Kim Junggil, Lim Jean Sun, Noh Heung-Ryoul, Kim Sang Kyu
Department of Chemistry, KAIST, Daejeon 34141, Republic of Korea.
Department of Physics, Chonnam National University, Gwangju 61186, Republic of Korea.
J Phys Chem Lett. 2020 Aug 20;11(16):6791-6795. doi: 10.1021/acs.jpclett.0c01918. Epub 2020 Aug 7.
Autler-Townes (AT) splitting has been experimentally observed in the optical transition between the zero-point levels of S and S for supersonically cooled 2-methoxythiophenol, 2-fluorothiophenol, and 2-chlorothiophenol. This is the first experimental observation of the light-dressed quantum states of polyatomic molecules ( > 3) in the electronic transition. In the resonance-enhanced ionization process involving the optically coupled states, if Rabi cycling is ensured within the nanosecond laser pulse, AT splitting is clearly observed for the open system for which the excited-state lifetime is shorter than hundreds of picoseconds. Semiclassical optical Bloch equations and a dressed-atom approach based on the three-level atomic model describe the experiment quite well, giving deep insights into the light-matter interaction in polyatomic molecular systems.
在超声冷却的2-甲氧基硫酚、2-氟硫酚和2-氯硫酚的S和S零点能级之间的光学跃迁中,已通过实验观察到奥特勒-汤斯(AT)分裂。这是首次在电子跃迁中对多原子分子(>3)的光修饰量子态进行实验观察。在涉及光耦合态的共振增强电离过程中,如果在纳秒激光脉冲内确保拉比循环,则对于激发态寿命短于数百皮秒的开放系统,可以清楚地观察到AT分裂。基于三能级原子模型的半经典光学布洛赫方程和修饰原子方法能很好地描述该实验,为多原子分子系统中的光与物质相互作用提供了深刻见解。