LaFeO chalcocite precursor was prepared by solid-phase milling method, and LaFeO-type chalcocite composite catalyst, referred to as LFCN catalyst, was synthesized by in situ doping of carbon and nitrogen (urea, melamine, dicyandiamide, and carbon powder), The catalytic performance of the catalysts was investigated by the different mass ratios of LaFeO chalcocite precursor and carbon and nitrogen (1:1, 1:2, and 2:1) and the degradation mechanism. Various characterization analyses, such as X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Brunauer-Emmett-Teller (BET), showed that the doped composite LFCN catalysts exhibited a hemispherical network structure with a larger specific surface area than that of the pure phase LaFeO material. In addition, the LaFeO material adjusted the electronic structure of the original LaFeO chalcogenide material to a certain extent after in situ doping with organic C and N elements, which enhanced its lattice oxygen oxidation ability. In the study of the catalytic degradation of sodium humate solution under natural light conditions, the catalytic performance was significantly improved compared to that of the pure phase LaFeO, and 10 mg of the catalyst degraded 30 mg/L of sodium humate solution in 50 min, with a degradation rate increasing from 40 to 98%. The degradation rate increased from 40 to 98% after 4 applications, indicating that the LFCN catalyst has good stability and significant catalytic degradation performance.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10633878 | PMC |
http://dx.doi.org/10.1021/acsomega.3c06161 | DOI Listing |
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