CN105914374B - Composite material of nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure and its preparation method and application - Google Patents

Composite material of nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure and its preparation method and application Download PDF

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CN105914374B
CN105914374B CN201610379503.3A CN201610379503A CN105914374B CN 105914374 B CN105914374 B CN 105914374B CN 201610379503 A CN201610379503 A CN 201610379503A CN 105914374 B CN105914374 B CN 105914374B
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nitrogen
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doped carbon
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CN105914374A (en
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夏新辉
谢东
***
涂江平
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Zhejiang University ZJU
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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
    • H01M4/62Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H01M4/624Electric conductive fillers
    • H01M4/625Carbon or graphite
    • 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
    • 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

Composite material the invention discloses a kind of nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure and its preparation method and application, this method includes:Selenium powder is dissolved in hydrazine hydrate, forms solution A;Sodium Molybdate Dihydrate is dissolved in water, forms solution B;Solution is mixed, reaction solution is formed, the vertical graphene collector material for being grown in carbon cloth is placed in the reaction solution, carries out hydro-thermal reaction, it is washed afterwards, dry, obtain VG MoSe2Nucleocapsid array structure;Dopamine hydrochloride is taken to be dissolved in water, then by VG MoSe2Nucleocapsid array structure is immersed in Dopamine hydrochloride aqueous solution, water-bath polymerization, washed drying;By dopamine polymerize nucleocapsid array structure, under hot conditions under protective atmosphere be carbonized to get.When the composite material of the structure is used as sodium ion negative material, with high reversible charge/discharge capacity, long circulation life and excellent high rate performance.

Description

The composite material of nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure And its preparation method and application
Technical field
The present invention relates to anode material of lithium-ion battery technical fields, and in particular to and a kind of nitrogen-doped carbon cladding selenizing molybdenum/ Composite material of graphene nucleocapsid array interlayer structure and preparation method thereof and the application as anode material of lithium-ion battery.
Background technology
Energy crisis and environmental problem are the two big challenges that current mankind society faces, and reproducible New Energy is cleaned in exploitation Source has become the active demand of today's society.Among current various new energy source technologies, lithium rechargeable battery is due to high energy Metric density, high working voltage, advantages of environment protection have captured rapidly portable electronic market, and as electric vehicle and greatly The primary selection of scale energy-storage system.But since lithium resource reserves are limited and are unevenly distributed, resulting in it can not effectively meet pair The huge needs of power lithium-ion rechargeable battery, and the price with lithium associated materials has further been raised, increase its battery Cost, so as to hinder the development of novel energy industry.Therefore the related energy storage technology of honest alternative lithium ion battery is developed It is crucial as urgent problem.
Sodium is resourceful, and development cost is low, and sodium has the characteristics that similar insertion and abjection mechanism to lithium so that sodium ion Secondary cell becomes the first choice of alternative lithium rechargeable battery, and as the research hotspot of today's society.But due to sodium from Sub- radiusCompare lithium ionGreatly, sodium ion migrates slowly in electrode material, and deintercalation process is complicated, leads Cause reversible capacity and high rate performance poor.Therefore the sodium-ion battery material with high reversible capacity and good circulation stability is explored Material has great importance to the development of sodium ion secondary battery of new generation.The MoSe of layer structure2, due to larger layer Spacing (0.67nm) is conducive to the insertion and abjection of sodium ion, and can be embedded in for sodium ion and provide big space, avoids embedding sodium When volume expansion, so as to maintain the stabilization of structure, while there is higher storage sodium capacity (400-800mA hg-1), therefore MoSe2Research as sodium ion negative material has become current research hotspot.But two-dimensional structure MoSe2Material is due to layer With the van der Waals interaction of interlayer, easily reunite during charge discharge, cause the effective of electrolyte and active material Contact reduces, electrode reversible capacity rapid decay.In addition, pure MoSe2Electronic conductivity is not high so that it is as sodium ion two High rate performance is relatively low during primary cell cathode, it is difficult to bear the charge and discharge of larger current density.Therefore, two-dimensional layer MoSe is improved2 Structural stability and improve electronic conductivity be MoSe2Material is as sodium ion secondary battery negative material using urgently to be resolved hurrily Key scientific problems.
At present, by by layer structure MoSe2It is compound with reduced graphene, inhibit its reunion, increase its electric conductivity, improve Sodium ion diffusion rate.In addition, to MoSe2Surface modification or cladding are carried out, inhibits more selenizings of its charge and discharge process generation The dissolving of object stores up the stability and high rate performance of sodium so as to improve it.Layer structure selenides surface is modified, carbon bag It covers, the thickness of carbon thin layer, microstructure, doping situation, affects its interlayer spacing, electric conductivity and its electronics transfer speed Rate stores up sodium performance so as to affect it.Although above method can improve MoSe to a certain extent2As sodium ion cathode Chemical property, but the chemical properties such as its reversible capacity and high rate performance from industrial applications also there are a distance, It is still necessary to improve.
The content of the invention
Object of the present invention is to provide a kind of nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structures Composite material and its preparation method and application, when the composite material of the structure is used as sodium ion negative material, with high reversible Charge/discharge capacity, long circulation life and excellent high rate performance.
A kind of nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure sodium ion negative material and its preparation side Method, the MoSe2Nanometer sheet intersecting vertical is grown in vertical graphene array, and uniformly coats the carbon of one layer of N doping Layer forms interlayer structure, and the carbon thickness of the N doping of the cladding is 5-10nm.
The present invention by with vertical graphene (VG) be skeleton, MoSe2Nanometer sheet intersecting vertical is grown in vertical graphene On array, the carbon (NC) of N doping is cladding layer building nucleocapsid array interlayer structure VG MoSe2@NC composite materials, so as to obtain High reversible capacity and excellent high rate performance.
A kind of preparation method of the composite material of nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure, bag Include following steps:
(1) selenium powder is dissolved in hydrazine hydrate, forms solution A;
(2) Sodium Molybdate Dihydrate is dissolved in water, forms solution B;
(3) solution A with solution B is uniformly mixed, forms reaction solution, the vertical graphene collector material of carbon cloth will be grown in Material is placed in the reaction solution, carries out hydro-thermal reaction, washed afterwards, dry, obtains VG-MoSe2Nucleocapsid array structure;
(4) Dopamine hydrochloride is taken to be dissolved in water, formed hydrochloric acid aqueous dopamine solution, then by step (3) obtained by VG- MoSe2Nucleocapsid array structure is immersed in Dopamine hydrochloride aqueous solution, water-bath polymerization, and washed drying obtains dopamine polymerization Nucleocapsid array structure;
(5) by the nucleocapsid array structure of dopamine polymerization obtained by step (4), carbonization is calcined under protective atmosphere, obtains nitrogen Adulterate the composite material of carbon coating selenizing molybdenum/graphene nucleocapsid array interlayer structure, i.e. VG MoSe2@NC。
The preferred technical solution of the present invention is used as below:
In step (1), the concentration of selenium is 0.2-0.6mmolmL in the solution A-1(i.e. mmol/mL).
In step (2), the concentration of sodium molybdate is 0.02-0.1mmolmL in the solution B-1
In step (3), the molar ratio of selenium and sodium molybdate in solution B is 1.5~2.5 in the solution A:1, it is further excellent Choosing is 2:1.Further preferably, when 160-200 DEG C of progress hydro-thermal reaction 12-24 is small.
In step (4), the concentration of dopamine is 3-7mg mL in the Dopamine hydrochloride aqueous solution-1, at 70 DEG C -90 DEG C When water-bath polymerization 12-24 is small, further preferably, water-bath temperature is 80 DEG C.
In step (5), either argon gas is under nitrogen or argon gas protection for nitrogen for the protective atmosphere, calcining heat For 500-800 DEG C, when calcination time is 2-6 small.
The composite material of the nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure, MoSe2Content is 0.2-0.5mg cm-2
The composite material of nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure is particularly as sodium-ion battery Negative material, the VG@MoSe that will be obtained2The directly small section of@NC composite materials is as sodium-ion battery cathode assembled battery.Cathode Preparation be by VG@MoSe obtained by step (5)2@NC composite materials are cut into slices, and membrane is using Whatman glass fibres, electrolysis Liquid is with 1molL-1NaClO4For solute, volume ratio 1:1 ethylene carbonate (EC) is solvent with dimethyl carbonate (DMC), And the fluorinated ethylene carbonate of 5.0wt.% is added in, cathode uses sodium piece, and the assembling process of battery is all full of argon gas And water oxygen content is completed in the glove box less than 0.1ppm.
The lithium ion battery that assembles place 24 it is small when after carry out constant current charge-discharge test, charging/discharging voltage for 3.0V~ 0.01V, capacity, charge-discharge performance and the multiplying power property of Xun Huan measurement negative electrode of lithium ion battery in 25 ± 1 DEG C of environment.
Compared with prior art, the invention has the advantages that:
(1) method that the present invention is combined using hydro-thermal, water-bath with calcining, the flexible nitrogen-doped carbon cladding selenizing molybdenum of preparation/ Graphene nucleocapsid array interlayer structure sodium ion negative material, of low cost, preparation process is simple, it is easy to accomplish a large amount of metaplasias Production.
(2) the VG@MoSe prepared by2@NC are flexible nucleocapsid array interlayer structure, and nitrogen-doped carbon clad is thick for 5-10nm Degree is conducive to improve the electric conductivity of material and the dissolving of more selenides during effective charge and discharge.
(3) the VG@MoSe prepared by2@NC are prepared into sodium ion cathode, then are direct shearing, eliminate the preparation of slurry, The cumbersome electrode preparation process such as coating, drying.
(4) the VG@MoSe prepared by2@NC composite materials, vertical graphene skeleton provide good electron-transport and lead to Road, the carbon coating layer of N doping improve the electric conductivity of electrode and inhibiting generated in charge and discharge process the dissolvings of more selenides from And overcome the fast inferior position of decaying, realize with high circulation stability, high rate capability, high charge-discharge capacity sodium-ion battery Cathode.
(5) this method is easy to operate, yield is big, and clad is uniform.The sandwich nucleocapsid array structure VG@that the present invention prepares MoSe2@NC sodium ions negative material has flexible support, high specific discharge capacity, long circulating stability and excellent high rate performance etc. Advantage has broad application prospects in novel energy field.
Description of the drawings
Fig. 1 is the composite wood of nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure prepared by embodiment 1 The process schematic of material, wherein, (a) is to be grown in the vertical graphene (VG) of carbon cloth in Fig. 1, and (b) is VG-MoSe in Fig. 12Core Shell array structure, (c) is VG@MoSe in Fig. 12@NC。
Fig. 2 is that the nitrogen-doped carbon prepared in embodiment 1 coats the composite wood of selenizing molybdenum/graphene nucleocapsid array interlayer structure The XRD spectra of material.
Fig. 3 is the nucleocapsid array structure VG@MoSe prepared in embodiment 12Different multiples SEM figure, wherein, in Fig. 3 (a) For the nucleocapsid array structure VG@MoSe prepared in embodiment 12Low range SEM figures, (b) is what is prepared in embodiment 1 in Fig. 3 Nucleocapsid array structure VG@MoSe2High magnification SEM figure.
Fig. 4 is that the composite material that nitrogen-doped carbon coats selenizing molybdenum/graphene nucleocapsid array interlayer structure is prepared in embodiment 1 Different multiples SEM figures and its photo in kind, wherein, (a) coats selenizing molybdenum/stone to prepare nitrogen-doped carbon in embodiment 1 in Fig. 4 The low range SEM of the composite material of black alkene nucleocapsid array interlayer structure schemes, and (b) is to prepare nitrogen-doped carbon bag in embodiment 1 in Fig. 4 The high magnification SEM figures of the composite material of selenizing molybdenum/graphene nucleocapsid array interlayer structure are covered, (c) is to be made in embodiment 1 in Fig. 4 The photo in kind of the composite material of standby nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure.
Fig. 5 is that the composite material that nitrogen-doped carbon coats selenizing molybdenum/graphene nucleocapsid array interlayer structure is prepared in embodiment 1 The circulating battery stability of preparation.
Fig. 6 is that the composite material that nitrogen-doped carbon coats selenizing molybdenum/graphene nucleocapsid array interlayer structure is prepared in embodiment 1 The battery high rate performance of preparation.
Specific embodiment
The present invention is made below by embodiment and further being illustrated, but the invention is not limited in following realities Example.
Embodiment 1
(1) the selenium powder dispersing and dissolving of 4mmol is taken among the hydrazine hydrate of 10mL, under the conditions of 25 DEG C of room temperature, stirring 30min, forms the solution A of claret, and the concentration of selenium is 0.4mmolmL in solution A-1
(2) 2mmol Sodium Molybdate Dihydrates is taken to be dissolved in 60mL deionized waters, form solution B, molybdic acid na concn in solution B For 0.33mmolmL-1
(3) solution A of 10mL and the solution B of 60mL are taken, is mixed evenly, is transferred among reaction kettle, then by 5 × Vertical graphene (VG) collector material that 5cm is grown in carbon cloth is placed in one, and when 200 DEG C of hydro-thermal reactions 24 are small, washs, does It is dry, obtain VG-MoSe2Nucleocapsid array structure;
(4) Dopamine hydrochloride of 0.2g is weighed, is dissolved in 30mL deionized waters and forms solution, then by VG-MoSe2Core Shell array structure impregnates wherein, when 80 DEG C of polymerisations 24 of water-bath are small, wash drying, obtains the nucleocapsid array that dopamine polymerize Composite material;
(5) for the nucleocapsid array composite material polymerizeing dopamine under argon atmosphere, 600 DEG C of high temperature cabonizations 4 are small When, obtain the composite material of nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure, i.e. VG@MoSe2@NC;
(6) by VG@MoSe2@NC composite materials are directly cut to small pieces, as sodium-ion battery electrode.By assembling button Sodium ion half-cell, with VG@MoSe2@NC composite materials are half-cell anode, using whatman glass fibres as half-cell membrane, With 1mol L-1NaClO4For solute, volume ratio 1:1 ethylene carbonate (EC) is solvent with dimethyl carbonate (DMC), and is added Enter the fluorinated ethylene carbonate of 5.0wt.% for electrolyte, using sodium piece as button half-cell cathode, the assembling process of battery is all It is completed in full of the glove box of argon gas and water oxygen content less than 0.1ppm.
With reference to hydro-thermal, water-bath prepares nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array with calcining the method being combined The preparation process of interlayer structure as shown schematically in fig. 1, wherein, (a) is to be grown in the vertical graphene (VG) of carbon cloth in Fig. 1, (b) is VG-MoSe in Fig. 12Nucleocapsid array structure, (c) is VG@MoSe in Fig. 12@NC。
Nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure sodium ion negative material passes through X-ray diffraction Spectrum test (XRD), as shown in Fig. 2, preparing VG@MoSe for the present embodiment 12The XRD spectrum of@NC composite materials.It can according to Fig. 2 Know, VG@MoSe prepared by the present embodiment 12@NC composite materials have the diffraction maximum of VG, with MoSe2Diffraction maximum (JCPDS Card No.29-0914).As shown in Fig. 3 (a-b), the carbon-coating VG-MoSe of uncoated N doping2SEM pictures, maintain vertical graphite The structure of alkene array, and growing the vertical MoSe of one layer of cross-bridging on graphene film2Nanometer sheet, nanoscale twins thickness For 20-30 nanometers.After foring carbon coating layer with carbonization by dopamine polymerization, as shown in Fig. 4 (a-b), it can be seen that vertical The MoSe being grown on graphene2Nanometer sheet is thickening, and lamellar structure is difficult to distinguish, forms carbon-coated MoSe2.Such as Fig. 4 c institutes Show, VG@MoSe2@NC have good flexibility.According to calculating of poor quality before and after reaction, nitrogen-doped carbon cladding selenizing can be calculated Molybdenum/graphene nucleocapsid array interlayer structure sodium ion negative material (i.e. nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array folder The composite material of core structure) in MoSe2Content be about 0.27mg cm-2
Assembled lithium ion battery place 24 it is small when after carry out constant current charge-discharge test, charging/discharging voltage section is 3.0V~0.01V, capacity, charge-discharge performance and the multiplying power of Xun Huan measurement sodium-ion battery cathode in 25 ± 1 DEG C of environment Characteristic.
After being assembled into lithium ion battery, various electrochemical property tests are carried out.As seen from Figure 5, sodium-ion battery exists 200mA g-1There is 785.6mAh g under current density-1Discharge capacity for the first time, by 400 times cycle after its discharge capacity still So there are 534.8mAh g-1, coulombic efficiency maintains more than 99%, shows excellent capacity retention ratio and cyclical stability. Fig. 6 show the high rate performance figure of negative material manufactured in the present embodiment, which shows very excellent high rate performance, 0.2,0.5,1.0 with 2.0A g-1Capacity respectively reaches 538,470,395 and 300mAh g under current density-1.When electric current from 2.0A g-1Return to 0.2A g-1When, and cycle 100 times after, battery capacity returns to 535mAh g-1
Embodiment 2
(1) the selenium powder dispersing and dissolving of 3mmol is taken among the hydrazine hydrate of 10mL, under the conditions of 25 DEG C of room temperature, stirring 30min, forms the solution A of claret, and the concentration of selenium is 0.3mmolmL in solution A-1
(2) 1.5mmol Sodium Molybdate Dihydrates is taken to be dissolved in 50mL deionized waters, form solution B, sodium molybdate is dense in solution B It spends for 0.03mmolmL-1
(3) solution A of 10mL and the solution B of 50mL are taken, is mixed evenly, is transferred among reaction kettle, then by 3 × Vertical graphene (VG) collector material that 3cm is grown in carbon cloth is placed in one, and when 200 DEG C of hydro-thermal reactions 16 are small, washs, does It is dry, obtain VG-MoSe2Nucleocapsid array structure;
(4) Dopamine hydrochloride of 0.15g is weighed, is dissolved in 30mL deionized waters and forms solution, then by VG-MoSe2 Nucleocapsid array structure impregnates wherein, when 80 DEG C of water-bath polymerisations 18 are small, wash drying, obtains the nucleocapsid battle array that dopamine polymerize Row composite material;
(5) the nucleocapsid array composite material polymerizeing dopamine is when calcining 3 is small at 700 DEG C under nitrogen protection atmosphere, Obtain nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array composites sandwich structures, i.e. VG@MoSe2@NC;
(6) by VG@MoSe2@NC composite materials are directly cut to small pieces, as electrode.By assembling half electricity of button sodium ion Pond, with VG@MoSe2@NC composite materials are half-cell anode, using whatman glass fibres as half-cell membrane, with 1molL- 1NaClO4For solute, volume ratio 1:1 ethylene carbonate (EC) is solvent with dimethyl carbonate (DMC), and is added in 5.0wt.% fluorinated ethylene carbonates are electrolyte, and using sodium piece as button half-cell cathode, the assembling process of battery is all being filled Full argon gas and water oxygen content are completed in the glove box less than 0.1ppm.
According to calculating of poor quality before and after reaction, it is sandwich that nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array can be calculated MoSe in structure sodium ion negative material2Content be about 0.25mg cm-2
By nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure sodium ion cathode prepared by the present embodiment After material is assembled into sodium ion secondary battery, various electrochemical property tests are carried out.Sodium-ion battery is in 200mA g-1Electric current is close Degree is lower to have 789.3mAh g-1Discharge capacity for the first time, by 400 times cycle after its discharge capacity still have 536.8mAh g-1, coulombic efficiency maintains more than 99%, shows excellent capacity retention ratio and cyclical stability.It is prepared from the present embodiment Negative material high rate performance figure in, which shows very excellent high rate performance, in 0.2,0.5,1.0 and 2.0A g-1 Capacity respectively reaches 539,471,394 and 302mAh g under current density-1.When electric current is from 2.0A g-1Return to 0.2A g-1When, and After Xun Huan 100 times, battery capacity returns to 534mAh g-1
Embodiment 3
(1) the selenium powder dispersing and dissolving of 6mmol is taken among the hydrazine hydrate of 10mL, under normal temperature condition, stirs 30min, shape Into the solution A of claret, the concentration of selenium is 0.6mmolmL in solution A-1
(2) Sodium Molybdate Dihydrate of 3mmol is taken to be dissolved in 60mL deionized waters, forms solution B, sodium molybdate is dense in solution B It spends for 0.05mmolmL-1
(3) solution A of 10mL and the solution B of 60mL are taken, is mixed evenly, is transferred among reaction kettle, then by 6 × Vertical graphene (VG) collector material that 6cm is grown in carbon cloth is placed in one, and when 200 DEG C of hydro-thermal reactions 12 are small, washs, does It is dry, obtain VG-MoSe2Nucleocapsid array structure;
(4) Dopamine hydrochloride of 0.3g is weighed, is dissolved in 30mL deionized waters and forms solution, then by VG-MoSe2Core Shell array structure impregnates wherein, when 80 DEG C of water-bath polymerisations 12 are small, wash drying, obtains the nucleocapsid array that dopamine polymerize Composite material;
(5) the nucleocapsid array composite material polymerizeing dopamine is when calcining 2 is small at 800 DEG C under argon atmosphere, Obtain nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array composites sandwich structures, i.e. VG@MoSe2@NC;
(6) by VG@MoSe2@NC composite materials are directly cut to small pieces, as electrode.By assembling half electricity of button sodium ion Pond, with VG@MoSe2@NC composite materials are half-cell anode, using whatman glass fibres as half-cell membrane, with 1mol L- 1NaClO4For solute, volume ratio 1:1 ethylene carbonate (EC) is solvent with dimethyl carbonate (DMC), and is added in 5.0wt.% fluorinated ethylene carbonates are electrolyte, and using sodium piece as button half-cell cathode, the assembling process of battery is all being filled Full argon gas and water oxygen content are completed in the glove box less than 0.1ppm.
According to calculating of poor quality before and after reaction, it is sandwich that nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array can be calculated MoSe in structure sodium ion negative material2Content be about 0.26mg cm-2
By nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure sodium ion cathode prepared by the present embodiment After material is assembled into sodium ion secondary battery, various electrochemical property tests are carried out.Sodium-ion battery is in 200mA g-1Electric current is close Degree is lower to have 783.5mAh g-1Discharge capacity for the first time, by 400 times cycle after its discharge capacity still have 535.8mAh g-1, coulombic efficiency maintains more than 99%, shows excellent capacity retention ratio and cyclical stability.It is prepared from the present embodiment Negative material high rate performance figure in, which shows very excellent high rate performance, in 0.2,0.5,1.0 and 2.0A g-1 Capacity respectively reaches 538,474,396 and 301mAh g under current density-1.When electric current is from 2.0A g-1Return to 0.2A g-1When, and After Xun Huan 100 times, battery capacity returns to 537mAh g-1
A kind of flexible nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure sodium ion in Examples 1 to 3 Its maximum discharge capacity in difference under current density is as shown in table 1 after negative material is assembled into sodium-ion battery:
Table 1

Claims (10)

1. a kind of preparation method of the composite material of nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure, special Sign is, comprises the following steps:
(1) selenium powder is dissolved in hydrazine hydrate, forms solution A;
(2) Sodium Molybdate Dihydrate is dissolved in water, forms solution B;
(3) solution A with solution B is uniformly mixed, forms reaction solution, the vertical graphene collector material for being grown in carbon cloth is put In the reaction solution, hydro-thermal reaction is carried out, it is washed afterwards, dry, obtain VG-MoSe2Nucleocapsid array structure;
(4) Dopamine hydrochloride is taken to be dissolved in water, formed hydrochloric acid aqueous dopamine solution, then by step (3) obtained by VG-MoSe2 Nucleocapsid array structure is immersed in Dopamine hydrochloride aqueous solution, and water-bath polymerization, washed drying obtains the nucleocapsid of dopamine polymerization Array structure;
(5) by the nucleocapsid array structure of dopamine polymerization obtained by step (4), carbonization is calcined under protective atmosphere, obtains N doping The composite material of carbon coating selenizing molybdenum/graphene nucleocapsid array interlayer structure.
2. the composite material of nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure according to claim 1 Preparation method, which is characterized in that in step (1), in the solution A concentration of selenium be 0.2-0.6mmolmL-1
3. the composite material of nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure according to claim 1 Preparation method, which is characterized in that in step (2), in the solution B concentration of sodium molybdate be 0.02-0.1mmolmL-1
4. the composite material of nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure according to claim 1 Preparation method, which is characterized in that in step (3), in the solution A in selenium and solution B the molar ratio of sodium molybdate for 1.5~ 2.5:1.
5. the composite material of nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure according to claim 1 Preparation method, which is characterized in that in step (3), 160-200 DEG C carry out hydro-thermal reaction 12-24 it is small when.
6. the composite material of nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure according to claim 1 Preparation method, which is characterized in that in step (4), in the Dopamine hydrochloride aqueous solution concentration of dopamine be 3-7mg mL-1
7. the composite material of nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure according to claim 1 Preparation method, which is characterized in that in step (4), when 70 DEG C of -90 DEG C of water-baths polymerization 12-24 are small.
8. the composite material of nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure according to claim 1 Preparation method, which is characterized in that in step (5), the protective atmosphere be nitrogen or argon gas, calcining heat 500- 800 DEG C, calcination time 2-6h.
9. the nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid prepared according to claim 1~8 any one of them preparation method The composite material of array interlayer structure.
10. the composite material of nitrogen-doped carbon cladding selenizing molybdenum/graphene nucleocapsid array interlayer structure according to claim 9 Application as anode material of lithium-ion battery.
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