CN102517481A - High-capacity germanium-cobalt alloy lithium ion battery anode material and preparation method thereof - Google Patents

Abstract

The invention discloses a high-capacity germanium-cobalt alloy lithium ion battery anode material and a preparation method thereof, which belong to an alloy powder material of a lithium ion battery anode and a preparation method thereof. In the method, carbon powder is taken as oxidants of reduced Ge and Co for generating a Ge-Co binary alloy or a binary intermetallic compound. A compound consists of polycrystalline particles of 1-100 micrometers, the reversible capacity is up to 900 mAh/g in maximum and is more than or equal to 750 mAh/g after circulation of 40 times, and the specific content is kept at 83.3 percent. The preparation method comprises the following steps of: preparing oxidants of Ge and Co according to the Ge-Co proportion of a generated alloy; mixing uniformly with carbon powder by milling; putting into inertia gas and heating to 600-1,200 DEG C; preserving heat; and switching off for cooling to the room temperature along with a furnace. The material has high specific capacity, stable performance, a simple preparation process, low cost and an industrial prospect.

Description

A kind of heavy body germanium cobalt alloy lithium ion battery cathode material and preparation method

Technical field

The invention belongs to the alloy powder material that is used for lithium ion battery negative, and adopt the method for carbothermic method by the preparation of metal oxides alloy powder material.

Background technology

The global energy and environmental problem are just impelling that automobile industry is constantly accelerated restructuring, the paces of industrial upgrading; Power truck of energy-saving and environmental protection (EV) and hybrid electric vehicle (HEV) become the developing direction of automobile industry, and people predict that generally the power supply of the high-energy-density of EV and HEV will become one of big industry in 10 years the most potential ten future.As the present lithium ion battery of practicability, it is the secondary cell with highest energy density, and its maximization will become EV and HEV key of success.After the world climate conference of Copenhagen, the Chinese government promises to undertake the year two thousand twenty, and the per GDP CO2 emissions were thandecline 40%-50% in 2005.New-energy automobile is as the important component part of national energy-saving and emission-reduction, and quilt is accelerated one of seven great strategy property new industries of cultivation and development during being classified as " 12 ", will continue to give the emphasis support in fund and policy aspect.

Because the exploitation leeway of lithium ion heavy body novel anode material is very little, the lithium ion battery negative material performance becomes the important factor that improves energy capacity of battery and cycle life.Yet the actual capacity of present business-like carbon negative pole material is near its theoretical value (372 mAhg^-1, 800 mAhcc^-1), thereby further develop or to improve the potentiality of embedding lithium capacity of this material very little.On the other hand, the embedding lithium current potential of graphite-based negative pole (is approximately 10 near the metallic lithium current potential and lithium velocity of diffusion therein is lower^-9--10^-11Cm²s^-1), the possibility that when high magnification charges, exists lithium to separate out on the surface is unfavorable for the security of battery.Therefore, seek the current potential higher slightly than carbon negative pole current potential and embed lithium, the preparation specific storage is high, and the reliable new type lithium ion battery negative material of safety performance becomes the research direction of industry and academia.

The storage lithium theoretical specific capacity of germanium is up to 1600mAh/g, and far above the graphite-like negative material, and the velocity of diffusion of lithium ion in germanium is 400 times in silicon.But Li and single metal form alloy Li_xDuring M (being removal lithium embedded), can be attended by 2-3 volumetric expansion doubly, this will cause electrode cycle performance variation, thereby hinder the practical application of alloy anode.Forming alloy Li for suppressing or relaxing_xThe volume change of being followed in the M process is taken off the electrode matrix of embedding with binary or multicomponent alloy as Li usually, is about to activity and implants mutually in the nonactive phase carrier; Form activity/nonactive alloy; Mostly one of metal is ductility inactive substance preferably in the alloy, the variation of volume is had stronger flexibility, when Li takes off embedding; Can cushion the mechanical stress of bringing owing to the active substance volume change; Thereby make alloy or intermetallic compound base negative material have good cyclical stability, Ge-Cu wherein, Ge-Sb etc. show better electrochemical performance.

The employing high energy ball mill methods such as Hun-Joon Sohn of Korea S Seoul National University are prepared the negative pole that the Ge-Cu thin-film material is used for lithium ion battery; Showing higher lithium storage content is 710mAh/g (Yoon Hwa; Cheol-Min Park, Sukeun Yoon, Hun-Joon Sohn; Electrochimica Acta, 55 (2010): 3324 – 3329).The Chang-Mook Hwang of Korea S Hanyang University; The method of employing magnetron sputterings such as Jong-Wan Park is prepared the Ge-Si film on Copper Foil sinks to the bottom; Maximum reversible capacity is 2099mAh/g (Chang-Mook Hwang; Jong-Wan Park, Journal of Power Sources, 196 (2011): 6772-6780).Domestic still do not have lithium ion battery and report with the ground correlative study of Ge base alloy anode.

Research shows: the metal Co quality is hard, good ductility is arranged, and is incorporated into the ductility that can improve alloy in other metal.The former higher hardness can be alloy and improves firm skeleton, and latter's good ductility can effectively cushion the mechanical swelling of system in the electrochemical process.

On preparation technology, the compound method of Ge base negative pole adopts physical sputtering more, high-energy ball milling, galvanic deposit or chemical pyrolysated method, and complex process, length consuming time, cost is high, and productive rate is low.Thereby, research and develop a kind of electrochemical specific capacity height, good cycling stability, and cost is low, is convenient to the multicomponent alloy negative material that industrialization is produced, for promoting the practical application of alloy material in lithium ion battery to have great importance.

Summary of the invention

The object of the invention at first is to provide a kind of lithium ion battery negative material of germanium cobalt binary alloy, and the uniform particles of this material germanium cobalt-base alloy powder is tiny, and percent crystallinity is good, and the germanium cobalt lithium ion battery negative material specific storage of preparing is high, good cycling stability.

The present invention proposes a kind of method that adopts carbothermic method by the lithium ion battery negative material of preparation of metal oxides germanium cobalt binary alloy simultaneously, and not only preparation process is simple for this method, cost is low, and has the prospect of industrialized development.

The object of the invention is realized in the following manner:

(1) heavy body germanium cobalt alloy lithium ion battery cathode material

This material adopt carbothermic method with carbon dust as reductive agent, the oxide compound of reduction Ge and Co, metal Ge that restores and Co alloying, generation has compound between Ge-Co binary alloy or the binary metal of stabilization of bony shelf structure.

Compound is 1 micron～100 microns a polycrystalline particle between said material Ge-Co binary alloy or binary metal, and percent crystallinity is high, and reversible capacity is up to 900mAh/g, circulates still to remain on more than the 750mAh/g after 40 times.

(2) a kind of method for preparing heavy body germanium cobalt alloy lithium ion battery cathode material

May further comprise the steps:

(1) with raw material GeO₂With Co₃O₄Or Co₂O₃Or CoO and gac or carbon black powder carry out the proportioning weighing, and above raw material is micron order or submicron order or nano level powder, GeO₂With Co₃O₄Or Co₂O₃Or the atomic ratio 7:1-1:5 that the add-on of CoO is pressed Ge/Co calculates, and the add-on of gac or carbon black is calculated by chemical formula (1) or (2) or (3) respectively:

With Co₃O₄During for the Co source:

xGeO₂?+yCo₃O₄?+?(2x+4y)C?→?Co_3yGe_x?+?(2x+4y)CO↑ （1）

With Co₂O₃During for the Co source:

xGeO₂?+yCo₂O₃+?(2x+3y)C?→?Co_2yGe_x?+?(2x+3y)CO↑ （2）

When being the Co source with CoO:

xGeO₂?+yCoO+?(2x+y)C?→?Co_yGe_x?+?(2x+y)CO↑ （3）

(2) adopt mechanical dry method mixed or wet mixing that the raw materials mix of proportioning weighing is even; Place the process furnace of flowing nitrogen or argon gas or CO gas; Temperature rise rate with 5 ℃/min～30 ℃/min reaches temperature required 600 ℃～1200 ℃, is incubated 1～6 hour; Outage naturally cools to room temperature with furnace temperature then.

Among the said preparation method, the consumption of gac or carbon black can excessiveatomic percent 2～30%, and is oxidized to prevent system.

Said preparation method further is with GeO₂With Co₃O₄Or CoO and activated carbon be initial feed, and initial feed is micron order, and 3:1:10～2:1:5 prepares burden in molar ratio; The atomic ratio that is Ge:Co is 1:1～2:1; After grinding mixture evenly, place that the temperature rise rate with 5 ℃/min is elevated to 800 ℃ under the mobile argon gas atmosphere, be incubated 4～5 hours; Outage naturally cools to room temperature then.

According to calculation of thermodynamics; The oxide compound of Ge and Co (460～800 ℃) under relatively low temperature can be metal Ge, Co by carbon reducing agent; The metal Ge that restores has higher activity, is prone to generate Ge-Co alloy or the intermetallic compound with stabilization of bony shelf structure with the Co alloying.And as lithium ion battery binary alloy electrode materials, Ge can close with lithiumation, and shows higher lithium storage content; Co is non-active element with respect to lithium, in the electrochemistry working cycle, and the various volume change of Co in can buffer electrode, thus improve the structural stability of electrode materials.

The present invention adopts the pyrochemistry reduction technique; Utilize carbon dust as reductive agent; The ratio of germanium oxide and powder blue with germanium oxide, powder blue and carbon dust uniform mixing, places the sintering oven that is connected with under the protective atmosphere to carry out sintering in the control starting raw material; Be incubated and obtain final product Ge-Co alloy composite materials with the furnace temperature naturally cooling after 1-6 hour, and the ratio of element is consistent with the starting raw material ratio in the gained Ge-Co alloy product.

The distinguishing feature that has through evidence the present invention with progress is:

As lithium ion battery negative material, specific storage is high with the Ge-Co alloy composite materials in the present invention, stable cycle performance.

The present invention adopts the preparation method of carbothermic method by preparation of metal oxides Ge-Co alloy powder material; To synthesize Ge-Co alloy percent crystallinity high; It is 1 micron～100 microns polycrystalline particle; Specific surface area is lower, is difficult for serious reunion and surface oxidation take place, thereby has reduced the irreversible capacity of negative material.Simultaneously; There is inactive buffering phase in the structural pattern of binary alloy; Cushioned the volume change of material in the removal lithium embedded process, thereby improved the cyclical stability of material, the Ge-Co lithium ion battery negative material specific storage of preparing is high, stable cycle performance; Reversible capacity is up to 900mAh/g, circulates still to remain on more than the 750mAh/g after 40 times.

Technological process of the present invention simple, consuming time less, productive rate is high, thereby, the development prospect that Ge-Co alloy that is proposed by the present invention and preparation method have industrialization.

Description of drawings

Fig. 1 is the XRD figure of carbothermic reduction synthetic Ge-Co powdered alloy of the present invention, and the atomic ratio of Ge, Co is 1:1, and synthesis temperature is 800 ℃, is incubated 4 hours.

Fig. 2 is the specific storage-cycle index curve of carbothermic reduction synthetic Ge-Co alloy anode of the present invention, and the atomic ratio of Ge, Co is 1:1, and synthesis temperature is 800 ℃, is incubated 4 hours.

Below in conjunction with embodiment the present invention is further specified, embodiment comprises but the scope that do not limit the present invention and protected.

Embodiment

Embodiment 1:

With GeO₂(Chun Du>99.9%) Co,₃O₄(Chun Du>99.9%) activated carbon (Chun Du>99%) is initial feed; Initial feed is micron order, and 3:1:10 prepares burden (atomic ratio that is equivalent to Ge:Co is 1:1) in molar ratio, after mixture grinding evenly; Place that the temperature rise rate with 5 ℃/min is elevated to 800 ℃ under the mobile argon gas atmosphere; Be incubated 4 hours, outage naturally cools to room temperature then.Like Fig. 1, the XRD material phase analysis result of gained sample shows that synthetic product is the CoGe/Ge alloy complex, does not have the existence of any oxide impurity phase.

The synthetic material is added the static eliminator acetylene black of 10 wt%, and the sticker PVDF of 10 wt% processes slurry, evenly is applied on the Copper Foil; After the oven dry; Block circular pole piece, form test cell, carry out the constant current charge-discharge experiment with metallic lithium; Charging and discharging currents is 100 mA/g, and the charging/discharging voltage scope is controlled between the 0.01-2.0 V.The maximum reversible capacity of germanium cobalt negative material of preparation is 900mAh/g, and the specific storage that circulates after 40 times is 750mAh/g, and capability retention is 83.3% (like Fig. 2).

Embodiment 2:

With GeO₂(Chun Du>99.9%) CoO (Chun Du>99.9%) and activated carbon (Chun Du>99%) be initial feed, initial feed is micron order, in molar ratio 2:1:5 prepare burden (atomic ratio that is equivalent to Ge:Co is 2:1); After grinding mixture evenly; Place under the mobile carbon monoxide atmosphere, be elevated to 900 ℃, be incubated 5 hours with the temperature rise rate of 10 ℃/min; Outage naturally cools to room temperature then.The XRD material phase analysis of gained sample shows that synthetic product is CoGe/Ge/CoGe₂Alloy complex does not have the existence of any oxide impurity phase.

The synthetic material is added the static eliminator acetylene black of 10 wt%, and the sticker PVDF of 10 wt% processes slurry, evenly is applied on the copper platinum; After the oven dry; Block circular pole piece, form test cell, carry out the constant current charge-discharge experiment with metallic lithium; Charging and discharging currents is 100mA/g, and the charging/discharging voltage scope is controlled between the 0.01-1.5V.The maximum reversible capacity of the Ge-Co alloy composite anode material of preparation is 700mAh/g.The specific storage that circulates after 20 times is 650mAh/g, and capability retention is 92.8%.

Embodiment 3:

With GeO₂(Chun Du>99.9%) Co,₂O₃(Chun Du>99.9%) and activated carbon (Chun Du>99%) be initial feed, initial feed is micron order, in molar ratio 10:1:23 prepare burden (atomic ratio that is equivalent to Ge:Co is 5:1); After grinding mixture evenly; Place under the mobile carbon monoxide atmosphere, be elevated to 1200 ℃, be incubated 1 hour with the temperature rise rate of 20 ℃/min; Outage naturally cools to room temperature then.Synthetic product is Ge/CoGe₂The existence of alloy complex and a small amount of Ge, Co oxide impurity phase.

The synthetic material is added the static eliminator acetylene black of 10 wt%, and the sticker PVDF of 10 wt% processes slurry, evenly is applied on the copper platinum; After the oven dry; Block circular pole piece, form test cell, carry out the constant current charge-discharge experiment with metallic lithium; Charging and discharging currents is 100mA/g, and the charging/discharging voltage scope is controlled between the 0.01-1.5V.The maximum reversible capacity of the Ge-Co alloy composite anode material of preparation is 500mAh/g.The specific storage that circulates after 20 times is 315mAh/g, and capability retention is 63%.

Embodiment 4:

With GeO₂(Chun Du>99.9%) CoO (Chun Du>99.9%) and activated carbon (Chun Du>99%) be initial feed, initial feed is micron order, in molar ratio 2:1:5 prepare burden (atomic ratio that is equivalent to Ge:Co is 2:1); After grinding mixture evenly; Place under the mobile carbon monoxide atmosphere, be elevated to 600 ℃, be incubated 6 hours with the temperature rise rate of 30 ℃/min; Outage naturally cools to room temperature then.The XRD material phase analysis of gained sample shows that synthetic product is CoGe/Ge/CoGe₂Alloy complex does not have the existence of any oxide impurity phase.

The synthetic material is added the static eliminator acetylene black of 10 wt%, and the sticker PVDF of 10 wt% processes slurry, evenly is applied on the copper platinum; After the oven dry; Block circular pole piece, form test cell, carry out the constant current charge-discharge experiment with metallic lithium; Charging and discharging currents is 100mA/g, and the charging/discharging voltage scope is controlled between the 0.01-1.5V.The maximum reversible capacity of the Ge-Co alloy composite anode material of preparation is 820mAh/g.The specific storage that circulates after 20 times is 700mAh/g, and capability retention is 85.3%.

Claims (5)

1. heavy body germanium cobalt alloy lithium ion battery cathode material; It is characterized in that this material adopt carbothermic method with carbon dust as reductive agent; The oxide compound of reduction Ge and Co; Metal Ge that restores and Co alloying generate compound between Ge-Co binary alloy with stabilization of bony shelf structure or binary metal.

2. lithium ion battery negative material according to claim 1; It is characterized in that compound between this material Ge-Co binary alloy or binary metal is 1 micron～100 microns a polycrystalline particle; And percent crystallinity is high; Reversible capacity is up to 900mAh/g, circulates still to remain on more than the 750mAh/g after 40 times.

3. method for preparing like the said material of claim 1～2 may further comprise the steps:

(1) with raw material GeO₂With Co₃O₄Or Co₂O₃Or CoO and gac or carbon black powder carry out the proportioning weighing, and above raw material is micron order or submicron order or nano level powder, GeO₂With Co₃O₄Or Co₂O₃Or the atomic ratio 7:1-1:5 that the add-on of CoO is pressed Ge/Co calculates, and the add-on of gac or carbon black is calculated by chemical formula (1) or (2) or (3) respectively:

With Co₃O₄During for the Co source:

xGeO₂?+yCo₃O₄?+?(2x+4y)C?→?Co_3yGe_x?+?(2x+4y)CO↑ （1）

With Co₂O₃During for the Co source:

xGeO₂?+yCo₂O₃+?(2x+3y)C?→?Co_2yGe_x?+?(2x+3y)CO↑ （2）

When being the Co source with CoO:

xGeO₂?+yCoO+?(2x+y)C?→?Co_yGe_x?+?(2x+y)CO↑ （3）

(2) adopt mechanical dry method mixed or wet mixing that the raw materials mix of proportioning weighing is even; Place the process furnace of flowing nitrogen or argon gas or CO gas; Temperature rise rate with 5 ℃/min～30 ℃/min reaches temperature required 600 ℃～1200 ℃, is incubated 1～6 hour; Outage naturally cools to room temperature with furnace temperature then.

4. preparation method according to claim 1 is characterized in that the consumption of active carbon powder or carbon black powders can excessive atomic percent 2%～30%, and is oxidized to prevent system.

5. preparation method according to claim 1 and 2 is characterized in that further with GeO₂With Co₃O₄Or CoO and activated carbon be initial feed, and initial feed is micron order, and 3:1:10～2:1:5 prepares burden in molar ratio; The atomic ratio that is Ge:Co is 1:1～2:1; After grinding mixture evenly, place that the temperature rise rate with 5 ℃/min is elevated to 800 ℃ under the mobile argon gas atmosphere, be incubated 4～5 hours; Outage naturally cools to room temperature then.

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