4.8 Article

Facile synthesis of ultrathin two-dimensional graphene-like CeO2-TiO2mesoporous nanosheet loaded with Ag nanoparticles for non-enzymatic electrochemical detection of superoxide anions in HepG2 cells

Journal

BIOSENSORS & BIOELECTRONICS
Volume 184, Issue -, Pages -

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2021.113236

Keywords

Two-dimensional; Metal oxides; Ag nanoparticles; Superoxide anions; Electrocatalytic reduction

Funding

  1. Natural Science Foundation of Shanghai [19ZR1412000]
  2. Science and Technology Commission of Shanghai Municipality (STCSM) [20520712500]
  3. Fundamental Research Funds for the Central Universities [50321102117022]

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A new facile strategy was presented to fabricate ultrathin 2D metal oxide nanosheets using polydopamine-coated graphene as a template under simply wet-chemical conditions. The resulting nanosheets, loaded with Ag nanoparticles, exhibited excellent properties for electrochemical detection of superoxide anion, showing potential for practical applications in biological sample analysis.
Here we presented a new facile strategy to fabricate ultrathin two-dimensional (2D) metal oxide nanosheets, by using polydopamine-coated graphene (rGO@PDA) as a template under simplywet-chemicalconditions. Based on the strategy, graphene-like CeO2-TiO(2)mesoporousnanosheet (MNS-CeO2-TiO2) was prepared and was loaded with dispersive Ag nanoparticles (AgNPs) to obtain effective electrocatalysts (denoted asAg/MNS-CeO2-TiO2) forelectrochemical detectionof superoxide anion (O-2(center dot & minus;)). Characterizations demonstrated that MNS-CeO2-TiO(2)exhibited ultrathin thickness, larger specific surface area, andpore volumein comparison with its bulk counterpart. The above properties of MNS-CeO2-TiO(2)shorten electron transmission distance, promotes mass transfer, and is conducive to the dispersion of post-modified AgNPs. Therefore, the recommended Ag/MNS-CeO2-TiO(2)sensors (denoted asAg/MNS-CeO2-TiO2/SPCE) exhibited satisfactory properties, including the sensitivity of 737.1 mu Acm(& minus;2)mM(& minus;1), the detection limit of 0.0879 mu M (S/N=3), and good selectivity. Meanwhile, the sensors also successfully realized in the online monitoring of O(2)(center dot & minus;)released from HepG2 cells, meaning the prepared sensors had practical application potential towards the analysis of O(2)(center dot & minus;)in biological samples.

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