Abstract
ZnO coupled Bi-doped porous LaFeO3 nanocomposites have successfully been fabricated via a wet-chemical method. It is confirmed that Bi3+ enters into the crystal lattice of PLFO and substitute La3+, while the ZnO with diameter of similar to 15 nm is coupled to the Bi-doped PLFO. It is shown that the amount-optimized 5Zn/7Bi-PLFO nanocomposite exhibits greatly improved visible-light activities for 2,4-dichlorophenol (2,4-DCP) degradation and CO2 conversion, compared to the unmodified PLFO with rather high photoactivity due to its large specific surface area. Based on the measurements of valence band XPS spectra, steady-state surface photovoltage spectra, transient-state surface photovoltage responses, photoelectrochemical I-V curves, fluorescence spectra related to produced center dot OH amount and photocurrent action spectra, it is clearly demonstrated that the significantly improved visible-light activities are attributed to the enhanced utilization of visible-light-excited high-level-energy electrons (HLEEs) by coupling with nanocrystalline ZnO to introduce a new energy platform for accepting electrons and to the extended visible-light absorption by doping Bi3+ to create surface states. Interestingly, it is proved that under UV-vis irradiation, the amount-optimized nanocomposite exhibit much higher photoactivity for 2,4-DCP degradation compared to the commercially available P25 TiO2. Moreover, it is confirmed by means of radical trapping experiments that the dominant radicals to decompose 2,4-DCP on PLFO could be modulated by doping Bi3+ and coupling ZnO. Furthermore, the possible decomposition pathways, respectively related to the -OH and O-2(center dot-), of 2,4-DCP over the amount-optimized Bi-doped PLFO and ZnO coupled Bi-doped PLFO samples are proposed by means of the liquid chromatography tandem mass spectrometry analysis of the intermediates, especially with the used isotopic D2O.