Preparation Method and Application for Metal Sulfide Hollow Microspheres with Enriched Sulfur Vacancies

Abstract

Disclosed is a hollow sulfide microsphere with enriched sulfur vacancies, which is prepared by a method comprising the steps of: dissolving cobalt nitrate and nickel nitrate in a mixed solution of N, N-dimethylformamide and acetone with an equal volume; then adding a chelating agent thereto, subjecting a resulting mixture to a solvothermal reaction to obtain a coordination polymer microsphere; dissolving the coordination polymer microsphere and a sulfurization agent in an organic solvent, and reacting to obtain a hollow sulfide microsphere; and subjecting the hollow sulfide microsphere to reduction treatment with sodium borohydride, centrifuging, washing and drying to obtain the hollow sulfide microsphere with enriched sulfur vacancies having a particle size of 1-2.5 μm, a shell thickness of 15-30 nm and a specific capacity of the material of 763.4 C g.sup.−1 (current density is 1 A g.sup.−1).

Claims

1. A sulfide hollow microsphere with enriched sulfur vacancies prepared through the following steps: 1) dissolving cobalt nitrate and nickel nitrate in a mixed solution of N, N-dimethylformamide and acetone to obtain a solution A; 2) dissolving a chelating agent with a carboxylate group in the solution A to obtain a solution B; 3) transferring the solution B into a stainless-steel autoclave lined Teflon and reacting at 140-160° C. for 1-5 h, cooling, centrifuging, washing and drying to obtain a coordination polymer microsphere; 4) dissolving the coordination polymer microsphere and a sulfurization agent in an organic solvent, reacting at 120-160° C. for 0.5-6 h, cooling, centrifuging, washing and drying to obtain a sulfide hollow microsphere; 5) dispersing the hollow sulfide microsphere in a sodium borohydride solution, stirring for 0.5-2 h, centrifuging, washing and drying to obtain sulfide hollow microspheres with enriched sulfur vacancies.

2. The sulfide hollow microspheres with enriched sulfur vacancies according to claim 1, wherein in step 1), a volume ratio of N, N-dimethylformamide and acetone is 1:1, and a molar ratio of cobalt nitrate and nickel nitrate is 2-4:1-2.

3. The sulfide hollow microspheres with enriched sulfur vacancies according to claim 1, wherein in step 2), the chelating agent is selected from the group including isophthalic acid, trimesic acid, terephthalic acid, and 3,5-pyridinedicarboxylic acid; the chelating agent is dissolved in the solution A and stirred for 6 h, and a molar ratio of the chelating agent to a total amount of cobalt nitrate and nickel nitrate is 1-2:2-4.

4. The sulfide hollow microspheres with enriched sulfur vacancies according to claim 1, wherein in step 3), the washing treatment is conducted with absolute ethanol, and the drying is under vacuum.

5. The sulfide hollow microspheres with enriched sulfur vacancies according to claim 1, wherein in step 4), the sulfurization agent is selected from the group including thioacetamide, thiourea, L-cysteine, and sodium sulfide, a mass ratio of the coordination polymer microsphere to the sulfurization agent is 2-4:1-8, the organic solvent is absolute ethanol, and the dispersion is performed with ultrasonic treatment for 15 min.

6. The sulfide hollow microspheres with enriched sulfur vacancies according to claim 1, wherein in step 4), the washing treatment is conducted with absolute ethanol, and the drying is under vacuum.

7. The sulfide hollow microspheres with enriched sulfur vacancies according to claim 1, wherein in step 5), a concentration of the sodium borohydride aqueous solution is 0.5-2 mol/L, preferably 1 mol/L, the washing is conducted by deionized water, and the drying is under vacuum.

8. The sulfide hollow microspheres with enriched sulfur vacancies according to claim 1, wherein a particle size and a shell thickness of the hollow microsphere is 1-2.5 μm and 15-30 nm, respectively.

9. An application of the sulfide hollow microspheres with enriched sulfur vacancies according to claim 1 for preparing electrode materials.

10. The application according to claim 9, wherein in step 1), a volume ratio of N, N-dimethylformamide and acetone is 1:1, and a molar ratio of cobalt nitrate and nickel nitrate is 2-4:1-2.

11. The application according to claim 9, wherein in step 2), the chelating agent is selected from the group consisting of isophthalic acid, trimesic acid, terephthalic acid, and 3,5-pyridinedicarboxylic acid, the chelating agent is dissolved in the solution A and stirred for 6 h, and a molar ratio of the chelating agent to a total amount of cobalt nitrate and nickel nitrate is 1-2:2-4.

12. The application according to claim 9, wherein in step 3), the washing is conducted with absolute ethanol, and the drying is vacuum drying.

13. The application according to claim 9, wherein in step 4), the sulfurization agent is selected from the group consisting of thioacetamide, thiourea, L-cysteine, and sodium sulfide, a mass ratio of the coordination polymer microsphere to the sulfurization agent is 2-4:1-8, the organic solvent is absolute ethanol, and the dispersion is ultrasonic dispersion for 15 min.

14. The application according to claim 9, wherein in step 4), the washing is conducted by washing with absolute ethanol, and the drying is under vacuum.

15. The application according to claim 9, wherein in step 5), a concentration of the aqueous sodium borohydride solution is 0.5-2 mol/L, preferably 1 mol/L, the washing is conducted with deionized water, and the drying is under vacuum.

16. The application according to claim 9, wherein a particle size and a shell thickness of the hollow microsphere is 1-2.5 μm and 15-30 nm, respectively.

17. The application according to claim 9, wherein the electrode material is a battery-type electrode material.

18. The application according to claim 10, wherein the electrode material is a battery-type electrode material.

19. The application according to claim 11, wherein the electrode material is a battery-type electrode material.

20. The application according to claim 12, wherein the electrode material is a battery-type electrode material.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0028] FIG. 1 is a SEM image of the sulfide hollow microspheres with enriched sulfur vacancies prepared in Example 5 of the present disclosure;

[0029] FIG. 2 is a TEM image of the sulfide hollow microspheres with enriched sulfur vacancies prepared in Example 5 of the present disclosure;

[0030] FIG. 3 is a XRD pattern of the sulfide hollow microspheres with enriched sulfur vacancies prepared in Example 5 and the sulfide prepared in Example 2;

[0031] FIG. 4 is a XPS spectrum of the sulfide hollow microspheres with enriched sulfur vacancies prepared in Example 5 and a high-resolution XPS spectrum of S element.

[0032] FIG. 5 is a CV curve of Example 6 under different scanning rates;

[0033] FIG. 6 is a GCD curve of Example 6 under different current densities;

[0034] FIG. 7 shows the specific capacity of Example 6 under different current densities;

[0035] FIG. 8 is a graph showing the specific capacity and Coulombic efficiency of Example 6 after 5000 cycles.

DETAILED DESCRIPTION OF THE EMBODIMENTS

[0036] In the present disclosure, the chemical raw materials used were purchased from Beijing Tongguang Fine Chemical Co., Ltd. and were of analytical grade.

Example 1

[0037] 0.2 mmol of cobalt nitrate and 0.1 mmol of nickel nitrate were dissolved in a mixed solution of 15 mL of N, N-dimethylformamide and 15 mL of acetone; 0.15 mmol of isophthalic acid was added into the above solution, stirred at room temperature for 6 h, and transferred to a stainless-steel autoclave lined Teflon to perform a solvothermal reaction at a temperature of 160° C. for 4 h; after cooling down to room temperature, a resulting product was subjected to centrifuging, washing and vacuum drying to obtain nickel-cobalt coordination polymer microspheres, solid spheres with a particle size of about 1-2 μm.

Example 2

[0038] 0.2 mmol of cobalt nitrate and 0.1 mmol of nickel nitrate were dissolved in a mixed solution of 15 mL of N, N-dimethylformamide and 15 mL of acetone; 0.15 mmol of isophthalic acid was added into the above solution, stirred at room temperature for 6 h, and transferred to a stainless-steel autoclave lined Teflon to perform a solvothermal reaction at a temperature of 160° C. for 4 h; after cooling down to room temperature, a resulting product was subjected to centrifuging, washing and vacuum drying to obtain nickel-cobalt coordination polymer microspheres; 30 mg of nickel-cobalt coordination polymer microspheres and 60 mg of thioacetamide were dissolved in 30 mL of absolute ethanol; the mixture was subjected to ultrasonic treatment for 15 min, and transferred to a stainless-steel autoclave lined Teflon to perform a solvothermal reaction at a temperature of 160° C. for 2 h to obtain the sulfide core-shell microspheres with an average size of 1-2 μm and rough surface.

Example 3

[0039] 0.133 mmol of cobalt nitrate and 0.067 mmol of nickel nitrate were dissolved in a mixed solution of 15 mL of N, N-dimethylformamide and 15 mL of acetone; 0.2 mmol of isophthalic acid was added into the above solution, stirred at room temperature for 6 h, and transferred to a stainless-steel autoclave lined Teflon to perform a solvothermal reaction at a temperature of 160° C. for 4 h; after cooling, a resulting product was subjected to centrifuging, washing and vacuum drying to obtain nickel-cobalt coordination polymer microspheres; 30 mg of nickel-cobalt coordination polymer microspheres and 60 mg of thioacetamide were weighed, and dispersed in 30 ml of absolute ethanol; the mixture was subjected to ultrasonic treatment for 15 min, and transferred to the hydrothermal kettle to perform a solvothermal reaction at a temperature of 160° C. for 6 h to obtain the sulfide hollow microspheres with the average size of 1-2 μm and the shell thickness of about 20-30 nm; at the same time, according to the peak area fitted in X-ray spectrum, a relative content of sulfur vacancies in the product is 31.24%.

Example 4

[0040] 0.133 mmol of cobalt nitrate and 0.067 mmol of nickel nitrate were dissolved in a mixed solution of 15 mL of N, N-dimethylformamide and 15 mL of acetone; 0.2 mmol of isophthalic acid was added into the above solution, stirred at room temperature for 6 h, and transferred to a stainless-steel autoclave lined Teflon to perform a solvothermal reaction at a temperature of 160° C. for 4 h; after cooling, a resulting product was subjected to centrifuging, washing and vacuum drying to obtain nickel-cobalt coordination polymer microspheres; 30 mg of nickel-cobalt coordination polymer microspheres and 60 mg of thioacetamide were weighed, and dispersed in 30 ml of absolute ethanol; the mixture was subjected to ultrasonic treatment for 15 min, and transferred to a stainless-steel autoclave lined Teflon to perform a solvothermal reaction at a temperature of 160° C. for 6 h to obtain a hollow sulfide; 30 mg of the hollow sulfide was dispersed into a 1 mol/L aqueous sodium borohydride solution, stirred at room temperature for 1 h, then the resulting product was subjected to centrifuging, washing with deionized water and vacuum drying to obtain sulfide hollow microspheres with enriched sulfur vacancies. The product reduced by sodium borohydride has a microspherical morphology, with a particle size of 1-2.5 μm and a slightly reduced crystallinity; according to the peak area fitted by the X-ray spectrum, the relative content of sulfur vacancies in the product is 45.64%.

Example 5

[0041] 0.133 mmol of cobalt nitrate and 0.067 mmol of nickel nitrate were dissolved in a mixed solution of 15 mL of N, N-dimethylformamide and 15 mL of acetone; 0.2 mmol of isophthalic acid was added into the above solution, stirred at room temperature for 6 h, and transferred to a stainless-steel autoclave lined Teflon to perform a solvothermal reaction at a temperature of 160° C. for 4 h; after cooling, a resulting product was subjected to centrifuging, washing and vacuum drying to obtain nickel-cobalt coordination polymer microspheres; 30 mg of nickel-cobalt coordination polymer microspheres and 60 mg of thioacetamide were weighed, and dispersed in 30 ml of absolute ethanol; the mixture was subjected to ultrasonic treatment for 15 min, and transferred to a stainless-steel autoclave lined Teflon to perform a solvothermal reaction at a temperature of 160° C. for 6 h to obtain a hollow sulfide; 30 mg of the hollow sulfide was dispersed into a 1 mol/L aqueous sodium borohydride solution, stirred at room temperature for 2 h, then the resulting product was subjected to centrifuging, washing with deionized water and vacuum drying to obtain sulfide hollow microspheres with enriched sulfur vacancies. The product reduced by sodium borohydride maintains a microspherical morphology, with a particle size of 1-2 μm, and a shell thickness of 15-25 nm; according to the peak area fitted in the X-ray spectrum, the relative content of sulfur vacancies in the product is 65.34%.

[0042] SEM results in FIG. 1 show that the diameter of the sulfide hollow microspheres with enriched sulfur vacancies is about 1-2 μm, and the surface of the microspheres is rough; The TEM results of the sample in FIG. 2 show that the microspheres have a hollow structure with the shell thickness of 10-20 nm; XRD results (FIG. 3) show that the diffraction peaks of the sulfide hollow microspheres with enriched sulfur vacancies coincides with the standard PDF card (JPCDS: #20-0278) after reduction treatment; XPS results show that Ni, Co and S elements exist in the sulfide hollow microspheres with enriched sulfur vacancies, and according to the high-resolution XPS spectrum of S, the relative content of S vacancies (2p½) reaches to 65.34%.

Example 6

[0043] The sulfide hollow microspheres with enriched sulfur vacancies prepared in Example 5, acetylene black and polytetrafluoroethylene were mixed according to a mass ratio of 7:2:1, and the slurry was coated on a 1×1 cm.sup.2 nickel foam, dried at 80° C. under vacuum for 12 h to acquire a working electrode. Cyclic voltammetry and galvanostatic charge-discharge tests were performed with an electrochemical workstation using a 3 M KOH aqueous solution as an electrolyte, a Hg/HgO electrode as a reference electrode, and a Pt electrode as a counter electrode.

[0044] It can be seen from FIG. 5 that the curve shows an obvious redox peaks. With the increase of a CV scan rate, anionic and cathodic peaks exhibit slight shifts for positive and negative direction, respectively; secondly, during the charge-discharge process, the GCD curve of the sample (FIG. 6) shows an obvious charge-discharge plateau, showing a typical behavior of battery-like electrode materials; when the current density is 1 A g.sup.−1, the specific capacity is 763.4 C g.sup.−1 (specific capacitance is 1526.8 F g.sup.−1, FIG. 7). The capacity retention of the electrode remains above 90%, and the Coulombic efficiency maintains 100% without decaying after 5000 cycles under a current density of 10 A g.sup.−1, as shown in FIG. 8.