Wire bonding remains widely used in semiconductor packaging, but combined degradation can occur at bond pad-wire interfaces during use or storage due to humidity, acidity, and ionic contamination, leading to galvanic corrosion, oxidation, and sulfidat...
Wire bonding remains widely used in semiconductor packaging, but combined degradation can occur at bond pad-wire interfaces during use or storage due to humidity, acidity, and ionic contamination, leading to galvanic corrosion, oxidation, and sulfidation. In particular, Al pad-wire and ENIG Au pad-wire structures contain Al, Ni, Au, Cu, and intermetallic compounds (IMCs), so localized galvanic corrosion can be concentrated at specific regions in sulfuric acid-containing sulfate environments. In this thesis, packaging structures composed of sputtered Al pads and ENIG Au pads on 4-inch Si wafers, combined with Au, Cu, Cu-Pd alloy (Cu1Pd), and Pd-coated Cu (PCC) wires, were systematically investigated in de-aerated 1 % Na₂SO₄ solutions with varying H₂SO₄ concentrations (x = 0, 0.1, 1, 10 %). Individual polarization and electrochemical galvanic tests were conducted to obtain the corrosion potential (Ecorr), corrosion current density (icorr), galvanic potential/current density, and corrosion rate estimated from the total charge. In addition, Temperature-Humidity Tests (85 °C / 85 % RH) were performed under 1 % Na₂SO₄ + 0 % or 1 % H₂SO₄ conditions using FR-4 PCB unit specimens in which a 1st ball bond was formed on an Al pad and a 2nd stitch bond on an Au pad with Au, Cu, Cu1Pd, or PCC wires, and the surface morphology and elemental distribution around ball bonds, stitch bonds, and wires were examined using a 3D optical microscope and FE-SEM/EDS. By correlating electrochemical results with THT observations, the effects of sulfuric acid concentration and pad-wire material combinations on galvanic corrosion behavior, the difference in corrosion resistance between Au and Cu wires, and the effects and limitations of Pd alloying/coating in Cu-based wires were elucidated.