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具有可调谐等离子体热点的压电驱动自供电传感器,用于增强表面增强拉曼光谱性能。

Piezoelectric-driven self-powered sensor with tunable plasmonic hotspots for enhanced SERS performance.

作者信息

Chen Ke, Sun Mei, Hu Hanmei, Zhang Jingyan, Zhou Haiou, Yang Mingdi

机构信息

School of Materials and Chemical Engineering, Anhui Jianzhu University, Hefei 230601, PR China; Anhui Province Key Laboratory of Advanced Building Materials, Anhui Jianzhu University, Hefei 230601, PR China.

School of Materials and Chemical Engineering, Anhui Jianzhu University, Hefei 230601, PR China; Anhui Province Key Laboratory of Advanced Building Materials, Anhui Jianzhu University, Hefei 230601, PR China.

出版信息

J Colloid Interface Sci. 2026 Jan;701:138642. doi: 10.1016/j.jcis.2025.138642. Epub 2025 Aug 5.

Abstract

Electrically Modulated Surface-enhanced Raman spectroscopy (E-SERS) technology can effectively increase Raman signal intensity. Compared with conventional E-SERS, self-powered E-SERS sensors provide an electric field through energy conversion, which reduces the dependence on external power sources and thus facilitates the development of portable real sample detection. Herein, high-performance piezoelectric lead zirconate titanate (PZT) with dopamine-functionalized reduced graphene oxide (rGO@PDA) was embedded into a polyvinylidene fluoride-trifluoroethylene (PVDF-TrFE) matrix, which was innovatively used for E-SERS technology. In particular, by applying external pressure to the PVDF-TrFE/PZT-rGO@PDA/Ag self-powered sensors, the surface localized electromagnetic field can be efficiently enhanced, which combines with the localized surface plasmon resonance (LSPR) effect of the Ag nanoparticles (NPs) to achieve highly tunable signal enhancement. As a proof-of-concept, voltage and current signals were generated by pressing the substrate, and Raman signal enhancement was also realized for molecules such as Rhodamine 6G (R6G) and Methyl Orange (MO). The self-powered sensor exhibits ultra-high sensitivity and excellent reproducibility for a wide range of probe molecules, especially thiram, with a low limit of detection (LOD) of 10 M, determining a low variation of 8.5 %. Additionally, the substrate successfully detected 10 M malachite green (MG) fungicide residue on fish skin and 10 M sulfamonomethoxine (SMM) antibiotic residue in chicken breast by pressing, proving its great potential for application in food contaminant monitoring.

摘要

电调制表面增强拉曼光谱(E-SERS)技术可以有效提高拉曼信号强度。与传统的E-SERS相比,自供电E-SERS传感器通过能量转换提供电场,这减少了对外部电源的依赖,从而促进了便携式实际样品检测的发展。在此,将具有多巴胺功能化还原氧化石墨烯(rGO@PDA)的高性能压电锆钛酸铅(PZT)嵌入聚偏二氟乙烯-三氟乙烯(PVDF-TrFE)基体中,创新性地用于E-SERS技术。特别是,通过对PVDF-TrFE/PZT-rGO@PDA/Ag自供电传感器施加外部压力,可以有效增强表面局域电磁场,该电磁场与银纳米颗粒(NPs)的局域表面等离子体共振(LSPR)效应相结合,实现高度可调的信号增强。作为概念验证,通过按压基底产生了电压和电流信号,并且对罗丹明6G(R6G)和甲基橙(MO)等分子也实现了拉曼信号增强。该自供电传感器对多种探针分子表现出超高灵敏度和优异的重现性,尤其是福美双,其检测限低至10⁻⁹ M,测定的低变异系数为8.5%。此外,该基底通过按压成功检测到鱼皮上10⁻⁸ M的孔雀石绿(MG)杀菌剂残留和鸡胸肉中10⁻⁸ M的磺胺间甲氧嘧啶(SMM)抗生素残留,证明了其在食品污染物监测中的巨大应用潜力。

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