According to the types of dental ceramic, various surface treatment techniques have been tried for adhesive cementation, but each treatment has its shortcomings. A simple and universal surface treatment for intraoral and chair-side adhesion promotion is needed for resin cements. This study investigated whether hexamethyldisiloxane (HMDSO) and benzene, when deposited using a low-power non-thermal atmospheric pressure dielectric barrier discharge jet, were effective precursor monomers in dental ceramic adhesion. Their effect on adhesion was evaluated with shear bond strength test (SBS), contact angle measurement, X-ray photoelectron spectroscopy, and Fourier transform infra-red spectrophotometer in an attenuated total reflectance mode. The bonded interfaces and fractured surfaces were evaluated using a scanning electron microscope. Plasma polymerization of HMDSO resulted in formation of a siloxane network (Si2 peak), but its surface hydrophobicity hindered adhesive wetting. Additional deposition of benzene onto the HMDSO-coated ceramic surface increased the C1 peak, which partly corresponded to the C=C double bonds, and the hydrophilic peaks (C-O, C=O and O-C=O bonds). Benzene deposition itself improved the adhesion between the ceramic and the overlying adhesive through the chemical interaction of C=C double bonds and the increased hydrophilic groups. Additional deposition of HMDSO before benzene mediated the chemical adhesion of benzene to the ceramic surface and led to an additional increase of bond strength. Plasma polymerization of benzene and HMDSO/benzene increased the bond strength of composite resin to dental ceramic by improving wettability and adaptation with hydrophilic ether, carbonyl and ester groups, and chemical bonding with active species, such as C=C double bonds and silanol groups.