Fabrication of Efficient and Non-Enzymatic Electrochemical Sensors for the Detection of Sucrose

Author:

Asghar Nazia12,Mustafa Ghulam13,Jabeen Nawishta4ORCID,Dawood Asadullah5ORCID,Rida 6,Jabeen Zeenat7,Malik Qaiser Hameed5,Khan Muhammad Asad8ORCID,Khan Muhammad Usman9ORCID

Affiliation:

1. Sulaiman Bin Abdullah Aba Al-Khail Centre for Interdisciplinary Research in Basic Sciences (SA-CIRBS), Faculty of Basic and Applied Sciences, International Islamic University Islamabad, Islamabad 44000, Pakistan

2. Department of Chemistry, Rawalpindi Women University, Rawalpindi 46300, Pakistan

3. Department of Chemistry, University of Okara, Okara 56300, Pakistan

4. Department of Physics, Fatima Jinnah Women University Rawalpindi, Rawalpindi 46000, Pakistan

5. Department of Physics, National Excellence Institute (University), Islamabad 04524, Pakistan

6. Department of Chemistry, University of Sargodha, Sargodha 40100, Pakistan

7. Department of Physics, COMSATS University Lahore Campus, Lahore 54000, Pakistan

8. Department of Mathematics and Physics, University of Campania “Luigi Vanvitelli”, 81100 Caserta, Italy

9. National Key Laboratory of Tunable Laser Technology, Institute of Optoelectronics, Department of Electronics Science and Technology, Harbin Institute of Technology, Harbin 150080, China

Abstract

Molecularly imprinted polymers have been used for the creation of an electrochemical sensor for the detection of sucrose, which are modified by using functionalized graphene (fG). Using AIBN as the free radical initiator and sucrose as the template, imprinted polymers are synthesized. The monomer, 4,4′-diisocyanatodiphenylmethane (DPDI), has both proton donor groups (N-H or O-H) and lone-pair donor groups (C=O). By creating H-bonds with electron donor groups (C=O), the proton donor group in this polymer may interact with the sugar molecule serving as its template. The sensor signals have improved as a result of the interaction between the monomer and the template. Thermogravimetric and differential thermal analysis (TGA/DTA) curves, scanning electron microscopy (SEM), and FT-IR spectroscopy have been employed to characterize the fabricated receptors. The fabricated sensor has exhibited a limit of detection of 16 ppb for the target analyte that is highly sensitive, linear, reversible, regenerative, and selective. Moreover, the sensor’s stability, reproducibility, and reusability have been evaluated for six months, following the device’s manufacturing, and the results revealed similar responses with the percentage error of less than 1%. Most importantly, this sensor has demonstrated a quick response time, which is very sensitive, stable, and selective.

Publisher

MDPI AG

Subject

Electrical and Electronic Engineering,Biochemistry,Instrumentation,Atomic and Molecular Physics, and Optics,Analytical Chemistry

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