Ultrasensitive detection of crystal violet using a molybdenum sulfide–silver nanostructure-based sensing platform: roles of the adsorbing semiconductor in SERS signal enhancement

结晶紫 基质(水族馆) 银纳米粒子 拉曼散射 吸附 检出限 材料科学 纳米复合材料 分子 纳米技术 拉曼光谱 化学工程 化学 纳米颗粒 有机化学 色谱法 光学 物理 地质学 工程类 病理 海洋学 医学
作者
Minh Khanh Pham,Dao Thi Nguyet Nga,Mai Quan Doan,T. V. Manh,Nguyen Quang Hoa,Vũ Đình Lãm,Ha Anh Nguyen,Anh‐Tuan Le
出处
期刊:Analytical Methods [The Royal Society of Chemistry]
卷期号:15 (39): 5239-5249 被引量:7
标识
DOI:10.1039/d3ay01374j
摘要

Crystal violet (CV) is an organic dye that is stabilized by the extensive resonance delocalization of electrons over three electron-donating amine groups. This prevents the molecule from being linked to a metal surface, and therefore, reduces the sensitivity of surface-enhanced Raman scattering (SERS) sensors for this toxic dye. In this work, we improved the sensing performance of a silver-based SERS sensor for CV detection by modifying the active substrate. Molybdenum sulfide (MoS2) nanosheets were employed as a scaffold for anchoring electrochemically synthesized silver nanoparticles (e-AgNPs) through a single step of ultrasonication, leading to the formation of MoS2/Ag nanocomposites. As an excellent adsorbent, MoS2 promoted the adsorption of CV onto the surface of the substrate, allowing more CV molecules to be able to experience the SERS effect originating from the e-AgNPs. Hence, the SERS signal of CV was significantly enhanced. In addition, the effects of the MoS2 content of the nanocomposites on their SERS performance were also taken into account. Using MoS2/Ag with the most optimal MoS2 content of 10%, the SERS sensor exhibited the best enhancement of the SERS signal of CV with an impressive detection limit of 1.17 × 10-11 M in standard water and 10-9 M in tap water thanks to an enhancement factor of 2.9 × 106, which was 11.2 times higher than that using pure e-AgNPs.

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