The major difference between semiconductor quantum dots and bulk semiconductors is in the quantum confinement effect. It results the controllable exciton¡¦s absorption and emission spectra by tuning the size of the quantum dot. Moreover, multi-exciton states are reported to be observed in the highly symmetric quantum dot systems. In this dissertation, we use the single molecule fluorescence measurement to study the power dependence of multi-exciton state in single CdSe/ZnS semiconductor quantum dots. At low excitation fluence, anti-bunching behavior, and nearly single exponential relaxation dynamics are observed. By increasing the laser power, bi-exponential fluorescence decay dynamics as well as bunching behaviors from the same QD indicate the fast PL dynamics due to the relaxation from multi-exciton. The results indicate certain threshold energy level for multi-exciton generation. In addition, the multiple step cascade radiative relaxation processes are observed. Besides, we modulate linear polarization light to study the excitation orientation dependence. The results indicate the emission dipole of multi-exciton is similar to the single exciton, having a two dimensional transition dipole plane with c-axis symmetry. However, the absorption dipole of multi-exciton exhibits different orientation dependence from the single exciton.

We have constructed a single molecule detection system with the capability to simultaneously measure many parameters, including transient fluorescence intensity, fluorescence lifetime, and photon anti-bunching behavior via the Hanbury Brown-Twiss photon-correlation technique. In addition, we apply the system to study the single DiI (1, 1 '- dioctadecyl- 3, 3 , 3 ', 3 ' - tetramethylindocarbocyanine perchlorate) molecule, to characterize the photo-physical behaviors. Cyanine dyes are the molecules that constitute of two nitrogen centers, one of which is positive charged, and is linked by a conjugated chain with odd number of carbon atoms to the other nitrogen center. Cyanine dyes are interested in the photo sensitization, optical recording media, nonlinear optics, laser dyes, and many interesting photophysical and photochemical behaviors. Among them, DiI plays an important role in single molecule fluorescence investigations. The high photo-stability, good QE, and low inter-system crossing rates, make it a pioneer for the widely investigations in single molecule studies. Our experimental goal is to understand the characteristic of the monitored single molecule by the measuring photo-physical parameters. Our results include the typical behaviors in DiI molecules: clear on-off blinking, fluorescence anti-bunching, one-step photo-bleaching, and consistent fluorescence polarization orientation. In addition, we also observed some change during measurement, which indicates the corresponding change of structure. Few molecules also exhibit non-zero probability around the zero delay time, which indicates the simultaneous existence of more than one quantum emitters in the detected region. These results demonstrate that the parameters are essential for understanding and characterizing the observed molecules in single molecule level.