Oxygen reference electrode

An extensive review on oxygen reference electrodes with solid electroytes is available [OOMal]. 

Oxygen reference electrodes are useful for the study of the thermodynamic and electrochemical properties of oxyanionic melts [96,97],... 

Table 2.24 Breakdown potentials (mV) for 316 stainless steel, titanium and cobalt-chromium-molybdenum alloy in oxygen-free 0.17 m NaCl solution at 37°C using a silver/ silver chloride reference electrode.

Several significant electrode potentials of interest in aqueous batteries are listed in Table 2 these include the oxidation of carbon, and oxygen evolution/reduction reactions in acid and alkaline electrolytes. For example, for the oxidation of carbon in alkaline electrolyte, E° at 25 °C is -0.780 V vs. SHE or -0.682 V (vs. Hg/HgO reference electrode) in 0.1 molL IC0 2 at pH [14]. Based on the standard potentials for carbon in aqueous electrolytes, it is thermodynamically stable in water and other aqueous solutions at a pH less than about 13, provided no oxidizing agents are present. 

When a solid electrolyte component is interfaced with two electronically conducting (e.g. metal) films (electrodes) a solid electrolyte galvanic cell is formed (Fig. 3.3). Cells of this type with YSZ solid electrolyte are used as oxygen sensors.8 The potential difference U R that develops spontaneously between the two electrodes (W and R designate working and reference electrode, respectively) is given by ... 

Figure 5.25. Redhead plot for oxygen desorption from a Pt film deposited on YSZ for various catalyst film potentials vs Au reference electrode. The slope of each line is equal to Ed/R.7 Reprinted with permission from Academic Press.

Thus if the working and reference electrodes are made of different metals, and there is negligible adsorption of oxygen on the two metals, in which case Or=o,m and Ow=eO0lM then equation (7.19) gives the cpd (contact potential difference) of the two metals ... 

Checking the absence of internal mass transfer limitations is a more difficult task. A procedure that can be applied in the case of catalyst electrode films is the measurement of the open circuit potential of the catalyst relative to a reference electrode under fixed gas phase atmosphere (e.g. oxygen in helium) and for different thickness of the catalyst film. Changing of the catalyst potential above a certain thickness of the catalyst film implies the onset of the appearance of internal mass transfer limitations. Such checking procedures applied in previous electrochemical promotion studies allow one to safely assume that porous catalyst films (porosity above 20-30%) with thickness not exceeding 10pm are not expected to exhibit internal mass transfer limitations. The absence of internal mass transfer limitations can also be checked by application of the Weisz-Prater criterion (see, for example ref. 33), provided that one has reliable values for the diffusion coefficient within the catalyst film. 

Description of the cell composition is based - as far as possible - on the Stockholm convention (1953), i.e. the left-hand electrode constitutes the negative terminal of the cell. Cells are listed according to the metallic constituent of the electrode mentioned first which is involved in the electrode reaction establishing the respective electrode potential. Contact materials and conductive additives may be mentioned first before the actual element of interest only for the sake of correct materials sequence. The sequence of electrode components is stated as reported in the original publications. When an oxygen electrode is used as reference electrode an oxygen partial pressure of 0.21 atm is assumed. 

Reference electrodes of Pt-air and In-In203 are useful to measure oxygen in sodium at 700-1100 K. Problems in the stability of the electrolyte tubes require the use of Th02 and 203 . 

The discharge curve for Air electrode, which was measured using additional third Ag AgCl reference electrode, is ideally horizontal since it is determined by the oxygen reduction potential in according medium... 

The partial oxygen pressure was checked with an OP-210/3 microanalyser [20] before and after the bubbling of oxygen through the electrolyte. The potential was measured against an Ag/AgCl reference electrode. 

Commonly used cells use Pt/C>2 or Pt/air as reference electrodes. At very low partial pressures of oxygen, care must be taken to avoid direct permeation of oxygen through stabilized zirconia from the air (or reference electrode) [74, 75]. The effect may be avoided by applying reference electrodes with activity near that observed at the working electrode. A well-defined buffer system like a metal-metal... 

In soil analysis, pH, specific ion, oxidation-reduction (redox), electrical conductivity (EC) cells, and oxygen electrodes are commonly used. For each of these measurements, a different specific electrode along with a separate or integral reference electrode is needed. In some cases, with extended use or long exposure to soil or soil-water suspensions, electrodes may become polarized. When this happens, erroneous results will be obtained and depolarization will need to be carried out using the electrode manufacturers directions [3],... 

The dissolved oxygen content of a solution can be determined by measuring the diffusion current that results at a selected voltage. The Clark electrode was developed for this purpose and various modifications have subsequently been introduced. It consists basically of a platinum electrode separated from the sample by a membrane which is permeable to oxygen, e.g. Teflon or polyethylene. A reference electrode of silver/silver chloride in potassium chloride is used to complete the system (Figure 4.21). When a voltage that is sufficient to give the... 

---