Journal
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
Volume 30, Issue 17, Pages 51356-51367Publisher
SPRINGER HEIDELBERG
DOI: 10.1007/s11356-023-25981-y
Keywords
Rare earths doping; Ceria; CeCO3OH; Oxygen vacancies; Photocatalysis
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Chemical reducing or rare earth cations (RE) doping were used to enhance the photocatalytic performance of ceria, but surprisingly hindered the photodegradation of methylene blue (MB). The excess oxygen vacancies (OVs) formed in RE-doped ceria reduced the separation efficiency of photo-excited e(-)/h(+). The recombination of e(-)/h(+), promoted by RE dopants and excess OVs, weakened the generation of active species and ultimately weakened the photocatalytic activity of ceria.
Chemical reducing or rare earth cations (RE) doping was normally employed to promote the photocatalytic performance of ceria, aimed to evaluate their cooperation influences, ceria was obtained by decomposing homogenously RE (RE = La, Sm, and Y)-doped CeCO3OH in H-2. XPS and EPR results evidenced that the excess oxygen vacancies (OVs) were formed in RE-doped CeO2 compared to the un-doped ceria. However, all the RE-doped ceria unexpectedly showed an impeded photocatalytic activity towards to methylene blue (MB) photodegradation. The 5% Sm-doped ceria had the best MB photodegradation ratio of 81.47% after 2-h reaction in all RE-doped samples, which was lower than that of 87.24% for the un-doped ceria. After doping RE cations and chemical reducing, the band gap of ceria were almost narrowed, while the PL spectra and photo-electro characterizations indicated that the separation efficiency of photo-excited e(-)/h(+) (electrons/holes) was reduced. The RE dopants and formed excess OVs including inner and surface OVs was proposed to promote the recombination of e(-)/h(+) which further hindered the generation of active species of center dot O-2(-) and center dot OH, and finally weakened the photocatalytic activity of ceria.
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