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• BaTiO 3 is conjugated by phosphate ester for small-sized ceramic capacitors. • Solvation of phosphate esters-BaTiO 3 under organic solvents is simulated. • Solvation declines with increasing the hydrophobicity of solvent molecules. • Solvation has a linear correlation with the experimental zeta potential. [Display omitted] Tetragonal BaTiO 3 is a key material for manufacturing multi-layer ceramic capacitors (MLCCs), and a highly dispersed BaTiO 3 suspension, where the surfaces are conjugated by phosphate ester dispersants, is an essential technology for the production of ultra-thin films and small-sized ceramic capacitors. Therefore, understanding the interactions of conjugated polymers with solvents is critical to designing improved dispersants and solvents for commercial MLCC applications. In this work, we theoretically investigate the solvation and inter-chain interactions of mono-alkyl and ethoxy phosphate esters under methanol, ethanol, isopropanol, 1-butanol, and toluene, on tetragonal BaTiO 3 (0 0 1) using the ab initio molecular dynamics (AIMD) simulations. Our results show that the total number of solvent molecules surrounding mono-alkyl and ethoxy phosphate esters decreases in the order of methanol > ethanol > isopropanol > 1-butanol > toluene, indicating that solvation via van der Waals forces and hydrogen bonding declines with increasing the hydrophobicity of solvent molecules. Also, the solvation interaction energy has a linear correlation with the experimental differential of zeta potential, suggesting that the calculated energy is associated with electrostatic environment at the dispersant/solvent/BaTiO 3 interface. Therefore, the solvation interaction energy is an important factor that describes the liquid–solid interfaces as well as a dispersion stability of BaTiO 3 suspension. [ABSTRACT FROM AUTHOR]