Process for producing a solid electrolyte layer on a substrate, in a fuel cell, and in a sensor

1. A method for producing a solid electrolyte layer, of a fully stabilized zirconium oxide layer on a substrate, which comprises:

applying a zirconium oxide starting material to the substrate together with a sintering additive as a green layer, the sintering additive being boron nitride;

forming a liquid phase of the sintering additive by subsequently heating the sintering additive; and

densifying the green layer with a liquid-phase sintering operation at a reduced sintering temperature as compared to a sintering temperature required without the sintering additive.

2. The method according to claim 1 , which further comprises selecting process parameters, including at least one of heating rate, sintering temperature, and holding time, to cause the liquid phase to still be present when the reduced sintering temperature is reached and to cause the

densified layer to be substantially free of sintering additive.

3. The method according to claim 1 , which further comprises setting a maximum sintering temperature of less than 1,400° C.

4. The method according to claim 1 , which further comprises setting a maximum sintering temperature of less than 1,300° C.

5. The method according to claim 1 , which further comprises setting a maximum sintering temperature to a value between approximately 1,100° C. and approximately 1,300° C.

6. The method according to claim 1 , which further comprises setting a heating rate of approximately 4 to approximately 7 K/min.

7. The method according to claim 1 , which further comprises applying to the substrate:

a green layer including the sintering additive; and

a zirconium oxide layer that does not include the sintering additive.

8. The method according to claim 1 , which further comprises forming a gastight zirconium oxide layer with a porosity of less than 5% by volume.

9. The method according to claim 8 , which further comprises forming the gastight layer with a layer thickness of between approximately 5 and approximately 300 μm.

10. The method according to claim 8 , which further comprises forming the gastight layer with an air permeability of ≦10 −3 mbar·l/s·cm 2 .

11. The method according to claim 8 , which further comprises forming the gastight layer with an air permeability of approximately 2·10 −4 mbar·l/s·cm 2 .

12. The method according to claim 8 , which further comprises:

providing a fuel cell having an electrode; and

coating the electrode with the zirconium oxide layer as a solid electrolyte layer.

13. The method according to claim 8 , which further comprises:

providing a gas sensor; and

applying the zirconium oxide layer to the gas sensor as a solid electrolyte layer.

14. A method for producing a solid electrolyte layer, of a fully stabilized zirconium oxide layer on a substrate, which comprises:

applying to the substrate a green layer including a sintering additive and a zirconium oxide layer that does not include the sintering additive;

forming a liquid phase of the sintering additive by subsequently heating the sintering additive; and

densifying the green layer to form a densified layer with a liquid-phase sintering operation at a reduced sintering temperature compared to a sintering temperature required without the sintering additive, in which operation process parameters, including at least one of heating rate, sintering temperature, and holding time, are selected to cause the liquid phase to still be present when the reduced sintering temperature is reached and to cause the densified layer to be substantially free of the sintering additive, the reduced sintering temperature being higher than a sintering temperature required for a sintering operation with sintering additive.

15. The method according to claim 14 , which further comprises setting a maximum sintering temperature of less than 1,400° C.

16. The method according to claim 14 , which further comprises setting a maximum sintering temperature of less than 1,300° C.

17. The method according to claim 14 , which further comprises setting a maximum sintering temperature to a value between approximately 1,100° C. and approximately 1,300° C.

18. The method according to claim 14 , which further comprises setting a heating rate of approximately 4 to approximately 7 K/min.

19. The method according to claim 14 , which further comprises forming a gastight zirconium oxide layer with a porosity of less than 5% by volume.

20. The method according to claim 19 , which further comprises forming the gastight layer with a layer thickness of between approximately 5 and approximately 100 μm.

21. The method according to claim 19 , which further comprises forming the gastight layer with an air permeability of ≦10 −3 mbar·l/s·cm 2 .

22. The method according to claim 19 , which further comprises forming the gastight layer with an air permeability of approximately 2·10 −4 mbar·l/s·cm 2 .

23. The method according to claim 19 , which further comprises:

providing a fuel cell having an electrode; and

coating the electrode with the zirconium oxide layer as a solid electrolyte layer.

24. The method according to claim 19 , which further comprises:

providing a gas sensor; and

applying the zirconium oxide layer to the gas sensor as a solid electrolyte layer.

25. A method for producing a solid electrolyte layer, of a fully stabilized zirconium oxide layer on a substrate, which comprises:

applying to the substrate:

a zirconium oxide starting material as a green layer with the sintering additive; and

a zirconium oxide starting material as a green layer without the sintering additive;

forming a liquid phase of the sintering additive by subsequently heating the sintering additive; and

densifying the green layer with a liquid-phase sintering operation at a reduced sintering temperature compared to a sintering temperature required without the sintering additive.

26. The method according to claim 25 , which further comprises selecting process parameters, including at least one of heating rate, sintering temperature, and holding time, to cause the liquid phase to still be present when the reduced sintering temperature is reached and to cause the densified layer to be substantially free of sintering additive.

27. The method according to claim 25 , which further comprises setting a maximum sintering temperature of less than 1,400° C.

28. The method according to claim 25 , which further comprises setting a maximum sintering temperature of less than 1,300° C.

29. The method according to claim 25 , which further comprises setting a maximum sintering temperature to a value between approximately 1,100° C. and approximately 1,300° C.

30. The method according to claim 25 , which further comprises setting a heating rate of approximately 4 to approximately 7 K/min.

31. The method according to claim 25 , which further comprises applying to the substrate:

a green layer including the sintering additive; and

a zirconium oxide layer that does not include the sintering additive.

32. The method according to claim 25 , which further comprises forming a gastight zirconium oxide layer with a porosity of less than 5% by volume.

33. The method according to claim 32 , which further comprises forming the gastight layer with a layer thickness of between approximately 5 and approximately 100 μm.

34. The method according to claim 32 , which further comprises forming the gastight layer with an air permeability of ≦10 −3 mbar·l/s·cm 2 .

35. The method according to claim 32 , which further comprises forming the gastight layer with an air permeability of approximately 2·10 −4 mbar·l/s·cm 2 .

36. The method according to claim 32 , which further comprises:

providing a fuel cell having an electrode; and

coating the electrode with the zirconium oxide layer as a solid electrolyte layer.

37. The method according to claim 32 , which further comprises:

providing a gas sensor; and

applying the zirconium oxide layer to the gas sensor as a solid electrolyte layer.