Guyot-Sionnest Philippe, Wehrenberg Brian, Yu Dong
James Franck Institute, 5640 South Ellis Avenue, Chicago, Illinois 60637, USA.
J Chem Phys. 2005 Aug 15;123(7):074709. doi: 10.1063/1.2004818.
The intraband relaxation between the 1Pe and 1Se state of CdSe colloidal quantum dots is studied by pump-probe time-resolved spectroscopy. Infrared pump-probe measurements with approximately 6-ps pulses show identical relaxation whether the electron has been placed in the 1Se state by above band-gap photoexcitation or by electrochemical charging. This indicates that the intraband relaxation of the electrons is not affected by the photogenerated holes which have been trapped. However, the surface ligands are found to strongly affect the rate of relaxation in colloid solutions. Faster relaxation (<8 ps) is obtained with phosphonic acid and oleic acid ligands. Alkylamines lead to longer relaxation times of approximately 10 ps and the slowest relaxation is observed for dodecanethiol ligands with relaxation times approximately 30 ps. It is concluded that, in the absence of holes or when the holes are trapped, the intraband relaxation is dominated by the surface and faster relaxation correlates with larger interfacial polarity. Energy transfer to the ligand vibrations may be sufficiently effective to account for the intraband relaxation rate.
通过泵浦-探测时间分辨光谱研究了CdSe胶体量子点1Pe和1Se态之间的带内弛豫。使用约6皮秒脉冲的红外泵浦-探测测量表明,无论电子是通过带隙以上光激发还是通过电化学充电置于1Se态,弛豫情况均相同。这表明电子的带内弛豫不受被俘获的光生空穴的影响。然而,发现表面配体对胶体溶液中的弛豫速率有强烈影响。使用膦酸和油酸配体可获得更快的弛豫(<8皮秒)。烷基胺导致弛豫时间更长,约为10皮秒,而对于十二烷硫醇配体,观察到最慢的弛豫,弛豫时间约为30皮秒。得出的结论是,在没有空穴或空穴被俘获的情况下,带内弛豫由表面主导,更快的弛豫与更大的界面极性相关。能量转移到配体振动可能足以解释带内弛豫速率。