Understanding the intricate bonding mechanism between coral reef surfaces and C–S–H is crucial for advancing large-scale engineering applications. This study conducts a comprehensive analysis of the impact of coral powder (CP) on cement paste. Initially, zeta potential experiments were performed to probe ion adsorption from the cement pore solution at the CP interface. We propose a novel model to quantify the adsorption of Ca2+ by CP. Subsequently, the study delves into the morphological properties of C–S–H nucleation and growth at this interface and formulates an equation elucidating the CP and Ca2+ adsorption relationship. Then, the crack extension behavior of cementitious materials was scrutinized. Finally, an examination of CP effects on the rheological properties of fresh cement pastes is presented. The findings indicate that CP particles exhibit a notably weaker adsorption affinity with Ca2+ compared to their interaction with SO42−. Compared to limestone (LP), CP exhibited a 32.1 % reduction in Ca2+ adsorption in Ca(OH)2 solutions, 44.2 % reduction in Ca(OH)2 + 10 mmol/L K2SO4, and 40.6 % reduction in Ca(OH)2 + 50 mmol/L K2SO4 solutions. Higher zeta potential values correspond to stronger Ca2+ adsorption and broader surface coverage of Ca2+. The inferior surface characteristics of CP hinder C–S–H nucleation and growth, leading to a low CH orientation index in cement paste containing CP. These pastes exhibit cracks more frequently between CP and hydration products. An attractive force is observed between CP and cement particles, decreasing cement paste flowability.