JPH04115153A - Oxygen gas sensor - Google Patents

Oxygen gas sensor

Info

Publication number
JPH04115153A
JPH04115153A JP2236241A JP23624190A JPH04115153A JP H04115153 A JPH04115153 A JP H04115153A JP 2236241 A JP2236241 A JP 2236241A JP 23624190 A JP23624190 A JP 23624190A JP H04115153 A JPH04115153 A JP H04115153A
Authority
JP
Japan
Prior art keywords
oxygen gas
electrode
gas
solid electrolyte
oxygen
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2236241A
Other languages
Japanese (ja)
Other versions
JP2946697B2 (en
Inventor
Shigeki Kuwata
桑田 茂樹
Norio Miura
則雄 三浦
Noboru Yamazoe
昇 山添
Masami Ando
正美 安藤
Chiaki Nakayama
千秋 中山
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Toto Ltd
Original Assignee
Toto Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Toto Ltd filed Critical Toto Ltd
Priority to JP2236241A priority Critical patent/JP2946697B2/en
Publication of JPH04115153A publication Critical patent/JPH04115153A/en
Application granted granted Critical
Publication of JP2946697B2 publication Critical patent/JP2946697B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Measuring Oxygen Concentration In Cells (AREA)

Abstract

PURPOSE:To achieve a simplified construction and a smaller size by forming an opposed pole comprising an inert material to an oxygen gas on the surface of a solid electrolyte, a part exposed to a gas to be inspected containing the oxygen gas being separated from a detection electrode. CONSTITUTION:A detection electrode 3 and an opposed pole 4 are formed on one side of a solid electrolyte 2 being separated from each other and a Pt wire 5 is connected to the electrodes 3 and 4. The electrolyte 2 employs a single crystal of LaF3, the electrode 3 employs Pt and the opposed pole 4 employs a material inert to an oxygen gas near a normal temperature, for example, Au, Ag or Sn. With such an arrangement, an electromotive force increases in proportion to an oxygen partial pressure in the detection gas. Thus, a product thus obtained can be used as oxygen gas sensor. The opposed pole 4 is formed by evaporation or sputtering of Au, Ag or Sn and the electrode 3 is formed by making a thin film of Pt on the surface of the LaF3 by evaporation or sputtering.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は酸素ガスを検知するセンサに関する。[Detailed description of the invention] (Industrial application field) The present invention relates to a sensor for detecting oxygen gas.

(従来の技術) 酸素ガスを検知するセンサとして、第4図に示すような
積層型センサが知られている。この積層型センサは固体
電解質11の一面側にエポキシ樹脂12によってガラス
チューブ13の一端を当て、このガラスチューブ13に
て固体電解質11の一面側に形成した参照電極14を囲
んで被検ガス雰囲気から遮断し、更に固体電解質11の
他面側に検知電極15を形成し、これら参照電極14及
び検知電極15にpt線16を接続している。
(Prior Art) A laminated sensor as shown in FIG. 4 is known as a sensor for detecting oxygen gas. In this stacked sensor, one end of a glass tube 13 is applied to one side of a solid electrolyte 11 using an epoxy resin 12, and the glass tube 13 surrounds a reference electrode 14 formed on one side of the solid electrolyte 11 to prevent the gas from being detected from the atmosphere. Further, a sensing electrode 15 is formed on the other side of the solid electrolyte 11, and a PT wire 16 is connected to the reference electrode 14 and the sensing electrode 15.

(発明が解決しようとする課題) 上述した積層型センサにあっては、参照電極が被検ガス
から遮断される構造としているため、参照電極へ参照ガ
スを導入するか、固体参照電極を用いなければならず、
センサ自体の構造の簡略化の妨げになっている。
(Problems to be Solved by the Invention) In the above-mentioned stacked sensor, the reference electrode has a structure that is shielded from the sample gas, so it is necessary to introduce a reference gas into the reference electrode or use a solid reference electrode. Not necessarily,
This hinders the simplification of the structure of the sensor itself.

(課題を解決するための手段) 上記課題を解決すべく本発明は、固体電解質の表面で且
つ酸素ガスを含んだ被検ガスに晒される部分に酸素ガス
に対して不活性な材料からなる対極を検知電極と離して
形成した。
(Means for Solving the Problems) In order to solve the above problems, the present invention provides a counter electrode made of a material inert to oxygen gas on the surface of a solid electrolyte and at a portion exposed to a test gas containing oxygen gas. was formed separately from the sensing electrode.

(作用) AuXAg又はSn等の酸素ガスに対して不活性な材料
で対極を構成すれば、検知ガス中の酸素分圧に比例して
起電力が増加する。
(Function) If the counter electrode is made of a material that is inert to oxygen gas, such as AuXAg or Sn, the electromotive force will increase in proportion to the oxygen partial pressure in the detection gas.

(実施例) 以下に本発明の実施例を添付図面に基いて説明する。(Example) Embodiments of the present invention will be described below with reference to the accompanying drawings.

第1図は本発明に係る酸素ガスセンサとしての平面型セ
ンサの断面図であり、平面型センサ1は固体電解質2の
一面側に検知電極3及び対極4を離間して形成し、これ
ら検知電極3及び対極4にPt線5.5を接続している
FIG. 1 is a sectional view of a planar sensor as an oxygen gas sensor according to the present invention. The planar sensor 1 has a sensing electrode 3 and a counter electrode 4 spaced apart from each other on one side of a solid electrolyte 2. A Pt wire 5.5 is connected to the counter electrode 4.

ここで、固体電解質2としてはLaF3(フッ化ランタ
ン)の単結晶を用い、検知電極3としてはPt(プラチ
ナ)を用い、対極4としてはAu(金)、Ag(銀)又
はSn(スズ)のように常温付近で酸素ガスに対して不
活性な材料を用いる。
Here, a single crystal of LaF3 (lanthanum fluoride) is used as the solid electrolyte 2, Pt (platinum) is used as the detection electrode 3, and Au (gold), Ag (silver) or Sn (tin) is used as the counter electrode 4. Use a material that is inert to oxygen gas at around room temperature, such as.

第2図は従来の積層型センサの検知電極をPtとAuで
構成した場合の100℃と25℃における酸素分圧(対
数)と起電力との関係を示すグラフであり、このグラフ
から明らかなように、100℃では検知電極としてPt
、Auのいずれを用いても検知ガス中の酸素分圧に比例
して起電力が増加するが、25℃においてはAuを検知
電極の材料とした場合には酸素分圧変化に対する起電力
変化は殆んと見られず、Auは常温付近では酸素ガスに
対して不活性といえる。従って、常温付近であればAu
を検知電極ではなく対極として用いればこの酸素ガスセ
ンサとしては対極を被検ガスから遮断する必要はなくな
る。
Figure 2 is a graph showing the relationship between oxygen partial pressure (logarithm) and electromotive force at 100°C and 25°C when the detection electrode of a conventional multilayer sensor is composed of Pt and Au. As shown, at 100°C, Pt is used as the sensing electrode.
or Au, the electromotive force increases in proportion to the oxygen partial pressure in the sensing gas, but at 25°C, when Au is used as the material for the sensing electrode, the electromotive force changes with respect to the oxygen partial pressure change. It is hardly seen, and it can be said that Au is inert to oxygen gas at around room temperature. Therefore, if the temperature is around room temperature, Au
If this oxygen gas sensor is used as a counter electrode instead of a sensing electrode, there is no need to isolate the counter electrode from the gas to be detected.

更にAg及びSnについても同様の実験を行なった結果
、Auと同様に常温付近では酸素ガスに対して不活性で
あった。したがって、Ag及びSnを平面型センサ1の
対極4の材料として用いてもよい。
Further, similar experiments were conducted with respect to Ag and Sn, and the results showed that, like Au, they were inert to oxygen gas at around room temperature. Therefore, Ag and Sn may be used as the material for the counter electrode 4 of the flat sensor 1.

また対極4はAu、Ag又はSnを蒸着またはスパッタ
リングすることで形成し、検知電極3は例えばLaF3
の表面にPtの薄膜を蒸着またはスパッタリングするこ
とで形成する。
Further, the counter electrode 4 is formed by vapor deposition or sputtering of Au, Ag, or Sn, and the sensing electrode 3 is formed by, for example, LaF3.
A thin film of Pt is formed by vapor deposition or sputtering on the surface of the Pt.

(効果) 以上に説明したように本発明によれば、LaF3(フッ
化ランタン)からなる固体電解質の表面で且つ酸素ガス
を含んだ被検ガスに晒される部分に、Au、Ag又はS
n等の酸素ガスに対して不活性な材料からなる対極を形
成したので、検知ガス中の酸素分圧に比例して起電力が
増加し、したがって十分に酸素ガスセンサとして使用す
ることができる。
(Effects) As explained above, according to the present invention, Au, Ag, or S
Since the counter electrode is made of a material that is inert to oxygen gas such as n, the electromotive force increases in proportion to the partial pressure of oxygen in the detection gas, so that it can be used satisfactorily as an oxygen gas sensor.

しかも、従来のごとく参照電極を被検ガスから遮断する
構造にする必要がないので構造が簡略になり、センサ自
体の小型化を達成できる。
Moreover, since there is no need to create a structure in which the reference electrode is isolated from the sample gas as in the conventional case, the structure is simplified and the sensor itself can be miniaturized.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明に係る酸素ガスセンサの断面図、第2図
は積層型酸素ガスセンサを用いて温度と酸素ガスに対す
る活性度との関係を示すグラフ、第3図は本発明に係る
酸素ガスセンサを用いた場合の酸素分圧と起電力との関
係を示すグラフ、第4図は従来の酸素ガスセンサの断面
図である。 尚、図面中1は本発明に係る平面型センサ、2は固体電
解質、3は検知電極、4は対極、5はPt線である。 第1図
FIG. 1 is a cross-sectional view of the oxygen gas sensor according to the present invention, FIG. 2 is a graph showing the relationship between temperature and activity for oxygen gas using a stacked oxygen gas sensor, and FIG. 3 is a graph showing the oxygen gas sensor according to the present invention. FIG. 4 is a graph showing the relationship between oxygen partial pressure and electromotive force when used, and is a sectional view of a conventional oxygen gas sensor. In the drawings, 1 is a flat sensor according to the present invention, 2 is a solid electrolyte, 3 is a detection electrode, 4 is a counter electrode, and 5 is a Pt wire. Figure 1

Claims (2)

【特許請求の範囲】[Claims] (1)LaF_3(フッ化ランタン)からなる固体電解
質の表面に検知電極を形成し、この検知電極と離れた固
体電解質の表面で且つ被検ガスに晒される部分に酸素ガ
スに対して不活性な材料からなる対極を形成したことを
特徴とする酸素ガスセンサ。
(1) A sensing electrode is formed on the surface of a solid electrolyte made of LaF_3 (lanthanum fluoride), and a portion of the solid electrolyte that is remote from the sensing electrode and exposed to the test gas is inert to oxygen gas. An oxygen gas sensor characterized by forming a counter electrode made of a material.
(2)前記検知電極はPtから構成され、対極はAu、
Ag又はSnから構成されることを特徴とする請求項(
1)に記載の酸素ガスセンサ。
(2) The sensing electrode is made of Pt, and the counter electrode is made of Au.
Claim characterized in that it is composed of Ag or Sn (
The oxygen gas sensor described in 1).
JP2236241A 1990-09-06 1990-09-06 Oxygen gas sensor Expired - Lifetime JP2946697B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2236241A JP2946697B2 (en) 1990-09-06 1990-09-06 Oxygen gas sensor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2236241A JP2946697B2 (en) 1990-09-06 1990-09-06 Oxygen gas sensor

Publications (2)

Publication Number Publication Date
JPH04115153A true JPH04115153A (en) 1992-04-16
JP2946697B2 JP2946697B2 (en) 1999-09-06

Family

ID=16997873

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2236241A Expired - Lifetime JP2946697B2 (en) 1990-09-06 1990-09-06 Oxygen gas sensor

Country Status (1)

Country Link
JP (1) JP2946697B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0677741A2 (en) * 1994-04-12 1995-10-18 Matsushita Electric Industrial Co., Ltd. Oxygen sensor
WO2002042756A3 (en) * 2000-11-22 2003-02-27 Panametrics Thin film ppb oxygen sensor
JP2008043943A (en) * 2006-07-21 2008-02-28 Nippon Soken Inc Catalyst material, electrode for gas sensor including the same, gas sensor and manufacturing method for them

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0677741A2 (en) * 1994-04-12 1995-10-18 Matsushita Electric Industrial Co., Ltd. Oxygen sensor
EP0677741A3 (en) * 1994-04-12 1996-05-01 Matsushita Electric Ind Co Ltd Oxygen sensor.
WO2002042756A3 (en) * 2000-11-22 2003-02-27 Panametrics Thin film ppb oxygen sensor
US6557393B1 (en) 2000-11-22 2003-05-06 Panametrics, Inc. Thin film ppb oxygen sensor
JP2008043943A (en) * 2006-07-21 2008-02-28 Nippon Soken Inc Catalyst material, electrode for gas sensor including the same, gas sensor and manufacturing method for them

Also Published As

Publication number Publication date
JP2946697B2 (en) 1999-09-06

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