Method for operating a sensor element

• US 20030164023A1
• Filed: 03/27/2003
• Published: 09/04/2003
• Est. Priority Date: 05/04/2001
• Status: Abandoned Application

• Current Assignee: Robert Bosch GmbH
• Original Assignee: Robert Bosch GmbH
• Inventors: Schumann, Bernd, Thiemann-Handler, Sabine, Gruenwald, Werner
• Application Number:
  US10/311,945
• Publication Number:
  US 20030164023A1
• Time in Patent Office: Days
• US Class Current: 73/23.31
• CPC Class Codes: F02D 41/146 the characteristics being an NOx content or concentration
• CPC Class Codes: F02D 41/1476 Biasing of the sensor
• CPC Class Codes: G01N 27/419 Measuring voltages or currents with a combination of oxygen pumping cells and oxygen concentration cells

Abstract

A method for operating a sensor element (10) for determining at least one gas component of a gas, in particular of an exhaust gas of a combustion engine, is proposed. A measured gas space (35) that is in communication with the gas located outside the sensor element (10) is introduced into the sensor element (10). A first electrode (31) and a second electrode (32) are provided in the measured gas space (35) on an oxygen-ion-conducting solid electrolyte (21), and a third electrode (33) is provided outside the measured gas space (35). The second electrode (32) is electrically connected by the solid electrolyte (21) to the third electrode (33), so that oxygen is pumpable by application of a voltage between the second electrode (32) and the third electrode (33). A lower voltage is present between the second and the third electrode (32, 33) in a first time interval than outside the first time interval, so that under constant external conditions, the oxygen partial pressure in the measured gas space (35) is greater, at least when averaged over the durations, during a first time interval than during a second time interval.

Claims

1. A method for operating a sensor element (10) for determining at least one gas component of a gas, in particular of an exhaust gas of a combustion engine, comprising a measured gas space (35), introduced into the sensor element (10), that is in communication with the gas located outside the sensor element (10), a first electrode (31) and a second electrode (32) being provided in the measured gas space (35) on an oxygen-ion-conducting solid electrolyte (21), and a third electrode (33) being provided outside the measured gas space (35), and oxygen being pumpable by application of a voltage between the second electrode (32) and the third electrode (33), wherein at least one predefined first time interval is provided;

and a lower voltage is applied between the second and the third electrode (32, 33) in the first time interval than outside the first time interval.

2. The method as recited in claim 1, wherein the voltage present in the first time interval between the second and the third electrode (32, 33) is selected so that under constant external conditions, the oxygen partial pressure in the measured gas space (35) is greater during the first time interval than outside the first time interval.

3. The method as recited in claim 1 or 2, wherein a means for accumulation of the gas component to be analyzed is provided in the vicinity of the first electrode (31) and/or in the first electrode (31).

4. The method as recited in claim 3, wherein the means for accumulation of the gas component to be analyzed is a material accumulating the gas component.

5. The method as recited in claim 3 or 4, wherein the gas component to be determined is accumulated by chemical adsorption in the form of a chemical compound at least partially containing the gas component to be analyzed, or by physical adsorption.

6. The method as recited in at least one of the preceding claims, wherein during the first time interval, there exists at the first electrode (31) a potential at which the gas component to be analyzed is not decomposed or is only slight decomposed;

and during a predetermined second time interval located outside the first time interval, there exists at the first electrode (31) a potential by which the gas component to be analyzed is decomposed.

7. The method as recited in at least one of the preceding claims, wherein the voltage between the second (32) and the third electrode (33) is selected so that the gas component to be analyzed is not decomposed during the first time interval at the second electrode (32) and can arrive at the first electrode (31);

and during the second time interval, the molecular oxygen present at the first electrode (31) is negligible compared to the oxygen deriving from decomposition of the gas component to be analyzed.

8. The method as recited in at least one of the preceding claims, wherein during the second time interval, the pump voltage between the second and the third electrode (32, 33) is selected so that limit current conditions exist.

9. The method as recited in at least one of claims 3 through 8, wherein within the second time interval, at least the majority of the gas component to be analyzed that has accumulated in the first electrode (31) or in the vicinity of the first electrode (31) is decomposed, the oxygen released upon decomposition being pumped off by the first electrode (31) and the concentration of the gas component to be analyzed being ascertained on the basis of the pump current.

10. The method as recited in claim 8 or 9, wherein during the second time interval, the potential at the first electrode bringing about decomposition of the gas component to be analyzed is not applied until limit current conditions exist.

11. The method as recited in at least one of the preceding claims, wherein the method steps occurring in the first and the second time interval are utilized in recurring time intervals.

12. The method as recited in at least one of the preceding claims, wherein the oxygen partial pressure during the second time interval is at least intermittently less than 10⁻

14 bar.

13. The method as recited in at least one of the preceding claims, wherein in the first time interval a voltage in the range from 0.1 to 0.25 V, preferably 0.2 V, is present between the second and the third electrode (32, 33), and a voltage in the range from 0 to 0.1 V, preferably 0 V, is present between the first and the third electrode (31, 33).

14. The method as recited in at least one of the preceding claims, wherein in the second time interval, at least while limit current conditions exist, a voltage of 1.2 to 1.5 V, preferably 1.4 V, is present between the first and the third electrode (31, 33).

15. The method as recited in at least one of the preceding claims, wherein in the second time interval, at least intermittently and in particular in order to establish limit current conditions, a voltage of 0.8 to 1.5 V, preferably 1.4 V, is present between the second electrode (32) and the third electrode (33).

16. The method as recited in at least one of the preceding claims, wherein the partial pressure of the gas component to be analyzed is ascertained by integrating the pump current flowing through the first electrode (31) during the second time interval.

17. The method as recited in at least one of claims 1 through 15, wherein the partial pressure of the gas component to be analyzed is ascertained by way of the maximum pump current flowing through the first electrode (31) during the second time interval.

18. The method as recited in at least one of the preceding claims, wherein the first time interval lasts 0.2 to 20 seconds, preferably 2 seconds, and the second time interval lasts 0.1 to 2 seconds, preferably 0.5 second.

19. The method as recited in at least one of the preceding claims, wherein the second electrode (32) is in contact with a region (36) of the measured gas space (35) located between the diffusion resistance (34) and the first electrode (31).

20. The method as recited in at least one of the preceding claims, wherein the third electrode (33) is in contact with the exhaust gas located outside the sensor element (10), or is in contact with a reference gas.

21. The method as recited in at least one of the preceding claims, wherein a further electrode that is in contact with a reference gas is provided.

22. The method as recited in at least one of the preceding claims, wherein the first electrode (31) and the third electrode (33), and the solid electrolyte positioned between the first and third electrodes (31, 33), constitute a pump cell.

23. The method as recited in claim 21, wherein the first electrode (31) and the further electrode, and the solid electrolyte positioned between the first electrode (31) and the further electrode, constitute a pump cell.

24. The method as recited in at least one of the preceding claims, wherein the gas component to be analyzed is an oxygen compound, for example NO_x and/or CO₂ and/or SO₂.

25. The method as recited in at least one of the preceding claims, wherein the first electrode (31) contains an oxide of the fifth subgroup, in particular V₂O₅, or a mixture of oxides of the fifth subgroup;

and the solid electrolyte (21) contains ZrO₂ doped with Y₂O₃.

26. The method as recited in claim 25, wherein the length of the first time interval is 0.5 to 3 seconds, preferably 1 second, and the length of the second time interval is 0.1 to 1 second, preferably 0.5 second.

27. The method as recited in at least one of the preceding claims, wherein the first electrode (31) contains barium and/or cerium and/or magnesium in the form of nitrates, oxides, or sulfates.

28. The method as recited in claim 27, wherein the length of the first time interval is 3 to 10 seconds, preferably 5 seconds, and the length of the second time interval is 0.1 to 2 seconds, preferably 0.5 second.

29. The method as recited in at least one of the preceding claims, wherein a means for temperature regulation is provided;

the means for temperature regulation encompasses a heating apparatus (41); and

during the first time interval, there exists at the first electrode (31) a lower temperature than during the second time interval.

30. The method as recited in claim 29, wherein at the first electrode, during the first time interval a temperature of 400 to 600 degrees Celsius, preferably 500 degrees Celsius, is established, and during the second time interval a temperature of 600 to 900 degrees Celsius, preferably 780 to 850 degrees Celsius, is established.