Yang J P, Kappes M M, Hippler H, Unterreiner A N
Lehrstuhl für Physikalische Chemie Mikroskopischer Systeme, Universität Karlsruhe, 76128 Karlsruhe, Germany.
Phys Chem Chem Phys. 2005 Feb 7;7(3):512-7. doi: 10.1039/b415524f.
Femtosecond one- and two-colour pump-probe spectroscopy of single-walled carbon nanotubes (SWNTs) individual in aqueous surfactant suspensions has been used to assess the "intrinsic" lifetime of the lowest excited states. We demonstrate that such measurements can be perturbed by several competing photophysical processes thus making lifetime deconvolution difficult. Furthermore we show how these effects, arising primarily from sample heterogeneity, can be reduced. Measurements of induced transients in the near IR yield lifetimes of (35 +/- 10) ps and (56 +/- 10) ps, for nanotubes having mean diameters of 0.95 and 1.2 nm, respectively. Furthermore, a fast decay component in the ps to sub-ps regime is also observed. We tentatively attribute this to relaxation in SWNT bundle components.
利用飞秒单双色泵浦-探测光谱技术,对水性表面活性剂悬浮液中单个的单壁碳纳米管(SWNTs)进行研究,以评估最低激发态的“本征”寿命。我们证明,此类测量可能会受到几种相互竞争的光物理过程的干扰,从而使寿命反卷积变得困难。此外,我们展示了如何减少这些主要由样品不均匀性引起的影响。对于平均直径分别为0.95和1.2 nm的纳米管,近红外诱导瞬态测量得出的寿命分别为(35±10) ps和(56±10) ps。此外,还观察到在皮秒到亚皮秒范围内的快速衰减成分。我们初步将此归因于单壁碳纳米管束成分中的弛豫。