Herrera Felipe, Litinskaya Marina
Department of Physics, Universidad de Santiago de Chile, Av. Ecuador, 3493 Santiago, Chile.
Department of Physics & Astronomy, University of British Columbia, Vancouver, British Columbia V6T 1Z1, Canada.
J Chem Phys. 2022 Mar 21;156(11):114702. doi: 10.1063/5.0080063.
We propose to use molecular picocavity ensembles as macroscopic coherent nonlinear optical devices enabled by nanoscale strong coupling. For a generic picocavity model that includes molecular and photonic disorder, we derive theoretical performance bounds for coherent cross-phase modulation signals using weak classical fields of different frequencies. We show that strong coupling of the picocavity vacua with a specific vibronic sideband in the molecular emission spectrum results in a significant variation of the effective refractive index of the metamaterial relative to a molecule-free scenario due to a vacuum-induced Autler-Townes effect. For a realistic molecular disorder model, we demonstrate that cross-phase modulation of optical fields as weak as 10 kW/cm is feasible using dilute ensembles of molecular picocavities at room temperature, provided that the confined vacuum is not resonantly driven by the external probe field. Our work paves the way for the development of plasmonic metamaterials that exploit strong coupling for optical state preparation and quantum control.
我们提议将分子微腔集合用作由纳米级强耦合实现的宏观相干非线性光学器件。对于一个包含分子和光子无序的通用微腔模型,我们使用不同频率的弱经典场推导了相干交叉相位调制信号的理论性能界限。我们表明,由于真空诱导的奥特勒-汤斯效应,微腔真空与分子发射光谱中特定的振动边带的强耦合导致超材料的有效折射率相对于无分子情况有显著变化。对于一个实际的分子无序模型,我们证明,在室温下使用分子微腔的稀集合,只要受限真空不被外部探测场共振驱动,10 kW/cm 这样弱的光场的交叉相位调制是可行的。我们的工作为开发利用强耦合进行光学态制备和量子控制的等离子体超材料铺平了道路。