CN107394177B - Nickel bicarbonate/graphene composite material for sodium-ion battery cathode and preparation method and application thereof - Google Patents

Nickel bicarbonate/graphene composite material for sodium-ion battery cathode and preparation method and application thereof Download PDF

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CN107394177B
CN107394177B CN201710652052.0A CN201710652052A CN107394177B CN 107394177 B CN107394177 B CN 107394177B CN 201710652052 A CN201710652052 A CN 201710652052A CN 107394177 B CN107394177 B CN 107394177B
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nickel
composite material
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ion battery
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顾鑫
赵学波
闫春柳
代鹏程
李良军
刘丹丹
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China University of Petroleum East China
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/362Composites
    • H01M4/366Composites as layered products
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00Nanotechnology for materials or surface science, e.g. nanocomposites
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/05Accumulators with non-aqueous electrolyte
    • H01M10/054Accumulators with insertion or intercalation of metals other than lithium, e.g. with magnesium or aluminium
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/48Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/485Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
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    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/58Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates
    • H01M4/583Carbonaceous material, e.g. graphite-intercalation compounds or CFx
    • H01M4/587Carbonaceous material, e.g. graphite-intercalation compounds or CFx for inserting or intercalating light metals
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/62Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H01M4/624Electric conductive fillers
    • H01M4/625Carbon or graphite
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

Abstract

The invention provides a nickel bicarbonate/graphene composite material for a sodium-ion battery cathode, and a preparation method and application thereof. The invention adopts a hydrothermal method, takes graphene oxide, divalent nickel salt, a reducing agent and water-soluble carbonate or urea as raw materials, and prepares the ferrous carbonate/graphene composite material. The composite material has uniform size, is applied to a sodium ion cathode, has good electrochemical performance, and has excellent rate performance and cycle stability. In addition, the preparation method of the invention has strong operability and good reproducibility, and the obtained product has stable quality.

Description

Nickel bicarbonate/graphene composite material for sodium-ion battery cathode and preparation method and application thereof
Technical Field
The invention relates to a nickel bicarbonate/graphene composite material for a sodium ion battery cathode, and a preparation method and application thereof, and belongs to the technical field of electrochemistry.
Background
Compared with the lithium ion battery, the sodium ion battery has the advantages of abundant sodium resource reserves and low raw material price, and has a wide application prospect in the field of large-scale energy storage. The negative electrode material of the sodium ion battery, which is one of important components of the battery, has important influence on the performance of the battery. At present, the sodium storage negative electrode material of the intercalation mechanism is concerned more because of the higher cycle stability, and mainly comprises hard carbon and Na2Ti3O7And Li4Ti5O12And the like. Among these sodium-storing negative electrode materials, Na2Ti3O7And Li4Ti5O12The specific capacity of (A) is usually less than 200mAh g-1And the requirement of a high-capacity energy storage battery is difficult to meet. The sodium storage capacity of the hard carbon can reach 300mAh g-1But its rate capability is poor and most of its capacity is below 0.1V (vs. Na/Na) at discharge voltage+) The potential is very close to the precipitation potential of metallic sodium, which can cause the formation of sodium dendrites on the surface of the electrode and bring about a serious safety hazard. Therefore, the search for a novel sodium-electricity negative electrode material with high specific capacity, better rate performance, better cycling stability and high safety is of great significance.
At present, in the prior art, it has been reported that the specific capacity, rate capability and cycle performance of a sodium ion battery are improved by preparing a graphene composite material and applying the graphene composite material to a sodium ion battery cathode material. For example, chinese patent document CN105789592A discloses a three-dimensional graphene composite electrode, which uses three-dimensional porous nickel foam as a substrate, and graphene is directly grown on the substrate, and flower-like Ni is directly grown on the graphene3S2. The three-dimensional graphene-based composite electrode prepared by the method does not contain any conductive agent and binder, and is prepared by firstly carrying out a chemical vapor deposition method and then carrying out hydrothermal treatmentThe preparation method is adopted to obtain; but the steps are more complicated, and the prepared material has poor specific capacity when being used for the sodium ion battery.
Nickel hydrogen carbonate is a negative electrode material of a conversion mechanism lithium ion battery which is researched more at present, and has higher theoretical capacity (300 mAh g) of lithium storage-1Based on conversion reactions
Figure BDA0001368305350000011
) Proper discharge voltage (1.0V), easy preparation, less environmental pollution and other advantages. However, there is no report on the application of nickel bicarbonate to the negative electrode material of sodium ion battery. However, nickel bicarbonate as a negative electrode material of a sodium ion battery has the defects of unstable structure and low conductivity caused by large volume change in the circulation process.
Accordingly, the present invention has been made to solve the above problems.
Disclosure of Invention
In order to make up for the defects of the conventional sodium-ion battery cathode material, the invention provides a nickel bicarbonate/graphene composite material for a sodium-ion battery cathode and a preparation method thereof. The preparation method of the composite material is simple, the operability is strong, the reproducibility is good, and the obtained product has stable quality.
The invention also provides an application of the nickel bicarbonate/graphene composite material, and the composite material applied to the negative electrode material of the sodium-ion battery can effectively improve the charge-discharge rate and the cycle performance.
The technical scheme of the invention is as follows:
a nickel bicarbonate/graphene composite material for a sodium ion battery cathode is a composite powder material of nickel bicarbonate and graphene, and the mass content of the nickel bicarbonate in the composite powder material is 60-95%.
According to the invention, the composite powder material preferably contains 80-95% of nickel bicarbonate by mass.
According to the invention, the preferable micro-morphology of the nickel bicarbonate/graphene composite material is as follows: the nickel bicarbonate nanoparticles are uniformly loaded on the graphene sheet; the particle size of the nickel bicarbonate nano particles is 10 nm-5 mu m; preferably, the particle size of the nickel bicarbonate nanoparticles is 10-500 nm.
The preparation method of the nickel bicarbonate/graphene composite material for the negative electrode of the sodium-ion battery comprises the following steps:
dispersing graphene oxide in deionized water, adding a divalent nickel salt, a reducing agent and water-soluble carbonate or urea, and uniformly mixing to obtain a reaction solution; carrying out hydrothermal reaction for 1-48 hours at the temperature of 70-200 ℃, and washing and drying to obtain the nickel bicarbonate/graphene composite material.
According to the present invention, the graphene oxide may be commercially available or prepared according to the prior art.
According to the present invention, it is preferable that the ratio of the mass of the graphene oxide to the amount of the divalent nickel salt substance in the reaction solution is 1: 0.01-0.5 g/mol; preferably, the ratio of the mass of the graphene oxide to the amount of the divalent nickel salt substance is 1: 0.02-0.2 g/mol.
According to the invention, the molar concentration of the divalent nickel salt in the reaction liquid is preferably 0.01-0.25 mol/L; preferably, the divalent nickel salt has a molar concentration of 0.025 to 0.125 mol/L.
According to the present invention, it is preferable that the amount ratio of the reducing agent, the water-soluble carbonate or urea and the divalent nickel salt in the reaction liquid is 0.5 to 1.5: 5-25: 1-5; preferably, the ratio of the amounts of the reducing agent, water-soluble carbonate or urea and divalent nickel salt is 0.5-1.5: 5-10: 1-3.
According to the present invention, preferably, the divalent nickel salt is one of nickel nitrate, nickel chloride, nickel sulfate or nickel acetate.
Preferably, according to the present invention, the reducing agent is one of citric acid, glucose or ascorbic acid.
Preferably according to the invention, the water-soluble carbonate is ammonium carbonate or sodium carbonate; preferably, the water-soluble carbonate is ammonium carbonate.
According to the invention, the water-soluble carbonate is preferably used in a molar concentration of 0.05 to 1.25mol L-1The water-soluble carbonate aqueous solution of (1).
Preferably, the preparation method of the reaction solution comprises the following steps: dispersing graphene oxide in deionized water, adding a divalent nickel salt and a reducing agent, dissolving and mixing uniformly, quickly adding a carbonate aqueous solution, and mixing uniformly to obtain a reaction solution.
According to the invention, the hydrothermal reaction temperature is preferably 160-180 ℃, and the reaction time is preferably 2-6 hours.
Preferably according to the invention, the drying conditions are: drying at 60-90 deg.C for 6-24 hr in air or vacuum.
The application of the nickel bicarbonate/graphene composite material for the negative electrode of the sodium-ion battery is used as a negative electrode material of the sodium-ion battery to be applied to the sodium-ion battery; the sodium ion battery comprises a negative electrode made of a nickel bicarbonate/graphene composite material, a positive electrode capable of releasing sodium ions and an electrolyte between the negative electrode and the positive electrode.
The mass percentage of nickel bicarbonate in the nickel bicarbonate/graphene composite material can be regulated and controlled by controlling the mass molar ratio of graphene oxide to divalent nickel salt.
The invention also provides a preparation method of the nickel bicarbonate, which comprises the following steps:
dissolving a divalent nickel salt, a reducing agent and water-soluble carbonate or urea in deionized water, and uniformly mixing to obtain a reaction solution; carrying out hydrothermal reaction for 1-48 hours at the temperature of 70-200 ℃, and washing and drying to obtain nickel bicarbonate;
the molar concentration of the divalent nickel salt in the reaction liquid is 0.01-0.25 mol/L; preferably, the divalent nickel salt has a molar concentration of 0.025 to 0.125 mol/L.
The mass ratio of the reducing agent, the water-soluble carbonate or urea and the divalent nickel salt is 0.5-1.5: 5-25: 1-5; preferably, the ratio of the amounts of the reducing agent, water-soluble carbonate or urea and divalent nickel salt is 0.5-1.5: 5-10: 1-3.
The divalent nickel salt is one of nickel nitrate, nickel chloride, nickel sulfate or nickel acetate;
the water-soluble carbonate is ammonium carbonate or sodium carbonate; preferably, the water-soluble carbonate is ammonium carbonate;
the water-soluble carbonate is used at a molar concentration of 0.05-1.25mol L-1An aqueous solution of a water-soluble carbonate salt of (4).
Preferably, the preparation method of the reaction solution comprises the following steps: dissolving a divalent nickel salt and a reducing agent in deionized water, quickly adding a carbonate aqueous solution, and uniformly mixing to obtain a reaction solution.
The nickel bicarbonate is applied to the sodium ion battery as a negative electrode material of the sodium ion battery.
The invention has the following technical characteristics and beneficial effects:
(1) the reducing agent is added in the preparation process, and is used for reducing graphene oxide into graphene in the reaction process and inhibiting oxidation of divalent nickel. The carbonate aqueous solution is quickly poured into the preparation method, mainly because carbonate and metal ions can quickly form a carbonate precursor, the particle size of the precursor can be reduced by quickly pouring the carbonate and the metal ions into the preparation method, and meanwhile, a uniform carbonate precursor and graphene oxide composite material is obtained, and finally, the nickel bicarbonate/graphene composite material obtained through hydrothermal reaction has the characteristic of uniform distribution of components. The micro-morphology of the composite material prepared by the invention is that nickel bicarbonate nano-particles with the particle size of 50-150nm are uniformly loaded on graphene sheets.
(2) The nickel bicarbonate can generate reversible electrochemical conversion reaction with sodium ions
Figure BDA0001368305350000031
Figure BDA0001368305350000032
Theoretical capacity of 300mAh g-1) The graphene modified nickel bicarbonate can inhibit the volume effect and improve the conductivity of the material, thereby further improving the specific capacity, the multiplying power and the cycle performance of the material.
(3) The nickel bicarbonate/graphene composite material is synthesized by a hydrothermal method in one step, the preparation method is simple, the cost is low, the method has strong operability and good reproducibility, and the obtained product has stable quality.
(4) When the nickel bicarbonate/graphene composite material prepared by the invention is applied to a sodium ion battery cathode material, the surprising discovery that the nickel bicarbonate/graphene composite material shows excellent specific capacity, cycle performance and rate capability, and simultaneously shows good rate and cycle performance under the condition of large current charging and discharging is surprisingly found, and the specific capacity of the nickel bicarbonate/graphene composite material reaches 107mAh/g under the current density of 2A/g; after 50 cycles under 100mA/g, the specific capacity of 266mAh/g can be kept; the method provides a new choice for the application of the sodium-ion battery cathode material, lays a foundation for the possible high-current charge and discharge application of the sodium-ion battery cathode material, and can further provide application products for high-current charge and discharge on electric vehicles.
Drawings
Fig. 1 is an XRD spectrum of the nickel bicarbonate/graphene composite material prepared in example 1 of the present invention.
Fig. 2 is a scanning electron micrograph of the nickel bicarbonate/graphene composite material prepared in example 1 of the present invention.
Fig. 3 is a graph comparing the electrochemical performance rate performance of nickel bicarbonate and nickel bicarbonate/graphene composite material in application example 1 of the present invention.
Fig. 4 is a graph comparing electrochemical cycle performance of nickel bicarbonate and nickel bicarbonate/graphene composite material in application example 1 of the present invention.
Detailed Description
The present invention will be further described with reference to the following examples, but is not limited thereto.
Meanwhile, the experimental methods described in the following examples are all conventional methods unless otherwise specified; the reagents and materials are commercially available, unless otherwise specified.
Graphene oxide is commercially available from Shandonghai chemical group in the examples.
Example 1
A nickel bicarbonate/graphene composite material for a sodium ion battery cathode is a composite powder material of nickel bicarbonate and graphene, wherein the mass content of nickel bicarbonate in the composite powder material is 92%.
The preparation method of the nickel bicarbonate/graphene composite material for the negative electrode of the sodium-ion battery comprises the following steps:
taking 6mg of graphene oxide, ultrasonically dispersing in 35mL of deionized water, then adding 1mmol of nickel chloride and 0.2g of ascorbic acid, stirring for 15 minutes at room temperature, and finally quickly adding 5mL of ammonium carbonate aqueous solution (1mol L)-1) Mixing evenly, transferring into a 50mL polytetrafluoroethylene reaction kettle, and reacting for 5 hours at the temperature of 160 ℃. And washing the obtained product, and drying the product in the air at the temperature of 80 ℃ for 6 hours to obtain the nickel bicarbonate/graphene composite material.
The XRD spectrum of the nickel bicarbonate/graphene composite material prepared in this example is shown in fig. 1, and it can be seen from fig. 1 that the prepared composite material is a composite of nickel bicarbonate and graphene.
A scanning electron micrograph of the nickel bicarbonate/graphene composite material prepared in this example is shown in fig. 2, and it can be seen from fig. 2 that nickel bicarbonate nanoparticles having a micro-morphology of about 60nm are loaded on graphene sheets.
Example 2
A preparation method of a nickel bicarbonate/graphene composite material for a sodium-ion battery cathode comprises the following steps:
taking 6mg of graphene oxide, ultrasonically dispersing in 35mL of deionized water, then adding 2mmol of nickel chloride and 0.2g of ascorbic acid, stirring for 15 minutes at room temperature, and finally quickly adding 5mL of ammonium carbonate aqueous solution (1mol L)-1) Mixing evenly, transferring into a 50mL polytetrafluoroethylene reaction kettle, and reacting for 3 hours at the temperature of 180 ℃. And washing the obtained product, and drying the product in the air at the temperature of 80 ℃ for 6 hours to obtain the nickel bicarbonate/graphene composite material.
Example 3
A preparation method of a nickel bicarbonate/graphene composite material for a sodium-ion battery cathode comprises the following steps:
taking 6mg of graphene oxide, ultrasonically dispersing in 35mL of deionized water, then adding 3mmol of nickel acetate and 0.2g of glucose, stirring for 15 minutes at room temperature, and finally quickly adding 5mL of ammonium carbonate aqueous solution (1mol L)-1) Mixing ofMixing evenly, transferring the mixture into a 50mL polytetrafluoroethylene reaction kettle, and reacting for 5 hours at the temperature of 160 ℃. And washing the obtained product, and drying the product in the air at the temperature of 80 ℃ for 6 hours to obtain the nickel bicarbonate/graphene composite material.
Example 4
A preparation method of nickel bicarbonate comprises the following steps:
1mmol of nickel chloride and 0.2g of ascorbic acid were added to 35mL of deionized water, and 5mL of an aqueous ammonium carbonate solution (1mol L) were rapidly added-1) Then, the mixture was stirred at room temperature for 15 minutes, and then transferred to a 50mL polytetrafluoroethylene reaction vessel to be reacted at 160 ℃ for 5 hours. And washing and drying the obtained product in air at 80 ℃ for 6 hours to obtain the nickel bicarbonate material.
Application example 1
The materials prepared in example 1 and example 4 were applied as active materials to negative electrode materials of sodium ion batteries, and electrochemical properties thereof were tested. The preparation method of the electrode comprises the following steps: mixing a conductive agent: adhesive: the active material (material prepared in example 1 and example 5) was mixed at a ratio of 10: 10: 80 to prepare slurry (acetylene black is adopted as a conductive agent, CMC is adopted as a binder), and the slurry is uniformly coated on the copper foil current collector by controlling a certain thickness. Cutting electrode plates with proper sizes, baking at 80 ℃ for 12 hours in vacuum, forming a button cell in a glove box, taking a sodium plate as a counter electrode, and adding 1mol/L NaClO4EC/DMC (volume ratio 1:1) is electrolyte, and the diaphragm is glass fiber filter paper, so as to form the button cell (CR 2032). The working interval of the battery is 0.01V-3.0V.
Fig. 3 is a graph showing the rate performance of the nickel bicarbonate prepared in example 4 and the nickel bicarbonate/graphene composite material prepared in example 1, and as can be seen from fig. 3, under a current density of 2A/g, the specific capacity of the nickel bicarbonate/graphene composite material reaches 107mAh/g, the specific capacity of the nickel bicarbonate is 64mAh/g, which is greatly improved compared with that of a single nickel bicarbonate, so that the specific capacity and the rate performance of the nickel bicarbonate material are greatly improved by introducing the graphene.
Fig. 4 is a comparison graph of cycle performance of the nickel bicarbonate prepared in example 4 and the nickel bicarbonate/graphene composite material prepared in example 1 at 100mA/g, the nickel bicarbonate/graphene composite material can maintain a specific capacity of 266mAh/g after 50 cycles, the nickel bicarbonate can maintain a specific capacity of 147mAh/g, and the nickel bicarbonate/graphene composite material shows significantly enhanced electrochemical stability compared with a single nickel bicarbonate material. Most of the capacity of the invention is realized at about 1.0V of discharge voltage.

Claims (3)

1. The application of the nickel bicarbonate/graphene composite material for the negative electrode of the sodium-ion battery is used as the negative electrode material of the sodium-ion battery to be applied to the sodium-ion battery; the sodium ion battery comprises a cathode made of a nickel bicarbonate/graphene composite material, an anode capable of releasing sodium ions and an electrolyte between the cathode and the anode;
the composite material is a composite powder material of nickel bicarbonate and graphene, and the mass content of the nickel bicarbonate in the composite powder material is 80-95%; the micro-morphology of the nickel bicarbonate/graphene composite material is as follows: the nickel bicarbonate nanoparticles are uniformly loaded on the graphene sheet; the particle size of the nickel bicarbonate nano particles is 10-500 nm;
the preparation method comprises the following steps:
dispersing graphene oxide in deionized water, adding a divalent nickel salt and a reducing agent, dissolving and mixing uniformly, quickly adding a carbonate aqueous solution, and mixing uniformly to obtain a reaction solution; carrying out hydrothermal reaction for 2-6 hours at the temperature of 160-180 ℃, and washing and drying to obtain a nickel bicarbonate/graphene composite material;
the divalent nickel salt is one of nickel nitrate, nickel chloride, nickel sulfate or nickel acetate; the reducing agent is one of citric acid, glucose or ascorbic acid; the ratio of the mass of the graphene oxide to the amount of the divalent nickel salt in the reaction solution is 1: 0.02-0.2 g/mol; the molar concentration of the divalent nickel salt in the reaction liquid is 0.01-0.25 mol/L; the mass ratio of the reducing agent, the carbonate and the divalent nickel salt in the reaction solution is 0.5-1.5: 5-25: 1-5.
2. The use of the nickel bicarbonate/graphene composite material for the negative electrode of the sodium-ion battery according to claim 1, wherein the ratio of the amounts of the reducing agent, the carbonate and the divalent nickel salt is 0.5-1.5: 5-10: 1-3.
3. The use of the nickel bicarbonate/graphene composite material for the negative electrode of the sodium-ion battery according to claim 1, wherein the carbonate is ammonium carbonate or sodium carbonate; the molar concentration of the carbonate aqueous solution is 0.05-1.25mol L-1
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