Efficient electrocatalytic nitrate reduction via boosting oxygen vacancies of TiO2 nanotube array by highly dispersed trace Cu doping

Nitrate pollution of water bodies is a serious global-scale environmental problem. The electrocatalytic nitrate reduction reaction (NO3RR) using Cu-based electrodes allows excellent nitrate removal; however, its long-term operation results in copper leaching, leading to health risks. This study proposes a strategy for efficient nitrate removal through the activation of oxygen vacancies on a highly dispersed Cu-doped TiO(2 )nanotube array (Cu/ TNTA) cathode via electrodeposition. The mechanism underlying the activation of oxygen vacancies and enhancement in charge transfer at the cathode-pollutant interface upon trace (0.02 wt%) Cu doping is elucidated by electron paramagnetic resonance analysis, UV-visible diffuse reflection spectroscopy, and Raman spectroscopy. The Cu/TNTA-300 exhibits a nitrate removal rate of 84.3% at 12 h; the electrode activity did not decrease after 10 cycles, and no Cu2+ was detected in the solution. Electrochemical characterization and density functional theory calculations demonstrate that Cu doping promotes efficient charge transfer between nitrate and the electrode and reduces the energy barrier of the nitrate reduction reaction. This work provides a platform for novel design of cathodes for use in efficient and safe electrocatalytic nitrate reduction in environmental water bodies.

Automated summary

This study proposes a strategy for efficient nitrate removal through the activation of oxygen vacancies on a highly dispersed Cu-doped TiO(2 )nanotube array (Cu/ TNTA) cathode via electrodeposition. The results show that trace Cu doping promotes efficient charge transfer between nitrate and the electrode, leading to enhanced nitrate removal rate and stability.