Patent Application
20230322563
Object of the invention are amorphous silicon carbon composite particles comprising the components silicon, carbon and hydrogen, wherein the silicon and carbon content gradually changes from the centre of the particles to the surface, and wherein the silicon content rises from the surface to the centre of the amorphous particles and the carbon content diminishes from the surface to the centre.
The use of silicon-based materials can increase the energy density of lithium ion batteries by at least 20% compared to the conventional graphite-based anodes. However, silicon-containing anodes are susceptible to rapid degradation due to severe volume changes on lithiation/dilithiation reaction during cycling. This challenge triggers the development of silicon-based materials with a different structure to minimize this degradation during lithiation/dilithiation in silicon-based anodes and to pursue higher capacities and longer cycle life of batteries, in particular, of lithium ion batteries (LIB).
Therefore, active electrode materials of anodes and cathodes play a crucial role in maximizing the total specific energy of the cell, Ecell, given by
E
cell
=C
cell
U
cell, (1)
where Ccell is the total cell capacity and Ucell is the nominal voltage of the cell. The total cell capacity can be calculated as
with Cc and Ca being the specific capacity of the cathode (also called positive electrode, i.e. electrode operating at a higher electrode potential) and anode (electrode operating at a lower potential), respectively, and 1/Qm being the specific mass of inactive battery components (electrolyte, separator, additives, current collector, casing etc.) in g/Ah. Thus, in order to maximise the energy stored in a cell it is necessary to maximise the reversible specific capacity and the difference between operating potentials of the cathode and anode (usually achieved by selecting a cathode with a high potential). High capacity, high rates capacity electrodes and high potential cathodes allow the production of smaller LIBs.
The state-of-the-art anode material used in LIB is graphite with rather low specific capacity of about 370 mAh/g. On the other hand, lithium is known to form alloys with a number of elements including silicon. Useful are compounds that are stable at room temperature, have the highest specific and volumetric capacity, adequate operating potential (i.e. anode material potential must be low enough to maintain a large potential difference between the cathode and anode, but above the potential of the metallic lithium to minimise Li plating during rapid charge) and are preferably non-toxic and abundant.
While lithium metal has intrinsically the lowest potential versus Li/Li+ and the highest specific capacity of 3862 mAh/g, in liquid organic electrolytes, lithium is not coated homogeneously, but forms Li deposits with a high surface area (e.g. dendrites) posing high safety risks. Among the known alloying elements silicon has the highest specific capacity: full lithiation of silicon near room temperature results in the formation of the Li15Si4 phase corresponding to the specific capacity of about 3600 mAh/g.
A serious problem of the combination of silicon as an anode material and lithium is the extremely large volume expansion of about 300% (for comparison, graphite expansion on lithiation is limited to about 10%).
The volume expansion/contraction during lithiation/dilithiation leads to fracture of the (coarse) particles and subsequent decrepitation of the electrode, loss of electric contact between the particles and current collector and repeated disruption of the so-called solid electrolyte interphase (SEI), i.e. a passivation layer formed as a result of the electrolyte decomposition on the particle surface, which continuously consumes the electrolyte and leads to a continuous lithium loss. All of them force a rapid capacity fade and cell failure. The fracture of silicon hinders the use of bulk silicon and coarse silicon powders as anode material in LIB.
This behavior can be explained by strongly inhomogeneous stresses arising as a result of a solid-state amorphization that occurs on the first lithiation of the crystalline silicon (c-Si) materials, when an amorphous lithiated LixSi shell (a-LixSi, with x close to 3.4) moves from the surface towards the non-lithiated crystalline Si core and results in crack initiation at the particle surface. Whereas in the amorphous silicon (a-Si) the lithiation also proceeds by the movement of a sharp phase boundary between the unlithiated a-Si and amorphous a-LixSi phase (x≈2.5-3.75), in contrast to c-Si the hydrostatic stress in a-Si is of lower magnitude and, thus, a higher stability can be expected in the amorphous silicon materials.
The capacity fade in Si-based electrodes is connected to the formation of the crystalline c-Li15Si4 phase. Avoiding the formation of c-Li15Si4 allows more stable cycling.
The suppression of the c-Li15Si4 formation was realised in particles comprising an active Si phase and an inactive matrix phase, such as found in Si-transition metal or Si—SiOx (x≤2) alloys [D. S. M. Iaboni and M. N. Obrovac, J. Electrochem. Soc. 163 (2016) A255]. However, the inactive phase reduces the specific capacity of the material greatly or/and can irreversibly trap Li during the first cycle, i.e. significantly reduce first cycle Coulombic efficiency (CE), and is, therefore, disadvantageous.
Object of the invention was therefore the design of a silicon-based material with minimized degradation during lithiation/dilithiation, furnishing a higher capacity for batteries with a longer cycle life. Therefore, another object of the invention was the design of a material suppressing the formation of detrimental crystalline Li15Si4 phase, in particular for a certain time during their use in batteries. A further object was providing a silicon-based material with a high specific capacity in the first cycle and the following cycles. A further object was to provide a silicon-based material with a high first cycle Coulombic efficiency. A further object was to provide a silicon-based material which allows a higher silicon content in matrix materials of anodes, such as in graphite anodes, in particular, without compromising their cyclability. In addition, the silicon-based material shall be producible in a large scale and cost-efficient process.
It is believed that the silicon carbon particles of the invention comprise silicon alloyed with carbon, in particular the carbon content of the particles is usually in a range to enable the formation of amorphous silicon phase alloyed with carbon, in particular the carbon is at least partially distributed on the atomic scale or as small domains of carbon atoms in amorphous silicon. It is believed that the silicon carbon particles of the invention exist with an inclusion of atomically distributed carbon in amorphous silicon, in particular in the silicon carbon composite.
In addition, a certain carbon content may not be present as an alloy with silicon. Further, due to the condition of synthesis a certain content of hydrogen, in particular at the surface of the silicon carbon particles, is present. The silicon carbon composite particles of the invention have beneficial effects on the performance of the particles in battery applications, combining the conductivity and cyclability of the carbon with the high capacity of the silicon.
The specific carbon content of the amorphous silicon carbon composite particles of the invention stabilizes the amorphous phase and inhibits the formation of a crystalline phase for a certain time at elevated temperature. Further, it was recognized that a higher carbon content of the silicon carbon composite particles allows an increased suppression of the crystalline phase formation at elevated temperature. For example, in the amorphous silicon (pure amorphous silicon, Si-am) annealing at 690° C. results in the complete transformation to the crystalline phase of silicon within one hour, whereas the amorphous silicon carbon composite particles resist crystallization at least three to four times longer, depending on the carbon content of the particles. The particles of the invention undergo only a partial phase transformation from the amorphous state into the crystalline state by 20 wt.-% with a carbon content of 14.2 wt.-% compared to 40 wt.-% of crystalline phase observed in particles comprising 6.3 wt.-% carbon. The degree of the crystallization can thus be correlated to the carbon content (s.
It is believed that the silicon alloyed with carbon and/or in combination with the carbon content of silicon carbon particles suppress the formation of crystalline Li15Si4 from the amorphous LixSi, x=2.5 to 3.75, in particular from the amorphous Li15Si4 phase.
The reason for this behaviour may be the altered atomic environment in the amorphous silicon carbon composite particles. The addition of carbon may disturb the local atomic environment in the amorphous phase and thus suppress the transformation to the crystalline c-Li15Si4 modification.
For the amorphous silicon carbon composite particles, in particular comprising carbon distributed at atomic scale or in domains of carbon atoms in amorphous silicon, it was observed that the stability of the particles increases with increasing carbon content.
It is further preferred, that the silicon carbon composite particles have no detectable aromatic bonding. The observed broad signal in CPMAS (
A particular advantage of the process of the invention is a one-step synthesis, suitable for scale-up. Further, inhomogeneities during synthesis resulting from mixing peculiarities do not play a role in the process of the invention.
Object of the invention are silicon carbon composite particles comprising the components 85 to 99.63 wt.-% silicon content,
0.3 to 15 wt.-% carbon content, in particular atomically distributed carbon in amorphous silicon, and at least 0.04 wt.-% hydrogen content, preferably at least 0.05 wt.-% hydrogen content and optionally 0 to 1 wt.-% oxygen content, wherein the components sum up to 100 wt.-%, and wherein the carbon content in the area beneath the surface of the particles starting with the surface, in particular at 0 nm, and reaching up to at least 30 nm from the surface in direction to the centre of the particles is at least 3 wt.-% higher than in the area of the centre of the particles, wherein the area of the centre is the remaining part of the particles and is directly joined to the area beneath the surface.
According to a preferred aspect of the invention the carbon content in the area beneath the surface of the particles starting with the surface, in particular at 0 nm, and reaching up to at least 30 nm from the surface in direction to the centre of the particles is from 5 wt.-% to 15 wt.-%, preferred are 6 wt.-% to 13 wt.-%, in relation to the remaining components that sum up to 100 wt.-% in the area beneath the surface of the particles.
According to a preferred aspect of the invention the proportion of the carbon content in relation to the silicon content as weight ratio in the area beneath the surface of the particles starting with the surface, in particular at 0 nm, and reaching up to at least 30 nm from the surface in direction to the centre of the particles is from 1:1 to 1:11, in particular from 1:5 to 1:11, preferred from 1:5 to 2:21. And optionally the proportion of the carbon content in relation to the silicon content in the area of the centre of the particles, is from 1:8 to 1:20, preferred from 1:11 to 1:20, wherein the area of the centre is the remaining part of the particles and is directly joined to the area beneath the surface
In addition, the silicon to carbon proportion in the silicon carbon composite particles (Si/C)total is greater than 5, preferred greater than 5,6.
In addition, optionally, the specific surface of the particles is from 3 to 35 m/g, particularly from 3 to 12 m/g, preferred from 4 to 9 m/g.
In a most preferred embodiment of the invention the average particle size of the primary particles is less than 300 nm, in particularly less than 250 nm. The primary particles may be agglomerated and/or aggregated, preferably the primary particles are agglomerated but not sintered, wherein the size of the agglomerates is from 150 to 1500 nm, in particular from 250 to 700 nm. Preferably about 10 to 90%, in particular 80 to 90% of the particles are not sintered.
The position of the surface of the particles is located at zero nm (0 nm). It is preferred that the particles comprise atomically distributed carbon in amorphous silicon, wherein the atomically distributed carbon decreases from the surface of the particles to the centre of the particles.
Particularly preferred are silicon carbon composite particles comprising: 85 to 97 wt.-% silicon content, 1.05 to 15 wt.-% carbon content, and at least 0.05 wt.-% to 5 wt.-% hydrogen content and optionally 0 to 1 wt.-% oxygen content, wherein the components sum up to 100 wt.-% optionally, wherein the specific surface of the particles is from 3 to 35 m/g, particularly from 3 to 10 m/g, preferred from 4 to 9 m/g.
Also preferred are silicon carbon composite particles comprising: 85 to 95 wt.-% silicon content, 1.03 to 15 wt.-% carbon content, and at least 0.07 wt.-% to 5 wt.-% hydrogen content and optionally 0 to 1 wt.-% oxygen content, wherein the components sum up to 100 wt.-% optionally, wherein the specific surface of the particles is from 3 to 35 m/g, particularly from 3 to 10 m/g, preferred from 4 to 9 m/g.
According to a further object of the invention also preferred are silicon carbon composite particles comprising: 85 to 92.93 wt.-% silicon content, 7 to 15 wt.-% carbon content, and at least 0.07 wt.-% to 5 wt.-% hydrogen content and optionally 0 to 1 wt.-% oxygen content, wherein the components sum up to 100 wt.-%, wherein the particles are particularly preferred from 98% to 100% amorphous particles, and optionally, wherein the specific surface of the particles is from 3 to 35 m/g, particularly from 3 to 10 m/g, preferred from 4 to 9 m/g.
More preferred are silicon carbon composite particles comprising 85 to 97 wt.-% silicon content, 2.5 to 15 wt.-% carbon content, and at least 0.1 wt.-% to 5 wt.-% hydrogen content and optionally 0 to 1 wt.-% oxygen content, wherein the components sum up to 100 wt.-%, optionally, wherein the specific surface of the particles is from 3 to 35 m/g, particularly 3 to 10 m/g, preferred from 4 to 9 m/g.
According to a particularly preferred further object of the invention also preferred are silicon carbon composite particles comprising: 93.5 to 92.93 wt.-% silicon content, 0.7 to 1.5 wt.-%, preferred 1.0 to 1.5 wt.-% carbon content, and at least 0.07 wt.-% to 5 wt.-% hydrogen content and optionally 0 to 1 wt.-% oxygen content, wherein the components sum up to 100 wt.-%, wherein the particles are particularly preferred from 98% to 100% amorphous particles, and optionally, wherein the specific surface of the particles is from 3 to 35 m/g, particularly from 3 to 10 m/g, preferred from 4 to 9 m/g.
Per definition in particular the centres of the particles are located at half-width of a diameter of each particle, preferred of spherically particles, wherein the carbon content decreases from the surface to the centre gradually. The same applies for non-spherical particles, for which at least two diameters are selected to locate the centre.
It is particularly preferred that the silicon carbon composite particles possess an amorphous content of more than 90%, in particular of more than 98%, more preferred up to 100%. In this regard it is preferred that the silicon carbon composite particles are amorphous from 95% or 97% up to 100%. Particularly preferred the silicon carbon composite particles are amorphous from 98% up to 100%, most preferred from 99% up to 100%. The amorphous content is measured with x-ray powder diffraction (XRPD).
Preferred atomic concentrations in at.-% in the following three parts of the particles are
In a preferred embodiment of the invention the silicon carbon composite particles are free from a chlorine content, in particular the chlorine content is below 0.7 ppm-wt, preferred below 0.4 ppm-wt., more preferred from 0.01 ppb.-wt. to 0.4 ppm-wt.
According to one aspect of the invention the silicon carbon composite particles possess an average particle size of the primary particle of less than 300 nm, in particularly less than 250 nm. Typically, the carbon silicon composite particles have a primary particle size from 30 nm to 250 nm, preferred from 80 nm to 150 nm. Optionally the particles may form agglomerates, wherein the size of agglomerates of the primary particles is preferred to be less than 1500 nm, wherein the particles are obtainable or formed in a) a gaseous stream comprising precursor silane, and b) a gaseous stream comprising precursor olefinic hydrocarbon, at a reaction temperature in the range of 400° C. to 700° C., in particular 400° C. to 670° C., preferred 490 to 640° C., within a time frame of 500 milliseconds to 20 seconds, optionally they are formed within a tubular inert gas stream, particularly the silicon carbon particles are obtained within a reaction zone that is located within the tubular inert gas stream, and optionally the tubular inert gas stream possesses a temperature of 400 to 670° C., preferred 430 to 650° C., and optionally the reaction mixture is quenched with an inert gas possessing a lower temperature than the reaction mixture, and the silicon carbon composite particles are collected. According to a further aspect of the invention preferably the particles do not form aggregates, i.e. the particles are not sintered to aggregates due to their formation.
A further aspect of the invention is that the particles may have a content of silicon, in particular amorphous silicon, comprising hydrogen, SiH-species and/or (poly-[SiH2]—), and optionally wherein the hydrogen content in the particles is at least 0.05 wt.-%, and wherein the components sum up to 100 wt.-%, in particular the hydrogen content is at least 0.1 wt.-%, preferably 0.3 wt.-%, particularly preferred at least 0.5 wt.-% in the particles.
According to a further aspect of the invention the swelling of the volume of the particles induced by lithiation is less than 250%, preferred less than 300%, in particular at a specific capacity of at least 3000 mAh/g, preferred less than 230%, compared to particles without lithiation.
It is preferred that the particles are spherical particles, wherein the ratio of a first diameter in relation to a second diameter of at least 10 wt.-% of the particles is 0.9 to 1.1, wherein the first and second diameter are arranged perpendicular to each other.
The surface area of the particles in a powder is preferred to be in the range from 3 to m/g, particularly from 3 to 15 m/g, in particular from 5 to 9 m/g, preferred are 6 to 8 m/g.
According to a further aspect of the invention the content of metals apart from silicon in the silicon carbon particles is preferred to be less than 10 ppm-wt., in particular less than 7 ppm-wt., wherein the metals may be selected from Al, Ca, Fe, Co, Zn, Na, Mg, K, most preferred the content of metals in the silicon carbon composite particles is less than 7 ppm-wt. In addition, the content of halogens may be less than 0.7 ppm-wt, preferred below 0.4 ppm-wt., more preferred from 0.01 ppb.-wt. to 0.4 ppm-wt.
According to a further aspect of the invention it is preferred that the reactivity with electrolyte defined as a ratio of the lithiation capacity at cycle (x) to dilithiation capacity at cycle (x−1) is less than 1.02, wherein per definition the reactivity with electrolyte is as a rule above 1 meaning that a reaction with electrolyte takes place; the closer this value to 1 the lower the reactivity with electrolyte.
Further, silicon carbon composite particles are preferred, wherein the silicon content of the particles increases gradually from the area beneath the surface of the particles, wherein the area beneath the surface of the particles starts with the surface, in particular at 0 nm, and reaches up to 30 nm from the surface in direction to the centre of the particles, and wherein the area of the centre is joined to the area beneath the surface, and wherein the carbon content decreases gradually from the surface of the particles to the centre of the particles by at least 3 wt.-%, in particular at least by 4 wt.-% to 20 wt.-%, in correlation to the particular total carbon content of the particles, in particular the carbon is atomically distributed carbon in amorphous silicon, in particular the centre of the particles is located at half-width of a diameter of the particles, wherein the carbon content decreases. In particular the area beneath the surface of the particles comprises the surface of the particles from 0 nm to 30 nm distance in direction of a diameter of the particles.
In addition, it is preferred that the silicon content of the particles is at least 0.5 wt.-% to 30 wt.-%, preferred from 2.5 wt.-% to 20 wt.-%, more preferred from 4 to 10 wt.-%, higher in the area of the centre of the particles than in the area beneath the surface of the particles, and, wherein the area of the centre is joined to the area beneath the surface, wherein the area beneath the surface of the particles starts with the surface, in particular at 0 nm, and reaches up to 30 nm from the surface in direction to the centre of the particles.
A particularly preferred embodiment of the invention comprises particles, wherein the silicon content of the particles is at least 0.5 wt.-% and optionally to 30 wt.-%, preferred from at least 0.7 wt.-%, more preferred 1.5 wt.-% to 20 wt.-%, more preferred from 2.0 wt.-% to 15 wt.-%, higher in the area of the centre of the particles, in particular the silicon content is at least 2.5 wt.-% to 10 wt.-%, in particular 2.5 wt.-% to 5 wt.-%, higher in the area of the centre of the particles, than in the area beneath the surface of the particles, and wherein the area of the centre is joined to the area beneath the surface, wherein the area beneath the surface of the particles starts with the surface, in particular at 0 nm, and reaches up to 30 nm from the surface in direction to the centre of the particles.
In particular, in all events the area beneath the surface of the particles comprises the surface of the particles from 0 nm to 30 nm distance in direction of a diameter of the particles.
According to a further preferred aspect of the invention the carbon content of the particles is from at least 3 wt.-% to optionally 30 wt.-%, in particular from 4 wt.-% to 20 wt.-% higher in the area beneath the surface than in the in the area of the centre of the particles, wherein the area of the centre is joined to the area beneath the surface, wherein the area beneath the surface of the particles starts with the surface, in particular at 0 nm, and reaches up to 30 nm from the surface in direction to the centre of the particles. It is particularly preferred that the silicon content increases reciprocally to the decreasing carbon content.
According to a further preferred aspect of the invention it is preferred that the carbon content of the particles, here total carbon content of the particles, is at least from 1 wt.-% to 15 wt.-%, preferred 2 wt.-% to 14 wt.-%, in particular 2 wt.-% to 10 wt.-% or 2 wt.-% to 8 wt.-%, particular preferred from 3 wt.-% to 6 wt.-%, wherein the components of the particles sum up to 100 wt.-%. According to a further object the carbon content is preferred from 6 to 14 wt.-%, wherein the remaining components sum up to 100 wt.-%. According to another preferred object the carbon content is preferred from 0.7 to 1.5 wt.-%, wherein the remaining components sum up to 100 wt.-%.
Further, the particles may contain a content of aliphatic carbon-hydrogen compounds, in particular wherein the content of aliphatic-carbon hydrogen compounds is from 0.05 wt.-% to 5 wt.-%, in particular 0.05 wt.-% to 3 wt.-%, and optionally the carbon content is comprised in the carbon content of the particles. Preferably the aliphatic-carbon hydrogen compounds comprise alkyl and/or alkenyl groups.
Silicon carbon composite particles according to the invention preferably have a density from 1.8 to. 2.25 g/cm3, particularly ca. 2 g/cm3 (density of crystalline Si is about 2.3 g/cm3).
According to a further aspect of the invention the particles or an anode comprising the particles of the invention particularly exhibit capacity (mAh/g) versus potential versus Li/Li+ (Volt) curves, wherein the curves of the particles possess no plateau extending from 750 mAh/g to 2000 mAh/g between 0.4 Volt and 0.5 Volt due to formation of crystalline Li15Si4 (c-Li15Si4) during at least the first cycle, and in particular until at least the twentieth cycle, more preferred during at least 100 cycles, in particular during the first cycle of lithiation in a secondary cell. According to a further aspect of the invention the particles or an anode comprising the particles preferably possess a dilithiation capacity (mAh/g) of at least 2500 mAh/g at 0.6 Volt, in particular of at least 2900 mAh/g at 0.8 Volt in the first cycle, in particular first cycle of lithiation in a secondary cell, measured as capacity (mAh/g) versus potential versus Li/Li+ (Volt) curves.
According to a further aspect of the invention the swelling of an anode comprising the particles induced by lithiation is less than 180% at a specific capacity of at least 3000 mAh/g, in particular less than 170% compared to the anode without lithiation. In particular the swelling of an anode comprising the particles in a single layer laminate full cell configuration with NMC111 cathode is less than 180% at a specific capacity of at least 3000 mAh/g, in particular less than 170% compared to the anode without lithiation.
According to a further aspect of the invention the particles or an anode comprising the particles preferably have particles possessing differential capacity (dQ/dV) versus voltage curves with a peak corresponding to the crystalline Li15Si4 (c-Li15Si4) formation, whereby the ratio of the area of this peak to the area of the differential capacity (dQ/dV) in the range between 0.38 and 0.8 V is in the range of 0 to 0.1 during at least first cycle, and in particular until at least the twentieth cycle, more preferred during at least 100 cycles.
According to a further aspect of the invention the particles or an anode comprising the particles have at the first cycle a Coulombic efficiency of at least 89% in the silicon carbon composite particles (synonym to Si/C powders of this invention).
Object of the invention is also a process for the production of silicon carbon composite particles, and in particular the particles obtainable according to the process, comprising the steps of
Particularly the olefinic hydrocarbons and alkines may be selected from linear, branched and/or cyclic olefinic hydrocarbons and alkines, such as alkenes, cyclo-alkenes, alkines and cyclo-alkines.
In general, the hydrocarbons may comprise hydrocarbon with 1 to 100 C-atoms, preferred are 1 to 20 C-atoms.
Optionally gaseous by-products are collected, too.
It is preferred that the reaction takes place in (ii) within a tubular reactor at a reaction temperature of 400° C. to 700° C., preferred at 490° C. to 670° C., particular preferred at 490° C. to 645° C., most preferred are 490° C. to 610° C., (iii) wherein the reaction mainly takes place within a heated tubular inert gas stream during a time frame of 500 milliseconds and 20 seconds, preferred are 500 milliseconds to 15 seconds, wherein the reaction takes place at 0.8 to 5 barabs, in particular at 1 to 3 barabs., preferred at 1.2 to 3.0 barabs.
The reaction temperature is defined as the temperature of the reaction, in particular of the reaction zone, within the heated tubular inert gas stream, in particularly within a time frame of 500 milliseconds to 20 seconds.
According to a particularly preferred process (iii) the reaction takes place within a reaction zone that is located within the heated tubular inert gas stream during a time frame of 500 milliseconds to seconds, and wherein the heated tubular inert gas stream possesses an outer circumference and an inner circumference, wherein the inner circumference is joined with the reaction zone which is within the heated tubular inert gas stream, wherein the radial distance from the inner circumference to the outer circumference of the tubular inert gas stream has a ratio of 2:1 to 1:10 in relation to the radius of the reaction zone within the tubular inert gas stream, preferred is 1:1 to 1:5. The radius of the reaction zone may vary over the reaction time, in particular the radius may increase after the injection of the precursor gas streams or a mixture of the precursor streams. In addition it is most preferred that in (iii) the reaction takes place within a reaction zone that is located within the heated tubular inert gas stream during a time frame of 500 milliseconds to 20 seconds, and wherein the heated tubular inert gas stream possesses a temperature of about 400 to 520° C. when the precursor silane, the precursor hydrocarbon, in particularly the precursor olefinic hydrocarbon, or a mixture thereof is injected into the reaction zone of the tubular reactor. The injection of the precursors direct into the centre of the tubular inert gas stream leading to a confinement of the reaction in the center of the reaction tube. Due to the very specific reaction conditions, forming a reaction zone comprising at least two reaction sections within the tubular inert gas stream, wherein the first reaction section comprises the injection of the gaseous precursor stream comprising precursor silane and precursor hydrocarbon, in particularly the precursor olefinic hydrocarbon, being injected axially into the reaction zone that has a temperature from 400° C. to 520° C., preferred from 430° C. to below 490° C. Wherein the reaction zone comprises at least two reaction sections along the axis of the tubular reactor, wherein the second reaction section follows behind the first reaction section. The second reaction section having a reaction temperature from 490° C. to 700° C., in particular from 490 to 650° C. The carbon source will not be consumed by 100% in the reaction.
The heated tubular inert gas stream possesses in particular a concentric outer circumference and a concentric inner circumference, wherein the inner circumference is joined with the reaction zone which is within the heated tubular inert gas stream, wherein the concentric radial distance from the inner circumference to the outer circumference of the tubular inert gas stream has a ratio of 2:1 to 1:10. Concentric means having a common centre at the length axis of the tubular reactor.
It is further preferred that a) a gaseous stream comprising precursor silane of at least one precursor silane, and b) a gaseous stream comprising precursor hydrocarbon, in particularly olefinic hydrocarbon, are injected into the tubular reactor at a volume flow of 1 to 15 Nm3/h, in particular at a volume flow of 1 to 5 Nm3/h, preferably at a volume flow of 1.1 to 5 Nm3/h. According to a particular preferred embodiment, the precursor silane, the precursor hydrocarbon, in particularly olefinic hydrocarbon, or a mixture thereof is injected into the tubular reactor at a volume flow of 1 to 15 Nm3/h, in particular 1 to 10 Nm3/h, preferably from 1 to 5 Nm3/h. a) and b) can be mixed before they are injected into the reactor.
According to a further aspect a) a gaseous stream comprising precursor silane of at least one precursor silane, and b) a gaseous stream comprising precursor hydrocarbon, in particularly olefinic hydrocarbon, are injected into the tubular reactor at a volume flow of 1 to 15 Nm3/h, in particular at a volume flow of 1 to 5 Nm3/h, preferably at a volume flow of 1.1 to 5 Nm3/h, wherein the proportion of a) to b) is from 20:1 to 1:1, preferred from 10:1 to 1:1, optionally the reaction takes place at 1.2 to 3.0 barabs.
Further, it is preferred that the reaction mainly takes place within a heated tubular inert gas stream comprising Argon, Helium and/or Neon, in particular Argon, during a time frame of 500 milliseconds and 15 seconds.
According to a further aspect of the invention the inert gas is selected from Argon, Helium, Neon and Nitrogen, in particular the inert gas stream is selected from Argon and/or the inert gas for quenching is selected from Nitrogen and Argon.
It is further preferred that the inert gas stream has a volume flow of 0.5 to 25 Nm3/h, in particular from 1 to 10 Nm3/h, in particular 2 to 8 Nm3/h, a preferred inert gas is Argon.
It is further preferred that the heated tubular inert gas stream has a volume flow of 0.5 to 25 Nm3/h, in particular from 1 to 10 Nm3/h, in particular 2 to 8 Nm3/h and, wherein the temperature of the inert gas stream is 490° C. to 670° C. A preferred inert gas is Argon.
According to a particular preferred embodiment, the precursor silane, the precursor olefinic hydrocarbon or a mixture thereof is injected into the tubular reactor at a lower volume flow, in particular with a volume flow of 1 to 5 Nm3/h, than the heated tubular inert gas stream, in particular with a volume flow of 3 to 15 Nm3/h, particularly wherein the heated tubular inert gas stream possesses a temperature of about 400 to 520° C. when the precursor silane, the precursor olefinic hydrocarbon or a mixture thereof being injected into the reaction zone of the tubular reactor.
According to a particular preferred embodiment, the precursor silane, the precursor olefinic hydrocarbon or a mixture thereof is injected into the tubular reactor at a lower volume flow, in particular with a volume flow of 1 to 4 Nm3/h, than the heated tubular inert gas stream, particularly wherein the tubular inert gas stream has a volume flow of more than 4 to Nm3/h.
According to an further aspect, the reaction may take place in the presence of hydrogen, in particular the gaseous stream comprising precursor silane may contain in addition hydrogen, more preferred hydrogen (H2) at a volume flow of 0.2 to 15 Nm3/h, and/or b) the gaseous stream comprising precursor olefinic hydrocarbon may in addition contain hydrogen (H2), more preferred hydrogen at a volume flow of 0.2 to 15 Nm3/h, and/or the heated tubular inert gas stream may in addition contain hydrogen, more preferred hydrogen (H2) at a volume flow of 0.2 to 15 Nm3/h. It may be preferred that hydrogen is injected, preferred into the tubular reactor, at a volume flow of 0.2 to 15 Nm3/h optionally as a mixture with at least one or both precursors and/or as a mixture with the inert gas.
Object of the invention is also an anode, in particular anode for use in a cell in a secondary lithium ion battery (LIB) comprising silicon carbon composite particles, wherein the anode optionally comprising at least a binder and optionally comprising acetylene black, carbon black, graphite or a mixture of these components. A preferred composition of an anode may comprise 2 to 90 wt.-%, in particular 40 to 65 wt.-%, of silicon and/or silicon carbon composite particles, preferred are silicon carbon composite particles, 5 to 97 wt.-%, 5 to 30 wt.-%, preferred 0.5 to 25 wt.-% graphite or acetylene black, carbon black, graphite or a mixture of these components and 0.5 to 30 wt.-% binder, in particular 5 to 25 wt.-% binder, wherein the composition sum up to 100 wt.-%.
A typical anode composition may comprise 10 wt. % carbon black, 15 wt.-% graphite and 15 wt.-% polyacrylic acid binder (PAA) and sum up to 100 wt.-% with silicon carbon composite particles.
Preferred binders comprise polyacrylic acid (PAA), polyvinyl alcohol (PVA), polyacrylonitrile (PAN), styrene butadiene rubber (SBR), carboxyl methylcellulose (CMC), alginate (Alg), gum arabic (GA), guar gum (GG), chitosan, starch, polyimide, olyethyleneimine (PEI), poly(1-pyrenemethyl methacrylate), poly(9,9-dioctylfluorene-co-fluorenone-co-methylbenzoic ester), b-cyclodextrin polymer (b-CDp), PEDOT:PSS, xanthan gum (XG), chitosan-glutaraldehyde (CS-GA), polyvinylidene fluoride (PVDF) or mixtures thereof.
A further object of the invention is a battery, in particular a secondary battery, more preferred for use in a lithium ion battery (LIB) comprising at least one anode, in particular an anode comprising silicon carbon composite particles of the invention, preferred amorphous silicon carbon composite particles comprising atomically distributed carbon in amorphous silicon. In addition, it is preferred that the battery comprises at least two or more than two secondary cells, in particular up to 1000 secondary cells.
Particular embodiments of the invention are described below without restricting the invention to the specific examples.
Experimental: A tubular reactor made of quartz (length to be heated 500 mm or 1000 mm, diameter 120 mm). The precursor silane and the precursor olefinic hydrocarbon were injected in the tubular reactor through a nozzle. Inert gas was injected in a tubular way around the nozzle of the tubular reactor. Heating elements were arranged outside of the quartz glass reactor and could be controlled along the reactor length. The nozzle was located at the axis of the reactor in the reaction zone in the first reaction section. The reaction was performed at 1 barabs, if not mentioned otherwise.
Analytical Methods:
Specific Surface Area Determination
Specific surface area was determined by nitrogen absorption using Brunauer, Emmett and Teller (BET) method (instrument: TriStar II Plus, Micromeretics). Prior to the measurement samples were dried under vacuum at 150° C. for 20 min.
Carbon, hydrogen and oxygen content determination: Total carbon, hydrogen and oxygen content is defined as the concentration averaged over the whole powder volume and is determined using elemental analysis by combustion. For carbon content determination Leco CS744 analyzer was employed. Elemental analysis of oxygen and hydrogen was performed using Leco ONH836 element analyzer. For oxygen and hydrogen content determination, the measurement was carried after and without air contact. For measurements without air contact, samples were filled into capsules in a glove box under protective atmosphere, sealed and discharged from the glove box in transport containers. These transport containers were placed on an attachment, which is flushed with a gas, placed into the analyzer, passed into the incinerator and the measurement was subsequently performed.
X-ray photospectroscopy (XPS): Carbon, oxygen and silicon contents are determined by x-ray photoelectron spectroscopy (XPS) using ESCALAB 250xi ThermoFisher Scientific spectrometer equipped with a monochromatic Al Kα source as a function of the distance from the surface using a depth profiling method revealing subsurface information. The powders were placed on the XPS sample holder and XPS spectra were collected first from the sample surface. The binding energy is referenced to C1s at 284.6 eV. A sequence of Argon ion gun etching and spectrum acquisition is repeated until profiling has proceeded to the required depth.
X-ray diffraction (XRD): The phase composition and structure parameters were determined by Rietveld refinement of x-ray diffraction data collected in the 2theta range of 15-110° with a step of 0.05° using Philips X'Pert Pro diffractometer (Cu Kα radiation) operated at 40 kV and 40 mA.
Transmission electron microscopy (TEM): Structure and powder morphology study were performed using transmission electron microscopy (TEM). The used instruments include a FEI Tecnai F20 operated at 200 kV and a Cs corrected JEOL JEM-2200FS TEM/STEM using an acceleration voltage of 200 kV. The nanoparticles were dispersed in ethanol and deposited on holey carbon TEM sample grids.
Differential scanning calorimetry (DSC): To determine the thermal properties of the powders as well as characteristic temperatures of the phase transformations occurring on heat treatment of the samples, DCS measurements were performed using Netzsch STA 449 F1 Jupiter TG/DSC. The samples were studied in the temperature range between 30 and 1100° C. with a heating rate of 10 K/min.
Solid state NMR: For NMR measurements a spectrometer operating at frequencies of 400 MHz (H1) was used (BrukerAvance III HD) and fitted with Bruker CP/MAS probe. Samples were placed into (ZrO2 rotors (4 mm diameter) and spun at 5 kHz (Si29)/9 kHz (C13). Field-induction decays (FIDs) were acquired with a relaxation delay of 5 s (C13 and Si29), spectral width of 32 kHz (Si29)/29.8 kHz (C13), and Fourier transformed with 100 Hz(Si)/50 Hz(C13) line broadening.
In a tubular reactor made of quartz (length to be heated outside of reactor 500 mm or 1000 mm, diameter 120 mm) precursor silane and the precursor olefinic hydrocarbon were injected through a nozzle located at the axis of the reactor (see table 1). Inert gas was injected in a tubular way around the nozzle of the tubular reactor. In a hot wall reactor, silane is injected into the reactor to obtain pure Si powders, whereas for the synthesis of silicon carbon composite particles as a powder a mixture of monosilane and ethylen as carbon precursor are used. The choice of appropriate gas-phase reaction conditions is guided by envisaged structure and microstructure design aimed at improving material performance in the LIB anode applications (s. table 1).
A lower reaction temperature (around or below 700° C.) favours the formation of the amorphous phase. Increasing temperature at and above 700° C. results in an increase of the crystalline Si fraction. At 850° C., fully crystalline Si is obtained at otherwise identical reaction conditions (Si-cr).
The collected silicon carbon particles were analysed by XRD, the silicon, carbon, hydrogen and oxygen contents were detected. Further, XRPD confirmed that the particles were produced as 100% amorphous particles at reaction temperatures of and below 690° C. The results are discussed below.
The following figures show in detail the chemical and physical properties of the silicon carbon particles as well as their electrical properties as material in anodes.
a:
13C-CP/MAS spectrum 9.091 pp/cm, 914.7 Hz/cm. No aromatic bonding is observed, the broad signal is purely due to the instrument background.
b:
29Si-CP/MAS spectrum 9.091 ppm/cm, 727.7 Hz/cm.
The chemical and physical properties of the silicon carbon particles as well as their electrochemical properties as material in anodes of the
The silicon carbon particles were analysed by Rietveld analysis of XRPD, the silicon, carbon, hydrogen and oxygen contents were determined by elemental analysis (Table 2). XRPD confirmed that the particles were produced as amorphous particles, with the amount of the amorphous phase from 99 wt.-% to 100 wt.-%.
29Si-CP/MAS signals and their correlation
29Si [ppm]
With 29Si (High performance decoupling) the observed signal is also broad but less intensive and shifted to a higher field (neg. chem. Shift). In 13C-NMR spectra (CP/MAS, CP: cross polarisation) the signal occurs at +14 ppm with a Gaussian profile verifying pure aliphatic carbon signals. The broad signals are also typical for amorphous systems. Therefore, the 29Si-NMR and 13C-NMR spectra both prove that the amorphous silicon carbon composite particles are free from crystalline phases and free from polymeric SiC. Crystalline SiC possesses three very sharp signals at −16 ppm, −20 ppm and 27 ppm in 29Si-NMR spectra as well as in 13C-NMR spectra a set of three sharp signals at 27 ppm, 20 ppm and 15 ppm.
The electrochemical feature of the c-Li15Si4 formation is a characteristic voltage plateau near 0.42 V in the voltage versus capacity curves or a corresponding peak in the differential capacity curves dQ/dV at about 0.42 V during dilithiation (
Both crystalline and amorphous silicon show this plateau/peak at around 0.42 V indicating the formation of c-Li15Si4 (
In electrodes containing the silicon carbon composite particles (synonym to amorphous silicon carbon composite particles), the formation of c-Li15Si4 is effectively suppressed, as confirmed by the absence of the characteristic voltage plateau in the voltage versus capacity curves and absent or only a weak peak in the differential capacity dQ/dV curves around 0.42 V (
The ratio of the area of the peak in the differential capacity corresponding to the formation of the crystalline c-Li15Si4, A[c-Li15Si4], to the area of the differential capacity (dQ/dV) in the range between 0.38 and 0.8 V, A[c-Li15Si4+a-Si″ ], for pure crystalline Si (from Alfa Aesar), amorphous silicon (Si-am) and amorphous silicon carbon composite particles is shown in
The first cycle Coulombic efficiency (CE) is retained at a high level of 89.2% in the amorphous silicon carbon composite powders; for comparison, the first cycle CE of Si-am is 90.2% and that of pure crystalline Si (from Alfa Aesar) is 77.2% (the corresponding lithiation/dilithiation curves are shown in
Remarkably, the suppression of the c-Li15Si4 phase formation is observed in silicon carbon composite particles at particle sizes around 200 nm and without the addition of FEC (
Thus, the design of silicon carbon composite particles represents the new concept for suppressing the c-Li15Si4 formation.
The reaction between silane and ethylene at 640° for 5 s leads to fully (100%) amorphous silicon carbon composite particles with a characteristic amorphous halo in the x-ray diffraction patterns independent of the silane and ethylene concentration in the gas mixture (
To study the distribution of carbon within the silicon carbon composite particles (Si/C nanoparticles), XPS spectra of carbon were collected from the amorphous Si (Si-am) and amorphous silicon carbon composite particles and depth profiles were measured using sputtering. Amorphous Si (Si-am) shows a low but constant background carbon concentration, which is commonly observed for samples that have been handled under environmental conditions. In contrast, a clear carbon concentration gradient is observed in the silicon carbon composite particles. The higher the carbon content in the silicon carbon composite particles determined by elemental analysis, the steeper is the depth-dependent carbon concentration gradient. The structure of the silicon carbon composite particles can thus be described as C-lean in the particle center and C-rich closer to the particle surface. This particular Si/C structure in silicon carbon composite particles of the invention is distinctly different from the conventional Si+C composites, where Si is coated by/embedded in a carbon layer.
DSC curves of silicon and silicon carbon composite powders show several distinct features (
The presence of carbon in the amorphous silicon carbon composite particles modifies the dealloying reaction and has a stabilization effect against silicon particle degradation, as qualitatively shown by scanning TEM (STEM) analysis (
The electrochemical capacity and the Coulombic efficiency of the amorphous silicon carbon composite particles were compared to those of the crystalline Si materials (Si-cr) (
The initial capacity is around 3500 mAh/g for pure crystalline silicon and about 3070 mAh/g in case of the amorphous silicon carbon composite particles. In both materials the capacity drops to about 2200 mAh/g after the second cycle. However, the Coulombic efficiency of amorphous silicon carbon composite particles is high in contrast to the pure crystalline silicon and reaches 85 and 92% for the first and second formation cycle, respectively, and levels at >99.5% in the subsequent cycles. We attribute the high Coulomb efficiency to reduced formation of a solid electrolyte interphase because of the carbon content, especially at the particle surface. The high initial capacity is due to the high overall content of silicon and indicates that the silicon is electrically well connected. The amorphous silicon carbon composite particles show a good performance during the first 120 cycles together with high specific capacity. After 120 cycles the capacity is at 1700 mA/g, whereas that for pure crystalline silicon is around 415 mAh/g.
Further modification of the synthesis of the silicon carbon composite particles at lower temperature in a well-defined reaction zone within a tubular inert gas stream, that surrounds the precursor silane and precursor olefinic hydrocarbon at a lower temperature of about 490° C. to 640° C. within a short time frame of 500 milliseconds to 20 seconds, preferred to 10 seconds results in silicon carbon particles of very uniform, spherical particles of a particle size of less than 250 nm, preferred 90 to 230 nm. The tubular inert gas stream is in particular a laminar inert gas stream. Due to the very specific reaction conditions, forming a reaction zone within the tubular inert gas stream of a temperature from 400° C. to 670° C., preferred from 430° C. to 500° C. where the gaseous stream comprising precursor silane and precursor olefinic hydrocarbon is injected into the reaction zone 100% amorphous silicon carbon particles comprising a carbon content decreasing from the area beneath the surface to the area of the centre of the particles can be obtained, which possess a high capacity of suppression of crystalline Li15Si4 phase formation.
| Number | Date | Country | Kind |
|---|---|---|---|
| 20194092.1 | Sep 2020 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2021/073465 | 8/25/2021 | WO |
