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Dynamic observation of the microstructure evolution of Sn2.5Ag0.7Cu0.1RE/Cu solder joints and the relationship between the interfacial intermetallic compound (IMC) and the mechanical properties of the solder joints were investigated during isothermal aging. The results showed that the original single scallop-type Cu6Sn5 IMC gradually evolved into a planar double-layer IMC consisting of Cu6Sn5 and Cu3Sn IMCs with isothermal aging. In particular, the Cu3Sn IMC grew towards the Cu substrate and the solder seam sides; growth toward the Cu substrate side was dominant during the isothermal aging process. The growth of Cu3Sn IMC depended on the accumulated time at a certain temperature, where the growth rate of Cu3Sn was higher than that of Cu6Sn5. Additionally, the growth of the interfacial IMC was mainly controlled by bulk diffusion mechanism, where the activation energies of Cu6Sn5 and Cu3Sn were 74.7 and 86.6 kJ/mol, respectively. The growth rate of Cu3Sn was slightly faster than that of Cu6Sn5 during isothermal aging. With increasing isothermal aging time, the shear strength of the solder joints decreased and showed a linear relationship with the thickness of Cu3Sn. The fracture mechanism of the solder joints changed from ductile fracture to brittle fracture, and the fracture pathway transferred from the solder seam to the interfacial IMC layer.

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A tactic for the synthesis of Ni-modified graphene nanosheets (Ni-GNSs) as a high-performance reinforcement of a lead-free solder is proposed and achieved via an environmentally friendly and controllable pyrolysis method. The segmented pyrolysis processes of an Ni(CH3COO)2∙4H2O@GNSs hybrid are discussed. The morphology, microstructure, phase transition, and adsorption strength of nanoparticles on the surface of GNSs with various theoretical Ni loadings are characterized. The adsorption mechanism of a single Ni atom on the surface of perfect graphene and defective graphene was studied based on density functional theory. The corresponding underlying formation mechanisms of Ni-GNSs are analyzed. The results show that the grain size, distribution and phase composition of the nanoparticles on GNSs could be controlled by changing the theoretical Ni loading level. The morphology and dispersity of Ni nanoparticles on GNSs did not significantly change after long-time or high-power ultrasonic treatment, suggesting that the adsorption strength between Ni nanoparticles and GNSs was relatively large and belonged to chemical adsorption based on first-principle calculation. Ni atoms tend to adsorb in the center of the carbon six-membered ring. The obtained Ni-GNSs nanohybrid exhibited a small size, fewer defects, and higher crystallinity and adsorption strength when the theoretical Ni loading was 17 mol %. The results have potential applications in the design of the reinforced phase of composites.

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