Since the Industrial Revolution, increasing greenhouse gas emissions have intensified global efforts to mitigate climate change. Carbon Capture and Storage (CCS) technology has emerged as a prominent strategy for reducing carbon emissions. Among CCS processes, the capture step constitutes the majority of overall operational costs, underscoring the necessity for efficient carbon dioxide (CO₂) separation technologies. Adsorption is one such promising separation method, with optimal adsorption temperatures and adsorbents varying based on specific process requirements. For instance, calcium oxide (CaO)-based adsorbents selectively capture CO₂ at high temperatures ranging from approximately 500 to 700°C; however, repeated use leads to performance degradation due to sintering caused by particle agglomeration. To address this issue, cerium (Ce), a metal capable of inhibiting particle agglomeration was introduced into the CaO-based adsorbent. Incorporating Ce is expected to enhance cyclic adsorption performance significantly. Furthermore, the introduction of Ce can induce oxygen vacancies, potentially further improving CO₂ adsorption efficiency. Therefore, this study focused on optimizing CO₂ adsorption performance by varying the molar ratio of metal precursors (Ca/Ce).