CNR ExploRA

Articolo in rivista, 2021, ENG, 10.1039/d0ra09964c

Pristine graphene covalent functionalization with aromatic aziridines and their application in the sensing of volatile amines - an ab initio investigation

Baachaoui S.; Aldulaijan S.; Raouafi F.; Besbes R.; Sementa L.; Fortunelli A.; Raouafi N.; Dhouib A.

Laboratoire de Chimie Analytique et Electrochimie (LR99ES15), Departement de Chimie, Faculté des Sciences de Tunis, Université de Tunis El Manar, Tunis El Manar, 2092, Tunisia; Department of Chemistry, College of Science, Imam Abdulrahman Bin Faisal University, Dammam, 31113, Saudi Arabia; Institut Préparatoire aux Etudes Scientifiques et Techniques (IPEST), Université de Carthage, La Marsa, Institut Préparatoire aux Etudes Scientifiques et Techniques (IPEST), Université de Carthage, La Marsa, Tunisia; Consiglio Nazionale delle Ricerche, CNR-ICCOM & IPCF, Pisa, 56124, Consiglio Nazionale delle Ricerche, Italy

Food quality is of paramount importance for public health safety. For instance, fish freshness can be assessed by sensing the volatile short chain alkylamines produced by spoiled fish. Functionalized graphene is a good candidate for the design of gas sensors for such compounds and therefore of interest as the basic material in food quality sensor devices. To shed theoretical insight in this direction, in the present work we investigateviafirst-principles density functional theory (DFT) simulations: (i) graphene functionalizationviaaziridine appendages and (ii) the adsorption of short chain alkylamines (methylamine MA, dimethylamine DMA, and trimethylamine TMA) on the chemically functionalized graphene sheets. Optimal geometries, adsorption energies, and projected density of states (PDOS) are computed using a DFT method. We show that nitrene reactive intermediates, formed by thermal or photo splitting of arylazides -p-carboxyphenyl azide (1a),p-carboxyperfluorophenyl azide (1b), andp-nitrophenyl azide (1c) - react with graphene to yield functionalized derivatives, with reaction energies >-1.0 eV and barriers of the order of 2.0 eV, and open a ~0.3 to 0.5 eV band gap which is in principle apt for applications in sensing and electronic devices. The interaction between the amines and functionalized graphene, as demonstrated from the calculations of charge density differences showing regions of charge gain and others of charge depletion between the involved groups, occurs through hydrogen bonding with interaction energies ranging from -0.04 eV to -0.76 eV, and induce charge differences in the system, which in the case ofp-carboxyperfluorophenyl azide (1b) are sizeable enough to be experimentally observable in sensing.

RSC advances 11 (12), pp. 7070–7077