Cobalt phosphate and molybdenum trioxide composite nanorod array three-dimensional electrode material and preparation method and application thereof
A cobalt phosphate molybdenum trioxide, nanorod array technology, applied in electrodes, nanotechnology, electrolysis components, etc., can solve the problems of inability to achieve good cycle stability, poor cycle stability, and overall structural damage at the same time, and achieve excellent HER activity, Improves performance, boosts dynamics
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Embodiment 1
[0040] Pretreatment of nickel foam:
[0041] The nickel foam was ultrasonically treated in 3mol / L hydrochloric acid for 10 minutes to remove surface impurities, then washed with deionized water and ethanol for more than three times, and dried in an oven at 60°C to obtain pretreated nickel foam NF.
Embodiment 2
[0043] Pretreatment of nickel foam:
[0044] The nickel foam was ultrasonically treated in 3mol / L hydrochloric acid for 10 minutes to remove surface impurities, then washed with deionized water and ethanol for more than three times, and dried in an oven at 60°C to obtain pretreated nickel foam NF.
[0045] CoO 4 -NiMoO 4 Preparation of / NF nanorods:
[0046] 0.05M Co(NO 3 ) 2 ·6H 2 O and 0.01M (NH 4 ) 2 MoO 4 2H 2 O was dissolved in 30 mL of deionized water and vigorously stirred until dissolved, then the mixed solution and NF were transferred to a Teflon-lined stainless steel autoclave and kept at 180 °C for 6 h. After the heating reaction was completed, it was washed with deionized water and dried under vacuum at 60 °C for 12 h to obtain the purple precursor CoMoO 4 -NiMoO 4 / NF samples.
Embodiment 3
[0048] Pretreatment of nickel foam:
[0049] The nickel foam was ultrasonically treated in 3mol / L hydrochloric acid for 10 minutes to remove surface impurities, then washed with deionized water and ethanol for more than three times, and dried in an oven at 60°C to obtain pretreated nickel foam NF.
[0050] CoO 4 -NiMoO 4 Preparation of / NF nanorods:
[0051] 0.05M Co(NO 3 ) 2 ·6H 2 O and 0.01M (NH 4 ) 2 MoO 4 2H 2 O was dissolved in 30 mL of deionized water and vigorously stirred until dissolved, then the mixed solution and NF were transferred to a Teflon-lined stainless steel autoclave and kept at 180 °C for 6 h. After the heating reaction was completed, it was washed with deionized water and dried under vacuum at 60 °C for 12 h to obtain the purple precursor CoMoO 4 -NiMoO 4 / NF samples.
[0052] CoP 4 -MoO 3 Preparation of / NF:
[0053] The precursor CoMoO 4 -NiMoO 4 / NF sample is placed downstream of the tube furnace, and 1.5gNaH is placed upstream 2 PO ...
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