Journal
NEW JOURNAL OF CHEMISTRY
Volume 46, Issue 9, Pages 4090-4102Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1nj05243h
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Funding
- King Saud University, Riyadh, Saudi Arabia [RSP-2021/306]
- National Taipei University of Technology [NTUT-NJUST-110-01, NSFC51872141]
- Nanjing University of Science and Technology
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In this study, a nitrogen-doped carbon quantum dot decorated gadolinium oxide nanocomposite was synthesized through hydrothermal synthesis for the first time. The nanocomposite exhibited a nanoseed-like structure and showed excellent performance as an electrode material for the electrochemical detection of an antibiotic drug. The developed sensor demonstrated a low detection limit, high sensitivity, and good stability, repeatability, and reproducibility in real sample analysis.
Here we present the hydrothermal synthesis of nitrogen-doped carbon quantum dot (N-CQD) decorated gadolinium oxide (N-CQD@Gd2O3) nanocomposite for the first time. The nanocomposite features a nanoseed-like structure rather than the typical Gd2O3 nanorod-like structure. The presence of N-CQDs plays a dynamic role in the specific structural formation of the nanocomposite, which has been evaluated through physiochemical characterizations. Also, for the first time, the nanocomposite was employed as an electrode material for the sensitive electrochemical detection of an antibiotic drug, clioquinol (CQL), using an amperometric technique. Based on the oxidation peak current response of CQL, the influence of experimental factors such as the nanocomposite loading concentration/volume, scan rate, sample concentration, and accumulation time were investigated. As a consequence, the developed N-CQD@Gd2O3/GCE sensor exhibits a low detection limit of 2.1 nM and a high sensitivity of 3.6 mu A mu M-1 cm(-2) for the detection of CQL. Furthermore, the developed sensor has a high level of stability, repeatability, and reproducibility. Furthermore it performed well in real sample analysis with good recovery results, suggesting its practical applicability.
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