A nano-spherical α-mno 2 /bi 2 o 3 Materials and their preparation methods and applications
A spherical and nanotechnology, applied in nanotechnology, nanotechnology, nanotechnology for materials and surface science, etc., can solve the problem of affecting the practical application of manganese dioxide materials, reducing the electrochemical stability of products, and reducing the particle size of manganese dioxide. Uneven distribution and other problems, to achieve the effect of more electrochemical active sites, improved cycle stability, and low requirements for equipment parameters and functions
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[0036] The invention relates to a nano-spherical α-MnO with good crystallization properties 2 / Bi 2 o 3 A material and a preparation method thereof belong to the field of zinc ion batteries. The nano-spherical α-MnO 2 / Bi 2 o 3 The material is made of α-MnO 2 The main phase (or "nano-spherical α-MnO 2 composition") and Bi 2 o 3 The second phase (or "Bi 2 o 3 Material composition") composition, the Bi 2 o 3 The content of the second phase is 0.5-10wt.%, and the nano-spherical α-MnO 2 / Bi 2 o 3 The particle size of the material is 5-500nm. Preparation of α-MnO 2 / Bi 2 o 3 The material is prepared by mixing the solution A containing potassium permanganate and foaming agent with the solution B containing low-priced manganese salt and bismuth salt in a certain way under mild conditions, and it is prepared by liquid phase co-precipitation reaction method α-MnO 2 / Bi 2 o 3 The precursor powder of the material, and its crystallization performance is improved by h...
Embodiment 1
[0052] (1) Weigh 0.4mol of potassium permanganate and 0.4mol of sodium carbonate and dissolve them in 2L of deionized water, disperse evenly, and record it as solution A; in addition, weigh 0.61mol of manganese chloride and 0.05mol of bismuth citrate to dissolve Disperse evenly in 2L of deionized water, and record it as solution B. Use an emulsifying disperser to disperse solution B, and at the same time drop solution A into solution B at a rate of 100 drops / minute, and then add 0.1 mol of ammonia water to adjust the pH to be alkaline. After the reaction was complete, the reacted mixed solution was left to stand for 24 hours, the precipitate was suction filtered and washed, and the resulting precipitated product was collected.
[0053] (2) The precipitated product of step (1) was dried in an oven at 110°C for 10 hours to obtain nano-spherical α-MnO 2 / Bi 2 o 3 The precursor powder of the material, with Figure 1a , 1b The SEM image and XRD image of its microstructure, resp...
Embodiment 2
[0057] (1) Weigh 0.35mol of potassium permanganate and 0.5mol of potassium carbonate and dissolve them in 2L of deionized water, disperse evenly, and record it as solution A; in addition, weigh 0.52mol of manganese nitrate and 0.05mol of bismuth citrate and dissolve in 2L of deionized water, dispersed evenly, recorded as solution B. Disperse solution B by ultrasonic stirring and dispersing, and drop solution A into solution B at the same time, control the dropping rate to 80 drops / min, then add 0.05mol sodium hydroxide to adjust the pH to be alkaline. After the reaction was complete, the reacted mixed solution was left to stand for 24 hours, the precipitate was suction filtered and washed, and the resulting precipitated product was collected.
[0058] (2) The precipitated product of step (1) was dried in an oven at 100°C for 10 hours to obtain nano-spherical α-MnO 2 / Bi 2 o 3 The precursor powder of the material.
[0059] (3) the nano-spherical α-MnO obtained in step (2) ...
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