Molecular engineering of piezoelectricity in collagen-mimicking peptide assemblies

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作者
Santu Bera
Sarah Guerin
Hui Yuan
Joseph O’Donnell
Nicholas P. Reynolds
Oguzhan Maraba
Wei Ji
Linda J. W. Shimon
Pierre-Andre Cazade
Syed A. M. Tofail
Damien Thompson
Rusen Yang
Ehud Gazit
机构
[1] Tel Aviv University,George S. Wise Faculty of Life Sciences, Shmunis School of Biomedicine and Cancer Research
[2] University of Limerick,Department of Physics, Bernal Institute
[3] Xidian University,School of Advanced Materials and Nanotechnology
[4] Swinburne University of Technology,ARC Training Centre in Biodevices, Faculty of Science, Engineering and Technology
[5] La Trobe University,Department of Chemistry and Physics, La Trobe Institute for Molecular Science
[6] Weizmann Institute of Science,Department of Chemical Research Support
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摘要
Realization of a self-assembled, nontoxic and eco-friendly piezoelectric device with high-performance, sensitivity and reliability is highly desirable to complement conventional inorganic and polymer based materials. Hierarchically organized natural materials such as collagen have long been posited to exhibit electromechanical properties that could potentially be amplified via molecular engineering to produce technologically relevant piezoelectricity. Here, by using a simple, minimalistic, building block of collagen, we fabricate a peptide-based piezoelectric generator utilising a radically different helical arrangement of Phe-Phe-derived peptide, Pro-Phe-Phe and Hyp-Phe-Phe, based only on proteinogenic amino acids. The simple addition of a hydroxyl group increases the expected piezoelectric response by an order of magnitude (d35 = 27 pm V−1). The value is highest predicted to date in short natural peptides. We demonstrate tripeptide-based power generator that produces stable max current >50 nA and potential >1.2 V. Our results provide a promising device demonstration of computationally-guided molecular engineering of piezoelectricity in peptide nanotechnology.
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