CN109264783A - A kind of hollow VS of polycrystal nanobelt self assembled three-dimensional4Microballoon and the preparation method and application thereof - Google Patents
A kind of hollow VS of polycrystal nanobelt self assembled three-dimensional4Microballoon and the preparation method and application thereof Download PDFInfo
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Abstract
A kind of hollow VS of polycrystal nanobelt self assembled three-dimensional4Microballoon and the preparation method and application thereof prepares the hollow VS of polycrystal nanobelt self assembled three-dimensional by simple one step hydro thermal method4Microballoon, and entire reaction process Template-free method auxiliary.When above-mentioned product is applied to lithium/anode material of lithium-ion battery, excellent chemical property can be shown, and lesser powder phenomenon-tion is shown in charge and discharge process.The powder is made of the micron ball that diameter is 0.5~2 μm, micron ball has nanobelt with the three-dimensional hollow structure of canoe self assembly, the diameter of nanobelt is about 50~100nm and is polycrystalline structure, and the interplanar distance of (110) crystal face can reach 0.581nm.By the hollow VS of polycrystal nanobelt self assembled three-dimensional made of preparation method of the invention4Microballoon is applied in lithium/sodium-ion battery field, and unique architectural characteristic can make it show excellent chemical property.
Description
Technical field
The present invention relates to a kind of VS4Nano-powder and the preparation method and application thereof, and in particular to a kind of polycrystal nanobelt from
Assemble three-dimensional hollow VS4Microballoon and the preparation method and application thereof.
Background technique
Lithium/sodium-ion battery has many advantages, such as low cost and high efficiency, in the application of large scale energy storage system
It is widely used in various electronic equipments and electric tool [Pan H, Hu Y-S, Chen L.Room-temperature
stationary sodium-ion batteries for large-scale electric energy
storage.Energy&Environmental Science.2013;6:2338-60.].With deepening continuously for application, people
To lithium/sodium-ion battery performance, more stringent requirements are proposed.As a very important part in lithium/sodium-ion battery,
The low performance of negative electrode material limits further applying for they.In order to find performance more preferably negative electrode material, researcher is carried out
A large amount of exploration.It has been reported that negative electrode material in, researchers generally believe the mineral VS with high theoretical capacity4It is
A kind of very potential candidate, and its nanostructure is regulated and controled further improve its chemical property.
However, the pure phase VS reported at present4Poor chemical property is shown, and the problem of there is easy dusting, this is significantly
Limit its application.Meanwhile the VS reported at present4Nanometer rods dispersed structure and self assembly solid construction are mostly shown.
Summary of the invention
The purpose of the present invention is to provide a kind of hollow VS of polycrystal nanobelt self assembled three-dimensional4Microballoon and preparation method thereof with
Using preparing the hollow VS of polycrystal nanobelt self assembled three-dimensional by simple one step hydro thermal method4Microballoon, and entirely reacted
Journey Template-free method auxiliary.When above-mentioned product is applied to lithium/anode material of lithium-ion battery, excellent electrification can be shown
Performance is learned, and shows lesser powder phenomenon-tion in charge and discharge process.
In order to achieve the above objectives, of the invention the preparation method is as follows:
Step 1: taking 0.9~1.1g sodium metavanadate and 3.5~3.7g thioacetamide at the same be added to 58~62ml go from
Magnetic agitation or ultrasonic disperse obtain half clear solution A in sub- water;
Step 2: the sodium hydroxide solution B of 2.8~3.2mol/L of configuration, solution B, which is added in solution A, reaches its pH
To 10.1~10.3, solution C is obtained;
Solution C: being poured into sealing after reacting in liner by step 3, is then placed on liner homogeneously loaded on fixed in outer kettle
It reacts in instrument, then under the speed conditions of 5~10r/min, 17.5~18.5h is reacted at 95~105 DEG C;
Step 4: hydro-thermal reaction terminates, and reaction kettle is naturally cooled to room temperature, then takes the product cooled down after reaction
Out, product is collected after water, alcohol alternately clean;
Step 5: the product of collection being placed in the cold well of freeze drier and freezed, then by the product after freezing
Be placed in pallet, cover seal closure, be evacuated down to 10~20Pa, collected after dry 12~18h product to get polycrystal nanobelt from
Assemble three-dimensional hollow VS4Microballoon.
Step 1) the magnetic agitation or ultrasonic disperse carry out at room temperature, and the revolving speed of magnetic agitation is 400~600r/
min。
The solvent of sodium hydroxide solution is deionized water in the step 2), and sodium hydroxide solution B is in continuous magnetic force
It under conditions of stirring, is added dropwise in solution A, that is, after 1 drop sodium hydroxide solution is added, stirring is until pH value of solution reaches steady
It is fixed, it is constantly repeated with this, until pH value of solution is adjusted to 10.1~10.3.
The packing ratio that the step 3) solution C pours into reaction liner is 58~62%.
Step 4) the water, alcohol alternately clean each 2~5 times, and product is collected by way of filtering or being centrifuged.
The freezing conditions of the step 5) are as follows: -60~-40 DEG C, freeze 2~5 hours.
Step 5) the product is sealed it before being put into pallet and being dried, with preservative film, and to preservative film
It carries out pricking hole processing.
By the hollow VS of polycrystal nanobelt self assembled three-dimensional made of preparation method of the invention4Microballoon, the powder are by straight
The micron ball that diameter is 0.5~2 μm forms, and micron ball has nanobelt with the three-dimensional hollow structure of canoe self assembly, nanometer
The diameter of band is about 50~100nm and is polycrystalline structure, and the interplanar distance of (110) crystal face can reach 0.581nm.
By the hollow VS of polycrystal nanobelt self assembled three-dimensional made of preparation method of the invention4Microballoon apply lithium/sodium from
Sub- field of batteries, unique architectural characteristic can make it show excellent chemical property.
Specifically have the beneficial effect that:
(1) final product is directly synthesized using a step hydro-thermal reaction due to the present invention, thus there is low synthesis temperature
Degree, simple synthesis path do not need large scale equipment and harsh reaction condition;
(2) vanadium source used in the present invention is sodium metavanadate, sulphur source is thioacetamide, both raw materials are common materials,
It is cheap and easy to get, at low cost, yield is high.
(3) present invention is added without any template, is reacted easily-controllable, is not necessarily to post-processing, environmentally friendly, can be suitble to big
Large-scale production;
(4) product chemistry composition prepared by the present invention is uniform, with high purity, pattern is uniform, negative as lithium/sodium-ion battery
Excellent performance can be shown when the material of pole;
(5) present invention passes through Collaborative Control vanadium source, the concentration and proportion, reacting solution pH value, reaction temperature, reaction of sulphur source
The parameters such as time, reaction-filling ratio and drying mode, realize the hollow VS of polycrystal nanobelt self assembled three-dimensional4The controllable conjunction of microballoon
At control precision with higher.Particularly, the structure of two parameters on product of pH value in reaction and reaction temperature has decisive
Influence.
(6) under excessively high and too low pH value condition, all it is unable to get the hollow VS of polycrystal nanobelt self assembled three-dimensional4Microballoon knot
Structure.
(7) under the conditions of excessively high and too low reaction temperature, also it is unable to get the hollow VS of polycrystal nanobelt self assembled three-dimensional4It is micro-
Spherical structure.
(8) concentration that the sodium hydroxide solution of pH value of solution is adjusted in the present invention must be strictly controlled in 2.8~3.2mol/L,
Excessively high concentration is unfavorable for the formation of uniform hollow structure, and too low concentration can seriously affect reaction-filling ratio, equally also not
Conducive to the formation of hollow structure.
(9) product prepared by the present invention has unique self-assembled structures, wherein in self assembly construct between nanobelt
Unique physics confinement effect and the unique volume buffering effect of hollow structure, can effectively inhibit charge and discharge process VS4Knot
Structure collapses, so as to promote the cyclical stability of material.
(10) there is product prepared by the present invention unique hollow structure it to be made to show lesser mass density, thus
It can be made to show high specific capacity.
(11) VS in product prepared by the present invention4Nanobelt has unique polycrystalline structure, can be in charge and discharge process
Li+/Na+Storage more active sites are provided, also can be Li+/Na+Transmission more infiltration lanes are provided, so as to
It is enough set to show higher capacity and rate capability.
(12)VS4The big chain pitch structure of nanobelt, can not only store more Li+/Na+, additionally it is possible to it is Li+/Na+?
The disengaging of interchain provides more smoothly channel, can finally cooperate with and improve VS4Capacity and high rate performance.
Detailed description of the invention
Fig. 1 is the X-ray diffractogram that the embodiment of the present invention 1 prepares product.Diffraction maximum can be very as can be observed from Figure
Matching criteria card PDF#72-1294 well illustrates that the product of synthesis is monoclinic phase VS4.It is worth noting that, entire diffraction pattern
Spectrum has more burr, it is meant that lower crystallinity.
Fig. 2 is the low power scanning electron microscope (SEM) photograph that the embodiment of the present invention 1 prepares product.It can be seen from the figure that products therefrom is
It is made of the three-dimensional self assembly micron ball that diameter is about 0.5~2 μm.
Fig. 3 is the high power scanning electron microscope (SEM) photograph that the embodiment of the present invention 1 prepares product.It can be seen from the figure that micron ball has
Nanobelt is about 50~100nm with the three-dimensional structure of canoe self assembly, the diameter of nanobelt.
Fig. 4 is the transmission electron microscope picture of product prepared by the embodiment of the present invention 1.Products therefrom VS can be determined from figure4It is micro-
Rice ball has hollow structure.
Fig. 5 is that the embodiment of the present invention 1 prepares VS4The selective electron diffraction figure of nanobelt.Being able to observe that from figure has
The diffraction ring of different radii shows that nanobelt is polycrystalline structure.
Specific embodiment
Embodiment 1:
Step 1: 1g sodium metavanadate and 3.6g thioacetamide are taken while being added in 60ml deionized water, at room temperature
Half clear solution A is obtained with 500r/min magnetic agitation;
Step 2: configuring the sodium hydroxide solution B of 3mol/L with deionized water, under conditions of continuous magnetic agitation, by
It is added dropwise in solution A, that is, after 1 drop sodium hydroxide solution B is added, stirring reaches stable up to pH value of solution, it is constantly repeated with this,
Until pH value of solution is adjusted to 10.2, solution C is obtained;
Step 3: sealing after pouring into solution C in reaction liner by 60% packing ratio, then by liner loaded in outer kettle
Fixation is placed in homogeneous reaction instrument, then under the speed conditions of 10r/min, reacts 18h at 100 DEG C;
Step 4: hydro-thermal reaction terminates, and reaction kettle is naturally cooled to room temperature, then takes the product cooled down after reaction
Out, replace each cleaning 3 times by water, alcohol and collect product in a manner of suction filtration;
Step 5: the product of collection being placed in the cold well of -50 DEG C of freeze drier and freezed 3 hours, then will freezing
Product afterwards is placed in pallet, is sealed with preservative film to it, and carries out pricking hole processing to preservative film, is covered seal closure, is taken out
Vacuum collects product after drying 12h to 16Pa to get the hollow VS of polycrystal nanobelt self assembled three-dimensional4Microballoon.
It can be observed that diffraction maximum can be well matched with standard card PDF#72-1294 from Fig. 1, illustrate the production of synthesis
Object is monoclinic phase VS4.It is worth noting that, entire diffracting spectrum has more burr, it is meant that lower crystallinity.
From figure 2 it can be seen that products therefrom is made of the three-dimensional self assembly micron ball that diameter is about 0.5~2 μm.
From figure 3, it can be seen that micron ball has nanobelt with the three-dimensional structure of canoe self assembly, nanobelt it is straight
Diameter is about 50~100nm.
Products therefrom VS can be determined from Fig. 44Micron ball has hollow structure.
It is able to observe that the diffraction ring with different radii from Fig. 5, shows that nanobelt is polycrystalline structure.
Embodiment 2:
Step 1: 1.1g sodium metavanadate and 3.7g thioacetamide are taken while being added in 58ml deionized water, in room temperature
Under half clear solution A obtained with 400r/min magnetic agitation;
Step 2: configuring the sodium hydroxide solution B of 2.8mol/L with deionized water, under conditions of continuous magnetic agitation,
It is added dropwise in solution A, that is, after 1 drop sodium hydroxide solution B is added, stirring is until pH value of solution reaches stable, with this continuous weight
It is multiple, until pH value of solution is adjusted to 10.1, obtain solution C;
Step 3: sealing after pouring into solution C in reaction liner by 58% packing ratio, then by liner loaded in outer kettle
Fixation is placed in homogeneous reaction instrument, then under the speed conditions of 5r/min, reacts 18.5h at 95 DEG C;
Step 4: hydro-thermal reaction terminates, and reaction kettle is naturally cooled to room temperature, then takes the product cooled down after reaction
Out, product is collected in eccentric fashion by water, each cleaning of alcohol alternating 2 times;
Step 5: the product of collection being placed in the cold well of -60 DEG C of freeze drier and freezed 5 hours, then will freezing
Product afterwards is placed in pallet, is sealed with preservative film to it, and carries out pricking hole processing to preservative film, is covered seal closure, is taken out
Vacuum collects product after drying 18h to 10Pa to get the hollow VS of polycrystal nanobelt self assembled three-dimensional4Microballoon.
Embodiment 3:
Step 1: 0.9g sodium metavanadate and 3.5g thioacetamide are taken while being added in 62ml deionized water, in room temperature
Under half clear solution A obtained with 600r/min magnetic agitation;
Step 2: configuring the sodium hydroxide solution B of 3.2mol/L with deionized water, under conditions of continuous magnetic agitation,
It is added dropwise in solution A, that is, after 1 drop sodium hydroxide solution B is added, stirring is until pH value of solution reaches stable, with this continuous weight
It is multiple, until pH value of solution is adjusted to 10.3, obtain solution C;
Step 3: sealing after pouring into solution C in reaction liner by 61% packing ratio, then by liner loaded in outer kettle
Fixation is placed in homogeneous reaction instrument, then under the speed conditions of 8r/min, reacts 17.5h at 105 DEG C;
Step 4: hydro-thermal reaction terminates, and reaction kettle is naturally cooled to room temperature, then takes the product cooled down after reaction
Out, replace each cleaning 5 times by water, alcohol and collect product in a manner of suction filtration;
Step 5: the product of collection being placed in the cold well of -40 DEG C of freeze drier and freezed 2 hours, then will freezing
Product afterwards is placed in pallet, is sealed with preservative film to it, and carries out pricking hole processing to preservative film, is covered seal closure, is taken out
Vacuum collects product after drying 12h to 20Pa to get the hollow VS of polycrystal nanobelt self assembled three-dimensional4Microballoon.
Embodiment 4:
Step 1: 1.05g sodium metavanadate and 3.7g thioacetamide are taken while being added in 59ml deionized water, in room temperature
Lower ultrasonic disperse obtains half clear solution A;
Step 2: configuring the sodium hydroxide solution B of 2.9mol/L with deionized water, under conditions of continuous magnetic agitation,
It is added dropwise in solution A, that is, after 1 drop sodium hydroxide solution B is added, stirring is until pH value of solution reaches stable, with this continuous weight
It is multiple, until pH value of solution is adjusted to 10.2, obtain solution C;
Step 3: sealing after pouring into solution C in reaction liner by 59% packing ratio, then by liner loaded in outer kettle
Fixation is placed in homogeneous reaction instrument, then under the speed conditions of 9r/min, reacts 18h at 98 DEG C;
Step 4: hydro-thermal reaction terminates, and reaction kettle is naturally cooled to room temperature, then takes the product cooled down after reaction
Out, product is collected in eccentric fashion by water, each cleaning of alcohol alternating 4 times;
Step 5: the product of collection being placed in the cold well of -55 DEG C of freeze drier and freezed 3 hours, then will freezing
Product afterwards is placed in pallet, is sealed with preservative film to it, and carries out pricking hole processing to preservative film, is covered seal closure, is taken out
Vacuum collects product after drying 16h to 13Pa to get the hollow VS of polycrystal nanobelt self assembled three-dimensional4Microballoon.
Embodiment 5:
Step 1: 0.95g sodium metavanadate and 3.6g thioacetamide are taken while being added in 61ml deionized water, in room temperature
Lower ultrasonic disperse obtains half clear solution A;
Step 2: configuring the sodium hydroxide solution B of 3.1mol/L with deionized water, under conditions of continuous magnetic agitation,
It is added dropwise in solution A, that is, after 1 drop sodium hydroxide solution B is added, stirring is until pH value of solution reaches stable, with this continuous weight
It is multiple, until pH value of solution is adjusted to 10.1, obtain solution C;
Step 3: sealing after pouring into solution C in reaction liner by 62% packing ratio, then by liner loaded in outer kettle
Fixation is placed in homogeneous reaction instrument, then under the speed conditions of 7r/min, reacts 18h at 103 DEG C;
Step 4: hydro-thermal reaction terminates, and reaction kettle is naturally cooled to room temperature, then takes the product cooled down after reaction
Out, replace each cleaning 3 times by water, alcohol and collect product in a manner of suction filtration;
Step 5: the product of collection being placed in the cold well of -45 DEG C of freeze drier and freezed 4 hours, then will freezing
Product afterwards is placed in pallet, is sealed with preservative film to it, and carries out pricking hole processing to preservative film, is covered seal closure, is taken out
Vacuum collects product after drying 15h to 18Pa to get the hollow VS of polycrystal nanobelt self assembled three-dimensional4Microballoon.
Claims (9)
1. a kind of hollow VS of polycrystal nanobelt self assembled three-dimensional4The preparation method of microballoon, it is characterised in that:
Step 1: 0.9~1.1g sodium metavanadate and 3.5~3.7g thioacetamide are taken while being added to 58~62ml deionized water
Middle magnetic agitation or ultrasonic disperse obtain half clear solution A;
Step 2: the sodium hydroxide solution B of 2.8~3.2mol/L of configuration, solution B, which is added in solution A, reaches its pH
10.1~10.3, obtain solution C;
Step 3: liner is then placed on homogeneous reaction loaded on fixation in outer kettle by sealing after solution C is poured into reaction liner
In instrument, then under the speed conditions of 5~10r/min, 17.5~18.5h is reacted at 95~105 DEG C;
Step 4: hydro-thermal reaction terminates, and reaction kettle is naturally cooled to room temperature, then takes out the product cooled down after reaction, warp
It crosses after water, alcohol alternately clean and collects product;
Step 5: the product of collection is placed in the cold well of freeze drier and is freezed, be then placed in the product after freezing
In pallet, seal closure is covered, is evacuated down to 10~20Pa, product is collected after dry 12~18h to get polycrystal nanobelt self assembly
Three-dimensional hollow VS4Microballoon.
2. the hollow VS of polycrystal nanobelt self assembled three-dimensional according to claim 14The preparation method of microballoon, it is characterised in that:
Step 1) the magnetic agitation or ultrasonic disperse carry out at room temperature, and the revolving speed of magnetic agitation is 400~600r/min.
3. the hollow VS of polycrystal nanobelt self assembled three-dimensional according to claim 14The preparation method of microballoon, it is characterised in that:
The solvent of sodium hydroxide solution is deionized water in the step 2), and sodium hydroxide solution B is the item in continuous magnetic agitation
It under part, is added dropwise in solution A, that is, after 1 drop sodium hydroxide solution is added, stirring is until pH value of solution reaches stable, not with this
It is disconnected to repeat, until pH value of solution is adjusted to 10.1~10.3.
4. a kind of hollow VS of polycrystal nanobelt self assembled three-dimensional according to claim 14The preparation method of microballoon, feature
Be: the packing ratio that the step 3) solution C pours into reaction liner is 58~62%.
5. the hollow VS of polycrystal nanobelt self assembled three-dimensional according to claim 14The preparation method of microballoon, it is characterised in that:
Step 4) the water, alcohol alternately clean each 2~5 times, and product is collected by way of filtering or being centrifuged.
6. the hollow VS of polycrystal nanobelt self assembled three-dimensional according to claim 14The preparation method of microballoon, it is characterised in that:
The freezing conditions of the step 5) are as follows: -60~-40 DEG C, freeze 2~5 hours.
7. the hollow VS of polycrystal nanobelt self assembled three-dimensional according to claim 14The preparation method of microballoon, it is characterised in that:
Step 5) the product is sealed it before being put into pallet and being dried, with preservative film, and carries out bundle hole to preservative film
Processing.
8. the hollow VS of polycrystal nanobelt self assembled three-dimensional made of a kind of preparation method as described in claim 14Microballoon, it is special
Sign is: the powder is made of the micron ball that diameter is 0.5~2 μm, and micron ball has nanobelt with canoe self assembly
Three-dimensional hollow structure, the diameter of nanobelt is about 50~100nm and for polycrystalline structure, and the interplanar distance of (110) crystal face can
Reach 0.581nm.
9. the hollow VS of polycrystal nanobelt self assembled three-dimensional made of a kind of preparation method as described in claim 14Microballoon is applied
Lithium/sodium-ion battery field, unique architectural characteristic can make it show excellent chemical property.
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109888223A (en) * | 2019-02-26 | 2019-06-14 | 陕西科技大学 | A kind of preparation method and application of four vanadic sulfides@redox graphene composite granule |
CN109904422A (en) * | 2019-02-26 | 2019-06-18 | 陕西科技大学 | A kind of preparation method and application of four vanadic sulfides@Super P composite granule |
CN110282660A (en) * | 2019-07-03 | 2019-09-27 | 中国计量大学 | A kind of four vanadic sulfide powder of nano bar-shape and its preparation method and application |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20140117189A (en) * | 2013-03-26 | 2014-10-07 | 국립대학법인 울산과학기술대학교 산학협력단 | Synthesis method of hybrid consisting of vanadium sulfide and reduced graphite oxide and lithium ion battery comprising the hybrid |
CN105923652A (en) * | 2016-04-29 | 2016-09-07 | 陕西科技大学 | Multilevel-structured VS4 nano-powder, and preparation method and application thereof |
CN106960955A (en) * | 2017-05-31 | 2017-07-18 | 中南大学 | Ternary cathode material of lithium ion battery of vanadium sulfide cladding and preparation method thereof |
CN107381636A (en) * | 2017-07-11 | 2017-11-24 | 陕西科技大学 | A kind of vanadic sulfide powder of nano-particles self assemble three dimensional micron cauliflower-shaped four and its preparation method and application |
CN108598432A (en) * | 2018-05-02 | 2018-09-28 | 电子科技大学 | A kind of preparation method of four vanadic sulfides/graphene composite material for sodium-ion battery electrode |
-
2018
- 2018-10-10 CN CN201811176050.XA patent/CN109264783B/en active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20140117189A (en) * | 2013-03-26 | 2014-10-07 | 국립대학법인 울산과학기술대학교 산학협력단 | Synthesis method of hybrid consisting of vanadium sulfide and reduced graphite oxide and lithium ion battery comprising the hybrid |
CN105923652A (en) * | 2016-04-29 | 2016-09-07 | 陕西科技大学 | Multilevel-structured VS4 nano-powder, and preparation method and application thereof |
CN106960955A (en) * | 2017-05-31 | 2017-07-18 | 中南大学 | Ternary cathode material of lithium ion battery of vanadium sulfide cladding and preparation method thereof |
CN107381636A (en) * | 2017-07-11 | 2017-11-24 | 陕西科技大学 | A kind of vanadic sulfide powder of nano-particles self assemble three dimensional micron cauliflower-shaped four and its preparation method and application |
CN108598432A (en) * | 2018-05-02 | 2018-09-28 | 电子科技大学 | A kind of preparation method of four vanadic sulfides/graphene composite material for sodium-ion battery electrode |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109888223A (en) * | 2019-02-26 | 2019-06-14 | 陕西科技大学 | A kind of preparation method and application of four vanadic sulfides@redox graphene composite granule |
CN109904422A (en) * | 2019-02-26 | 2019-06-18 | 陕西科技大学 | A kind of preparation method and application of four vanadic sulfides@Super P composite granule |
CN109888223B (en) * | 2019-02-26 | 2021-08-10 | 陕西科技大学 | Preparation method and application of vanadium tetrasulfide @ reduced graphene oxide composite powder |
CN109904422B (en) * | 2019-02-26 | 2022-05-20 | 陕西科技大学 | Preparation method and application of vanadium tetrasulfide @ Super P composite powder |
CN110282660A (en) * | 2019-07-03 | 2019-09-27 | 中国计量大学 | A kind of four vanadic sulfide powder of nano bar-shape and its preparation method and application |
CN110282660B (en) * | 2019-07-03 | 2022-02-11 | 中国计量大学 | Nano rod-shaped vanadium tetrasulfide powder and preparation method and application thereof |
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