Design, synthesis, and evaluation of novel arecoline-linked amino acid derivatives for insecticidal and antifungal activities.

A series of arecoline derivatives with amino acid moieties were designed and synthesised using an acylamide condensation strategy, taking arecoline as the foundational structure. The insecticidal efficacy of these compounds against Aphis craccivora and Tetranychus cinnabarinus was evaluated. Notably, derivatives 3h and 3i demonstrated superior insecticidal activity compared with arecoline. Additionally, 3h and 3i showed good fungicidal effectiveness against two types of plant fungi. Moreover, molecular docking analyses suggested that 3h and 3i could affect the nervous systems of A. craccivora and T. cinnabarinus by binding to neuronal nicotinic acetylcholine receptors. These findings suggest that compounds 3h and 3i represent promising leads for further development in insecticide and fungicide research.

Fluorescent Probes Based on Ag NPs@N/GQDs and Molecularly Imprinted Polymer for Sensitive Detection of Noradrenaline in Bananas.

Fluorescence intensity and selective recognition ability are crucial factors in determining the analytical techniques for fluorescent probes. In this study, a core-shell fluorescent material, composed of silver nanoparticles@nitrogen-doped graphene quantum dots (Ag NPs@N/GQDs), was synthesised using mango leaves as the raw material through a thermal cracking method, resulting in strong fluorescence luminescence intensity. By employing noradrenaline as a template molecule and using a surface molecular imprinting technique, a molecularly imprinted membrane (MIP) was formed on the surface of the fluorescent material, that was subsequently eluted to obtain a highly specific, fluorescent probe capable of recognising noradrenaline. The probe captured various concentrations of noradrenaline using the MIP, which decreased the fluorescence intensity. Then a method for detecting trace amounts of noradrenaline was established. This method exhibited a linear range from 0.5 -700 pM with a detection limit of 0.154 pM. The proposed method was implemented in banana samples. Satisfactory recoveries were confirmed at four different concentrations. The method presented a relative standard deviation (RSD) of less than 5.0%.

Anthracene-based dual channel donor-acceptor triazine-containing covalent organic frameworks for superior photoelectrochemical sensing.

Covalent organic frameworks (COFs) exhibit excellent photoelectrically active structures and serve as channels for photon capture and charge carrier transport. However, their relatively high charge-carrier recombination rates and lack of specific recognition sites limit their application in photoelectrochemical sensing. This paper reports a functionalized donor-acceptor (D-A) COF comprising electron-rich polycyclic aromatic moieties and electron-deficient triazines (Tz) incorporating boronic acid through ligand exchange. The number of aromatic rings in the polycyclic aromatic moiety is crucial for establishing an efficient D-A system within COF. In the absence of an external electron donor, the anthracene-based COF exhibited a five-fold enhancement in photocurrent compared to the naphthalene-based COF. The resulting anthracene-based D-A COF exhibited enhanced orbital overlap and electron push-pull interactions, facilitating more effective charge separation. Furthermore, introducing boronic acid enabled the selective enrichment of low-concentration external electron donors, such as dopamine, in the inner Helmholtz plane. This ingenious approach establishes a unique dual-channel D-A system that allows direct measurement of dopamine in serum. Under optimized conditions, the test platform achieves good correspondence for dopamine at 1 to 100 nM and 0.5 to 100 µM with a detecting limit of 0.36 nM (3σ/S, n = 11). This strategy introduces a novel dimension to photoelectrochemical sensing, focusing on the effect of spatial separation between the external electron donor and the photoelectrode interface that intricately shapes the behavior and enhances the performance of the photoelectric system.

Synergistic co-catalytic nanozyme system for highly efficient one-pot colorimetric sensing at neutral pH: Combining molybdenum trioxide and Fe(III)-Modified covalent triazine framework.

This study investigates the co-catalytic capabilities of MoO3 nanosheets in enhancing the enzyme-like catalytic activity of a two-dimensional ultrathin Fe(III)-modified covalent triazine framework (Fe-CTF) under neutral pH conditions. The unique physicochemical surface properties and two-dimensional structures of Fe-CTF enable the direct immobilization of native enzymes (glucose oxidase (GOD) and xanthine oxidase (XOD)) through adsorption, eliminating the need for chemical processes. Efficient immobilization of the native enzymes within the Fe-CTF/GOD(XOD) hybrid is achieved through multipoint attachment involving various interactions. The Fe-CTF/MoO3 co-catalytic system exhibits enzyme-mimicking activity at neutral pH and, when combined with the high catalytic activity of the immobilized native enzymes, enables the development of a colorimetric method for glucose detection. This method demonstrates excellent facilitation, rapidity, sensitivity, and selectivity, with a linear detection range of 50-1000 µM and a limit of detection of 8.8 µM for glucose. Furthermore, a straightforward one-pot colorimetric method is established for screening XOD inhibitors. The inhibitory potential of a crude extract derived from Chinese water chestnut peel on XOD activity is evaluated using this method. The findings of this study pave the way for the utilization of nanozyme/native enzyme hybrids in pH-neutral conditions for one-pot colorimetric sensing. This work contributes to the advancement of enzyme-based sensing technologies and holds promise for various applications in biosensing and biomedical research.

MOF@Au NPs/aptamer fluorescent probe for the selective and sensitive detection of thiamethoxam.

The luminescence performance of fluorescent reagents plays a crucial role in fluorescence analysis. Therefore, in this study, a novel bi-ligand Zn-based metal-organic framework, Au nanoparticle (NP) fluorescent material was synthesized using a hydrothermal method with Zn as the metal source. Simultaneously, a DNA aptamer was introduced as a molecular recognition element to develop a Zn-based MOF@Au NPs/DNA aptamer fluorescent probe for the ultra-trace detection of thiamethoxam residues in agricultural products. The probe captured different concentrations of the target molecule, thiamethoxam, through the DNA aptamer, causing a conformational change in the DNA aptamer and bursting the fluorescence of the probe, therefore establishing a fluorometric method for thiamethoxam detection. This method is highly sensitive due to the excellent luminescence properties of the Zn-based MOF@Au NPs, and the DNA aptamer can specifically recognize thiamethoxam, offering high selectivity. The linear range of the method was 2.5-6000 × 10-11  mol L-1 , with a detection limit of 8.33 × 10-12  mol L-1 . This method was applied to the determination of actual samples, such as bananas, and the spiked recovery rate was found to be in the range 84.05-109.07%. Overall, the proposed probe has high sensitivity, high selectivity, and easy operation for the detection of thiamethoxam residues in actual samples.

Electrochemical chiral sensor for levofloxacin detection base on Cu/Fe-BTC amplification.

The key to developing sensors for chiral drug determination is to exclude interference from enantiomers. In this study, metal-organic frameworks (MOFs) and molecularly imprinted polymer (MIP) were introduced to prepare a chiral sensor for levofloxacin detection. The MIP was electropolymerised on the surface of the Cu/Fe-benzene-1,3,5-tricarboxylate MOF (Cu/Fe-BTC)-modified Au electrode using levofloxacin as a template molecule. After eluting the levofloxacin, a chiral sensor with recognition sites for levofloxacin was obtained. With this site as a switch, a novel method for detecting levofloxacin was established. Because of the enhanced recognition effect, the sensor can effectively exclude the enantiomeric interference of d-ofloxacin. Moreover, Cu/Fe-BTC can effectively amplify the current response signal and improve the sensitivity of the sensor. The linear range of the sensor was 5 to 4000 × 10-11 mol L-1, and the detection limit was 2.07 × 10-11 mol L-1. When applied to detecting levofloxacin in actual samples, the sensor showed a 92.7-109.8% recovery.

Reusable molecularly imprinted electrochemiluminescence assay for kanamycin based on ordered mesoporous carbon loaded with indium oxide nanoparticles and carbon quantum dots.

A highly sensitive kanamycin electrochemiluminescence (ECL) switch sensor was constructed. A signal element consisting of ordered mesoporous carbon loaded with indium oxide nanoparticles/carbon quantum dots (OMC/In2O3/C-dots) was assembled on the surface of a gold electrode. Then, a molecularly imprinted polymer (MIP) was prepared on the modified electrode surface using kanamycin as the template molecule and o-aminophenol as the functional monomer. After kanamycin elution, the prepared sensor retained specific kanamycin recognition sites. OMC/In2O3 effectively amplified the ECL signal of the C-dots, thereby enhancing the detection sensitivity, whereas kanamycin quenched the signal. Therefore, the imprinted sites acted as a switch, providing a new method for detecting kanamycin. Under the optimal experimental conditions, the concentration of kanamycin was proportional to the degree of ECL quenching within a linear range of 5-4500 × 10-12 mol L-1 at 0.8 V (vs. Ag/AgCl electrode electrode), and the detection limit was 5.8 × 10-13 mol L-1. When applied to the detection of kanamycin in actual samples, such as chicken, duck, pork, and milk, the recovery for spiked samples was in the range 92.7-110%.

Correction: Microflower-like Co9S8@MoS2 heterostructure as an efficient bifunctional catalyst for overall water splitting.

[This corrects the article DOI: 10.1039/D2RA04086G.].

Microflower-like Co9S8@MoS2 heterostructure as an efficient bifunctional catalyst for overall water splitting.

The development of a distinguished and high-performance catalyst for H2 and O2 generation is a rational strategy for producing hydrogen fuel via electrochemical water splitting. Herein, a flower-like Co9S8@MoS2 heterostructure with effective bifunctional activity was achieved using a one-pot approach via the hydrothermal treatment of metal-coordinated species followed by pyrolysis under an N2 atmosphere. The heterostructures exhibited a 3D interconnected network with a large electrochemical active surface area and a junctional complex with hydrogen evolution reaction (HER) catalytic activity of MoS2 and oxygen evolution reaction (OER) catalytic activity of Co9S8, exhibiting low overpotentials of 295 and 103 mV for OER and HER at 10 mA cm-2 current density, respectively. Additionally, the catalyst-assembled electrolyser provided favourable catalytic activity and strong durability for overall water splitting in 1 M KOH electrolyte. The results of the study highlight the importance of structural engineering for the design and preparation of cost-effective and efficient bifunctional electrocatalysts.

Ligand-variable metal clusters charge transfer in Ce-Por-MOF/AgNWs and their application in photoelectrochemical sensing of ronidazole.

A photoelectrochemical sensing platform based on ligand-variable metal clusters charge transfer was established for the quantitative assay of ronidazole (RNZ) using Ce-porphyrin-metal-organic frameworks/silver nanowires (Ce-Por-MOFs/AgNWs). Rod-like Ce-Por-MOFs and well-dispersed sub-50 nm AgNWs were prepared using a hydrothermal method and polyol strategy, and then through simple drop coating to yield Ce-Por-MOFs/AgNWs nanocomposites. We investigated the intrinsic semiconducting properties of the composites. More importantly, it was found that the variable-valence metal node can provide electronic defect states similar to those caused by multi-metal doping, synergizing with the surface plasmon effect of AgNWs, which significantly improved the photoelectric conversion efficiency, thereby resulting in excellent optoelectronic properties. In combination with molecular imprinting, a competitive type trace photoelectrochemical sensor for RNZ was constructed using Fe2+ as the electron donor and probe. Under optimal conditions, the sensor response is proportional to the logarithm of RNZ concentration in the range 0.1-104 nM with a detected limit of 0.038 nM. The recoveries ranged from 87.2 to 116% with relative standard deviations (RSDs) < 6.5% (n = 3) in milk sample. This work reveals the charge-transfer process of variable-valence metal nodes in MOFs during photoelectrochemical processes, which will provide new insights for the sensing application of variable-valence metal MOFs.

Determination of trichlorfon using a molecularly imprinted electrochemiluminescence sensor on multi-walled carbon nanotubes decorated with silver nanoparticles.

Considering the limitations associated with existing methods for the detection of trace amounts of trichlorfon, this paper proposes a novel molecularly imprinted electrochemiluminescence (ECL) sensor for the detection of trichlorfon by utilizing the double enhancement effect of trichlorfon and Ag nanoparticles supported by multi-walled carbon nanotubes (MWCNTs/Ag NPs) in a luminol-H2O2 ECL system. Here, trichlorfon was electropolymerized on the surface of the MWCNT/Ag NP-modified gold nanoelectrode with o-phenylenediamine to prepare the molecularly imprinted polymer-based sensor. After eluting the trichlorfon, imprinted holes for the identification of trichlorfon were retained on the sensor, which were used as signal switches to obtain different ECL intensities through the adsorption of different concentrations of trichlorfon. The ECL signal of the sensitized luminol-H2O2 was doubly enhanced by the MWCNTs/Ag and trichlorfon, improving the sensitivity of the sensor. The trichlorfon concentration was positively correlated with the enhanced ECL intensity of the sensor in the range 5.0 × 10-8-5.0 × 10-11 mol L-1, and the detection limit of trichlorfon was 3.9 × 10-12 mol L-1. Moreover, the proposed sensor was successfully applied to the detection of trichlorfon residues in real samples, and the recovery ranged between 91.8 and 109%. A molecularly imprinted electrochemiluminescence sensor for trichlorfon detection by utilizing the double enhancement effect of trichlorfon and Ag nanoparticles supported by multi-walled carbon nanotubes in a luminol-H2O2 ECL system. The dual enhancement of the ECL signal improved the sensitivity of the sensor.

Microfluidic paper-based chip for parathion-methyl detection based on a double catalytic amplification strategy.

The rapid detection of insecticides such as parathion-methyl (PM) requires methods with high sensitivities and selectivities. Herein, a dual catalytic amplification strategy was developed using Fe3O4 nanozyme-supported carbon quantum dots and silver terephthalate metal-organic frameworks (Fe3O4/C-dots@Ag-MOFs) as current amplification elements. Based on this strategy, a novel electrochemical microfluidic paper-based chip was designed to detect PM. Fe3O4/C-dots@Ag-MOFs were synthesised by a hydrothermal method, and a molecularly imprinted polymer (MIP) was then synthesised on the surface of Fe3O4/C-dots@Ag-MOFs using PM as a template molecule. Finally, the reaction zone of a chip was modified with MIP/Fe3O4/C-dots@Ag-MOFs. PM from a sample introduced into the reaction zone was captured by the MIP, which generated a reduction current response at - 0.53 V in a three-electrode system embedded in the chip. Simultaneous catalysis by Fe3O4/C-dots and Ag-MOFs significantly enhanced the signal. The chip had a detection limit of 1.16 × 10-11 mol L-1 and was successfully applied to the determination of PM in agricultural products and environmental samples with recovery rates ranging from 82.7 to 109%, with a relative standard deviation (RSD) of less than 5.0%. This approach of combining a dual catalytic amplification strategy with an MIP significantly increased the sensitivity as well as selectivity of chips and can potentially be used to detect a wide variety of target analytes using microfluidic paper-based chips.

Biomimetic Synthesis of Ultrafine Mixed-Valence Metal-Organic Framework Nanowires and Their Application in Electrochemiluminescence Sensing.

Metal-organic frameworks (MOFs) prepared via typical procedures tend to exhibit issues like poor water stability and poor conductivity, which hinder their application in electrochemical sensing. Herein, we report a strategy for the preparation of mixed-valence ultrafine one-dimensional Ce-MOF nanowires based on a micelle-assisted biomimetic route and subsequent investigation into their growth mechanism. The prepared mixed-valence Ce-MOF nanowires exhibited a typical size of ∼50 nm and were found to present good water stability and high conductivity. On this basis, we examined the introduction of these nanowires into the luminol hydrogen peroxide luminescence system and proposed a novel dual-route self-circulating electrochemiluminescence (ECL) catalytic amplification mechanism. Finally, in combination with molecular imprinting, a MOF-based ECL sensor was developed for the detection of trace amounts of imidacloprid in plant-derived foods. This sensor exhibited a linearity of 2-120 nM and a detection limit of 0.34 nM. Thus, we proposed not only a novel route to MOF downsizing but also a facile and robust methodology for the design of a MOF-based molecular imprinting ECL sensor.

Novel chloramphenicol sensor based on aggregation-induced electrochemiluminescence and nanozyme amplification.

Combining electrochemiluminescence (ECL) with nanozyme amplification provides unique advantages for the detection of antibiotic residues. Herein, a molecularly imprinted chloramphenicol (CAP) sensor was established based on aggregation-induced (AI)-ECL and nanozyme amplification. Covalent organic framework materials with AI-ECL groups (COF-AI-ECL) and nanozyme Co3O4 were synthesised as the signal element and the amplification element, respectively. Subsequently, using CAP as a template molecule, a molecularly imprinted polymer (MIP) was fabricated on the electrode surface modified with COF-AI-ECL and Co3O4. The ECL signal of COF-AI-ECL was catalytically amplified by Co3O4, whereas CAP effectively quenched this signal. Consequently, the ECL signal was controlled by the elution and adsorption of CAP by the MIP, thus establishing a new method for CAP detection. Unlike traditional ECL reagent, COF-AI-ECL exhibited a stable and strong ECL signal. Therefore, COF-AI-ECL in combination with the MIP provided greater sensitivity and enhanced selectivity. The linear range of the developed CAP sensor was 5 × 10-13 to 4 × 10-10 mol/L, with a detection limit of 1.18 × 10-13 mol/L. Moreover, the recoveries range of 85.0%-106.2% were obtained for the detection of CAP in real honey, milk, and chicken samples, indicating the potential of this sensor design for the detection of trace antibiotic residues in food safety applications.

Novel molecularly imprinted amoxicillin sensor based on a dual recognition and dual detection strategy.

The use of dual recognition and multiple detection modes is an attractive strategy for realising sensors with improved selectivity and accuracy. Herein, a molecularly imprinted polymer (MIP)-based sensor is developed for amoxicillin detection based on two detection modes (fluorescence and electrochemiluminescence) and dual recognition. First, graphene oxide loaded with CdTe quantum dots/gold nanoparticles (GO/CdTe/Au NPs) is coated onto an indium tin oxide (ITO) electrode. Then, 4-mercapto-calix[6]arene is bonded to GO/CdTe/Au NPs as the first recognition element, which then form a host-guest complex with the target molecule amoxicillin. Subsequently, as the second recognition element, an MIP is prepared on the ITO electrode. After amoxicillin is removed from the MIP, specific identification sites for amoxicillin are obtained. Furthermore, the GO/CdTe/Au NPs can generate fluorescence and electrochemiluminescence signals that are effectively quenched by amoxicillin. Therefore, on/off switching of these signals can be achieved through the elution or adsorption of amoxicillin. The dual detection modes are complementary and provide mutual authentication, which can improve the detection accuracy and application scope. Moreover, the dual recognition sites for amoxicillin, improve detection selectivity. The fluorescence and electrochemiluminescence modes have detection ranges of 5-1000 × 10-11 mol L-1 and 5-1500 × 10-11 mol L-1, respectively, with detection limits of 9.2 × 10-12 mol L-1 and 8.3 × 10-12 mol L-1, respectively.

Chiral drug fluorometry based on a calix[6]arene/molecularly imprinted polymer double recognition element grafted on nano-C-dots/Ir/Au.

A luminescent double recognition nanoprobe is described as a new strategy for the selective determination of chiral molecules. C-dots/Ir/Au fluorescent nanoparticles, synthesised under hydrothermal conditions, are used as a high-performance probe in combination with a molecularly imprinted polymer (MIP) and calix[6]arene as a double recognition element. Thiolated calix[6]arene is grafted on C-dots/Ir/Au as the first recognition element, which then forms a host-guest complex with the target molecule levodopa (L-DOPA). Subsequently, an MIP is prepared on the C-dots/Ir/Au (MIP/C-dots/Ir/Au) by chemical polymerisation. After the removal of L-DOPA, double recognition imprinting cavities are formed. The fluorescence intensity at 478 nm of the nanoprobe is effectively quenched by adsorption of L-DOPA on MIP/C-dots/Ir/Au, which provides a method for L-DOPA determination. Owing to the double recognition strategy, this method has excellent selectivity which can effectively avoid interference from enantiomer D-DOPA, and a imprinting factor of 7.1 is obtained for L-DOPA. This accurate and reliable method, with a wide linear range (5 × 10-10 to 1.2 × 10-7 mol L-1) and a low limit of detection (1.45 × 10-10 mol L-1), was successfully applied to the determination of L-DOPA in real samples, giving standard recoveries of 89.7-110.0%. Thus, the proposed sensing method provides a viable approach for the determination of a single enantiomer. Graphical abstract Schematic presentation of the MIP/C-dots/Ir/Au for L-DOPA detection. A fluorescence double chiral recognition nanoprobe is prepared of C-dots/Ir/Au nanoparticles as signal probe, and a molecularly imprinted polymer (MIP) and calix[6]arene as a double recognition element. Owing to the double recognition strategy, this method has strong specificity and can effectively avoid interference from enantiomers and racemates.

A strategy for construction of highly sensitive glycosyl imprinted electrochemical sensor based on sandwich-like multiple signal enhancement and determination of neural cell adhesion molecule.

A novel electrochemical sensor for a neural cell adhesion molecule (CD56) was constructed by glycosyl imprinting. A sandwich-like multi-signal generation strategy was first proposed in glycosyl imprinting sensors via boric acid affinity. Glycosyl-imprinted polymers were formed by electro-polymerization with poly-sialic acid (PolySia) as a template molecule and p-aminobenzeneboronic (p-ABA) acid as a functional monomer. Methods such as scanning electron microscope (SEM), Fourier transform infrared spectrum (FT-IR), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS) were used to characterize the successful formation of imprinted membranes. Confirmed by both simulation calculation and experimental results, a signal-amplified effect based on macromolecules was introduced for the first time. After re-absorption, aminobenzene borate was linked to the surface of the sensor by boric acid affinity due to the rich hexadoxyl structure of the CD56-terminal chain as a signal probe. Under optimal conditions, the detection limit of the sensor is as low as 0.47 ng/L, and it can be successfully applied to the detection of CD56 in human serum.

Fluorometric aptasensor for cadmium(II) by using an aptamer-imprinted polymer as the recognition element.

A fluorometric assay is described for the determination of Cd(II) in environmental and agricultural samples. It is making use of a molecularly imprinted polymer (MIP) and aptamer as dual recognition units, while carbon quantum dots (co-doped with sulphur and nitrogen) and gold nanoparticles (SN-CQD/Au) act as the fluorophores. The aptamer-modified MIP was placed on an SN-CQD/Au-modified indium tin oxide glass electrode. Cd(II) was detected with high selectivity by the recognition sites of the aptamer in the MIP. Fluorescence, with excitation/emission peaks at 370/430 nm, is quenched by Cd(II). Response is linear in the 20 pM to 12 nM concentration range. The detection limit is 1.2 pM. The sensor is selective for Cd(II), and recoveries from spiked waters, soils and vegetables real-world samples range between 82.1 and 113.9%. Graphical abstractA fluorescence sensor composed of a molecularly imprinted polymer and an aptamer as a dual identification system for Cd2+ coupled with and carbon quantum dots (co-doped with sulphur and nitrogen) and gold nanoparticles (SN-CQDs/Au) as fluorescent element that can detect Cd2+ with high selectivity by a dual-recognition mechanism.

Synthesis of Zr-coordinated amide porphyrin-based two-dimensional covalent organic framework at liquid-liquid interface for electrochemical sensing of tetracycline.

Highly-conductive two-dimensional covalent organic framework (COF) displays prominent applications in various fields of science and technology. This paper reports the design and liquid-liquid interface synthesis of a novel Zr-coordinated amide porphyrin-based 2D COF (Zr-amide-Por-based 2D COF). The COF adopts a graphene-like multilayer structure with the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) band gap of 1.6 eV. The ordered multilayer structure of the amide COF was confirmed through a series of characterization techniques, including scanning electron microscopy, high-resolution transmission electron microscopy, atomic force microscopy, Fourier-transform infrared spectroscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. In particular, the inherent-ordered structure of Zr-amide-Por-based 2D COF with Zr as the catalytically active center confers several distinct advantages to the material, such as high conductivity and high electrocatalysis performance. A molecularly imprinted tetracycline electrochemiluminescence sensor was constructed based on the Zr-amide-Por-based 2D COF, and gate control effect was used as a signal-generation mechanism. Under optimal conditions, the sensor showed a good linear relationship with tetracycline in the concentration range of 5-60 pM, with a detection limit of 2.3 pM. Because the sensor is rapid, cost-efficient, highly sensitive, and specific, it can be considered as a viable platform for veterinary drug residue monitoring.

Molecularly imprinted electroluminescence switch sensor with a dual recognition effect for determination of ultra-trace levels of cobalt (II).

A dual selection/recognition effect is described for cobalt (II) ions (Co2+). It is based on bovine serum albumin-metal-Co2+ coordination (BSA-Co2+) and the use of a molecularly imprinted polymer (MIP). An electrochemiluminescence (ECL) switch sensor was designed for detecting nanomolar levels of Co2+. The BSA-Co2+ coordination complex was chosen as a template to prepare a MIP modified switch sensor. The coordination reaction between BSA and Co2+ provides the first step in recognition, and MIP provides the second step for Co2+. This leads to a strong improvement in selectivity of the sensor. A multi-walled carbon nanotube/Cu nanoparticles/carbon quantum dots nanocomposite (MWCNT/Cu/C-dots) acts as an ECL device, and the BSA-Co2+ complex quenches the ECL signal. Therefore, the elution and resorption of BSA-Co2+ can be used as a switch to control ECL. Additionally, a method was established to detect Co2+, with the detection limit as low as 3.07 × 10-10 mol/L. The method was applied to the analysis of spiked environmental water, soil samples, and agricultural products. The recovery rates of the method were in the range of 87.5-111.3%.