Short-lived memory in multidimensional spectra encodes full signal evolution

TL;DR

This paper introduces the spectral generalized master equation (GME), a novel technique that reconstructs full 2D spectra evolution from short-waiting time data, reducing experimental costs and noise.

Contribution

The spectral GME method enables high-resolution spectral evolution analysis from minimal data, overcoming limitations of traditional multidimensional spectroscopy.

Findings

Reduces experimental cost by orders of magnitude.

Accurately removes statistical noise from spectra.

Demonstrated on both theoretical and experimental spectra.

Abstract

Ultrafast multidimensional spectroscopies are powerful tools that can access charge and energy flow in complex materials, shifting chemical kinetics, and even many-body interactions in correlated matter. However, current implementations typically involve complex apparatuses and long averaging times. As a result, these methods have been limited to detailed mechanistic investigations of a few samples, precluding the broad characterization of molecular systems and/or the optimization of material ones. For example, converging the statistical noise in 2D spectra becomes exponentially expensive with increasing waiting times, and extended laser exposure heightens the probability of sample degradation. We address this fundamental challenge by developing a new technique, the spectral generalized master equation (GME), that enables one to employ short-waiting time 2D spectra to determine the full evolution of 2D spectra over arbitrary waiting times with high temporal resolution. In addition to reducing the cost of experiments by multiple orders of magnitude, our approach accurately removes statistical noise, reducing the need for time averaging, while circumventing the increasing convergence costs with longer waiting times. We provide a rigorous theoretical footing for the spectral GME and demonstrate its applicability on theoretically generated and experimentally measured 2D electronic and 2D infrared spectra. We anticipate that this advance has the potential to enable the investigation of systems that are too delicate for study with current multidimensional spectroscopies and accelerate the progress of 2D spectroscopy-based microscopies that can offer highly resolved excitation dynamics with spatial resolution over heterogeneous environments.