CAM) in its lithiated form, that is, as present in a discharged cell. In its delithiated form, when the cell is charged, it is the only cell component that is contributing to storing energy (in conjunction with a hypothetical in situ lithiumplated anode formed during charging), thus making it the material required to be present in large quantity to achieve a high-performing cell. All other components, which may be required for large scale processing, only decrease the specific energy of the cell and are, therefore, engineered to minimize their content without affecting the function of the cell. This is evident in the research efforts made to increase the CAM content in the cathode layer, decrease the separator thickness as much as possible, and the pursuit to plate lithium metal in situ (in "anode-free" cells, which are more correctly described as "zero excess lithium metal" cells) without the use of an anode active material. [4] Thus, the CAM type and content in the cell ultimately determine the maximum specific energy that the system can provide.Moreover, the CAM contributes a significant proportion to the overall cell costs, [5] hence the necessity of steady tailoring toward reduced costs and higher energy density. So far, CAM development has mainly targeted performance optimization with LEs in LIBs. For instance, cathode electrolyte interface (CEI) formation, [6] Solid-state batteries (SSBs) currently attract great attention as a potentially safe electrochemical high-energy storage concept. However, several issues still prevent SSBs from outperforming today's lithium-ion batteries based on liquid electrolytes. One major challenge is related to the design of cathode active materials (CAMs) that are compatible with the superionic solid electrolytes (SEs) of interest. This perspective, gives a brief overview of the required properties and possible challenges for inorganic CAMs employed in SSBs, and describes stateof-the art solutions. In particular, the issue of tailoring CAMs is structured into challenges arising on the cathode-, particle-, and interface-level, related to microstructural, (chemo-)mechanical, and (electro-)chemical interplay of CAMs with SEs, and finally guidelines for future CAM development for SSBs are proposed.