A Supramolecular Wire Able to Self‐Assemble on Gold Surface: Controlling the Film Length to Optimize the Device Lifetime and Electron Transfer Efficiency
Abstract A chemical “lego nanoset” has been used to realize different structures on gold surfaces. Three building blocks have been designed, in order to chemically link the surface and self‐assemble in an ordered manner. Self‐assembled films are arranged on a gold surface into 3D suprastructures via...
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Format: | Article |
Language: | English |
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Wiley-VCH
2025-02-01
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Series: | Advanced Materials Interfaces |
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Online Access: | https://doi.org/10.1002/admi.202400418 |
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author | Sascha Kubitzky Raffaella Lettieri Elena Passaretti Mariano Venanzi Marta De Zotti Claudia Mazzuca Ernesto Placidi Emanuela Gatto |
author_facet | Sascha Kubitzky Raffaella Lettieri Elena Passaretti Mariano Venanzi Marta De Zotti Claudia Mazzuca Ernesto Placidi Emanuela Gatto |
author_sort | Sascha Kubitzky |
collection | DOAJ |
description | Abstract A chemical “lego nanoset” has been used to realize different structures on gold surfaces. Three building blocks have been designed, in order to chemically link the surface and self‐assemble in an ordered manner. Self‐assembled films are arranged on a gold surface into 3D suprastructures via consecutive deposition of different mono‐layers, taken together by thymine‐adenine hydrogen bonds. Three films, composed of one, two, and three helical peptide layers, both containing a zinc‐tetraphenylporphyrin dye as an external sheet, are built and characterized by spectro‐electrochemical and spectroscopic techniques. All films are found to generate current under illumination, and their photoresponse and stability are studied as a function of the number of peptide layers. The efficiency of the photoconversion process has been correlated to the molecular organization of the porphyrin dyes in the film and to the templating role of the bridge between the porphyrin and the gold surface. |
format | Article |
id | doaj-art-3c1890f8f971416eac9496291d8b428a |
institution | Kabale University |
issn | 2196-7350 |
language | English |
publishDate | 2025-02-01 |
publisher | Wiley-VCH |
record_format | Article |
series | Advanced Materials Interfaces |
spelling | doaj-art-3c1890f8f971416eac9496291d8b428a2025-02-03T13:24:05ZengWiley-VCHAdvanced Materials Interfaces2196-73502025-02-01123n/an/a10.1002/admi.202400418A Supramolecular Wire Able to Self‐Assemble on Gold Surface: Controlling the Film Length to Optimize the Device Lifetime and Electron Transfer EfficiencySascha Kubitzky0Raffaella Lettieri1Elena Passaretti2Mariano Venanzi3Marta De Zotti4Claudia Mazzuca5Ernesto Placidi6Emanuela Gatto7Department of Chemical Science and Technologies University of Rome Tor Vergata Rome 00133 ItalyDepartment of Chemical Science and Technologies University of Rome Tor Vergata Rome 00133 ItalyInstitute for Building Materials Eidgenössische Technische Hochschule Zürich 8093 SwitzerlandDepartment of Chemical Science and Technologies University of Rome Tor Vergata Rome 00133 ItalyDepartment of Chemical Sciences University of Padova Padova 35131 ItalyDepartment of Chemical Science and Technologies University of Rome Tor Vergata Rome 00133 ItalyDepartment of Physics Sapienza University of Rome Rome 00185 ItalyDepartment of Chemical Science and Technologies University of Rome Tor Vergata Rome 00133 ItalyAbstract A chemical “lego nanoset” has been used to realize different structures on gold surfaces. Three building blocks have been designed, in order to chemically link the surface and self‐assemble in an ordered manner. Self‐assembled films are arranged on a gold surface into 3D suprastructures via consecutive deposition of different mono‐layers, taken together by thymine‐adenine hydrogen bonds. Three films, composed of one, two, and three helical peptide layers, both containing a zinc‐tetraphenylporphyrin dye as an external sheet, are built and characterized by spectro‐electrochemical and spectroscopic techniques. All films are found to generate current under illumination, and their photoresponse and stability are studied as a function of the number of peptide layers. The efficiency of the photoconversion process has been correlated to the molecular organization of the porphyrin dyes in the film and to the templating role of the bridge between the porphyrin and the gold surface.https://doi.org/10.1002/admi.202400418peptidesphotocurrent generationself assembled monolayerssupramolecular chemistrythymine‐adenine interactions |
spellingShingle | Sascha Kubitzky Raffaella Lettieri Elena Passaretti Mariano Venanzi Marta De Zotti Claudia Mazzuca Ernesto Placidi Emanuela Gatto A Supramolecular Wire Able to Self‐Assemble on Gold Surface: Controlling the Film Length to Optimize the Device Lifetime and Electron Transfer Efficiency Advanced Materials Interfaces peptides photocurrent generation self assembled monolayers supramolecular chemistry thymine‐adenine interactions |
title | A Supramolecular Wire Able to Self‐Assemble on Gold Surface: Controlling the Film Length to Optimize the Device Lifetime and Electron Transfer Efficiency |
title_full | A Supramolecular Wire Able to Self‐Assemble on Gold Surface: Controlling the Film Length to Optimize the Device Lifetime and Electron Transfer Efficiency |
title_fullStr | A Supramolecular Wire Able to Self‐Assemble on Gold Surface: Controlling the Film Length to Optimize the Device Lifetime and Electron Transfer Efficiency |
title_full_unstemmed | A Supramolecular Wire Able to Self‐Assemble on Gold Surface: Controlling the Film Length to Optimize the Device Lifetime and Electron Transfer Efficiency |
title_short | A Supramolecular Wire Able to Self‐Assemble on Gold Surface: Controlling the Film Length to Optimize the Device Lifetime and Electron Transfer Efficiency |
title_sort | supramolecular wire able to self assemble on gold surface controlling the film length to optimize the device lifetime and electron transfer efficiency |
topic | peptides photocurrent generation self assembled monolayers supramolecular chemistry thymine‐adenine interactions |
url | https://doi.org/10.1002/admi.202400418 |
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