Preparation method of anti-sulfide-poisoning fuel cell cathode catalyst
A fuel cell cathode and anti-sulfide technology, applied in physical/chemical process catalysts, metal/metal oxide/metal hydroxide catalysts, battery electrodes, etc., can solve problems such as easy sulfide poisoning, and the method is simple and easy Excellent anti-sulfide poisoning performance, the effect of overcoming easy sulfide poisoning
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Embodiment 1
[0037] (1) Functionalization of carbon supports
[0038] Weigh 1 gram of commercially available Vulcan XC-72 carbon powder, add 150 ml of a mixed solution of 30% hydrogen peroxide and concentrated sulfuric acid with a volume ratio of 1:4, stir ultrasonically for 3 hours, dilute with ultrapure water, and let stand After 24 hours, the supernatant was filtered out, washed by centrifugation for several times, dried, and ground to obtain functionalized Vulcan XC-72 carbon powder.
[0039] (2)MoO 3 Preparation of / C catalyst
[0040] According to functionalized Vulcan XC-72 carbon powder: ammonium molybdate mass ratio is 1: 0.05 to take the functionalized VulcanXC-72 carbon powder and ammonium molybdate of step (1) gained, then take deionized water as solvent under ultrasonic stirring condition Oscillate evenly, continue to stir for 12 hours, and evaporate to dryness at 80°C. After grinding, keep the mixture powder at 180°C in a nitrogen atmosphere for 30 minutes, then continue to...
Embodiment 2
[0046] Step (1) is the same as step (1) in Example 1.
[0047] (2)MoO 3 Preparation of / C catalyst
[0048] Take the functionalized VulcanXC-72 carbon powder and molybdenum chloride obtained in step (1) by weighing the functionalized Vulcan XC-72 carbon powder: molybdenum chloride mass ratio of 1: 0.01, then use deionized water as a solvent under ultrasonic stirring conditions Shake evenly under the hood, continue to stir for 15 hours, evaporate to dryness at 60°C, keep the mixture powder at 120°C in an argon atmosphere for 60 minutes after grinding, then continue to heat up to 450°C and keep it for 8 hours, and obtain MoO after cooling 3 / C Catalyst.
[0049] (3) Preparation of Pt-MoO 3 / C Catalyst
[0050] Chloroplatinic acid: sodium citrate: MoO 3 The mass ratio of / C is 1: 3: 1 and takes by weighing the MoO obtained from chloroplatinic acid, sodium citrate and step (2) 3 / C catalyst, adding all MoO to excess ethylene glycol solvent 3 / C catalyst, sodium citrate and ...
Embodiment 3
[0054] Step (1) is the same as step (1) in Example 1.
[0055] (2)MoO 3 Preparation of / C catalyst
[0056] Weigh the functionalized VulcanXC-72 carbon powder and molybdic acid obtained in step (1) according to the functionalized Vulcan XC-72 carbon powder: molybdic acid mass ratio of 1:0.1, and then use deionized water as a solvent to vibrate under ultrasonic stirring conditions Evenly, continue to stir for 24 hours, evaporate to dryness at 95°C, keep the mixture powder at 100°C in a nitrogen atmosphere for 40 minutes after grinding, then continue to heat up to 400°C and keep for 4 hours, and obtain MoO after cooling 3 / C Catalyst.
[0057] (3) Preparation of Pt-MoO 3 / C Catalyst
[0058] Chloroplatinic acid: sodium citrate: MoO 3 The mass ratio of / C is 1: 1: 4 and takes by weighing the MoO obtained from chloroplatinic acid, sodium citrate and step (2) 3 / C catalyst, adding all MoO to excess ethylene glycol solvent 3 / C catalyst, sodium citrate and chloroplatinic acid...
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