Graphene nanosheets-supported Ag nanoparticles for ultrasensitive detection of TNT by surface-enhanced Raman spectroscopy

被引:129
作者
Liu, Minmin [1 ,2 ]
Chen, Wei [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Jilin, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100039, Peoples R China
基金
中国国家自然科学基金;
关键词
Silver nanoparticles; Graphene; Nitrated explosives; Chemical sensor; Surface enhanced Raman scattering; P-AMINOTHIOPHENOL; TRANSITION-METALS; CHEMICAL SENSORS; AU NANOPARTICLES; ROOM-TEMPERATURE; SCATTERING; SILVER; EXPLOSIVES; TRINITROTOLUENE; SUBSTRATE;
D O I
10.1016/j.bios.2013.01.073
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Sensitive and selective detection of 2,4,6-trinitrotoluene (TNT) has attracted considerable attention due to the wide applications of TNT as explosive material. Many efforts have been made to develop various sensors for detecting TNT in recent years. We herein report a novel sensor based on p-aminothiophenol (PATP) functionalized silver nanoparticles supported on graphene nanosheets (Ag/GNs), which was found to be a kind of effective chemosensor for the ultratrace detection of TNT by using surface enhanced Raman scattering (SERS). In the present hybrid material, PATP is paired together to form a corresponding azo compound p, p'-dimercaptoazobenzene (DMAB) and thus can be used as a model Raman probe. The pi-donor-acceptor interaction between pi-acceptor TNT and pi-donor DMAB-Ag/GNs complex can effectively induce the "hot spots" for SERS. The intense spectral resonance from the DMAB-TNT-DMAB bridges formed between the Ag/GNs nanosheets could result in enhanced Raman signals of DMAB molecules with the presence of ultratrace TNT. SERS measurements demonstrated that TNT with concentration as low as 10(-11) M can be detected by using the present SERS platform. The present study not only provides a facile method for ultrasensitive and selective detection of TNT but also could develop a graphene-based SERS platform. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:68 / 73
页数:6
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