Development of visible-light-driven Ca2Fe1-xSmxBiO6 double perovskites for decomposition of Rhodamine 6G dye

被引:26
作者
Feraru, S. [1 ]
Borhan, A. I. [1 ]
Samoila, P. [2 ]
Mita, C. [1 ]
Cucu-Man, S. [1 ]
Iordan, A. R. [1 ]
Palamaru, M. N. [1 ]
机构
[1] Alexandru Ioan Cuza Univ, Fac Chem, Iasi 700506, Romania
[2] Petru Poni Inst Macromol Chem, Iasi 700487, Romania
关键词
Double perovskite; Rhodamine; 6G; Sol-gel chemistry; Visible light photocatalyst; IR-SPECTROSCOPIC CHARACTERIZATION; PHOTOCATALYTIC DEGRADATION; TIO2; PERFORMANCE; ADSORPTION; REMOVAL; IONS;
D O I
10.1016/j.jphotochem.2015.04.004
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The main objective of this work was to investigate, for the first time, the photocatalytic activity of double perovskite materials Ca2Fe1-xSmxBiO6 (x= 0, 0.2, 0.4, 0.6, 0.8, 1) in degradation of Rhodamine 6G under visible irradiation. For the synthesis was used sol-gel auto-combustion method with citric acid as combustion agent and ammonium bistmuth citrate as a source for bistmuth cation. Synthesized photocatalysts were structurally investigated by FT-IR spectroscopy to follow the M-O characteristic bands of double perovskite structure and X-ray diffraction (XRD) to confirm the pure phase of catalysts. The catalyst microstructure was characterized by SEM and BET surface areas were measured at the liquid nitrogen temperature by nitrogen adsorption. The Sm concentration optimization yielded an efficient photocatalyst. Surprisingly, the two ends of the series, i.e., Ca2FeBiO6 and Ca2SmBiO6 photocatalysts, are much more active in visible light to the degradation of pollutant Rhodamine 6G than samarium substituted Ca2FeBiO6 materials in different percentages. At an optimum composition of Sm as x = 1 in Ca2Fe1-xSmxBiO6, the photocatalyst exhibited 3.58 times the degradation yield for Rh6G dye in presence of visible light, than its intermediare counterpart. (C) 2015 Elsevier B.V. All rights reserved.
引用
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页码:1 / 8
页数:8
相关论文
共 38 条
[1]   The design and development of highly reactive titanium oxide photocatalysts operating under visible light irradiation [J].
Anpo, M ;
Takeuchi, M .
JOURNAL OF CATALYSIS, 2003, 216 (1-2) :505-516
[2]  
Antonov V. N., 2004, Condensed Matter Physics, V7, P211, DOI 10.5488/CMP.7.2.211
[3]   Photodegradation of Rhodamine 6G and phenol red by nanosized TiO2 under solar irradiation [J].
Asiri, Abdullah M. ;
Al-Amoudi, Muhammed S. ;
Al-Talhi, Tariq A. ;
Al-Talhi, Abdullah D. .
JOURNAL OF SAUDI CHEMICAL SOCIETY, 2011, 15 (02) :121-128
[4]   Synthesis and Characterization of Ca2CoTaO6, a New Monoclinically Distorted Double Perovskite [J].
Elisabet Lavat, Araceli ;
Jose Baran, Enrique .
MATERIALS RESEARCH-IBERO-AMERICAN JOURNAL OF MATERIALS, 2011, 14 (04) :472-474
[5]   Influence of the B-site cation nature on dielectric properties of Ca2XBiO6 (X = Dy, Fe, Al) double perovskite [J].
Feraru, Simona ;
Samoila, Petrisor ;
Nica, Valentin ;
Iordan, Alexandra R. ;
Palamaru, Mircea N. .
CHEMICAL PAPERS, 2013, 67 (10) :1311-1316
[6]   Visible-light-induced degradation of rhodamine B by nanosized Bi2WO6 [J].
Fu, HB ;
Pan, CS ;
Yao, WQ ;
Zhu, YF .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (47) :22432-22439
[7]   Photocatalytic degradation of Rhodamine 6G on mesoporous titania films: Combined effect of texture and dye aggregation forms [J].
Ghazzal, M. N. ;
Kebaili, H. ;
Joseph, M. ;
Debecker, D. P. ;
Eloy, P. ;
De Coninck, J. ;
Gaigneaux, E. M. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2012, 115 :276-284
[8]   Kinetic and adsorption study of acid dye removal using activated carbon [J].
Gomez, V. ;
Larrechi, M. S. ;
Callao, M. P. .
CHEMOSPHERE, 2007, 69 (07) :1151-1158
[9]   TiO2 photocatalysis:: A historical overview and future prospects [J].
Hashimoto, K ;
Irie, H ;
Fujishima, A .
JAPANESE JOURNAL OF APPLIED PHYSICS PART 1-REGULAR PAPERS BRIEF COMMUNICATIONS & REVIEW PAPERS, 2005, 44 (12) :8269-8285
[10]  
Hyun G.K., 1999, CHEM COMMUN, V107, P1077