Kinetics of intermetallic phase formation at the interface of Sn-Ag-Cu-X (X = Bi, In) solders with Cu substrate

The effects of Bi and In additions on intermetallic phase formation in lead-free solder joints of Sn-3.7Ag-0.7Cu; Sn-1.0Ag-0.5Cu-1.0Bi and Sn-1.5Ag-0.7Cu-9.5In (composition given in weight %) with copper substrate are studied. Soldering of copper plate was conducted at 250 °C for 5 s. The joints were subsequently aged at temperatures of 130-170 °C for 2-16 days in a convection oven. The aged interfaces were analyzed by optical microscopy and energy dispersive X-ray spectroscopy (EDX) microanalysis. Two intermetallic layers are observed at the interface - Cu₃Sn and Cu₆Sn₅. Cu₆Sn₅ is formed during soldering. Cu₃Sn is formed during solid state ageing. Bi and In decrease the growth rate of Cu₃Sn since they appear to inhibit tin diffusion through the grain boundaries. Furthermore, indium was found to produce a new phase - Cu₆(Sn,In)₅ instead of Cu₆Sn₅, with a higher rate constant. The mechanism of the Cu₆(Sn,In)₅ layer growth is discussed and the conclusions for the optimal solder chemical composition are presented.     

Suppressing effect of 0.5 wt.% nano-TiO2 addition into Sn-3.5Ag-0.5Cu solder alloy on the intermetallic growth with Cu substrate during isothermal aging

This study investigated the effects of adding 0.5 wt.% nano-TiO₂ particles into Sn3.5Ag0.5Cu (SAC) lead-free solder alloys on the growth of intermetallic compounds (IMC) with Cu substrates during solid-state isothermal aging at temperatures of 100, 125, 150, and 175 °C for up to 7 days. The results indicate that the morphology of the Cu₆Sn₅ phase transformed from scallop-type to layer-type in both SAC solder/Cu joints and Sn3.5Ag0.5Cu-0.5 wt.% TiO₂ (SAC) composite solder/Cu joints. In the SAC solder/Cu joints, a few coarse Ag₃Sn particles were embedded in the Cu₆Sn₅ surface and grew with prolonged aging time. However, in the SAC composite solder/Cu aging, a great number of nano-Ag₃Sn particles were absorbed in the Cu₆Sn₅ surface. The morphology of adsorption of nano-Ag₃Sn particles changed dramatically from adsorption-type to moss-type, and the size of the particles increased.The apparent activation energies for the growth of overall IMC layers were calculated as 42.48 kJ/mol for SAC solder and 60.31 kJ/mol for SAC composite solder. The reduced diffusion coefficient was confirmed for the SAC composite solder/Cu joints.     

微小互连Cu-Sn界面钎焊及接头剪切行为

针对Cu-Sn-Cu三明治结构,进行0.06 MPa恒压钎焊. 基于Cu-Sn二元相图,选定了不同的钎焊温度与钎焊时间. 钎焊完成后,根据不同相组成可将接头分为残余锡,Cu₃Sn-Cu₆Sn₅-Cu₃Sn,Cu-Cu₃Sn-Cu三类. 为研究三种不同相组成接头抗剪强度之间的关系,进行1 mm/min加载速率的剪切试验,并对断口进行形貌分析. 结果表明,随着Sn与Cu₆Sn₅相继耗尽,接头抗剪强度不断升高. 残余锡接头,Cu₃Sn-Cu₆Sn₅-Cu₃Sn接头,Cu-Cu₃Sn-Cu接头抗剪强度分别为23.26,33.59,51.83 MPa. 分析断口形貌发现,在残余Sn接头断口中,可以分辨出Sn,Cu₆Sn₅,Cu₃Sn形貌,说明其断裂路径穿过了Cu₆Sn₅与Cu₃Sn两相. 在Cu₃Sn-Cu₆Sn₅-Cu₃Sn接头断口中,可分辨出Cu₆Sn₅,Cu₃Sn形貌,其断裂路径穿过了Cu₃Sn相. 全Cu₃Sn相接头断口中仅可分辨出Cu₃Sn相断裂形貌.     

Microstructure, kinetic analysis and hardness of Sn-Ag-Cu-1 wt% nano-ZrO2 composite solder on OSP-Cu pads

Nano-sized, nonreacting, noncoarsening ZrO₂ particle-reinforced Sn-Ag-Cu composite solders were prepared by mechanically dispersing ZrO₂ nano-particles into Sn-Ag-Cu solder and the interfacial morphology between the solder and organic solderability preservative (OSP)-Cu pads were characterized metallographically. At their interfaces, island-shaped Cu₆Sn₅ and Cu₃Sn intermetallic compound (IMC) layers were found in solder joints with and without the ZrO₂ particles and the IMC layer thickness was substantially increased with reaction time and temperature. In the solder ball region, needle-shaped Ag₃Sn and spherically-shaped Cu₆Sn₅ IMC particles were found to be uniformly distributed in the β-Sn matrix. However, after the addition of ZrO₂ nano-particles, Ag₃Sn and Cu₆Sn₅ IMC particles appeared with a fine microstructure and retarded the growth rate of the IMC layers at their interfaces. From a kinetic analysis, the calculated activation energies for the total (Cu₆Sn₅ + Cu₃Sn) IMC layers for Sn-Ag-Cu and Sn-Ag-Cu-1 wt% ZrO₂ composite solder joints on OSP-Cu pads were about 53.2 and 59.5 kJ/mol, respectively. In addition, solder joints containing ZrO₂ nano-particles displayed higher hardness due to the uniform distribution of ZrO₂ nano-particles as well as the refined IMC particles. The hardness values of the plain Sn-Ag-Cu solder joint and solder joints containing 1 wt% of ZrO₂ nano-particles after 5 min reaction at 250 °C were about 15.0 Hv and 17.1 Hv, respectively. On the other hand, their hardness values after 30 min reaction were about 13.7 Hv and 15.5 Hv, respectively.     

Enthalpy of formation of Au-Sn intermetallic phases. Part II

The technique of solution calorimetry with liquid Sn has been used for the determination of enthalpy of formation of intermetallic compounds from the Au-Sn system. The intermetallic phases were prepared and homogenized in a glow-box operated in high purity argon. They were analyzed by an X-ray diffraction method before the calorimetric investigations to confirm their crystallographic structure. The obtained experimental values of enthalpy of formation were −5.8 ± 0.3 and −1.3 ± 0.4 kJ/mole of atoms for ζ′-Au₅Sn, and ζ-Au₅Sn of the composition Au₈₉Sn₁₁, respectively. Using the DTA technique the transition temperatures were measured for the following phases: η-AuSn₄, ?-AuSn₂, δ-AuSn, ζ′-Au₅Sn and ζ-Au₅Sn (Au₈₉Sn₁₁). It was found that the obtained data in the study agreed very well with the results previously presented in literature, except for the ζ-Au₅Sn (Au₈₉Sn₁₁) intermetallic phase, for which a difference of about 50° was observed for the liquidus temperature.     

Intermetallic compound growth suppression at high temperature in SAC solders with Zn addition on Cu and Ni-P substrates

The effect of adding 0.5-1.5 wt.% Zn to Sn-3.8Ag-0.7Cu (SAC) solder alloy during reflow and solid state ageing has been investigated. In particular, the role of the Zn addition in suppressing interfacial Intermetallic Compound (IMC) growth on Cu and Ni-P substrates has been determined. Solder-substrate couples were aged at 150 °C and 185 °C for 1000 h. In the case of 0.5-1.0 wt.% Zn on Cu substrate, Cu₃Sn IMC was significantly suppressed and the morphology of Cu₆Sn₅ grains was changed, leading to suppressed Cu₆Sn₅ growth. In the SAC-1.5Zn/Cu substrate system a Cu₅Zn₈ IMC layer nucleated at the interface followed by massive spalling of the layer into the solder, forming a barrier layer limiting Cu₆Sn₅ growth. On Ni-P substrates the (Cu,Ni)₆Sn₅ IMC growth rate was suppressed, the lowest growth rate being found in the SAC-1.5Zn/Ni-P system. In all cases the added Zn segregated to the interfacial IMCs so that Cu₆Sn₅ became (Cu,Zn)₆Sn₅ and (Cu,Ni)₆Sn₅ became (Ni,Cu,Zn)₆Sn₅. The effect of Zn concentration on undercooling, wetting angles and IMC composition changes during ageing are also tabulated, and a method of incorporating Zn into the solder during reflow without compromising solder paste reflow described.     

Effect of adding 1 wt% Bi into the Sn–2.8Ag–0.5Cu solder alloy on the intermetallic formations with Cu-substrate during soldering and isothermal aging

Intermetallic compound (IMC) formations of Sn–2.8Ag–0.5Cu solder with additional 1 wt% Bi were studied for Cu-substrate during soldering at 255 °C and isothermal aging at 150 °C. It was found that addition of 1 wt% Bi into the Sn–2.8Ag–0.5Cu solder inhibits the excessive formation of intermetallic compounds during the soldering reaction and thereafter in aging condition. Though the intermetallic compound layer was Cu₆Sn₅, after 14 days of aging a thin Cu₃Sn layer was also observed for both solders. A significant increase of intermetallic layer thickness was observed for both solders where the increasing tendency was lower for Bi-containing solder. After various days of aging, Sn–2.8Ag–0.5Cu–1.0Bi solder gives comparatively planar intermetallic layer at the solder–substrate interface than that of the Sn–2.8Ag–0.5Cu solder. The formation of intermetallic compounds during aging for both solders follows the diffusion control mechanism and the diffusion of Cu is more pronounced for Sn–2.8Ag–0.5Cu solder. Intermetallic growth rate constants for Sn–2.8Ag–0.5Cu and Sn–2.8Ag–0.5Cu–1.0Bi solders were calculated as 2.21 × 10⁻¹⁷ and 1.91 × 10⁻¹⁷ m²/s, respectively, which had significant effect on the growth behavior of intermetallic compounds during aging.     

Interface reaction systematics in the Cu/In–48Sn/Cu system bonded by diffusion soldering

An alternative lead-free solder alloy In–48 at%Sn with a melting point of 120 °C and its implementation to bond Cu substrates in a diffusion soldering joining method are presented. According to the EPMA, TEM/EDX and electron diffraction analyses, two different behaviors were observed in the interconnection zone depending on the temperature range: (i) a single layer consisting of η phase below 200 °C; (ii) a Cu-poor region consisting of η phase and a Cu-rich layer formed by a mixture of thin alternate regions of ζ-Cu₁₀Sn₃ and δ-Cu₇In₃ phases perpendicular to the interconnection plane above 200 °C. The η layer shows two morphologies: large grains and fine grains at the η/In–48Sn (liquid) and at the η/Cu-rich interfaces, respectively. Additionally, the η region shows a gradual change in composition, suggesting a change from the Cu₆Sn₅ to the Cu₂In structures. Thermal stability tests indicate that the thermal resistance of the bonds is about 750 °C.     

Interfacial reactions and mechanical properties between Sn-4.0Ag-0.5Cu and Sn-4.0Ag-0.5Cu-0.05Ni-0.01Ge lead-free solders with the Au/Ni/Cu substrate

Sn-4.0Ag-0.5Cu (SAC) and Sn-4.0Ag-0.5Cu-0.05Ni-0.01Ge (SACNG) lead-free solders reacting with the Au/Ni/Cu multi-layer substrate were investigated in this study. All reaction couples were reflowed at 240 and 255 °C for a few minutes and then aged at 150 °C for 100-500 h. The (Cu, Ni, Au)₆Sn₅ phase was formed by reflowing for 3 min at the interface. If the reflowing time was increased to 10 min, both (Cu, Ni, Au)₆Sn₅ and (Ni, Cu, Au)₃Sn₄ phases formed at the interface. The AuSn₄ phase was found in the solder for all reaction couples. An addition of Ni and Ge to the solder does not significantly affect the IMC formation. After a long period of heat-treatment, the thickness of the (Cu, Ni, Au)₆Sn₅ and (Ni, Cu, Au)₃Sn₄ phases increased and the intermetallic compounds (IMCs) growth mechanism obeyed the parabolic law and the IMC growth mechanism was diffusion-controlled. The mechanical strengths for both the soldered joints decreased with increasing thermal aging time. The SACNG/Au/Ni/Cu couple had better mechanical strength than that in the SAC/Au/Ni/Cu couple.     

Evolution of CuSn intermetallics between molten SnAgCu solder and Cu substrate

The evolution of SnCu intermetallic compounds (IMCs) between a molten SnAgCu alloy and the Cu under-bump metallization (UBM) throughout reflow is presented based on interruption of soldering reactions in experiments by removing the liquid solder from the substrate. This allows to capture and visualize interfacial reactants at arbitrary moments of the soldering process, and to gain an insight into their formation characteristics. The results show that the interfacial Cu₆Sn₅/Cu₃Sn structure is formed at an early stage of reflow and is maintained throughout the process. Based on the experiments, formation mechanisms of interfacial CuSn IMCs are discussed.     

Thermo-electrochemical activation of Cu3Sn negative electrode for lithium-ion batteries

A Cu₃Sn film electrode (thickness = ca. 3 μm) is prepared by DC magnetron sputtering deposition of Sn on Cu substrate and subsequent annealing at 300 °C for 30 h. At 25 °C, this Cu-Sn binary intermetallic compound is inactive for lithiation, but becomes active at elevated temperatures due to facilitation of Cu-Sn bond cleavage for the conversion-type lithiation. The lithiated product at 120 °C is the most Li-rich Li-Sn alloy (Li₁₇Sn₄). Upon de-lithiation, the Cu-Sn intermetallics of different compositions are generated by the reaction between the metallic Sn that is restored from Li₁₇Sn₄ and the idling metallic Cu. The nature of the resulting intermetallics is dependent on the de-lithiation temperature: Cu₁₀Sn₃ at 120 °C and Cu₆Sn₅ at 25 °C. Only the latter is active for lithiation in the subsequent room-temperature cycling. That is, Cu₃Sn is thermo-electrochemically activated to be Cu₆Sn₅ by lithiation at 120 °C and subsequent de-lithiation at 25 °C. The higher lithiation activity observed with the more Sn-rich phase (Cu₆Sn₅) compared to the initial one (Cu₃Sn) has been accounted for by the higher equilibrium lithiation potential (thermodynamic consideration) and smaller number of Cu-Sn bonds to be broken (kinetic consideration).     

Morphology and growth kinetics of Ag3Sn during soldering reaction between liquid Sn and an Ag substrate

For the soldering of recycled Ag sputtering targets, the interfacial reaction between liquid Sn and an Ag substrate at temperatures ranging from 250 –425°C has been investigated. Experimental results show that a scallop-shaped layer of Ag₃Sn intermetallic compounds formed during the soldering reaction. Kinetics analysis indicated that the growth of such interfacial Ag₃Sn intermetallic compounds is diffusion-controlled with activation energy of 70.3kJ/mol. During the reaction, the Ag substrate dissolves into the molten Sn solder and causes the appearance of needle-shaped Ag₃Sn precipitates in the Sn matrix.     

The structural,elastic, electronic and thermodynamic properties of hexagonal η-Cu6−xNixSn5 (x = 0, 0.5, 1, 1.5 and 2) intermetallic compounds

Based on first-principles calculations, the effects of various Ni concentrations on the structural, elastic, electronic and thermodynamic properties of hexagonal η-Cu₆Sn₅ compound have been systematically investigated. The results demonstrate that higher Ni concentration in the η-Cu_6−xNi_xSn₅ (x = 0, 0.5, 1, 1.5 and 2) leads to thermodynamically stable compounds, and Ni atoms preferentially occupy Cu₂ + Cu_1c sites forming the η-Cu₄Ni₂Sn₅ compound. It is also found that the unit cell volume and lattice parameter of the ‘a’ axis decrease with increasing Ni concentration, which are consistent with the other experimental results. Furthermore, the polycrystalline elastic properties are obtained from single-crystal elastic constants. Our results indicate that the addition of Ni enhances the mechanical stability, brittleness, modulus and Debye temperatures of η-Cu₆Sn₅ compound. Analyzing the electronic structure and charge density distribution provides the explanation that Ni develops distinct bonding energy to Cu and Sn in the structure.     

Ni segregation in the interfacial (Cu,Ni)6Sn5 intermetallic layer of Sn-0.7Cu-0.05Ni/Cu ball grid array (BGA) joints

Ni segregation in the interfacial (Cu,Ni)₆Sn₅ intermetallic layer of Sn-0.7Cu-0.05Ni/Cu BGA solder joints was investigated by using synchrotron micro X-ray fluorescence (XRF) analysis and synchrotron X-ray diffraction (XRD). Compared to Sn-0.7Cu/Cu BGA joints, Ni containing solder show suppressed Cu₃Sn growth in both reflow and annealed conditions. In as-reflowed Sn-0.7Cu-0.05Ni/Cu BGA joints, Ni was relatively homogenously distributed within interfacial (Cu,Ni)₆Sn₅. During subsequent annealing, the diffusion of Ni in Cu₆Sn₅ was limited and it remained concentrated adjacent the Cu substrate where it contributes to the suppression of Cu₃Sn formation at the interface between the Cu substrate and Cu₆Sn₅ intermetallics.     

Composition and heat-treatment effects on the adhesion strength of Sn-Zn-Al solders on Cu substrate

Intermetallic layer growth at the solder/substrate interface during soldering and subsequent aging in service can affect bond strength and dimensional stability. In this work, interfacial structure and bonding strength studies were performed on lead-free, Sn-Zn-Al solders as a function of composition and aging time. With the x value of Sn-x(5Al-Zn) solder increasing from 5 wt.% to 40 wt.%, the adhesion strength of bonding decreased from 11.2±0.5 MPa to 3.3±0.9 MPa while the thickness of the γ-Cu₅Zn₈ intermetallic compound layer increased from less than 1 μm to about 2 μm. Simultaneously, the adhesion strength of Sn-x(5Al-Zn) solders with x=5, 9, 20, 30, and 40 decreased as the aging time at 150°C increased from 0 to 1,000 hours. For more information, contact M.-C. Wang, National Kaohsiung Institute of Technology, Department of Mechanical Engineering, 415 Chien-Kung Road, Kaohsiung 80782, Taiwan; telephone 886-6-258-5663; fax 886-6-250-2734.     

Reaction diffusions of Cu<Subscript>6</Subscript>Sn<Subscript>5</Subscript> and Cu<Subscript>3</Subscript>Sn intermetallic compound in the couple of Sn-3.5Ag eutectic solder and copper substrate

The growth kinetics of intermetallic compound layers formed between Sn-3.5Ag solder and Cu substrate were investigated as a consequence of solid-state isothermal aging. Isothermal aging was carried out in a temperature range between 70°C and 200°C for 0 to 60 days. A quantitative analysis of the intermetallic compound layer thickness as a function of time and temperature was performed. The diffusion couples showed a composite intermetallic layer comprised of Cu₆Sn₅ and Cu₃Sn. The growth of intermetallic compounds followed diffusion-controlled kinetics and the layer thickness reached only 9 μm after 60 day of aging at 150°C. The apparent activation energies were calculated for the growth of the total intermetallic compound (Cu₆Sn₅+Cu₃Sn); Cu₆Sn₅ and Cu₃Sn intermetallic are 65.4, 55.4 and 75.7 kJ/mol, respectively.     

Growth Behavior of Intermetallic Compounds at SnAgCu/Ni and Cu Interfaces

The growth behavior of reaction-formed intermetallic compounds (IMCs) at Sn3.5Ag0.5Cu/Ni and Cu interfaces under thermal-shear cycling conditions was investigated. The results show that the morphology of (Cu _x Ni_1–x )₆Sn₅ and Cu₆Sn₅ IMCs formed both at Sn3.5Ag0.5Cu/Ni and Cu interfaces gradually changed from scallop-like to chunk-like, and different IMC thicknesses developed with increasing thermal-shear cycling time. Furthermore, Cu₆Sn₅ IMC growth rate at the Sn3.5Ag0.5Cu/Cu interface was higher than that of (Cu _x Ni_1–x )₆Sn₅ IMC under thermal-shear cycling. Compared to isothermal aging, thermal-shear cycling led to only one Cu₆Sn₅ layer at the interface between SnAgCu solder and Cu substrate after 720 cycles. Moreover, Ag₃Sn IMC was dispersed uniformly in the solder after reflow. The planar Ag₃Sn formed near the interface changed remarkably and merged together to large platelets with increasing cycles. The mechanism of formation of Cu₆Sn₅, (Cu _x Ni_1–x )₆Sn₅ and Ag₃Sn IMCs during thermal-shear cycling process was investigated.     

Interfacial reactions between Sn–8Zn–3Bi–xAg lead-free solders and Cu substrate

The formation and the growth of the intermetallic compounds (IMCs) at the interface between the Sn–8Zn–3Bi–xAg (x = 0, 0.5, and 1 wt.%) lead-free solder alloys and Cu substrate soldered at 250 °C for different durations from 5 to 60 min were investigated. It was found that Cu₅Zn₈ and CuZn₅ formed at Sn–8Zn–3Bi/Cu interface, and Cu₅Zn₈ and AgZn₃ formed at the solder/Cu interface when the solder was added with Ag. The thickness of IMC layers in different solder/Cu systems increased with increasing the soldering time. And the growth of the IMCs was found to be mainly controlled by a diffusion mechanism. Additionally, the growth of the IMC layers decreased with increasing content of Ag in the soldering process.     

Evolution of Ag3Sn at Sn-3.0Ag-0.3Cu-0.05Cr/Cu joint interfaces during thermal aging

The intermetallic compounds (IMC) in the solder and at the interface of Sn-3.0Ag-0.5Cu (SAC)/Cu and Sn-3.0Ag-0.3Cu-0.05Cr (SACC)/Cu joints were investigated after isothermal aging at 150 °C for 0, 168 and 500 h. Different shaped Ag₃Sn phases were found near the IMC layer of the latter joint. Interestingly, fine rod-shaped and branch-like Ag₃Sn were detected near the interface after soldering and long Ag₃Sn changed into shorter rods and small particles during aging. It is investigated that the Cr addition and thermal aging have effect on the evolution of Ag₃Sn morphologies and it is controlled by interfacial diffusion. Energy minimization theory and the redistribution of elements are used to explain the morphological evolution of Ag₃Sn. Small Ag₃Sn particles were also found on the IMC layer after aging, unlike the large Ag₃Sn at that of SAC/Cu joints. In conclusion, a favorable morphology of the joint interface leads to better bonding properties for SACC/Cu joints against thermal aging than that for SAC/Cu.     

Effects of in situ nickel particle addition on the microstructure and microhardness of Sn–Ag solder

Abstract

In this study, various amounts of Ni particles were added in situ to Sn–3·5 wt-%Ag lead free solder to form new composite solders. Copper substrates were then dipped into these solders and aged at 150°C for 0, 25, 225, or 1000 h. The microstructure and microhardness of the as solidified solder and the aged solder/copper couples were investigated. Experimental results revealed that the addition of Ni particles increased the microhardness of the composite solder. Ni additions of less than 3 wt-% yielded a microstructure of β-Sn grains surrounded by a eutectic mixture of Ag₃Sn and a Sn rich matrix. An intermetallic compound of Ni₃Sn₄ particles was dispersed throughout the eutectic. For 5 wt-%Ni addition, the Ni₃Sn₄ phase and the remaining Ni particles were agglomerated. In the case of copper substrate dipped with a thick layer of composite solder, water quenched and then aged at 150°C, the induced (Ni, Cu)₃Sn₄ particles coarsened and agglomerated. Additionally, the intermetallic (Cu, Ni)₆Sn₅ compound layer formed at the solder/Cu interface thickened with increasing Ni content.