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用于连续流动中表面增强拉曼光谱法检测硝酸盐的自组装半胱胺报告配体

Self-Assembled Cysteamine Reporter Ligands for SERS Nitrate Detection in Continuous Flow.

作者信息

Küster Timo, Bothun Geoffrey D

机构信息

Department of Chemical, Biomolecular, and Materials Engineering, University of Rhode Island, 2 East Alumni Ave, Kingston, Rhode Island 02881, United States.

出版信息

Langmuir. 2025 Jun 17;41(23):14669-14676. doi: 10.1021/acs.langmuir.4c05378. Epub 2025 Jun 3.

Abstract

Elevated nitrate concentrations in aquatic environments can contribute to the formation of harmful algal blooms, which lead to eutrophication. In this work, cysteamine self-assembled monolayers (SAMs) on two-dimensional gold nanostructured substrates were investigated for the capture and detection of nitrate anions by surface enhanced Raman scattering (SERS) under continuous fluid flow. An indirect detection strategy is demonstrated where cysteamine Raman activity and SAM reconfiguration change due to nitrate adsorption. Nitrate adsorption, as well as SAM reconfiguration based on the to conformation ratio, were dependent upon the cysteamine protonation state. The terminating amine of cysteamine was Raman active when protonated near the expected SAM p and the gold-thiol bond was increasingly Raman active above the expected p. Highly charged SAMs (pH 3) were not responsive to nitrate, suggesting that nitrate detection is reliant upon the dynamic interplay between protonation, charge state, and nitrate adsorption. Cysteamine SAMs responded to nitrate concentrations spanning 10 to 10 nanomolar (10 to 10 parts per billion), which are considerably lower than those previously reported for direct detection of nitrate using cationic SAMs. This work demonstrates the potential for indirect SERS detection of anionic pollutants using rationally selected capture + reporter ligands.

摘要

水生环境中硝酸盐浓度升高会导致有害藻华的形成,进而引发富营养化。在这项工作中,研究了二维金纳米结构基底上的半胱胺自组装单分子层(SAMs),用于在连续流体流动下通过表面增强拉曼散射(SERS)捕获和检测硝酸根阴离子。展示了一种间接检测策略,即由于硝酸根吸附导致半胱胺拉曼活性和SAM重构发生变化。硝酸根吸附以及基于 到 构象比的SAM重构取决于半胱胺的质子化状态。当在预期的SAM p附近质子化时,半胱胺的末端胺具有拉曼活性,并且在预期的p以上,金 - 硫醇键的拉曼活性越来越高。高电荷的SAMs(pH 3)对硝酸根无响应,这表明硝酸根检测依赖于质子化、电荷状态和硝酸根吸附之间的动态相互作用。半胱胺SAMs对浓度范围为10至10纳摩尔(十亿分之10至10)的硝酸根有响应,这比先前报道的使用阳离子SAMs直接检测硝酸根的浓度要低得多。这项工作展示了使用合理选择的捕获 + 报告配体间接SERS检测阴离子污染物的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f45/12422535/3d63525e69bb/la4c05378_0001.jpg

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