INTERMEDIATE PRODUCT OF SOLID ELECTROLYTE, SOLID ELECTROLYTE USING SAME, SECONDARY BATTERY INCLUDING SAME, AND METHOD FOR MANUFACTURING SAME

Abstract

Provided is an intermediate product of a solid electrolyte. The intermediate product of a solid electrolyte may comprise: a compound in which a cation including thiophenium or thiazolium and an anion including fluorohydrogenate are bound, and a solvent in which the compound is mixed.

Claims

1. An intermediate product of a solid electrolyte, comprising a compound in which a cation including thiophenium or thiazolium and an anion including fluorohydrogenate are bound; and a solvent in which the compound is mixed.

2. The intermediate product of the solid electrolyte of claim 1, wherein the intermediate product of the solid electrolyte including the compound and the solvent is in a liquid or gel state.

3. The intermediate product of the solid electrolyte of claim 1, wherein the solvent comprises at least any one of acetonitrile, tetrahydrofuran, DMSO, or DMF.

4. The intermediate product of the solid electrolyte of claim 1, wherein the cation comprises the thiophenium, and the compound comprises a methyl group bonded with a sulfur element of the thiophenium.

5. The intermediate product of the solid electrolyte of claim 1, wherein the cation comprises the thiazolium, and the compound comprises an ethyl group bonded with a nitrogen element of the thiazolium.

6. A method for preparing a solid electrolyte, the method comprising: preparing an intermediate product of a solid electrolyte according to claim 1; and removing and drying the solvent included in the intermediate product of the solid electrolyte to prepare a solid electrolyte.

7. A secondary battery comprising: a positive electrode; a solid electrolyte disposed on the positive electrode and prepared according to claim 6; and a negative electrode disposed on the solid electrolyte.

8. The secondary battery of claim 7, wherein a positive electrode active material of the positive electrode comprises lithium, phosphorus, and iron, and a negative electrode active material of the negative electrode comprises lithium.

9. A cation source for preparing a solid electrolyte comprising a compound in which a cation and an anion are bound, wherein the cation source includes: a solution including an alkyl group; and thiophene or thiazoline mixed in the solution including the alkyl group.

10. The cation source of claim 9, wherein thiophene is mixed in the solution including the alkyl group, and the solution including the alkyl group includes dichloromethane and acetonitrile.

11. The cation source of claim 9, wherein thiazoline is mixed in the solution comprising the alkyl group, and the solution comprising the alkyl group comprises ethyl chloride and acetonitrile.

12. An anion source for preparing a solid electrolyte comprising a compound in which a cation and an anion are bound, wherein the anion source includes: a solvent including water; and hydrofluoric acid mixed in the solvent.

13. The anion source for preparing the solid electrolyte of claim 12, further comprising: lithium salt in addition to the solvent and the hydrofluoric acid.

Description

DESCRIPTION OF DRAWINGS

[0030] FIG. 1 is a graph showing an ion conductivity of compounds according to Experimental Examples 1-1, 11-7, 11-8, 11-15, 11-17 and 11-18 of the present application as measured depending on a temperature.

[0031] FIG. 2 is a differential scanning calorimetry (DSC) graph showing a compound according to Experimental Example 1-1 and a solid electrolyte according to Experimental Example 12-3 of the present application.

[0032] FIG. 3 is a DSC graph showing a compound according to Experimental Examples 11-7 and 11-8 of the present application.

[0033] FIGS. 4 and 5 are graphs showing an X-ray diffraction (XRD) pattern of a compound according to Experimental Example 1-1 of the present application depending on a temperature.

[0034] FIG. 6 is a graph showing an NMR analysis result of a solid electrolyte according to Experimental Example 12-1 of the present application.

[0035] FIG. 7 is a graph showing a chemical shift and a diffusion coefficient of a solid electrolyte according to Experimental Example 12-1 of the present application as measured depending on a temperature.

[0036] FIG. 8 is a graph showing an XRD pattern of a compound according to Experimental Example 1-1 and a solid electrolyte according to Experimental Example 12-2 of the present application.

[0037] FIG. 9 is a view for explaining a crystal structure of a solid electrolyte according to Experimental Examples 12-1 to 12-3 of the present application.

[0038] FIG. 10 is a graph showing an ion conductivity of a compound according to Experimental Example 1-1 and a solid electrolyte according to Experimental Examples 12-1 to 12-3 of the present application depending on a temperature.

[0039] FIG. 11 is a picture of a electrolyte membrane coated with a solid electrolyte according to Experimental Example 12-1 of the present application.

[0040] FIGS. 12 and 13 are graphs showing results of a cycle test of a secondary battery including a solid electrolyte according to Experimental Example 12-2 of the present application.

[0041] FIG. 14 is a graph showing a capacity retention rate depending on a charge/discharge rate of a secondary battery including a solid electrolyte according to Experimental Example 12-2 of the present application.

[0042] FIG. 15 is a graph showing an impedance depending on a cycle test of a secondary battery including a solid electrolyte according to Experimental Example 12-2 of the present application.

MODE FOR INVENTION

[0043] Hereinafter, preferred embodiments of the present application will be described in detail with reference to the accompanying drawings. However, the technical idea of the present application is not limited to the embodiments described herein and may be implemented in other forms. Rather, the embodiments introduced herein are provided to sufficiently deliver the spirit of the present application to those skilled in the art so that the disclosed contents may become thorough and complete.

[0044] When it is mentioned in the specification that one element is on another element, it means that the first element may be directly formed on the second element or a third element may be interposed between the first element and the second element. Further, in the drawings, the thicknesses of the membrane and areas are exaggerated for efficient description of the technical contents.

[0045] Further, in the various embodiments of the present specification, the terms such as first, second, and third are used to describe various elements, but the elements are not limited to the terms. These terms are used only to distinguish one component from another component. Accordingly, an element mentioned as a first element in one embodiment may be mentioned as a second element in another embodiment. The embodiments described and illustrated herein also include their complementary embodiments. Further, the term “and/or” in the specification is used to include at least one of the elements enumerated in the specification.

[0046] In the specification, the terms of a singular form may include plural forms unless otherwise specified. Further, the terms “including” and “having” are used to designate that the features, the numbers, the steps, the elements, or combinations thereof described in the specification are present, and are not to be understood as excluding the possibility that one or more other features, numbers, steps, elements, or combinations thereof may be present or added.

[0047] Further, in the following description of the present application, a detailed description of known functions or configurations incorporated herein will be omitted when it may make the subject matter of the present invention unnecessarily unclear.

[0048] An intermediate product of a solid electrolyte according to an embodiment of the present application will be described.

[0049] According to an embodiment of the present application, the intermediate product of the solid electrolyte may include a compound in which a cation and an anion are bound, and a solvent in which the compound is mixed.

[0050] According to one embodiment, the cation may be thiophenium represented by <Formula 1> below. The compound may include an alkyl group (R1) bonded with a sulfur element of the thiophenium.

##STR00001##

[0051] For example, the cation may have a methyl group represented by <Formula 2> below, an ethyl group represented by <Formula 3>, a propyl group represented by <Formula 4>, or a butyl group represented by <Formula 5>.

##STR00002##

[0052] According to another embodiment, the cation may be thiazolium represented by <Formula 6> below. The compound may include an alkyl group (R1) bonded with a nitrogen element of the thiazolium.

##STR00003##

[0053] For example, the cation may have a methyl group represented by <Formula 7> below, an ethyl group represented by <Formula 8>, a propyl group represented by <Formula 9>, or a butyl group represented by <Formula 10>.

##STR00004##

[0054] The anion may include fluorohydrogenate represented by <Formula 11>.

##STR00005##

[0055] The compound may include a compound in which a cation including the thiophenium and an anion including the fluorohydrogenate are bound, or may include a compound in which a cation including the thiazolium and an anion including the fluorohydrogenate are bound.

[0056] The compound may be provided in a state in which the compound is dispersed or dissolved in the solvent. The solvent may include at least any one of acetonitrile, tetrahydrofuran, DMSO, or DMF.

[0057] The intermediate product of the solid electrolyte including the compound and the solvent may be in a liquid or get state. The intermediate product of the solid electrolyte in a liquid or gel state may be stored, transported and distributed.

[0058] The solid electrolyte may be prepared by removing and drying the solvent included in the intermediate product of the solid electrolyte. The solid electrolyte may include a compound in which the cation including the thiophenium or the thiazolium and the anion including the fluorohydrogenate are bound, may be in a flexible solid state, and may have crystallinity. In other words, the solid electrolyte may be in a flexible and crystalline solid state having a high ion conductivity, in which the cation and the anion are bound.

[0059] The solid electrolyte may be provided between a positive electrode and a negative electrode to configure a secondary battery. In this case, according to one embodiment, a positive electrode active material included in the positive electrode may include lithium, phosphorus, and iron, and a negative electrode active material included in the negative electrode may include lithium.

[0060] A method for preparing an intermediate product of the solid electrolyte, a cation source for preparing the solid electrolyte, and an anion source for preparing the solid electrolyte may be described.

[0061] A cation source and an anion source for preparing the solid electrolyte including the compound in which the cation and the anion are bound may be provided.

[0062] If the cation is thiophenium, the cation source may include a solution containing an alkyl group, and thiophene. In this case, the cation source may include thiophenium salt. Alternately, if the cation is thiazolium, the cation source may include a solution containing an alkyl group, and thiazoline. In this case, the cation source may include thiazolium salt.

[0063] According to one embodiment, the solution containing the alkyl group may be prepared by adding an alkyl group precursor into a solvent and stirring at room temperature. For example, the solvent may be acetonitrile. Specifically, for example, the alkyl group precursor may include any one of dichloromethane represented by <Formula 12> below, ethyl chloride represented by <Formula 13> below, propyl chloride represented by <Formula 14> below, or butyl chloride represented by <Formula 15> below.

##STR00006##

[0064] The cation source may be prepared by dripping and reacting the thiophene or the thiazoline into the solution containing the alkyl group. Unlike the above, if a large amount of the thiophene or the thiazoline is added into the solution containing the alkyl group at one time, the reactivity between the thiophene or the thiazoline and the solution containing the alkyl group may decrease, and thus it may not be easy to prepare the cation source.

[0065] Accordingly, as described above, the thiophene or the thiazoline may be dripped into the solution containing the alkyl group, and thus the reactivity between the solution containing the thiophene or the thiazoline and the alkyl group may increase to enhance an yield of the thiophenium salt or the thiazoline salt.

[0066] According to one embodiment, as a length of a chain of the alkyl group in the solution containing the alkyl group increases, a reaction time may increase. Thus, as the length of the chain of the alkyl group increases, a temperature of the reaction may increase. Accordingly, a manufacturing process time for the cation source may be shortened and a manufacturing cost may be reduced, and thus mass production may be facilitated.

[0067] As described above, the thiophenium salt may include an alkyl group bonded with a sulfur atom of the thiophenium as represented by <Formula 1> to <Formula 5>. For example, the thiophenium salt may include thiophenium chloride containing any one of a methyl group, an ethyl group, a propyl group or a butyl group.

[0068] Specifically, for example, if the solution containing the alkyl group includes dichloromethane represented by <Formula 12>, the thiophene may be dripped into the solution containing the dichloromethane, and reacted at room temperature, and the thiophenium salt may include one in which a carbon element of the dichloromethane is bonded with a sulfur element of the thiophene as represented by <Formula 16>.

##STR00007##

[0069] As another example, if the solution containing the alkyl group includes ethyl chloride represented by <Formula 13>, the thiophene may be dripped into the solution containing the ethyl chloride, and reacted at a temperature higher than room temperature and the thiophenium salt may include one in which a carbon element of the ethyl chloride is bonded with a sulfur element of the thiophene as represented by <Formula 17>.

##STR00008##

[0070] As still another example, if the solution containing the alkyl group includes propyl chloride represented by above <Formula 14>, the thiophene may be dripped into the solution containing the propyl chloride, and reacted at a temperature higher than room temperature and the thiophenium salt may include one in which a carbon element of the propyl chloride is bonded with a sulfur element of the thiophene as represented by <Formula 18>.

##STR00009##

[0071] As still another example, if the solution containing the alkyl group includes butyl chloride represented by above <Formula 15>, the thiophene may be dripped into the solution containing the butyl chloride, and reacted at a temperature higher than room temperature and the thiophenium salt may include one in which a carbon element of the butyl chloride is bonded with a sulfur element of the thiophene as represented by <Formula 19>.

##STR00010##

[0072] The thiazolium salt may include an alkyl group bonded with a nitrogen atom of the thiazolium as represented by <Formula 6> to <Formula 10>. For example, the thiazolium salt may include thiazolium chloride containing any one of a methyl group, an ethyl group, a propyl group or a butyl group.

[0073] Specifically, for example, if the solution containing the alkyl group includes dichloromethane represented by above <Formula 12>, the thiazoline may be dripped into the solution containing the dichloromethane, and reacted at room temperature, and the thiazolium salt may include one in which a carbon element of the dichloromethane is bonded with a nitrogen element of the thiazoline as represented by <Formula 20>.

##STR00011##

[0074] As another example, if the solution containing the alkyl group includes ethyl chloride represented by above <Formula 13>, the thiazoline may be dripped into the solution containing the ethyl chloride, and reacted at a temperature higher than room temperature and the thiazolium salt may include one in which a carbon element of the ethyl chloride is bonded with a nitrogen element of the thiazoline as represented by <Formula 21>.

##STR00012##

[0075] As still another example, if the solution containing the alkyl group includes propyl chloride represented by above <Formula 14>, the thiazoline may be dripped into the solution containing the propyl chloride, and reacted at a temperature higher than room temperature and the thiazolium salt may include one in which a carbon element of the propyl chloride is bonded with a nitrogen element of the thiazoline as represented by <Formula 22>.

##STR00013##

[0076] As still another example, if the solution containing the alkyl group includes butyl chloride represented by above <Formula 15>, the thiazoline may be dripped into the solution containing the butyl chloride, and reacted at a temperature higher than room temperature and the thiazolium salt may include one in which a carbon element of the butyl chloride is bonded with a nitrogen element of the thiazoline as represented by <Formula 23>.

##STR00014##

[0077] The anion source may include a solvent including water and hydrofluoric acid mixed in the solvent. Specifically, the anion source prepared by stirring hydrofluoric acid and water may be a fluorohydrogenate precursor.

[0078] According to one embodiment, the anion source may further include lithium salt in addition to the solvent and the hydrofluoric acid. For example, the lithium salt may include lithium chloride. In this case, the anion source may be a lithium fluorohydrogenate precursor.

[0079] The cation source and the anion source may be stored, transported, and distributed in a liquid state while being provided in a container. The container may include an air conditioner which creates an environment suitable for storing the cation source and the anion source, and thus a temperature, humidity, and pressure inside the container may be adjusted.

[0080] An intermediate product of the solid electrolyte may be prepared by mixing the cation source and the anion source.

[0081] Specifically, the intermediate product of the solid electrolyte may be prepared by preparing a mixed solution in which the cation source and the anion source are mixed, and reacting the mixed solution. The mixed solution may be reacted at a temperature lower than room temperature (e.g., −70° C.).

[0082] Unlike the above, if the mixed solution is reacted at room temperature, the fluorohydrogenate precursor may be evaporated. Specifically, the fluorohydrogenate precursor may have a boiling point at a temperature equal to or lower than room temperature, and thus may be volatilized at room temperature.

[0083] Thus, as described above, if the mixed solution is reacted at a temperature lower than room temperature, the intermediate product of the solid electrolyte may be easily prepared. In addition, as a temperature of the reaction decreases, a loss of the fluorohydrogenate precursor may decrease, and thus a reaction time may decrease.

[0084] According to an embodiment of the present application, the intermediate product of the solid electrolyte may be provided in a liquid or gel state, and the cation source and the anion source for preparing the solid electrolyte may be provided in a liquid state. Thus, compared to those provided in a solid state, the intermediate product of the solid electrolyte, the cation source, and the anion source may be easily stored, distributed, and transported. Accordingly, the cost for preparing the solid electrolyte may be saved, and mass production of the solid electrolyte may be facilitated.

[0085] Hereinafter, according to specific experimental examples of the present application, a solid electrolyte including a compound in which various cations and anions are bound, and results of evaluating their properties will be described.

[0086] Preparing of Compound According to Experimental Example 1-1

[0087] Acetonitrile was provided into a conical flask, after which dichloromethane was added and stirred at room temperature for 10 minutes to prepare a solution containing an alkyl group. In this case, the preparation of the solution containing the alkyl group was performed in a glove box without moisture.

[0088] Thiophene was dripped into the solution containing the alkyl group while being stirred, after which a uniformly mixed solution was slowly stirred at room temperature for four days so as to prepare thiophenium salt having a methyl group which is a cation source.

[0089] A washing process was performed by providing the thiophenium salt and a solvent of ethyl acetate and diethyl ether into a rotary concentrator.

[0090] 1M hydrofluoric acid and extra water were added into a conical flask and stirred for 10 minutes to prepare a fluorohydrogenate precursor which is an anion source.

[0091] Thiophenium salt was added into the fluorohydrogenate precursor to prepare a mixed solution. The mixed solution was left alone at a temperature of −70° C. for 24 hours, so as to prepare a compound in which thiazolium salt and the fluorohydrogenate were bound as an intermediate product of the solid electrolyte.

[0092] The compound was provided into a glove box under a nitrogen atmosphere and left alone at room temperature for two to three hours, so that volatile gas was removed. After that, a drying process was performed by providing the compound into the rotary concentrator, so as to prepare a compound according to Experimental Example 1-1, in which a thiophenium cation having a methyl group (R1) and a fluorohydrogenate anion are bound.

[0093] Preparing of Compound According to Experimental Example 1-2

[0094] A compound was prepared by the same method as described above in Experimental Example 1-1. However, ethyl chloride was provided instead of dichloromethane. In addition, in the preparing of thiophenium, a reaction was performed at a temperature of 60 to 80° C. for two to three days instead of the reaction at room temperature for four days, so as to prepare the compound according to Experimental Example 1-2, in which a thiophenium cation having an ethyl group (R1) and a fluorohydrogenate anion are bound.

[0095] Preparing of Compound According to Experimental Example 1-3

[0096] A compound was prepared by the same method as described above in Experimental Example 1-1. However, propyl chloride was provided instead of dichloromethane. In addition, in the preparing of thiophenium, a reaction was performed at a temperature of 60 to 80° C. for two to three days instead of the reaction at room temperature for four days, so as to prepare the compound according to Experimental Example 1-3, in which a thiophenium cation having a propyl group (R1) and a fluorohydrogenate anion are bound.

[0097] Preparing of Compound According to Experimental Example 1-4

[0098] A compound was prepared by the same method as described above in Experimental Example 1-1. However, butyl chloride was provided instead of dichloromethane. In addition, in the preparing of thiophenium, a reaction was performed at a temperature of 60 to 80° C. for two to three days instead of the reaction at room temperature for four days, so as to prepare the compound according to Experimental Example 1-4, in which a thiophenium cation having a butyl group (R1) and a fluorohydrogenate anion are bound.

[0099] Preparing of Compound According to Experimental Example 2-1

[0100] A compound was prepared by the same method as described above in Experimental Example 1-1, but thiazoline was added into a solution containing an alkyl group so as to prepare thiazolium salt as a cation source.

[0101] After that, thiazolium salt and a fluorohydrogenate precursor were reacted by the same method as described above in Experimental Example 1-1, so as to prepare the compound according to Experimental Example 2-1, in which a thiazolium cation having a methyl group (R1) and a fluorohydrogenate anion are bound.

[0102] Preparing of Compound According to Experimental Example 2-2

[0103] A compound was prepared by the same method as described above in Experimental Example 1-2, but thiazoline was added into a solution containing an alkyl group so as to prepare thiazolium salt as a cation source.

[0104] After that, thiazolium salt and a fluorohydrogenate precursor were reacted by the same method as described above in Experimental Example 1-2, so as to prepare the compound according to Experimental Example 2-2, in which a thiazolium cation having an ethyl group (R1) and a fluorohydrogenate anion are bound.

[0105] Preparing of compound according to Experimental Example 2-3

[0106] A compound was prepared by the same method as described above in Experimental Example 1-3, but thiazoline was added into a solution containing an alkyl group so as to prepare thiazolium salt as a cation source.

[0107] After that, thiazolium salt and a fluorohydrogenate precursor were reacted by the same method as described above in Experimental Example 1-3, so as to prepare the compound according to Experimental Example 2-3, in which a thiazolium cation having a propyl group (R1) and a fluorohydrogenate anion are bound.

[0108] Preparing of Compound According to Experimental Example 2-4

[0109] A compound was prepared by the same method as described above in Experimental Example 1-4, but thiazoline was added into a solution containing an alkyl group so as to prepare thiazolium salt as a cation source.

[0110] After that, thiazolium salt and a fluorohydrogenate precursor were reacted by the same method as described above in Experimental Example 1-4, so as to prepare the compound according to Experimental Example 2-4, in which a thiazolium cation having a butyl group (R1) and a fluorohydrogenate anion are bound.

[0111] Preparing of Compound According to Experimental Example 3-1

[0112] Phospholanium represented by <Formula 24> below was provided as a cation, and fluorohydrogenate prepared according to Experimental Example 1-1 as described above was used as an anion, so as to prepare the compound according to Experimental Example 3-1, in which a phospholanium cation having a methyl group (R1) and an ethyl group (R2) and a fluorohydrogenate anion are bound.

##STR00015##

[0113] Preparing of Compound According to Experimental Example 3-2

[0114] A compound was prepared by the same method as described above in Experimental Example 3-1, so as to prepare the compound according to Experimental Example 3-2, in which a phospholanium cation having a methyl group (R1) and a propyl group (R2) and a fluorohydrogenate anion are bound.

[0115] Preparing of Compound According to Experimental Example 3-3

[0116] A compound was prepared by the same method as described above in Experimental Example 3-1, so as to prepare the compound according to Experimental Example 3-3, in which a phospholanium cation having a methyl group (R1) and a butyl group (R2) and a fluorohydrogenate anion are bound.

[0117] Preparing of Compound According to Experimental Example 3-4

[0118] A compound was prepared by the same method as described above in Experimental Example 3-1, so as to prepare the compound according to Experimental Example 3-4, in which a phospholanium cation having an ethyl group (R1) and a butyl group (R2) and a fluorohydrogenate anion are bound.

[0119] Preparing of Compound According to Experimental Example 3-5

[0120] A compound was prepared by the same method as described above in Experimental Example 3-1, so as to prepare the compound according to Experimental Example 3-5, in which a phospholanium cation having a methyl group (R1) and a methyl group (R2) and a fluorohydrogenate anion are bound.

[0121] Preparing of Compound According to Experimental Example 4-1

[0122] Oxathiolanium represented by <Formula 25> below was provided as a cation, and fluorohydrogenate prepared according to Experimental Example 1-1 as described above was used as an anion, so as to prepare the compound according to Experimental Example 4-1, in which an oxathiolanium cation having a methyl group (R1) and a fluorohydrogenate anion are bound.

##STR00016##

[0123] Preparing of Compound According to Experimental Example 4-2

[0124] A compound was prepared by the same method as described above in Experimental Example 4-1, so as to prepare the compound according to Experimental Example 4-2, in which an oxathiolanium cation having an ethyl group (R1) and a fluorohydrogenate anion are bound.

[0125] Preparing of Compound According to Experimental Example 4-3

[0126] A compound was prepared by the same method as described above in Experimental Example 4-1, so as to prepare the compound according to Experimental Example 4-3, in which an oxathiolanium cation having a propyl group (R1) and a fluorohydrogenate anion are bound.

[0127] Preparing of Compound According to Experimental Example 4-4

[0128] A compound was prepared by the same method as described above in Experimental Example 4-1, so as to prepare the compound according to Experimental Example 4-4, in which an oxathiolanium cation having a butyl group (R1) and a fluorohydrogenate anion are bound.

[0129] Preparing of Compound According to Experimental Example 5-1

[0130] Ammonium was provided as a cation, and fluorohydrogenate prepared according to Experimental Example 1-1 as described above was used as an anion, so as to prepare the compound according to Experimental Example 5-1, in which an ammonium cation having a tetraethyl group and a fluorohydrogenate anion are bound.

[0131] Preparing of Compound According to Experimental Example 5-2

[0132] A compound was prepared by the same method as described above in Experimental Example 5-1, so as to prepare the compound according to Experimental Example 5-2, in which an ammonium cation having a tetrabutyl group and a fluorohydrogenate anion are bound.

[0133] Preparing of Compound According to Experimental Example 5-3

[0134] A compound was prepared by the same method as described above in Experimental Example 5-1, so as to prepare the compound according to Experimental Example 5-3, in which an ammonium cation having a trimethyl group and a fluorohydrogenate anion are bound.

[0135] Preparing of Compound According to Experimental Example 5-4

[0136] A compound was prepared by the same method as described above in Experimental Example 5-1, so as to prepare the compound according to Experimental Example 5-4, in which an ammonium cation having a diethylmethyl group and a fluorohydrogenate anion are bound.

[0137] Preparing of Compound According to Experimental Example 6-1

[0138] Sulphonium was provided as a cation, and fluorohydrogenate prepared according to Experimental Example 1-1 as described above was used as an anion, so as to prepare the compound according to Experimental Example 6-1, in which a sulphonium cation having a trimethyl group and a fluorohydrogenate anion are bound.

[0139] Preparing of Compound According to Experimental Example 6-2

[0140] A compound was prepared by the same method as described above in Experimental Example 6-1, so as to prepare the compound according to Experimental Example 6-2, in which a sulphonium cation having a trimethyl group and a fluorohydrogenate anion are bound.

[0141] Preparing of Compound According to Experimental Example 7-1

[0142] Phosphonium was provided as a cation, and fluorohydrogenate prepared according to Experimental Example 1-1 as described above was used as an anion, so as to prepare the compound according to Experimental Example 7-1, in which a phosphonium cation having a trimethyl group and a fluorohydrogenate anion are bound.

[0143] Preparing of Compound According to Experimental Example 7-2

[0144] A compound was prepared by the same method as described above in Experimental Example 7-1, so as to prepare the compound according to Experimental Example 7-2, in which a phosphonium cation having a triethyl group and a fluorohydrogenate anion are bound.

[0145] Preparing of Compound According to Experimental Example 7-3

[0146] A compound was prepared by the same method as described above in Experimental Example 7-1, so as to prepare the compound according to Experimental Example 7-3, in which a phosphonium cation having a tributyldecyl group and a fluorohydrogenate anion are bound.

[0147] Preparing of Compound According to Experimental Example 8-1

[0148] Thiazolidinium represented by <Formula 26> below was provided as a cation, and fluorohydrogenate prepared according to Experimental Example 1-1 as described above was used as an anion, so as to prepare the compound according to Experimental Example 8-1, in which a thiazolidinium cation having a methyl group (R1) and an ethyl group (R2) bound to a nitrogen element, and two methyl groups bound to a sulfur element, and a fluorohydrogenate anion are bound.

##STR00017##

[0149] Preparing of Compound According to Experimental Example 8-2

[0150] A compound was prepared by the same method as described above in Experimental Example 8-1, so as to prepare the compound according to Experimental Example 8-2, in which a thiazolidinium cation having a methyl group (R1) and a propyl group (R2) bound to a nitrogen element, and two methyl groups bound to a sulfur element, and a fluorohydrogenate anion are bound.

[0151] Preparing of Compound According to Experimental Example 8-3

[0152] A compound was prepared by the same method as described above in Experimental Example 8-1, so as to prepare the compound according to Experimental Example 8-3, in which a thiazolidinium cation having a methyl group (R1) and a butyl group (R2) bound to a nitrogen element, and two methyl groups bound to a sulfur element, and a fluorohydrogenate anion are bound.

[0153] Preparing of Compound According to Experimental Example 8-4

[0154] A compound was prepared by the same method as described above in Experimental Example 8-1, so as to prepare the compound according to Experimental Example 8-4, in which a thiazolidinium cation having an ethyl group (R1) and a butyl group (R2) bound to a nitrogen element, and two methyl groups bound to a sulfur element, and a fluorohydrogenate anion are bound.

[0155] Preparing of Compound According to Experimental Example 9-1

[0156] Imidazolium represented by <Formula 27> below was provided as a cation, and fluorohydrogenate prepared according to Experimental Example 1-1 as described above was used as an anion, so as to prepare the compound according to Experimental Example 9-1, in which an imidazolium cation having a methyl group (R1) and an ethyl group (R2) and a fluorohydrogenate anion are bound.

##STR00018##

[0157] Preparing of Compound According to Experimental Example 9-2

[0158] A compound was prepared by the same method as described above in Experimental Example 9-1, so as to prepare the compound according to Experimental Example 9-2, in which an imidazolium cation having a methyl group (R1) and a propyl group (R2) and a fluorohydrogenate anion are bound.

[0159] Preparing of Compound According to Experimental Example 9-3

[0160] A compound was prepared by the same method as described above in Experimental Example 9-1, so as to prepare the compound according to Experimental Example 9-3, in which an imidazolium cation having a methyl group (R1) and a butyl group (R2) and a fluorohydrogenate anion are bound.

[0161] Preparing of Compound According to Experimental Example 9-4

[0162] A compound was prepared by the same method as described above in Experimental Example 9-1, so as to prepare the compound according to Experimental Example 9-4, in which an imidazolium cation having an ethyl group (R1) and a butyl group (R2) and a fluorohydrogenate anion are bound.

[0163] Preparing of Compound According to Experimental Example 10-1

[0164] Pyrrolidinium represented by <Formula 28> below was provided as a cation, and fluorohydrogenate prepared according to Experimental Example 1-1 as described above was used as an anion, so as to prepare the compound according to Experimental Example 10-1, in which an pyrrolidinium cation having a methyl group (R1) and an ethyl group (R2) and a fluorohydrogenate anion are bound.

##STR00019##

[0165] Preparing of Compound According to Experimental Example 10-2

[0166] A compound was prepared by the same method as described above in Experimental Example 10-1, so as to prepare the compound according to Experimental Example 10-2, in which a pyrrolidinium cation having a methyl group (R1) and a propyl group (R2) and a fluorohydrogenate anion are bound.

[0167] Preparing of Compound According to Experimental Example 10-3

[0168] A compound was prepared by the same method as described above in Experimental Example 10-1, so as to prepare the compound according to Experimental Example 10-3, in which a pyrrolidinium cation having a methyl group (R1) and a butyl group (R2) and a fluorohydrogenate anion are bound.

[0169] Preparing of Compound According to Experimental Example 10-4

[0170] A compound was prepared by the same method as described above in Experimental Example 10-1, so as to prepare the compound according to Experimental Example 10-4, in which a pyrrolidinium cation having an ethyl group (R1) and a butyl group (R2) and a fluorohydrogenate anion are bound.

[0171] Preparing of Compound According to Experimental Example 10-5

[0172] A compound was prepared by the same method as described above in Experimental Example 10-1, so as to prepare the compound according to Experimental Example 10-5, in which a pyrrolidinium cation having a methyl group (R1) and a methyl group (R2) and a fluorohydrogenate anion are bound.

[0173] The ion conductivity of the compounds according to Experimental Examples 1-1 to 10-5 was measured at room temperature, and the ion molecular weight of cations and the state information of the compounds according to Experimental Examples 1-1 to 10-5 are summarized as shown in <Table 1>.

TABLE-US-00001 TABLE 1 Ion molecular Ion weight conductivity Classification Cation Alkyl group (g/mol) State (mS/cm.sup.2) Experimental Thiophenium Methyl group 99.15 Crystalline 126 Example 1-1 solid Experimental Ethyl group 113.14 Crystalline 103 Example 1-2 solid Experimental Propyl group 127.15 Crystalline 68 Example 1-3 solid Experimental Butyl group 142.16 Crystalline 46 Example 1-4 solid Experimental Thiazolium Methyl group 101.13 Crystalline 45 Example 2-1 solid Experimental Ethyl group 114.14 Crystalline 74 Example 2-2 solid Experimental Propyl group 126.15 Crystalline 18.9 Example 2-3 solid Experimental Butyl group 143.13 Crystalline 6.8 Example 2-4 solid Experimental Phospholanium Methyl group/ 130.97 Crystalline 2 Example 3-1 Ethyl group solid Experimental Methyl group/ 143.1 Crystalline 35 Example 3-2 Propyl group solid Experimental Methyl group/ 159.9 Crystalline 16 Example 3-3 Butyl group solid Experimental Ethyl group/ 174 Crystalline 45 Example 3-4 Butyl group solid Experimental Methyl group/ 117 Crystalline 24 Example 3-5 Methyl group solid Experimental Oxathiolanium Methyl group 106.06 Crystalline 12 Example 4-1 solid Experimental Ethyl group 120.07 Crystalline 17.5 Example 4-2 solid Experimental Propyl group 132.06 Crystalline 26.5 Example 4-3 solid Experimental Butyl group 149.06 Crystalline 21.1 Example 4-4 solid Experimental Ammonium Tetraethyl group 130.25 Crystalline 12.5 Example 5-1 solid Experimental Tetrabutyl group 242.46 Crystalline 10.1 Example 5-2 solid Experimental Tetramethyl 59.11 Ionic liquid 9.4 Example 5-3 group Experimental Diethylmethyl 88.9 Ionic liquid 8.1 Example 5-4 group Experimental Sulfonium Trimethyl 77.04 Ionic liquid 8.4 Example 6-1 group Experimental Triethyl group 119.06 Crystalline 5.6 Example 6-2 solid Experimental Phosphonium Trimethyl group 77.09 Ionic liquid 5.7 Example 7-1 Experimental Triethyl group 119.16 Crystalline 4.9 Example 7-2 solid Experimental Tributyldecyl 343.59 Crystalline 2.8 Example 7-3 group solid Experimental Thiazolidinium Methyl group/ 99.15 Crystalline 60 Example 8-1 Ethyl group solid Methyl group/ Methyl group Experimental Methyl group/ 113.14 Crystalline 19.6 Example 8-2 Propyl group solid Methyl group/ Methyl group Experimental Methyl group/ 127.15 Crystalline 28.7 Example 8-3 Butyl group solid Methyl group/ Methyl group Experimental Ethyl group/ 142.16 Crystalline 5.8 Example 8-4 Butyl group solid Methyl group/ Methyl group Experimental Imidazolium Methyl group/ 112.07 Crystalline 14 Example 9-1 Ethyl group solid Experimental Methyl group/ 124.08 Crystalline 6.5 Example 9-2 Propyl group solid Experimental Methyl group/ 141.08 Crystalline 8.9 Example 9-3 Butyl group solid Experimental Ethyl group/ 155.07 Crystalline 2.5 Example 9-4 Butyl group solid Experimental Pyrrolidinium Methyl group/ 115.12 Crystalline 7 Example 10-1 Ethyl group solid Experimental Methyl group/ 127.13 Crystalline 5.3 Example 10-2 Propyl group solid Experimental Methyl group/ 144.12 Crystalline 14.5 Example 10-3 Butyl group solid Experimental Ethyl group/ 158.12 Crystalline 20 Example 10-4 Butyl group solid Experimental Methyl group/ 101.13 Crystalline 0.9 Example 10-5 Methyl group solid

[0174] As can be understood from <Table 1>, it can be confirmed that compounds have a high ion conductivity, if thiophenium is included as a cation (Experimental Examples 1-1 to 1-4), if thiazolium having a methyl group, an ethyl group, or a propyl group is included (Experimental Examples 2-1 to 2-3), if phospholanium having a methyl group/propyl group, a methyl group/butyl group, an ethyl group/butyl group, or a methyl group/methyl group is included (Experimental Examples 3-2 to 3-5), if oxathiolanium having an ethyl group, a propyl group, or a butyl group is included (Experimental Examples 4-2 to 4-4), and if a thiazolidinium having a methyl group/ethyl group, a methyl group/propyl group, and a methyl group/butyl group is included (Experimental Examples 8-1 to 8-3).

[0175] Thiophenium having a methyl group identified as having the highest ion conductivity in <Table 1> was fixed as a cation and a type of anion was varied to prepare a compound for a solid electrolyte according to Experimental Examples 11-1 to 11-18.

[0176] Preparing of Compound According to Experimental Example 11-1

[0177] Chlorine ion was provided as an anion so as to prepare a compound according to Experimental Example 11-1 in which a thiophenium cation having a methyl group according to Experimental Example 1-1 as described above and a chlorine anion are bound.

[0178] Preparing of Compound According to Experimental Example 11-2

[0179] Cyanate was provided as an anion so as to prepare a compound according to Experimental Example 11-2 in which a thiophenium cation having a methyl group according to Experimental Example 1-1 as described above and a cyanate anion are bound.

[0180] Preparing of Compound According to Experimental Example 11-3

[0181] Oxohydrogenate was provided as an anion so as to prepare a compound according to Experimental Example 11-3 in which a thiophenium cation having a methyl group according to Experimental Example 1-1 as described above and an oxohydrogenate anion are bound.

[0182] Preparing of Compound According to Experimental Example 11-4

[0183] SCN was provided as an anion so as to prepare a compound according to Experimental Example 11-4 in which a thiophenium cation having a methyl group according to Experimental Example 1-1 as described above and an SCN anion are bound.

[0184] Preparing of Compound According to Experimental Example 11-5

[0185] Nitrogen was provided as an anion so as to prepare a compound according to Experimental Example 11-5 in which a thiophenium cation having a methyl group according to Experimental Example 1-1 as described above and a nitrogen anion are bound.

[0186] Preparing of Compound According to Experimental Example 11-6

[0187] N(CN).sub.2 was provided as an anion so as to prepare a compound according to Experimental Example 11-6 in which a thiophenium cation having a methyl group according to Experimental Example 1-1 as described above and an N(CN).sub.2 anion are bound.

[0188] Preparing of Compound According to Experimental Example 11-7

[0189] Cyano(nitroso)methanide was provided as an anion so as to prepare a compound according to Experimental Example 11-7 in which a thiophenium cation having a methyl group according to Experimental Example 1-1 as described above and a cyano(nitroso)methanide anion are bound.

[0190] Preparing of Compound According to Experimental Example 11-8

[0191] Tetrazolidine was provided as an anion so as to prepare a compound according to Experimental Example 11-8 in which a thiophenium cation having a methyl group according to Experimental Example 1-1 as described above and a tetrazolidine anion are bound.

[0192] Preparing of Compound According to Experimental Example 11-9

[0193] Bromine was provided as an anion so as to prepare a compound according to Experimental Example 11-9 in which a thiophenium cation having a methyl group according to Experimental Example 1-1 as described above and a bromine anion are bound.

[0194] Preparing of Compound According to Experimental Example 11-10

[0195] BF.sub.4 was provided as an anion so as to prepare a compound according to Experimental Example 11-10 in which a thiophenium cation having a methyl group according to Experimental Example 1-1 as described above and a BF.sub.4 anion are bound.

[0196] Preparing of Compound According to Experimental Example 11-11

[0197] Dihydrogen phosphate was provided as an anion so as to prepare a compound according to Experimental Example 11-11 in which a thiophenium cation having a methyl group according to Experimental Example 1-1 as described above and a dihydrogen phosphate anion are bound.

[0198] Preparing of Compound According to Experimental Example 11-12

[0199] Hydrogensulfate was provided as an anion so as to prepare a compound according to Experimental Example 11-12 in which a thiophenium cation having a methyl group according to Experimental Example 1-1 as described above and a hydrogensulfate anion are bound.

[0200] Preparing of Compound According to Experimental Example 11-13

[0201] Dimethyl phosphate was provided as an anion so as to prepare a compound according to Experimental Example 11-13 in which a thiophenium cation having a methyl group according to Experimental Example 1-1 as described above and a dimethyl phosphate anion are bound.

[0202] Preparing of Compound According to Experimental Example 11-14

[0203] Iodine was provided as an anion so as to prepare a compound according to Experimental Example 11-14 in which a thiophenium cation having a methyl group according to Experimental Example 1-1 as described above and an iodine anion are bound.

[0204] Preparing of Compound According to Experimental Example 11-15

[0205] PF.sub.6 was provided as an anion so as to prepare a compound according to Experimental Example 11-15 in which a thiophenium cation having a methyl group according to Experimental Example 1-1 as described above and a PF.sub.6 anion are bound.

[0206] Preparing of Compound According to Experimental Example 11-16

[0207] Trifluoromethanesulfonate was provided as an anion so as to prepare a compound according to Experimental Example 11-16 in which a thiophenium cation having a methyl group according to Experimental Example 1-1 as described above and a trifluoromethanesulfonate anion are bound.

[0208] Preparing of Compound According to Experimental Example 11-17

[0209] FSI was provided as an anion so as to prepare a compound according to Experimental Example 11-17 in which a thiophenium cation having a methyl group according to Experimental Example 1-1 as described above and an FSI anion are bound.

[0210] Preparing of Compound According to Experimental Example 11-18

[0211] TFSI was provided as an anion so as to prepare a compound according to Experimental Example 11-18 in which a thiophenium cation having a methyl group according to Experimental Example 1-1 as described above and a TFSI anion are bound.

[0212] The ion conductivity of the compounds according to Experimental Examples 11-11 to 11-17 was measured at room temperature, and the molecular weight of anions, the state information of the compounds according to Experimental Examples 11-1 to 11-17, pH of anions, and an entropy of fusion of the compounds according to Experimental Examples 11-1 to 11-17 are summarized as shown in <Table 2>.

TABLE-US-00002 TABLE 2 Ion Molecular Ion Entropy weight conductivity of fusion Classification Anion (g/mol) State (mS/cm.sup.2) pH (J/Kmol) Experimental Chlorine 35.45 Ionic liquid 3.6 More 9.3 Example 11-1 than 3 Experimental Cyanate 42 Ionic liquid 4.3 8.1 Example 11-2 Experimental Oxohydrogenate 48 Ionic liquid 5.8 7.6 Example 11-3 Experimental SCN 58.08 Ionic liquid 3.9 6.4 Example 11-4 Experimental Nitrogen 62 Crystalline 4.1 Less 36 Example 11-5 solid than 3 Experimental Fluorohydrogenate 63 Crystalline 126 23.6 Example 1-1 solid Experimental N(CN).sub.2 66 Crystalline 3.6 36 Example 11-6 solid Experimental Cyano(nitro)methanide 69 Crystalline 48.6 24.9 Example 11-7 solid Experimental Tetrazolidine 72 Crystalline 69.4 24.3 Example 11-8 solid Experimental Bromine 79.90 Crystalline 2.6 35.6 Example 11-9 solid Experimental BF.sub.4 86.81 Crystalline 6.9 38.1 Example 11-10 solid Experimental Dihydrogen phosphate 96.98 Crystalline 3.3 43.2 Example 11-11 solid Experimental Hydrogen sulfate 97.07 Crystalline 16.9 47.6 Example 11-12 solid Experimental Dimethyl phosphate 126.05 Crystalline 8.1 49.3 Example 11-13 solid Experimental Iodine 126.9 Crystalline 5.1 45.2 Example 11-14 solid Experimental PF.sub.6 145 Crystalline 23 39.8 Example 11-15 solid Experimental Trifluoromethanesulfonate 164.1 Crystalline 12.6 42.8 Example 11-16 solid Experimental FSI 180.13 Crystalline 35 41.7 Example 11-17 solid Experimental TFSI 280.135 Crystalline 29 46.9 Example 11-18 solid

[0213] As can be understood from <Table 2>, it can be confirmed that compounds have a high ion conductivity, if fluorohydrogenate is included as an anion (Experimental Example 1-1), if cyano(nitroso)methanide is included (Experimental Example 11-7), and if tetrazolidine is included (Experimental Examples 11-8). In addition, if a molecular weight of the anion is 60 g/mol % or less (more specifically, 58.08 g/mol % or less), and if a pH of the anion is greater than 3, it can be confirmed that a compound in which a cation and an anion are bound is not a crystalline solid but an ionic liquid. In other words, if a molecular weight of the anion is more than 60 g/mol (more specifically, 62 g/mol % or less), and if a pH of the anion is less than 3, it can be confirmed that a compound in which a cation and an anion are bound is maintained as a crystalline solid.

[0214] In addition, if a molecular weight of the anion is more than 60 g/mol (more specifically, 62 g/mol % or more), and if a pH of the anion is less than 3 and an entropy of fusion is 15-25 J/Kmol (more specifically, more than 9.3 J/Kmol and less than 35.6 J/Kmol), it can be confirmed that a compound has a high ion conductivity.

[0215] Preparing of Solid Electrolyte According to Experimental Example 12-1

[0216] A 1M hydrofluoric acid aqueous solution and lithium chloride (LiCl) were added into a container and left alone at a temperature of −70° C. for 24 hours, so as to prepare lithium fluorohydrogenate.

[0217] A compound having a methyl group according to Experimental Example 1-1 described above was heated to 60° C. and lithium fluorohydrogenate was added in an amount of 1 mol % at the same time and reacted for two hours, so as to prepare a solid electrolyte according to Experimental Example 12-1.

[0218] Preparing of Solid Electrolyte According to Experimental Example 12-2

[0219] A solid electrolyte was prepared by the same method as described above in Experimental Example 12-1. However, lithium fluorohydrogenate was added in an amount of 5 mol % instead of 1 mol %, so as to prepare a solid electrolyte according to Experimental Example 12-2.

[0220] Preparing of Solid Electrolyte According to Experimental Example 12-3

[0221] A solid electrolyte was prepared by the same method as described above in Experimental Example 2-1. However, lithium fluorohydrogenate was added in an amount of 10 mol % instead of 1 mol %, so as to prepare a solid electrolyte according to Experimental Example 12-3.

[0222] FIG. 1 is a graph showing an ion conductivity of compounds according to Experimental Examples 1-1, 11-7, 11-8, 11-15, 11-17 and 11-18 of the present application as measured depending on a temperature.

[0223] Referring to FIG. 1, an ion conductivity of compounds according to Experimental Examples 1-1, 11-7, 11-8, 11-15, 11-17 and 11-18 of the present application was measured depending on a temperature.

[0224] As can be understood from FIG. 1, it may be confirmed that a compound has the highest ion conductivity, in case of including fluorohydrogenate as an anion according to Experimental Example 1-1, and it can be confirmed that a compound has the highest ion conductivity, in case of including cyano(nitro)methanide and tetrazolidine as an anion according to Experimental Examples 11-7 and 11-8.

[0225] FIG. 2 is a differential scanning calorimetry (DSC) graph showing a compound according to Experimental Example 1-1 and a solid electrolyte according to Experimental Example 12-3 of the present application.

[0226] Referring to FIG. 2, a solid-liquid or solid-solid state change depending on a temperature may be observed in the compound according to Experimental Example 1-1 and the solid electrolyte according to Experimental Example 12-3.

[0227] As shown in FIG. 2, a solid-liquid state change was observed at 90° C. in the compound of Experimental Example 1-1. In contrast, a solid-liquid state change was observed at 70° C. in the solid electrolyte of Experimental Example 12-3.

[0228] In addition, a solid-solid state change was observed twice in the compound of Experimental Example 1-1, and specifically it can be seen that the compound of Experimental Example 1-1 has a first crystal phase in a temperature range of 28 to 90° C. and a second crystal phase in a temperature range of 22 to 28° C. In contrast, a solid-solid state change was observed once in the solid electrolyte of Experimental Example 12-3, and it can be confirmed that the solid electrolyte has one crystal phase in a temperature range of 22 to 70° C.

[0229] FIG. 3 is a DSC graph showing a compound according to Experimental Examples 11-7 and 11-8 of the present application.

[0230] Referring to FIG. 3, a state change of compounds according to Experimental Examples 11-7 and 11-8 was observed depending on a temperature.

[0231] As can be understood from FIG. 3, it can be confirmed that the compounds according to Experimental Examples 11-7 and 11-8 stably maintain a solid crystal phase in a relatively wide range of temperatures. Specifically, it can be confirmed that the compound according to Experimental Example 11-7 and the compound according to Experimental Example 11-8 stably maintain a solid crystal phase −15 to 98° C. and at −59 to 129° C., respectively. In addition, the compounds according to Experimental Examples 11-7 and 11-8 have a somewhat low ion conductivity compared to the compound according to Experimental Example 1-1, but stably maintain a crystal phase in a range of temperatures wider than the range of temperatures (28 to 90° C.) in which the compound according to Experimental Example 1-1 stably maintains a first crystal phase as shown in FIG. 2. Accordingly, the compounds according to Experimental Examples 11-7 and 11-8 can be useful in military or space fields, or low-temperature environments such as a polar region.

[0232] FIGS. 4 and 5 are graphs showing an X-ray diffraction (XRD) pattern of a compound according to Experimental Example 1-1 of the present application depending on a temperature.

[0233] Referring to FIGS. 4 and 5, an XRD pattern of a compound according to Experimental Example 1-1 depending on a temperature was measured in the range of −50 to 80° C.

[0234] As can be understood from FIGS. 4 and 5, it can be confirmed that a main peak moves to the left as a temperature increases in the area of 20 to 80° C., and a peak corresponding to 2θ 53.6° and 85.4° disappears at a temperature of 70° C. or higher.

[0235] In addition, as a temperature increases, it can be observed that one peak changes to two peaks, and it can be understood that a peak intensity value decreases. In other words, as the temperature increases, it can be confirmed that a short range disordered amorphous crystal structure increases and thus sequentially changes to phase III (−50 to 25° C.), phase II (25 to 30° C.), and phase I (30° C. or higher) as shown in FIG. 5, and phase III, phase II, and phase I of FIG. 5 correspond to solid phase III, phase II, and phase I of FIG. 2, respectively.

[0236] FIG. 6 is a graph showing an NMR analysis result of a solid electrolyte according to Experimental Example 12-1 of the present application.

[0237] Referring to FIG. 6, an NMR analysis was performed for a solid electrolyte according to Experimental Example 12-1. (a) of FIG. 6 may be 6.sup.1H NMR spectra, (b) of FIG. 6 may be 8.sup.19 F NMR spectra, and (c) of FIG. 6 may be 7.sup.7 Li NMR spectra.

[0238] It can be confirmed from (a), (b), and (c) of FIG. 6 that lithium is doped onto the compound in which a cation and an anion are bound through lithium fluorohydrogenate.

[0239] FIG. 7 is a graph showing a chemical shift and a diffusion coefficient of a solid electrolyte according to Experimental Example 12-1 of the present application as measured depending on a temperature.

[0240] Referring to FIG. 7, a chemical shift of Li, H, and F of the solid electrolyte according to Experimental Example 12-1 was measured depending on a temperature, and a diffusion coefficient of Li ions, cations, and anions of the solid electrolyte according to Experimental Example 12-1 was measured.

[0241] As can be understood from FIG. 7, a diffusion coefficient of Li ions of the solid electrolyte of Experimental Example 12-1 was measured to be 10.sup.−8 to 10.sup.−9 m.sup.2s.sup.−1, which is generally at a remarkably high level compared to the solid electrolyte in which a cation and an anion are bound.

[0242] FIG. 8 is a graph showing an XRD pattern of a compound according to Experimental Example 1-1 and a solid electrolyte according to Experimental Example 12-2 of the present application.

[0243] Referring to FIG. 8, a change in a crystal structure of the solid electrolyte according to Experimental Example 12-2 may be observed compared to the compound according to Experimental Example 1-1.

[0244] As shown in FIG. 8, it was confirmed that the compound of Experimental Example 1-1 and the solid electrolyte of Experimental Example 12-2 have the same position of main peaks. In contrast, different peak intensities were observed, and it can be seen that the solid electrolyte of Experimental Example 12-2 further includes a lithium-rich phase.

[0245] FIG. 9 is a view for explaining a crystal structure of a solid electrolyte according to Experimental Examples 12-1 to 12-3 of the present application.

[0246] Referring to FIG. 9, the solid electrolytes according to Experimental Examples 12-1 to 12-3 may include a thiophenium cation, a fluorohydrogenate anion and lithium salt.

[0247] A unit cell of the compound in which a thiophenium cation and a fluorohydrogenate anion are bound may have an orthorhombic crystal structure, in which the thiophenium cation may be provided at a vertex of the crystal structure and at a center of a face thereof, and the fluorohydrogenate anion may be provided in a middle of an edge of the crystal structure. In this case, the solid electrolyte of Experimental Examples 12-1 to 12-3 may have the lithium salt optionally provided at interstitial sites of the crystal structure. Specifically, the lithium salt may include lithium fluorohydrogenate.

[0248] The lithium salt may be provided at the interstitial sites of the crystal structure of the compound, and thus may easily move within the crystal structure. Accordingly, an ion conductivity may increase as an addition amount of the lithium fluorohydrogenate, which is lithium salt, increases.

[0249] FIG. 10 is a graph showing an ion conductivity of a compound according to Experimental Example 1-1 and a solid electrolyte according to Experimental Examples 12-1 to 12-3 of the present application depending on a temperature.

[0250] Referring to FIG. 10, a lithium ion conductivity was measured with regard to a compound according to Experimental Example 1-1 and a solid electrolyte according to Experimental Examples 12-1 to 12-3. As described above with reference to FIG. 9, lithium fluorohydrogenate may be optionally provided at interstitial sites in the crystal structure of the compound of the solid electrolyte of Experimental Examples 12-1 to 12-3. Accordingly, it was observed that lithium fluorohydrogenate may easily move within the crystal structure, and thus, when an addition amount of lithium fluorohydrogenate is increased, an ion conductivity becomes higher.

[0251] In this case, lithium fluorohydrogenate may move to interstitial sites in the crystal structure where lithium fluorohydrogenate is not provided, and may exhibit a high ion conductivity. Thus, as the interstitial sites provided with lithium fluorohydrogenate increase, a rate of increase in ion conductivity may reach saturation. In other words, as shown in FIG. 10, it can be confirmed that the ion conductivity substantially reaches saturation, if an addition amount of the lithium fluorohydrogenate is 5 mol % or more.

[0252] FIG. 11 is a picture of a electrolyte membrane coated with a solid electrolyte according to Experimental Example 12-1 of the present application.

[0253] Referring to FIG. 11, a picture was taken of a solid electrolyte membrane in the form of a film in which a solid electrolyte according to Experimental Example 12-1 of the present application is coated on a polytetrafluoroethylene (PTFE) resin. In this case, it was confirmed that the solid electrolyte membrane maintains the softness and transparency of the resin.

[0254] FIGS. 12 and 13 are graphs showing results of a cycle test of a secondary battery including a solid electrolyte according to Experimental Example 12-2 of the present application.

[0255] Referring to FIGS. 12 and 13, a secondary battery was manufactured by using the solid electrolyte according to Experimental Example 12-2 of the present application, LiFePO.sub.4 as the positive electrode, and lithium metal as the negative electrode, and charge/discharge properties were evaluated.

[0256] Charge and discharge were performed at a rate of 1 C, and the secondary battery showed a coulombic efficiency of 99.5% and a capacity of 158.6 mAh/g. In a 250th cycle, it can be confirmed that the secondary battery showed a coulomb efficiency of 98% and a capacity of 155.5 mAh/g. It can be confirmed that a secondary battery having a long life, high stability and high reliability may be implemented by using the solid electrolyte according to the implementation of the present application.

[0257] FIG. 14 is a graph showing a capacity retention rate depending on a charge/discharge rate of a secondary battery including a solid electrolyte according to Experimental Example 12-2 of the present application.

[0258] Referring to FIG. 14, charge/discharge was performed at a rate of 0.1 to 5 C for the secondary battery manufactured with reference to FIGS. 12 to 13. Specifically, a charge/discharge rate of the secondary battery increased to 0.1 to 5 C, and again decreased to 1 C. If the charge/discharge rate was 0.1, 0.5, 1, 2, 3 and 5 C, a discharge capacity was measured to be 161.0, 160.5, 158.6, 156.4, 153.8 and 148.9 mAh/g, respectively.

[0259] In other words, it can be confirmed that a secondary battery stably operable in a high-speed charge/discharge condition may be implemented by using the solid electrolyte according to the implementation of the present application.

[0260] FIG. 15 is a graph showing an impedance depending on a cycle test of a secondary battery including a solid electrolyte according to Experimental Example 12-2 of the present application.

[0261] Referring to FIG. 15, in the secondary battery manufactured with reference to FIGS. 12 and 13, an interphase impedance (R.sub.SEI) and an electron transfer impedance (R.sub.CT) in the first cycle and the 250th cycle was measured. The interphase impedance and the electron transfer impedance in the first cycle were calculated to be 1.65 and 11.22Ω), respectively. In addition, the interphase impedance and the electron transfer impedance in the 250th cycle were calculated to be 1.75 and 11.65Ω), respectively. In the secondary battery, as the number of charge/discharge cycles increases, elements included in the components of the secondary battery may be subject to movement and diffusion. Accordingly, resistance in the secondary battery may increase, and charge/discharge properties of the secondary battery may decrease. However, it was observed that the secondary battery including the solid electrolyte according to an embodiment of the present application shows a relatively low increase in the impedance in the 250th cycle. Thus, it can be confirmed that the secondary battery including the solid electrolyte according to an embodiment of the present application has excellent chemical stability.

[0262] Although the present application has been described in detail with reference to exemplary embodiments, the scope of the present application is not limited to a specific embodiment and should be interpreted by the attached claims. In addition, those skilled in the art should understand that many modifications and variations are possible without departing from the scope of the present application.

INDUSTRIAL APPLICABILITY

[0263] The solid electrolyte according to an embodiment of the present application may be used as an electrolyte for a secondary battery, a super capacitor or the like.