Figures & data
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Table 1. Crystalline, interplanar spacing, particle sizes and lattice constant of MFe2O4 nanostructures calcined at 973 K for 24 h.
Figure 3. SEM images of (a) NiFe2O4; (b) CoFe2O4; (c) CuFe2O4; (d) ZnFe2O4, calcined at 973 K for 24 h.
![Figure 3. SEM images of (a) NiFe2O4; (b) CoFe2O4; (c) CuFe2O4; (d) ZnFe2O4, calcined at 973 K for 24 h.](/cms/asset/f8a35f8a-d23b-43d7-a062-18af7f4109d0/tusc_a_2134696_f0003_ob.jpg)
Figure 4. EDS analysis of (a) NiFe2O4; (b) CoFe2O4; (c) CuFe2O4; (d) ZnFe2O4, calcined at 973 K for 24 h.
![Figure 4. EDS analysis of (a) NiFe2O4; (b) CoFe2O4; (c) CuFe2O4; (d) ZnFe2O4, calcined at 973 K for 24 h.](/cms/asset/6c5c343e-2334-40c3-a5d3-035fc76ee077/tusc_a_2134696_f0004_oc.jpg)
Figure 5. HRTEM results and particle size distributions of (a) NiFe2O4; (b) CoFe2O4; (c) CuFe2O4; (d) ZnFe2O4, calcined at 973 K for 24 h.
![Figure 5. HRTEM results and particle size distributions of (a) NiFe2O4; (b) CoFe2O4; (c) CuFe2O4; (d) ZnFe2O4, calcined at 973 K for 24 h.](/cms/asset/0b5b0df7-0956-4a2b-b74c-95709ad0d5c4/tusc_a_2134696_f0005_ob.jpg)
Figure 6. Particle size distributions of (a) NiFe2O4; (b) CoFe2O4; (c) CuFe2O4; (d) ZnFe2O4, calcined at 973 K for 24 h.
![Figure 6. Particle size distributions of (a) NiFe2O4; (b) CoFe2O4; (c) CuFe2O4; (d) ZnFe2O4, calcined at 973 K for 24 h.](/cms/asset/b064ffb8-b606-4425-8ac7-80485c5b751f/tusc_a_2134696_f0006_oc.jpg)
Figure 7. Nitrogen adsorption-desorption isotherms and pore size distribution of MFe2O4 photocatalysts.
![Figure 7. Nitrogen adsorption-desorption isotherms and pore size distribution of MFe2O4 photocatalysts.](/cms/asset/5354af64-caac-4e69-a749-2a7d92f7cf98/tusc_a_2134696_f0007_oc.jpg)
Table 2. Textural properties of MFe2O4 nanoparticles.
Figure 11. (a) Effect of calcination temperature of ZnFe2O4. (b) Effect of calcination duration upon photocatalytic activity of ZnFe2O4 (1:2) nanoparticles calcined at 873 K on the photodegradation of CV dye using 15 mg of photocatalyst, 10 ml of 10-ppm CV solution in sunlight and pH 7.
![Figure 11. (a) Effect of calcination temperature of ZnFe2O4. (b) Effect of calcination duration upon photocatalytic activity of ZnFe2O4 (1:2) nanoparticles calcined at 873 K on the photodegradation of CV dye using 15 mg of photocatalyst, 10 ml of 10-ppm CV solution in sunlight and pH 7.](/cms/asset/54ed75a3-ebb6-4413-8d48-88f8aef02a1e/tusc_a_2134696_f0011_oc.jpg)
Figure 12. (a) effect of ratio of Zn/Fe, (b) effect of load of ZnFe2O4 (1:2) nanoparticles calcined at 873 K on the photodegradation of CV dye using 15 mg of photocatalysts, 10 ml of 10 ppm CV solution under sunlight radiation and at pH 7 for 30 min.
![Figure 12. (a) effect of ratio of Zn/Fe, (b) effect of load of ZnFe2O4 (1:2) nanoparticles calcined at 873 K on the photodegradation of CV dye using 15 mg of photocatalysts, 10 ml of 10 ppm CV solution under sunlight radiation and at pH 7 for 30 min.](/cms/asset/0824fd8d-f8d4-43cd-b5ac-4d5949a3d1cd/tusc_a_2134696_f0012_oc.jpg)
Figure 13. Time-dependent spectral changes to CV dye solution (a) dark reaction catalyzed by ZnFe2O4, calcined at 973 K; (b) blank reaction; (c) catalyzed reaction by ZnFe2O4, calcined at 873 K; (d) catalyzed reaction by ZnFe2O4, calcined at 973 K.
![Figure 13. Time-dependent spectral changes to CV dye solution (a) dark reaction catalyzed by ZnFe2O4, calcined at 973 K; (b) blank reaction; (c) catalyzed reaction by ZnFe2O4, calcined at 873 K; (d) catalyzed reaction by ZnFe2O4, calcined at 973 K.](/cms/asset/035b6307-65cb-4b0b-8cf5-1f31953ccf02/tusc_a_2134696_f0013_oc.jpg)
Figure 14. (a) C/Co vs time plot for the photocatalytic degradation of CV dye, and (b) the plot of ln (C/Co) vs time for the kinetic study by MFe2O4 photocatalysts.
![Figure 14. (a) C/Co vs time plot for the photocatalytic degradation of CV dye, and (b) the plot of ln (C/Co) vs time for the kinetic study by MFe2O4 photocatalysts.](/cms/asset/0d3a36c2-a5a0-47d6-9ce5-895d21e9801a/tusc_a_2134696_f0014_oc.jpg)
Table 3. Kinetic studies of photocatalytic degradation of CV dye using MFe2O4 nanostructures.
Figure 15. Degradation efficiency ZnFe2O4 per run, measured as the percentage of CV dye degraded by photocatalysts.
![Figure 15. Degradation efficiency ZnFe2O4 per run, measured as the percentage of CV dye degraded by photocatalysts.](/cms/asset/65f19aae-b70d-4150-b41d-ec5d376f17f9/tusc_a_2134696_f0015_oc.jpg)
Figure 16. (a) XPS spectra; (b) Mott–Schottky plots; (c) scheme of energy with reduction potentials vs. NHE of ZnFe2O4 photocatalyst.
![Figure 16. (a) XPS spectra; (b) Mott–Schottky plots; (c) scheme of energy with reduction potentials vs. NHE of ZnFe2O4 photocatalyst.](/cms/asset/5b9ec010-7d93-4455-8c7e-da588b05d277/tusc_a_2134696_f0016_oc.jpg)
Data availability statement
Not applicable.