Nitrogen-containing graphitized carbon material adopting double-metal MOFs (metal organic frameworks)
A graphitized carbon and bimetallic technology, applied in non-metallic elements, metal processing equipment, carbon preparation/purification, etc., can solve the problems of limited application of electrode materials, poor degree of graphitization, and low metal-nitrogen structure ratio, etc. Achieved the effect of excellent activity, excellent product performance and high specific surface area
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Embodiment 1
[0027] Step 1: Weigh 3.7 g of 2-methylimidazole, stir and dissolve it in 80 mL of methanol at room temperature to form solution A. Weigh 1.233 g of cobalt nitrate hexahydrate and 0.42 g of zinc nitrate hexahydrate, stir and dissolve in 80 mL of methanol at room temperature to form solution B. Slowly pour B into A, stir for 5 min, and stand at room temperature for 24 h. The mixture is centrifuged at 10,000 rpm, washed with methanol three times, vacuum-dried at low temperature for 12 h, and vacuum-activated at 200°C for 24 h. A CoZn-ZIF precursor is obtained.
[0028] Step 2: Synthesis of Co-CNT@NC: Weigh 200 mg of CoZn-ZIF from Step 1 and put it into a tube furnace, heat it up to 900°C at a rate of 5°C / min under an argon atmosphere, and calcinate for 3 h, 35.5 mgCo-CNT@NC was obtained.
[0029] Step 3: Synthesis of P-Co-CNT@NC: Weigh 25 mg of Co-CNT@NC in Step 2 and 5 mg of triphenylphosphine in 10 mL of methanol and mix and stir for 24 h, then drain the methanol to obtain T...
Embodiment 2
[0031] Step 1: Weigh 3.7 g of 2-methylimidazole, stir and dissolve it in 80 mL of methanol at room temperature to form solution A. Weigh 0.822 g of cobalt nitrate hexahydrate and 0.84 g of zinc nitrate hexahydrate, stir and dissolve in 80 mL of methanol at room temperature to form solution B. Slowly pour B into A, stir for 5 min, and stand at room temperature for 24 h. The mixture is centrifuged at a speed of 10,000 rpm, washed with methanol for 3 times, vacuum-dried at low temperature for 12 h, and vacuum-activated at 200°C for 24 h. A CoZn-ZIF precursor is obtained.
[0032] Step 2: Synthesis of Co-CNT@NC: Weigh 200 mg of CoZn-ZIF from Step 1 and put it into a tube furnace, heat it up to 900°C at a rate of 5°C / min under an argon atmosphere, and calcinate for 3 h, 28.4 mgCo-CNT@NC was obtained.
[0033] Step 3: Synthesis of P-Co-CNT@NC: Weigh 25 mg of Co-CNT@NC in Step 2 and 5 mg of triphenylphosphine in 10 mL of methanol and mix and stir for 24 h, then drain the methanol t...
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