TY - JOUR
T1 - Metal-free inorganic ligands for colloidal nanocrystals
T2 - S2-, HS-, Se2-, HSe-, Te2-, HTe -, TeS32-, OH-, and NH 2- as surface ligands
AU - Nag, Angshuman
AU - Kovalenko, Maksym V.
AU - Lee, Jong Soo
AU - Liu, Wenyong
AU - Spokoyny, Boris
AU - Talapin, Dmitri V.
PY - 2011/7/13
Y1 - 2011/7/13
N2 - All-inorganic colloidal nanocrystals were synthesized by replacing organic capping ligands on chemically synthesized nanocrystals with metal-free inorganic ions such as S2-, HS-, Se2-, HSe-, Te2-, HTe-, TeS32-, OH- and NH2-. These simple ligands adhered to the NC surface and provided colloidal stability in polar solvents. The versatility of such ligand exchange has been demonstrated for various semiconductor and metal nanocrystals of different size and shape. We showed that the key aspects of Pearsons hard and soft acids and bases (HSAB) principle, originally developed for metal coordination compounds, can be applied to the bonding of molecular species to the nanocrystal surface. The use of small inorganic ligands instead of traditional ligands with long hydrocarbon tails facilitated the charge transport between individual nanocrystals and opened up interesting opportunities for device integration of colloidal nanostructures.
AB - All-inorganic colloidal nanocrystals were synthesized by replacing organic capping ligands on chemically synthesized nanocrystals with metal-free inorganic ions such as S2-, HS-, Se2-, HSe-, Te2-, HTe-, TeS32-, OH- and NH2-. These simple ligands adhered to the NC surface and provided colloidal stability in polar solvents. The versatility of such ligand exchange has been demonstrated for various semiconductor and metal nanocrystals of different size and shape. We showed that the key aspects of Pearsons hard and soft acids and bases (HSAB) principle, originally developed for metal coordination compounds, can be applied to the bonding of molecular species to the nanocrystal surface. The use of small inorganic ligands instead of traditional ligands with long hydrocarbon tails facilitated the charge transport between individual nanocrystals and opened up interesting opportunities for device integration of colloidal nanostructures.
UR - http://www.scopus.com/inward/record.url?scp=79960047171&partnerID=8YFLogxK
U2 - 10.1021/ja2029415
DO - 10.1021/ja2029415
M3 - Article
AN - SCOPUS:79960047171
SN - 0002-7863
VL - 133
SP - 10612
EP - 10620
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 27
ER -