High-performance metal-air battery positive electrode catalyst and preparation method thereof
An air battery and catalyst technology, applied in the field of electrocatalytic materials, can solve single problems and achieve the effect of simple preparation methods
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Embodiment 1
[0045] CoN-CoO x / C composite preparation
[0046] (1) Surface functionalization of mesoporous carbon: Disperse 80 mg of mesoporous carbon (CMK-3) in 15 mL of 1mol L -1 Nitric acid aqueous solution, stirred at room temperature for 1 h; the dispersion was transferred to a 25 mL reaction kettle with Teflon lining, and kept at 150 ° C for 4 h; after cooling to room temperature, the kettle was opened, and the mesoporous carbon sample was centrifuged and separated with deionized Water and absolute ethanol were centrifuged and washed three times respectively; finally, the samples were vacuum-dried at 60 °C for 12 h to obtain surface-functionalized mesoporous carbons.
[0047] (2) Metal ion Co 2+ and metal ammonia complex ions Co(NH 3 ) 6 2+ Co-adsorption on mesoporous carbon: First, soak 50 mg of surface-functionalized mesoporous carbon in 20 mL of 3 mmol L -1 CoCl 2 In the aqueous solution, stir at room temperature for 1 h; centrifuge and wash the treated mesoporous carbon w...
Embodiment 2
[0058] CoN-CoO x Preparation and testing of / C composite materials:
[0059] (1) Surface functionalization treatment of mesoporous carbon: same as Example 1;
[0060] (2) Metal ion Co 2+ and metal ammonia complex ions Co(NH 3 ) 6 2+ Co-adsorption on mesoporous carbon: same as Example 1;
[0061] (3) heat treatment to obtain CoN-CoO x / C composite material: Co(NH 3)6 2+ &Co 2+ / C sample in N 2 Atmosphere, at 1°C min -1 The heating rate was raised from room temperature to 800 °C, and kept for 1 hour to obtain a high-performance metal-air battery cathode catalyst sample, labeled as CoN-CoO x / C-800.
[0062] The SEM image of the obtained sample is as Figure 8 As shown, it can be seen that the morphology of mesoporous carbon is destroyed when the calcination temperature is increased to 800 °C.
[0063] Figure 9 is the XRD pattern of the sample, by Figure 9 It can be seen that, compared to CoN-CoO x / C-700, CoN-CoO obtained by calcination at 800°C x The vast ma...
Embodiment 3
[0067] CoN-CoO x Preparation and testing of / C composite materials:
[0068] (1) Surface functionalization treatment of mesoporous carbon: same as Example 1;
[0069] (2) Metal ion Co 2+ and metal ammonia complex ions Co(NH 3 ) 6 2+ Co-adsorption on mesoporous carbon: same as Example 1;
[0070] (3) heat treatment to obtain CoN-CoO x / C composite material: Co(NH 3)6 2+ &Co 2+ / C sample in N 2 Atmosphere, at 1°C min -1 The heating rate was raised from room temperature to 600°C and kept for 1 hour to obtain a high-performance metal-air battery cathode catalyst sample, labeled as CoN-CoO x / C-600.
[0071] The SEM image of the obtained sample is as Figure 12 It can be seen that the morphology of mesoporous carbon will not be destroyed when the calcination temperature is 600 °C.
[0072] Figure 13 is the XRD pattern of the sample, except that there are two steamed bread peaks at about 24° and 44° (indicating the localized graphitization of mesoporous carbon), no d...
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