Table 1.
Methods | Advantages | Disadvantages | |
---|---|---|---|
Top-down | Electrochemical oxidation | High purity, high yield, controllable size, good reproducibility, low cost | Complicated operation, especially when doping with heteroatoms |
Laser ablation | Simple experimental setup, can produce particles with different sizes and controllable morphology by changing experimental parameters | Low yield and high cost | |
Chemcial oxidation | Inexpensive equipment and can produce c-dots are a large scale | Numerous tedious steps, usually requires toxic reagents and strong acid/base. Non-uniform size distribution |
|
Ultrasonic synthesis | Easy operation | High energy cost and instrumental wastage | |
Bottom-up | Hydrothermal treatment | Low cost, with simple control of key parameters such as temperature, time and pressure of the reaction vessel. The produced c-dots also have a high quantum efficiency and are non-toxic. | Long synthesis duration and at a low yield |
Microwave synthesis | Short reaction time and it is easy to control the size of the particles with the c-dots produced being uniform in size distribution. | High energy cost | |
Thermal decomposition | Easy operation, solvent-free, low cost and can produce c-dots at a large scale | Low yield |