4.8 Article

One-Step Electrodeposition of Silver Nanostructures on 2D/3D Metal-Organic Framework ZIF-67: Comparison and Application in Electrochemical Detection of Hydrogen Peroxide

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 12, Issue 37, Pages 41960-41968

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c11269

Keywords

electrochemical sensor; electrodeposition; electrocatalysis; zeolite imidazolate framework-67; hydrogen peroxide; liver cancer cells

Funding

  1. National Natural Science Foundation of China [21675177, 81803521]
  2. National Student's Innovation Training Program [201910573006]
  3. Project of Educational Commission of Guangdong Province [2018KTSCX108]
  4. Natural Science Foundation of Guangdong Province [2020A1515010075, 2019A1515010273, 2018A030310142]

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Metal-organic frameworks (MOFs) have been widely used as supporting materials to load or encapsulate metal nanoparticles for electrochemical sensing. Herein, the influences of morphology on the electrocatalytic activity of Co-containing zeolite imidazolate framework-67 (ZIF-67) as supporting materials were studied. Three types of morphologies of MOF ZIF-67 were facilely synthesized by changing the solvent because of the influence of the polar solvent on the nucleation and preferential crystal growth. Two-dimensional (2D) ZIF-67 with microplate morphology and 2D ultrathin ZIF-67 nanosheets were obtained from pure H2O (H-ZIF-67) and a mixed solution of dimethylformamide and H2O (D-ZIF-67), respectively. Three-dimensional ZIF-67 with rhombic dodecahedron morphology was obtained from pure methanol (M-ZIF-67). Then, one-step electrodeposition of silver nanostructures on ZIF-67-modified glassy carbon electrode (Ag/ZIF-67/GCE) was performed for the reduction of hydrogen peroxide (H2O2). Cyclic voltammetry can be used to investigate the electrocatalytic activity of Ag/ZIF-67/GCE, and Ag/H-ZIF-67/GCE displayed the best electrocatalytic property than Ag/D-ZIF-67/GCE and Ag/M-ZIF-67/GCE. The electrochemical H2O2 sensor showed two wide linear ranges of 5 mu M to 7 mM and 7 to 67 mM with the sensitivities of 421.4 and 337.7 mu A mM(-1) cm(-2) and a low detection limit of 1.1 mu M. In addition, the sensor exhibited good selectivity, high reproducibility, and stability. Furthermore, it has been utilized for real-time detection of H2O2 from HepG2 human liver cancer cells. This work provides a novel strategy for enhancing the detection performance of electrochemical sensors by changing the crystalline morphologies of supporting materials.

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