We pr
esent studi
es on femtosecond to nanosecond fluor
escence dynamics of aqueous solutions of cadmium telluride (CdTe) quantum dots (QDs) with diameters of 3.1 and 3.6 nm. Ultrafast tim
es in the range 200–320 fs and 1.6 ps were determined, and assigned to electron relaxation to the bottom of the conduction band and to recombination of trapped electrons and hol
es. Th
ese tim
es are common to the relaxation mechanisms of QDs in solution, and therefore sugg
ests that intrinsic mechanisms for electron and hole relaxation dominate over surface effects, in agreement with other reports. Additionally, tim
es of
![](http://www.sciencedirect.com/scidirimg/entiti<font color=)
es/223c.gif" alt="not, vert, similar" title="not, vert, similar" border="0">40 ps,
![](http://www.sciencedirect.com/scidirimg/entiti<font color=)
es/223c.gif" alt="not, vert, similar" title="not, vert, similar" border="0">600 ps and
![](http://www.sciencedirect.com/scidirimg/entiti<font color=)
es/223c.gif" alt="not, vert, similar" title="not, vert, similar" border="0">20 ns due to radiative transitions were recorded. Th
ese r
esults are relevant to understanding the photodynamics of CdTe and other QDs in water which should play a fundamental role in their signal when used in biological media.