The patent pertains to the structure of a portable nano-optical chip based on the principle of generating plasmons and on the modification of a plasmonic nanoparticle surface. The nano-optical chip detects very low concentrations of substances/molecules in the environment (water, air, soil), food, and biological systems.
Plasmons are oscillations of electron plasma that are excited by light on metal nanoparticles; the excitation results in generating a significantly enhanced electromagnetic field (EF) on the surface of the nanoparticles. SERS (Surface-enhanced Raman spectroscopy) is a technique based on significant enhancement of EF on metal nanostructures and subsequent increase in the intensity of Raman signal. Such increased Raman signal transforms Raman spectroscopy from a structural analytical method into a structurally sensitive nano-probe able to detect very low concentration of molecules down to the single-molecule level.
At present, SERS is the only single-molecule detection option with a simultaneous analysis of the chemical structure. Technically, SERS depends on the existence of the so-called “hot spots” (HS) found in the structure of plasma nanoparticles. We recognize two different types of HS: a) gaps between metallic nanoparticles and b) spikes of nanoparticle surface exhibiting a high surface curvature. In both cases, the EF is strongly enhanced by the excitation light. Thus, enhanced EF significantly increases Raman signal from the molecules found in these HS.
Description of the Nano-Optical Chip:
Plasmonic nanoparticle surface created by physical methods, such as pulsed laser deposition, functionalized by specific molecular linkers and by the deposition of additional layer/layers of nanoparticles of various shapes.
FIGURE: Schematic representation of the structure of the nano-optical chip
The nano-optical chip integrates two different parts: the plasmonic nanoparticle surface consisting of plasmonic nanoparticles deposited on the substrate and the molecular functionalization of the plasmonic nanoparticle surface.
The plasmonic nanoparticle surface 2 comprises suitably shaped and spaced plasmonic nanoparticles 5 (NPs 5) immobilized on the substrate 1. Depending on the type of NPs 5 deposited on the substrate 1 and the spacing between them, an optimal amount of HS 4 is generated, where the EF is strongly enhanced by the interaction between the light and plasmons.
Both selectivity and sensitivity of thus created plasmonic nanoparticle surface 2 for the detection of substances/molecules are increased by the molecular functionalization 3 of the plasmonic nanoparticle surface 2. The most suitable functionalization is achieved using the following linkers: i) cavitand linkers (CL) containing internal cavities in their structure. CL molecules are bound directly to the surface and they lead to highly specific recognition and binding of the molecules to be detected; ii) bifunctional linkers (BL) containing aliphatic chains or other molecules creating favorable conditions for the selective binding of the molecules to be detected.
The subsequent increase in the sensitivity and selectivity of the nano-optical chip lies in the possibility of attaching a second layer of NPs 5 with different morphology (shape), such as round NPs, pyramidal NPs, star-like NPs to the primary functionalized plasmonic nanoparticle surface 2. The aim is to increase the size of the surface available for binding the substances/molecules to be detected while increasing the number of HS in the nano-optical chip. In addition, the functionalization of the second layer of NPs 5 creates favorable conditions for the binding of other molecules to be detected.
Nano-optical chips can detect the substances/molecules in the environment (water, air, soil), food, and biological systems. The detection and identification of these substances/molecules by certified techniques (mass spectrometry or gas chromatography) is time-consuming and expensive. In comparison with the certified methods (mass spectrometry or gas chromatography), the detection of substances/molecules by nano-optical chips is cheaper, faster, more sensitive and performed on the spot (without the need for pre-treatment of samples in the laboratory).
EF Electromagnetic field
SERS Surface-enhanced Raman spectroscopy
HS Hot spots, (areas of high-intensity of EF)
PLD Pulsed laser deposition
NPs Plasmonic nanoparticles
BL Bifunctional linkers
CL Cavitand linkers
Number | Date | Country | Kind |
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PP 127-2017 | Dec 2017 | SK | national |
Filing Document | Filing Date | Country | Kind |
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PCT/IB18/60065 | 12/13/2018 | WO | 00 |