Photonics and Optoelectronics Group, Physics Department and CeNS, Ludwig-Maximilians-Universität München, Amalienstrasse 54, 80799 München, Germany.
Phys Rev Lett. 2013 May 24;110(21):217406. doi: 10.1103/PhysRevLett.110.217406. Epub 2013 May 23.
We report a femtosecond transient spectroscopy study in the near to middle infrared range, 0.8-0.35 eV photon energy, on graphene and few layer graphene single flakes. The spectra show an evolving structure of photoinduced absorption bands superimposed on the bleaching caused by Pauli blocking of the interband optically coupled states. Supported by tight-binding model calculations, we assign the photoinduced absorption features to intersubband transitions as the number of layers is increased. Interestingly, the intersubband photoinduced resonances show a longer dynamics than the interband bleaching, because of their independence from the absolute energy of the carriers with respect to the Dirac point. The dynamic of these intersubband transitions reflects the lifetime of the hot carriers and provides an elegant method to access it in this important class of semimetals.
我们报告了在近中红外范围(0.8-0.35 eV 光子能量)对石墨烯和少层石墨烯单片中的飞秒瞬态光谱研究。光谱显示出光致吸收带的演变结构,这些吸收带叠加在由带间光耦合态的 Pauli 阻塞引起的漂白上。通过紧束缚模型计算的支持,我们将光致吸收特征分配给随着层数的增加而发生的子带间跃迁。有趣的是,由于其与相对于狄拉克点的载流子的绝对能量无关,因此子带间光致共振的动力学比带间漂白更长。这些子带间跃迁的动力学反映了热载流子的寿命,并提供了一种在这种重要的半导体中访问它的优雅方法。