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量子效应进入基于半导体的 SERS:多共振 MoO·HO 量子点实现对小无机分子的直接、灵敏 SERS 检测。

Quantum Effects Enter Semiconductor-Based SERS: Multiresonant MoO·HO Quantum Dots Enabling Direct, Sensitive SERS Detection of Small Inorganic Molecules.

机构信息

School of Nano-Tech and Nano-Bionics, University of Science and Technology of China, Hefei 230026, China.

Key Lab of Nanodevices and Applications, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou 215123, China.

出版信息

Anal Chem. 2022 Mar 29;94(12):5048-5054. doi: 10.1021/acs.analchem.1c05142. Epub 2022 Mar 17.

DOI:10.1021/acs.analchem.1c05142
PMID:35297614
Abstract

There is keen research interest in building highly effective semiconductor-based surface-enhanced Raman scattering (SERS) platforms, due to their selectivity for many probe molecules and suitability for complex scenario applications. However, current tuning approaches have not yet been successful in creating semiconductor-based SERS sensors for small inorganic molecules, due to the challenge of creating sufficient SERS enhancement in semiconductors. Here, we demonstrate the use of MoO·HO quantum dots (QDs), to achieve direct and sensitive fingerprinting of the inorganic species hydrazine, which is a first attempt in semiconductor-based SERS research, as well as various other probe molecules. The resulting SERS platform that uses QDs with average size of 2.2 nm could successfully detect the signal of hydrazine with a limit of detection estimated to be around 4 × 10 M, significantly lowering the detectable concentration by at least 1000-fold, in sharp contrast to the weak performance of 10 and 100 nm particles, demonstrating that quantum size effect triggered by small particle size below the Bohr radius is crucially responsible for high SERS activity. The significantly enhanced SERS activity is a result of vibronically coupled multipathway, highly efficient charge-transfer resonances induced by the divergence of energy states in quantum-sized MoO·HO. This is a proof-of-concept demonstration of the exploitation of quantum size effect, toward significantly enhanced intrinsic SERS activity in semiconductor-based SERS materials.

摘要

由于对许多探针分子具有选择性,并且适用于复杂场景应用,因此人们对构建高效的基于半导体的表面增强拉曼散射(SERS)平台非常感兴趣。然而,由于在半导体中产生足够的 SERS 增强存在挑战,当前的调谐方法尚未成功用于创建基于半导体的 SERS 传感器来检测小的无机分子。在这里,我们展示了使用 MoO·HO 量子点(QD)来实现对无机物种肼的直接和灵敏的指纹识别,这是基于半导体的 SERS 研究中的首次尝试,以及各种其他探针分子。所使用的平均尺寸为 2.2nm 的 QD 制成的 SERS 平台能够成功地检测到肼的信号,其检测限估计约为 4×10 M,与 10nm 和 100nm 颗粒的微弱性能相比,至少降低了 1000 倍的可检测浓度,这表明由小于玻尔半径的小颗粒尺寸引起的量子尺寸效应对于高 SERS 活性至关重要。显著增强的 SERS 活性是由振动耦合多途径和由量子尺寸 MoO·HO 中的能级发散引起的高效电荷转移共振导致的。这是对量子尺寸效应的概念验证,表明可以在基于半导体的 SERS 材料中显著提高内在的 SERS 活性。

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