Photoelectrocatalytic (PEC) degradation
of organic pollutants into
CO2 and H2O is a promising strategy for addressing
ever-growing environmental problems. Titanium dioxide (TiO2) has been widely studied because of its good performance and environmental
benignancy; however, the PEC activity of TiO2 catalyst
is substantially limited due to its fast electron–hole recombination.
Herein, we report a TiO2 nanocone-based photoelectrocatalyst
with superior degradation performance and outstanding durability.
The unique conical catalyst can boost the PEC degradation of 4-chlorophenol
(4-CP) with 99% degradation efficiency and higher than 55% mineralization
efficiency at a concentration of 20 ppm. The normalized apparent rate
constant of a nanocone catalyst is 5.05 h–1 g–1 m2, which is 3 times that of a nanorod
catalyst and 6 times that of an aggregated particle catalyst, respectively.
Further characterizations reveal that the conical morphology of TiO2 can make photogenerated charges separate and transfer more
efficiently, resulting in outstanding PEC activity. Moreover, computational
fluid dynamics simulations indicate that a three-dimensional conical
structure is beneficial for mass transfer. This work highlights that
tuning the morphology of a photoelectrocatalyst at the nanometer scale
not only promotes the charge transfer but also facilitates the mass
transportation, which jointly enhance the PEC performance in the degradation
of persistent pollutants.