In recent years, surface-enhanced Raman scattering (SERS) of a molecule/metal-semiconductor hybrid system has attracted considerable interest and regarded as the synergetic contribution of the electromagnetic and chemical enhancements from the incorporation of noble metal into semiconductor nanomaterials. However, the underlying mechanism is still to be revealed in detail. Herein, we report an irreversible accumulated SERS behavior induced by near-infrared (NIR) light irradiating on a 4-mercaptobenzoic acid linked with silver and silver-doped titanium dioxide (4MBA/Ag/Ag-doped TiO2) hybrid system. With increasing irradiation time, the SERS intensity of 4MBA shows an irreversible exponential increase, and the Raman signal of the Ag/Ag-doped TiO2 substrate displays an exponential decrease. A microscopic understanding of the time-dependent SERS behavior is derived based on the microanalysis of the Ag/Ag-doped TiO2 nanostructure and the molecular dynamics, which is attributed to three factors: (1) higher crystallinity of Ag/Ag-doped TiO2 substrate; (2) photo-induced charge transfer; (3) charge- induced molecular reorientation.

Irreversible accumulated SERS behavior of the molecule-linked silver and silver-doped titanium dioxide hybrid system

Lucia Petti;Pasquale Mormile
2020

Abstract

In recent years, surface-enhanced Raman scattering (SERS) of a molecule/metal-semiconductor hybrid system has attracted considerable interest and regarded as the synergetic contribution of the electromagnetic and chemical enhancements from the incorporation of noble metal into semiconductor nanomaterials. However, the underlying mechanism is still to be revealed in detail. Herein, we report an irreversible accumulated SERS behavior induced by near-infrared (NIR) light irradiating on a 4-mercaptobenzoic acid linked with silver and silver-doped titanium dioxide (4MBA/Ag/Ag-doped TiO2) hybrid system. With increasing irradiation time, the SERS intensity of 4MBA shows an irreversible exponential increase, and the Raman signal of the Ag/Ag-doped TiO2 substrate displays an exponential decrease. A microscopic understanding of the time-dependent SERS behavior is derived based on the microanalysis of the Ag/Ag-doped TiO2 nanostructure and the molecular dynamics, which is attributed to three factors: (1) higher crystallinity of Ag/Ag-doped TiO2 substrate; (2) photo-induced charge transfer; (3) charge- induced molecular reorientation.
2020
Istituto di Scienze Applicate e Sistemi Intelligenti "Eduardo Caianiello" - ISASI
Inglese
11-1785
1
10
10
https://www.nature.com/articles/s41467-020-15484-6
Esperti anonimi
SERS
PLASMONICS
Lavoro a carattere fortemente interdisciplinare e Internazionale frutto di una Collaborazione tra 1 il Department of Microelectronic Science and Engineering, School of Physical Science and Technology, Ningbo University,China. 2 Center for Terahertz Waves and College of Precision Instrument and Optoelectronics Engineering, Tianjin University, China. 3 Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, China. 4 Hefei National Laboratory for Physical Sciences at the Microscale, and Synergetic Innovation Center of Quantum Information and Quantum Physics, University of Science and Technology of China, China. 5 Key Laboratory of Transparent and Opto-functional Inorganic Materials, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 201800, China. 6 Department of Electrical Engineering and State Key Laboratory of Terahertz and Millimeter Waves, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon Tong, Hong Kong, China. 7Department of Electrical and Electronic Engineering, Southern University of Science and Technology, Shenzhen 518055, China. 8 Institute of Applied Sciences and Intelligent Systems-ISASI, CNR, Via Campi Flegrei, 34, 80078 Pozzuoli, Italy. 9 School of Information Science and Engineering, Xinjiang University, Urumqi 830046 Xinjiang, China
Internazionale
Elettronico
16
info:eu-repo/semantics/article
262
Zhou, Lu; Zhou, Jun; Lai, Wei; Yang, Xudong; Meng, Jie; Su, Liangbi; Gu, Chenjie; Jiang, Tao; Yue Bun Pun, Edwin; Shao, Liyang; Petti, Lucia; Wei Sun,...espandi
01 Contributo su Rivista::01.01 Articolo in rivista
open
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/377386
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