Detection of P(O/sub 2/)-changes within a few milliseconds using sputtered strontium titanate

J. Gerblinger, H. Meixner
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引用次数: 4

Abstract

Between 700 and 1100 degrees C the electrical conductivity of undoped SrTiO/sub 3/ changes from p-type to n-type as P(O/sub 2/) decreases from 1 to 10/sup -15/ bar. For bulk materials the response time t/sub R90/ of the oxygen sensor upon changes of the oxygen partial pressure in the surrounding atmosphere decreases quadratically with the thickness of the sensitive material. Thick samples show a diffusion-controlled dependence of their response time. Thin films of about 1 mu m exhibit response times in the range of a few milliseconds at temperatures of 1000 degrees C. Comparing the activation energy with values given in the literature for bulk materials shows that for great changes of the oxygen partial pressure the response time of the sputtered films is controlled by the diffusion of the oxygen vacancies in the sensitive material. The lower activation energies for oxygen diffusion in and out of the sensitive material at above 800 degrees C indicate an effect where the response time of the oxygen sensor is dominated by the reaction of the oxygen molecules on the surface of the sensitive material.<>
利用溅射钛酸锶在几毫秒内检测P(O/sub 2/)-变化
在700 ~ 1100℃之间,当P(O/sub 2/)从1降到10/sup -15/ bar时,未掺杂的SrTiO/sub 3/的电导率由P型变为n型。对于块状材料,氧传感器对周围大气中氧分压变化的响应时间t/sub R90/随敏感材料厚度呈二次曲线递减。厚样品显示其响应时间的扩散控制依赖性。在1000℃的温度下,1 μ m左右的薄膜的响应时间在几毫秒的范围内,将活化能与文献中给出的块状材料的活化能进行比较表明,当氧分压发生较大变化时,溅射薄膜的响应时间受敏感材料中氧空位的扩散控制。在800℃以上,氧气在敏感材料内外扩散的活化能较低,表明氧传感器的响应时间主要由敏感材料表面氧分子的反应决定。
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