This paper reports on how the surface chemistry of boron-doped nanocrystalline diamond (BDD) thin-film electrodes (H vs O) affects the wettability and electrochemical properties in two room-temperature ionic liquids (RTILs): [BMIM]­[PF6] and [HMIM]­[PF6]. Comparative measurements were made in 0.5 mol L–1 H2SO4. The BDD electrodes were modified by microwave or radio-frequency (RF) plasma treatment in H2 (H-BDD), Ar (Ar-BDD), or O2 (O-BDD). These modifications produced low-, medium-, and high-oxygen surface coverages. Atomic O/C ratios, as determined by X-ray photoelectron spectroscopy (XPS), were 0.01 for H-BDD, 0.08 for Ar-BDD, and 0.17 for O-BDD. The static contact angle of ultrapure water on the modified electrodes decreased from 110° (H-BDD) to 41° (O-BDD) with increasing surface oxygen coverage, as expected as the surface becomes more hydrophilic. Interestingly, the opposite trend was seen for both RTILs as the contact angle increased from 20° (H-BDD) to 50° (O-BDD) with increasing surface oxygen coverage. The cyclic voltammetric background current and potential-dependent capacitance in both RTILs were largest for BDD electrodes with the lowest O/C ratio (H-BDD) and smallest contact angle. Slightly larger voltammetric background currents and capacitance were observed in [HMIM]­[PF6] than in [BMIM]­[PF6]. Capacitance values ranged from 8 to 16 μF cm–2 over the potential range for H-BDD and from 4 to 6 μF cm–2 for O-BDD. The opposite trend was observed in H2SO4 as the voltammetric background current and capacitance were largest for BDD electrodes with the highest O/C ratio (O-BDD) and smallest contact angle. In summary, reducing the surface oxygen on BDD electrodes increases the wettability to two RTILs and this increases the voltammetric background current and capacitance.