Table 1 Plant extracts used for the synthesis of SnO2NPs with their shape, size and brief experimental condition
Plant (part) | Precursors | Synthesis conditions | Shape | Size | Applications | Ref |
---|---|---|---|---|---|---|
Annona squamosa (peel) | SnCl2·2H2O | Reaction: 60 °C, 3 h Drying: 160 °C, 1 h | Spherical | 27.5 nm | Cytotoxic activity | [64] |
Aspalathus linearis (leaf) | SnCl4·5H2O | Drying: 80 °C, Annealing: 400–900 °C, 4 h | Quasi-spherical | 2.5–11.40 nm | Efficient photocatalyst against methylene blue, congo red, eosin Y | [51] |
Brassica oleracea L. var. botrytis (leaf) | SnCl2·2H2O | Reaction: 60 °C, 6 h Drying: 75 °C, Annealing: 300–450 °C, 4 h | Spherical | 3.1–6.34 nm | Excellent photocatalyst against methylene blue | [52] |
Camellia sinensis (leaf) | SnCl2 | Reaction: 80 °C, 30 min Drying: 80 °C, Annealing: 200–800 °C | Spherical | 5–30 nm | – | [53] |
Calotropis gigantean (leaf) | SnCl2·5H2O | Drying: microwave oven; Calcination: 400 °C, 3 h | Spherical | 30–40 nm | Photocatalytic activity against methyl orange dye | [62] |
Catunaregam spinosa (root) | SnCl2 | Reaction: 60 °C, 2 h Annealing: 450 °C, 2 h | Spherical | 47 nm | Efficient photocatalyst against congo red dye | [57] |
Cyphomandra betacea (fruit) | SnCl2 | Reaction: 80 °C, 3 h Annealing: 300 °C, 3 h | Spherical | 20–50 nm | Excellent photocatalytic activity against methylene blue | [65] |
Daphne alpina (leaf) | SnCl4·5H2O | Reaction: 60 °C, Drying: 120 °C | Elongated shape | 19–27 nm | As adsorbent for Cd2+ ions | [66] |
Lisea cubeba (fruit) | SnCl2·2H2O | Reaction: room temp., 10 min, Drying: 50 °C, 2 h; | Irregular | 30 nm | Antioxidant activity Excellent photocatalytic activity against congo red | [67] |
Persia Americana (seed) | SnCl2 | Reaction: 60 °C, 12 h; Calcination: 300 °C, 2 h | Flake-like | 4 nm | Excellent photocatalytic activity against phenolsulfonphthalein dye | [68] |
Piper betle (leaf) | SnCl2·2H2O | Heating: 60 °C, 4 h Calcination: 400 °C, 4 h | Spherical | 8.4 nm | Excellent photocatalytic activity against reactive yellow 186 dye | [63] |
Piper nigrum (seed) | SnCl2·2H2O | Drying: 60 °C, Calcination: 300–900 °C, 1 h | Tetragonal | 5–30 nm | Cytotoxic activity | [69] |
Pruni spinosae flos | SnCl2·2H2O | Reaction: 80 °C,1 h | Spherical | 9 nm | Biocidal against bacteria and fungi | [70] |
Psidium guajava (leaf) | SnCl4 | Stirring: 60 °C, 4 h Calcination: 400 °C, 4 h | Spherical | 8–10 nm | Photocatalytic activity against reactive yellow 186 | [61] |
Saccharum officinarum (stem) | SnCl2·2H2O, AgNO3, | Reaction: 100 °C, 4 h Drying: 60 °C, Calcination: 200 °C, 400 °C, 2 h | Spherical | 8–10 nm | Antibacterial activity against P. aeruginosa, E. coli, B. subtillis and S. pneumonia Antioxidant activity | [71] |
Trigonelle foenum-graecum (seed) | SnCl4·5H2O | Reaction: room temp., 5 min; Annealing: 300–900 °C, 1 h | Spherical | 2.2–3.3 nm | Antibacterial activity against E. coli Antioxidant activity against DPPH | [72] |