Satellite DNA (satDNA) is among the fastest evolving elements in the genome and is highly abundant in some eukaryotic genomes. Its highly repetitive nature means it is challenging to assemble, and thus underrepresented in most assemblies and often understudied as a result. Birds are an ideal model organism for the study of satDNA and its evolution, since the large amount of available sequenced genomes of this clade allows for dense sampling across various evolutionary timescales, and the low number of satDNA families within their satellitomes facilitates their study and comparison between species. Here, we characterize satDNA and its evolution across Passeriformes, an avian clade containing two-thirds of all bird species spanning ~50 million years of evolution. With this goal we use both short-read data and long-read assemblies of species representative of over 30 passerine families in this clade to shed light on the evolution of its satellitome. We focus on examining the phylogenetic relationships between satellites common to most species as well as characterizing satellite array structure and location in genome assemblies. We also analyse satellite abundance in each genome, focusing on differences in the satellite content between male and female individuals to look for satellites present in the female-specific W sex chromosome and the germline-restricted chromosome. Seven satDNA families shared by a quarter of the species were found, that were likely present in an ancestral species shared by most, if not all the species of Passeriformes. We observed that satDNA evolution is complex and does not follow species phylogeny and that satellite arrays generally have a simple head-to-tail conformation, with evidence in four of the sampled species of satDNA arrays with higher-order repeats. We also found two satDNA families with fairly consistent monomer length and conserved regions that we hypothesise to might be functional.