Dickerson Claire E, Guo Han, Shin Ashley J, Augenbraun Benjamin L, Caram Justin R, Campbell Wesley C, Alexandrova Anastassia N
Department of Chemistry and Biochemistry, University of California Los Angeles, Los Angeles, California 90095, USA.
Department of Physics, Harvard University, Cambridge, Massachusetts 02138, USA.
Phys Rev Lett. 2021 Mar 26;126(12):123002. doi: 10.1103/PhysRevLett.126.123002.
Laser induced electronic excitations that spontaneously emit photons and decay directly to the initial ground state ("optical cycling transitions") are used in quantum information and precision measurement for state initialization and readout. To extend this primarily atomic technique to large, organic compounds, we theoretically investigate optical cycling of alkaline earth phenoxides and their functionalized derivatives. We find that optical cycle leakage due to wave function mismatch is low in these species, and can be further suppressed by using chemical substitution to boost the electron-withdrawing strength of the aromatic molecular ligand through resonance and induction effects. This provides a straightforward way to use chemical functional groups to construct optical cycling moieties for laser cooling, state preparation, and quantum measurement.
激光诱导的电子激发会自发发射光子并直接衰减到初始基态(“光学循环跃迁”),被用于量子信息和精密测量中的态初始化与读出。为了将这种主要基于原子的技术扩展到大型有机化合物,我们从理论上研究了碱土金属苯氧化物及其功能化衍生物的光学循环。我们发现,在这些物种中,由于波函数失配导致的光学循环泄漏较低,并且可以通过化学取代来进一步抑制,即通过共振和诱导效应提高芳香族分子配体的吸电子强度。这提供了一种直接的方法,利用化学官能团构建用于激光冷却、态制备和量子测量的光学循环部分。