Surface Enhanced on Infrared Absorption (SEIRAS) and Raman Spectroscopy (SERS) are nondestructive analytic techniques used to detect low concentrations and recognize the fingerprints of molecules. The recognition of the absorption from samples by conventional infrared spectroscopy (IR) via Attenuated Total Reflection (ATR) is difficult for molecules with a low signal strength. However, developed structures with SERS and SEIRAS effect present problems such as high cost, low stability, and low compatibility. Research into new media to obtain greater amplification is largely based on the creation of nanoscale structures with symmetrical arrangements and reproducible distances, resulting in aggregates of nanoparticles that help generate hot spots which are active for amplification. The sol-gel and electrospinning method for the obtention of ceramics provides an alternative means by which to produce said substrates. Fibers of nanometric scale provide an increase of surface area which allows more contact to occur with analytes. Consequently, in this study, a silica-titania-silver nanostructured support that amplifies signal intensity for Raman and infrared spectroscopy was developed. The silica-titania support was developed by sol-gel and electrospinning techniques, and the as spun fibers were treated at 800 °C. Then, the ceramic fibrous membrane was placed on conductive indium tin oxide plastic to be doped with silver using an electroplating technique, varying the silver nitrate concentration (5, 10 and 20 mM), as well as electrodeposition times (1, 2, 5 and 10 min), with a constant voltage (1 V). Twelve different supports were obtained that showed amplification. The enhancement of infrared signals from pyridine and crystal violet molecules adsorbed on silica-titania-silver (SiO2–TiO2–Ag) nanofibers was studied in situ by Attenuated Total Reflection-Fourier Transformed Infrared Spectroscopy (ATR-FTIR). The highest amplification was obtained by the support doped at 10 min in a 10 mM concentration, with an amplification factor of 2.74 in the band localized at 3301 cm−1. In Raman spectroscopy, the highest amplification factor was 27.03, on the support doped for 5 min at a concentration of 5 mM.
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