Quartz crystal microbalance combined with x-ray photoelectron spectroscopy has been used to study thin corrosion films of electroplated Ni and electroplated Sn or Au on Ni, with Sn-and Au-thicknesses within the range used for electrical contact materials. Results are presented which show that mass changes can be measured in situ during corrosion at atmospheric pressure conditions. Based on quartz crystal microbalance measurements, the influence of SO~ and NO., on the kinetics of atmospheric corrosion has been investigated. Introduction of sub-ppm concentrations of SO~ or NO., alone results in a minor increase in corrosion rates on Ni-coated surfaces and in no significant increase in corrosion rates on Sn-coated surfaces. Introduction of the same concentration of SO~ and NO.2 simultaneously, however, results in significant increases in corrosion rates on all Ni-, Sn-, as well as Au-coated surfaces.The atmospheric corrosion of materials and components for electrical and electronic applications has for a long time been of wide economical interest. With recent advances in small size component technology, it has become obvious that even minor quantities of adsorbed moisture films or corrosion products can result in significant changes in performance or in premature failure of electronic components.The rapid growth of surface analytical techniques during the last two decades has greatly extended the possibilities of studying minute amounts of corrosion products in electronic equipment. Most surface sensitive techniques available today for studies of the corrosion of electronic materials (e.g., Auger electron spectroscopy, x-ray photoelectron spectroscopy, secondary ion mass spectroscopy, electrical contact resistance, and electrolytic reduction) are based on ex situ analysis. Under operating conditions, however, it is of great practical and fundamental interest to be able to continuously monitor the instant corrosion rate. Hence, it is of vital importance to extend the diversification of surface analytical techniques also to those based on in situ analyses.The quartz crystal microbalance (QCM) method can easily measure mass changes of less than 10 -s g/cm 2 during actual exposure conditions (1). The method is based on a piezoelectric quartz crystal which oscillates at its resonance frequency. Deposition of material on the crystal results in a change in resonance frequency which is dependent on the mass of deposited material. In addition to its high sensitivity and the possibilities of performing in situ analysis, the QCM method offers advantages, such as rapid measurements and the absence of any influence of mechanical shaking or vibrations, over volumetric methods.Despite its obvious advantages, the QCM method has found relatively few applications in the study of surface phenomena related to corrosion kinetics of metals. A limited number of QCM studies under atmospheric pressure conditions have been reported, e.g., in connection with the adsorption of moisture films (2-5), atmospheric corrosion in the presence of humi...