Table 1.
Method | Cu Source | Solvent | Reducing Agent | Other Organics Added | Reaction Temperature and Duration | Length of CuNWs | Refs. |
---|---|---|---|---|---|---|---|
Hydrothermal reduction | CuCl2 | water | glucose | hexadecylamine | 120°C for 2 h | several microns | [13] |
CuCl2 | water | glucose | hexadecylamine | 120°C for 12 h | tens of microns | [5] | |
Cu(NO3)2 | water | ethylene glycol | polyvinyl pyrrolidone | 160°C for 24 h | tens of microns | [20] | |
CuCl2 | water | octadecylamine | - | 165°C for 140 h | hundreds of microns | [6] | |
CuCl2 | water | glucose | ethanol, oleic acid, and oleylamine | 116 °C for 2–12 h | tens of microns | [7] | |
Aqueous solution reduction | Cu(NO3)2 | water | hydrazine | ethylenediamine | 40–80 °C for 25 min–15 h | tens of microns | [1,2,4,21,22] |
Cu(OH)2 | water | hydrazine | ethylenediamine | 70 °C for 1 h | tens of microns | [23] | |
Cu(NO3)2 | water | hydrazine | propanediamine | 80 °C for 1 h | tens of microns | [24] | |
CuCl2 | water | glucose | hexadecylamine | 100 °C for 6 h | hundreds of microns | [25] | |
CuCl2 | water–alcohol | L-ascorbic acid | oleylamine | 55–85 °C for 12 h | hundreds of microns | [8] | |
Non-aqueous synthesis | CuCl | oleylamine | via disproportionation reaction | - | 200 °C 30 min | tens of microns | [26] |
CuCl2 | oleylamine | in the presence of catalytic Ni2+ | - | 175 °C for 10 h | tens of microns | [9] | |
Cu(acac)2 | hexadecylamine | in the presence of catalytic Pt | cetyltriamoninum bromide | 180 °C for 10 h | hundreds of microns | [3] | |
CuCl2 | oleylamine | tris(trimethylsilyl)silane | oleic acid | 165 °C for 10 h | tens of microns | [10] |