| 總結: | The most relevant technique for portable (on-chip) sensors is Surface Enhanced Raman Scattering (SERS). This strategy crashes in the case of large (biorelevant) molecules and nano-objects, whose SERS spectra are irreproducible for “homeopathic” concentrations. We suggested solving this problem by SERS-mapping. We analyzed the distributions of SERS parameters for relatively “small” (malachite green (MG)) and “large” (phthalocyanine, H<sub>2</sub>Pc*) molecules. While fluctuations of spectra for “small” MG were negligible, noticeable distribution of spectra was observed for “large” H<sub>2</sub>Pc*. We show that the latter is due to a random arrangement of molecules with respect to “hot spot” areas, which have limited sizes, thus amplifying the lines corresponding to vibrations of different molecule parts. We have developed a method for engineering low-cost SERS substrates optimized for the best enhancement efficiency and a measurement protocol to obtain a reliable Raman spectrum, even for a countable number of large molecules randomly distributed over the substrate.
|
|---|
