阅读说明：本技术 一种可调控开关的光电化学传感器及其制备方法和应用 (Photoelectric chemical sensor capable of regulating and controlling switch and preparation method and application thereof ) 是由 赵啟元 王锦 陈婷婷 周琳 卑佳丽 于 2020-12-24 设计创作，主要内容包括：本发明公开了一种可调控开关的光电化学传感器及其制备方法和应用,以氯金酸为氧化剂,柠檬酸、二水合柠檬酸三钠为还原剂,用高效、快速的方法合成金纳米粒子(Au NPs)和水溶性柱五芳烃(WP5)的复合物(Au NPs@WP5),并通过SEM、TEM、HRTEM、XRD分析验证了其形貌,考察了复合材料的组成和结构,并将纯玻碳电极(GCE)和Au NPs@WP5修饰的电极相比,Au NPs@WP5修饰的GCE对咖啡酸(CA)具有较高的电催化活性。在可见光下的检测效果也有了显著的提高,通过Au NPs@WP5修饰后的GCE对CA的线性检测范围为0.025μM-370μM。(The invention discloses a photoelectric chemical sensor capable of regulating a switch, and a preparation method and application thereof, wherein chloroauric acid is used as an oxidant, citric acid and trisodium citrate dihydrate are used as a reducing agent, a compound (Au NPs @ WP 5) of gold nanoparticles (Au NPs) and water-soluble column pentaarene (WP 5) is synthesized by a high-efficiency and rapid method, the morphology of the compound is verified by SEM, TEM, HRTEM and XRD analysis, the composition and the structure of the compound material are examined, and a pure Glassy Carbon Electrode (GCE) is compared with an Au NPs @ WP5 modified electrode, and the Au NPs @ WP5 modified GCE has higher electrocatalytic activity on Caffeic Acid (CA). The detection effect under visible light is also obviously improved, and the linear detection range of the GCE modified by Au NPs @ WP5 to CA is 0.025 mu M-370 mu M.)

1. The utility model provides a photoelectrochemistry sensor of adjustable switch which characterized in that: a compound formed by compounding gold nanoparticles and water-soluble pillared penta-arene is modified on the glassy carbon electrode; the gold nanoparticles are prepared by reducing chloroauric acid, the water-soluble pillaraarene is compounded on the surfaces of the gold nanoparticles to obtain a compound, and the compound is modified on the surfaces of the glassy carbon electrodes; the structural formula of the water-soluble penta-arene is shown as the formula I:

2. a method for manufacturing a photoelectric chemical sensor of an adjustable switch according to claim 1, comprising the steps of:

the first step is as follows: preparing gold nanoparticles, and reducing chloroauric acid to obtain gold nanoparticles;

the second step is that: preparing water-soluble penta-arene;

thirdly, compounding water-soluble pillared penta-arene on the surface of the gold nano particles to obtain a compound: subjecting gold nanoparticles and water-soluble pillaraarene (n Au NPs: n WP5 ═ 1:1) uniformly dispersed in Phosphate Buffered Saline (PBS) at pH 7 by ultrasound for 3 hours to obtain a complex Au NPs @ WP 5;

the fourth step: modifying the Au NPs @ WP5 obtained in the third step on the surface of the GCE by a dropping method;

the fifth step: and carrying out photoelectrochemical detection on the object to be detected by utilizing an electrochemical workstation, a visible light source simulated by a xenon lamp and the GCE obtained in the fourth step.

3. The photoelectric sensor of claim 1, wherein: the complex is Au NPs @ WP 5.

4. Use of a photoelectric electrochemical sensor of the controllable switch according to claim 1 for detecting caffeic acid in red wine.

5. The photoelectric chemical sensor of claim 1, wherein: the specific reduction method and reduction steps of the chloroauric acid are as follows: h3Cit (0.9mL,0.1M), Na3Cit (2.1mL,0.1M), and deionized H2O (150mL) were boiled, stirred for 15 minutes, injected into HAucl4(1mL,25.4mM), stirred for 3 minutes, and subjected to ice-water bath to obtain AuNPs.

6. The photoelectric chemical sensor of claim 1, wherein: the specific compounding method comprises the following steps: au NPs (0.2mL,1.4224mL), WP5(6.47mg) and PBS (4.8mL) were mixed and sonicated for 3 hours to give Au NPs @ WP5 nanoparticles.

7. The method for manufacturing a photoelectric chemical sensor of an adjustable switch according to claim 2, wherein: the water-soluble pillaraarene comprises the following specific synthetic steps:

Technical Field

The invention relates to the technical field of photoelectrochemistry, in particular to a photoelectrochemical sensor with an adjustable switch and a preparation method and application thereof.

Background

With the improvement of living standard, the requirements of people on diet and physical health are more and more strict, and the imbalance of food and the content of caffeic acid in the body affects the health of people. Excessive caffeine in foods and medicines can cause cancer, and appropriate amount of caffeine can be used for preventing heart disease, preventing cancer, reducing cell mutation, resisting various viruses, and relieving inflammation. The existing detection methods for caffeic acid in red wine, such as ultraviolet visible absorption photometry, high performance liquid chromatography, gas chromatography, capillary electrophoresis, electrochemical detection and the like, are limited in aspects of low sensitivity, limited detection range, expensive instruments, requirement of special operators and the like. Therefore, the establishment of a sensitive, efficient, simple and green method for detecting caffeic acid in red wine not only can deeply discuss the theoretical efficacy mechanism, but also has extremely important significance for disease diagnosis. Gold nanoparticles (Au NPs) play an important role in the fields of nanoscience, nanotechnology, and the like, and have attracted continuous research interest of people due to their unique optical and electrical properties. Their potential applications in physicochemical properties, sensor biomedicine and catalysis have caused strong repercussions. Au NPs become an important component of novel hybrid nano materials due to the characteristics of easy synthesis, high chemical stability, easy surface functionalization and the like. Meanwhile, macrocyclic hosts (cyclodextrins, calixarenes, cucurbiturils, etc.) have unique size-inaccessible luminal structures and exhibit special properties. Based on the host-guest interaction, self-assembly, drug/gene delivery, isolation, sensing, etc. have been applied. The framework structure of the pillared [ n ] arenes is formed by the connection of hydroquinone or derivatives thereof at the 2 and 5 positions by methylene (-CH2-) bridges. Compared with crown ether and calixarene, the pillared arene has a stronger rigid structure; on the other hand, pillared [ n ] arenes are more easily modified than cyclodextrins and cucurbitenes. As a new macrocyclic arene host family, the pillared [ n ] arenes are widely concerned by the characteristics of novel rigid symmetrical columnar structures, hydrophobic electron supply cavities, unique and excellent host guest functions, edges with adjustable functions and the like. Due to these unique properties, pillared [ n ] arenes are promising as building blocks for assembling supramolecular structures and supramolecular sensing platforms. In recent years, the preparation of noble metal nano-doped organic materials has attracted great interest due to their advanced electronic, optical and biological properties. Column

The synthesis, derivatization, subject-object chemistry, supramolecular self-assembly and the like of [ n ] arene are widely researched, but the combination of column [ n ] arene and Au NPs and the application of nano substance composition thereof are rarely reported. Therefore, the coupling of Au NPs and the column [ n ] arene not only provides a novel hybrid nano material, but also is expected to bring new performance, functions and application. Due to the local surface plasma effect of the gold nanoparticles under visible light, the gold nanoparticles can improve the sensitivity of caffeic acid detection. Meanwhile, the water-soluble column aromatic hydrocarbon used in the experiment has strong complexation with the caffeic acid as the substance to be detected. Therefore, the gold nanoparticles with high conductivity and local surface plasmon resonance effect and the water-soluble pillared aromatic hydrocarbon can play a synergistic role, and the sensitivity of electrochemical detection on caffeic acid detection is improved.

Disclosure of Invention

The invention provides a photoelectrochemical sensor with an adjustable switch and a preparation method and application thereof, and solves the technical problems of low sensitivity, limited detection range, serious environmental pollution, expensive instruments, special operators, low efficiency, low speed, difficult operation and the like of the conventional detection technology.

The invention adopts the following technical scheme:

the photoelectrochemical sensor of the adjustable switch is characterized in that a compound formed by compounding gold nanoparticles and water-soluble pentacene is modified on a glassy carbon electrode; the gold nanoparticles are prepared by reducing chloroauric acid, the water-soluble pillaraarene is compounded on the surfaces of the gold nanoparticles to obtain a compound, and the compound is modified on the surfaces of the glassy carbon electrodes; the structural formula of the water-soluble penta-arene is shown as the formula I:

a method for preparing a photoelectric chemical sensor capable of regulating a switch comprises the following steps:

the first step is as follows: preparing gold nanoparticles, and reducing chloroauric acid to obtain gold nanoparticles;

the second step is that: preparing water-soluble penta-arene;

thirdly, compounding water-soluble pillared penta-arene on the surface of the gold nano particles to obtain a compound: subjecting gold nanoparticles and water-soluble pillaraarene (n Au NPs: n WP5 ═ 1:1) uniformly dispersed in Phosphate Buffered Saline (PBS) at pH 7 by ultrasound for 3 hours to obtain a complex Au NPs @ WP 5;

the fourth step: modifying the Au NPs @ WP5 obtained in the third step on the surface of the GCE by a dropping method;

the fifth step: and carrying out photoelectrochemical detection on the object to be detected by utilizing an electrochemical workstation, a visible light source simulated by a xenon lamp and the GCE obtained in the fourth step.

As a preferred technical scheme of the invention: the complex is Au NPs @ WP 5.

As a preferred technical scheme of the invention: the specific reduction method and reduction steps of the chloroauric acid are as follows: h3Cit (0.9mL,0.1M), Na3Cit (2.1mL,0.1M), and deionized H2O (150mL) were boiled, stirred for 15 minutes, injected into HAucl4(1mL,25.4mM), stirred for 3 minutes, and subjected to ice-water bath to obtain AuNPs.

As a preferred technical scheme of the invention: the specific compounding method comprises the following steps: au NPs (0.2mL,1.4224mL), WP5(6.47mg) and PBS (4.8mL) were mixed and sonicated for 3 hours to give Au NPs @ WP5 nanoparticles.

As a preferred technical scheme of the invention: the water-soluble pillaraarene comprises the following specific synthetic steps:

the application also protects the application of the photoelectric chemical sensor capable of regulating the switch in the detection of the caffeic acid in the red wine.

Advantageous effects

Compared with the prior art, the photoelectric chemical sensor with the adjustable switch and the preparation method and application thereof adopt the technical scheme, and have the following technical effects:

1. the advantages of the local surface plasmon resonance effect of Au NPs under the irradiation of visible light, the strong complexation effect of WP5 and caffeic acid and the like are utilized;

2. the sensor modified by the Au NPs @ WP5 nano composite material can detect caffeic acid rapidly, sensitively, intelligently and greenly by regulating a switch of visible light;

3. the lowest detection limit in the existing literature is 80nM, the detection limit of the photoelectrochemical sensor disclosed by the invention to CA reaches 10nM, and the photoelectrochemical sensor has obvious advantages compared with the detection limit in the existing literature.

Drawings

FIG. 1 is a UV-vis diagram of Au NPs @ WP5 in the present application.

FIG. 2 is a graph of CV curves for AuNPs modified GCE of various sizes in this application in 5mM K3[ Fe (CN)6] + K4[ Fe (CN)6] and 0.5M KCl.

Fig. 3 is a graph of CV curves for Au NPs modified GCE of different sizes at 0.5mM CA (pH 2.0) in the present application.

Fig. 4 is a graph of DPV measured in 0.5mM CA (pH 2.0) under visible light irradiation and dark conditions, respectively, for GCE modified with AuNPs according to the present application.

Figure 5 is a graph of DPV measured in 0.5mM CA (pH 2.0) under visible light and dark conditions, respectively, for GCE modified with Au NPs @ WP5 according to the present application.

Figure 6 is a graph of DPV of GCE modified with AuNPs, WP5, and AuNPs @ WP5 for the present application at 0.5mM CA (pH 2.0) under visible light.

Fig. 7 is a DPV plot of Au NPs @ WP5 detected at 0.5mM CA (PH 2.0) under visible light irradiation, obtained by compounding AuNPs and WP5 in the presence of water, PBS having PH 2, and PBS having PH 7 as solvents, respectively, according to the present application of Au NPs: WP5: 1: 25.

FIG. 8 is a drawing of the present application H1-H3Cit + Na3Cit-WP5 Au NPs 0.075: 1; H2-H3Cit + Na3Cit-WP5 Au NPs: -20: 1; N1-NaBH4-WP5 Au NPs 0.075: 1; N2-H3Cit + Na3Cit-WP5 Au NPs obtained at 20:1 and WP5 gave DPV profiles of Au NPs @ WP5 at 0.5mM CA (pH 2.0) under visible light illumination.

FIG. 9 is a DPV profile of Au NPs @ WP5 modified GCE of the present application at various pHs of 0.5mM CA.

FIG. 10 is a graph of LSV of the Au NPs @ WP5 modified GCE of the present application at different scan speeds for 0.5mM CA.

FIG. 11 is a diagram of a method for synthesizing water-soluble pillaraarenes according to the present application.

FIG. 12 is a TEM image of Au NPs of the present application.

Detailed Description

The present invention is further described with reference to the following examples, which are intended to be illustrative only and not to be limiting of the scope of the claims, and other alternatives which may occur to those skilled in the art are within the scope of the claims.

Example 1:

a method for preparing a photoelectric chemical sensor capable of regulating a switch comprises the following steps:

step one, preparing gold nanoparticles: h3Cit (0.9mL,0.1M), Na3Cit (2.1mL,0.1M), and deionized H2O (150mL) were boiled, stirred for 15 minutes, HAuCl4(1mL, X25.4 mM) was injected, stirring was continued for 3 minutes, and the Au NPs were obtained by ice-water bath.

Second, Au NPs @ WP5 preparation: WP5 was prepared using the method described in figure 11; synthesis of Au NPs @ WP5 Au NPs (0.2mL,1.4224mM) and WP5(6.47mg) were added to 4.8mL of PBS (pH 7) and sonicated for 3 hours to give Au NPs @ WP 5.

Example 2

Preparing a photoelectric chemical sensor with an adjustable switch:

coating 20 microliters of the Au NPs @ WP5 obtained in the above example 1 on the surface of the GCE in a dropwise manner, drying the GCE at 45 ℃ to obtain an Au NPs @ WP5 modified GCE, dissolving caffeic acid in PBS with PH of 2 as an object to be detected, irradiating the surface of the GCE electrode with a xenon lamp simulated visible light source by a traditional three-electrode method, controlling the shading interval time as an adjustable switch, and performing photoelectrochemical detection by using an electrochemical workstation.

Example 3

Au NPs, WP5 and Au NPs @ WP5 were characterized by TEM and UV-vis using different volumes of reducing agent to obtain uniform Au particle size. To better control the shape of the Au NPs, different volumes of reducing agent were optimized. The reducing agent (0.9mL citric acid) is critical for the preparation of well-defined Au NPs. Representative TEM images show no change in shape and size of Au @ WP5 and an average diameter of about 15nm after self-assembly by WP 5. The sharp lattice fringes in fig. 12 show the good crystallinity of typical spherical gold. The lattice spacing was 0.234 and 0.232nm, respectively, consistent with the crystal planes of Au NPs.

Comparing UV-vis with single Au NPs and Au NPs @ WP5, it is apparent that SPR peak of Au NPs is about 528 nm. Combining the Au NPs and WP5, the SPR peaks underwent blue shifts of 528 and 302 nm. The phenomenon shows that the absorption intensity of the Au NPs @ WP5 is higher than that of the Au NPs, and the composite material has higher sensitivity and greater advantage for photoelectrochemical detection.

Example 4

Photoelectrochemical detection of Au NPs and Au NPs @ WP5:

FIG. 2 shows the detection of a mixed solution of 5mM K3(Fe (CN)6) +5mM K4 (Fe (CN)6) and 0.5M potassium chloride in Au NPs modified GCE of different sizes. AuNPs made from 0.9mL HAuCl4 had higher peak current intensity and better absorption of light, and similarly, in fig. 3, the AuNPs made from 0.9mL HAuCl4 had higher peak current intensity and better absorption of light, when measured photoelectrochemically against 0.5mM CA (pH 2.0). Therefore, 0.9mL of Au NPs prepared by HAucl4 was selected for the entire experiment.

FIGS. 4 and 5 show that the electrochemical response of the Au NPs, whether the Au NPs are single or Au NPs @ WP5, is better than that of the Au NPs in a dark environment under the irradiation of visible light, and the Au NPs have the local surface plasmon resonance effect under the irradiation of visible light.

FIG. 6 shows that the composite Au NPs @ WP5 has better electrochemical response than single Au NPs and WP5 under irradiation of visible light. Meanwhile, the Au NPs have the local surface plasmon resonance effect under the irradiation of visible light, so the electric signal of the Au NPs is stronger than that of WP 5.

Fig. 7 shows that when Au NPs and WP5 are compounded, the responses of different solvents and different PH values of the same solvent to Au NPs @ WP5 modified GCE to the photo-generated current are strong and weak, and the compounded Au NPs @ WP5 in PBS at PH 7 is obviously superior, and the compounded Au NPs @ WP5 in PBS at PH 7 is used as the final material of the modified GCE.

FIG. 8 is a DPV graph of Au NPs @ WP5 obtained by reducing chloroauric acid with the same reducing agent in different proportions and Au NPs @ WP5 obtained by reducing chloroauric acid with the same reducing agent in different proportions and compounding the Au NPs and WP5 in the same reducing agent in different proportions, and when 0.5mM CA (pH is 2.0) is detected under visible light irradiation, it is clear that the electric signal is stronger when 0.5mM CA (pH is 2.0) is detected under visible light irradiation by the Au NPs @ WP5 obtained by compounding the Au NPs and WP5 obtained when the H1-H3Cit + Na3Cit-WP5: the Au NPs ═ 0.075:1, so the Au NPs @ WP5 is prepared by the scheme of H3Cit + Na3Cit-WP5: the Au NPs ═ 0.075: 1.

Example 5

Effect of scan speed and PH on Au NPs @ WP5 detection of CA:

fig. 9 shows the response of different PH values in PBS to the photo-generated current when CA was detected, PH 2 has absolute advantage in photoelectrochemical detection compared to other PH values, thus confirming that CA was photoelectrochemically detected in PH 2 environment with Au NPs @ WP5 finally obtained in example 4.

The linear increase in oxidation peak current density with increasing scan speed is shown in fig. 10, indicating that the Au NPs modified GCE detection of CA redox reaction is a diffusion-controlled process.

Example 6

Stability, reproducibility, interference resistance and detection limit of Au @ WP5 modified GCE.

And detecting the anti-interference capability of other similar molecules which can coexist in the Au NPs @ WP5 in the red wine solution, such as NaCl, ascorbic acid, citric acid, gallic acid, glucose and the like on CA detection. The photocurrent response of Au NPs @ WP5/GCE was obtained in 0.5mM CA solution (Ipa) and 0.5mM CA +5mM interfering substance (Ip), respectively. The relative photo-current response (Ipa/Ip) shows the weak signal change (104.2% -105.25%) when the interference exists, which indicates that the Au NPs @ WP5 sensor has good anti-interference performance for CA sensing.

Stability is an important parameter for evaluating the fabricated sensors by performing the corresponding photocurrent switching cycle test on the fabricated Au NPs @ WP5 sensors in 0.5mM CA solution. After cycling for about 700 seconds, the photocurrent did not change. In addition, after 10 days at room temperature, the photocurrent signal on the PEC sensor retained-91.68% of the initial photocurrent value, confirming acceptable stability of the Au NPs @ WP5 PEC sensor.

The reproducibility of the prepared PEC sensors was evaluated by measuring 0.5mM CA solutions on five parallel Au NPs @ WP5 electrodes under the same conditions. The Relative Standard Deviation (RSD) was calculated to be 4.21%, which illustrates the excellent reproducibility of the PEC sensor.

Example 7

And (3) real sample analysis:

to evaluate the effectiveness of the Au NPs @ WP5 nanocomposite, red wine containing CA was selected as the subject. Red wine was first diluted 1mL to 25mL with PBS (PH 2) and then 10 mM caffeic acid 25 μ L was added sequentially using standard addition methods and CA in red wine was detected by DPVs curves. This illustrates the usefulness of the Au NPs @ WP5 nanocomposite as a commercial test.

The embodiments described above are described to facilitate an understanding and use of the invention by those skilled in the art. It will be readily apparent to those skilled in the art that various modifications to these embodiments may be made, and the generic principles described herein may be applied to other embodiments without the use of the inventive faculty. Therefore, the present invention is not limited to the above embodiments, and those skilled in the art should make improvements and modifications within the scope of the present invention based on the disclosure of the present invention.