ABSTRACT
Primary zinc-silver batteries are widely employed in military, aerospace, and marine applications. However, the development of secondary zinc-silver batteries is still a subject of on-going research. For example, these batteries suffer from rapid capacity loss during cycling due to instabilities of the zinc anode and the silver cathode. While there is a large body of work on the Zn anode, there is limited work toward stabilizing the Ag electrode and thereby achieving a long cycle life. In this work, we propose a gold-silver nanostructure where gold acts as a scaffolding material and improves the retention of structural integrity during cell cycling. We show that this nanostructure improves battery capacity as well as capacity retention after 35 cycles. Our work emphasizes the role of nanostructuring in enabling a newer secondary battery chemistry based on existing primary ones.
ABSTRACT
Self-assembling molecular systems often display amplified chirality compared to the monomeric state, which makes the molecular recognition more sensitive to chiral analytes. Herein, we report the almost absolute enantioselective recognition of a chiral perylenediimide (PDI) molecule by chiral supramolecular nanofibers of a bichromophoric naphthalenediimide (NDI) derivative. The chiral recognition was evaluated through the Förster resonance energy transfer (FRET) from the NDI-based host nanofibers to the guest PDI molecules. The excitation energy was successfully transferred to the guest molecule through efficient energy migration along the host nanofiber, thus demonstrating the light-harvesting capability of these hybrid systems. Furthermore, circularly polarized luminescence (CPL) was enantioselectively sensitized by the guest molecule as the wavelength band and sign of the CPL signal were switched in response to the chiral guest molecule.
