Preparation method of CuO-Cu2O/CM nanowire array heterostructure and application
A technology of nanowire arrays and heterogeneous structures, applied in measuring devices, material analysis through optical means, instruments, etc., can solve expensive and time-consuming problems, achieve low detection limits, good detection stability, and good stability Effect
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Embodiment 1
[0034] (1) Dissolve 3.2g NaOH and 0.91g ammonium persulfate in 25mL deionized water respectively, mix NaOH solution and ammonium persulfate solution, and stir for 5 minutes to obtain a clear solution; place the pretreated copper grid in the above clear solution Soak in medium for 20 minutes; take out the sample, wash with deionized water and ethanol respectively, and air-dry at 60°C to obtain Cu(OH) 2 precursor.
[0035] (2) The Cu(OH) prepared in step (1) 2 The precursors were calcined at 350 °C for 15 min in air. Take out the copper grid, and finally the obtained sample (CuO-Cu 2 O / CM) were washed several times with deionized water and dried in air.
Embodiment 2
[0037] (1) Dissolve 3.5g NaOH and 1.0g ammonium persulfate in 20mL deionized water respectively, mix NaOH solution and ammonium persulfate solution, and stir for 10 minutes to obtain a clear solution; place the pretreated copper grid in the above clear solution Soak in medium for 25 minutes; take out the sample, wash with deionized water and ethanol respectively, and air-dry at 60°C to obtain Cu(OH) 2 precursor.
[0038] (2) The Cu(OH) prepared in step (1) 2 The precursors were calcined at 350 °C for 20 min in air. Take out the copper grid, and finally the obtained sample (CuO-Cu 2 O / CM) were washed several times with deionized water and dried in air.
Embodiment 3
[0040] (1) Dissolve 3.3g NaOH and 0.95g ammonium persulfate in 23mL deionized water respectively, mix NaOH solution and ammonium persulfate solution, and stir for 8 minutes to obtain a clear solution; place the pretreated copper grid in the above clear solution Soak in medium for 23 minutes; take out the sample, wash with deionized water and ethanol respectively, and air-dry at 60°C to obtain Cu(OH) 2 precursor.
[0041] (2) The Cu(OH) prepared in step (1) 2 The precursors were calcined at 350 °C for 18 min in air. Take out the copper grid, and finally the obtained sample (CuO-Cu 2 O / CM) were washed several times with deionized water and dried in air.
[0042] photoelectrochemical biosensor
[0043] The photoelectrochemical biosensor of the present invention comprises a working electrode connected to an electrochemical workstation, a reference electrode (Ag|AgCl|Cl - ), the counter electrode (platinum electrode), using a xenon lamp as a simulated light source, the working...
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