Hey, everyone. So here we're going to say that potentiometry uses electrodes to measure voltages that also provide vital chemical information on their solutions. We're going to say the difference in potential between the two electrodes provides an analysis for the composition of the analyte and we're going to see if the measurement of the voltage at an electrode relative to the reference is done in the absence of current flow. So no current or electricity is being run through this. It's going to say we're going to say here that our nonstandard cell potential equals the potential of our indicator electrode minus the potential of our reference electrode plus the potential of our junction potential.
Now, the junction potential arises from both ends of our salt bridge. We're going to say this is a result of a type of imbalance in the ions from one side to another. It could also be an imbalance or difference in ionic size for the salts, the neutral salts used within our salt bridge. But we can say that by fine-tuning the types of ions and the size of ions being used, we can make our potential or sub potential for our junction potential negligible, meaning that it gets close to 0. And if it's close to 0 we can ignore it. Now, we're going to say that when it comes to the salt bridge to do this we typically use potassium chloride. So we have our chloride ions here and our potassium ions here. Remember, chloride ions are negative ions would flow towards the anode side and our potassium ions would flow towards the cathode side. The reason that this is the ideal combination of ions is that they're pretty close in size and because of that they're the best types of ions used within our salt bridge. Doing this would help us get to our cell potential for our junction potential being close to 0.
Now, here if we take a look at this, we have our typical electrochemical cell. In this electrochemical cell, we see that we have our silver chloride, this our saturated solution of potassium chloride solution. We can say here, that we can create a solid and here the solid would actually be AgCl. That will be our precipitate that forms when silver and chloride are allowed to connect together. We're going to say here that this side is our reference electrode and because it's the anode side we can say that these two are connected together. So our anode here is represented by our reference electrode. On this side here we have our indicator electrode, which is connected to our cathode.
Now, here remember our reference electrode, this is the part of the cell that is held constant, so it's not changing in terms of concentration. The indicator electrode, this is the part of the cell that contains the analyte being analyzed. So the portion of the solution that we want to focus all our attention on determining its composition. Now the half reactions are given as we have silver chloride solid and here we're going to say that we have an electron. This electron is being given to the chloride ion, and by doing this, our silver goes from being plus 1 to being neutral. So here we have silver solid being created, a precipitate. We know that this is the anode from this notation of minus because here our minus sign is indicative of the anode. And then here we have Fe3+ absorbs an electron to become Fe2+ this is indicative of a cathode. Notice here we don't form a precipitate which is why within our image we don't have an iron electrode, instead, we have a platinum electrode. This platinum electrode serves as an inert electrode within this reaction.
Now with this information we can say that the Nernst equation provides a mathematical relationship between the electrode potential and an analyte reduced and oxidized forms. Now here we're going to say the difference in potential is based on only one of the half solid concentrations because remember, our reference electrode is held constant. So here, we would have this side represented for the cathode because here we're dealing with our positive electrode which is the cathode. Here we're dealing with the negative electrode which is our anode. And we're going to say here that remember that your nonstandard cell potential equals in this case E positive minus E negative, cathode minus anode, which in this case since we're dealing with indicator and reference electrodes would be, cell potential of our indicator electrode minus cell potential of our reference electrode. So when it comes to this whole process, we're basically making sure that one of our half reactions is done with the reference electrode, but we know its value based on literature, and all we're doing is examining the analyte, the one that has a varying concentration. From this, we can obtain a plethora of information that gives us a lot of detail in terms of the composition of that particular analyte. And again, this can be based on different concentrations as well as the cell potentials that are being created.
