传统上，RuO₂/TiO₂复合电极制备是通过在TiO₂/Ti基体上多次涂覆含Ru前驱体溶液和随后热分解（TD）来实现的. 为克服上述方法中Ru用量大和利用率低之不足, 本工作主要基于循环伏安法（CV）在TiO₂纳米管阵列（TNA）上电沉积RuO₂制备RuO₂^CV/TNA复合电极. SEM、GIXRD和CV结果表明， 电沉积的RuO₂为无定型结构, 所制备电极中的Ru用量约为传统的RuO₂^TD/TNA电极中Ru用量的1/30. 尽管两电极催化CO₂还原产物的法拉第效率接近, 但是RuO₂^CV/TNA电极比RuO₂^TD/TNA电极展示了更高的还原电流, 较正的初始还原电位和更好的稳定性. 与磷酸盐缓冲溶液中电还原CO₂相比，RuO₂^CV/TNA电极在0.1 mol•L^-1 KHCO₃中电还原CO₂除生成更高法拉第效率的甲酸根和甲烷外，还检测到CO的生成.

RuO₂/TiO₂ composite materials have multitude of electrocatalytic applications including but not limited to CO₂ reduction reaction (CO₂RR). RuO₂/TiO₂ electrodes were previously prepared by repetitive coating and thermal decomposition (TD) of a Ru(III) precursor solution on Ti substrate. In this work, electrochemical potential cycling is applied to deposit amorphous RuO₂ (α-RuO₂) layers onto TiO₂ nanotube array (TNA) (RuO₂^CV/TNA) preformed on Ti foil. SEM, GIXRD, and voltammetry are applied to characterize the structures of the resulting Ru_O2^CV/TNA. Ru loading on the RuO₂^CV/TNA electrode is ca. 1/30 of that on the conventional RuO₂^TD/TNA electrode. Although both electrodes yield similar faradaic efficiencies (FEs) for the reduction products, the RuO₂^CV/TNA electrode displays a much higher reduction current, a more positive initial reduction potential and a better durability than the RuO₂^TD/TNA one. In addition to higher FEs for formate and CH₄, the RuO₂^CV/TNA electrode yields the product of CO for the CO₂RR in 0.1 mo•lL^-1 KHCO₃, which is not available in a PBS solution with pH 7.