{"title":"多肽碳点杂化物的界面组装可实现光诱导电子转移并改善光响应","authors":"Pramita Mondal, Umesh, Niladri Hazra, Joydeep Datta, Sharmistha De Dalui, Anashmita Ghosh, Somobrata Acharya, Santanu Bhattacharya","doi":"10.1021/acs.langmuir.4c03597","DOIUrl":null,"url":null,"abstract":"Assemblies at the interface represent a powerful tool for integrating organic and inorganic components into hybrid nanostructures. Carbon dots are both excellent electron donors and acceptors, offering opportunities for their potential uses in light-harvesting applications. To further improve their functions, integration of acceptor carbon dots into donor organic nanostructures is of great interest for improving photophysical properties useful for photoinduced electron transfer. Here, a one-step protocol for the interfacial assembly of a two-component hybrid consisting of carbon dots and perylene containing an <span>l</span>-phenylalanine-based dipeptide through noncovalent bonding is developed. The perylene-containing dipeptide derivative formed micrometer-long nanofibers on the water surface through J-aggregate formation. Spectroscopic studies reveal photoluminescence quenching of the donor dipeptide upon increasing the concentration of acceptor carbon dots in the hybrid, suggesting photoinduced electron transfer from the donor peptides to acceptor carbon dots. The hybrids integrated in a planar device architecture show a significantly improved photoresponse because of the favorable interactions between the donor–acceptor components. The one-step integration of donor–acceptor hybrids on the water surface offers opportunities for light harvesting and related applications.","PeriodicalId":50,"journal":{"name":"Langmuir","volume":null,"pages":null},"PeriodicalIF":3.7000,"publicationDate":"2024-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Interfacial Assembly of Peptide Carbon Dot Hybrids Enables Photoinduced Electron Transfer with Improved Photoresponse\",\"authors\":\"Pramita Mondal, Umesh, Niladri Hazra, Joydeep Datta, Sharmistha De Dalui, Anashmita Ghosh, Somobrata Acharya, Santanu Bhattacharya\",\"doi\":\"10.1021/acs.langmuir.4c03597\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Assemblies at the interface represent a powerful tool for integrating organic and inorganic components into hybrid nanostructures. Carbon dots are both excellent electron donors and acceptors, offering opportunities for their potential uses in light-harvesting applications. To further improve their functions, integration of acceptor carbon dots into donor organic nanostructures is of great interest for improving photophysical properties useful for photoinduced electron transfer. Here, a one-step protocol for the interfacial assembly of a two-component hybrid consisting of carbon dots and perylene containing an <span>l</span>-phenylalanine-based dipeptide through noncovalent bonding is developed. The perylene-containing dipeptide derivative formed micrometer-long nanofibers on the water surface through J-aggregate formation. Spectroscopic studies reveal photoluminescence quenching of the donor dipeptide upon increasing the concentration of acceptor carbon dots in the hybrid, suggesting photoinduced electron transfer from the donor peptides to acceptor carbon dots. The hybrids integrated in a planar device architecture show a significantly improved photoresponse because of the favorable interactions between the donor–acceptor components. The one-step integration of donor–acceptor hybrids on the water surface offers opportunities for light harvesting and related applications.\",\"PeriodicalId\":50,\"journal\":{\"name\":\"Langmuir\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2024-11-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Langmuir\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.langmuir.4c03597\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Langmuir","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.langmuir.4c03597","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Interfacial Assembly of Peptide Carbon Dot Hybrids Enables Photoinduced Electron Transfer with Improved Photoresponse
Assemblies at the interface represent a powerful tool for integrating organic and inorganic components into hybrid nanostructures. Carbon dots are both excellent electron donors and acceptors, offering opportunities for their potential uses in light-harvesting applications. To further improve their functions, integration of acceptor carbon dots into donor organic nanostructures is of great interest for improving photophysical properties useful for photoinduced electron transfer. Here, a one-step protocol for the interfacial assembly of a two-component hybrid consisting of carbon dots and perylene containing an l-phenylalanine-based dipeptide through noncovalent bonding is developed. The perylene-containing dipeptide derivative formed micrometer-long nanofibers on the water surface through J-aggregate formation. Spectroscopic studies reveal photoluminescence quenching of the donor dipeptide upon increasing the concentration of acceptor carbon dots in the hybrid, suggesting photoinduced electron transfer from the donor peptides to acceptor carbon dots. The hybrids integrated in a planar device architecture show a significantly improved photoresponse because of the favorable interactions between the donor–acceptor components. The one-step integration of donor–acceptor hybrids on the water surface offers opportunities for light harvesting and related applications.
期刊介绍:
Langmuir is an interdisciplinary journal publishing articles in the following subject categories:
Colloids: surfactants and self-assembly, dispersions, emulsions, foams
Interfaces: adsorption, reactions, films, forces
Biological Interfaces: biocolloids, biomolecular and biomimetic materials
Materials: nano- and mesostructured materials, polymers, gels, liquid crystals
Electrochemistry: interfacial charge transfer, charge transport, electrocatalysis, electrokinetic phenomena, bioelectrochemistry
Devices and Applications: sensors, fluidics, patterning, catalysis, photonic crystals
However, when high-impact, original work is submitted that does not fit within the above categories, decisions to accept or decline such papers will be based on one criteria: What Would Irving Do?
Langmuir ranks #2 in citations out of 136 journals in the category of Physical Chemistry with 113,157 total citations. The journal received an Impact Factor of 4.384*.
This journal is also indexed in the categories of Materials Science (ranked #1) and Multidisciplinary Chemistry (ranked #5).