Fe-modified perovskite-type NaMgF3 photocatalyst: Synthesis and photocatalytic properties. (15th August 2018)

• Record Type: Journal Article
• Authors: Nie, Kun; Yang, Hanpei; Gao, Zhao; Wu, Junming
• Is Part Of: Materials science in semiconductor processing. Volume 83(2018)
• Page Start: 12
• Page End: 17
• Publication Date: 2018-08-15
• Subjects: NaMgF3 -- Iron modification -- Photocatalysis -- Rhodamine B -- Promotion mechanism; Semiconductors -- Periodicals; Integrated circuits -- Materials -- Periodicals; Semiconducteurs -- Périodiques; Circuits intégrés -- Matériaux -- Périodiques; Electronic journals; 621.38152
• DOI: 10.1016/j.mssp.2018.04.001
• Languages: English
• ISSNs: 1369-8001

Abstract

Abstract: Fe-modified perovskite-type NaMgF3 photocatalysts were synthesized via a microemulsion method followed by calcinations. The as-prepared catalysts were characterized via X-ray diffraction (XRD), scanning electron microscopy (SEM), Transmission electron microscopy (TEM), Brunauer–Emmett–Teller specific surface areas (BET) measurements, Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), UV–vis diffuse reflectance spectroscopy (UV–vis DRS), and Photoluminescence spectroscopy (PL). The photocatalytic activity of as-prepared materials was obtained via degradation of aqueous Rhodamine B. Results demonstrate that the Mg 2+ in NaMgF3 may be substituted by a low amount of Fe 3+, forming a finite solid solution NaMg1-x Fex F3 ( x = 0–0.3), while the perovskite-type framework of NaMgF3 remains unchanging. Simultaneously, α-Fe2 O3 is formed to construct an efficient heterostructure. The Fe-modification inside of the lattice of NaMgF3 can suppress growth and aggregation of NaMgF3 crystallion, thus improving the light response and inhibiting the recombination of phtogenerated hole/electron pairs by forming a donor level of impurities and shallow traps in their lattice matrix. α-Fe2 O3 formed outside of NaMg1-x Fex F3 can tightly bond to construct an efficient heterostructure between α-Fe2 O3 and NaMg1-x Fex F3, which is also an important factor of optical absorbance improvement and phtogenerated hole/electron pair separation, due to the migration and jumping of electrons or holes between the two semiconductors. The photocatalytic degradation rate of Rhodamine B on the modified catalyst under optimal content of Fe 3+ (10 mol%) reached to 93% within 1 h, and about 7.6 times of the rate constant of that on raw NaMgF3 was observed. The results show that h + as well as ∙OH play dominant roles of the photodegradation of Rhodamine B. After the 5th photocatalytic experiment, the photocatalytic degradation rate of Rhodamine B retains more than 90% of the original value.