Dielectric ceramic materials and associated methods
View Patent ↗Ceramic dielectric materials that can be utilized as electronic components, such as dielectric resonators are disclosed. The material can have a formula Ba 12 M′ (28+a/3) Ti (54−a-b) M″ a Ge b O 162 , wherein M′ is at least one rare earth element selected from the group consisting of lanthanum, neodymium, samarium, gadolinium, and yttrium, M″ is at least one element selected from the group consisting of aluminum, gallium, chromium, indium, scandium, and ytterbium, 0≦a≦6, and 0≦b≦3. The ceramic dielectric material can also have a formula Ba 12 M′ (28+2x/3) Ti (54−x−y) M′″ x Ge y O 162 , wherein M′ is at least one rare earth element selected from the group consisting of lanthanum, neodymium, samarium, gadolinium, and yttrium, M′″ is at least one metal selected from the group consisting of magnesium, zinc, nickel, and cobalt, 0≦x≦3, and 0≦y≦3. One or more aspects of the present invention pertain to methods of fabricating a dielectric component. Methods of synthesizing the disclosed ceramic dielectric materials are also disclosed.
1. A dielectric composition comprising a material with a formula
Ba 12 M′ (28+a/3) Ti (54−a-b) M″ a Ge b O 162
where M′ is at least one rare earth element selected from the group consisting of lanthanum, neodymium, samarium, gadolinium, and yttrium, M″ is at least one element selected from the group consisting of aluminum, gallium, chromium, indium, scandium, and ytterbium, 0≦a≦6, and 0≦b≦3.
2. The dielectric composition of claim 1 wherein b is about 3.
3. The dielectric composition of claim 1 wherein b is about 0.1.
4. The dielectric composition of claim 1 further comprising a material selected from the group consisting of BaTi 4 O 9 , Ba 2 Ti 9 O 20 , TiO 2 , and Nd 2 Ti 2 O 7 .
5. The dielectric composition of claim 1 wherein M′ is at least one of neodymium, samarium, and yttrium, and M″ is one of aluminum and gallium.
6. The dielectric composition of claim 5 wherein M′ is neodymium and samarium, M″ is aluminum, and b is about 0.3.
7. A dielectric composition comprising a material with a formula
Ba 12 M′ (28+2x/3) Ti (54−x-y) M′″ x Ge y O 162
where M′ is at least one rare earth element selected from the group consisting of lanthanum, neodymium, samarium, gadolinium, and yttrium, M′″ is at least one metal selected from the group consisting of magnesium, zinc, nickel, and cobalt, 0≦x≦3, and 0≦y≦3.
8. The dielectric composition of claim 7 wherein y is about 3.
9. The dielectric composition of claim 7 wherein y is about 0.1.
10. The dielectric composition of claim 7 further comprising a material selected from the group consisting of BaTi 4 O 9 , Ba 2 Ti 9 O 20 , TiO 2 , and Nd 2 Ti 2 O 7 .
11. A method of fabricating a dielectric component comprising:
blending a precursor mixture of compounds including a barium source, a titanium source, at least one rare earth element source, and at least one metal source;
promoting reaction of the compounds to from a green material;
comminuting the green material into green dielectric particles having a maximum target diameter;
forming a green dielectric member from the green dielectric particles; and
sintering the green dielectric member to produce the dielectric component, the dielectric component including a dielectric material having a formula of
Ba 12 M′ (28+a/3) Ti (54−a-b) M″ a Ge b O 162
with 0≦a≦6 and 0≦b≦3
or
Ba 12 M′ (28+2x/3) Ti (54−x-y) M′″ x Ge y O 162 ,
with 0≦x≦3 and 0≦y≦3
where M′ is at least one rare earth element selected from the group consisting of lanthanum, neodymium, samarium, gadolinium, and yttrium, M″ is at least one element selected from aluminum, gallium, chromium, indium, scandium, and ytterbium, and M′″ is at least one metal selected from the group consisting of magnesium, zinc, cobalt, and nickel.
12. The method of claim 11 further comprising adding a binder to the green dielectric particles prior to forming the green dielectric member from the green dielectric particles.
13. The method of claim 12 wherein promoting reaction of the compounds comprises:
heating the precursor mixture at a first heating rate of less than or equal to about 300° C. per hour to a reaction temperature that is in a range of about 1,000° C. to about 1,400° C.;
exposing the precursor mixture to the reaction temperature for a period in a range of between about four hours and about twelve hours to form a first product; and
cooling the first product to about room temperature at a first cooling rate in a range of about 100° C. per hour to about 600° C. per hour to form the green material.
14. The method of claim 13 wherein sintering the green dielectric member to produce the dielectric component comprises:
heating the green dielectric member at a second heating rate of less than or equal to about 200° C. per hour to a sintering temperature that is in a range of about 1,300° C. to about 1,500° C.;
exposing the green dielectric member to the sintering temperature for a sintering period in a range of between about two hours and about eight hours to form a sintered dielectric product; and
cooling the sintered dielectric product to about room temperature at a second cooling rate in a range of 50° C. per hour to about 200° C. per hour to produce the dielectric component.
15. The method of claim 14 wherein forming the green dielectric particles into the dielectric member comprises:
adding a binder to the green dielectric particles; and
shaping the green dielectric particles into the dielectric member to a green density that is at least about 50% of the theoretical density of the dielectric material.
16. The method of claim 15 further comprising machining the dielectric component into a dielectric resonator having at least one target physical characteristic.
17. The method of claim 11 wherein the maximum target diameter is less than or equal to about 10 microns.
18. The method of claim 11 further comprising providing the precursor mixture of compounds in target relative stoichiometric amounts to produce the dielectric material having M′ as at least one of neodymium and samarium, and M″ as aluminum.