So when we talk about electrolysis, we're going to say that electrolysis deals with passing an electrical current through a substance in order to produce chemical changes. Now because we're using outside energy, we're going to say that processes dealing with electrolysis are non-spontaneous. Remember, non-spontaneous things do not occur naturally and therefore require this outside energy in order to drive the reaction forward. Now here, we're going to say a good example of electrolysis. We have the passing of an electric current through water.
This helps to generate the standard components of water. Here, we have water as a liquid. We drive electricity through it and as a result, we produce oxygen gas and hydrogen gas. This is not a natural thing. We need that outside energy in the form of the current in order to force the reaction to occur.
Some of these concepts we've seen before. But just to revisit, remember we deal with electrical current. We're going to say here the units for electrical currents are in amperes or amps. So if we are given 15 amps, we'd say an amp is equal to coulombs per second. This would be equal to 15C/s.
Remember, when we're talking about current, we can use the variable I. I here, which is current equals q/t. So q here would be our charge. Here, this would be our time. If we're talking about moles of electrons, we can say the moles of electrons within a reaction are determined by molesofelectrons=I·t/F, where F is Faraday's constant.
Remember, current is coulombs per second. Time here will be in seconds. Faraday's constant has the units of coulombs over moles of electrons. So if you see, coulombs cancel out, seconds cancel out, and that's how you're left with moles of electrons at the end. Now with non-spontaneous processes, we should realize that our cell potential will be negative.
It'll be less than 0. We have to take into account that with non-spontaneous processes, our current is not negligible. It's a necessary part of the whole process. Because of this, we're going to have to take into account three other terms. We're going to have ohmic potential, which we're going to say is e.
It's the voltage necessary to overcome resistance R when the current I is flowing. Remember here, we'd say I=e/R. So I again is our current, e here is our voltage, and R here is our resistance. We're going to also have another term, over potential.
This is the voltage required to overcome the activation energy for the reaction in the given electrode. It's a non-spontaneous process, so the activation energy has to be overcome in order to drive the reaction forward. Next, we have concentration polarization, which occurs when there is a difference in the concentration of reactants on the surface of the electrode when compared to the solution itself. So the concentration of ions could be a very different number when it's close to the metal surface of our electrode or inert electrode as opposed to within the bulk solution itself.
Now we're going to say here, electrolysis is made more difficult by these different values because here, your potential here is subtracting from our total, and our overpotentials are subtracting from our total. Our concentration polarization is found here between these two. So all these concepts help to make our overall cell potential more negative. Remember, the more negative and smaller your cell potential becomes, the more non-spontaneous your process, the more current you need to supply in order to drive the reaction forward. So remember, when we're talking about electrolysis, we're basically running current through a substance to elicit a response and we have to do this because the whole process in itself is not a spontaneous one.