Liu Kaihui, Hong Xiaoping, Choi Sangkook, Jin Chenhao, Capaz Rodrigo B, Kim Jihoon, Wang Wenlong, Bai Xuedong, Louie Steven G, Wang Enge, Wang Feng
Department of Physics, University of California, Berkeley, CA 94720;State Key Laboratory for Mesoscopic Physics, School of Physics, Peking University, Beijing 100871, China;
Department of Physics, University of California, Berkeley, CA 94720;
Proc Natl Acad Sci U S A. 2014 May 27;111(21):7564-9. doi: 10.1073/pnas.1318851111. Epub 2014 May 12.
Optical absorption is the most fundamental optical property characterizing light-matter interactions in materials and can be most readily compared with theoretical predictions. However, determination of optical absorption cross-section of individual nanostructures is experimentally challenging due to the small extinction signal using conventional transmission measurements. Recently, dramatic increase of optical contrast from individual carbon nanotubes has been successfully achieved with a polarization-based homodyne microscope, where the scattered light wave from the nanostructure interferes with the optimized reference signal (the reflected/transmitted light). Here we demonstrate high-sensitivity absorption spectroscopy for individual single-walled carbon nanotubes by combining the polarization-based homodyne technique with broadband supercontinuum excitation in transmission configuration. To our knowledge, this is the first time that high-throughput and quantitative determination of nanotube absorption cross-section over broad spectral range at the single-tube level was performed for more than 50 individual chirality-defined single-walled nanotubes. Our data reveal chirality-dependent behaviors of exciton resonances in carbon nanotubes, where the exciton oscillator strength exhibits a universal scaling law with the nanotube diameter and the transition order. The exciton linewidth (characterizing the exciton lifetime) varies strongly in different nanotubes, and on average it increases linearly with the transition energy. In addition, we establish an empirical formula by extrapolating our data to predict the absorption cross-section spectrum for any given nanotube. The quantitative information of absorption cross-section in a broad spectral range and all nanotube species not only provides new insight into the unique photophysics in one-dimensional carbon nanotubes, but also enables absolute determination of optical quantum efficiencies in important photoluminescence and photovoltaic processes.
光吸收是表征材料中光与物质相互作用的最基本光学性质,并且最容易与理论预测进行比较。然而,由于使用传统透射测量时消光信号较小,确定单个纳米结构的光吸收截面在实验上具有挑战性。最近,利用基于偏振的零差显微镜成功实现了单个碳纳米管光学对比度的显著提高,其中纳米结构的散射光波与优化的参考信号(反射/透射光)发生干涉。在这里,我们通过在透射配置中将基于偏振的零差技术与宽带超连续激发相结合,展示了针对单个单壁碳纳米管的高灵敏度吸收光谱。据我们所知,这是首次在单管水平上对50多个具有明确手性的单壁纳米管在宽光谱范围内进行高通量和定量测定纳米管吸收截面。我们的数据揭示了碳纳米管中激子共振的手性依赖行为,其中激子振子强度与纳米管直径和跃迁阶数呈现出普遍的标度律。激子线宽(表征激子寿命)在不同纳米管中变化很大,并且平均而言它随跃迁能量线性增加。此外,我们通过外推数据建立了一个经验公式,以预测任何给定纳米管的吸收截面光谱。宽光谱范围内和所有纳米管种类的吸收截面定量信息不仅为一维碳纳米管中独特的光物理提供了新的见解,而且还能够绝对确定重要的光致发光和光伏过程中的光学量子效率。