Enhanced visible light photocatalytic activity of magnetic cobalt doped BiFeO3open access
- Authors
- Ponraj, Caroline; Kumar, P. Santhosh; Sarkar, Sumit; Krishnamoorthi, C.; Manikandan, N.; Vinitha, G.; Daniel, Joseph
- Issue Date
- Jul-2022
- Publisher
- Elsevier
- Keywords
- Photocatalyst; Combustion synthesis; Environmental remediation; BiFe 1-xCoxO3; AcidRed-85; Visible light and ferro magnetic property
- Citation
- Surfaces and Interfaces, v.31, pp 1 - 12
- Pages
- 12
- Indexed
- SCIE
SCOPUS
- Journal Title
- Surfaces and Interfaces
- Volume
- 31
- Start Page
- 1
- End Page
- 12
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/2897
- DOI
- 10.1016/j.surfin.2022.102050
- ISSN
- 2468-0230
2468-0230
- Abstract
- Photocatalysis is drawing considerable research attention because of its extensive applications in the field of environmental remediation and renewable energy. In this work, synthesis and activity of magnetic BiFe1-xCoxO3 (x = 0, 0.025, 0.05, 0.075 & 0.10) photocatalysts under visible light irradiation is reported. The photocatalyst materials were synthesized using the Gel combustion method assisted by citric acid as fuel. The X-ray diffraction studies reported distorted rhombohedral structure with decreasing crystallite size and increasing dopant concentrations. The X-ray Photoelectron spectroscopy studies confirmed that Bi, Fe and Co are in 3+ states. The optical band gap showed a decrease in the bandgap, which might be due to the presence of oxygen vacancies in the system. The infra-red spectroscopic studies exhibited similar vibrating modes of BiFeO3. Morphological studies also show a decrease in crystallite size. An increase in magnetic property was observed for all samples, with the highest magnetic behaviour seen in the 5% cobalt doped BiFeO3. The influences of Co doping content on photocatalytic activity of BiFeO3 were investigated. The photocatalytic degradation of Acid Red-85 dye followed pseudo-first-order kinetics, with the greatest performance found in BiFe0.925Co0.075O3 with 93.79% degradation after 2 h of light exposure. Photoluminescence and photocurrent studies validate efficient charge separation for enhanced photocatalytic behaviour.
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