The apparent piezoelectricity of biological materials
is not yet fully understood at the molecular level. In particular,
dynamic noncovalent interactions, such as host−guest binding, are
not included in the classical piezoelectric model, which limits the
rational design of eco-friendly piezoelectric supramolecular
materials. Here, inspired by the conformation-dependent mecha noresponse of the Piezo channel proteins, we show that guest−
host interactions can amplify the electromechanical response of a
conformationally mobile peptide metal−organic framework
(MOF) based on the endogenous carnosine dipeptide, demon strating a new type of adaptive piezoelectric supramolecular
material. Density functional theory (DFT) predictions validated by
piezoresponse force microscopy (PFM) measurements show that
directional alignment of the guest molecules in the host carnosine−zinc peptide MOF channel determines the macroscopic
electromechanical properties. We produce stable, robust 1.4 V open-circuit voltage under applied force of 25 N with a frequency of
0.1 Hz. Our findings demonstrate that the regulation of host−guest interactions could serve as an efficient method for engineering
sustainable peptide-based power generators.
History
Publication
Journal of the American Chemical Society;144 (8), pp. 3468-3476
Publisher
American Chemical Society
Note
peer-reviewed
Other Funding information
Irish Centre for High-End Computing (ICHEC), National Natural Science Foundation of China, Natural Science Foundation of Shaanxi Province, SFI