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用于超灵敏表面增强拉曼散射检测的纯金属1T相钪掺杂的螺旋状二硫化钼形态

Pure metallic 1T phase Sc-doped MoS Fusilli morphology for ultra-sensitive SERS detection.

作者信息

Xu Hongquan, Li Baizhi, Wang Zhong, Wang Jingshu, Wei Maobin, Zhang Yong, Liu Huilian, Gao Ming

机构信息

Key Laboratory of Functional Materials Physics and Chemistry of the Ministry of Education, Jilin Normal University, Changchun 130103, PR China; National Demonstration Centre for Experimental Physics Education, Jilin Normal University, Siping 136000, PR China; Key Laboratory of Preparation and Application of Environmental Friendly Materials, Jilin Normal University, Ministry of Education, Changchun 130103, PR China.

School of pharmaceutical sciences, Jilin University, Changchun 130012, PR China.

出版信息

J Hazard Mater. 2025 Jul 5;491:138043. doi: 10.1016/j.jhazmat.2025.138043. Epub 2025 Mar 24.

Abstract

Surface-enhanced Raman spectroscopy (SERS) offers great potential for sensitive molecular detection in fields ranging from environmental science to healthcare diagnostics, but its efficacy is limited by the low enhancement factors and sensitivity of semiconductor substrates. In this study, we synthesized scandium-doped 1T-phase molybdenum disulfide (Sc-doped 1T-MoS) substrates and measured their performance against standard 2H-phase molybdenum disulfide (2H-MoS) and undoped 1T-MoS. Here, the substrate-analyte molecule interaction was amplified by doping metallic MoS with Sc, which resulted in a notable rise in SERS enhancement for non-metal-sulfide semiconductor materials. The modified 0.4Sc-MoS substrate not only maintains the metal-like conductivity and stability inherent to the 1 T phase but also significantly enhances SERS sensitivity. The doped substrates demonstrated significantly improved SERS enhancement factors and reduced detection limits to 5.3 × 10 M for aspartame (APM) and 5.0 × 10 M for thiabendazole (TBZ). To validate and understand the mechanism behind these phenomena, density functional theory (DFT) calculations have been used to study the interaction of methylene blue (MB) molecules with xSc-MoS, 2H-MoS and 1T-MoS. Our findings not only improve the understanding of physicochemical interactions within Raman-enhancing substrates but also pave the way for developing high-performance semiconductor-based substrates for Raman spectroscopy. This advancement is a critical step toward the practical implementation of these materials in a wide range of sensing applications.

摘要

表面增强拉曼光谱(SERS)在从环境科学到医疗诊断等诸多领域的灵敏分子检测方面具有巨大潜力,但其功效受到半导体基底的低增强因子和灵敏度的限制。在本研究中,我们合成了钪掺杂的1T相二硫化钼(Sc掺杂的1T-MoS)基底,并测量了它们相对于标准2H相二硫化钼(2H-MoS)和未掺杂的1T-MoS的性能。在此,通过用Sc掺杂金属性的MoS放大了基底-分析物分子间的相互作用,这导致了非金属硫化物半导体材料的SERS增强显著提高。改性的0.4Sc-MoS基底不仅保持了1T相固有的类金属导电性和稳定性,还显著提高了SERS灵敏度。掺杂后的基底表现出显著提高的SERS增强因子,阿斯巴甜(APM)的检测限降至5.3×10⁻⁸ M,噻苯达唑(TBZ)的检测限降至5.0×10⁻⁸ M。为了验证并理解这些现象背后的机制,已使用密度泛函理论(DFT)计算来研究亚甲基蓝(MB)分子与xSc-MoS、2H-MoS和1T-MoS之间的相互作用。我们的研究结果不仅增进了对拉曼增强基底内物理化学相互作用的理解,还为开发用于拉曼光谱的高性能半导体基底铺平了道路。这一进展是朝着在广泛的传感应用中实际应用这些材料迈出的关键一步。

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