WO2011129256A1 - ボンディングワイヤ - Google Patents

ボンディングワイヤ Download PDF

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Publication number
WO2011129256A1
WO2011129256A1 PCT/JP2011/058786 JP2011058786W WO2011129256A1 WO 2011129256 A1 WO2011129256 A1 WO 2011129256A1 JP 2011058786 W JP2011058786 W JP 2011058786W WO 2011129256 A1 WO2011129256 A1 WO 2011129256A1
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WIPO (PCT)
Prior art keywords
wire
coating layer
core material
bonding
added
Prior art date
Application number
PCT/JP2011/058786
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English (en)
French (fr)
Inventor
長谷川 剛
Original Assignee
タツタ電線株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Publication date
Application filed by タツタ電線株式会社 filed Critical タツタ電線株式会社
Priority to JP2012510635A priority Critical patent/JPWO2011129256A1/ja
Priority to CN2011800188602A priority patent/CN102884615A/zh
Publication of WO2011129256A1 publication Critical patent/WO2011129256A1/ja

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23KSOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
    • B23K35/00Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
    • B23K35/02Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by mechanical features, e.g. shape
    • B23K35/0222Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by mechanical features, e.g. shape for use in soldering, brazing
    • B23K35/0227Rods, wires
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    • H01L2924/20753Diameter ranges larger or equal to 30 microns less than 40 microns
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2924/00Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
    • H01L2924/20Parameters
    • H01L2924/207Diameter ranges
    • H01L2924/20754Diameter ranges larger or equal to 40 microns less than 50 microns

Definitions

  • the present invention relates to a bonding wire for connecting an electrode on an integrated circuit element such as an IC, LSI, transistor or the like to a conductor wiring of a circuit wiring board such as a lead frame, a ceramic substrate, or a printed circuit board by a ball bonding method, and its manufacture. It is about the method.
  • connection method by this kind of ball bonding method is generally in the form shown in FIGS. 1A to 1H, and the wire W shown in FIG. 1A is inserted into the capillary 10a and a ball is attached to the tip thereof. From the state where (FAB: Free Air Ball) b is formed, the clamp 10b is opened, and the capillary 10a is lowered toward the electrode a of the integrated circuit element. At this time, the ball (FAB) b is captured in the capillary 10a and bonded to the electrode a.
  • (FAB: Free Air Ball) b Free Air Ball
  • the capillary 10a grips the ball b and applies heat, weight, and ultrasonic waves to the ball b, whereby the ball b and the electrode a Solid-phase bonding is performed to form a 1st bond and adhere to the electrode a (1st bonding, FIG. 1B).
  • the capillary 10a moves up to a certain height (FIG. (C)) and then moves to a position directly above the conductor wiring c (FIGs. (D) to (e)).
  • a special movement is performed on the capillary 10a so that the wire W is attached with a “string” (see the solid line from the chain line in FIG. 4D).
  • Capillary 10a that reaches directly above the conductor wiring c descends toward the conductor wiring c and presses the wire W against the conductor wiring (2nd target) c ((e) to (f) in the figure). At the same time, heat, weight, and ultrasonic waves are applied to the pressed portion, thereby deforming the wire W, and stitches for joining the wire W onto the conductor wiring c, and a tail for securing the tail in the next step. A bond is formed (2nd junction, FIG. 1 (f)).
  • the capillary 10a rises with the wire W remaining, and after securing a tail of a certain length at the tip of the capillary 10a, the clamp 10b is closed (by grabbing the wire W), and the tail The wire W is torn off from the bond portion (FIG. 1 (g)).
  • the capillary 10a stops when it rises to the required height, and a high voltage is applied to the tip of the wire W secured at the tip of the capillary 10a with the discharge rod g to discharge (discharge) the spark.
  • the wire W is melted, and the melted wire material becomes a spherical ball b by the surface tension and hardens (FIG. 1 (h)).
  • a gold wire is mainly used as the bonding wire W.
  • an inexpensive copper wire having a copper purity of 99.9% by mass or more (3N) has recently been used. It is made to use.
  • a core material 1 made of copper wire is coated with an oxidation resistant metal 2 as shown in FIG. Is used.
  • the coating metal (coating layer) 2 gold (Au), platinum (Pt), palladium (Pd), silver (Ag), nickel (Ni) or the like is employed (Patent Documents 1 to 3).
  • the ball b In the bonding wire W made of a metal-coated copper wire, the ball b needs to be made smaller with the miniaturization of integrated circuit elements due to the recent miniaturization of electronic components.
  • the diameter L is preferably 50 ⁇ m or less (paragraph 0009 in Patent Document 1).
  • the ball b when the ball b is in a downward bowl shape (reverse conical shape) in connection to the electrode a of the integrated circuit element, the electrode b is pressed by the sharp end of the ball b when the ball b is pressed against the electrode a.
  • the ball b is preferably a true sphere as much as possible.
  • the thickness t of the covering layer 2 is set to 0.001 or less of the core wire diameter (Patent Document 1, Claim 1), and the thickness t of the covering layer 2 is set to 0.001 to The thickness is set to 0.02 ⁇ m (Claim 1 of Patent Document 3), or the coating layer 2 is formed of an oxidation-resistant metal having a melting point higher than that of copper of the core material 1 (paragraph 0014 of Patent Document 2).
  • phosphorus (P), boron (B), bismuth (Bi), tin (Sn), silver (Ag), and manganese (Mg) are added to the copper of the core material 1, and a peel test (peeling test) is performed.
  • a technique for increasing the sphericity of a ball by increasing the breaking elongation of the ball and synergistic with the oxidation-resistant metal forming the coating layer 2 by an additive metal such as P when the ball is melted is disclosed ( Patent Document 4, paragraph 0055).
  • the bonding wire W coated with a copper wire with an oxidation-resistant metal has been well-received in various ways and has been well received.
  • the speed of work based on the recent cost reduction has been increased.
  • further work stability for example, the following continuous bonding property, FAB stability, and the like are required.
  • P or the like can be selected.
  • sparking during FAB formation can be performed in a low current and in a short time.
  • the P or the like is added, the oxidation resistance may be deteriorated.
  • the capillary 10a shown in FIGS. 1E to 1F descends toward the conductor wiring c, and the wire W is transferred to the conductor wiring (2nd target).
  • the cover layer 2 may be cracked along with the bending. If the cover layer 2 is cracked, the oxidation resistance of the cracked portion is deteriorated, and a problem arises in the formation of the true sphere when the ball b is formed in FIG.
  • the first object of the present invention is to increase the electric resistance value of the bonding wire W and prevent the deterioration of the oxidation resistance, and the second problem is to suppress the deterioration of the oxidation resistance as much as possible even if the crack occurs. To do.
  • the present invention first adds P among P, B, Bi, Sn, Ag, and Mg, which are considered to increase the electric resistance value.
  • P increases the electrical resistance value
  • the FAB can be formed by supplying the spark during FAB formation stably at a low current for a short time.
  • P has processing heat stability and is generally sold as a Cu—P alloy, so that it is easy to obtain and it is easy to obtain a required addition amount.
  • B is poor in thermal stability, addition is difficult, Bi is not preferable from the environmental point of view, Sn has a problem that it can be wrinkled by dissolution, and Ag is easy to oxidize.
  • Mg has a problem that it is difficult to add Mg due to its low vapor pressure.
  • the oxidation resistant material Au, Pt, Pd, Ag, Ni, Fe (iron), Cr (chromium), Mn, and the like can be considered. Of these, Ag, Ni, Fe, and Mn are easy. In addition, P and a compound (Ag—P, Ni—P, Fe—P, Cr—P, Mn—P) are produced, so even if added, they do not contribute to the improvement of oxidation resistance. Therefore, at least one or more of the platinum group (Pt group) of Au or Ru, Rh, Pd, Os, Ir, and Pt that does not combine with P even when melted is added. At this time, 1 type is more preferable from the ease of addition of a required amount, and it is preferable to use at most 2 types. Thus, if it is Au or Pt group which does not combine with P, while improving the electrical resistance value by addition of P, the oxidation resistance improvement by addition of Au etc. can be aimed at.
  • the addition amount of P and the addition amount of Au or the like may be appropriately determined by experiments or the like as long as the effect can be obtained.
  • the addition amount of Au is 2 to 250 ppm, such as Au. Is 1 to 100 ppm in total.
  • P is less than 2 ppm, an improvement in electric resistance cannot be expected and the effect of forming a ball at a low current and in a short time may not be obtained.
  • the function as a bonding wire for transmitting a signal from the element (electrode a) to the lead (conductor wiring c) may be hindered, and a crack (chip crack) may occur in the electrode a at the time of the first bonding.
  • the strength of the wire W becomes too high, which may cause chip cracks at the time of the first bonding, and if it is less than 1 ppm, the oxidation resistance effect may not be expected.
  • the range in which ball formation is particularly stable is 10 ppm or more.
  • a more preferable range of the addition amount of P and the addition amount of Au or the like is 50 ppm or less for P and 1 ppm or more and 50 ppm or less in total for Au or the like.
  • a specific configuration of the present invention is a bonding wire having a wire diameter of 12 ⁇ m or more and 50.8 ⁇ m or less for connecting an electrode of an integrated circuit element and a conductor wiring of a circuit wiring board by a ball bonding method, and is an Au or Pt group
  • the bonding wire is made of copper having a purity of 99.99% by mass or more.
  • the wire diameter L of the bonding wire W is set to 50.8 ⁇ m or less in the above-mentioned Patent Document 1 in which the diameter L is set to 50 ⁇ m or less, but if it is 50.8 ⁇ m or less, it is 50 ⁇ m or less. This is because the above-mentioned ball b can be made even smaller.
  • the lower limit of the wire diameter L is set to 12 ⁇ m or more because if it is less than 12 ⁇ m, it becomes difficult for an operator to pass the wire W through the capillary 10a before bonding, and workability is deteriorated.
  • the reason why the copper purity of the core material 1 is 99.9% by mass (3N) or more is to ensure high conductivity of copper.
  • the present invention first adds P to the core material in order to increase the electric resistance value, and at least one or more of Au or Pt group in order to improve oxidation resistance.
  • the FAB can be formed stably at a low current and in a short time, and the core material itself is made oxidation resistant.
  • the addition of P increases the electric resistance value without causing deterioration of oxidation resistance, and stably supplies the spark during FAB formation at a low current and in a short time. By doing so, the FAB can be formed.
  • an oxidation resistant Pt or Pd thickness t of 0.02 to 0.09 ⁇ m was formed on the entire outer periphery of the core material. Since Pt or Pd does not form a compound with P as described above, the compound is not formed even when the coating layer is dissolved, and the electrical resistance value and the oxidation resistance are improved. Moreover, since Pd and Pt have higher melting points than copper, the sphericity of the ball b can be expected to increase. In addition, even if a crack occurs in the wire (coating layer) at the time of the 2nd bonding or the like, since the crack is usually slight, the addition amount of Au or the like into the core material 1 can sufficiently suppress the oxidation. To do.
  • a bonding wire having a wire diameter of 12 ⁇ m or more and 50.8 ⁇ m or less for connecting an electrode of an integrated circuit element and a conductor wiring of a circuit wiring board by a ball bonding method, the core material of which is In addition, at least one or more of gold or platinum group is added to improve oxidation resistance, and P is added to improve electrical resistance, and is made of copper with a purity of 99.9% by mass or more.
  • the bonding wire has a structure in which an oxidation-resistant Pt or Pd coating layer having a thickness of 0.02 to 0.09 ⁇ m is formed on the entire surface.
  • the wire diameter is 12 ⁇ m or more and 50.8 ⁇ m or less and the purity is 99.9% by mass or more for the same reason as described above.
  • the thickness t of the coating layer 2 is decreased, the hardness of the ball b is decreased, and the possibility of damage to the Si chip (electrode a) is decreased.
  • the degree to which copper is exposed is increased, and only the stitch bondability as high as that of a copper wire not having the coating layer 2 can be exhibited.
  • the thickness t of the coating layer 2 shall be 0.02 micrometer or more from the experimental result of the Example and a comparative example.
  • the thickness t is set to 0.04 ⁇ m or more from the experimental results of the continuous bonding property.
  • the stage temperature is lowered, the load required for stitch bond bonding increases, and when the thickness t of the coating layer 2 is in the range of 0.02 ⁇ m or more to less than 0.04 ⁇ m, the degree of exposure of the core copper increases and the continuous bonding property increases. This is because may be damaged.
  • the coating layer 2 is thick, the hardness of the ball b increases and the possibility of damage to the Si chip (electrode a) increases. For this reason, the thickness t of the coating layer 2 shall be 0.09 micrometer or less from the experimental result of a postscript Example and a comparative example.
  • the thickness t of the coating layer 2 is 0.04 ⁇ m or more, machine troubles are reduced even at a stage temperature of 150 ° C.
  • Pd is adopted for the coating layer 2 and the thickness t of the coating layer 2 is 0.05 ⁇ m. It has been confirmed that no machine trouble occurs even when the stage temperature is set at a lower temperature of 130 ° C. This is considered to be based on the synergistic effect that the difference in melting time between Cu and Pd is small in the case of the palladium coating layer 2 and it is more likely to become a true sphere.
  • the copper purity of the core material is 99.99 mass% (4N) or higher, and further 99.999 mass% (5N) or higher, the possibility of damage to the Si chip (electrode a) is reduced. This is because the FAB hardness can be further reduced by setting the copper purity to 99.99% by mass or more, and further to 99.999% by mass or more.
  • the entire outer periphery of the core material 1 made of copper having a purity of 99.9% by mass or more is coated with one or more of Pt and Pd.
  • the wire is drawn to a wire diameter of 12 ⁇ m to 50.8 ⁇ m, and the tensile elongation is 8% or more. In this way, a tempering heat treatment is performed so that the thickness t of the coating layer 2 is 0.02 to 0.09 ⁇ m.
  • the coating layer 2 is formed by a known means such as electrolytic plating, electroless plating, vapor deposition, etc.
  • the wire W is predetermined by sequentially passing a copper rod having a large wire diameter through a tool called a die. Therefore, the coating layer 2 is formed by the above means with an appropriate wire diameter in the middle of this process.
  • the wire diameter of the core material 1 at the time of coating is determined by workability and cost, but is generally 0.2 to 0.8 mm due to the limitation of the manufacturing apparatus.
  • a coated wire coated with a metal such as Pd on the entire outer surface is subjected to a diffusion heat treatment at 200 to 500 ° C.
  • the thickness t of the coating layer 2 can be set to 0.02 to 0.09 ⁇ m by performing a tempering heat treatment so that the wire is drawn to 50.8 ⁇ m or less and further has a tensile elongation of 8% or more. The reason why the tensile elongation is 8% or more is to improve the stitch bondability and obtain more stable bonding properties.
  • the above copper added with the required amount of P can be adopted.
  • the step of forming the covering layer 2 is omitted.
  • the FAB since the electrical resistance value is increased as described above, the FAB can be stably formed in a low current and in a short time, and oxidation can be suppressed as much as possible. Moreover, in the wire provided with the coating layer, even if a crack occurs in the coating layer 2, it is possible to suppress the deterioration of oxidation resistance due to the crack as much as possible.
  • Examples 1 to 20 and Comparative Examples 1 to 12 shown in Table 1 are manufactured, and the bonding wire W has a continuous bonding property, HTST (High Temperature Storage Test), FAB stability, and a Si chip (electrode a) ) Was tested (confirmed) (Table 2). That is, first, an 8 mm diameter copper alloy wire was prepared by adding required ppm of Au, Ru, Rh, Pd, Os, Ir, Pt, and P to pure copper (4N) having a copper purity of 99.99 mass%. The alloy wire was coated with Pd and Pt by an electrolytic plating method, the coated wire was rewound, passed through an annealing furnace, and then wound again with a winding reel to perform continuous diffusion heat treatment.
  • the annealing furnace an electric furnace having a furnace core tube having a furnace length of 1 m was used, and nitrogen gas was allowed to flow through the furnace core tube.
  • the furnace temperature was 500 ° C. to 800 ° C.
  • the temperature of the coated wire (copper alloy wire) was 200 to 500 ° C.
  • the traveling speed of the coated wire was 5 to 60 m / min.
  • the wire is drawn to a wire diameter of 15 to 50 ⁇ m and further tempered so that the tensile elongation is 8% or more.
  • Heat treatment was performed to obtain bonding wires W (Examples 3 to 15 and Comparative Examples 1 to 10) having a thickness t of the coating layer 2 of 0.011 to 0.134 ⁇ m.
  • Table 2 shows the results of the following evaluation on each bonding wire W.
  • Depth analysis was performed by Auger spectroscopy. In the depth analysis, the concentration of Pd or Pt was measured while sputtering with Ar ions, and the distance from the surface layer was calculated in terms of SiO2. The thickness of the surface coating layer was defined as the thickness of the surface coating layer up to a point at which the concentration was half the measured value of the Pd or Pt concentration of the surface layer (see FIG. 3). [Analysis of additive elements] ICP analysis was used.
  • A Evaluation of continuous bonding property is A at both 200 ° C. and 150 ° C., and other evaluations are also A.
  • B Evaluation of continuous bonding property is A at 200 ° C., B at 150 ° C., and other evaluations. Evaluation is also A.
  • C Evaluation of continuous bonding property is C at 130 ° C., and other evaluation is A or B.
  • D At least one of D. Among these A, B, C, D, A and B were good and C could be used.
  • the FAB is a stable result in a perfect spherical shape (Examples 1 to 20, Comparative Examples 1 to 5, 7, 8, 10 to 12). ). Further, when the addition amount is 10 ppm or more, the result is very stable and the FAB shape is good (Examples 1, 3 to 9, 11 to 20, Comparative Examples 1 to 5, 7, 11, 12). On the other hand, when the addition amount is less than 2 ppm, the FAB shape is deteriorated (Comparative Examples 6 and 9). When the addition amount exceeds 50 ppm, the coating layer thickness t is 0.09 ⁇ m or less and the addition amount of Au or Pt group is small.

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Abstract

 被覆層(2)に亀裂が生じても芯材(1)の耐酸化性の劣化を極力抑制する。集積回路素子の電極(a)と回路配線基板の導体配線(c)をボールボンディング法によって接続するための線径(L)12μm以上50.8μm以下のボンディングワイヤ(W)である。99.99質量%以上の銅からなる芯材(1)にAu又は白金族の少なくとも1種以上を耐酸化性を向上するために添加し、Pを電気抵抗向上のために添加し、その芯材(1)の外周全面に耐酸化性のPt又はPdの厚み(t)0.02~0.09μmの被覆層(2)を形成したものとする。このボンディングワイヤは、Pの添加によって電気抵抗値が高くなり、スパークが低電流・短時間で、安定したFABが形成できる。このとき、芯材(1)にAu又は白金族が添加されているため、Pと化合物を生成せず、耐酸化性の向上効果を担保する。このため、その被覆層に亀裂が生じても、その亀裂による芯材の耐酸化性の劣化を極力抑制する。

Description

ボンディングワイヤ
 この発明は、IC、LSI、トランジスタ等の集積回路素子上の電極と、リードフレーム、セラミック基板、プリント基板等の回路配線基板の導体配線とをボールボンディング法によって接続するためのボンディングワイヤ及びその製造方法に関するものである。
 この種のボールボンディング法による接続方法は、図1(a)~(h)に示す態様が一般的であり、同図(a)に示す、ワイヤWがキャピラリー10aに挿通されてその先端にボール(FAB:Free  Air  Ball)bが形成された状態から、クランプ10bが開いて、キャピラリー10aが集積回路素子の電極aに向かって降下する。このとき、ボール(FAB)bはキャピラリー10a内に捕捉され、電極aにボンディングされる。
 ターゲットである電極aにボールbが接触すると(キャピラリー10aが電極aに至ると)キャピラリー10aがボールbをグリップし、ボールbに熱・加重・超音波を与え、それによってボールbと電極aが固相接合され、1stボンドが形成されて電極aと接着する(1st接合、図1(b))。
 1stボンドが形成されれば、キャピラリー10aは、一定高さまで上昇した後(同図(c))、導体配線cの真上まで移動する(同図(d)~(e))。このとき、安定したループを形成するため、キャピラリー10aに特殊な動きをさせてワイヤWに「くせ」を付ける動作をする場合がある(同図(d)の鎖線から実線参照)。
 導体配線cの真上に至ったキャピラリー10aは、導体配線cに向かって降下し、ワイヤWを導体配線(2ndターゲット)cに押付ける(同図(e)~(f))。これと同時に、その押付け部位に熱・加重・超音波を与え、それによってワイヤWを変形させ、ワイヤWを導体配線c上に接合させるためのステッチボンドと、次のステップでテイルを確保するテイルボンドを形成する(2nd接合、図1(f))。
 その両ボンドを形成した後、キャピラリー10aはワイヤWを残したまま上昇し、キャピラリー10aの先端に一定の長さのテイルを確保した後、クランプ10bを閉じて(ワイヤWをつかんで)、テイルボンドの部分からワイヤWを引きちぎる(図1(g))。
 キャピラリー10aは、所要の高さまで上昇すると停止し、そのキャピラリー10aの先端に確保されたワイヤWの先端部分に、放電棒gでもって高電圧を掛けて火花を飛ばし(放電し)、その熱でワイヤWを溶かし、この溶けたワイヤ素材は表面張力によって球状に近いボールbになって固まる(図1(h))。
 以上の作用で一サイクルが終了し、以後、同様な作用によって、電極aと導体配線cのボールボンディング法による接続がなされる。
 このボールボンディング法による接続において、ボンディングワイヤWには、金線が主に使用されるが、金は高価であるため、近年、銅純度99.9質量%以上(3N)の安価な銅線を使用することが行われている。そのとき、銅は裸のままでは、表面の酸化が起こり易いことから、その酸化が問題となる場合、図2に示すように、銅線からなる芯材1に耐酸化金属2を被覆したものが使用されている。
 その被覆金属(被覆層)2としては、金(Au)、白金(Pt)、パラジウム(Pd)、銀(Ag)、ニッケル(Ni)等が採用されている(特許文献1~3)。
特開2003-133361号公報 特開2004-64033号公報 特開2007-12776号公報 特開2009-140953号公報
 この金属被覆の銅線からなるボンディングワイヤWにおいて、近年の電子部品の小型化等による集積回路素子間の極小化に伴い、上記ボールbもより小さくする必要から、ボンディングワイヤWにも小径のものが望まれ、そのためには、その径Lを50μm以下とするのが好ましいとされている(特許文献1段落0009)。
 また、集積回路素子の電極aへの接続において、ボールbが下向き槍状(逆円錐状)になっていると、上記ボールbの電極aへの押付け時、そのボールbの尖鋭端によって電極aを損傷させる恐れがあるため、ボールbはできるだけ、真球であることが好ましい。そのボールbの真球度を高めるために、上記被覆層2の厚みtを芯線径の0.001以下としたり(特許文献1請求項1)、同じく被覆層2の厚みtを0.001~0.02μmとしたり(特許文献3請求項1)、芯材1の銅よりも高融点の耐酸化金属で被覆層2を形成したりしている(特許文献2段落0014)。
 さらに、有機基板をベースにしたBGA(Ball  Grid  Array)などでは加熱温度(ステージ温度)を高くすると、反りが発生してボンディング性が著しく悪化する。このため、上記ワイヤWと電極a又は導体配線cとの接合時の加熱温度(ステージ温度)を低く、例えば、150℃程度にしても、十分な接合強度を担保するための種々の工夫、例えば、熱処理後に伸線する加工等もされている(特許文献3段落0020、同0054等)。
 また、芯材1の銅に、リン(P)、ボロン(B)、ビスマス(Bi)、錫(Sn)、銀(Ag)、マンガン(Mg)を添加して、ピール試験(剥離試験)での破断伸びを増加させると共に、ボールの溶融時にそのP等の添加金属が被覆層2を形成する耐酸化性金属との相乗効果によって、ボールの真球性を向上させる技術も開示されている(特許文献4段落0055)。
 以上のように、耐酸化金属で銅線を被覆したボンディングワイヤWは、従来から、種々の工夫がなされてそれなりに好評を得ているが、近年の低コスト化に基づく、作業の高速化の要求の中で、より一層の作業の安定性、例えば、下記連続ボンディング性、FABの安定性等が求められている。
 その作業の安定性の向上には、芯材1の電気抵抗値を高めることが考えられ、その場合、上記P等を選択し得る。その電気抵抗値を高めることで、FAB形成の際のスパークを低電流・短時間で行うことができる。しかし、そのP等を添加した場合、耐酸化性が劣化する恐れがある。
 また、作業を高速化すると、上記ボールボンディング法による接続において、図1(e)~(f)に示した、キャピラリー10aが導体配線cに向かって降下し、ワイヤWを導体配線(2ndターゲット)cに押付けて、ワイヤWを海老の尻尾のように屈曲させると(同図(f)参照)、その屈曲に伴って被覆層2に亀裂が入る場合がある。被覆層2に亀裂が入れば、その亀裂個所の耐酸化性が劣化することとなり、同図(h)におけるボールbの形成時、その真球の形成に問題が生じる。
 この発明は、ボンディングワイヤWの電気抵抗値を高めるとともに耐酸化性の低下を防止することを第1の課題、上記亀裂が生じても耐酸化性の劣化を極力抑えることを第2の課題とする。
 上記第1課題を達成するために、この発明は、まず、上記の電気抵抗値を高めると考えるP、B、Bi、Sn、Ag、Mgの内、Pを添加することとしたのである。
 このPの添加によって電気抵抗値が高くなり、FAB形成の際のスパークを低電流・短時間で安定して供給することによってそのFABの形成ができる。
 Pは、添加しても加工熱安定性がある上に、一般的にCu-P合金として販売されていて、その入手も容易である上に、所要の添加量を得やすい。これに対し、Bは熱安定性が悪いことから、添加が困難であり、Biは環境面から好ましくなく、Snは溶解によって煤ができる問題があり、Agは酸化し易いことから、信頼性が劣り、Mgは蒸気圧が低いことから添加し難い問題がある。
 つぎに、上記耐酸化材として、上記Au、Pt、Pd、Ag、NiやFe(鉄)、Cr(クロム)、Mn等が考えられるが、これらの内、Ag、Ni、Fe、Mnは容易にPと化合物(Ag-P、Ni-P、Fe-P、Cr-P、Mn-P)を作るため、添加しても耐酸化性の向上に寄与しなくなる。このため、溶融してもPと化合しない、Au又はRu、Rh、Pd、Os、Ir、Ptの白金族(Pt族) の少なくとも1種以上を添加することとしたのである。このとき、所要量の添加のし易さから、1種がより好ましく、多くても2種にすることが好ましい。
 このように、Pと化合しないAu又はPt族であれば、Pの添加による電気抵抗値の向上を得ることができるとともに、Au等の添加による耐酸化性の向上を図ることができる。
 このPの添加量及びAu等の添加量は、その効果を得ることができる範囲で実験等によって適宜に定めれば良いが、例えば、Pにあっては、2~250ppm、Au等にあっては、合計で1~100ppmとする。P:2ppm未満では、電気抵抗値の向上が望めず、低電流・短時間によるボール形成の効果を得ることができない場合があり、250ppmを越えると、電気抵抗値が上がりすぎてSiチップ等の素子(電極a)からリード(導体配線c)に信号を伝えるというボンディングワイヤとしての機能を阻害する恐れがあるとともに、上記1st接合時の電極aにクラック(チップクラック)が生じる恐れがある。Au等が100ppmを越えると、ワイヤWの強度が高くなりすぎて、1st接合時のチップクラックの原因となる恐れがあり、1ppm未満では耐酸化性の効果を望めない恐れがある。また、Pにあっては、ボール形成が特に安定する範囲は10ppm以上である。
 さらに、最近ではより脆弱な電極aが使われることがあるため、チップクラックに対してはより要求が厳しくなっている。そのため、Pの添加量及びAu等の添加量についてはより好ましい範囲はPにあっては、50ppm以下、Au等にあっては合計で1ppm以上50ppm以下とする。この範囲であれば、上記の効果が得られるとともに、ボールbが硬くなりすぎないため、より脆弱な電極aにもチップクラックを生じることなく、1st接合できる。一方でPが50ppmを超えて250ppm以下またはAu等が50ppmを超えて100ppm以下添加されると、ボールbが硬くなって、脆弱な電極aに用いることができなくなる。
 この発明の具体的な構成としては、集積回路素子の電極と回路配線基板の導体配線をボールボンディング法によって接続するための線径12μm以上50.8μm以下のボンディングワイヤであって、Au又はPt族から少なくとも1種を耐酸化性を向上するために添加するとともに、Pを電気抵抗向上のために添加した純度99.99質量%以上の銅からなる構成のボンディングワイヤとしたのである。
 この構成において、ボンディングワイヤWの線径Lを、50.8μm以下としたのは、上述の特許文献1ではその径Lを50μm以下としているが、50.8μm以下であれば、50μm以下とかわらない程度でもって、上記ボールbをより小さくできるからである。
 また、線径Lの下限を12μm以上としたのは、12μm未満ではボンディング前にオペレータがワイヤWをキャピラリー10aに通すのが困難になり、作業性が悪くなるからである。
 芯材1の銅純度を99.9質量%(3N)以上としたのは、銅の高導電性を担保するためである。
 上記第2の課題を達成するために、この発明は、まず、芯材に電気抵抗値を高めるためにPを添加するとともに、耐酸化性を向上させるためにAu又はPt族の少なくとも1種以上を添加したものとして、FAB形成の際のスパークを低電流・短時間で安定してそのFABの形成ができるとともに、芯材そのものを耐酸化性のものとしたのである。
 このようにすれば、上記と同様に、Pの添加によって、耐酸化性の劣化を招くことなく、電気抵抗値が高くなり、FAB形成の際のスパークを低電流・短時間で安定して供給することによってそのFABの形成ができる。
 つぎに、芯材の外周全面に耐酸化性のPt又はPdの厚みtが0.02~0.09μmの被覆層を形成したのである。
 このPt又はPdは、上記のように、Pとは化合物を生成しないため、被覆層が溶けてもその化合物ができることがなく、電気抵抗値及び耐酸化性の向上は図られる。
 また、Pd、Ptは、その融点が銅の融点より高いため、ボールbの真球度が増すことが期待できる。
 なお、上記2nd接合時等において、ワイヤ(被覆層)に亀裂が生じても、その亀裂は、通常僅かであるため、上記芯材1中へのAu等の添加量でその酸化を十分に抑制する。
 この発明の具体的な構成としては、集積回路素子の電極と回路配線基板の導体配線をボールボンディング法によって接続するための線径12μm以上50.8μm以下のボンディングワイヤであって、その芯材が、金又は白金族から少なくとも1種以上を耐酸化性を向上するために添加するとともに、Pを電気抵抗向上のために添加した純度99.9質量%以上の銅からなり、その芯材の外周全面に、耐酸化性のPt又はPdの厚み0.02~0.09μmの被覆層を形成した構成のボンディングワイヤとしたのである。
 この構成において、線径12μm以上50.8μm以下、純度99.9質量%以上としたのは、上記と同一の理由である。
 また、被覆層2の厚みtは薄いほど、ボールbの硬度が低くなり、Siチップ(電極a)の損傷の可能性が低くなるが、薄すぎると、ステッチボンド接合の際に芯材1の銅が露出する度合いが大きくなり、被覆層2を有さない銅ワイヤ程度のステッチボンド接合性しか発現できない。例えば、後記実施例と比較例の実験結果から理解できるように、2回以上のマシンストップが生じる恐れがある。このため、その実施例と比較例の実験結果から、被覆層2の厚みtは0.02μm以上とする。
 なお、ステージ温度:150℃程の低温度でのボールボンディングの時には、連続ボンディング性の実験結果からその厚みtを0.04μm以上とする。ステージ温度を低くすると、ステッチボンド接合に要する加重が大きくなり、被覆層2の厚みtが0.02μm以上から0.04μm未満の範囲では芯材の銅が露出する度合いが大きくなり、連続ボンディング性が損なわれることがあるからである。
 一方、被覆層2が厚いと、ボールbの硬度が高くなり、Siチップ(電極a)の損傷の可能性が高くなる。このため、後記実施例と比較例の実験結果から、被覆層2の厚みtは0.09μm以下とする。
 また、被覆層2の厚みtを0.04μm以上とした場合、ステージ温度150℃でもマシントラブルが少なくなるが、特に、Pdを被覆層2に採用し、被覆層2の厚みtを0.05μm以上とした時にはステージ温度をより低温の130℃としたときでもマシントラブルが起こらないことも確認されている。これは、パラジウム被覆層2の場合、CuとPdの溶融時間差が小さく、より真球になりやすいこととの相乗効果に基づくものと考える。
 さらに、上記芯材の銅純度を99.99質量%(4N)以上、さらに、同99.999質量%(5N)以上とすれば、Siチップ(電極a)の損傷の可能性が低くなる。これは、銅純度を99.99質量%以上、さらに、同99.999質量%以上とすることで、FAB硬度をより低減できるからである。
 これらの構成のボンディングワイヤWの製造方法には種々のものが採用できるが、例えば、純度99.9質量%以上の銅からなる芯材1の外周全面に、Pt、Pdの1種以上による被覆層2を形成し、その被覆線を拡散熱処理して芯材と被覆層の密着性を高めた後、線径12μm以上50.8μm以下まで伸線し、さらに、引張伸びが8%以上となるように調質熱処理を行って、被覆層2の厚みtを0.02~0.09μmとした構成を採用できる。
 その被覆層2は、電解めっき、無電解めっき、蒸着法等の周知の手段によって形成され、一般に、ワイヤWは大きな線径の銅ロッドをダイスと呼ばれるツールに順次貫通させていくことにより、所定の線径に仕上げられるため、この工程途中の適宜な線径で被覆層2を前記手段により形成する。このとき、被覆する際の芯材1の線径は作業性・コストにより決定されるが、製造装置の制限から0.2~0.8mmが一般的である。外周全面にPd等の金属を被覆された被覆線は200~500℃(被覆線の温度)で拡散熱処理を施して前記芯材1と被覆層2の密着性を高めた後、線径12μm以上50.8μm以下まで伸線し、さらに、引張伸びが8%以上となるように調質熱処理を行って、被覆層2の厚みtを0.02~0.09μmとすることができる。
 引張伸びを8%以上とするのは、ステッチボンド接合性を上げ、より安定したボンディング性を得るためである。
 以上のボンディングワイヤWの製造方法において、前記銅に上記所要量のPを添加したものを採用できる。このとき、被覆層2を有しないワイヤWにあっては、その被覆層2を形成する工程を省略する。
 この発明は、以上のようにして電気抵抗値を高めたので、低電流・短時間で安定してそのFABの形成ができるうえに、酸化を極力抑えることができる。また、被覆層を設けたワイヤにあっては、仮に、被覆層2に亀裂が生じても、その亀裂による耐酸化性の劣化を極力抑制することができる。
ボールボンディング接続法の説明図であり、(a)~(h)はその途中図 この発明に係るボンディングワイヤの断面図 オージェピーク強度と被覆層(めっき層)深さの関係図
 表1に示す実施例1~20及び比較例1~12を製作し、そのボンディングワイヤWの連続ボンディング性、HTST(High Temperature Storage Test)、FABの安定性及び1st接合部のSiチップ(電極a)の損傷度合の試験(確認)を行った(表2)。
 すなわち、まず、銅純度99.99質量%の純銅(4N)に、Au、Ru、Rh、Pd、Os、Ir、Pt及びPを所要ppm添加した8mm径の銅合金線を作製し、その銅合金線にPd、Ptを電解めっき法によって被覆し、その被覆線を巻き戻し、焼鈍炉を通したのち、再び巻き取り用リールで巻き取ることによって連続拡散熱処理を行った。焼鈍炉は炉長1mの炉芯管を有する電気炉を用い、炉芯管には窒素ガスを流した。その炉温度は500℃以上800℃以下として被覆線(銅合金線)の温度を200~500℃とし、その被覆線の走行速度は5~60m/分とした。
 以上の拡散熱処理を施して銅線(芯材)1と被覆層2の密着性を高めた後、線径15~50μmまで伸線し、さらに、引張伸びが8%以上となるように調質熱処理を行って、被覆層2の厚みt:0.011~0.134μmのボンディングワイヤW(実施例3~15及び比較例1~10)を得た。
 つぎに、この各ボンディングワイヤWにおいて、下記の評価を行った結果を表2に示す。
 〔表面被覆層の厚み〕
 オージェ分光分析法による深さ分析を行った。深さ分析はArイオンでスパッタしながらPdまたはPtの濃度を測定し、SiO2換算して表層からの距離を算出した。表面被覆層の厚みは、表層のPdまたはPt濃度の測定値の1/2の濃度になる点までを表面被覆層の厚みとした(図3参照)。
 〔添加元素の分析〕
 ICP分析を用いた。
 〔連続ボンディング性〕
 ボンディングマシンで、10,000回の連続ボンディングを行い、マシンストップが発生しなければA、1回のマシンストップでB、2回以上のマシンストップが起こればDとした。
 連続ボンディングはステージ温度が低くなれば困難になることから、200℃、150℃の2水準で行った。
 また、ステージ温度130℃でも同様の連続ボンディングを行った。このときの評価については、マシンストップの発生なしの場合をA、1回のマシンストップではB、2~3回のマシンストップでC、3回以上のマシンストップが起こればDとした。
 〔HTST〕
 ボンディング後、200℃に加熱された大気炉にリードフレームを入れ、1000hr経過後のワイヤWの状態を光学顕微鏡500倍の倍率で確認した。酸化が進んでいないものはA、キズが発生し、Cuが露出することによってワイヤWに酸化部が点在しているものはDとした。
 〔FABの安定性〕
 100個のFABを作製し、95%以上が真球状ならA、90%以上95%未満が真球状ならB、90%未満ならDとした。
 〔1st接合部のSiチップ損傷〕
 ボンディング後、1stボール接合部直下のSiチップ損傷を評価するために、ボール接合部および電極膜を王水で溶解し、Siチップのクラックを走査型電子顕微鏡(SEM)500倍で観察した。
 100個の接合部を観察して5μm未満の微小なピットが1個もしくはまったく見られない場合はA、5μm未満の微小なピットが2~5個ある場合はB、5μm以上のクラックが2個以上もしくは5μm未満の微小なピットが6個以上認められた場合をDとした。
 〔総合評価〕
 A:連続ボンディング性の評価が200℃、150℃ともにAであり、かつ他の評価もAであるもの
 B:連続ボンディング性の評価が200℃ではA、150℃ではBであり、かつ他の評価もAであるもの
 C:連続ボンディング性の評価が130℃でCであり、かつ他の評価がA又はBのもの
 D:ひとつでもDのあるもの
 このA、B、C、Dの内、A、Bを良好とし、Cは使用し得るものとした。
Figure JPOXMLDOC01-appb-T000001
Figure JPOXMLDOC01-appb-T000002
 この試験結果から、被覆層厚tが0.02μm未満であると、200℃及び150℃の両連続ボンディング性が低下し(比較例1、3、7)、0.02μm以上0.04μm未満になると、前者の連続ボンディング性が満足できるものとなり(実施例1、3、10、17、比較例8)、0.04μm以上となると、両者の連続ボンディング性が満足できる(良好な)ものとなることが理解できる(実施例2、4~9、11~16、18~20、比較例2、4~6、9~12)。また、被覆層にPdを用い、被覆層厚tが0.05μm以上となると、130℃での連続ボンディング性が満足できるものとなることがわかる(実施例2、4、5、7~9、11、13、14、比較例4~6)。
 一方、被覆層厚tが0.09μmを越えると、ボールbが硬くなって、Siチップ(電極a)の損傷が認められるようになる(比較例2、9、11、12)。
 また、芯材1にAuまたはPt族を1ppm以上添加したものはHTSTの結果が良好になり(実施例1~20、比較例1、2、5、7、9~12)、1ppm未満のものは耐酸化性が低くなる(比較例3、4、6、8)。これらにおいて、同50ppmを超えたものについては、被覆層厚tが0.09μm以下であっても、ボールbが硬くなるため、電極aに若干の損傷が認められるようになる(比較例1、7)。同100ppmを超えたものについては、被覆層厚tが0.09μm以下であっても、電極aに損傷が生じ、使用上問題が起こる(比較例5、9、10)。
 P添加については、添加量が2ppm以上10ppm未満であれば、FABが安定して真球状になる良好な結果である(実施例1~20、比較例1~5、7、8、10~12)。また、添加量が10ppm以上であれば、非常に安定してFAB形状が良好な結果となる(実施例1、3~9、11~20、比較例1~5、7、11、12)。一方、添加量が2ppm未満であるとFAB形状が悪くなり(比較例6、9)、添加量が50ppmを超えると、被覆層厚tが0.09μm以下でかつAuまたはPt族の添加量が50ppm以下であっても、電極aに若干の損傷が認められるようになる(実施例1、5、16、20)。さらに、添加量が250ppmを超えると、被覆層厚tが0.09μm以下でかつAuまたはPt族の添加量が50ppm以下であっても、ボールbが硬くなって、電極aの損傷が認められるようになる(比較例3、4)。
W ボンディングワイヤ
1 芯材
2 被覆層
a 集積回路素子の電極
b ボンディングボール
c 回路配線基板の導体配線

Claims (5)

  1.  集積回路素子の電極(a)と回路配線基板の導体配線(c)をボールボンディング法によって接続するための線径(L):12μm以上50.8μm以下のボンディングワイヤ(W)であって、
     その芯材(1)が、金又は白金族から少なくとも1種以上を耐酸化性を向上するために添加するとともに、リンを電気抵抗向上のために添加した純度99.9質量%以上の銅からなり、
     その芯材(1)の外周全面に、耐酸化性の白金又はパラジウムの厚み(t):0.02~0.09μmの被覆層(2)を形成したことを特徴とするボンディングワイヤ。
  2.  上記被覆層(2)の厚み(t)を0.04~0.09μmとしたことを特徴とする請求項1に記載のボンディングワイヤ。
  3.  上記被覆層(2)の厚み(t)を0.05~0.09μmとしたことを特徴とする請求項1に記載のボンディングワイヤ。
  4.  上記リンの添加量:2~250ppm、上記金又は白金族から少なくとも1種にあっては、その合計添加量:1~100ppmとしたことを特徴とする請求項1乃至3の何れかに記載のボンディングワイヤ。
  5.  上記リンの添加量:10~50ppm、上記金又は白金族から少なくとも1種にあっては、その合計添加量:1~50ppmとしたことを特徴とする請求項1乃至3の何れかに記載のボンディングワイヤ。
PCT/JP2011/058786 2010-04-14 2011-04-07 ボンディングワイヤ WO2011129256A1 (ja)

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