Detection of Low-Concentration Contaminants in Solution by Exploiting Chemical Derivatization in Surface-Enhanced Raman Spectroscopy

被引:19
作者
Hardy, Mike [1 ]
Doherty, Matthew D. [1 ]
Krstev, Igor [2 ]
Maier, Konrad [2 ]
Moller, Torgny [3 ]
Mueller, Gerhard [2 ]
Dawson, Paul [1 ]
机构
[1] Queens Univ Belfast, Sch Math & Phys, Ctr Nanostruct Media, Belfast BT7 1NN, Antrim, North Ireland
[2] Airbus Grp Innovat, D-81663 Munich, Germany
[3] Serstech AB, SE-22370 Lund, Sweden
基金
欧盟第七框架计划;
关键词
AQUEOUS SULFURIC-ACID; SERS; GOLD; DEPENDENCE; SCATTERING; SPECTRA;
D O I
10.1021/ac5014095
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A simple derivatization methodology is shown to extend the application of surface-enhanced Raman spectroscopy (SERS) to the detection of trace concentration of contaminants in liquid form. Normally in SERS the target analyte species is already present in the molecular form in which it is to be detected and is extracted from solution to occupy sites of enhanced electromagnetic field on the substrate by means of chemisorption or drop-casting and subsequent evaporation of the solvent. However, these methods are very ineffective for the detection of low concentrations of contaminant in liquid form because the target (ionic) species (a) exhibits extremely low occupancy of enhancing surface sites in the bulk liquid environment and (b) coevaporates with the solvent. In this study, the target analyte species (acid) is detected via its solid derivative (salt) offering very significant enhancement of the SERS signal because of preferential deposition of the salt at the enhancing surface but without loss of chemical discrimination. The detection of nitric acid and sulfuric acid is demonstrated down to 100 ppb via reaction with ammonium hydroxide to produce the corresponding ammonium salt. This yields an improvement of similar to 4 orders of magnitude in the low-concentration detection limit compared with liquid phase detection.
引用
收藏
页码:9006 / 9012
页数:7
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