Direct measurement of high-lying vibrational repumping transitions for molecular laser cooling

TL;DR

This paper introduces a novel high-resolution spectroscopy method to identify vibrational repumping transitions in molecules for laser cooling, using optically-driven chemical reactions and frequency-modulated absorption, demonstrated on YbOH.

Contribution

The authors develop a general, optical cycling-free spectroscopy technique for high-lying vibrational states, enabling efficient identification of repumping transitions in molecules for laser cooling.

Findings

Measured the spectrum of the $ ilde{A}^2\Pi_{1/2}(1,0,0)- ilde{X}^2\Sigma^+(3,0,0)$ band in YbOH.

Identified key vibrational repump transitions necessary for photon cycling.

Determined spectral constants of the $ ilde{X}^2\Sigma^+(3,0,0)$ state.

Abstract

Molecular laser cooling and trapping requires addressing all spontaneous decays to excited vibrational states that occur at the $\gtrsim 10^{-4} - 10^{-5}$ level, which is accomplished by driving repumping transitions out of these states. However, the transitions must first be identified spectroscopically at high-resolution. A typical approach is to prepare molecules in excited vibrational states via optical cycling and pumping, which requires multiple high-power lasers. Here, we demonstrate a general method to perform this spectroscopy without the need for optical cycling. We produce molecules in excited vibrational states by using optically-driven chemical reactions in a cryogenic buffer gas cell, and implement frequency-modulated absorption to perform direct, sensitive, high-resolution spectroscopy. We demonstrate this technique by measuring the spectrum of the $\tilde{A}^2\Pi_{1/2}(1,0,0)-\tilde{X}^2\Sigma^+(3,0,0)$ band in $^{174}$YbOH. We identify the specific vibrational repump transitions needed for photon cycling, and combine our data with previous measurements of the $\tilde{A}^2\Pi_{1/2}(1,0,0)-\tilde{X}^2\Sigma^+(0,0,0)$ band to determine all of the relevant spectral constants of the $\tilde{X}^2\Sigma^+(3,0,0)$ state. This technique achieves high signal-to-noise, can be further improved to measure increasingly high-lying vibrational states, and is applicable to other molecular species favorable for laser cooling.