ALL SOLID-STATE ELECTROLYTE COMPOSITE BASED ON FUNCTIONALIZED METAL-ORGANIC FRAMEWORK MATERIALS FOR LITHIUM SECONDARY BATTERY AND METHOD FOR MANUFACTURING THE SAME

Abstract

A safe all-solid-state lithium secondary battery using a functionalized Metal-organic framework (MOFs)-based sol-id-state electrolyte composite and methods for manufacturing that electrolyte are provided. Specifically, that solid-state electrolyte composite includes MOFs material and traditional polymer, which are mixed and electrospining into a solid thin film. The solid-state electrolyte could significantly reduce the safety risk as well as enhance the Li+ conductivity rate through reducing the degree of crys-tallinity for polymer and coupling the polymer within the oriented and uniform pore structures in MOFs, thus improving the ionic conductivity and enhancing the Li batteries performance. The procedure involves only one step, and it is expected to be easy for scale-up.

Claims

1. An all-solid-state electrolyte composition for a secondary Li battery comprising: (a) functionalized MOFs; and (b) a polymer electrolyte.

2. The all-solid-state electrolyte composition of claim 1, wherein a weight percentage of the functionalized MOFs is 0.1%-20%, and the weight percentage of the polymer electrolyte is 80%-99.9%.

3. The all-solid-state electrolyte composition of claim 1, wherein the functionalized MOFs are selected from at least one of ZIF-8, ZIF-67, MOF-5, UIO-66, UIO-67, MIL-100 (Fe), MIL-53 (Al), DUT-5, DUT-4, MIL-101 (Cr), MIL-10INDC, HKUST-1 and PCN-14.

4. The all-solid-state electrolyte composition of claim 1, wherein functionalized groups for MOFs are selected from at least one of sulfonates, sulfonylimides, tetrahedral borates, and their derivatives.

5. The all-solid-state electrolyte composition of claim 1, wherein the polymer is selected from at least one of Polyethylene oxide (PEO), polymethyl methacrylate (PMMA), polyacrylonitrile (PAN), polyvinylidene difluoride (PVDF), polyvinylidene fluoride-hexafluoropropylene (PVDF-HFP) and their derivates.

6. The all-solid-state electrolyte composition of claim 1, wherein a type of the functionalized MOFs is one or two.

7. The all-solid-state electrolyte composition of claim 1, wherein the polymer electrolyte composite is selected from pure PEO or mixtures of PEO and another kind of polymer.

8. The all-solid-state electrolyte composition of claim 1, wherein the weight percentage of the functionalized MOFs ranges from 1.5% to 10%.

9. A process for manufacturing the all-solid-state electrolyte composition according to claim 1, wherein the process comprises: (a) pouring a certain amount of polymer powder into a Dimethylformamide (DMF) solvent at room temperature, and stirring it for 5-90 hours at 60-100° C. to form a clear solution A; (b) adding a certain amount of MOFs powder into the solution A, and stirring it for 8-90 hours at 50-100° C. to form a clear solution B; (c) pouring the solution B into a syringe and removing the air inside, then starting to electrospin at a certain rate and electric intensity to form a solid film; (d) drying the solid film at 60-100° C. to obtain the desired solid-state electrolyte.

10. The process for manufacturing the all-solid-state electrolyte composition of claim 9, wherein the electric intensity, injection rate and the injection time in procedure (c) range from 1 to 1.5 kV/cm, 1.2-1.5 mL/h and 3-5 hours, respectively.

11. The all-solid-state electrolyte composition of claim 3, wherein a type of the functionalized MOFs is one or two.

12. The all-solid-state electrolyte composition of claim 4, wherein the polymer electrolyte composite is selected from pure PEO or mixtures of PEO and another kind of polymer.

13. The all-solid-state electrolyte composition of claim 3, wherein the weight percentage of the functionalized MOFs ranges from 1.5% to 10%.

Description

BRIEF DESCRIPTION OF FIGURES

[0026] FIG. 1 is the SEM image of ZIF-8(SO.sub.3H)-PEO solid-state electrolyte in example 1.

[0027] FIG. 2 is the cross-sectional SEM image of ZIF-8(SO.sub.3H)-PEO solid-state electrolyte in example 1.

[0028] FIG. 3 is the SEM image of ZIF-8(SO.sub.3H, 10%)-PEO solid-state electrolyte in which the weight percentage of ZIF-8 in the whole electrolyte is 10% in example 2.

[0029] FIG. 4 is the SEM image of functionalized UIO-66 (SO.sub.3H)/ZIF-8(SO.sub.3H)-PEO mixed MOFs-based solid-state electrolyte in example 3.

[0030] FIG. 5 is the EIS results of the batteries in example 1 and comparative example 1.

[0031] FIG. 6 is the ion conductivity performance of the solid-state electrolytes in example 1 and comparative example 2.

[0032] FIG. 7 is the performance of the all-solid-state Li—S battery in example 1 and comparative example 2.

[0033] FIG. 8 is the stability performance of the all-solid-state Li—S battery in example 1 and comparative example 2.

[0034] FIG. 9 is the rate discharge curve of the all-solid-state Li-ion battery under 0.2 C CC/CV (constant current/constant voltage) charge to 4.2 V. Cut off 0.05 C; 0.2 C/0.5 C/1 C/1.5 C discharge from 4.2 V to 3.0 V.

[0035] FIG. 10 is the charge-discharge curve under 0.2 C CC/CV charge to 4.2V. Cut off 0.05 C; 0.2 C discharge from 4.2 V to 3.0 V.

[0036] FIG. 11 shows the standard charging and discharging curves of all-solid-state Li-ion battery at 0.2 C, the profile is 0.2 C CC/CV charge to 4.2V. Cut off 0.05 C; 0.2 C/0.5 C/1 C/1.5 C discharge from 4.2 V to 3.0 V.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

[0037] Hereinafter, the present invention will be described batteries in more detail based on examples. Meanwhile, the present invention is not interpreted to be limited thereto.

Example 1

[0038] I. Production of Solid-State Electrolyte

[0039] Weigh polymer PEO powder and DMF 1.2 g, 5.4 g, respectively. Then the PEO powder was poured into the DMF solvent at room temperature, and stirring it for 5 hr at 80° C. to form a clear solution. The functionalized ZIF-8 powder of 0.018 g was added into the above solution, and stirring it for 8 hr at 80° C. to form a clear solution. The weight percentage of functionalized ZIF reaches 1.5%. That solution was poured into the syringe and removed the air bubble inside. Then started to electrospin for the rate of 1.2 mL/h and with the electric intensity of 1 kV/cm for 5 hours to form a solid film. The above film was dried at 80° C. to obtain the desired solid-state electrolyte.

[0040] II. Electrochemical Characterization of the Solid-State Electrolyte

[0041] The ion conductivity was tested at different temperatures.

[0042] III. Production of Li—S all-Solid-State Battery

[0043] Such electrolyte was then immersed in 70% S/CS2 solution at 155° C. for 6 hours to obtain carbonaceous fabrics, which were mixed with carbon black (wt.10%) and PVDF (10%) as the cathode material. Assembling it with Li metal and commercialized Celegard 2500 separator to Li—S battery. The battery performance was then tested at room temperature.

[0044] IV. Production of Li-Ion all-Solid-State Battery

[0045] The commercialized ternary cathode material of Nickel Cobalt Manganese (NCM523), graphite as the positive and negative electrode, respectively. While the obtained all-solid-state material is used as the electrolyte. The cell is assembled and tested under open air condition.

Example 2

[0046] In Example 2, the weight percentage of functionalized MOFs in the whole solid-state electrolyte was adjusted.

[0047] I. Production of Solid-State Electrolyte

[0048] Weigh polymer PEO powder and DMF 1.2 g, 5.4 g, respectively. Then the PEO powder was poured into the DMF solvent at room temperature, and stirring it for 5 hr at 80° C. to form a clear solution. The functionalized ZIF-8 powder of 0.12 g was added into the above solution, and stirring it for 8 hr at 80° C. to form a clear solution. The weight percentage of functionalized ZIF reaches 10%. That solution was poured into the syringe and removed the air bubble inside. Then started to electrospin for the rate of 1.2 mL/h and with the electric intensity of 1 kV/cm for 5 hours to form a solid film. The above film was dried at 80° C. to obtain the desired solid-state electrolyte.

[0049] II. Electrochemical Characterization of the Solid-State Electrolyte

[0050] The ion conductivity was tested at different temperatures.

[0051] III. Production of Li—S Solid-State Battery

[0052] Such electrolyte was then immersed in 70% S/CS2 solution at 155° C. for 6 hours to obtain carbonaceous fabrics, which were mixed with carbon black (wt.10%) and PVDF (10%) as the cathode material. Assembling it with Li metal and commercialized Celegard 2500 separator to Li—S battery.

[0053] IV. The Performance of Li—S Solid-State Battery was Evaluated

[0054] The electrochemical characterization, rate performance and long-term cycling performance were then tested at room temperature.

[0055] V. Production of Li-Ion all-Solid-State Battery

[0056] The commercialized ternary cathode material of Nickel Cobalt Manganese (NCM523), graphite as the positive and negative electrode, respectively. While the obtained all-solid-state material is used as the electrolyte. The cell is assembled and tested under open air condition.

Example 3

[0057] In Example 3, the kind number of functionalized MOFs in the whole solid-state electrolyte was adjusted.

[0058] I. Production of Solid-State Electrolyte

[0059] Weigh polymer PEO powder and DMF 1.2 g, 5.4 g, respectively. Then the PEO powder was poured into the DMF solvent at room temperature, and stirring it for 5 hr at 80° C. to form a clear solution. The functionalized ZIF-8 powder of 0.012 g and UIO-66 of 0.006 g were added into the above solution, and stirring it for 8 hr at 80° C. to form a clear solution. The weight percentage of functionalized ZIF reaches 10%. That solution was poured into the syringe and removed the air bubble inside. Then started to electrospin for the rate of 1.2 mL/h and with the electric intensity of 1 kV/cm for 5 hours to form a solid film. The above film was dried at 80° C. to obtain the desired solid-state electrolyte.

[0060] II. Electrochemical Characterization of the Solid-State Electrolyte

[0061] The ion conductivity was tested at different temperatures.

[0062] III. Production of Li—S Solid-State Battery

[0063] Such electrolyte was then immersed in 70% S/CS2 solution at 155° C. for 6 hours to obtain carbonaceous fabrics, which were mixed with carbon black (wt.10%) and PVDF (10%) as the cathode material. Assembling it with Li metal and commercialized Celegard 2500 separator to Li—S battery.

[0064] IV. The Performance of Li—S Solid-State Battery was Evaluated

[0065] The electrochemical characterization, rate performance and long-term cycling performance were then tested at room temperature.

[0066] V. Production of Li-Ion all-Solid-State Battery

[0067] The commercialized ternary cathode material of Nickel Cobalt Manganese (NCM523), graphite as the positive and negative electrode, respectively. While the obtained all-solid-state material is used as the electrolyte. The cell is assembled and tested under open air condition.

Example 4

[0068] In Example 4, the electric intensity of the electrospining method was adjusted.

[0069] I. Production of Solid-State Electrolyte

[0070] Weigh polymer PEO powder and DMF 1.2 g, 5.4 g, respectively. Then the PEO powder was poured into the DMF solvent at room temperature, and stirring it for 5 hr at 80° C. to form a clear solution. The functionalized ZIF-8 powder of 0.018 g was added into the above solution, and stirring it for 8 hr at 80° C. to form a clear solution. The weight percentage of functionalized ZIF reaches 1.5%. That solution was poured into the syringe and removed the air bubble inside. Then started to electrospin for the rate of 1.2 mL/h and with the electric intensity of 1.5 kV/cm for 5 hours to form a solid film. The above film was dried at 80° C. to obtain the desired solid-state electrolyte.

[0071] II. Electrochemical Characterization of the Solid-State Electrolyte

[0072] The ion conductivity was tested at different temperatures.

[0073] III. Production of Li—S Solid-State Battery

[0074] Such electrolyte was then immersed in 70% S/CS2 solution at 155° C. for 6 hours to obtain carbonaceous fabrics, which were mixed with carbon black (wt.10%) and PVDF (10%) as the cathode material. Assembling it with Li metal and commercialized Celegard 2500 separator to Li—S battery. The battery performance was then tested at room temperature.

[0075] IV. Production of Li-Ion all-Solid-State Battery

[0076] The commercialized ternary cathode material of Nickel Cobalt Manganese (NCM523), graphite as the positive and negative electrode, respectively. While the obtained all-solid-state material is used as the electrolyte. The cell is assembled and tested under open air condition.

Example 5

[0077] In Example 5, the electrospinning rate of the electrospining method was adjusted.

[0078] I. Production of Solid-State Electrolyte

[0079] Weigh polymer PEO powder and DMF 1.2 g, 5.4 g, respectively. Then the PEO powder was poured into the DMF solvent at room temperature, and stirring it for 5 hr at 80° C. to form a clear solution. The functionalized ZIF-8 powder of 0.018 g was added into the above solution, and stirring it for 8 hours at 80° C. to form a clear solution. The weight percentage of functionalized ZIF reaches 1.5%. That solution was poured into the syringe and removed the air bubble inside. Then started to electrospin for the rate of 1.5 mL/h and with the electric intensity of 1.5 kV/cm for 5 hours to form a solid film. The above film was dried at 80° C. to obtain the desired solid-state electrolyte.

[0080] II. Electrochemical Characterization of the Solid-State Electrolyte

[0081] The ion conductivity was tested at different temperatures.

[0082] III. Production of Li—S Solid-State Battery

[0083] Such electrolyte was then immersed in 70% S/CS2 solution at 155° C. for 6 hours to obtain carbonaceous fabrics, which were mixed with carbon black (wt.10%) and PVDF (10%) as the cathode material.

[0084] Assembling it with Li metal and commercialized Celegard 2500 separator to Li—S battery. The battery performance was then tested at room temperature.

[0085] IV. Production of Li-Ion all-Solid-State Battery

[0086] The commercialized ternary cathode material of Nickel Cobalt Manganese (NCM523), graphite as the positive and negative electrode, respectively. While the obtained all-solid-state material is used as the electrolyte. The cell is assembled and tested under open air condition.

Comparative Example 1

[0087] The solid-state electrolyte is produced in the same manner as in the Example 1 except that the functionalized MOFs used in the Example 1 was not used.

Comparative Example 2

[0088] The CR2032 coin cells were assembled by using sulfur composite (S and Li2S, 1:1 by mole) electrode as cathode, Celgard 2500 membrane as separator, and lithium foil as anode in Ar-filled glove box with moisture and oxygen level lower than 0.5 ppm. The electrolyte contains 1M lithium bis(trifluoromethane) sulfonamide (LiTFSI) in a binary solvent of dimethoxymethane/1,3-dioxolane (DME/DOL, 1:1 by volume) with 2 wt. % LiNO3 as additive.

[0089] FIG. 1 is the scheme of the functionalized MOFs.

[0090] FIG. 2 shows that the functionalized ZIF-8-PEO solid-state electrolyte in present invention uniformly disperses on the fibers of PEO polymer, indicating the electrospinning method can mix the two composites well.

[0091] FIG. 3 shows that the thickness of functionalized ZIF-8-PEO solid-state electrolyte is 320 um.

[0092] FIG. 4 shows that the functionalized ZIF-8 particles mostly distribute on the PEO polymer fibers, indicating the weigh percentage is a little bit high.

[0093] FIG. 5 shows that the functionalized UIO-66 and functionalized to ZIF-8 particles were distributed uniformly on the PEO polymer fibers.

[0094] FIG. 6 shows that the battery resistance in Example 1 and Comparative Example 1 was 1250Ω, 1650Ω, respectively, indicating that the existence of functionalized MOFs particles is beneficial for reducing the resistance and improving the Li+ ion conductivity.

[0095] FIG. 7 shows that the ion conductivities at 25° C., 60° C., 70° C., 80° C. in Example 1 are higher than that in Comparative Example 1 and Comparative Example 2, demonstrating the ion conductivity is excellent in Example 1. It should be noted that the highest ion conductivity reaches as high as 0.18 mS/cm, showing the potential for commercialization.

[0096] FIG. 8 shows that the rate discharge curves at 0.1 C, 0.2 C, 0.5 C, 1 C in Example 1 are higher than that in Comparative Example 1 and Comparative Example 2. In addition, the performance when recycling at 0.1 C remains 93.1%, compared to that is only 77.2%, 73.6% in Comparative Example 1 and Comparative Example 2, respectively.

[0097] The charge-discharge curves of the all-solid-state Li—S battery in Example 1 is shown in FIG. 9. The results show the excellent cycling stability of the solid-state electrolyte with a high capacity retention of 83.3% even after 100 cycles, while it is only 69.2%, 52% in Comparative Example 1 and Comparative Example 2, respectively.

[0098] FIG. 10 shows the standard charging and discharging curves of all-solid-state Li-ion battery at 0.2 C, the profile is 0.2 C CC/CV (constant current/constant voltage) charge to 4.2V. Cut off 0.05 C; 0.2 C discharge from 4.2 V to 3.0 V.

[0099] FIG. 11 shows the standard charging and discharging curves of all-solid-state Li-ion battery at 0.2 C, the profile is 0.2 C CC/CV charge to 4.2V. Cut off 0.05 C; 0.2 C/0.5 C/1 C/1.5 C discharge from 4.2 V to 3.0 V.