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Abstract Conjugated ladder polymers (cLPs) represent an intriguing class of macromolecules, characterized by their multi‐stranded structure, with continuous fused π‐conjugated rings forming the backbone. Isotope substitution, such as deuteration and carbon‐13 labeling, offers unique approaches to address the significant challenges associated with elucidating the structure and solution phase dynamics of these polymers. For instance, selective deuteration can highlight parts of the polymer by controlling the scattering length density of specific molecular sections, thereby enhancing the contrast for neutron scattering experiments. In this context, deuteration of side‐chains in cLPs represents a promising approach to uncover the elusive polymer physics properties of their backbone. The synthesis of two distinct types of cLPs with perdeuterated side‐chains are reported here. During the synthesis,¹³C isotope labeling was also employed to verify the low levels of defects in the synthesized polymers. Demonstrating these synthetic successes lays the foundation for rigorous characterization of the defects, conformation, and dynamics of cLPs. 

The solubilization of conjugated polymers can be carefully quantified using static light scattering. Our findings reveal that the architecture of sidechains and backbones significantly influences polymer's conformation and aggregation. 

Abstract It has been proposed that biologically generated turbulence plays an important role in material transport and ocean mixing. Both experimental and numerical studies have reported evidence of the nonnegligible mixing by moderate Reynolds number swimmers, such as zooplankton, in quiescent water, especially at aggregation scales. However, the interaction between biologically generated agitation and the background flow, as a key factor in biologically generated turbulence that could reshape our previous knowledge of biologically generated turbulence, has long been ignored. Here, we show that the geometry between the biologically generated agitation and the background hydrodynamic shear can determine both the intensity and direction of biologically generated turbulent energy flux. Measuring the migration of a centimeter-scale swimmer—as represented by the brine shrimp Artemia salina—in a shear flow and verifying through an analog experiment with an artificial jet revealed that different geometries between the biologically generated agitation and the background shear can result in spectral energy transferring toward larger or smaller scales, which consequently intensifies or attenuates the large-scale hydrodynamic shear. Our results suggest that the long ignored geometry between the biologically generated agitation and the background flow field is an important factor that should be taken into consideration in future studies of biologically generated turbulence. 

Ladder-type structures can impart exceptional stability to polymeric electronic materials. This article introduces a new class of conductive polymers featuring a fully ladder-type backbone. A judicious molecular design strategy enables the synthesis of a low-defect ladder polymer, which can be efficiently oxidized and acid-doped to achieve its conductive state. The structural elucidation of this polymer and the characterization of its open-shell nature are facilitated with the assistance of studies on small molecular models. An autonomous robotic system is used to optimize the conductivity of the polymer thin film, achieving over 7 mS cm^−1. Impressively, this polymer demonstrates unparalleled stability in strong acid and under harsh UV-irradiation, significantly surpassing commercial benchmarks like PEDOT:PSS and polyaniline. Moreover, it displays superior durability across numerous redox cycles as the active material in an electrochromic device and as the pseudocapacitive material in a supercapacitor device. This work provides structural design guidance for durable conductive polymers for long-term device operation.