Preparation method and application of functionalized graphene modified glassy carbon electrode
A glassy carbon electrode and graphene technology, applied in the direction of material electrochemical variables, material analysis through electromagnetic means, instruments, etc., can solve the problems of slow electron transfer rate, easy adsorption of oxidation products, inaccurate detection results, etc., and achieve good results. reproducible effect
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Embodiment l
[0023] A preparation method for a functionalized graphene-modified glassy carbon electrode, comprising the steps of:
[0024] 1) Pretreatment of glassy carbon electrodes
[0025] The glassy carbon electrodes were sequentially coated with 1.0, 0.3, 0.05 μm Al 2 o 3 The powder was polished to a mirror surface, and then ultrasonically washed 3 times in twice distilled water and absolute ethanol, each time for 3 minutes, N 2 Dry and set aside for use to prepare a pretreated electrode.
[0026] 2) Activation of pretreatment electrodes
[0027] at 1.0 x 10 -3 mol / L K 3 [Fe(CN) 6 ] The pretreated electrode was electrochemically activated by cyclic voltammetry in the solution.
[0028] 3) Preparation of copper-doped γ-ureapropyltriethoxysilane functionalized graphene oxide
[0029] Weigh 1.00g of graphene oxide and dissolve it in 500mL of absolute ethanol, sonicate for 2 hours to obtain a graphene oxide solution, transfer it to a reaction kettle, and then add 0.15g of γ-ureapr...
Embodiment 2
[0033] A preparation method for a functionalized graphene-modified glassy carbon electrode, comprising the steps of:
[0034] 1) Pretreatment of glassy carbon electrodes
[0035] The glassy carbon electrodes were sequentially coated with 1.0, 0.3, 0.05 μm Al 2 o 3 The powder was polished to a mirror surface, and then ultrasonically washed 3 times in twice distilled water and absolute ethanol, each time for 3 minutes, N 2 Dry and set aside for use to prepare a pretreated electrode.
[0036] 2) Activation of pretreatment electrodes
[0037] at 1.0 x 10 -3 mol / L K 3 [Fe(CN) 6 ] The pretreated electrode was electrochemically activated by cyclic voltammetry in the solution.
[0038] 3) Preparation of nickel-doped γ-ureapropyltriethoxysilane functionalized graphene oxide
[0039]Weigh 1.00g of graphene oxide and dissolve it in 500mL of absolute ethanol, sonicate for 2 hours to obtain a graphene oxide solution, transfer it to a reaction kettle, and then add 0.18g of γ-ureapro...
Embodiment 3
[0043] A preparation method for a functionalized graphene-modified glassy carbon electrode, comprising the steps of:
[0044] 1) Pretreatment of glassy carbon electrodes
[0045] The glassy carbon electrodes were sequentially coated with 1.0, 0.3, 0.05 μm Al 2 o 3 The powder was polished to a mirror surface, and then ultrasonically washed 3 times in twice distilled water and absolute ethanol, each time for 3 minutes, N 2 Dry and set aside for use to prepare a pretreated electrode.
[0046] 2) Activation of pretreatment electrodes
[0047] at 1.0 x 10 -3 mol / L K 3 [Fe(CN) 6 ] The pretreated electrode was electrochemically activated by cyclic voltammetry in the solution.
[0048] 3) Preparation of iron-doped γ-ureapropyltriethoxysilane functionalized graphene oxide
[0049] Weigh 1.00g of graphene oxide and dissolve it in 500mL of absolute ethanol, sonicate for 2 hours to obtain a graphene oxide solution, transfer it to a reaction kettle, and then add 0.35g of γ-ureaprop...
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