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Investigation of the physico-chemical properties of Sr2FeNb1−x W x O6 (0.0 ≤ x ≤ 0.1) for visible-light photocatalytic water-splitting applications

Pramod H. BorseCenter for Nanomaterials, International Advanced Research Center for Powder Metallurgy and New Materials, Balapur PO, Hyderabad, AP, 500 005, IndiaKwon Taek LimDepartment of Imaging System Engineering, Pukyong National University, Busan, 609-735, KoreaJang‐Hee YoonDivision of High Technology Materials Research, Korea Basic Science Institute, Busan, 618-230, KoreaJong‐Seong BaeDivision of High Technology Materials Research, Korea Basic Science Institute, Busan, 618-230, KoreaMyoung Gyu HaDivision of High Technology Materials Research, Korea Basic Science Institute, Busan, 618-230, KoreaEun Hyuk ChungDivision of High Technology Materials Research, Korea Basic Science Institute, Busan, 618-230, KoreaEuh Duck JeongDivision of High Technology Materials Research, Korea Basic Science Institute, Busan, 618-230, KoreaH. G. KimDivision of High Technology Materials Research, Korea Basic Science Institute, Busan, 618-230, Korea
2014en
ABI

Abstract

Incorporation of the pentavalent W-ion has been investigated in Sr2FeNb1−x W x O6 for 0.0 ≤ x < 0.15. The synthesized double perovskite system was used to study its structural and optical properties. The optical, as well as structural, properties were found to change with the varying Nb:W stoichiometric ratio. The Sr2FeNb1−x W x O6 samples with 0.0 ≤ x < 0.1 were further investigated for visible-light photocatalytic water splitting. At an optimized value of ∼0.01, i.e., Sr2FeNb0.99W0.01O6, the perovskite lattice yielded an efficient photocatalyst, it displayed a moderately-altered direct band-gap of 2.17 eV, and gave twice the higher quantum yield for photosplitting in a H2O-CH3OH mixture compared to that for x ∼0 under visible light (λ ≥ 420 nm). For x > 0.1, the Sr2FeNb1−x W x O6 showed no change in the optical properties but crystal structure was drastically affected, exhibiting impurity phases and a disordered structure, thus yielding a degraded photocatalytic behavior. The higher absorption coefficient in the Sr2FeNb0.99W0.01O6 and a higher electron-density acquired by n-type lattice doping seems to be responsible for the better efficient charge separation in Sr2FeNb1−x W x O6 (0.01 ≤ x ≤ 0.20) and consequently the higher photocatalytic activity in co-catalyst loaded photocatalysts.

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