Method of preparing and application of carbon selenium composites
View Patent ↗Disclosed is method of preparing a selenium carbon composite material and a use of the selenium carbon composite material in a cathode of a lithium selenium secondary battery. A battery formed with a cathode of the disclosed selenium carbon composite material has high energy density and stable electrochemical performance. The disclosed selenium carbon composite material can effectively shorten the migration distance of lithium ions during charging and discharging of the battery and improve conductivity and utilization of selenium after compounding carbon and selenium. Multiple batteries formed with cathodes of the disclosed selenium carbon composite material can be assembled into a lithium selenium pouch-cell battery having stable electrochemical performance and high energy density.
1. A method of preparing a selenium carbon composite material, comprising:
(a) carbonizing an alkali metal organic salt or an alkaline earth metal organic salt at high temperature, washing with an acid, and drying to obtain a two-dimensional carbon nanomaterial;
(b) mixing the two-dimensional carbon material obtained in step (a) with an organic solvent and selenium, heating the mixture to evaporate the organic solvent, and then going through multistage heat ramping and soaking processes to achieve the two-dimensional selenium carbon composite material.
2. The method according to claim 1 , wherein, in step (a):
the alkali metal organic salt is selected from one or several of potassium citrate, potassium gluconate, and sucrose acid sodium;
the alkaline earth metal organic salt is selected from one or both of calcium gluconate and sucrose acid calcium; and
carbonization is performed at 600° C.-1000° C. for 1-10 hours.
3. The method according to claim 1 , wherein, in step (b):
the organic solvent is selected from one or several of ethanol, dimethylsulfoxide (DMSO), toluene, acetonitrile, N,N-dimethylformamide (DMF), carbon tetrachloride, diethyl ether or ethyl acetate;
the multistage-heat ramping and soaking process includes: heating 2° C.-10° C./min to 200° C.-300° C. and soaking for 3-10 hours; and
continue to heating to 400° C.-600° C. and soaking for 10-30 hours.
4. The method of claim 1 , wherein the acid is hydrochloric acid.
5. The method according to claim 1 , wherein, in step (a):
the alkali metal organic salt is selected from one or several of potassium citrate, potassium gluconate, and sucrose acid sodium;
the alkaline earth metal organic salt is selected from one or both of calcium gluconate and sucrose acid calcium; and
carbonization is performed at 700° C.-900° C.
6. The method according to claim 1 , wherein, in step (b):
the organic solvent is selected from one or several of ethanol, dimethylsulfoxide (DMSO), toluene, acetonitrile, N,N-dimethylformamide (DMF), carbon tetrachloride, diethyl ether or ethyl acetate; and
the multistage-heat ramping and soaking process includes: heating to 220° C.-280° C. and soaking at 220° C.-280° C.
7. A method of preparing a selenium carbon composite material, comprising:
(a) carbonizing an alkali metal organic salt or an alkaline earth metal organic salt at a temperature ≥600° C.;
(b) washing the carbonized salt of step (a) with an acid;
(c) drying the washed carbonized salt of step (b) to obtain a two-dimensional carbon nanomaterial;
(d) mixing the two-dimensional carbon nanomaterial of step (c) with selenium and an organic solvent;
(e) heating the mixture of step (d) to evaporate the organic solvent; and
(f) subjecting the organic solvent evaporated mixture of step (e) to a multistage heat ramping and soaking process to achieve a two-dimensional selenium carbon composite material.
8. The method of claim 7 , wherein in step (d) the two-dimensional carbon nanomaterial of step (c) is mixed with an organic solution of selenium and the organic solvent.
9. The method of claim 7 , wherein:
the alkali metal organic salt is one or more of potassium citrate, potassium gluconate, and sucrose acid sodium; or
the alkaline earth metal organic salt is one or both of calcium gluconate and sucrose acid calcium; or
step (a) is performed at 600° C.-1000° C.; or
step (a) is performed for 1-10 hours.
10. The method of claim 7 , wherein:
the organic solvent of step (d) is an organic solvent comprised of one or more of ethanol, dimethylsulfoxide (DMSO), toluene, acetonitrile, N,N-dimethylformamide (DMF), carbon tetrachloride, diethyl ether, and ethyl acetate; and
the multistage heat ramping and soaking process of step (f) includes:
(1) increasing the temperature by 2° C.-10° C./min to a temperature of 200° C.-300° C.;
(2) following step (1), soaking at the temperature of step (1) for 3-10 hours;
(3) following step (2), increasing the temperature to 400° C.-600° C.; and
(4) following step (3), soaking at the temperature of step (3) for 10-30 hours.
11. The method of claim 7 , wherein the acid is hydrochloric acid.
12. The method of claim 7 , wherein:
the alkali metal organic salt is one or more of potassium citrate, potassium gluconate, and sucrose acid sodium; or
the alkaline earth metal organic salt is one or both of calcium gluconate and sucrose acid calcium; or
step (a) is performed at 700° C.-900° C.
13. The method of claim 7 , wherein:
the organic solvent of step (d) is an organic solvent comprised of one or more of ethanol, dimethylsulfoxide (DMSO), toluene, acetonitrile, N,N-dimethylformamide (DMF), carbon tetrachloride, diethyl ether, and ethyl acetate; and
the multistage heat ramping and soaking process of step (f) includes:
(1) increasing the temperature to 220° C.-280° C.; and
(2) following step (1), soaking at the temperature of step (1).
14. The method of claim 13 , wherein the multistage heat ramping and soaking process of step (f) includes:
(3) following step (2), increasing the temperature to 430° C.-460° C.; and
(4) following step (3), soaking at the temperature of step (3).