WO2021047283A1 - 检测内源性h2s的电化学传感器的构建方法及其应用 - Google Patents

检测内源性h2s的电化学传感器的构建方法及其应用 Download PDF

Info

Publication number
WO2021047283A1
WO2021047283A1 PCT/CN2020/102261 CN2020102261W WO2021047283A1 WO 2021047283 A1 WO2021047283 A1 WO 2021047283A1 CN 2020102261 W CN2020102261 W CN 2020102261W WO 2021047283 A1 WO2021047283 A1 WO 2021047283A1
Authority
WO
WIPO (PCT)
Prior art keywords
rgo
solution
electrode
electrochemical
water
Prior art date
Application number
PCT/CN2020/102261
Other languages
English (en)
French (fr)
Inventor
赵媛
顾文秀
刘瀚
Original Assignee
江南大学
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 江南大学 filed Critical 江南大学
Publication of WO2021047283A1 publication Critical patent/WO2021047283A1/zh

Links

Classifications

    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/28—Electrolytic cell components
    • G01N27/30—Electrodes, e.g. test electrodes; Half-cells
    • G01N27/308—Electrodes, e.g. test electrodes; Half-cells at least partially made of carbon

Definitions

  • the invention belongs to the technical field of electrochemical analysis, and particularly relates to a construction method of an electrochemical sensor for detecting endogenous H 2 S.
  • Hydrogen sulfide gas in the natural environment is a high-risk gas.
  • hydrogen sulfide is an acidic corrosive gas, in terms of physics, it is an explosive and flammable gas, and in terms of biology, it is a nerve anesthetic, causing shock.
  • hydrogen sulfide has been proven to have many important roles in maintaining body health and dealing with diseases.
  • H 2 S in organisms is mainly composed of cystathionine- ⁇ -synthetase (CBS), cystathionine- ⁇ -lyase (CSE), fungal/yeast thiopyruvate thiotransferase (3-MST) three enzymes Catalyzes the production of cystine (Cys).
  • CBS cystathionine- ⁇ -synthetase
  • CSE cystathionine- ⁇ -lyase
  • 3-MST fungal/yeast thiopyruvate thiotransferase
  • the existing detection methods mainly include fluorescence, chromatography, and surface-enhanced Raman scattering spectroscopy.
  • these methods have disadvantages such as large environmental impact, expensive detection equipment, and cumbersome operation.
  • electrochemical methods have attracted widespread attention due to their high sensitivity, easy operation, and simple instruments.
  • ferrocene and Ag NPs are used as electrochemical beacons
  • sodium hydrosulfide and sodium sulfide are used as H 2 S substitutes to chemically react with the beacon to affect the electrochemical signal to achieve the purpose of detecting H 2 S.
  • the present application provides a construction method and application of an electrochemical sensor for endogenous H 2 S detection.
  • the invention is easy to operate, green and pollution-free, and has high sensitivity.
  • a construction method of an electrochemical sensor for endogenous H 2 S detection comprising the following steps:
  • step (1) Add the rGO/Fe 3 O 4 solution obtained in step (1) to the 0.01-0.012g/mL copper nitrate solution, sonicate for 30-40min, mix well, then add 80-100 ⁇ L 0.035-0.04mol while stirring /L NaOH solution, and continue to stir for 30-50min, then add 400-450mL 85-90mol/L hydrazine hydrate solution and stir for 40-50min, then solid-liquid separation to take the solid phase, the solid phase is washed and dried with water, and finally renewed Disperse in water to obtain 2-3mg/ml rGO/Fe 3 O 4 /Cu 2 O solution;
  • MGCE with a diameter of 4-10mm was polished on alumina powder with a particle size of 0.4-0.6mm and 0.025-0.03mm respectively, and then the polished electrode was cleaned with ethanol and water, and the cyclic voltammetry of the bare electrode was measured.
  • step (2) Take a certain amount of the rGO/Fe 3 O 4 /Cu 2 O dispersion obtained in step (2), add a series of different concentrations of NaHS and ammonia with a concentration of 5-7wt%, react for a certain period of time, and mix the reacted magnetic
  • the material is adsorbed by a magnet and the supernatant is removed to separate the magnetic hybrid nanomaterial, and the magnetic hybrid nanomaterial is re-dissolved and dispersed in ultrapure water, and then a certain amount of the obtained solution is dripped and applied in step (3).
  • electrochemical scanning is performed on the obtained electrode, the signal changes are recorded, and a standard curve between the electrochemical signal of the magnetic hybrid nanomaterial and the NaHS concentration after the reaction is established.
  • the concentration of the ethylene glycol solution of reduced graphene oxide in step (1) is 1-2w/v%, wherein the mass ratio of reduced graphene oxide, iron acetylacetonate and amine acetate is 30-60: 15-35:100-180.
  • step (2) the volume-to-volume ratio of the reduced graphene oxide dispersion, the copper nitrate solution, the NaOH solution and the hydrazine hydrate solution is 0.2-1.2:5-15:0.04-0.16:200-600.
  • the voltage range of the electrochemical scan in step (3) is -0.5v-0.3v.
  • step (4) The specific steps for constructing the electrochemical sensor described in step (4) are as follows: Take 5-12 parts of 20-30 ⁇ L of the rGO/Fe 3 O 4 /Cu 2 O dispersion obtained in step (2) in parallel and place them in a centrifuge tube. And add 100-150 ⁇ L of NaHS solution of different concentrations, and add 20-30 ⁇ L of ammonia water with a concentration of 5-7wt% at the same time, react for 50-70min, separate the reacted magnetic mixed nanomaterials, take them out and re-disperse them.
  • the concentration of the NaHS solution ranges from 0.5 to 100,000 nM.
  • the magnetic hybrid nano-material is a mixture of rGO/Fe 3 O 4 /Cu 2 O and rGO/Fe 3 O 4 /Cu 2 O-Cu 9 S 8 nano-materials.
  • An electrochemical sensor for the detection of endogenous H 2 S which is applied to the detection of endogenous H 2 S.
  • the nanomaterials used are low in cost and easy to obtain.
  • the principle of the present invention is to use the electroactive material rGO/Fe 3 O 4 /Cu 2 O to undergo oxidation-reduction reaction with NaHS to generate a sulfur-copper compound rGO/Fe 3 O 4 /Cu 2 O-Cu with a hole structure.
  • 9 S 8 the electrochemical signal of this sulfur-copper compound is weaker than that of rGO/Fe 3 O 4 /Cu 2 O.
  • the electrochemical signal of rGO/Fe 3 O 4 /Cu 2 O-Cu 9 S 8 Increased, the amount of rGO/Fe 3 O 4 /Cu 2 O decreased, which weakened the electrochemical signal of the overall magnetic hybrid nanomaterial.
  • the existing H 2 S detection method is mainly methylene blue method (detection limit is about 8 ⁇ M, detection range is 25 ⁇ M-1000 ⁇ M). Compared with methylene blue method, the detection limit of this electrochemical sensor is 230 pM, and the detection range is 500 pM. -500 ⁇ M, it can be seen that the detection limit of the present invention is low, the detection range is wide, and the sensitivity is high.
  • the electrode modification steps are greatly simplified, the cost of electrode modification is reduced, and the traditional electrode modification process is also reduced. error.
  • the material is magnetic, it can be repeatedly collected and tested, and the test results are highly reproducible.
  • Figure 1 is the intermediate product rGO/Fe 3 O 4 /Cu 2 O prepared in Example 1, the final reaction mixture rGO/Fe 3 O 4 /Cu 2 O and rGO/Fe 3 O 4 /Cu 2 O -Cu 9 S 8 XRD patterns of magnetic composite nanomaterials;
  • Figure 2 is the intermediate product rGO/Fe 3 O 4 /Cu 2 O prepared in Example 1, the final reaction mixture rGO/Fe 3 O 4 /Cu 2 O and rGO/Fe 3 O 4 /Cu 2 O -Cu 9 S 8 XPS spectrum of magnetic composite nanomaterials;
  • Example 3 is an AC impedance diagram and a cyclic voltammetry (CV) diagram of the electrochemical sensor prepared in Example 1;
  • Figure 4 is the DPV spectrum and verification UV spectrum of the electrochemical sensor
  • Fig. 5 shows the electrochemistry of rGO/Fe 3 O 4 /Cu 2 O and rGO/Fe 3 O 4 /Cu 2 O-Cu 9 S 8 magnetic hybrid nanomaterials measured by the electrochemical sensor prepared in Example 1.
  • MGCE with a diameter of 4mm was polished on alumina powder with a particle size of 0.5mm and 0.03mm respectively, and then the polished electrode was cleaned with ethanol and water, and the CV curve of the bare electrode was measured.
  • the oxidation peak and the reduction peak were When the potential difference is 85mV, the polishing is finished, and then the polished electrode is cleaned with ethanol and water, and the cleaned electrode is dried with nitrogen or argon for use;
  • the constructed electrochemical sensor system add 20 ⁇ L of the rGO/Fe 3 O 4 /Cu 2 O solution obtained in step (2), and add a series of different concentrations (0.5 nM, 1 nM, 10 nM, 100 nM, 1000 nM, 10000 nM, 100000 nM) NaHS and ammonia water with a concentration of 5wt%, react for 50 min, use magnetism to transfer the reacted rGO/Fe 3 O 4 /Cu 2 O and rGO/Fe 3 O 4 /Cu 2 O -Cu 9 S 8 magnetic composite nano-materials are adsorbed and separated, the resulting mixed nano-materials are re-dispersed in ultrapure water, and 10 ⁇ L of the resulting dispersion is dripped on the surface of the electrode obtained in step (3), and the obtained electrode is electrochemically Scan and record the signal changes, and establish the standard between the electrochemical signal and NaHS concentration of the reacted rGO/Fe 3 O 4 /
  • the electrochemical signal of the rGO/Fe 3 O 4 /Cu 2 O modified electrode gradually decreases.
  • the test blank group to obtain the standard deviation multiplied by 3, the lowest detection limit is 230 pM. It can be seen that the electrochemical biosensor designed by the present invention not only has a wide detection range for detecting H 2 S, but also has a high sensitivity.
  • 15 ⁇ L of the rGO/Fe 3 O 4 /Cu 2 O solution obtained in step (2) is added to a series of different concentrations (0.5 nM, 1 nM, 10 nM, 100 nM, 1000 nM, 10000 nM, 100000 nM) NaHS and 7 wt% ammonia water, react for 60 min, use magnetism to transfer the reacted rGO/Fe 3 O 4 /Cu 2 O and rGO/Fe 3 O 4 /Cu 2 O -Cu 9 S 8 magnetic composite nano-materials are adsorbed and separated, the resulting magnetic hybrid nano-materials are re-dispersed in ultrapure water, and 8 ⁇ L of the resulting dispersion is dripped on the surface of the electrode obtained in step (3), and the electrode is electrically charged.
  • concentrations 0.5 nM, 1 nM, 10 nM, 100 nM, 1000 nM, 10000 nM, 100000 nM
  • step (1) Add 1 mL of magnetic reduced graphene oxide (rGO/Fe 3 O 4 ) dispersion obtained in step (1) to 0.011 g/mL copper nitrate solution, sonicate for 35 min, mix well, and then add while stirring 90 ⁇ L of 0.037 mol/L NaOH solution, and continue to stir for 40 minutes, then add 430 mL of 87 mol/L hydrazine hydrate solution and stir for 45 minutes, then solid-liquid separation takes the solid phase, the solid phase is washed and dried with water, and finally renewed Disperse in water to obtain 2.5 mg/mL rGO/Fe 3 O 4 /Cu 2 O solution;
  • MGCE with a diameter of 6mm was polished on 0.4mm and 0.027mm alumina powder successively, and then the polished electrode was cleaned with ethanol and water, and the CV curve of the bare electrode was measured.
  • the oxidation peak and reduction peak potential difference is 82 mV That is, the polishing is completed, and then the polished electrode is cleaned with ethanol and water, and the cleaned electrode is dried with nitrogen or argon for use;
  • the constructed electrochemical sensor system add 25 ⁇ L of the rGO/Fe 3 O 4 /Cu 2 O solution obtained in step (2) to a series of different concentrations (0.5 nM, 1 nM, 10 nM, 100 nM, 1000 nM, 10000 nM, 100000 nM) NaHS and ammonia water with a concentration of 6 wt%, react for 40 minutes, and magnetically transfer the reacted rGO/Fe 3 O 4 /Cu 2 O and rGO/Fe 3 O 4 /Cu 2 O -Cu 9 S 8 magnetic composite nano-materials are adsorbed and separated, the resulting magnetic hybrid nano-materials are re-dispersed in ultrapure water, and 13 ⁇ L of the resulting dispersion is dripped on the surface of the electrode obtained in step (3), and the resulting electrode is electrically charged.
  • concentrations 0.5 nM, 1 nM, 10 nM, 100 nM, 1000 nM, 10000 nM, 100000
  • Example 2 the rGO/Fe 3 O 4 /Cu 2 O prepared in Example 1 and the nano-material rGO/Fe 3 O 4 / Cu 2 O obtained in the step (4) of Example 1 were studied by XPS measurement.
  • the XPS spectra confirmed the coexistence of Cu and O in the composite material before the reaction with NaHS. From the Cu 2p XPS spectrum, we can see that the XPS spectrum of the composite material has two peaks at 931.5eV and 951eV, which belong to Cu 2p1/2 and Cu 2p3/2 respectively .
  • the binding energy of 2p orbital basically matches Cu + .
  • the two peaks at 942.5 eV and 961.5 eV are attributed to the satellite peaks of Cu 2+ , and the two independent peaks at 931.1 eV and 950.4 eV binding energy are attributed to Cu 2p3/2 and Cu 2p1/2 respectively , which correspond to Cu + 2p orbital binding energy.
  • S 2p3/2 and S 2p1/2 of element S appear in the range of 159 eV-162 eV, and the peak at 167.8 eV is designated as the oxidation state orbital binding energy of S 2-.
  • the composition of the composite material after the reaction is rGO/Fe 3 O 4 /Cu 2 O-Cu 9 S 8 .
  • the material is modified on the electrode surface and the arc radius is found to be larger than rGO/Fe 3 O 4 /Cu 2 O, indicating that rGO/Fe 3 O 4 /Cu
  • the surface charge mobility of 2 O-Cu 9 S 8 is lower than that of rGO/Fe 3 O 4 /Cu 2 O.
  • the cyclic voltammetry (CV) diagrams of different modified electrodes are observed.
  • the changes of CV diagrams of different modified electrodes correspond to the change trend of EIS, which proves that rGO/Fe 3 O 4 /
  • the electrochemical signal of Cu 2 O-Cu 9 S 8 is weaker than that of rGO/Fe 3 O 4 /Cu 2 O.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Molecular Biology (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Compounds Of Iron (AREA)

Abstract

一种内源性H2S检测的电化学传感器的构建方法，属于电化学分析技术领域。包括：制备rGO/Fe3O4/Cu2O磁性纳米材料，并与H2S反应生成具有空穴结构的硫铜化合物rGO/Fe3O4/Cu2O-Cu9S8，利用rGO/Fe3O4/Cu2O-Cu9S8电化学信号弱的特点，构建了以rGO/Fe3O4/Cu2O和H2S(NaHS)为体系的电化学传感器，传感器具有检测限低、准确度高等优点，在内源性H2S的检测方面具有很好的应用前景。

Description

检测内源性H2S的电化学传感器的构建方法及其应用 技术领域
本发明属于电化学分析技术领域，尤其是涉及一种检测内源性H 2S的电化学传感器的构建方法。
背景技术
自然环境中的硫化氢气体是一种高危气体，在化学功能方面硫化氢是一种酸性腐蚀气体，在物理方面是一种易爆易燃气体，在生物方面是一种神经麻醉剂，导致人休克。但是，在生物体内，硫化氢已被证明对维持机体健康和处理疾病方面具有许多重要的作用。生物体内的H 2S主要由胱硫醚-β-合成酶（CBS），胱硫醚-γ-裂解酶（CSE），真菌/酵母巯基丙酮酸硫基转移酶（3-MST）三种酶催化胱氨酸（Cys）产生的。在正常的生物系统中，H 2S的存在有助于维持健康平衡的生理活动，但是一旦H 2S在生命体内的含量失衡，就标志着某些疾病的发生，例如宫颈癌、结肠癌以及一些肺部疾病等。因此，大量研究人员将H 2S作为某种生物指标去衡量健康状态，从而，对H 2S的检测尤为重要。
目前现有的检测方法主要有荧光法，色谱法，表面增强拉曼散射光谱法等，但是，这些法存在检测受环境影响大，检测仪器昂贵，操作繁琐等缺点。与这些检测方法相比较，电化学方法由于其灵敏度高、易操作、仪器简单等特点引起了人们的广泛关注。例如采用二茂铁，Ag NPs的作为电化学信标，通过硫氢化钠，硫化钠作为H 2S的替代物与信标发生化学反应从而影响电化学信号，来达到检测H 2S的目的。
在弱碱性的环境下，Cu 2O与H 2S发生氧化还原反应，生成具有空穴结构的硫铜化合物影响其电化学响应。同时，为了简化材料的收集以及电极的修饰过程，在传感器材料上映入了具有磁性的Fe 3O 4和可以改善电子传导的二维材料rGO，制备了rGO/Fe 3O 4/Cu 2O材料。利用其修饰传感器去检测外源性和内源性的H 2S得到的很好的应用。
技术问题
在此处键入技术问题描述段落。
 技术解决方案
在此处键入技术解决方案描述段落。本申请针对现有技术的不足，本发明提供了一种内源性H 2S检测的电化学传感器的构建方法及其应用。本发明操作简易，绿色无污染，灵敏度高。
本发明的技术方案如下：
一种内源性H 2S检测的电化学传感器的构建方法，所述构建方法包括如下步骤：
（1）磁性还原氧化石墨烯（rGO/Fe 3O 4）的合成：
将还原氧化石墨烯加入乙二醇中，混合溶解后加入乙酰丙酮铁，并将混合液超声处理30-40min，随后加入1.4-1.6g的乙酸胺，搅拌30-50min后，将搅拌所得混合液转移到反应釜中，190-210℃反应22-26 h，反应结束后冷却至室温，随后进行固液分离取固相，后用水和乙醇清洗固相，并用水重新将所得固相溶解分散，定容至浓度为2-4mg/mL，制得磁性还原氧化石墨烯溶液，即rGO/Fe 3O 4溶液；
（2）rGO/Fe 3O 4/Cu 2O溶液的合成：
将步骤（1）中所得rGO/Fe 3O 4溶液，加入到0.01-0.012g/mL的硝酸铜溶液中，超声处理30-40min，混合均匀，之后边搅拌边加入80-100µL 0.035-0.04mol/L的NaOH溶液，并持续搅拌30-50min，随后加入400-450mL 85-90mol/L的水合肼溶液并搅拌40-50min，随后固液分离取固相，将固相用水洗涤干燥，最后重新分散在水中，即得2-3mg/ml的rGO/Fe 3O 4/Cu 2O溶液；
（3）MGCE电极预处理：
将直径为4-10mm的 MGCE先后在粉末粒径为0.4-0.6mm和0.025-0.03mm的氧化铝粉上分别进行打磨，然后用乙醇和水清洗打磨后的电极，测裸电极的循环伏安曲线，当氧化峰和还原峰电位差小于90mV时即为打磨结束，之后再用乙醇和水清洗打磨后的电极，将清洗干净的电极用氮气或者氩气吹干待用；
（4）电化学传感器的构建：
取一定量步骤（2）所得的rGO/Fe 3O 4/Cu 2O分散液，加入一系列不同浓度的NaHS和浓度为5-7wt%的氨水，反应一定时间，将反应后的磁性混合纳米材料用磁铁吸附住，去除上清液，从而将磁性混合纳米材料分离出来，并将磁性混合纳米材料重新溶解分散在超纯水中，然后取一定量所得溶液滴涂在步骤（3）中所得电极表面，对所得电极进行电化学扫描，记录信号变化，建立反应后磁性混合纳米材料的电化学信号和NaHS浓度间的标准曲线。
步骤（1）中所述还原氧化石墨烯的乙二醇溶液浓度为1-2w/v%，其中还原氧化石墨烯、乙酰丙酮铁与乙酸胺的质量比为30-60: 15-35:100-180。
步骤（2）中还原氧化石墨烯分散液、硝酸铜溶液、NaOH溶液与水合肼溶液的体积用量比为0.2-1.2:5-15:0.04-0.16:200-600。
步骤（3）中所述电化学扫描的电压范围为-0.5v-0.3v。
步骤（4）中所述电化学传感器的构建，具体步骤如下：平行取5-12份20-30µL步骤（2）所得的rGO/Fe 3O 4/Cu 2O分散液置于离心管中，并分别加入100-150µL不同浓度的NaHS溶液，同时加入20-30µL浓度为5-7wt%的氨水，反应50-70min，分别将反应后的磁性混合纳米材料分离出来，取出来以后分别重新分散在20-30µL超纯水中，然后取8-12µL所得分散液滴涂在步骤（3）中所得电极表面，进行电化学扫描，记录信号变化，建立磁性混合纳米材料的电化学信号和NaHS浓度间的标准曲线。
所述NaHS溶液的浓度范围为0.5-100000nM。
所述磁性混合纳米材料为rGO/Fe 3O 4/Cu 2O与rGO/Fe 3O 4/Cu 2O-Cu 9S 8纳米材料的混合物。
一种内源性H 2S检测的电化学传感器，所述电化学传感器应用于内源性H 2S的检测。
有益效果
本发明有益的技术效果在于：
1、在构建的电化学传感器中，所用的纳米材料成本低廉，且简单易得。
2、本发明的原理是，利用电活性材料rGO/Fe 3O 4/Cu 2O与NaHS发生氧化还原反应，生成具有空穴结构的硫铜化合物rGO/Fe 3O 4/Cu 2O-Cu 9S 8，该硫铜化合物的电化学信号比rGO/Fe 3O 4/Cu 2O的电化学信号弱，反应过程中随着rGO/Fe 3O 4/Cu 2O-Cu 9S 8的增多，rGO/Fe 3O 4/Cu 2O量减少，使得整体磁性混合纳米材料的电化学信号减弱，通过建立整体磁性混合纳米材料电化学信号和NaHS浓度间的标准曲线，最终以达到检测H 2S的目的，实验原理简单。
3、现有的检测H 2S方法主要为亚甲基蓝法（检测限大约为8μM，检测范围25μM-1000μM），而与亚甲基蓝法相比，本电化学传感器的检测限为 230 pM，检测范围为 500 pM-500 μM，由此可见本发明的检测限较低，检测范围广且灵敏度高。
4、本发明中通过引入Fe 3O 4，利用材料的磁性吸附在磁电极表面，极大地简化了电极修饰的步骤，减少了电极修饰的成本，同时降低了传统电极修饰过程的所带来的误差。同时，由于材料具有磁性，可以重复收集检测，检测结果的重现性高。
5、还原氧化石墨烯改善传感器的电子传导能力，使结果更准确。
 附图说明
在此处键入附图说明描述段落。图1是实施例1制备所得中间产物rGO/Fe 3O 4/Cu 2O、反应最终混合物rGO/Fe 3O 4/Cu 2O和rGO/Fe 3O 4/Cu 2O -Cu 9S 8磁性复合纳米材料的XRD图谱；
图2是实施例1制备所得中间产物rGO/Fe 3O 4/Cu 2O、反应最终混合物rGO/Fe 3O 4/Cu 2O和rGO/Fe 3O 4/Cu 2O -Cu 9S 8磁性复合纳米材料的XPS图谱；
图3是实施例1中制备所得电化学传感器的交流阻抗图和循环伏安（CV）图；
图4是电化学传感器的DPV图谱和验证紫外图谱；
图5是实施例1制备得到的电化学传感器测得反应后的rGO/Fe 3O 4/Cu 2O和rGO/Fe 3O 4/Cu 2O-Cu 9S 8磁性混合纳米材料的电化学信号，随着NaHS浓度变化的DPV曲线图，以及在峰电流值与 NaHS 浓度对数值之间建立的标准曲线图。
本发明的最佳实施方式
在此处键入本发明的最佳实施方式描述段落。
 本发明的实施方式
下面结合附图和实施例，对本发明进行具体描述。
实施例1：
（1）磁性还原氧化石墨烯（rGO/Fe 3O 4）的合成：
将0.45g还原氧化石墨烯加入乙二醇中，混合溶解后加入0.23g乙酰丙酮铁，并将混合液超声处理30min，随后加入1.49g的乙酸胺，搅拌30min后，将搅拌所得混合液转移到反应釜中，200℃反应24h；反应结束后冷却至室温，随后进行固液分离取固相，后用水和乙醇清洗固相，并用水重新将所得固相溶解分散，定容至浓度为3 mg/mL，即得磁性还原氧化石墨烯（rGO/Fe 3O 4）溶液；
（2）rGO/Fe 3O 4/Cu 2O溶液的合成：
将步骤（1）中制备得到的1 mL rGO/Fe 3O 4溶液加入到10 mL浓度为0.01g/mL的硝酸铜溶液中，在室温下超声30 min，使溶液充分混合均匀，结束超声。在搅拌的作用下，将80 µL浓度为0.035 M的NaOH溶液加入到混合体系中持续搅拌30 min，接下来将400 mL浓度为85 mM的水合肼加入到溶液中，在室温下搅拌40 min，随后固液分离取固相，将固相用水洗涤干燥，最后重新分散在水中，即得2 mg/mL的rGO/Fe 3O 4/Cu 2O溶液，并利用XRD扫描仪对rGO/Fe 3O 4/Cu 2O产物进行结构表征，结果见图1（1）。
（3）MGCE电极预处理：
将直径为4mm的 MGCE先后在粉末粒径为0.5mm和0.03mm的氧化铝粉上分别进行打磨，然后用乙醇和水清洗打磨后的电极，测裸电极的CV曲线，当氧化峰和还原峰电位差为85mV时打磨结束，之后再用乙醇和水清洗打磨后的电极，将清洗干净的电极用氮气或者氩气吹干待用；
（4）电化学传感器的构建：
在已构建好的电化学传感器体系中，加入20 μL 步骤（2）所得的rGO/Fe 3O 4/Cu 2O溶液，加入一系列不同浓度（0.5 nM， 1 nM，10 nM， 100 nM， 1000 nM， 10000 nM， 100000 nM）的NaHS和浓度为5wt%的氨水，反应50 min，利用磁性将反应后的rGO/Fe 3O 4/Cu 2O和rGO/Fe 3O 4/Cu 2O-Cu 9S 8磁性复合纳米材料吸附分离出来，将所得混合纳米材料重新分散在超纯水中，取10 μL所得分散液滴涂在步骤（3）中所得电极表面，对所得电极进行电化学扫描，记录信号变化，建立反应后的rGO/Fe 3O 4/Cu 2O和rGO/Fe 3O 4/Cu 2O-Cu 9S 8磁性混合纳米材料的电化学信号和NaHS浓度间的标准曲线，结果如图5所示，在500 pM-500 μM浓度范围内，随着 NaHS 的浓度的不断增大，rGO/Fe 3O 4/Cu 2O 修饰电极的电化学信号逐渐降低。在峰电流和NaHS 的浓度对数之间建立标准曲线，Ip =5.96 lg[NaHS]-61.61，其线性相关系数R 2= 0.99275。利用检测空白组得出标准偏差乘3得出最低检测限为 230 pM。由此可见本发明所设计的电化学生物传感器对检测H 2S，不但具有较宽的检测范围，而且有较高的灵敏度。
实施例2
（1）磁性还原氧化石墨烯（rGO/Fe 3O 4）的合成：
将0.3g还原氧化石墨烯加入乙二醇中，混合溶解后加入0.15g乙酰丙酮铁，并将混合液超声处理40 min，随后加入1.6 g的乙酸胺，搅拌50min后，将搅拌所得混合液转移到反应釜中，210℃反应26 h；反应结束后冷却至室温，接着进行固液分离，取固相，后用水和乙醇清洗固相，随后用水重新将固体溶解，将溶液定容至4 mg/mL的溶液；
（2）rGO/Fe 3O 4/Cu 2O溶液的合成：
将步骤（1）中所得1 mL磁性还原氧化石墨烯（rGO/Fe 3O 4）分散液，加入到0.012 g/mL的硝酸铜溶液中，超声处理40 min，混合均匀，之后边搅拌边加入100 µL 0.04 mol/L的NaOH溶液，并持续搅拌50 min，随后加入450 mL 90 mol/L的水合肼溶液并搅拌50 min，随后固液分离取固相，将固相用水洗涤干燥，最后重新分散在水中，即得3 mg/mL的rGO/Fe 3O 4/Cu 2O溶液；
（3）MGCE电极预处理：
将直径为10 mm的 MGCE先后在0.6mm和0.025mm的氧化铝粉上进行打磨，然后用乙醇和水清洗打磨后的电极，测裸电极的CV曲线，当氧化峰和还原峰电位差83 mV时打磨结束。之后再用乙醇和水清洗打磨后的电极，将清洗干净的电极用氮气或者氩气吹干待用；
（4）电化学传感器的构建：
在已构建好的电化学传感器体系中，15 μL步骤（2）所得的rGO/Fe 3O 4/Cu 2O溶液，加入一系列不同浓度（0.5 nM， 1 nM，10 nM， 100 nM， 1000 nM， 10000 nM， 100000 nM）的NaHS和浓度为7 wt%的氨水，反应60 min，利用磁性将反应后的rGO/Fe 3O 4/Cu 2O和rGO/Fe 3O 4/Cu 2O-Cu 9S 8磁性复合纳米材料吸附分离出来，将所得磁性混合纳米材料重新分散在超纯水中，取8 μL所得分散液滴涂在步骤（3）中所得电极表面，对所得电极进行电化学扫描，记录信号变化，建立反应后的rGO/Fe 3O 4/Cu 2O和rGO/Fe 3O 4/Cu 2O-Cu 9S 8磁性混合纳米材料的电化学信号和NaHS浓度间的标准曲线。
实施例3
（1）磁性还原氧化石墨烯（rGO/Fe 3O 4）的合成：
将0.6g还原氧化石墨烯加入乙二醇中，混合溶解后加入0.35g乙酰丙酮铁，并将混合液超声处理35 min，随后加入1.4g的乙酸胺，搅拌40 min后，将搅拌所得混合液转移到反应釜中，190℃反应22 h；反应结束后冷却至室温，接着进行固液分离，取固相，后用水和乙醇清洗固相，随后用水重新将固体溶解，将溶液定容至2mg/ml的分散液，然后冷藏备用；
（2）rGO/Fe 3O 4/Cu 2O溶液的合成：
将步骤（1）中所得1 mL磁性还原氧化石墨烯（rGO/Fe 3O 4）分散液，加入到0.011 g/mL的硝酸铜溶液中，超声处理35 min，混合均匀，之后边搅拌边加入90 µL 0.037 mol/L的NaOH溶液，并持续搅拌40 min，随后加入430 mL 87 mol/L的水合肼溶液并搅拌45 min，随后固液分离取固相，将固相用水洗涤干燥，最后重新分散在水中，即得2.5 mg/mL的rGO/Fe 3O 4/Cu 2O溶液；
（3）MGCE电极预处理：
将直径为6mm的 MGCE先后在0.4mm和0.027mm的氧化铝粉上进行打磨，然后用乙醇和水清洗打磨后的电极，测裸电极的CV曲线，当氧化峰和还原峰电位差82 mV时即为打磨结束，之后再用乙醇和水清洗打磨后的电极，将清洗干净的电极用氮气或者氩气吹干待用；
（4）电化学传感器的构建：
在已构建好的电化学传感器体系中，25 μL步骤（2）所得的rGO/Fe 3O 4/Cu 2O溶液，加入一系列不同浓度（0.5 nM， 1 nM，10 nM， 100 nM， 1000 nM， 10000 nM， 100000 nM）的NaHS和浓度为6 wt%的氨水，反应40分钟，利用磁性将反应后的rGO/Fe 3O 4/Cu 2O和rGO/Fe 3O 4/Cu 2O-Cu 9S 8磁性复合纳米材料吸附分离出来，将所得磁性混合纳米材料重新分散在超纯水中，取13 μL所得分散液滴涂在步骤（3）中所得电极表面，对所得电极进行电化学扫描，记录信号变化，建立反应后的rGO/Fe 3O 4/Cu 2O和rGO/Fe 3O 4/Cu 2O-Cu 9S 8磁性混合纳米材料的电化学信号和NaHS浓度间的标准曲线。
测试例
1，实施例1中制备得到中间产物rGO/Fe 3O 4/Cu 2O、反应最终混合物rGO/Fe 3O 4/Cu 2O和rGO/Fe 3O 4/Cu 2O -Cu 9S 8磁性复合纳米材料的表征
A，利用XRD扫描仪对实施例1中制备得到的rGO/Fe 3O 4/Cu 2O产物进行结构表征，结果见图1（1），其中在X射线衍射图谱中，发现所得 rGO/Fe 3O 4/Cu 2O中的Cu 2O峰与标准立方体的 Cu 2O 很好地匹配，初步说明反应后产物得到的是rGO/Fe 3O 4/Cu 2O；同时利用XRD扫描仪对实施例1步骤（4）中rGO/Fe 3O 4/Cu 2O与NaHS反应过后的反应产物进行结构表征，所得结果见图1（2），其中，反应所得产物的X-射线衍射峰通过与标准的Cu 9S 8对比，发现所得反应产物中的峰与其匹配，初步可知得出反应后的样品为rGO/Fe 3O 4/Cu 2O -Cu 9S 8。
B，同时，通过XPS测量研究了实施例1中制备得到的rGO/Fe 3O 4/Cu 2O和实施例1步骤（4）中反应得到的纳米材料rGO/Fe 3O 4/ Cu 2O-Cu 9S 8中元素的化学组成和化学状态的变化；如图2（1）、（2）所示，研究XPS图谱证实了与NaHS反应前复合材料中Cu元素和O元素的共存。从中的Cu 2p XPS图谱中，我们可以看出复合材料的XPS光谱在931.5eV和951eV出现两个峰，分别属于Cu 2p1/2和Cu 2p3/2，2p轨道的结合能基本与Cu +相匹配。此外，在530 eV 出现一个宽峰，与O的1s轨道结合能相匹配。在材料与NaHS反应后，进一步的研究复合材料的XPS，结果如图2（3）、（4）所示，XPS图谱显示复合材料中Cu元素，O元素和S元素的共存，这与XRD的结果相复合。从Cu 2p XPS 图谱中可以看出，在933 eV和954 eV出现两个峰分别归属于Cu 2+的Cu 2p3/2和Cu 2p1/2轨道结合能。在942.5 eV和961.5 eV的两个峰归属于Cu 2+的卫星峰，位于931.1 eV和950.4 eV结合能的两个独立峰分别归因于Cu 2p3/2和Cu 2p1/2，它们对应于Cu + 2p轨道结合能。在S 2p的XPS图谱中在159 eV-162eV范围内出现了S元素的S 2p3/2和 S 2p1/2而在 167.8 eV处的峰值指定为S 2-的氧化态轨道结合能。综上进一步的证明了反应后复合材料的组成为rGO/Fe 3O 4/Cu 2O-Cu 9S 8。
2，为了达到电化学检测的目的，研究了反应前后材料的电化学性质，利用软件中的等效电路去处理交流阻抗数据得到传感器在0.1 M [Fe(CN) 6] 3-/4-溶液中的电子转移动力学图谱。如图3（1）所示，裸的 MGCE 呈现几乎平滑的直线，然而， MGCE/rGO/Fe 3O 4/Cu 2O可以观察到一个半弧形，说明 rGO/Fe 3O 4/Cu 2O 的存在阻碍了电子的传导，更进一步，与 NaHS反应后，将材料修饰在电极表面发现其圆弧半径要大于 rGO/Fe 3O 4/Cu 2O ，说明rGO/Fe 3O 4/Cu 2O-Cu 9S 8表面电荷的迁移率低于rGO/Fe 3O 4/Cu 2O。相应的，如图3（2）所示，不同修饰电极对应的循环伏安（CV）图，观察发现不同修饰电极的 CV图变化与EIS的变化趋势相照应，证明rGO/Fe 3O 4/Cu 2O-Cu 9S 8的电化学信号比rGO/Fe 3O 4/Cu 2O弱。
3，电化学传感器的验证紫外图谱和DPV图谱
为了更加进一步的准确检测内源性硫化氢，记录了rGO/Fe 3O 4/Cu 2O与NaHS反应前后紫外吸收变化，其结果如图4所示，发现在电压为-0.1 伏，rGO/Fe 3O 4/Cu 2O修饰的电极具有明显的DPV电流响应。rGO/Fe 3O 4/Cu 2O和500 µM的NaHS反应过后，利用磁性分离材料，用超水洗涤材料去除未反应的S 2-，重新定容，修饰在电极表面在-0.5伏~0.3伏的扫描范围，扫描DPV，发现电化学信号发生了明显的下降。同时，利用紫外吸收光谱研究实施例1中rGO/Fe 3O 4/Cu 2O纳米材料与NaHS反应前后光学性质的变化，如图4（2）所示，与rGO/Fe 3O 4/Cu 2O在500 nm处出现肩峰以及在及近红外区域（500-1000 nm）具有向下倾斜曲线相比，与500 nm的NaHS反应过后，混合物的吸收强度增大，同时随着波长的增加而表现出一种近红外区域的钩状吸收。
工业实用性
在此处键入工业实用性描述段落。
 序列表自由内容
在此处键入序列表自由内容描述段落。

Claims (7)

  1. 一种内源性H 2S检测的电化学传感器的构建方法，其特征在于，所述构建方法包括如下步骤：
    （1）磁性还原氧化石墨烯的合成：
    将还原氧化石墨烯加入乙二醇中，混合溶解后加入乙酰丙酮铁，并将混合液超声处理30-40min，随后加入1.4-1.6g的乙酸胺，搅拌30-50min后，将搅拌所得混合液转移到反应釜中，190-210℃反应22-26 h，反应结束后冷却至室温，随后进行固液分离取固相，后用水和乙醇清洗固相，并用水重新将所得固相溶解分散，定容至浓度为2-4mg/mL，制得磁性还原氧化石墨烯溶液，即rGO/Fe 3O 4溶液；
    （2）rGO/Fe 3O 4/Cu 2O溶液的合成：
    将步骤（1）中所得rGO/Fe 3O 4溶液，加入到0.01-0.012g/mL的硝酸铜溶液中，超声处理30-40min，混合均匀，之后边搅拌边加入80-100µL 0.035-0.04mol/L的NaOH溶液，并持续搅拌30-50min，随后加入400-450mL 85-90mol/L的水合肼溶液并搅拌40-50min，随后固液分离取固相，将固相用水洗涤干燥，最后重新分散在水中，即得2-3mg/ml的rGO/Fe 3O 4/Cu 2O溶液；
    （3）磁性玻碳电极MGCE预处理：
    将直径为4-10mm的 MGCE先后在粉末粒径为0.4-0.6mm和0.025-0.03mm的氧化铝粉上分别进行打磨，然后用乙醇和水清洗打磨后的电极，测裸电极的循环伏安曲线，当氧化峰和还原峰电位差小于90mV时即为打磨结束，之后再用乙醇和水清洗打磨后的电极，将清洗干净的电极用氮气或者氩气吹干待用；
    （4）电化学传感器的构建：
    取一定量步骤（2）所得的rGO/Fe 3O 4/Cu 2O溶液，加入一系列不同浓度的NaHS和浓度为5-7wt%的氨水，反应一定时间，将反应后的磁性混合纳米材料用磁铁吸附住，去除上清液，从而将磁性混合纳米材料分离出来，并将磁性混合纳米材料重新溶解分散在超纯水中，然后取一定量所得溶液滴涂在步骤（3）中所得电极表面，对所得电极进行电化学扫描，记录信号变化，建立反应后磁性混合纳米材料的电化学信号和NaHS浓度间的标准曲线；
    所述磁性混合纳米材料为rGO/Fe 3O 4/Cu 2O与rGO/Fe 3O 4/Cu 2O-Cu 9S 8纳米材料的混合物。
  2. 根据权利要求1所述的构建方法，其特征在于，步骤（1）中所述含有还原氧化石墨烯的乙二醇溶液浓度为1-2w/v%，其中还原氧化石墨烯、乙酰丙酮铁与乙酸胺的质量比为30-60: 15-35:100-180。
  3. 根据权利要求1所述的构建方法，其特征在于，步骤（2）中还原氧化石墨烯分散液、硝酸铜溶液、NaOH溶液与水合肼溶液的体积用量比为0.2-1.2:5-15:0.04-0.16:200-600。
  4. 根据权利要求1所述的构建方法，其特征在于，步骤（3）中所述电化学扫描的电压范围为-0.5v-0.3v。
  5. 根据权利要求1所述的构建方法，其特征在于，步骤（4）中所述电化学传感器的构建，具体步骤如下：平行取5-12份20-30µL步骤（2）所得的rGO/Fe 3O 4/Cu 2O分散液置于离心管中，并分别加入100-150µL不同浓度的NaHS溶液，同时加入20-30µL浓度为5-7wt%的氨水，反应50-70min，分别将反应后的磁性混合纳米材料分离出来，取出来以后分别重新分散在20-30µL超纯水中，然后取8-12µL所得分散液滴涂在步骤（3）中所得电极表面，进行电化学扫描，记录信号变化，建立磁性混合纳米材料的电化学信号和NaHS浓度间的标准曲线。
  6. 根据权利要求5所述的构建方法，其特征在于，所述NaHS溶液的浓度范围为0.5-100000nM。
  7. 一种权利要求1所述构建方法制得的内源性H 2S检测的电化学传感器，其特征在于，所述电化学传感器应用于内源性H 2S的检测。
PCT/CN2020/102261 2019-09-12 2020-07-16 检测内源性h2s的电化学传感器的构建方法及其应用 WO2021047283A1 (zh)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN201910862438.3 2019-09-12
CN201910862438.3A CN110554074B (zh) 2019-09-12 2019-09-12 检测内源性h2s的电化学传感器的构建方法及其应用

Publications (1)

Publication Number Publication Date
WO2021047283A1 true WO2021047283A1 (zh) 2021-03-18

Family

ID=68740045

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/CN2020/102261 WO2021047283A1 (zh) 2019-09-12 2020-07-16 检测内源性h2s的电化学传感器的构建方法及其应用

Country Status (2)

Country Link
CN (1) CN110554074B (zh)
WO (1) WO2021047283A1 (zh)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110554074B (zh) * 2019-09-12 2020-06-30 江南大学 检测内源性h2s的电化学传感器的构建方法及其应用
CN110615693B (zh) * 2019-09-19 2022-03-08 中国科学院合肥物质科学研究院 一种硫化氢气体传感材料、传感器及制备方法与使用方法

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108226234A (zh) * 2018-03-27 2018-06-29 上海第二工业大学 一种基于CuO/CuFe2O4气敏材料的H2S气体传感器的制备方法
CN109507267A (zh) * 2018-11-27 2019-03-22 临沂大学 用于生物硫化氢快捷检测的传感材料及其制备方法
CN109916966A (zh) * 2019-02-26 2019-06-21 华南理工大学 一种α-Fe2O3/TiO2纳米复合材料及由其制备的H2S气敏传感器
CN110554074A (zh) * 2019-09-12 2019-12-10 江南大学 一种内源性h2s检测的电化学传感器的构建方法及其应用

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20190107502A1 (en) * 2017-10-06 2019-04-11 William N. Carr Pixel for Thermal Transport and Electrical Impedance Sensing
CN105806815B (zh) * 2016-03-14 2019-04-05 首都师范大学 一种检测硫化氢的荧光纳米探针及其制备方法与应用
CN105928914B (zh) * 2016-04-15 2019-09-27 安徽师范大学 硫化氢检测传感器及其制备方法、硫化氢的定量检测方法和细胞内硫化氢的定性检测方法
US10830722B2 (en) * 2017-01-09 2020-11-10 King Abdullah Unviersity Of Science And Technology Gas sensors and methods of detecting gas
CN106885830B (zh) * 2017-01-24 2019-04-26 临沂大学 一种低温硫化氢气敏材料及制备方法
CN108802120A (zh) * 2018-05-25 2018-11-13 江南大学 一种基于Au@Ag核壳纳米粒子电化学检测硫化氢的方法
CN109540976B (zh) * 2018-11-27 2021-07-23 临沂大学 生物硫化氢快速检测元件的制备方法

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108226234A (zh) * 2018-03-27 2018-06-29 上海第二工业大学 一种基于CuO/CuFe2O4气敏材料的H2S气体传感器的制备方法
CN109507267A (zh) * 2018-11-27 2019-03-22 临沂大学 用于生物硫化氢快捷检测的传感材料及其制备方法
CN109916966A (zh) * 2019-02-26 2019-06-21 华南理工大学 一种α-Fe2O3/TiO2纳米复合材料及由其制备的H2S气敏传感器
CN110554074A (zh) * 2019-09-12 2019-12-10 江南大学 一种内源性h2s检测的电化学传感器的构建方法及其应用

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
ATAROD MONIREH; NASROLLAHZADEH MAHMOUD; MOHAMMAD SAJADI S.: "Green synthesis of Pd/RGO/Fe3O4nanocomposite usingWithania coagulansleaf extract and its application as magnetically separable and reusable catalyst for the reduction of 4-nitrophenol", JOURNAL OF COLLOID AND INTERFACE SCIENCE, ACADEMIC PRESS,INC., US, vol. 465, 2 December 2015 (2015-12-02), US, pages 249 - 258, XP029383226, ISSN: 0021-9797, DOI: 10.1016/j.jcis.2015.11.060 *
LIU LINGYU, ZHU XUDONG, ZENG YANBO, WANG HAILONG, LU YIXIA, ZHANG JIAN, YIN ZHENGZHI, CHEN ZHIDONG, YANG YIWEN, LI LEI: "An Electrochemical Sensor for Diphenylamine Detection Based on Reduced Graphene Oxide/Fe3O4-Molecularly Imprinted Polymer with 1,4-Butanediyl-3,3’-bis-l-vinylimidazolium Dihexafluorophosphate Ionic Liquid as Cross-Linker", POLYMERS, vol. 10, no. 12, pages 1329, XP055790077, DOI: 10.3390/polym10121329 *

Also Published As

Publication number Publication date
CN110554074A (zh) 2019-12-10
CN110554074B (zh) 2020-06-30

Similar Documents

Publication Publication Date Title
Zhou et al. Enhanced electrochemical performance for sensing Pb (II) based on graphene oxide incorporated mesoporous MnFe2O4 nanocomposites
Zhang et al. A non-enzymatic electrochemical biosensor based on Au@ PBA (Ni–Fe): MoS 2 nanocubes for stable and sensitive detection of hydrogen peroxide released from living cells
WO2021047283A1 (zh) 检测内源性h2s的电化学传感器的构建方法及其应用
Ensafi et al. Nickel-ferrite oxide decorated on reduced graphene oxide, an efficient and selective electrochemical sensor for detection of furazolidone
CN110133082B (zh) 一种适体传感器用电极材料，电化学适体传感器及其制备方法
Teng et al. Electrochemical detection of mobile zinc ions for early diagnosis of prostate cancer
Ensafi et al. Electrochemical sensing of flutamide contained in plasma and urine matrices using NiFe2O4/rGO nanocomposite, as an efficient and selective electrocatalyst
CN110618272B (zh) 一种汞离子荧光/电化学传感器的制备方法及其应用
Taei et al. Simultaneous determination of sunset yellow and tartrazine in soft drinks samples using nanocrystallites of spinel ferrite-modified electrode
Dinesh et al. Birnessite MnO2 decorated MWCNTs composite as a nonenzymatic hydrogen peroxide sensor
CN111707719A (zh) 聚l-半胱氨酸和还原氧化石墨烯负载纳米银修饰的玻碳电极及其应用
Khan et al. Electrochemiluminescence behaviour of silver/ZnIn2S4/reduced graphene oxide composites quenched by Au@ SiO2 nanoparticles for ultrasensitive insulin detection
Zeng et al. Design and synthesis of a vanadate-based ratiometric fluorescent probe for sequential recognition of Cu 2+ ions and biothiols
Mounesh et al. Detection of nanomolar concentrations H2O2 Using cobalt (II) phthalocyanine modified GCE with MWCNTs
CN109813787B (zh) 一种MnO2/Fe2O3@无定形碳复合材料、核酸适体传感器及其制备方法和应用
Xiao et al. The functionalization of gold nanoparticles as a novel platform for the highly efficient electrochemical detection of silver ions
Hasanpour et al. NiMnO3 nanoparticles anchored on graphene quantum dot: Application in sensitive electroanalysis of dobutamine
CN104090009B (zh) 一种基于石墨烯纳米片改性电极的电化学传感器的制备方法
Manjula et al. Electrochemical sensors for β-adrenoceptor agonist isoprenaline analysis in human urine and serum samples using manganese cobalt oxide-modified glassy carbon electrode
CN109781814A (zh) 一种光增强电化学传感器及其制备方法和应用
CN110927233A (zh) 一种检测肾上腺素的电化学传感器及其制备方法和应用
CN112362712B (zh) 一种可同时检测粮食中重金属铅和镉离子的电化学传感器电极
Yao et al. Preparation of Horseradish Peroxidase Modified Gold Nanoparticle/Coiled Carbon Nanotube Nanocomposite and its application for bromate and nitrite determination
Shen et al. Polypyrrole hollow nanotubes loaded with Au and Fe3O4 nanoparticles for simultaneous determination of ascorbic acid, dopamine, and uric acid
CN111474221B (zh) 一种基于金纳米笼/氟化石墨烯的电化学传感器及应用

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 20863631

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 20863631

Country of ref document: EP

Kind code of ref document: A1