Highly efficient piezoelectric field enhanced photocatalytic performance via in situ formation of BaTiO3 on Ti3C2Tx for phenolic compound degradation†
Abstract
The strategy of boosting the photocatalytic activity through an internal potential field has attracted wide attention. Therefore, the coupling of the piezoelectric effect and photocatalytic process promoted the separation of photogenerated carriers, thus increasing the piezo-photocatalytic activity. Herein, BaTiO3 nanoparticles were prepared on the Ti3C2Tx surface by an in situ hydrothermal method. The obtained BaTiO3/Ti3C2Tx piezo-photocatalysts exhibited rapid electron transfer, a low energy bandwidth of 2.18 eV, and a wide visible light response range of 400–800 nm. Their phenol degradation rate reached 94.3% within the first 60 min of reaction conducted under light irradiation and ultrasonic vibration. During the phenol degradation process, intermediate products were generated first and then mineralized into CO2 and H2O due to the influence of the piezoelectric potential of the BaTiO3/Ti3C2Tx photocatalysts. Furthermore, ultrasonic vibration produced a piezoelectric field on the BaTiO3/Ti3C2Tx, which enhanced the separation of photogenerated carriers, making hydroxyl radicals (˙OH) the most active species in the synergistic degradation of phenol. These results demonstrate that coupling piezoelectric and photocatalytic properties has broad application prospects in water pollution control.