4.8 Article

Diphenylalanine-Derivative Peptide Assemblies with Increased Aromaticity Exhibit Metal-like Rigidity and High Piezoelectricity

Journal

ACS NANO
Volume 14, Issue 6, Pages 7025-7037

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.0c01654

Keywords

aromatic-rich peptides; crystal engineering; energy harvesting; piezoelectricity; metallic Young's modulus; photoluminescence

Funding

  1. European Research Council under the European Union's Horizon 2020 research and innovation program (BISON, Advanced ERC Grant) [694426]
  2. Planning and Budget Committee, Israel
  3. National Natural Science Foundation of China [11804148]
  4. Natural Science Foundation of Jiangsu province [BK20180320]
  5. Fundamental Research Funds for the Central Universities [XJ2020013501]
  6. Echnological Innovation Foundation of Nanjing University [020414913413]
  7. Irish Research Council Embark Postgraduate Scholarship [GOIPG/2018/1161]
  8. SFI Opportunistic Fund [12/RI/2345/SOF]
  9. Science Foundation Ireland (SFI) [15/CDA/3491, 12/RC/2275]
  10. HHMI
  11. NIH [AG054022]
  12. Science Foundation Ireland (SFI) [12/RI/2345/SOF] Funding Source: Science Foundation Ireland (SFI)

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Diphenylalanine (FF) represents the simplest peptide building block that self-assembles into ordered nanostructures with interesting physical properties. Among self-assembled peptide structures, FF nanotubes display notable stiffness and piezoelectric parameters (Young's modulus = 19-27 GPa, strain coefficient d(33) = 18 pC/N). Yet, inorganic alternatives remain the major materials of choice for many applications due to higher stiffness and piezoelectricity. Here, aiming to broaden the applications of the FF motif in materials chemistry, we designed three phenyl-rich dipeptides based on the beta,beta-diphenyl-Ala-OH (Dip) unit: Dip-Dip, cyclo-Dip-Dip, and tert-butyloxycarbonyl (Boc)Dip-Dip. The doubled number of aromatic groups per unit, compared to FF, produced a dense aromatic zipper network with a dramatically improved Young's modulus of , similar to 70 GPa, which is comparable to aluminum. The piezoelectric strain coefficient d(33) of similar to 73 pC/N of such assembly exceeds that of poled polyvinylidene-fluoride (PVDF) polymers and compares well to that of lead zirconium titanate (PZT) thin films and ribbons. The rationally designed pi-pi assemblies show a voltage coefficient of 2-3 Vm/N, an order of magnitude higher than PVDF, improved thermal stability up to 360 degrees C (similar to 60 degrees C higher than FF), and useful photoluminescence with wide-range excitation-dependent emission in the visible region. Our data demonstrate that aromatic groups improve the rigidity and piezoelectricity of organic self-assembled materials for numerous applications.

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