US 4,576,697 AGrant
Synthesis of Carbon-Containing Intercalatable Layered Transition Metal Chalocogenides
Issue Date:1986-03-18
•4 Claims
Abstract
Carbon-containing intercalatable layered or lamellar transition metal chalcogenides having the general formula M.sub.n X.sub.2 C where M is a transition metal selected from the group consisting of Ti, V, Cr, Fe, Zr and Ta; X is sulfur; and n is 1-2; such as TiS.sub.2 C or Ti.sub.2 S.sub.2 C, usable as cathode active materials in alkali metal nonaqueous secondary batteries that can undergo alkali metal intercalation, are synthesized by ion implanting a substrate of the transition metal with sulfur and then carbon at implantation energies in the range of about 150-200 kiloelectron volts and at saturation dosages of 1.times.10.sup.12 to 1.times.10.sup.19 sulfur and carbon atoms/cm.sup.2.
Metadata
Assignee
- Combustion Engineering, Inc.
Inventor
- David N. Palmer
Application Information
Application Number:US 4871480
Filing Date:1983-04-21
Priority Date:1983-04-21
Art Unit:112
Classifications
IPC:
C23C 1500
Field of Search:
429204250218192 C;192 N;298194429.3
Patent Drawings
This patent does not have any drawings.
Description
The present invention relates to the synthesis of carbon-containing intercalatable layered or lamellar transition metal chalcogenides.
Layered or lamellar transition metal chalcogenides are well known to be useful as the cathode active material for alkali metal nonaqueous secondary batteries which operate upon the principle of intercalation. Typical examples of such materials and such batteries are those disclosed, for example, in U.S. Pat. Nos. 4,009,052; 4,049,879; 4,049,887; 4,198,476; 4,206,276; 4,207,245; 4,228,226; and 4,233,377.
The object of the present invention is to provide alternative cathode active materials having improved or greater conductivity and improved or reduced cell internal resistance and a process for their preparation.
In accordance with the present invention there is provided a process for the synthesis of carbon-containing intercalatable layered transition metal chalcogenides which comprises:
(a) forming a compound having the general formula M.sub.n X.sub.2 C where M is a transition metal selected from the group consisting of Ti, V, Cr, Fe, Zr and Ta; X is sulfur; and n is 1-2; by the steps of:
(a.sub.1) ion implanting sulfur at an implantation energy in the range of about 150-200 kiloelectron volts and at a saturation dosage of 1.times.10.sup.12 to 1.times.10.sup.19 sulfur atoms/ cm.sup.2 into a substrate of the transition metal; and
(a.sub.2) then ion implanting carbon at an implantation energy in the range of about 150-200 kilo electron volts and at a saturation dosage of 1.times.10.sup.12 to 1.times.10.sup.19 carbon atoms/cm.sup.2 into the sulfur-implanted substrate of the transition metal.
In a preferred embodiment of the process of the present invention, the ion-implanted substrate of the transition metal is annealed under a vacuum of from about 1.times.10.sup.-4 torr to about 1.times.10.sup.-6 torr at a temperature of from about 200.degree. C. to about 500.degree. C. for about 24 hours to about 48 hours. The annealing can be performed after each ion-implanting step or at the end of the ion-implanting steps.
The transition metals usable in the process of the present invention, as noted above, are titanium, vanadium, chromium, iron, zirconium and tantalum. The preferred transition metal is titanium.
The substrate of the transition metal can be, for example, a foam or a thin film, e.g., 1-10 .mu.m thickness.
The chalcogen usable in the process of the present invention, as also noted above, is sulfur.
Ion implantation in the process of the present invention can be achieved by using a conventional ion implantation apparatus wherein a source of the sulfur or carbon to be implanted is first ionized and then accelerated in an electric field to implantation energies which usually lie in the range of about 150-200 kiloelectron volts (keV) in a moderately hard vacuum (r 1 m Pa). Prior to impact on the transition metal substrate target, a particular ion species is discriminated by a magnetic field accelermeter.
The ion-implanted compounds MX.sub.2 C or M.sub.2 X.sub.2 C, such as TiS.sub.2 C or Ti.sub.2 S.sub.2 C, of the present invention can be used as cathode active materials in alkali metal nonaqueous secondary batteries that can undergo alkali metal intercalation. They have improved or greater conductivity than transition metal chalcogenides due to their carbon content. The substrate of the transition metal can serve as the current collector when the transition metal is a conductive metal. The products also have reduced cell internal resistance due to their carbon content, e.g., 0.09 ohms for a Ti.sub.2 S.sub.2 C cathode versus 0.3 ohms for a TiS.sub.2 cathode in comparable secondary cells.
The products of the present invention are not only useful as cathode active materials for nonaqueous intercalatable secondary batteries, but are also useful as catalysts and as photoactive materials. They can also be employed in the production of fuel cells, photogalvanic devices and photovoltaic devices.
The processes and products of the present invention will be further illustrated by the following representative examples thereof.
EXAMPLES
Pretreatment for all Foam Substrates
Specimens of Ti, V, Cr, Fe, Zr and Ta foams were ultrasonically cleaned in a detergent/water mixture at 25.degree. C. followed by a rinse and soak in acetone and cyclohexane. After solvent soak the specimens were vacuum dried at 1.times.10.sup.-4 torr for 2 hours at 25.degree. C.
Specimens of foams with the exception of those transition metals which hydride readily (e.g. Zr) were placed in a quartz reactor and evacuated to 1.times.10.sup.-6 torr for 30 minutes. At the 1.times.10.sup.-6 torr condition the reactor containing the foam was back filled with 90% He and 10% H.sub.2 to 1 atmosphere. The reactor was sealed to the environment and heated at a rate of 10.degree. C./minute to 500.degree. C. The specimens were held isothermally for 24 hours at 500.degree. C. and then slowly allowed to cool to 25.degree. C. The foams were removed from the quartz reactor in a controlled argon environment.
Ion Implantation of Foam Substrates
Depth dose studies were completed to find appropriate doses and energies for saturation range and straggling values were calculated and sputter yields were found for chalcogen (sulfur) implanted. All foam specimens were placed in a specially designed holder to continuously cool the specimen during implantation. If the foams are not properly cooled, melting or degradation of the foam structure can occur. Prior to implanation it was found that inert gas sputtering of the surface was not necessary, because >800 .ANG. of the foam fibril surfaces were removed by the impinging chalcogen (sulfur) ion stream prior to actual implant.
Chalcogen (sulfur) implanting was completed before carbon implantation. Dosages and implantation energy and depth are listed in Table 1 below.
The surfaces implanted with chalcogen (sulfur) were examined by scanning electron microscope (SEM) and by x-ray fluorescence analysis. X-ray analysis verified the following atom ratios on the implanted surfaces set forth in Table 2 below confirming atomic ratio values.
Table 2
Chalcogen (Sulfur) to Transition Metal Atom Ratio
S/Ti=2.0:1.0 (TiS.sub.2.0)
S/V=2.0:1.0 (VS.sub.2.0)
S/Cr=1.9:1.0 (CrS.sub.1.9)
S/Fe=2.0:1.0 (FeS.sub.2.0)
S/Zr=2.0:1.0 (ZrS.sub.2.0)
S/Ta=1.6:1.0 (TaS.sub.1.6)
Specimen weights of the foams prior to implantation are given in Table 3 below.
Table 3
Specimen Weights (grams) of Foam Prior to Implantation
(0.75".times.0.75" on edge by 0.25" thick)
Ti=0.3513
V=0.3735
Cr=0.3814
Fe=0.4096
Zr=0.4795
Ta=1.3271
As noted above, after implantation with the chalcogen (sulfur) carbon was implanted at 0.9.times.10.sup.18 atoms/cm.sup.2 and at 2.0.times.10.sup.18 atoms/cm.sup.2 at 150 KeV in all cases. Carbon analysis revealed the following data in Table 4 below.
All S as well as S+C implanted foams were annealed at 1.times.10.sup.-6 torr for 32 hours at 300.degree. C.
After implantation with S+C a Ti.sub.2 S.sub.2 C[(Ti+S)+C] foam was configured in a standard electrochemical cell configuration and tested for secondary battery characteristics. The conditions for the cell evaluations and cell results are listed in Table 5 below.
Data contained in Table 5 above indicate the following:
Based on the energy density data shown in Table 5, ion implanted TiS.sub.2 followed by a further carbon implant yielded a compound equivalent to Ti.sub.2 S.sub.2 C and not TiS.sub.2 +TiC. The Ti.sub.2 S.sub.2 C specimen displayed adequate secondary cell characteristics.
Claims
What is claimed is:
1. A process for treating the surface of a transition metal substrate to form into the surface a carbon-containing intercalatable layered transition metal chalcogenide having the general formula M.sub.n X.sub.2 C where M is a transition metal selected from the group consisting of Ti, V, Cr, Fe, Zr and Ta; X is sulfur; and n is 1-2; which comprises: ion implanting sulfur at an implantation energy in the range of about 150-200 kiloelectron volts and at a saturation dosage of about 10.sup.18 sulfur atoms/cm.sup.2 into the surface of the transition metal substrate to a depth of about 1000-2200 .ANG.; and then ion implanting carbon at an implantation energy in the range of about 150-200 kiloelectron volts and at a saturation dosage of about 10.sup.18 carbon atoms/cm.sup.2 into the surface of the sulfur-implanted transition metal substrate to a depth of about 1000-2200 .ANG..
2. A process according to claim 1 wherein M is Ti, X is S and n is 1.
3. A process according to claim 1 wherein M is Ti, X is S and n is 2.
4. A process according to claim 1 wherein the ion-implanted transition metal substrate is annealed under a vacuum of from about 1.times.10.sup.-4 torr to about 1.times.10.sup.-6 torr at a temperature of from about 200.degree. C. to about 500.degree. C. for from about 24 hours to about 48 hours.
Patent Citations (11)
| Patent | Date | Inventor | Cited By |
|---|---|---|---|
| US3806380 | 1974-04-01 | Kitada et al. | |
| US4089990 | 1978-05-01 | Walker | |
| US4278890 | 1981-07-01 | Gruen et al. | |
| US4281029 | 1981-07-01 | Takagi | |
| US4281030 | 1981-07-01 | Silfast | |
| US4299892 | 1981-11-01 | Dines | |
| US4366215 | 1982-12-01 | Coetzer | |
| US4390604 | 1983-06-01 | Evans et al. | |
| US4395467 | 1983-07-01 | Vossen et al. | |
| US4404233 | 1983-09-01 | Ikeda et al. | |
| US4440108 | 1984-04-01 | Little et al. |
Non-Patent Literature (8)
- Brec et al. Inorg. Chem. 16 (1977), pp. 660-665.
- Beckmann et al. Monat. Fur Chem. 101 (1970), pp. 945-955.
- Alberts et al. Chem. Abst. 98 (1983) #112023.
- Sartwell et al. Chem. Abst. 93 (1980) #171740.
- Belyi et al. Chem. Abst. 90 (1979) #172838.
- Kirk-Othmer Encyclopedia of Chemical Technology, vol. 13, 1981 (John Wiley & Sons) New York, N.Y., pp. 706-719.
- Murphy et al., "Vanadium Disulfide: Metal Substitution and Lithium Intercalation", J. of Solid State Chemistry, 29, 339-343 (1979).
- Whittingham, "Chemistry of Intercalation Compounds: Metal Guests in Chalcogenide Hosts", Prog. Solid State Chem., vol. 12, pp. 4-99 (1978).