Vanadium-doped cobalt phosphide nano-thorn catalytic material used for overall water-splitting reaction
A catalytic material, cobalt phosphide technology, applied in physical/chemical process catalysts, electrolysis processes, electrolysis components, etc., can solve the problems of expensive platinum-based precious metal water electrolysis catalysts and poor performance of non-precious metal water electrolysis catalysts, and achieve high performance. , good stability and repeatability, and the effect of high current density
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Embodiment 1
[0034] Step 1. Hydrothermal synthesis of vanadium-doped cobalt oxide cobalt hydroxide precursor grown on carbon cloth:
[0035] Cut the carbon cloth into a size of 1cm×4cm, take 30ml of concentrated nitric acid (68%) and put the cut carbon cloth into a stainless steel autoclave with polytetrafluoroethylene, transfer it to an electric blast drying oven, set The temperature is 90°C, and the holding time is 3 hours. After the waiting is over, the pretreatment of the carbon cloth is completed by ultrasonic cleaning with ethanol and deionization for 5 minutes respectively. Next is hydrothermal treatment, weigh 0.1mM VCl 3 (vanadium trichloride), 2mMCo(NO 3 ) 2 (cobalt nitrate hexahydrate), 6mMH 4 FN (ammonium fluoride), 10mMCH 4 N 2 O (urea) was sequentially added to 30 mL of deionized water, and magnetically stirred for 30 min to ensure that the raw materials were evenly mixed. After the precursor mixed solution is stirred evenly, add it and a piece of pretreated carbon clot...
Embodiment 2
[0039] Step 1. Hydrothermal synthesis of vanadium-doped cobalt oxide cobalt hydroxide precursor grown on carbon cloth:
[0040] Cut the carbon cloth into a size of 1cm×4cm, take 30ml of concentrated nitric acid and the cut carbon cloth into a stainless steel autoclave with polytetrafluoroethylene, transfer it to an electric blast drying oven, set the temperature at 90°C , the holding time is 3 hours, after the waiting is over, further ultrasonic cleaning with ethanol and deionization is performed, and the pretreatment of the carbon cloth is completed. Next is hydrothermal treatment, weigh 0.15mM VCl 3 (vanadium(III) chloride), 3mMCo(NO 3 ) 2 (cobalt nitrate hexahydrate), 9mMH 4 FN (ammonium fluoride), 15mMCH 4 N 2 O (urea) was sequentially added to 30 mL of deionized water, and magnetically stirred for 30 min to ensure that the raw materials were evenly mixed. After the precursor mixed solution is stirred evenly, add it and a piece of pretreated carbon cloth with a size ...
Embodiment 3
[0044] Step 1. Hydrothermal synthesis of vanadium-doped cobalt oxide cobalt hydroxide precursor grown on carbon cloth:
[0045] Cut the carbon cloth into a size of 1cm×4cm, take 30ml of concentrated nitric acid and the cut carbon cloth into a stainless steel autoclave with polytetrafluoroethylene, transfer it to an electric blast drying oven, set the temperature at 90°C , the holding time is 3 hours, after the waiting is over, further ultrasonic cleaning with ethanol and deionization is performed, and the pretreatment of the carbon cloth is completed. Next is hydrothermal treatment, weigh 0.1mM VCl 3 (vanadium(III) chloride), 2mMCo(NO 3 ) 2 (cobalt nitrate hexahydrate), 6mMH 4 FN (ammonium fluoride), 10mMCH 4 N 2 O (urea) was sequentially added to 30 mL of deionized water, and magnetically stirred for 30 min to ensure that the raw materials were evenly mixed. After the precursor mixed solution is stirred evenly, add it and a piece of pretreated carbon cloth with a size o...
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