In-situ SERS monitoring of reaction catalyzed by multifunctional Fe3O4@TiO2@Ag-Au microspheres

被引:73
作者
Shen, Jianhua [1 ]
Zhou, Ying [1 ]
Huang, Jianfei [1 ]
Zhu, Yihua [1 ]
Zhu, Jingrun [1 ]
Yang, Xiaoling [1 ]
Chen, Wei [1 ]
Yao, Yifan [1 ]
Qian, Shaohong [2 ]
Jiang, Hao [1 ]
Li, Chunzhong [1 ]
机构
[1] East China Univ Sci & Technol, Sch Mat Sci & Engn, Key Lab Ultrafine Mat, Minist Educ, Shanghai 200237, Peoples R China
[2] Fudan Univ, Dept Ophthalmol, EENT Hosp, 83 Fenyang Rd, Shanghai 200031, Peoples R China
基金
中国国家自然科学基金;
关键词
Multifunctional microspheres; Ag-Au bimetallic nanostructures; Noble metal catalyst; Surface-enhanced Raman scattering; Finite-difference time-domain; ENHANCED RAMAN-SCATTERING; NITROPHENOL REDUCTION; HETEROGENEOUS PHOTOCATALYSIS; METAL NANOPARTICLES; METHANOL OXIDATION; AU NANOPARTICLES; GOLD; 4-NITROPHENOL; NANOCRYSTALS; SPECTROSCOPY;
D O I
10.1016/j.apcatb.2016.12.010
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Multifunctional Fe3O4@TiO2@Ag-Au microspheres (MS) were synthesized by grafting Ag nanoparticles onto 3-Aminopropyltrimethoxysilane (APTMS) modified Fe3O4@TiO2 MS, followed by galvanic replacement approach to fabricate Ag-Au bimetallic nanostructures with variable bimetallic molar ratios. The composite with Au-to-Ag ratio of 1:1 exhibits optimal catalytic activity for reduction of 4-nitrophenol (4-NP). Furthermore, finite-difference time-domain (FDTD) simulation study shows that incorporating Au-Ag bimetallic nanostructures onto Fe3O4@TiO2 MS significantly increases the effect of the 'hot spot', offering stronger electromagnetic field enhancements. Indeed, the Fe3O4@TiO2@Ag-Au was demonstrated to be an excellent substrate material for in-situ surface-enhanced Raman scattering (SERS) monitoring of the reaction process. Combined with its good magnetic and photocatalytic performance allowing facile recovery, Fe3O4@TiO2@Ag-Au MS shows great potential for multifunctional platform for simultaneous catalysis and in-situ reaction monitoring. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:11 / 18
页数:8
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