UIO-66/Ag/TiO2 Nanocomposites as Highly Active SERS Substrates for Quantitative Detection of Hexavalent Chromium

Abstract

Sensitive determination of Cr(VI) is of great importance as this is one of the most toxic heavy metal ions in the environment. In this work, a metal–organic framework (MOF) material, UIO-66 (University of Oslo, UIO), was introduced for the first time to develop a composite substrate, UIO-66/Ag/TiO2, for the sensitive SERS detection of Cr(VI) in water. The composition, morphology, crystal structure and optical property of the UIO-66/Ag/TiO2 were characterized by SEM, XRD, EDX, UV-Vis and Raman spectroscopy. The control experiment revealed the introduction of UIO-66 and TiO2 can improve the adsorption to Cr ions and thus greatly enhance the SERS signal of Cr(VI) on this composite substrate. The SERS signal can also be tuned by changing the dosage of TiO2. Under optimized conditions, UIO-66/Ag/TiO2 was used to detect Cr(VI) in water with different concentrations, which showed high sensitivity and good stability. The SERS signals showed a linear increase as the concentration of Cr(VI) increases from 5 × 10−9 M to 5 × 10−6 M. The detection limit was 5 nM, which was lower than the safe drinking water standard of the US Environmental Protection Agency (1 μM). Detection of Cr(VI) in the range of 1 × 10−7 M to 5 × 10−6 M in real lake water was also achieved. These results demonstrate the great potential of UIO-66/Ag/TiO2 composites as SERS substrates for the trace determination of Cr(VI) in the environmental field.

Metal–Organic Frameworks–Based Surface–Enhanced Raman Scattering Substrates for Gas Sensing

“…This charge transfer arises from the CM mechanism of MOFs and offers superior selectivity compared to EM enhancement for target molecules. Therefore, by combining the excellent LSPR properties of NMNPs with the CT characteristics of MOFs, structure engineering strategies can create a heterogeneous SERS platform that synergistically enhances sensitivity and showcases superior selectivity for target analytes [44].…”