TY - JOUR
T1 - Photoluminescence and X-ray excited luminescence from glutathione- stabilized gold nanoparticles
AU - Yang, Chang
AU - Ma, Lun
AU - Maley, Jason
AU - Sammynaiken, Ramaswami
AU - Feng, Renfei
AU - Xiang, Guangya
AU - Chen, Wei
PY - 2013/9
Y1 - 2013/9
N2 - Au nanoparticles coated with glutathione (GSH) were prepared by the heat-assisted reduction of Au(I)-thiol complex at 1:1 or 5:4 molar ratio of Au to GSH. The 1:1 sample has three emissions at 610, 645 and 800 nm while the 5:4 sample has a dominant emission at 800 nm but the two emissions at 610 and 645 nm are very weak. It was found in separations that the 610 and 645 nm emissions are closely related while the 800 nm emission behaves in a different way. By adding NaOH, the 800 nm emission decreases while the red emission increases in intensity at low concentration, but both the red and the NIRL emissions are quenched at high concentrations. The luminescence lifetimes of the red emissions were on the nanosecond time scale while the 800 nm emission was on the microsecond time scale. Based on these observations, it is concluded that the red emission is from a single excited states while the 800 nm emission is originated from surface states. Also, for the first time, X-ray excited luminescence is reported here from Au nanoparticles and the applications of these nanoparticles for cell imaging is also investigated.
AB - Au nanoparticles coated with glutathione (GSH) were prepared by the heat-assisted reduction of Au(I)-thiol complex at 1:1 or 5:4 molar ratio of Au to GSH. The 1:1 sample has three emissions at 610, 645 and 800 nm while the 5:4 sample has a dominant emission at 800 nm but the two emissions at 610 and 645 nm are very weak. It was found in separations that the 610 and 645 nm emissions are closely related while the 800 nm emission behaves in a different way. By adding NaOH, the 800 nm emission decreases while the red emission increases in intensity at low concentration, but both the red and the NIRL emissions are quenched at high concentrations. The luminescence lifetimes of the red emissions were on the nanosecond time scale while the 800 nm emission was on the microsecond time scale. Based on these observations, it is concluded that the red emission is from a single excited states while the 800 nm emission is originated from surface states. Also, for the first time, X-ray excited luminescence is reported here from Au nanoparticles and the applications of these nanoparticles for cell imaging is also investigated.
KW - Cell imaging
KW - Decay lifetime
KW - Fluorescence
KW - Glutathione
KW - Gold nanoclusters
KW - X-ray excited luminescence
UR - http://www.scopus.com/inward/record.url?scp=84883726857&partnerID=8YFLogxK
U2 - 10.1166/jbn.2013.1688
DO - 10.1166/jbn.2013.1688
M3 - Article
C2 - 24059082
AN - SCOPUS:84883726857
SN - 1550-7033
VL - 9
SP - 1827
EP - 1836
JO - Journal of Biomedical Nanotechnology
JF - Journal of Biomedical Nanotechnology
IS - 11
ER -