A Novel Ultra‐Sensitive Semiconductor SERS Substrate Boosted by the Coupled Resonance Effect

Lili Yang(Chinese Academy of Sciences), Yusi Peng(Chinese Academy of Sciences), Yong Yang(Chinese Academy of Sciences), Jianjun Liu(Chinese Academy of Sciences), Haoliang Huang(University of Science and Technology of China), Bohan Yu(Chinese Academy of Sciences), Jimin Zhao(Chinese Academy of Sciences), Yalin Lü(University of Science and Technology of China), Zhengren Huang(Chinese Academy of Sciences), Zhi‐Yuan Li(South China University of Technology), John R. Lombardi(City College of New York)
Advanced Science
April 16, 2019
Cited by 295Open Access
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Abstract

Abstract Recent achievements in semiconductor surface‐enhanced Raman scattering (SERS) substrates have greatly expanded the application of SERS technique in various fields. However, exploring novel ultra‐sensitive semiconductor SERS materials is a high‐priority task. Here, a new semiconductor SERS‐active substrate, Ta 2 O 5 , is developed and an important strategy, the “coupled resonance” effect, is presented, to optimize the SERS performance of semiconductor materials by energy band engineering. The optimized Mo‐doped Ta 2 O 5 substrate exhibits a remarkable SERS sensitivity with an enhancement factor of 2.2 × 10 7 and a very low detection limit of 9 × 10 −9 m for methyl violet (MV) molecules, demonstrating one of the highest sensitivities among those reported for semiconductor SERS substrates. This remarkable enhancement can be attributed to the synergistic resonance enhancement of three components under 532 nm laser excitation: i) MV molecular resonance, ii) photoinduced charge transfer resonance between MV molecules and Ta 2 O 5 nanorods, and iii) electromagnetic enhancement around the “gap” and “tip” of anisotropic Ta 2 O 5 nanorods. Furthermore, it is discovered that the concomitant photoinduced degradation of the probed molecules in the time‐scale of SERS detection is a non‐negligible factor that limits the SERS performance of semiconductors with photocatalytic activity.


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