Boron-doped carbon material and preparation method and application thereof
A technology of boron doping and carbon materials, applied in electrical components, battery electrodes, circuits, etc., can solve the problems of difficult control of process conditions in the preparation process, unfavorable catalyst industrialization, complex preparation methods, etc., and achieve excellent stability and methanol resistance performance, good ORR catalytic activity, and high degree of graphitization
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Embodiment 1
[0069] (1) Synthesis of PTPB: Dissolve 62.3g (0.2mol) triphenyltriboroxane (TPB) in 2000mL nitrobenzene, then add 91.3g (1.2mol) dimethoxymethane (molecular weight 76) and 289.7g (1.2mol) of anhydrous aluminum trichloride, stirred at 45°C for 5h, then raised to 80°C and stirred for 19h; after the reaction was completed, poured into 10L of methanol for settling, filtered, washed with water (1000mL×2), and dried for later use; The polymer was characterized by infrared spectroscopy, as figure 1 shown;
[0070] (2) 2.5gPTPB in N 2 Heat treatment at 900°C for 2 hours in the atmosphere to obtain 1.5 g of boron-doped carbon-nonmetal oxygen reduction catalyst, which is designated as B-C-900.
[0071] Catalyst performance test method (the following each embodiment obtains catalyst and the commercial Pt / C (JohnsonMatthey) that is used for comparison all tests with this method)
[0072] (1) Weigh 2mg of the catalyst, add it to 1mL Nafion-ethanol (1.5 / 98.5vol / vol) solution, disperse it...
Embodiment 2
[0077] (1) Synthesis of PTPB: Dissolve 62.3g (0.2mol) triphenylboroxane (TPB) in 2000mL dichloroethane, then add 91.3g (1.2mol) dimethoxymethane and 289.7g ( 1.2mol) of anhydrous aluminum trichloride, stirred at 45°C for 5h, then raised to 80°C and stirred for 19h; after the reaction was completed, poured into 10L methanol for sedimentation, filtered, washed with water (1000mL×2), and dried for later use; the obtained polymer was Infrared spectroscopy was characterized as figure 1 shown;
[0078] (2) 2.5gPTPB in N 2 Heat treatment at 800°C for 2 hours in the atmosphere to obtain 1.2 g of boron-doped carbon-nonmetal oxygen reduction catalyst, which is designated as B-C-800.
Embodiment 3
[0080] (1) Synthesis of PTPB: Dissolve 62.3g (0.2mol) triphenyltriboroxane (TPB) in 2000mL nitrobenzene, then add 88.9g (1.2mol) diethyl ether (molecular weight 74), 45.6 g (0.6mol) dimethoxymethane and 194.6g (1.2mol) anhydrous ferric trichloride, stirred at 45°C for 5h, then raised to 80°C and stirred for 19h; after the reaction was completed, pour it into 10L methanol for sedimentation, filter, Washed with water (1000mL × 2), dried for subsequent use; The resulting polymer was characterized by infrared spectroscopy, as figure 1 shown;
[0081] (2) 2.5gPTPB in N 2 Heat treatment at 1000°C for 2 hours in the atmosphere to obtain 1.1 g of boron-doped carbon-nonmetal oxygen reduction catalyst, which is designated as B-C-1000.
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