We have studied carrier transfer to strain confined dots from a host q
uantum well, using selectively excited time-resolved photoluminescence
spectroscopy. We find that the photoluminescence decay rate after pic
osecond excitation is much slower when excitation is indirect, via tra
nsfer from the quantum well, then when it is directly into the dot, ev
en though the decay of the quantum well photoluminescence is fast. Thi
s result is inconsistent with a simple three level kinetic model of th
e transfer process. We propose a tentative model involving an intermed
iate nonradiative state, possibly the charge separated state predicted
theoretically. (C) 1996 Academic Press Limited