Journal
ACS SENSORS
Volume 2, Issue 12, Pages 1869-1875Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acssensors.7b00783
Keywords
lithography-free; dual-functional; electrochemical; SERS; paracetamol
Funding
- European Research Council under European Union's Seventh Framework Program [320535-HERMES]
- IDUN Center of Excellence - Danish National Research Foundation [DNRF122]
- Villum Foundation [9301]
- Villum Fonden [00009301] Funding Source: researchfish
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In this work, we present a dual-functional sensor that can perform surface-enhanced Raman spectroscopy (SERS) based identification and electrochemical (EC) quantification of analytes in liquid samples. A lithography-free reactive ion etching process was utilized to obtain nanostructures of high aspect ratios distributed homogeneously on a 4 in. fused silica wafer. The sensor was made up of three-electrode array, obtained by subsequent e-beam evaporation of Au on nanostructures in selected areas through a shadow mask. The SERS performance was evaluated through surface-averaged enhancement factor (EF), which was similar to 6.2 x 10(5), and spatial uniformity of EF, which was similar to 13% in terms of relative standard deviation. Excellent electrochemical performance and reproducibility were revealed by recording cyclic voltammograms. On nanostructured electrodes, paracetamol (PAR) showed an improved quasi-reversible behavior with decrease in peak potential separation (Delta E-p similar to 90 mV) and higher peak currents (I-pa/I-pc similar to 1), compared to planar electrodes (Delta E-p similar to 560 mV). The oxidation potential of PAR was also lowered by similar to 80 mV on nanostructured electrodes. To illustrate dual-functional sensing, quantitative evaluation of PAR ranging from 30 mu M to 3 mM was realized through EC detection, and the presence of PAR was verified by its SERS fingerprint.
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