Self-powered photoelectrochemical sensor based on molecularly imprinted polymer-coupled CBFO photocathode and AgS/SnS photoanode for ultrasensitive dimethoate sensing.

Anal Chim Acta

CAS Key Laboratory of Separation Sciences for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, PR China. Electronic address:

Published: February 2025


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Dimethoate (DIM) is one of the most extensively applied organophosphorus pesticides (OPs), which is used to boost farm productivity due to its high insecticidal efficacy. However, the excessive use of DIM can result in the extensive contamination of soil, groundwater and food. Monitoring of DIM in environmental and food samples is crucial in view of its potential health risks and environmental hazards from excessive residues. The expensive equipment and complex operations for current detection methods greatly limit their practical applications. Herein, a self-powered photoelectrochemical (PEC) sensing platform based on AgS/SnS photoanode, iron-doped cobalt borate (CBFO) photocathode, and molecularly imprinted polymers (MIPs) was proposed for the detection of DIM. The molecularly imprinted polymers at CBFO photocathode endow the self-powered PEC sensor with high selectivity. The AgS/SnS photoanode enhances the efficient of electron transfer between the photoanode and photocathode, contributing to the high sensitivity of PEC sensor. The self-powered molecularly imprinted PEC sensor exhibits outstanding sensitivity and selectivity for DIM at concentrations from 1 × 10 to 1 × 10 nM with a detection limit of 5.9 pM. Excellent recoveries (95.4 ± 2.6 %, 98.4 ± 2.3 %, 106.3 ± 3.3 %) were achieved in spiked crown pear samples, indicating that the molecularly imprinted PEC sensor is capable of detecting DIM in real samples. This research provides a novel simple, fast, highly selective and sensitive self-powered molecularly imprinted photoelectrochemical sensing platform for detection of DIM. The fabricated PEC sensor offers a promising candidate for the detection method of organophosphorus pesticides residues, which is of great significance for the fields of food safety and environmental protection.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.aca.2024.343556DOI Listing

Publication Analysis

Top Keywords

molecularly imprinted
24
pec sensor
20
cbfo photocathode
12
ags/sns photoanode
12
self-powered photoelectrochemical
8
organophosphorus pesticides
8
sensing platform
8
imprinted polymers
8
detection dim
8
self-powered molecularly
8

Similar Publications

Amplified electrochemical detection of sulfadiazine based on Cu-BTC-encapsulated FeNi dual-atom catalysts with improved catalytic efficiency.

Anal Methods

September 2025

College of Environmental Science and Engineering, Guangxi Key Laboratory of Environmental Pollution Control Theory and Technology, Niversity Engineering Research Center of Watershed Protection and Green Development, Guilin University of Technology, Guilin, 541006, China.

The amplification of detection signals is an important method for improving the sensitivity of electrochemical detection. This study presents an efficient strategy for preparing electrochemical catalytic materials using a simple self-assembly technique to encapsulate Fe single atoms (Fe-SAs) and Ni single atoms (Ni-SAs) in the Cu-benzene-1,3,5-tricarboxylic acid (Cu-BTC) metal-organic framework to form a Cu-BTC@FeNi-SAs catalytic system. Subsequently, Cu-BTC@FeNi-SAs was modified on the surface of a gold electrode, and sulfadiazine was used as a template to prepare a molecularly imprinted polymer (MIP) on the modified electrode.

View Article and Find Full Text PDF

Rutin is a potent antioxidant with therapeutic value in managing vascular and inflammatory conditions. Its accurate quantification is critical for pharmaceutical quality control and food safety. In this study, rutin was employed as a template to construct surface molecularly imprinted magnetic nanozymes (MIPs@FeO-CoNi).

View Article and Find Full Text PDF

A versatile fluorescent molecularly imprinted nanosensor (MIPs@O-CDs) for profiling ciprofloxacin (CIP) was innovatively developed using a controllable post-imprinting modification strategy. High-affinity molecularly imprinted polymers (MIPs) as recognition elements granted nanosensor favorable anti-interference. Bright orange-emission carbon dots (O-CDs) as signal transducers demonstrated prominent reverse fluorescence response to CIP due to inner filter effect, ameliorating detection sensitivity and accuracy.

View Article and Find Full Text PDF

The pervasive concern regarding veterinary drug residues in food necessitates advanced detection solutions, particularly addressing limitations of conventional methods reliant on large-scale instrumentation that incur prolonged analysis duration, complex sample preparation, and lack of real-time on-site capability. A portable "single response-on" molecularly imprinted ratiometric fluorescent paper-based sensor was developed for quantifying fleroxacin (FLX) residues in animal-derived foods, wherein B, N-co-doped MXene quantum dot (B, N-MQD) was synthesized and combined with BCP-Eu as dual-emission fluorophores, while FLX- molecularly imprinted polymer (FLX-MIP) was engineered using functionalized Nano-SiO as the carrier. Concentration-dependent fluorescence enhancement at 574 nm was exhibited with invariant reference signal at 411 nm, achieving a 36-fold lower detection limit (0.

View Article and Find Full Text PDF

Redox-Active Polyphenol Red Molecularly Imprinted Polymers on Porous Gold Electrodes for Ultrasensitive, AI-Assisted Detection of Alzheimer's Biomarkers in Undiluted Biofluids.

Adv Healthc Mater

September 2025

David Price Evans Global Health and Infectious Diseases Group, Pharmacology & Therapeutics, Institute of Systems Molecular and Integrative Biology, University of Liverpool, Crown Street, Liverpool, L69 7BE, UK.

Early diagnosis of Alzheimer's disease (AD) is hindered by the high cost, complexity, and centralization of current diagnostic platforms such as enzyme-linked immunosorbent assay (ELISA) and single-molecule array (SIMOA). Here, an integrated point-of-care (PoC) biosensing platform is reported based on redox-active polyphenol red molecularly imprinted polymers (pPhR MIPs) deposited on highly porous gold (HPG) electrodes for the ultrasensitive, reagent-free detection of phosphorylated tau 181 (p-tau 181) in undiluted plasma and serum. The unique electrochemical interface combines the signal-enhancing properties of HPG with the redox functionality of pPhR, eliminating the need for external redox probes.

View Article and Find Full Text PDF