Ultrafast Dynamics within the 1S Exciton Band of Colloidal PbSe Quantum Dots Using Multiresonant Coherent Multidimensional Spectroscopy

The simple particle-in-a-sphere model of quantum dot excitons is the basis for understanding the excitonic peak positions, line widths, and relaxation dynamics in many spectroscopic experiments. Recent multiresonant coherent multidimensional spectroscopy (CMDS) with picosecond excitation pulses measured the two-dimensional spectra of PbSe quantum dots and successfully used this simple model of an inhomogeneous distribution of spherically confined exciton and biexciton states and rate constants to describe the dephasing and population relaxation dynamics. The long excitation pulses prevented resolution of faster dynamics. This work reports the development of multiresonant CMDS with femtosecond excitation pulses to resolve the spectra and dynamics associated with the 1S exciton line shape of PbSe quantum dots. The experiments use different combinations of excitation frequencies, excitation pulse time delays, and a monochromator to display and measure correlations between the spectral features and their dynamics. Line-narrowing of the inhomogeneous distribution occurs at short time delays where the excitation excites a subset of the quantum dots within the 1S line shape and the last pulse probes this subset. The line-narrowing disappears at longer delay times. Three pulse photon echo peak shifts (3PEPS) also occur when the line-narrowing is present, but the shifts disappear as the correlation between the first and last coherence frequencies disappears. Wigner plots reveal the spectral dynamics accompanying the peak shift and the disappearance of the line-narrowing. This work shows there is rapid relaxation dynamics occurring within the line profile of the quantum confined excitonic states that is not consistent with current understanding of the excitonic line broadening. The data suggest that the relaxation dynamics play a more dominant role in defining the excitonic line widths than the inhomogeneous broadening of the quantum dot size distribution. These observations are consistent with other spectroscopic experiments on CdSe and PbS quantum dots. The experiments also show the presence of a higher energy feature that lies outside the 1S line shape and undergoes very rapid relaxation

Exploring Electronic Structure and Order in Polymers via Single-Particle Microresonator Spectroscopy

PEDOT:PSS, a transparent electrically conductive polymer, finds widespread use in electronic devices. While empirical efforts have increased conductivity, a detailed understanding of the coupled electronic and morphological landscapes in PEDOT:PSS has lagged due to substantial structural heterogeneity on multiple length-scales. We use an optical microresonator-based absorption spectrometer to perform single-particle measurements, providing a bottom-up examination of electronic structure and morphology ranging from single PEDOT:PSS polymers to nascent films. Using single-particle spectroscopy with complementary theoretical calculations and ultrafast spectroscopy, we demonstrate that PEDOT:PSS displays bulk-like optical response even in single polymers. We find highly ordered PEDOT assemblies with long-range ordering mediated by the insulating PSS matrix and reveal a preferential surface orientation of PEDOT nanocrystallites absent in bulk films with implications for interfacial electronic communication. Our single-particle perspective provides a unique window into the microscopic structure and electronic properties of PEDOT:PSS

Single-Crystal Thin Films of Cesium Lead Bromide Perovskite Epitaxially Grown on Metal Oxide Perovskite (SrTiO₃)

High-quality metal halide perovskite single crystals have low defect densities and excellent photophysical properties, yet thin films are the most sought after material geometry for optoelectronic devices. Perovskite single-crystal thin films (SCTFs) would be highly desirable for high-performance devices, but their growth remains challenging, particularly for inorganic metal halide perovskites. Herein, we report the facile vapor-phase epitaxial growth of cesium lead bromide perovskite (CsPbBr₃) continuous SCTFs with controllable micrometer thickness, as well as nanoplate arrays, on traditional oxide perovskite SrTiO₃(100) substrates. Heteroepitaxial single-crystal growth is enabled by the serendipitous incommensurate lattice match between these two perovskites, and overcoming the limitation of island-forming Volmer–Weber crystal growth is critical for growing large-area continuous thin films. Time-resolved photoluminescence, transient reflection spectroscopy, and electrical transport measurements show that the CsPbBr₃ epitaxial thin film has a slow charge carrier recombination rate, low surface recombination velocity (10⁴ cm s^–1), and low defect density of 10¹² cm^–3, which are comparable to those of CsPbBr₃ single crystals. This work suggests a general approach using oxide perovskites as substrates for heteroepitaxial growth of halide perovskites. The high-quality halide perovskite SCTFs epitaxially integrated with multifunctional oxide perovskites could open up opportunities for a variety of high-performance optoelectronics devices