CN106410152B - A kind of one-dimensional antimony trisulfide-carbon composite, preparation method and application - Google Patents

A kind of one-dimensional antimony trisulfide-carbon composite, preparation method and application Download PDF

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CN106410152B
CN106410152B CN201610964572.0A CN201610964572A CN106410152B CN 106410152 B CN106410152 B CN 106410152B CN 201610964572 A CN201610964572 A CN 201610964572A CN 106410152 B CN106410152 B CN 106410152B
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composite material
spinning
antimony trisulfide
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CN106410152A (en
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朱明强
张唯
余翔翔
喻能
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Huazhong University of Science and Technology
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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
    • 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y40/00Manufacture or treatment of nanostructures
    • 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
    • H01M10/052Li-accumulators
    • H01M10/0525Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
    • 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
    • H01M4/58Selection 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
    • H01M4/581Chalcogenides or intercalation compounds thereof
    • H01M4/5815Sulfides
    • 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
    • H01M4/58Selection 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
    • 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 discloses a kind of one-dimensional antimony trisulfide-carbon nanocoils composite material and preparation method, the one-dimensional Sb that the present invention is prepared2S3/ C nano line composite material, structure is uniform, antimony trisulfide particle rule is unified and is evenly distributed on inside carbon nanocoils and surface, preparation method have the advantages that raw material is simple and easy to get, cheap, synthetic method is simple, environmental-friendly;When the material is used as lithium ion battery negative material, good cycling stability, specific capacity height, the volume expansion that can effectively inhibit alloying in cyclic process, when being used for lithium ion battery negative material, in 100mA g‑1, 150 circle circulation after have up to 551mAh g‑1Capacity.

Description

A kind of one-dimensional antimony trisulfide-carbon composite, preparation method and application
Technical field
The present invention relates to energy storage material, new energy and electrochemical field, especially a kind of one-dimensional antimony trisulfide-carbon composite wood Material, preparation method and application.
Background technique
The energy and environment are two stern challenges that the mankind stride into that 21 century must face, tap a new source of energy with it is renewable Clean energy resource is most one of the technology of decisive influence in current world economy.Especially along with petroleum, coal, natural gas The environmental problem for gradually decreasing and getting worse of equal non-renewable energy resources, efficient, environmentally friendly, energy-saving novel energy resource material technology Research and application more seem important.Lithium ion battery has the characteristics that other secondary cells are incomparable, emerging portable Formula electronic product is such as: laptop computer, video camera and mobile phone etc. are widely used, related lithium ion battery Research also becomes hot spot concerned by people.
Nano metal sulfide material cures antimony has the characteristic of high capacity, theoretical due to there is two step lithium insertion process Particular capacity is very high, is 946mAh g–1.But the antimony trisulfide composite material that the prior art is used as lithium cell cathode material is to pass through Hydro-thermal prepares rodlike, pencil antimony trisulfide, and no and carbon compound, cyclical stability is poor, and capacity is low.In addition antimony trisulfide is received with carbon Mitron is compound to have production difficulty, expensive problem.
Summary of the invention
Aiming at the above defects or improvement requirements of the prior art, one-dimensional antimony trisulfide carbon nanocoils are mixed the present invention provides a kind of Composite material and preparation method and application, its object is to be designed by unique structure, using electrostatic spinning technique, SbCl3Reduction method and vacuum high-temperature vulcanize the mode combined, and active nano material cures antimony insertion carbon nanocoils are prepared into To lithium ion battery antimony trisulfide negative electrode material of the invention, the composite material of prior art antimony trisulfide is thus solved as lithium ion The problems such as cyclical stability present in cell negative electrode material is poor, specific capacity is low, compound difficult with carbon nanotube.
To achieve the above object, according to one aspect of the present invention, it is compound that a kind of one-dimensional antimony trisulfide-carbon nanocoils are provided The chemical formula group of material, the composite material becomes Sb2S3/ C, wherein antimony trisulfide particle distribution inside carbon nanocoils and surface, The mass percent of its antimony trisulfide is 33~41%, surplus C.
Preferably, the size of the carbon nanocoils is 150~300nm.
Preferably, the size of the antimony trisulfide particle is 15~30nm.
Preferably, when the composite material is used for lithium ion battery material, in 100mA g-1, 150 circle circulation after have 510~551mA h g-1Capacity.
Other side according to the invention provides a kind of preparation method of one-dimensional antimony trisulfide-carbon composite, including Following steps:
(1) by antimony chloride, polyacrylonitrile, N,N-dimethylformamide according to mass ratio be 0.07~0.11:0.07~ 0.11:1 is uniformly mixed, and antimonic salt spinning liquid as precursor is prepared;
(2) the spinning liquid as precursor spinning under high pressure for obtaining step (1), obtains presoma one-dimensional nano line;Wherein Spinning voltage is 18~22KV, and it is 0.2~1.0mm/min that rate is injected in spinning;
(3) one-dimensional nano line for obtaining step (2) is calcined in hydrogen/argon atmospher high temperature, obtains one-dimensional mixing antimony after cooling Carbon nanocoils;The calcination temperature is 550~750 DEG C, and calcination time is 6~10h;
(4) the one-dimensional of step (3) acquisition is mixed into antimony carbon nanocoils in a vacuum, vulcanization reaction 6 occurs at 300~350 DEG C ~10h obtains one-dimensional antimony trisulfide-carbon composite.
Preferably, spinning voltage described in step (2) is 20KV, and it is 0.6mm/min that rate is injected in spinning.
Preferably, the volume ratio of hydrogen and argon gas is 10:90 in step (3) hydrogen/argon atmospher.
Preferably, step (4) vulcanization reaction is to be carried out by the way that excessive sulphur powder is added.
Preferably, high-temperature calcination heating rate described in step (4) is 5~10 DEG C/min.
Other side according to the invention provides the one-dimensional antimony trisulfide carbon nanocoils composite material mixed described in one kind Using negative electrode material applied to lithium ion battery.
In general, through the invention it is contemplated above technical scheme is compared with the prior art, can obtain down and show Beneficial effect.
(1) one-dimensional antimony trisulfide-carbon nanocoils composite material for being prepared of the present invention, wherein Sb2S3The size of particle is 20 ~30nm or so, the size of carbon nanocoils are 150~300nm.When applied to ion cathode material lithium, stability is good, specific capacity Volume expansion that is high, can effectively inhibiting alloying in cyclic process.When for lithium ion battery negative material, in 100mA g-1, 150 circle circulation after have up to 521mAh g-1Capacity.
(2) one-dimensional antimony trisulfide-carbon nanocoils composite material provided by the invention during the preparation process there is synthesis material to close Simple at method, environmental-friendly, unique structure, and the material property synthesized is good, stablizes, pattern is uniform, high with specific capacity, The advantages of stable structure, small toxicity, mature production technology.
(3) one-dimensional antimony trisulfide-carbon nanocoils composite material prepared by the present invention, Sb2S3Nano particle and one-dimensional carbon fiber Composite material and pure Sb2S3Material is compared, by by Sb2S3It is prepared into equally distributed nano particle, rule is unified and uniform It is distributed in carbon nanocoils inside and surface, insertion and abjection of the lithium/sodium ion in charge and discharge process is effectively alleviated and causes Volume change, so that cycle performance and service life be made to be greatly improved, meanwhile, carbon fiber also provides for composite material Good electric conductivity and mechanical performance.
Detailed description of the invention
Fig. 1 is one-dimensional antimony trisulfide-carbon nanocoils composite material preparation technology flow chart of the invention;
Fig. 2 is one-dimensional antimony trisulfide-carbon nanocoils composite material SEM figure that the embodiment of the present invention 1 is prepared;
Fig. 3 is one-dimensional antimony trisulfide-carbon nanocoils composite material TEM figure that the embodiment of the present invention 1 is prepared;
Fig. 4 is one-dimensional antimony trisulfide-carbon nanocoils composite material X-ray diffractogram that the embodiment of the present invention 1 is prepared;
Fig. 5 is one-dimensional antimony trisulfide-carbon nanocoils composite material cycle performance figure that the embodiment of the present invention 1 is prepared.
Specific embodiment
In order to make the objectives, technical solutions, and advantages of the present invention clearer, with reference to the accompanying drawings and embodiments, right The present invention is further elaborated.It should be appreciated that the specific embodiments described herein are merely illustrative of the present invention, and It is not used in the restriction present invention.As long as in addition, technical characteristic involved in the various embodiments of the present invention described below Not constituting a conflict with each other can be combined with each other.
A kind of one-dimensional antimony trisulfide-carbon nanocoils composite material provided by the invention, chemical composition Sb2S3/ C, wherein Sb2S3Nanoparticle is evenly distributed on inside carbon nanocoils and surface, Sb2S3Mass percent be 33~41%, surplus is C, the size of the carbon nanocoils are 150~300nm, and the size of the antimony trisulfide particle is 15~30nm.
One-dimensional Sb of the invention2S3When/C nano line composite material is applied to lithium ion battery negative material, cyclical stability Good, specific capacity is high, can effectively inhibit the volume expansion of alloying in cyclic process.When for lithium ion battery material, 100mA g-1, 150 circle circulation after have 510~551mAh g-1Capacity.
The preparation method of one-dimensional antimony trisulfide-carbon nanocoils composite material proposed by the present invention, comprising the following steps:
(1) by antimony chloride, polyacrylonitrile, N,N-dimethylformamide according to mass ratio be 0.07~0.11:0.07~ 0.11:1 is uniformly mixed, and antimonic salt spinning liquid as precursor is prepared;
(2) the spinning liquid as precursor spinning under high pressure for obtaining step (1), obtains presoma one-dimensional nano line;Wherein Spinning voltage is 18~22KV, and preferably 20KV, it is 0.2~1.0mm/min, preferably 0.6mm/min that rate is injected in spinning;
(3) one-dimensional nano line for obtaining step (2) is calcined in hydrogen/argon atmospher high temperature, the hydrogen/argon-mixed volume Ratio is 10:90, obtains one-dimensional mixing antimony carbon nanocoils after cooling;The calcination temperature be 550~750 DEG C, calcination time be 6~ 10h;
(4) by step (3) obtain it is one-dimensional mix antimony carbon nanocoils in a vacuum, it is high temperature vulcanized with excessive sulphur powder, then with two Nitric sulfid washes away remaining sulphur powder, obtains one-dimensional antimony trisulfide-carbon nanocoils composite material, wherein heating rate be 5~10 DEG C/ Min, vulcanization reaction temperature are 300~350 DEG C, the vulcanization reaction time 20~for 24 hours.
The present invention is by by SbCl3It is reduced into antimony simple substance, then it is vulcanized by vacuum sealing tube high temperature sulphur powder as vulcanization Antimony, the preparation method is simple and feasible, synthetic product purity is high.
The present invention uses electrostatic spinning technique, uses SbCl for the first time3Reduction method and vacuum sealing tube is high temperature vulcanized combines Active material antimony trisulfide insertion carbon nanocoils are prepared one-dimensional antimony trisulfide-carbon nanocoils composite material, are applied to lithium by mode Ion battery antimony trisulfide negative electrode material shows superior performance, 100mA gUnder -1Circulation for the first time can be reached after 150 circle of circulation to hold The 86% of amount, and the antimony trisulfide lithium ion battery negative material that the method for prior art hydrothermal synthesis is prepared is in 100mA gUnder -1Its capacity is reduced to the 79% of circulation volume for the first time after 100 circle of circulation.
Step (1) selects SbCl3It is that many experiments are explored as a result, once attempting Sb (NO in test as antimony source3)3、Sb (CH3COO)3Equal antimonic salts find that its Sb particle in high-temperature calcination reduction process overflows carbon nanocoils, or even reunion is together, cannot Be prepared as described in the present invention it is one-dimensional mix antimony trisulfide carbon nanocoils composite material, this is because it was restored in high-temperature calcination It decomposes in journey and generates a large amount of NO2、CO2Caused by equal gases.And SbCl3It does not have decomposition and leads to the problem of gas, because This, selects SbCl3The antimony source that antimony trisulfide carbon nanocoils composite material synthesis process is mixed as the present invention, in reduction process, sulphur That changes that antimony can be stable is embedded in inside and outside carbon nanocoils, to be made uniform, be embedded in the vulcanization on inside carbon nanocoils and surface Antimony nanoparticle.
The following are embodiments:
Embodiment 1:
A kind of one-dimensional antimony trisulfide-carbon nanocoils composite material preparation method as shown in Figure 1, comprising the following steps:
(1) preparation of spinning precursor solution: weighing antimony chloride, PAN and DMF in mass ratio for 0.09:0.09:1, stirring For 24 hours, it is uniformly mixed it, obtains spinning precursor solution.
(2) preparation of nanowire precursor: by spinning precursor solution made from above-mentioned steps (1) in electrospinning device Voltage 20KV, middle spinning injects rate 0.6mm/min.
(3) above-mentioned (2) resulting nanowire precursor the preparation of one-dimensional Sb/C nanowire composite: is placed in tube furnace In be passed through hydrogen/argon-mixed calcining (10:90, Vol), 650 DEG C of calcination temperature, calcination time 6h, heating rate is 5 DEG C/min.
(4) one-dimensional antimony trisulfide-carbon nanocoils composite material preparation: the nano wire for the stable structure that step (3) are obtained With 30mg sulphur powder in 350 degree of vulcanization 22h of high temperature in vacuum sealing tube, then remaining sulphur powder is washed away with carbon disulfide and obtains Fig. 2, figure One-dimensional antimony trisulfide-carbon nanocoils composite material shown in 3.Fig. 2 is that one-dimensional antimony trisulfide-carbon that the present embodiment preparation process obtains is received The SEM of rice noodles composite material schemes, it can be seen that the width dimensions of the negative electrode material are 200nm or so;Fig. 3 is the present embodiment system One-dimensional antimony trisulfide-carbon nanocoils composite material TEM figure that standby technique obtains, it can be seen that Sb2S3Particle is uniform to be distributed in Inside carbon nanocoils and surface, Sb2S3The size of particle is 20~30nm, through analyzing Sb2S3The mass fraction of particle is 39%.
Through detecting, one-dimensional antimony trisulfide-carbon nanocoils composite material diffracting spectrum (XRD) that the present embodiment is prepared is such as Shown in Fig. 4, it was demonstrated that its object phase composition is Sb2S3/ C compound;Fig. 5 is one-dimensional antimony trisulfide-carbon nanometer that the present embodiment is prepared The cycle performance figure of the preparation of line composite material, it can be seen that after circulation 150 times, coulombic efficiency is still 99%;The material is used When making the negative electrode material of lithium ion battery, in 100mA g-1, 150 circle circulation after have up to 551mAh g-1Capacity.
Embodiment 2:
A kind of one-dimensional antimony trisulfide-carbon nanocoils composite material preparation method as shown in Figure 1, comprising the following steps:
(1) preparation of spinning precursor solution: weighing antimony chloride, PAN and DMF in mass ratio for 0.07:0.11:1, stirring For 24 hours, it is uniformly mixed it, obtains spinning precursor solution.
(2) preparation of nanowire precursor: by spinning precursor solution made from above-mentioned steps (1) in electrospinning device Voltage 18KV, middle spinning injects rate 0.2mm/min.
(3) above-mentioned (2) resulting nanowire precursor the preparation of one-dimensional Sb/C nanowire composite: is placed in tube furnace In be passed through hydrogen/argon-mixed calcining (10:90, Vol), 750 DEG C of calcination temperature, calcination time 10h, heating rate is 10 DEG C/ Min obtains one-dimensional Sb/C nanowire composite.
(4) one-dimensional antimony trisulfide-carbon nanocoils composite material preparation: the nano wire for the stable structure that step (3) are obtained For 24 hours, then with carbon disulfide remaining sulphur powder is washed away in 300 degree of high temperature vulcanizations with 33mg sulphur powder in vacuum sealing tube.Through detecting, this The one-dimensional Sb that embodiment is prepared2S3The width dimensions of/C nano line are 150~200nm or so, Sb2S3The size of particle is 20~30nm, through analyzing Sb2S3The mass fraction of particle is 33%.
One-dimensional antimony trisulfide-carbon nanocoils composite material that the present embodiment is prepared is for ion cathode material lithium and tests Its circulation volume, in 100mA g-1, 150 circle circulation after have up to 510mAh g-1Capacity.
Embodiment 3:
A kind of one-dimensional antimony trisulfide-carbon nanocoils composite material preparation method as shown in Figure 1, comprising the following steps:
(1) preparation of spinning precursor solution: weighing antimony chloride, PAN and DMF in mass ratio for 0.11:0.07:1, stirring For 24 hours, it is uniformly mixed it, obtains spinning precursor solution.
(2) preparation of nanowire precursor: by spinning precursor solution made from above-mentioned steps (1) in electrospinning device Voltage 22KV, middle spinning injects rate 1.0mm/min.
(3) preparation of one-dimensional Sb/C nano wire compound lithium ion, sodium ion negative electrode material: above-mentioned steps (2) are resulting Nanowire precursor, which is placed in tube furnace, is passed through hydrogen/argon-mixed calcining (10:90, Vol), and 550 DEG C of calcination temperature, calcination time 6h, heating rate are 5 DEG C/min, obtain one-dimensional Sb/C nanowire composite.
(4) one-dimensional antimony trisulfide-carbon nanocoils composite material preparation: the nano wire for the stable structure that step (3) are obtained Remaining sulphur powder is washed away in 350 degree of vulcanization 20h of high temperature, then with carbon disulfide with 27mg sulphur powder in vacuum sealing tube.It is detected, is made Standby obtained one-dimensional Sb2S3The width dimensions of/C nano line are 200~300nm or so, Sb2S3The size of particle is 20~30nm, Through analyzing Sb2S3The mass fraction of particle is 33%.
Through detecting, one-dimensional antimony trisulfide-carbon nanocoils composite material that the present embodiment is prepared is used for lithium ion battery material When expecting negative electrode material, in 100mA g-1, 150 circle circulation after have up to 541mAh g-1Capacity.
Embodiment 4:
A kind of one-dimensional antimony trisulfide-carbon nanocoils composite material preparation method as shown in Figure 1, comprising the following steps:
(1) the step of the present embodiment (1) is identical as (1) the step of embodiment 1.
(2) preparation of nanowire precursor: by spinning precursor solution made from above-mentioned steps (1) in electrospinning device Voltage 22KV, middle spinning injects rate 0.2mm/min.
(3) nano wire of above-mentioned (3) resulting stable structure the preparation of one-dimensional Sb/C nanowire composite: is placed in pipe Be passed through in formula furnace hydrogen/argon-mixed (10:90, Vol) calcining, 650 DEG C of calcination temperature, calcination time 6h, heating rate be 5 DEG C/ Min obtains Fig. 2, one-dimensional Sb/C nanowire composite shown in Fig. 3.
(4) one-dimensional antimony trisulfide-carbon nanocoils composite material preparation: the nano wire for the stable structure that step (3) are obtained Remaining sulphur powder is washed away in 300 DEG C of vulcanization 20h, then with carbon disulfide with 33mg sulphur powder in vacuum sealing tube.It is detected, is prepared into One-dimensional antimony trisulfide-carbon nanocoils composite material the size arrived is 200nm or so, Sb2S3The size of particle is on the left side 15~20nm The right side, through analyzing Sb2S3The mass fraction of particle is 38%.
Through detecting, one-dimensional antimony trisulfide-carbon nanocoils composite material that the present embodiment is prepared is used for lithium ion battery material When expecting negative electrode material, in 100mA g-1, 150 circle circulation after have up to 538mAh g-1Capacity.
By the above various embodiments as it can be seen that one-dimensional antimony trisulfide-carbon nanocoils composite material prepared by the present invention is used as lithium ion When cell negative electrode material, have many advantages, such as high comprehensive performance, unique structure, good cycle.
As it will be easily appreciated by one skilled in the art that the foregoing is merely illustrative of the preferred embodiments of the present invention, not to The limitation present invention, any modifications, equivalent substitutions and improvements made within the spirit and principles of the present invention should all include Within protection scope of the present invention.

Claims (6)

1. a kind of preparation method of one-dimensional antimony trisulfide-carbon composite, which comprises the following steps:
It (1) is 0.07~0.11:0.07~0.11:1 according to mass ratio by antimony chloride, polyacrylonitrile, N,N-dimethylformamide It is uniformly mixed, antimonic salt spinning liquid as precursor is prepared;
(2) the spinning liquid as precursor spinning under high pressure for obtaining step (1), obtains presoma one-dimensional nano line;Wherein spinning Voltage is 18~22KV, and it is 0.2~1.0mm/min that rate is injected in spinning;
(3) one-dimensional nano line for obtaining step (2) is calcined in hydrogen/argon atmospher high temperature, is obtained one-dimensional antimony carbon of mixing after cooling and is received Rice noodles;The calcination temperature of the high-temperature calcination is 550~750 DEG C, and calcination time is 6~10h;
(4) by step (3) obtain it is one-dimensional mix antimony carbon nanocoils in a vacuum, at 300~350 DEG C occur vulcanization reaction 20~ 24h。
2. the preparation method of composite material as described in claim 1, which is characterized in that spinning voltage described in step (2) is 20KV, it is 0.6mm/min that rate is injected in spinning.
3. the preparation method of composite material as described in claim 1, which is characterized in that hydrogen in step (3) hydrogen/argon atmospher The volume ratio of gas and argon gas is 10:90.
4. the preparation method of composite material as described in claim 1, which is characterized in that step (4) described vulcanization reaction is logical The excessive sulphur powder of addition is crossed to carry out.
5. the preparation method of composite material as described in claim 1, which is characterized in that high-temperature calcination liter described in step (4) Warm rate is 5~10 DEG C/min.
6. a kind of preparation method of one-dimensional antimony trisulfide-carbon composite as claimed in any one of claims 1 to 5, wherein is prepared Composite material application, which is characterized in that the negative electrode material applied to lithium ion battery.
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CN109768239A (en) * 2018-12-24 2019-05-17 肇庆市华师大光电产业研究院 A kind of anode material of lithium-ion battery and preparation method thereof
CN109768238B (en) * 2018-12-24 2021-01-15 肇庆市华师大光电产业研究院 Sb-C/S nanofiber composite material, preparation method and application
CN110729478B (en) * 2019-09-20 2021-08-17 中南大学 Antimony trisulfide nano-dot/sulfur-doped carbon composite material, preparation method thereof and application thereof in sodium/potassium ion battery
CN112072107B (en) * 2020-08-28 2022-07-05 中南大学 Antimony sulfide-based composite material and preparation method and application thereof
CN112186161B (en) * 2020-09-30 2021-05-18 青岛科技大学 Semi-filled one-dimensional nano longitudinal hole composite fiber membrane flexible electrode material and preparation method thereof
CN112909246B (en) * 2021-01-19 2022-07-08 广东工业大学 Bismuth telluride/carbon nanowire composite material and preparation method and application thereof
CN113292099B (en) * 2021-06-30 2022-10-28 湖南理工学院 Preparation method of bismuth sulfide single crystal/carbon nanowire composite material

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101898792A (en) * 2010-07-21 2010-12-01 陕西科技大学 Preparation method of Sb2S3 nanowire
WO2011149991A1 (en) * 2010-05-24 2011-12-01 The Regents Of The University Of California Inorganic nanostructure-organic polymer heterostructures useful for thermoelectric devices
WO2012112120A1 (en) * 2011-02-17 2012-08-23 Nanyang Technological University Inorganic nanorods and a method of forming the same, and a photoelectrode and a photovoltaic device comprising the inorganic nanorods
CN104600293A (en) * 2014-12-22 2015-05-06 桂林电子科技大学 Antimony sulfide negative electrode material with micro-nano structure for sodium-ion battery and preparation method of antimony sulfide negative electrode material

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011149991A1 (en) * 2010-05-24 2011-12-01 The Regents Of The University Of California Inorganic nanostructure-organic polymer heterostructures useful for thermoelectric devices
CN101898792A (en) * 2010-07-21 2010-12-01 陕西科技大学 Preparation method of Sb2S3 nanowire
WO2012112120A1 (en) * 2011-02-17 2012-08-23 Nanyang Technological University Inorganic nanorods and a method of forming the same, and a photoelectrode and a photovoltaic device comprising the inorganic nanorods
CN104600293A (en) * 2014-12-22 2015-05-06 桂林电子科技大学 Antimony sulfide negative electrode material with micro-nano structure for sodium-ion battery and preparation method of antimony sulfide negative electrode material

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Solvothermal synthesis of Sb2S3/C composite nanorods with excellent Li-storage performance;Xiaozhong Zhou et al;《Electrochimica Acta》;20130626;第108卷;18页右栏-19页左栏,附图2-3

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