Calculating EMF of a Cell: Ni(s) | Ni2+ (0.1M) || Au3+ (1.0M) | Au (s)

  • Thread starter Thread starter Krushnaraj Pandya
  • Start date Start date
  • Tags Tags
    Cell Emf
AI Thread Summary
The discussion focuses on calculating the EMF of the electrochemical cell Ni(s) | Ni2+ (0.1M) || Au3+ (1.0M) | Au(s) using standard reduction potentials and the Nernst equation. Participants clarify the correct application of the Nernst equation, emphasizing the importance of sign conventions and the proper formulation of the reaction quotient. A misunderstanding regarding the concentrations of the reactants led to confusion in calculating the cell potential. Suggestions include calculating the Nernst equation for each electrode separately and applying Le Chatelier's principle to understand the effects of concentration changes on cell potential. The conversation concludes with acknowledgment of the helpful tips provided.
Krushnaraj Pandya
Gold Member
Messages
697
Reaction score
73

Homework Statement


The EMF of the cell : Ni(s) | Ni2+ (0.1M) || Au 3+ (1.0M) | Au (s) is

[ given E°(Ni2+/Ni)= -0.25V; E° (Au3+ / Au )= +1.50V ]

Homework Equations


E°cell=E°(cathode)-E°(anode) For SRP.
Nernst equation

The Attempt at a Solution


SOP is given, therefore converting to SRP we take minus sign of both. Now Ni to Ni2+ is at anode and Au3+ to Au is at cathode. Therefore E(cell)= -1.5-0.25= -1.75V
Writing balanced reaction 3Ni+2Au3+ gives 3Ni2+ + 2Au, no. of electrons transferred=6.
Putting into nernst equation, EMF should be -1.75-(0.059/6)log(0.1)^3 which gives the wrong answer. Where am I wrong, I'd appreciate some help
 
Physics news on Phys.org
Why have you got log(0.1)^3 ? Write out the Nernst equation in full for this cell.
 
Ok, so we have E°=-1.75, RT/F=0.059, Q=[Ni2+]^3/[Au3+]^2=(0.1)^3/(1)^2=(0.1)^3
replacing in E=E°-2.303(RT/nF)logQ we get the equation I wrote in"Attempt at a solution"
 
Sorry, I misread the question, I thought [Au3+] was also 0.1M.
I think you've got the signs wrong. E for the cell is ER - EL by convention
Ecell = E(Au3+/Au) - E(Ni2+/Ni)
= E0(Au3+/Au) - E0(Ni2+/Ni) + RT/nF*log([Au3+]2/[Ni2+]3)
 
mjc123 said:
Sorry, I misread the question, I thought [Au3+] was also 0.1M.
I think you've got the signs wrong. E for the cell is ER - EL by convention
Ecell = E(Au3+/Au) - E(Ni2+/Ni)
= E0(Au3+/Au) - E0(Ni2+/Ni) + RT/nF*log([Au3+]2/[Ni2+]3)
The magnitude should remain the same (note that reversing the terms inside log reverses its sign)
 
Alright, I realized my mistake. I got confused in sign conventions. Thank you for your help :D
 
You might find it helpful
(i) to do the Nernst equation on each electrode separately; that way you ought to get the magnitude of the cell potential right, even if you get the sign convention wrong.
(ii) to think Le Chatelier - if I increase the concentration of X, will that pull the equilibrium to the right or left - increase or decrease cell potential?
 
mjc123 said:
You might find it helpful
(i) to do the Nernst equation on each electrode separately; that way you ought to get the magnitude of the cell potential right, even if you get the sign convention wrong.
(ii) to think Le Chatelier - if I increase the concentration of X, will that pull the equilibrium to the right or left - increase or decrease cell potential?
Very helpful tips, thank you
 
Back
Top