Single-crystalline Bi2Fe4O9 synthesized by low-temperature co-precipitation: performance as photo- and Fenton catalysts

被引:56
作者
Hu, Zhong-Ting [1 ]
Chen, Bo [2 ]
Lim, Teik-Thye [1 ,3 ]
机构
[1] Nanyang Technol Univ, Sch Civil & Environm Engn, Div Environm & Water Resources Engn, Singapore 639798, Singapore
[2] Nanyang Technol Univ, Sch Mat Sci & Engn, Singapore 639798, Singapore
[3] Nanyang Technol Univ, NEWRI, Singapore 637141, Singapore
关键词
MICROWAVE HYDROTHERMAL SYNTHESIS; BIFEO3; NANOPARTICLES; BISMUTH FERRITES; PHOTOCATALYTIC ACTIVITY; MAGNETIC-PROPERTIES; HYDROGEN-PEROXIDE; AQUEOUS-SOLUTION; THIN-FILM; DEPENDENCE; RADICALS;
D O I
10.1039/c4ra02555e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multi-functional, self-assembled mullite bismuth ferrites (Bi2Fe4O9) have been synthesized by a facile co-precipitation method at a low temperature of 95 degrees C. The Bi/Fe precursor molar ratio and the reaction time were investigated for their influences on the resulting Bi2Fe4O9 nanopads. The Bi2Fe4O9 nanopads were formed via self-assembled crystal growth along the (001) plane, with an average thickness of 170 nm. The most well crystalline nanopads were produced at a reaction time of 36 h, beyond which the nanopads started to dissolve. The produced pure Bi2Fe4O9 nanopads exhibit a high degree of elemental stoichiometry with uniform elemental distribution. The Bi2Fe4O9 exhibits double bandgaps of 1.9 and 2.3 eV, and shows surface area of 5.8 m(2) g(-1). It can be photoexcited by visible light of up to 656 nm. The Bi2Fe4O9 can be used as a photocatalyst and Fenton catalyst. Its catalytic activities were evaluated using bisphenol A (BPA) as the model pollutant. Under visible-light irradiation from a solar simulator, 34% of BPA could be removed (compared to only similar to 3% with Evonik P25) via visible-light photocatalysis. With addition of H2O2 (16 mM), 54% and 73% of BPA could be removed within 1 h via dark Fenton-like and visible-light photo-Fenton reactions, respectively. The Bi2Fe4O9 also exhibits a weak magnetism of 0.99 emu g(-1). The multi-functional Bi2Fe4O9 nanopad has the potential to be used for continuous solar catalytic treatment of wastewater over an alternating day/night cycle and is recoverable via magnetically-enhanced gravity separation.
引用
收藏
页码:27820 / 27829
页数:10
相关论文
共 52 条
[31]   Evidence for an additional oxidant in the photoassisted Fenton reaction [J].
Pignatello, JJ ;
Liu, D ;
Huston, P .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1999, 33 (11) :1832-1839
[32]   DARK AND PHOTOASSISTED FE3+-CATALYZED DEGRADATION OF CHLOROPHENOXY HERBICIDES BY HYDROGEN-PEROXIDE [J].
PIGNATELLO, JJ .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1992, 26 (05) :944-951
[33]   Theoretical investigation of magnetoelectric behavior in BiFeO3 [J].
Ravindran, P. ;
Vidya, R. ;
Kjekshus, A. ;
Fjellvag, H. ;
Eriksson, O. .
PHYSICAL REVIEW B, 2006, 74 (22)
[34]   THE RATE CONSTANT OF THE REACTION BETWEEN HYDROGEN PEROXIDE AND FERROUS IONS [J].
RIGG, T ;
TAYLOR, W ;
WEISS, J .
JOURNAL OF CHEMICAL PHYSICS, 1954, 22 (04) :575-577
[35]   DAS SYSTEM WISMUTOXYD-EISENOXYD IM BEREICH VON 0 BIS 55 MOL-PERCENT EISENOXYD [J].
ROYEN, P ;
SWARS, K .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1957, 69 (24) :779-779
[36]   On the Thermodynamic Stability of BiFeO3 [J].
Selbach, Sverre M. ;
Einarsrud, Mari-Ann ;
Grande, Tor .
CHEMISTRY OF MATERIALS, 2009, 21 (01) :169-173
[37]  
SHIMADZU, APPL NEWS SPECTR AN, VA428
[38]   Magnetic Bi25FeO40-graphene catalyst and its high visible-light photocatalytic performance [J].
Sun, Aiwu ;
Chen, Huan ;
Song, Chunyan ;
Jiang, Fang ;
Wang, Xin ;
Fu, Yongsheng .
RSC ADVANCES, 2013, 3 (13) :4332-4340
[39]   Visible Light-Induced Photocatalytic Oxidation of Phenol and Aqueous Ammonia in Flowerlike Bi2Fe4O9 Suspensions [J].
Sun, Songmei ;
Wang, Wenzhong ;
Zhang, Ling ;
Shang, Meng .
JOURNAL OF PHYSICAL CHEMISTRY C, 2009, 113 (29) :12826-12831
[40]   Study on visible light response and magnetism of bismuth ferrites synthesized by a low temperature hydrothermal method [J].
Sun, Yuxia ;
Xiong, Xiangyu ;
Xia, Zhao ;
Liu, Hongri ;
Zhou, Yong ;
Luo, Man ;
Wang, Chengyan .
CERAMICS INTERNATIONAL, 2013, 39 (04) :4651-4656