Table 1.
Method | Advantages | Disadvantages | Ref. | Examples |
---|---|---|---|---|
Laser Ablation Synthesis in Solution (LASiS) | Green synthesis Different structures and composition |
Difficult control of particle size and clustering | [27,28] | [29,30] |
Chemical vapor deposition (laser and spray pyrolysis) |
Easy to prepare Production of small particle size |
Expensive equipment Gaseous interferences |
[26,31,32,33] | [34,35,36,37] |
Co-precipitation | Green Low-cost Scalable Facile Efficient |
Difficult to control size Polydispersity Lack of precise stoichiometric phase control |
[26,28,31,32,38] | [39,40,41] |
Thermal decomposition | Small size particles Control of size and shape Monodisperse |
Requires multiple steps Toxic solvents Toxic and expensive precursors Laborious purification Requires surface treatment after synthesis |
[31,33] | [42,43] |
Hydrothermal (solvothermal) | Green Versatile Control of morphology |
Need of autoclave Control of dispersity Slow reaction kinetics |
[28,33] | [44,45] |
Sol-gel synthesis | Homogeneous Control of shape and length Low-cost High phase purity |
Requires post treatment By-products Safety Low efficiency |
[28,33] | [46,47] |
Sonochemical decomposition | Mild experimental conditions Good crystallinity Versatile |
Mechanism not still understood | [26,32,43] | [48,49] |
Microemulsion | Monodispersity Simple equipment High control of size and shape Room conditions Small sizes |
Removal of surfactants High solvent consumption Low-yield Difficult scale-up |
[26,28,31,33] | [50] |
Electrochemical synthesis | Control of particle size Simple and fast |
Lack of reproducibility | [32] | [51,52] |
Biosynthesis | High yield Reproducibility Scalability Low cost Room temperature |
Time-consuming Laborious |
[31,32] | [53,54] |