than about four inches and areas less than about 16 square inches, joining over larger lengths and areas presents particular challenges. It has been observed that for optimal joining it is advantageous that the surfaces to be joined be heated as uniformly, and as simultaneously, as possible. When the lengths and areas become larger, it is increasingly difficult to maintain the desired reaction simultaneity and uniformity from a single ignition point. In addition, larger joining region dimensions can exceed those of easily fabricated RCM's, requiring multiple pieces of reactive foil to cover the joint surface area. Even though the joining reaction spreads rapidly through the RCM, not every part of a large surface area joint area may be molten at the same time, possibly resulting in poor bonding between the components. Moreover, increasing the surface area to be joined presents increasingly stringent requirements for the uniform application of pressure to the components during the joining process.
In another aspect, the invention relates to the manufacture of targets for use in physical vapor deposition processes, and in particular, to a novel method of bonding metal or ceramic tiles or plates to metal backing plates for use as targets in physical vapor deposition processes (sputtering). Such targets are typically large area assemblies of temperature sensitive materials.
Differences in the coefficients of thermal expansion (CTE) between sputtering target materials and backing plate materials limit the use of conventional soldering processes. In such conventional processing, the entire bond assembly is heated above the melting temperature of the solder. On cooling, the excessive contraction of the component with the higher CTE relative to the component with the lower CTE results in severe residual stresses within the bond and in the components. This is generally true for all ceramic targets bonded to metal backing plates. The net result is that good quality bonds are limited to very small areas or else large area bonds are of very low quality, characterized by debonding, cracking and warping of the target and backing plate components. Indium solder or elastomer bonds are often used to mitigate these problems. Although indium is a very compliant material, it has low strength (tensile strength of 2 MPa) and has a very low melting temperature (157° C.). The resulting indium bonds are similarly weak and are unable to tolerate even moderate temperatures in service. Even if indium solder is used, locked in residual stresses during conventional bonding lead to poor bond quality and cracking of the ceramic target often results during service. Elastomer bonds on the other hand have higher strengths, but suffer from very low electrical and thermal conductivities and outgassing issues during service.
Bonding with reactive multilayer foil is a new joining technology that enables soldering without significantly heating the components being bonded. The reactive multilayer foils are magnetron sputtered and consist of thousands of alternating nanoscale layers, such as alternating layers of Ni and Al. The layers react exothermically when atomic diffusion between the layers is initiated by an external energy pulse, and release a rapid burst of heat in a self-propagating reaction. If the foils are sandwiched between layers of solder, the heat released by the foils can be harnessed to melt these layers. By controlling the properties of the foils the exact amount of heat released by the foils can be tuned to ensure there is sufficient heat to melt the solder layers, but at the same time the bulk of the components will be at or close to room temperature. The components therefore do not undergo any significant expansion or contraction during bonding despite differences in CTE. Bonding with reactive multilayer foil is thus a room temperature method that enables the formation of low stress, high quality metallic bonds between materials with dissimilar CTE's.
Accordingly, it would be advantageous to provide a reactive composite joining process for use in joining components over surface areas which are larger than the size of a single sheet of reactive composite material, and which result in a strong and relatively uniform bond between the component materials.
Briefly stated, the present invention provides a method for joining bodies of component material over regions of large dimensions by disposing a plurality of substantially contiguous RCM sheets between the component material bodies. Each of the substantially contiguous RCM sheets is coupled to at least one adjacent RCM sheet by a bridging material capable of transferring an energetic reaction from one sheet to another. An ignition reaction is initiated in one or more of the RCM sheets and enabled to spread through all remaining sheets via the bridging material, resulting in rapid localized heating of materials adjacent the sheets, which form a bond between the bodies of component material upon cooling.
In an embodiment of the present invention, a plurality of substantially contiguous RCM sheets disposed between component material bodies to be joined over a region of large dimension are coupled together by a bridging material. The bridging material may be in the form of a reactive foil, wire, layer, powder, or other material which is capable of conveying an ignition reaction from one sheet to another, either directly or by thermal conduction. The bridging material is reactive in response to an ignition of a first RCM sheet to ignite a second RCM sheet.
In an alternate embodiment of the present invention, a plurality of substantially contiguous RCM sheets disposed between component material bodies to be joined over a region of large dimension are coupled together by structural support tabs of fusible material to enable easy assembly, transport, and positioning of the multiple RCM sheets between the component bodies to be joined.
In a variation of the present invention, a plurality of substantially contiguous RCM sheets are disposed between component material bodies to be joined over a region of large dimensions, directly adjacent surfaces of the component material bodies to be joined.
In an alternate embodiment of the present invention, a plurality of substantially contiguous RCM sheets are disposed between component material bodies to be joined over a region of large dimensions. Sheets of fusible material such as solder or braze are disposed in proximity to the RCM sheets and to the component material bodies. The fusible material sheets can overlie, underlie, or sandwich the sheets of reactive composite materials. The fusible material sheets can be continuous across the boundaries of the contiguous RCM sheets, and may optionally function as connecting material to hold RCM sheets together.
A method of the present invention for joining bodies of component material over regions of large dimension disposes at least one RCM sheet between the component material bodies. An ignition reaction is initiated at a plurality of ignition points disposed about the RCM sheet, resulting in rapid localized heating of materials adjacent the sheets which form a bond between the bodies of component material upon cooling.
One application of the invention provides a novel method of bonding metal or ceramic tiles or plates to metal backing plates for use as targets in physical vapor deposition processes (sputtering). In one embodiment, the method utilizes reactive multilayer foil to heat the interface between the plates above the melting point of solder or braze layers pre-applied to the plates, allowing the solder or braze to fuse together and to the foil and join the plates. This method permits soldering or brazing of materials with large differences in coefficient of thermal expansion due to minimal heating of the plates.
A variation of the method of the present invention for joining bodies of component material over regions of large dimension disposes at least one RCM sheet between the component material bodies. At least one spacer plate is positioned between an external pressure source and the component bodies. Pressure is applied to the arrangement from the external pressure source, urging the component bodies towards each other to control the formation of a bond between the component bodies following initiation of an ignition reaction in the RCM sheets. The ignition reaction within the RCM sheets results in rapid localized heating of materials adjacent the sheets, which form a bond between the bodies of component material upon cooling.
The advantages, nature and various additional features of the invention will appear more fully upon consideration of the illustrative embodiments now to be described in detail in connection with the accompanying drawings. In the drawings:
Corresponding reference numerals indicate corresponding parts throughout the several figures of the drawings. It is to be understood that the drawings are for illustrating the concepts of the invention and are not to scale.
The following detailed description illustrates the invention by way of example and not by way of limitation. The description enables one skilled in the art to make and use the invention, and describes several embodiments, adaptations, variations, alternatives, and uses of the invention, including what is presently believed to be the best mode of carrying out the invention.
As used herein, the phrase “large dimension” is used to describe a joint or bonding region and is understood to mean a joint or bonding region which has an area or length which exceeds the area or length of a single sheet of reactive composite material utilized in the joining processes, which is sufficiently large enough that a single propagation wave front from an ignition reaction within a sheet of reactive composite material fails to achieve desired bond characteristics throughout the bonding region, or which exhibits a loading variation between the center and the edges of the joint or bonding region. For example, an area of at least 16.0 sq. inches or a length of at least 4.0 inches is considered to be a large dimension when utilizing a sheet of reactive composite material having an area of less than 16.0 sq. inches and a longest dimension of less than 4.0 inches.
As used herein, the phrase “reactive composite material” or “RCM” is understood by those of ordinary skill in the art to refer to structures, such as reactive multilayer foils, comprising two or more phases of materials spaced in a controlled fashion such that, upon appropriate excitation or exothermic reaction initiation, the materials undergo an exothermic chemical reaction which spreads throughout the composite material structure. These exothermic reactions may be initiated by electrical resistance heating, inductive heating, laser pulses, microwave energy, or ultrasonic agitation of the reactive composite material at one or more ignition points.
Referring to the drawings,
Next, as shown in Block B, two or more sheets 12 of reactive composite material in a substantially contiguous arrangement are disposed between the mating surfaces of the two component bodies 10A and 10B. As used herein, the term “contiguous” is understood by those of ordinary skill in the art to mean that any adjacent edges of the sheets 12 of reactive composite material are arranged as close together as necessary to form a substantially void-free bond and at least sufficiently close together such that adjacent sheets 12 of reactive composite material can be operatively connected together into a single assembly. Contiguous RCM sheets do not need to be in physical contact with each other.
To operatively connect adjacent RCM sheets 12, a number of structurally supporting bridges or tabs 20 are formed between the sheets 12 (as shown in
A structural support bridge or tab 20 can be in any one of several forms to secure contiguous RCM sheets 12 together in the assembly 24. In one exemplary embodiment, the structural support bridges or tabs 20 are in the form of a soft metal or fusible material sheet, for instance indium, which is cold-pressed or rolled onto the RCM sheets 12.
An ignition bridge or tab 22 formed from a reactive material is preferably selected such that it will either ignite or conduct thermal energy between the adjacent sheets 12 to enable a reaction initiated in a first sheet 12A to continue via the bridge or tab to the adjacent sheet 12B. The configuration of an ignition bridge or tab 22 can be in any one of several forms to assist propagation of reaction between contiguous RCM sheets 12. For example, the ignition bridge or tab 22 can be in the form of a reactive multilayer foil, similar or identical to that used for the RCM sheets 12, or a thin wire that contains regions or layers of materials with a large negative heat of mixing. These configurations of the ignition bridges or tabs 22 can be attached to one or both contiguous sheets 12 with a small amount of glue or with a small piece of fusible solder. In addition to conveying an initiated reaction, ignition bridges or tabs 22 may be structural in nature, i.e. providing structural support to an arrangement of sheets 12 of RCM, or may be non-structurally supporting in nature, For example, a non-structurally supporting ignitable bridge 22 can be in the form of a loose or compact powder mixture of materials with a large negative heat of mixing.
Advantageously, the various forms of both bridges and tabs 20, 22 are small in comparison to the size of the RCM sheets 12, and do not interfere with the flow of any fusible material present in the bonding region, or with the flatness of the component body mating surfaces during the joining process.
Turning to
Within a large area bonding region 26, the solder tabs 20 may be secured to the sheets 12 of the assembly 24 by pressing or with a minimal amount of glue. If it is undesirable to use a solder material for the tabs 20 which differs from the solder material used as a fusible material within the joint, due to concerns about alloying, small tabs of the desired solder could be glued to the reactive sheets, preferably minimizing the amount of glue.
Those of ordinary skill in the art will recognize that the number of RCM sheets 12 comprising the various assemblies 24 shown in
In lieu of assembly tabs 20, an assembly 24 of two or more RCM sheets 12 with ignition bridges 22 may be packaged as shown in
Once the assembly 24 is formed, with or without fusible layers 32A and 32B, it is disposed within the bonding region 26 between the components 10A and 10B to be joined. As shown in Block C of
The final step, shown in Block D of
Those of ordinary skill in the art will recognize that a variety of devices which are capable of simultaneous delivery of ignition energy to the ignition points may be used. For example, an electrical circuit consisting of a capacitor and a switch associated with each ignition point may be employed. All the switches are controlled by a master switch, such that the capacitors charge and discharge simultaneously. An electrical pulse travels from the capacitors, through the switches to the ignition points on the RCM sheets 12, and to an electrical ground through the press platens 36A and 36B, igniting the sheets 12 within the assembly 24 and ultimately forming the bond between components 10A and 10B. Alternatively, a single large capacitor and switch may be connected to all the ignition points in parallel, such that energy is discharged to all ignition points about the assembly 24 simultaneously from the capacitor to ignite each sheet 12.
During the bonding process, it is known that non-uniform load distribution between the component bodies 10A and 10B will result in poor quality bonds with the presence of air gaps (voids) following the ignition of the sheets 12 within the assembly 24. Uneven load distribution typically results when the press platens 36A and 36B of the loading mechanism are significantly oversized or undersized compared to the size of the bonding region 26. This problem may be exacerbated when one or both of the components 10A and 10B to be joined are relatively thin. In the case where the press platens 36A and 36B are oversized relative to the size of the bonding region 26, the resulting pressure near the peripheral edges of the bonding region 26 is greater than the pressure near the center of the bonding region 26, and thus voids may form near the center of the bonding region 26. This is illustrated by the white regions visible near the center of the top-plan ultrasonic acoustic image or C-scan of a bonding region 26 shown in
Conversely, in the case where the press platens 36A and 36B are undersized relative to the bonding region 26, the pressure near the center of the bonding region is greater than the pressure near the peripheral edges of the bonding region 26, and thus voids may appear about the peripheral edge as is shown by the white regions visible about the peripheral edges of the top-plan ultrasonic acoustic image or C-scan of a bonding region 26 shown in
In order to distribute the load from the press platens 36A and 36B in a uniform manner to the bonding region 26, one or more spacer plates 34 sized to match the bonding region 26 are placed between the components 10A, 10B, and the platen or platens 36A, 36B. The ideal thickness for the spacer plate or plates 34 may be determined by a sequential process, in which a test bond is initially formed without the use of any spacer plate or plates 34. The resulting bond between components 10A and 10B is evaluated to identify the presence of voids. For applications where the press platens 36A and 36B are larger than the bonding region 26, the bond quality may be characterized by a ratio of voided area in the center quarter of the bonding region 26 to the total area of the bonding region. To reduce the voided area, spacer plates 34 of increasingly greater thickness are employed in additional bonding test procedures between components 10A and 10B until the desired ratio of voided areas to bonding region area is achieved for a bonding procedure. Preferably, the thickness of the spacer plates 34 is doubled between each bonding test procedure until the desired ratio is achieved.
The procedure may be modified for large area joining applications where none or only a limited number of edge voids can be tolerated. For these applications the percentage of edge voids, defined as the ratio of voided area in the outer quarter of the bonding region 26 to the total joining area, may be tracked as described above. If the process of doubling the spacer plate thickness results in an acceptable percentage of center voids and no edge voids, then the optimal spacer plate thickness has been derived. If on the other hand, the process results in an acceptable percentage of center voids, but some percentage of edge voids are detected, then the spacer plate thickness should be reduced to the average thickness of the present and previous spacer plate thicknesses. This process is repeated until a spacer plate 34 having a determined thickness results in the minimum amount of center voids and the desired amount of edge voids. This is illustrated by the small white region near the center and the general lack of any white regions visible near the peripheral edges of the top-plan ultrasonic acoustic image or C-scan of a bonding region 26 shown in
For applications where the press platens 36A and 36B are undersized relative to the bonding region 26, the bond quality may be characterized by a ratio of voided area in the outer quarter of the bonding region 26 to the total area of the bonding region. To reduce the voided area, spacer plates 34 of increasingly greater thickness are employed in additional bonding test procedures between components 10A and 10B until the desired ratio of voided areas to bonding region area is achieved for the bonding procedure. Preferably, the thickness of the spacer plates 34 is doubled between each bonding test procedure until the desired ratio is achieved.
The methods of the present invention for joining component bodies 10A and 10B over a large dimension bonding region 26 are further illustrated by the following six examples.
In this example, reactive or ignition bridges 22 and assembly tabs 20 were disposed on an assembly 24 inside the peripheral edges of a bonding region 26 as is illustrated in
The brass disk 10B was placed on a flat surface with the pre-applied layer of tin-lead solder 32B facing upwards. The portions of the assembly 24 were positioned adjacent to each other with a minimum separation gap G on top of the brass disk 10B so that they completely covered the bond region 26. The nickel disk 10A was placed above the reactive multilayer foil with the pre-applied layer of tin-lead solder 32A facing down, in contact with the RCM sheets 12 (Ni—Al, 80 μm thick, reaction velocity 7 m/s) in the assembly 24. An aluminum spacer plate 34 0.75 inches thick, with a diameter of 17.7 inches, was positioned above and aligned with the nickel disk 10A. The spacer thickness was previously determined using the process described above, by making several joints with different sized spacer plates. A thin layer of hard rubber 38, with a matching surface area, was placed above the aluminum spacer plate 34 to accommodate any imperfections on the outside surfaces of the brass and nickel disks 10A and 10B and the surfaces of the platens of the press 36A, 36B used to apply a load during joining. The entire arrangement was transferred to a hydraulic press, where a load of 107,000 lbs was applied to the arrangement. The sheets 12 of the assembly 24 were then ignited electrically, simultaneously at twelve ignition points around the circumference identified by the arrows in
In this example, assembly tabs 20 were disposed on an assembly 24 inside the peripheral edges of a bonding region 26, while the reactive or ignition bridges 22 were disposed outside the peripheral edges of the bonding region 26, as is illustrated in
Next, the brass disk 10B was placed on a flat surface with the pre-applied layer of tin-lead solder 32B facing upwards. The portions of the assembly 24 were positioned adjacent to each other with a minimum separation gap on top of the brass disk 10B so that they completely covered the bond region 26. The nickel disk 10A was placed above the reactive multilayer foil with the pre-applied layer of tin-lead solder 32A facing down, in contact with the RCM sheets 12 in the assembly 24. An aluminum spacer plate 34 0.75 inches thick, with a diameter of 17.7 inches, was positioned above and aligned with the nickel disk 10A. The spacer thickness was previously determined using the process described above, by making several joints with different sized spacer plates. A thin layer of hard rubber 38, with matching surface area, was placed above the aluminum spacer plate 34 to accommodate any imperfections on the outside surfaces of the brass and nickel disks 10A and 10B, and the surfaces of the platens of the press 36A, 36B used to apply a load during joining. The entire arrangement was transferred to a hydraulic press, where a load of 107,000 lbs was applied to the arrangement. The sheets 12 of the assembly 24 were then ignited electrically, simultaneously at sixteen ignition points around the circumference identified by the arrows in
In this example, assembly tabs 20 and ignition bridges 22 were disposed on an assembly 24, both inside and outside of the peripheral edges of a bonding region 26, as is illustrated in
The resulting joined assembly was ultrasonically (acoustically) scanned to determine the quality of the bond. A representative acoustic scan is shown in
In this example, an assembly 24 of RCM sheets 12 is arranged with assembly tabs 20 disposed within a square bonding region 26, and with ignition bridges 22 outside of the peripheral edges of the square bonding region 26, as is illustrated in
The resulting joint between the component bodies 10A and 10B was ultrasonically scanned to determine the quality of the bond. An acoustic scan is shown in
In this example, an assembly 24 of RCM sheets 12 was utilized to simultaneously join a set of discrete component tiles 40A-40F to a single base component body 42, as shown schematically in
In this example, an assembly 24 of RCM sheets 12 was utilized to bond two curved component bodies 44A and 44B over matching non-planar (curved) surfaces, as illustrated in
The present disclosure provides a novel method of bonding metal or ceramic tiles or plates to metal backing plates for use as targets in physical vapor deposition processes (sputtering). In one embodiment, the method utilizes reactive multilayer foil to heat the interface between the plates above the melting point of solder or braze layers pre-applied to the plates, allowing the solder or braze to fuse together and to the foil and join the plates (
Targets bonded with this invention may be operated at powers 30 to 100% higher than targets bonded with elastomers or indium solder without cracking or separating from their backing plates. Targets bonded with this invention may also have superior bond line uniformity and thus may sputter more uniformly than targets bonded by other means.
Target materials that may be bonded in this manner include but are not limited to aluminum oxide, quartz, indium tin oxide, boron carbide, silicon carbide, silica glass, silicon, graphite, CVD diamond, aluminum nitride, zinc oxide, lanthanum manganese oxide, other oxides, other carbides, and other nitrides. Metals for targets or backing plates include but are not limited to lanthanum, zirconium, nickel, cobalt, tungsten, titanium, copper, brass, aluminum, titanium-tungsten alloys, copper-tungsten alloys, InCuSil® and other braze alloys. Solders that may be used to join the targets and backing plates include but are not limited to PbSn, SnAg, SnZn, and SAC.
The following case studies demonstrate the bonding with reactive multilayer foil of various sputtering target materials to backing plate materials. Residual stress analysis by finite element modeling (FEM) compares conventional bonding to bonding with reactive multilayer foil. Measured bond strength data is presented and bond quality is discussed. Furthermore, a side by side performance comparison between a conventionally bonded ceramic (B4C) target, using indium solder, and a ceramic (B4C) bonded target using reactive multilayer foils and higher melting temperature SnAg solder is presented. The B4C target bonded with reactive multilayer foil was run at double the power without any cracking or debonding from the backing plate compared to the conventionally bonded B4C target for a significantly longer duration.
Residual Stress Analysis
Finite Element Modeling (FEM) of the bonding of a ceramic target, B4C, to a metal backing plate, CuCr, was performed. The geometry consisted of a 6″×6″×0.25″ B4C target bonded with 96.5Sn3.5Ag solder to a 6″×6″×0.31″ Cu—Cr plate. Two separate cases were analyzed. The first case was a conventional bonding operation where the entire assembly was heated uniformly above the melting temperature of the solder and then cooled uniformly with a bond forming once the solder solidified (below 221° C.). The second case was a bonding operation using reactive multilayer foil as a heat source with non-uniform heating and cooling of the solder and the components. A cross-sectional temperature profile captured at the moment of solder solidification (
Bond Strength
The bond strengths of various configurations joined with reactive multilayer foil have been measured. Table 1 lists some shear strengths we have measured for bonding with different solders. The measured strengths are found to depend on the strength of the solder used and not on the combination of materials bonded. Hence bonds formed with indium solder are limited in strength by the strength of indium to 4-6 MPa (580-870 psi), while bonds formed with SnAg measure 23-28 MPa (3335-4060 psi) due to the higher strength of SnAg solder. Of further note is the fact that where it is possible to form conventional reflow bonds when the CTE mismatch between sputter target and backing plate is not significant, the measured strengths are generally about 10% lower than the bonds formed with reactive multilayer foil. This higher strength can be attributed to the refined microstructure formed due to the rapid cooling during bonding with reactive multilayer foil.
Bond Quality
The quality of large area sputtering target to backing plate bonds, up to 300 sq. inches, using reactive multilayer foil has been found to be consistently very good and beyond the capability of current commercial process. For any combination of sputter target, backing plate and solder, the required thickness and properties of the multilayer foil can be chosen by running custom written finite difference software that accounts for thermal transfer. This ensures that sufficient heat is transferred into the solder for melting, while not heating up the sputter target and backing plate.
The percentage bond coverage of sputter targets, including ceramic targets, bonded to backing plates using reactive multilayer foils exceeds the standard industry requirements of total coverage >95%, no single void >2% and no edge voids. The typical coverage for reactive multilayer foil bonds is greater than 98%.
Case Study
Boron carbide (B4C) sputtering targets were bonded to copper-chromium alloy backing plates by a conventional reflow solder process using indium and by a multilayer reactive foil approach using 96.5Sn3.5Ag. In both cases the bonded target was a 4 piece construction of 0.25 in thick B4C tiles with 90 degree butt joints bonded to a single backing plate. Each B4C tile measured 6.25 in long and 6 in wide so that the total bond area was 25 in long and 6 in wide.
The two B4C targets were evaluated by DC magnetron sputtering in identical cathodes in the same vacuum chamber. All sputtering parameters, except for power input, were also identical. The conventionally bonded target was run at 2 kW, while the target bonded with reactive multilayer foil was run at 4 kW. The conventionally bonded target cracked after the first use, running for less than 10 hours. These cracks can be seen in
ITO Case Study
Three identical Indium Tin Oxide (ITO) sputtering targets (7.6 cm diameter) were bonded to copper backing plates using three different bonding processes:
(1) Conventional reflow of InSn solder
(2) Elastomer bonding
(3) NanoBond® using NanoFoil® as a local heat source to melt a SnAg type solder
The three bonded ITO targets were then run sequentially in the same magnetron cathode under DC power. The power was ramped up in 100 W increments, holding for a minimum of 1 hour at each power setting to observe stable sputtering performance. A summary of each target's performance is given in Table 2 below. The target bonded with InSn solder using a conventional reflow process failed while ramping from 200 W to 300 W, when the InSn solder melted and dripped out of the bond, thereby shorting to the anode. Thus the maximum sustainable power recorded for this target was 200 W. The target bonded with elastomer started to exhibit small cracks when the power was ramped up from 200 W to 300 W, but seemed to remain stable operating at 300 W. However, when the power was ramped from 300 W to 400 W, the cracks became larger (see
Alumina Case Study
Two identical alumina (Al2O3) sputtering targets (7.6 cm diameter) were bonded to copper backing plates using two different bonding processes:
(1) Elastomer bonding
(2) NanoBond® using NanoFoil® as a local heat source to melt a SnAg type solder
The two bonded alumina targets were then run sequentially in the same magnetron cathode under RF power. The power was ramped up in 100 W increments, holding for a minimum of 1 hour at each power setting to observe stable sputtering performance. A summary of each target's performance is given in Table 3 below. The target bonded with elastomer started to crack at 300 W, but seemed to remain stable at this power. However, when the power was ramped to 400 W pieces of the target fell off from the backing plate (see
Boron Carbide Case Study
Two identical boron carbide (B4C) sputtering targets (63 cm×15 cm), consisting of four tile pieces, were bonded to copper backing plates using two different bonding processes:
(1) Conventional Reflow of ln Solder
(2) NanoBond® using NanoFoil® as a local heat source to melt a SnAg type solder
The two bonded boron carbide targets were run sequentially in the same magnetron cathode at DC power under production conditions. The target bonded with conventional reflow of ln solder was run at 2000 W. A summary of each target's performance is given in Table 4 below. After less than 10 hours of use, cracks appeared in the boron carbide as shown in
We have demonstrated a room temperature process of solder bonding sputtering targets to backing plates with no restrictions on the differences in CTE of the two materials. This is achieved by localized heating of solder layers by reactive multilayer foil that releases sufficient heat for melting the solder but not enough to heat up the sputtering target and backing plate. Bonding of ceramic targets to metal backing plates using solders with high melting temperatures can thus be achieved. High strength bonds are obtainable, limited only by the strength of the solder chosen. Bond quality is very good with bond coverage typically >98%. The net result of these high quality, strong metallic bonds, with high melting temperature solders and with good thermal and electrical conduction, is that the end user is provided with a durable bonded sputtering target that will not crack during use and can be run at significantly higher input powers that will result in vastly higher deposition rates.
The use of a NanoBond® sputtering target can lead to a 30-100% increase of sputtering rate (compared to a conventional ln solder reflow bond or elastomer bond). This can consequently lead to significant increases in production efficiency. Since the equipment costs in many sputtering production processes are very high, this translates to big cost reductions per production cycle due to a lowering of overhead costs (especially capital equipment depreciation). For a typical webcoating process, an increase in throughput of 25% could be achieved by halving the time spent on the ceramic coating part of the process. The overhead costs per production run would be reduced by a similar amount. A simple cost analysis shows that the savings can amount to $150,000-500,000 per year per sputtering system.
The present disclosure can be embodied in-part in the form of computer-implemented processes and apparatuses for practicing those processes. The present disclosure can also be embodied in-part in the form of computer program code containing instructions embodied in tangible media, such as floppy diskettes, CD-ROMs, hard drives, or an other computer readable storage medium, wherein, when the computer program code is loaded into, and executed by, an electronic device such as a computer, micro-processor or logic circuit, the device becomes an apparatus for practicing the present disclosure.
The present disclosure can also be embodied in-part in the form of computer program code, for example, whether stored in a storage medium, loaded into and/or executed by a computer, or transmitted over some transmission medium, such as over electrical wiring or cabling, through fiber optics, or via electromagnetic radiation, wherein, when the computer program code is loaded into and executed by a computer, the computer becomes an apparatus for practicing the present disclosure. When implemented in a general-purpose microprocessor, the computer program code segments configure the microprocessor to create specific logic circuits.
As various changes could be made in the above constructions and procedures without departing from the scope of the invention, it is intended that all matter contained in the above description or shown in the accompanying drawings shall be interpreted as illustrative and not in a limiting sense.
The present application is a continuation, and claims priority from, U.S. patent application Ser. No. 12/029,256 filed on Feb. 11, 2008, which in turn is a divisional of U.S. Ser. No. 11/393,055 filed Mar. 30, 2006 (now U.S. Pat. No. 7,354,659), which in turn is related to and claims priority from U.S. Provisional Application Ser. No. 60/666,179 filed on Mar. 30, 2005. The present application is further a continuation of U.S. patent application Ser. No. 11/851,003 filed on Sep. 6, 2007, which in turn is related and claims priority to U.S. Provisional Application Ser. No. 60/825,055 filed on Sep. 8, 2006, which is herein incorporated by reference. The '003 application is further related to and claims priority from, U.S. Provisional Application Ser. No. 60/915,823 filed on May 3, 2007. All of the above identified applications are incorporated herein by reference.
The United States government has certain rights in this invention pursuant to NSF Award DMI-034972.
Number | Date | Country | |
---|---|---|---|
60666179 | Mar 2005 | US | |
60825055 | Sep 2006 | US | |
60915823 | May 2007 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 11393055 | Mar 2006 | US |
Child | 12029256 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 12029256 | Feb 2008 | US |
Child | 12102764 | US | |
Parent | 11851003 | Sep 2007 | US |
Child | 11393055 | US |