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SERS Chemical Enhancement of 2,4,5-Trichlorophenoxyacetic Acid Adsorbed on Silver Substrate

Duy Quang DaoFaculty of Natural Sciences, Duy Tan University, Da Nang 550000, Viet NamThị Chinh NgoFaculty of Natural Sciences, Duy Tan University, Da Nang 550000, Viet NamThị Thùy Hương LêGraduate University of Science and Technology, Vietnam Academy of Science and Technology (VAST), Ha Noi 100000, Viet NamQuang Thang TrịnhInstitute of High Performance Computing (IHPC), Agency for Science Technology and Research (A*STAR), #16-16 Connexis, 1 Fusionopolis Way, Singapore 138632, SingaporeThi Lê Anh NguyenFaculty of Natural Sciences, Duy Tan University, Da Nang 550000, Viet NamBui The HuyDepartment of Chemistry, Changwon National University, Changwon 51140, Republic of KoreaNguyen Ngoc TriLaboratory of Computational Chemistry and Modelling (LCCM), and Department of Chemistry, Quy Nhon University, Quy Nhon 591300, Viet NamNguyễn Tiến TrungLaboratory of Computational Chemistry and Modelling (LCCM), and Department of Chemistry, Quy Nhon University, Quy Nhon 591300, Viet NamMinh Tho NguyenDepartment of Chemistry, KU Leuven, B-3001 Leuven, Belgium
2021en
ABI

Аннотация

Surface-enhanced Raman spectroscopy (SERS) was employed to gain an understanding of the chemical enhancement mechanism of 2,4,5-trichlorophenoxyacetic acid (2,4,5-T), an Agent Orange, adsorbed on a silver substrate surface. Experimental measurements were performed using a micro-Raman spectrophotometer with an excitation wavelength of 532 nm and successfully detected 2,4,5-T at a relatively low concentration of 0.4 nM. Density functional theory (DFT) calculations on the interactions of the 2,4,5-T molecule with some small silver clusters, Agn with n = 4, 8, and 20, as well as with extended Ag surfaces, demonstrate that the most stable adsorption configuration is formed via coordination of Cl9 sites and carbonyl C═O group on the 2,4,5-T ligand to the Ag atoms on surfaces. Analyses of charge transfer mechanism and frontier orbitals distributions show an electron transfer from 2,4,5-T to the cluster in the ground state, and an inversed trend occurs for the excited singlet state process, consequently leading to a chemical enhancement of SERS signals. The obtained results are of importance for subsequent work in guiding the design of mobile sensors specifically used for services of rapid screening and detection of these toxic compounds present in the environment, as well as agricultural and food products. Extensive computations pointed out that small silver clusters, in particular of Ag20 size, can be used as appropriate models for a metal nanoparticle surface.

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