Optimizing the Automated Assembly Process for Filled-Polymer Based Thermal Bondlines
Great efforts are expended by researchers to develop new and better thermal interface materials. In contrast,optimization of the performance of a given material is usually left to more empirical efforts. Unfortunately,interactions between the many parameters affecting performance make the design of experiments required for empirical optimization impractically large. We are conducting systematic mechanistic studies on the combined effects of materials selection and process parameters such as normal forces,assembly speeds,and thermal profiles on bondline macro/microstructure and thermal performance.
The most common type of medium/high-performance thermal interface material is undoubtedly that of polymers filled with
conductive particles,most often Ag. However,these materials rarely perform as well in a practical application as predicted based on manufacturer supplied data sheets. This is usually ascribed to defects such as voids,porosity and filler distribution heterogeneity. Such defects can be minimized by process optimization,but we also believe that we can learn to tailor some level of heterogeneity to our advantage. In fact,a thermal resistance two and a half times lower than that predicted based on the data sheet has already been demonstrated for one high-end commercial material. Moreover,this can be compatible with a practical manufacturing process.
The present paper offers a discussion of results of systematic process studies on commercial filled polymer materials,including correlations between process parameters,defects and final bondline thickness. Important insights were derived from a new technique allowing the in-situ measurement of bondline electrical resistance during processing. The indication is that the dominant pathways for heat transport are provided by chains of Ag particles in good electrical contact with each other. However,typical thermal conductivities of adhesives with,say,30% Ag (by volume) are lower than that of pure Ag by a factor of fifty or more. The reason for this is that a relatively small fraction of the Ag particles are in conducting chains; in many instances heat must travel through interfaces between the Ag and thin coatings or layers of polymer. Indications are that the fraction of metallic (electron) transport (transport through chains of Ag) can be enhanced in an optimized assembly process.