Cobalt-doped cerium oxide nanocrystals shelled 1D SnO2 structures for highly sensitive and selective xanthine detection in biofluids

被引:16
作者
Malhotra, Deepanshu [1 ]
Tran, Phan Khanh Linh [1 ]
Tran, Duy Thanh [1 ]
Kim, Nam Hoon [1 ]
Lee, Joong Hee [1 ,2 ]
机构
[1] Jeonbuk Natl Univ, Dept Nano Convergence Engn, Jeonju 54896, Jeonbuk, South Korea
[2] Jeonbuk Natl Univ, Ctr Carbon Composite Mat, Dept Polymer & Nano Sci & Technol, Jeonju 54896, Jeonbuk, South Korea
基金
新加坡国家研究基金会;
关键词
Cobalt-doped cerium oxides; 1D tin oxide nanorods; Core@shell electrocatalyst; Nonenzymatic xanthine detection; Sensitivity; PEROXIDASE-LIKE ACTIVITY; REDUCED GRAPHENE OXIDE; URIC-ACID; ELECTROCHEMICAL SENSOR; COLORIMETRIC DETERMINATION; PASTE ELECTRODE; NANOPARTICLES; HYPOXANTHINE; NANOSTRUCTURES; NANOCOMPOSITE;
D O I
10.1016/j.jcis.2021.05.024
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this study, we prepared a three-dimensional self-supported electrocatalyst based on a thin layer of cerium oxide nanocrystals doped with cobalt heteroatoms (CeO2-Co) and then uniformly shelled over one-dimensional tin oxide (SnO2) nanorods supported by carbon cloth substrate. The material was used as a binder-free sensor that could nonenzymatically detect xanthine (XA) with an excellent sensitivity of 3.56 mu A mu M (-1), wide linear range of 25 nM to 55 mu M, low detection limit of 58 nM, and good selectivity. A screen-printed electrode based on the material accurately detected XA in food samples as well. The achievements were resulted from synergistic effects coming from the unique core@shell formation and Co-doping strategy, which efficiently modified electronic structure of the material to expose more electroactive site numbers/types and fast charge transfer, thereby producing intrinsic catalytic properties for XA oxidation. These results suggested that the SnO2@CeO2-Co is potential for developing efficient sensor to detect XA with good sensitivity and accuracy in food-quality monitoring. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:299 / 309
页数:11
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