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Organic heterostructure modified carbon nitride as apprehension for Quercetin Biosensor.

Authors :
Hayat, Asif
Alrowaili, Z.A.
Taha, T.A.
Khan, Javid
Uddin, Ikram
Ali, Tariq
Raziq, Fazal
Ullah, Ikram
Hayat, Ashiq
Palamanit, Arkom
Irfan, Ahmad
Khan, Wasim Ullah
Source :
Synthetic Metals. Aug2021, Vol. 278, pN.PAG-N.PAG. 1p.
Publication Year :
2021

Abstract

An electrochemical quercetin (Q.R.) sensor based on carbon nitride (CN) copolymerized with 2,6-diaminoantandantquinone (DAQ) was assembled. The product has a humongous texture and excellent processability. The as-synthesized samples with uniform surface distribution were characterized by UV-Vis-spectroscopy, PL, XPS NMR, EPR, XRD, FT-IR, BET, and SEM. Furthermore, samples were electrochemically pickled in 0.1 MPBS solution via cyclic voltammetry (CV) for Q.R. electrochemical response, interference research, electrochemical active surface determination, stability, photocurrent and EIS. It was found that current response surges in a linear way with increasing Q.R. concentration from 0.015 µM to 260 µM with less than 2 s of response time and a recognition limit of 0.0025 µM. To assess this sample's feasibility to be used as a sensor, Q.R. content was determined in different real samples comprising green drink, fresh apple, lamella, and reasonable results were achieved. The current study proposed a new approach for identifying Q.R. as well as a novel breed of electrochemical detecting material. • We synthesized highly active and structurally uniform electrometric polymeric carbon nitride (PCN). • 2,6-diaminoantandantquinone (DAQ) was integrated into PCN to enhance its photocatalytic properties. • As-synthesized samples were characterized by UV-Vis-spectroscopy, PL, XPS, NMR, EPR, XRD, FT-IR, BET, and SEM. • Copolymerized samples demonstrate superior performances towards electrocatalytic oxidation of quercetin (QR). [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03796779
Volume :
278
Database :
Academic Search Index
Journal :
Synthetic Metals
Publication Type :
Academic Journal
Accession number :
151630761
Full Text :
https://doi.org/10.1016/j.synthmet.2021.116813