Structural Disorder at the Edges of Rubrene Crystals Enhances Singlet Fission.

Materials that undergo singlet fission are of interest for their use in light-harvesting, photocatalysis, and quantum information science, but their ability to undergo fission can be sensitive to local variations in molecular packing. Herein we employ transient absorption microscopy, molecular dynamics simulations, and electronic structure calculations to interrogate how structures found at the edges of orthorhombic rubrene crystals impact singlet fission. Within a micrometer-scale spatial region at the edges of rubrene crystals, we find that the rate of singlet fission increases nearly 4-fold. This observation is consistent with formation of a region at crystal edges with reduced order that accelerates singlet fission by disrupting the symmetry found in rubrene's orthorhombic crystal structure. Our work demonstrates that structural distortions of singlet fission materials can be used to control fission in time and in space, potentially offering a means of controlling this process in light harvesting and quantum information applications.

Progress and Prospects in Optical Ultrafast Microscopy in the Visible Spectral Region: Transient Absorption and Two-Dimensional Microscopy.

Ultrafast optical microscopy, generally employed by incorporating ultrafast laser pulses into microscopes, can provide spatially resolved mechanistic insight into scientific problems ranging from hot carrier dynamics to biological imaging. This Review discusses the progress in different ultrafast microscopy techniques, with a focus on transient absorption and two-dimensional microscopy. We review the underlying principles of these techniques and discuss their respective advantages and applicability to different scientific questions. We also examine in detail how instrument parameters such as sensitivity, laser power, and temporal and spatial resolution must be addressed. Finally, we comment on future developments and emerging opportunities in the field of ultrafast microscopy.

Single-shot transient absorption spectroscopy techniques and design principles.

Single-shot transient absorption (SSTA) spectroscopy is fundamentally identical to transient absorption (TA) spectroscopy but differs in its implementation to enable the measurement of sample response at a range of pump-probe time delays in a single laser shot. As in TA, a pump pulse in SSTA photoexcites a sample, inducing a change in the absorption of a probe pulse. Both commercial and home-built TA instruments typically execute serial measurements at a range of pump-probe time delays to yield transients that report on the dynamics of the photoexcited species, with the sample returning to the same relaxed state between each measurement. SSTA instruments acquire a range of pump-probe time delays simultaneously by somehow encoding the time delay into the profile of the probe beam. This dramatically reduces the time required for SSTA measurements, enabling the measurement of unstable systems undergoing irreversible processes that cannot be accurately characterized using typical TA instruments. The implementation of the encoded time delay must be appropriately designed and carefully calibrated to suit the targeted system and ensure accurate measurements. This review describes techniques used to encode the time delay and design principles for SSTA instruments. Strategies are presented to implement a broadband probe, account for spatial variations in pump and probe beam profiles that influence the intensity and noise of the spatially encoded signal, optimize detection, and correct for dynamic background signals. With these design principles in place, SSTA is capable of measuring an array of unstable and evolving systems that cannot be addressed using typical TA instruments.

Evolving Stark Effect During Growth of Perovskite Nanocrystals Measured Using Transient Absorption.

Methylammonium lead triiodide (MAPbI3) nanocrystals (NCs) are emerging materials for a range of optoelectronic applications. Photophysical characterization is typically limited to structurally stable NCs owing to the long timescales required for many spectroscopies, preventing the accurate measurement of NCs during growth. This is a particular challenge for non-linear spectroscopies such as transient absorption. Here we report on the use of a novel single-shot transient absorption (SSTA) spectrometer to study MAPbI3 NCs as they grow. Comparing the transient spectra to derivatives of the linear absorbance reveals that photogenerated charge carriers become localized at surface trap states during NC growth, inducing a TA lineshape characteristic of the Stark effect. Observation of this Stark signal shows that the contribution of trapped carriers to the TA signal declines as growth continues, supporting a growth mechanism with increased surface ligation toward the end of NC growth. This work opens the door to the application of time-resolved spectroscopies to NCs in situ, during their synthesis, to provide greater insight into their growth mechanisms and the evolution of their photophysical properties.

Broadband single-shot transient absorption spectroscopy.

The duration of transient absorption spectroscopy measurements typically limits the types of systems for which the excited state dynamics can be measured. We present a single-shot transient absorption (SSTA) instrument with a spatially encoded 60 ps time delay range and a 100 nm spectral range that is capable of acquiring a transient spectrum in 20 s. We describe methods to spatially overlap the flat-top pump and probe beams at the sample plane, calibrate the spatially encoded time delay, and correct for non-uniform excitation density. SSTA measurements of organic materials in solution and film demonstrate this technique.

In Situ Measurement of Exciton Dynamics During Thin-Film Formation Using Single-Shot Transient Absorption.

The exciton dynamics of pseudoisocyanine (PIC) is reported during the formation of a thin film dropcast from solution. Tilted pump pulses are used to spatially encode a pump-probe time delay, enabling the collection of a transient in a single shot. We demonstrate that a spatially encoded delay can be used to accurately measure exciton dynamics in thin-film samples, with a signal-to-noise ratio above 20 attained in 2 s. We report in situ linear absorption, fluorescence, and transient absorption measurements during the molecular aggregation of PIC. These measurements reveal a highly fluorescent intermediate stage during thin-film formation that we ascribe to J-aggregates, in contrast to the final, less fluorescent, dry thin film that exhibits photophysics indicative of disordered J-aggregates. The ability to measure exciton dynamics in situ during materials formation will provide a deeper understanding of how functional materials properties evolve, and will enable direct feedback for rational materials design.

Single-shot transient absorption spectroscopy with a 45 ps pump-probe time delay range.

We report a single-shot transient absorption apparatus that successfully uses a tilted pump pulse to spatially encode a 45 ps pump-probe time delay. The time delay range is significantly improved over other reported instruments by using a spatial light modulator to flatten the intensity of the excitation field at the sample position. The full time delay range of the instrument is demonstrated by measuring a long-lived dye. A signal-to-noise ratio of >35 is attained in 8 s. This advance will enable the measurement of excited state dynamics of systems that are not at structural equilibrium.