SERS-based portable single-wavelength Raman photometer
A single-wavelength, photometric technology, used in Raman scattering, material analysis by optical means, material excitation analysis, etc., can solve the problems of unassisted SERS sensing analysis efficiency, increased difficulty in instrument miniaturization, and prolonged testing time. , to achieve the effect of improving detection efficiency, flexible and diverse data recording formats, and reducing test costs
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Embodiment 1
[0035] Embodiment 1 uses a fiber laser with a center wavelength of 785 nm as the light source. Since the laser light emitted by the fiber probe has a large divergence angle, the present invention uses a collimator to make the beam close to a parallel beam; further, in the collimator A Galileo beam expander is introduced in the downstream optical path. In addition to further optimizing the divergence angle of the laser beam, it also expands the beam diameter so that a larger numerical aperture can be obtained during the focusing process of the sample. After the above “shaping”, the laser beam is reflected by the dichroic mirror at an angle of 90° and focused to the center of the sample cell by the lens; the SERS signal is collected by the same lens and passes through the dichroic mirror used to filter Rayleigh scattering , Through the pinhole used to shield the stray light of the environment, and then filter out the scattered light of specific wavelength by the interference filte...
Embodiment 2
[0054] Example 2: Quantitative detection performance test
[0055] Prepare AgNO 3 (10mM), OPE3 (2mM), L-ascorbic acid (10mM), trisodium citrate, gold nanorod sol, potassium thiocyanide, the SERS-based portable single-wavelength Raman photometer provided by the present invention.
[0056] (1) Preparation of gold nanorod sol:
[0057] ① Preparation of seeds
[0058] Take 10mL of 0.1M CTAB aqueous solution and add 250μL of 10mM HAuCl 4 , Stir for two minutes. Then, add 600μL 10mMNaBH 4 , Stir vigorously for 1 minute. Let stand for two hours to make NaBH 4 Completely decompose.
[0059] ②Growth solution preparation
[0060] Take 10mL of 0.1M CTAB aqueous solution and add 500μL of 10mM HAuCl 4 , Then add 200μL 1M HCl solution and 100μL 10mMAgNO 3 , Stir for 2 minutes.
[0061] ③Growth response
[0062] Add 100 μL of ascorbic acid to the growth solution to initiate the reaction, and stop after stirring for one minute. Take 50μL of seeds and add them to the growth solution and let stand for 24...
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