High efficiency and high sensitivity particle capture type terahertz sensing system
US-2021389228-A1 · Dec 16, 2021 · US
US12465927B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12465927-B2 |
| Application number | US-202217979249-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 2, 2022 |
| Priority date | Apr 18, 2022 |
| Publication date | Nov 11, 2025 |
| Grant date | Nov 11, 2025 |
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A method for detecting a nanoplastic using a vertical nanogap electrode and a Raman spectroscopic device, includes, in a state where a vertical nanogap electrode is provided in aquatic environment in which a nanoplastic exists, forming a nanoplastic aggregate having a size of 1 μm or more by applying an alternating voltage of a specific frequency to the vertical nanogap electrode, and collecting and concentrating the nanoplastic in a collector of the vertical nanogap electrode, and performing Raman spectroscopy on the nanoplastic aggregate concentrated in the collector of the vertical nanogap electrode to detect the nanoplastic constituting the nanoplastic aggregate.
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What is claimed is: 1 . A method for detecting a nanoplastic using a vertical nanogap electrode and a Raman spectroscopic device, comprising: in a state where a vertical nanogap electrode is provided in aquatic environment in which a nanoplastic exists, forming a nanoplastic aggregate having a size larger than a laser wavelength of a Raman spectroscopic device, by applying an alternating voltage of a specific frequency to the vertical nanogap electrode to collect and concentrate the nanoplastic in a collector of the vertical nanogap electrode, irradiating the nanoplastic aggregate with the Raman spectroscopic device, and performing Raman spectroscopy on the nanoplastic aggregate concentrated in the collector of the vertical nanogap electrode to detect the nanoplastic constituting the nanoplastic aggregate, the alternating voltage and a frequency of the corresponding alternating voltage are controlled so that a local minimum point of potential energy acting on the vertical nanogap electrode is located in a central region of the collector of the vertical nanogap electrode, the local minimum point of the potential energy acting on the vertical nanogap electrode due to interaction between AC-electroosmosis (ACEO) and dielectrophoresis (DEP) is located in the central region of the collector of the vertical nanogap electrode, in the aquatic environment in which the nanoplastic exists, a minimum size of the nanoplastic is 200 nm, and a limiting of detection (LoM) of the nanoplastic is 4.66 mg/L. 2 . The method according to claim 1 , wherein a size of the nanoplastic is smaller than a wavelength of a laser to be irradiated, and the Raman spectroscopy is performed on the nanoplastic aggregate having a size larger than the wavelength of the laser to detect a molecular type of an individual nanoplastic constituting the nanoplastic aggregate. 3 . The method according to claim 2 , wherein the vertical nanogap electrode comprises a substrate, a first electrode stacked on an entire surface of the substrate, an insulation film and a second electrode sequentially stacked on the first electrode, the insulation film and the second electrode are removed to expose the first electrode to form the collector, and the alternating voltage of the specific frequency is applied to the first electrode and the second electrode. 4 . The method according to claim 1 , wherein a size of the nanoplastic aggregate is 1 μm or more. 5 . The method according to claim 1 , wherein the vertical nanogap electrode comprises a substrate, a first electrode stacked on an entire surface of the substrate, an insulation film and a second electrode sequentially stacked on the first electrode, the insulation film and the second electrode are removed to expose the first electrode to form the collector, and the alternating voltage of the specific frequency is applied to the first electrode and the second electrode. 6 . A method for detecting a nanoplastic using a vertical nanogap electrode and a Raman spectroscopic device, comprising: in a state where a vertical nanogap electrode is provided in aquatic environment in which a nanoplastic exists, forming a nanoplastic aggregate having a size larger than a laser wavelength of a Raman spectroscopic device, by applying an alternating voltage of a specific frequency to the vertical nanogap electrode to collect and concentrate the nanoplastic in a collector of the vertical nanogap electrode, irradiating the nanoplastic aggregate with the Raman spectroscopic device, and performing Raman spectroscopy on the nanoplastic aggregate concentrated in the collector of the vertical nanogap electrode to detect the nanoplastic constituting the nanoplastic aggregate, wherein the alternating voltage and a frequency of the corresponding alternating voltage are controlled so that a local minimum point of potential energy acting on the vertical nanogap electrode is located in a central region of the collector of the vertical nanogap electrode, the local minimum point of the potential energy acting on the vertical nanogap electrode due to interaction between AC-electroosmosis (ACEO) and dielectrophoresis (DEP) is located in the central region of the collector of the vertical nanogap electrode a SERS (Surface-Enhanced Raman Scattering) particle is provided in advance in the collector of the vertical nanogap electrode, and when the alternating voltage of the specific frequency is applied to the vertical nanogap electrode, the SERS particle forms the aggregate together with the nanoplastic, the Raman spectroscopy is performed on the aggregate to detect the nanoplastic constituting the nanoplastic aggregate, wherein in the aquatic environment in which the nanoplastic exists, a minimum size of the nanoplastic is 30 nm, and a limit of detection (LoM) of the nanoplastics is 0.01 mg/L.
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