TY - JOUR
T1 - Time-resolved photoluminescence of solid state fullerenes
AU - Byrne, H. J.
AU - Maser, W.
AU - Rühle, W. W.
AU - Mittelbach, A.
AU - Hönle, W.
AU - von Schnering, H. G.
AU - Movaghar, B.
AU - Roth, S.
PY - 1993/3/26
Y1 - 1993/3/26
N2 - Time-resolved photoluminescence studies in films, powders and single crystals of C60 are reported. The observed spectra in all forms are consistent with those reported for steady state conditions and may be associated with an intramolecular process. The spectrum is largely temperature independent and, at low temperatures, the observed luminescence decays with a lifetime of 1.2 ns. No long-lived decay from the triplet is observed at these intensities.In the case of the films, both the emission spectrum and lifetime are independent of excitation intensity. In the powder and single crystallite, a dramatic increase in the lifetime as well as a red-shift and broadening of the spectrum is observed at higher intensities. The luminescence intensity is seen to increase with the cube of the input intensity. The behaviour is interpreted as an abrupt onset of emission from the highly populated triplet state resulting from a banding of the intramolecular triplet states, a process which is dependent on a critical excited state density.
AB - Time-resolved photoluminescence studies in films, powders and single crystals of C60 are reported. The observed spectra in all forms are consistent with those reported for steady state conditions and may be associated with an intramolecular process. The spectrum is largely temperature independent and, at low temperatures, the observed luminescence decays with a lifetime of 1.2 ns. No long-lived decay from the triplet is observed at these intensities.In the case of the films, both the emission spectrum and lifetime are independent of excitation intensity. In the powder and single crystallite, a dramatic increase in the lifetime as well as a red-shift and broadening of the spectrum is observed at higher intensities. The luminescence intensity is seen to increase with the cube of the input intensity. The behaviour is interpreted as an abrupt onset of emission from the highly populated triplet state resulting from a banding of the intramolecular triplet states, a process which is dependent on a critical excited state density.
UR - http://www.scopus.com/inward/record.url?scp=0001225062&partnerID=8YFLogxK
U2 - 10.1016/0009-2614(93)89187-M
DO - 10.1016/0009-2614(93)89187-M
M3 - Article
AN - SCOPUS:0001225062
SN - 0009-2614
VL - 204
SP - 461
EP - 466
JO - Chemical Physics Letters
JF - Chemical Physics Letters
IS - 5-6
ER -