Template-annealing-assisted fabrication of Au/TiO2/Ni nanopetal arrays as ultrasensitive and reproducible SERS substrates with super long-term stability

被引:0
|
作者
Lin, Qi [1 ]
Zheng, Chunfang [1 ]
Qian, Weicong [1 ]
Yuan, Ning [1 ]
Fu, Qun [1 ]
Lei, Yong [2 ,3 ]
机构
[1] Shanghai Univ, Inst Nanochem & Nanobiol, Shanghai 200444, Peoples R China
[2] Tech Univ Ilmenau, Inst Phys, Fachgebiet Angew Nanophys, D-98693 Ilmenau, Germany
[3] Tech Univ Ilmenau, IMN MacroNano, D-98693 Ilmenau, Germany
基金
中国国家自然科学基金;
关键词
ENHANCED RAMAN-SCATTERING; TIO2; NANOPARTICLES; GROWTH; NOBLE; SIZE;
D O I
10.1039/d4nj03674c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Although (Au or Ag)/TiO2 hybrid structures have been widely used for surface-enhanced Raman scattering (SERS) detection, nanostructured TiO2 still faces significant drawbacks of low response to visible light and the resulting poor Raman response. Template-annealing-assisted fabrication of three-dimensional (3D) petal-like Au/TiO2/Ni nanoarrays provides a way to realize ultrasensitive and reproducible SERS responses with super long-term stability for TiO2 in the visible-light region. Thermal annealing treatment of TiO2/Ni nanopillar arrays in an air atmosphere at high temperatures (particularly at 650 degrees C) brought about partial oxidation of Ni to NiO, transformation of amorphous TiO2 (a-TiO2) to non-stoichiometric TiO2-x, and a 3D petal-like morphology with a large specific surface area, which effectively increased visible-light absorption. Dense Au nanoparticles, ordered Ni nanoarrays, and the closely packed nanopetal-like morphology with numerous Raman active sites, as well as each component, including Au, Ni, TiO2-x, NiO, and a-TiO2, and their synergies, not only enabled the remarkable enhancement of surface plasmon resonance, but also strongly facilitated the photoinduced charge-transfer effect between the substrate and adsorbed molecules. 3D Au/TiO2/Ni nanopetal arrays exhibited an ultrasensitive and reproducible SERS response to rhodamine 6G (as low as 10-12 M) and crystal violet molecules (as low as 10-13 M) with super long-term stability (372 days) at 632.8-nm excitation. A lower concentration detection limit could be realized with precise regulation of the Au deposition thickness. This work presents a cost-effective and efficient alternative for optimizing the SERS performance of wide-bandgap oxides.
引用
收藏
页码:615 / 623
页数:9
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