| GO–CuO | 
(i) Hydrothermal synthesis | 
(i) Brilliant green | 
(i) 112
 | 
| (ii) CuO/Cu2O heterostructure (10–15 nm) | 
(ii) Tetracyclin, MOr | 
(ii) 116
 | 
| (iii) Catalytic property | 
(iii) Reduces –NO2 to –NH2
 | 
(iii) 113
 | 
| GO–AgO/Ag2O | 
(i) Synthesized by electrostatic interaction | 
(i) RhB | 
(i) 134
 | 
| (ii) Electrostatic interaction | 
(ii) MB | 
(ii) 137 and 141
 | 
| (iii) In situ green synthesis method | 
(iii) MB, RhB | 
(iii) 138
 | 
| (iv) GO–Ag/V/Mo heterostructure via precipitation method | 
(iv) RhB | 
(iv) 139
 | 
| GO–ZnO | 
(i) Chemical method, ZnO (∼15–20 nm) | 
MB | 
(i) 144, 146 and 147
 | 
| (ii) Solution method | 
(ii) 151 and 152
 | 
| (iii) Flower like morphology of ZnO | 
(iii) 145
 | 
| GO–Fe2O3, GO–Fe3O4
 | 
(i) Impregnation process, both α and γ phases are present | 
RhB, 4-nitrophenol, MB, Cu2+, fulvalic acid, NH4ClO4, AO7, Cd2+, Pb2+
 | 
166, 167, 169, 170, 172, 174, 175, 178 and 183
 | 
| (ii) In situ chemical deposition | 
| (iii) Core–shell structure (10–15 nm Fe3O4) | 
| GO–NiO | 
(i) Hydrothermal method, solution mixing | 
MB, 2-chlorophenol, methyl violet (MV) | 
186–190
 | 
| (ii) Radiofrequency sputtering | 
| (iii) In situ reduction, particle size ∼20 nm | 
| GO–CdO | 
Solution phase method without surfactant | 
MB, RhB | 
191
 | 
| GO–ZrO2
 | 
Hydrothermal and co-precipitation method | 
RhB, MB, As, Cr | 
195, 197 and 198
 | 
| GO–TiO2
 | 
Eco friendly synthesis using green alga | 
Congo red, crystal violet | 
202 and 203
 | 
| GO–MgO | 
Hydrothermal and solvothermal method | 
Congo red, phenol ozonolysis | 
206, 212 and 215
 | 
| GO–MgO | 
Co-precipitation | 
Pb2+, Cu2+
 | 
207 and 214
 | 
| GO–EDTA | 
Chemical (silanization) reaction | 
Pb2+, Cu2+, Ni2+, Hg2+
 | 
217–219
 | 
| GO–chitosan | 
Self-assembly, formation of 3D network | 
Pb2+, Cu2+, MB, RhB, Congo red, eosin Y | 
223–226
 | 
| GO–PAn | 
Chemical oxidation with APS | 
Cd2+ adsorption | 
260
 | 
| GO–PPy | 
Electrochemical deposition | 
Ag+, Cu2+, Pb2+, Cd2+, Fe3+ adsorption | 
270
 |