Low energy excited state vibrations revealed in conjugated copolymer PCDTBT

Low energy vibrations in the excited state have been hypothesized to play an important role in quickly and efficiently generating free charges in bulk heterojunctions of some conjugated polymer systems. While time-resolved vibrational spectroscopies seemingly are well poised to address the relationship between kinetics and vibrational motions after initial photoexcitation, uncertainty in the measurement arises due to overlapping signals and difficulties in assigning observed oscillatory signals to the molecular response. Here, we demonstrate a high sensitivity strategy to distinguish between signal oscillations originating from lab noise and those molecular in origin in order to isolate the low energy excited-state vibrations in the model conjugated copolymer PCDTBT. Furthermore, to distinguish modes that may be implicated in different kinetic pathways, coherent signal oscillations extracted from 2-dimensional electronic spectroscopy (2DES) are compared for the polymer in two solvents with different polarities resulting in different kinetics. We observe that the change in solvent affects dynamics on the >2 ps scale but not on the time scale required for free charge generation in heterojunctions (similar to 200 fs time scale). By the same token, the excited state vibrational modes that appear and disappear based on solvent polarity may also be associated with the slower kinetic process. The observation of low energy vibrational motions coupled to the excited state manifold that persists through the solvent change and thus can be associated with the fast kinetic process supports the hypothesis that direct polaron formation, rather than exciton formation and diffusion followed by interfacial charge separation, is a more likely route toward free charges in organic heterostructures. Published under license by AIP Publishing

Fixation can change the appearance of phase separation in living cells

Fixing cells with paraformaldehyde (PFA) is an essential step in numerous biological techniques as it is thought to preserve a snapshot of biomolecular transactions in living cells. Fixed-cell imaging techniques such as immunofluorescence have been widely used to detect liquid–liquid phase separation (LLPS) in vivo. Here, we compared images, before and after fixation, of cells expressing intrinsically disordered proteins that are able to undergo LLPS. Surprisingly, we found that PFA fixation can both enhance and diminish putative LLPS behaviors. For specific proteins, fixation can even cause their droplet-like puncta to artificially appear in cells that do not have any detectable puncta in the live condition. Fixing cells in the presence of glycine, a molecule that modulates fixation rates, can reverse the fixation effect from enhancing to diminishing LLPS appearance. We further established a kinetic model of fixation in the context of dynamic protein–protein interactions. Simulations based on the model suggest that protein localization in fixed cells depends on an intricate balance of protein–protein interaction dynamics, the overall rate of fixation, and notably, the difference between fixation rates of different proteins. Consistent with simulations, live-cell single-molecule imaging experiments showed that a fast overall rate of fixation relative to protein–protein interaction dynamics can minimize fixation artifacts. Our work reveals that PFA fixation changes the appearance of LLPS from living cells, presents a caveat in studying LLPS using fixation-based methods, and suggests a mechanism underlying the fixation artifact

Broadband Deep UV Spectra of Interfacial Aqueous Iodide.

The behavior of ions at aqueous interfaces influences vital processes in many fields but has long remained a subject of controversy. Over the past decade, counterintuitive surface concentration enhancement of several ions in aqueous solution has been demonstrated via nonlinear laser spectroscopy and mass spectrometry. While the evidence for significant ion enhancement at the air-water interface is convincing, the mechanism remains incompletely understood. Toward this end, we present the full broadband DUV-SFG spectrum of the charge-transfer-to-solvent (CTTS) band of interfacial aqueous iodide measured in a single laser shot with a newly developed broadband deep UV-SFG technique, clearly revealing a ∼8 nm redshift and a significant linewidth narrowing relative to bulk solution spectra. KI and NaI solutions yield indistinguishable results. Additionally, we observe a dramatic change in the relative intensities of the J = 3/2 and 1/2 CTTS transitions

Exciton–Phonon Spectroscopy of Quantum Dots Below the Single-Particle Homogeneous Line Width

We demonstrate that high-dimensionality coherent spectroscopy yields “super-resolved” spectra whereby peaks may be localized far below their homogeneous line width by resolving them across multiple, coherently coupled dimensions. We implement this technique using a fifth-order photon-echo spectroscopy called Gradient-Assisted Multidimensional Electronic–Raman Spectroscopy (GAMERS) that combines resonant and nonresonant excitation to disperse the optical response across three spectral dimensions: two involving excitonic transitions and one that encodes phonon energies. In analogy to super-resolution localization microscopies, which separate spatially overlapping signals in time, GAMERS isolates signals spectrally using combined electronic and nuclear resolution. Optical phonon lines in a colloidal solution of CdSe quantum dots at room temperature separated by less than 150 μeV are resolved despite the homogeneous line width of these transitions being nearly an order of magnitude broader. The frequency difference between these phonon modes is attributed to softening of the longitudinal phonon mode upon excitation to the lowest exciton state. Further, such phonon mode selectivity yields spectra with electronic line widths that approach the single particle limit. Through this enhanced spectral resolution, the GAMERS method yields insights into the nature of coupling between longitudinal optical and acoustic phonons and specific excitonic transitions that were previously hidden