Battery negative electrode material and preparation method and application thereof
A battery negative electrode, hydrothermal reaction technology, applied in the direction of electrode manufacturing, battery electrodes, negative electrodes, etc., can solve the problems of conductivity and specific surface area decline
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[0029] The present invention also provides a method for preparing the battery negative electrode material described in the above technical solution, comprising the following steps:
[0030] After mixing MXene, nickel salt, iron salt, weak base and water, a hydrothermal reaction is carried out to obtain the battery negative electrode material.
[0031] In the present invention, unless otherwise specified, all raw material components are commercially available products well known to those skilled in the art.
[0032] The present invention does not have any special limitation on the type of MXene, and the type well known to those skilled in the art can be used. In the present invention, the type of the MXene is more preferably Ti 3 C 2 MXene. The present invention does not have any special limitation on the source of the MXene, and it can be prepared by a preparation method well known to those skilled in the art.
[0033] In the present invention, the nickel salt is preferabl...
Embodiment 1
[0048] 1mmol (0.1676g) Ti 3 C 2 MXene and 70mL deionized water were mixed under ultrasonic conditions for 30min to obtain Ti 3 C 2 After MXene dispersion, mix with 0.75mmol NiCl under the condition of stirring 2 ·6H 2 O, 0.25mmol Fe(NO 3 ) 3 9H 2 O and 2 mmol urea were mixed and stirred for 30 minutes, then transferred to a hydrothermal reaction kettle, and carried out a hydrothermal reaction at a temperature of 120° C. for 18 hours. After cooling down to room temperature, centrifugal washing was performed with deionized water and dried to obtain the negative electrode material of the battery. (Ti 3 C 2 The molar ratio of MXene and NiFe-LDH is 1:1);
[0049] The negative electrode material of the battery is carried out XRD and SEM test, test result is as follows respectively figure 1 and figure 2 shown by figure 1 It can be seen that the battery negative electrode material described in the present invention includes MXene and NiFe-LDH.
Embodiment 2
[0051] 1.5mmol (0.2514g) Ti 3 C 2 MXene and 70mL deionized water were mixed under ultrasonic conditions for 30min to obtain Ti 3 C 2 After MXene dispersion, mix with 0.75mmol NiCl under the condition of stirring 2 ·6H 2 O, 0.25mmol Fe(NO 3 ) 3 9H 2 O and 2 mmol urea were mixed and stirred for 30 minutes, then transferred to a hydrothermal reaction kettle, and carried out a hydrothermal reaction at a temperature of 120° C. for 18 hours. After cooling down to room temperature, centrifugal washing was performed with deionized water and dried to obtain the negative electrode material of the battery. (Ti 3 C 2 The molar ratio of MXene to NiFe-LDH is 1.5:1);
[0052] figure 2 is the SEM image of the negative electrode material of the battery, composed of figure 2 It can be seen that the NiFe-LDH was successfully grown on the surface of the MXene.
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