Q.Differentiate between Electrochemical cell and Electrolytic cell. What are the importances of salt bridge in an electrochemical cell? [3 + 2]
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Cell Representation and the Nernst Equation: From Intuition to Precision
Imagine you have a Daniell cell — a zinc rod in zinc sulphate solution connected by a salt bridge to a copper rod in copper sulphate solution. You know it produces a voltage. But what happens if you dilute the copper sulphate solution? Or if you change the temperature? The voltage changes. The Nernst equation is the tool that tells you exactly how much it changes.
The Intuition First
A battery works because the two half-cells "want" to react — zinc wants to lose electrons, copper ions want to gain them. This "want" is measured as a tendency, or potential. But the strength of that tendency depends on how crowded the ions are.
Think of it like this: If you have a room full of people who all want to leave (like zinc ions wanting to form), the push to get out is stronger when the room is packed. If the room is nearly empty, the push is weaker. Similarly, for copper ions wanting to enter the metal (gain electrons), the pull is stronger when there are many copper ions around, and weaker when there are few.
The Nernst equation quantifies this: the actual cell potential depends on the concentrations (or activities) of the ions involved.
The Precise Statement
For a general cell reaction:
aA+bB→cC+dD
The cell potential E under non-standard conditions is given by:
E=E∘−nFRTlnQ
Where:
- E = cell potential under the given conditions (in volts)
- E∘ = standard cell potential (when all reactants/products are at 1 M, 1 atm, 25°C)
- R = universal gas constant (8.314 J/mol·K)
- T = temperature in Kelvin
- n = number of moles of electrons transferred in the balanced half-reactions
- F = Faraday constant (96,485 C/mol)
- Q = reaction quotient = [A]a[B]b[C]c[D]d (using concentrations for dilute solutions)
At 25°C (298 K), the equation simplifies to a very practical form:
E=E∘−n0.0591log10Q
The 0.0591 comes from F2.303RT at 298 K. Notice it uses log10 (common log), not natural log.
Cell Representation: How We Write It
In electrochemistry, we represent a cell with a shorthand notation. For the Daniell cell:
Zn(s)∣Zn2+(aq)∥Cu2+(aq)∣Cu(s)
The single vertical line ∣ represents a phase boundary (solid electrode | solution). The double line ∥ represents the salt bridge.
The anode (oxidation) is written on the left, the cathode (reduction) on the right. Electrons flow from left to right in the external circuit.
Applying the Nernst Equation to a Cell Representation
For the Daniell cell, the half-reactions are:
- Anode (oxidation): Zn(s)→Zn2+(aq)+2e−
- Cathode (reduction): Cu2+(aq)+2e−→Cu(s)
Overall: Zn(s)+Cu2+(aq)→Zn2+(aq)+Cu(s)
Here n=2 (two electrons transferred). The reaction quotient is:
Q=[Cu2+][Zn2+]
So the Nernst equation becomes:
E=E∘−20.0591log10[Cu2+][Zn2+]
Solids (Zn, Cu) do not appear in Q because their concentrations are constant (activity = 1).
A Worked Example
Suppose you have a Daniell cell where [Zn2+]=0.1 M and [Cu2+]=1.0 M at 25°C. E∘ for the cell is 1.10 V.
E=1.10−20.0591log101.00.1 …
Why this formula?
Cell Representation & the Nernst Equation: Why It Works
The Core Question
Why does a cell's voltage change when concentrations change? The Nernst equation answers this — but the reason lies in the link between chemical free energy and electrical work.
1. The Fundamental Link: Gibbs Free Energy & Cell Potential
A galvanic cell does electrical work. The maximum useful work a cell can do equals the change in Gibbs free energy (ΔG):
ΔG=−nFEcell
Where:
- n = moles of electrons transferred
- F = Faraday constant (96,485C mol−1)
- Ecell = cell potential (volts)
Why negative? A spontaneous reaction has ΔG<0 and Ecell>0 — the negative sign makes this consistent.
2. The Chemical Side: ΔG Depends on Concentration
For a general redox reaction:
aA+bB→cC+dD
The Gibbs free energy under non-standard conditions is:
ΔG=ΔG∘+RTlnQ
Where Q is the reaction quotient:
Q=[A]a[B]b[C]c[D]d
Why this form? It comes from the relationship between chemical potential and concentration — the entropy of mixing drives concentration dependence.
3. Combining Both Sides: The Derivation
Set the electrical work equal to the chemical free energy change:
−nFEcell=−nFEcell∘+RTlnQ
Divide both sides by −nF:
Ecell=Ecell∘−nFRTlnQ
This is the Nernst equation.
4. The "Why" in Plain Terms
| Concept | Physical Meaning |
|---|---|
| Ecell∘ | Voltage when all species are at 1 M (standard state) |
| −nFRTlnQ | Correction factor — adjusts voltage for real concentrations |
| Q | Tells you how far the reaction is from equilibrium |
Key insight: When Q=K (equilibrium), Ecell=0 — the battery is dead because no net reaction occurs.
5. The Common Form (log base 10)
At 25∘C (298K):
FRTln10≈0.0592V
So:
Ecell=Ecell∘−n0.0592log10Q
Why convert to log? Exam convenience — most concentration values are powers of 10.
--- …
The two kinds of electrochemical cells differ in the direction of energy conversion - one generates electricity from a spontaneous reaction, the other consumes electricity to force a non-spontaneous one - and the salt bridge is what keeps a galvanic cell like the Daniell cell actually working. …
Electrochemical cell: spontaneous redox -> produces electricity. Electrolytic cell: external electricity -> drives a non-spontaneous reaction. Salt bridge completes the circuit, keeps both solutions neutral and prevents junction potential.
Difference between electrochemical (galvanic) cell and electrolytic cell:
| Feature | Electrochemical (Galvanic/Voltaic) cell | Electrolytic cell |
|---|---|---|
| Energy conversion | Converts chemical energy into electrical energy | Converts electrical energy into chemical energy |
| Nature of reaction | Based on a spontaneous redox reaction (ΔG negative) | Based on a non-spontaneous reaction, forced by external current (ΔG positive) |
| Source of current | Produces electric current | Consumes electric current from an external source (battery) |
| Electrodes | Anode is negative, cathode is positive | Anode is positive, cathode is negative |
| Set-up | Two half-cells joined by a salt bridge | Single vessel with electrolyte and two electrodes dipping in it |
| Example | Daniell cell (Zn-Cu cell) | Electrolysis of water / molten NaCl, electroplating, electrorefining |
In both, oxidation occurs at the anode and reduction at the cathode.
Importance of the salt bridge in an electrochemical cell:
- It completes the internal electrical circuit by allowing the flow of ions between the two half-cells, so that the cell can operate continuously. …
Showing the 12 most recent of 14 on this concept.
- CBSE 2026Set ANNUAL1 markQ.What is the potential difference between the two electrodes of the galvanic cell called?
›Reveal solutionSolution
The potential difference between the two electrodes of a galvanic cell (measured when no current is drawn) is called the electromotive force (EMF) or cell potential, Ecell.
Concept. In a galvanic (voltaic) cell, the two half-cells are at different electrode potentials. The difference between the cathode and anode potentials is what pushes electrons through the external circuit:
Ecell=Ecathode−Eanode
…
- CBSE 2026Set ANNUAL1 markMCQQ.Consider the following statements about a reaction at equilibrium: A(g) + B(g) ↔ C(g). Statement I: Adding an inert gas at constant volume will shift the equilibrium to the right. Statement II: A catalyst changes the position of equilibrium.(a) i) Both statement I and II are correct(b) ii) Both statement I and II are incorrect(c) iii) Statement I is correct and statement II is incorrect(d) iv) Statement I is incorrect and statement II is correct
›Reveal solutionSolution
[!TLDR]
ii) Both statement I and II are incorrect
Why
Adding an inert gas at constant volume does not change partial pressures/concentrations of reacting species, so it does not shift equilibrium (Statement I false). A catalyst speeds up attainment of equilibrium equally in …
- CBSE 2025Set ANNUAL1 markQ.For the electrochemical cell Zn(s)+Cu2+(aq)→Zn2+(aq)+Cu(s) the cell produces an electrical potential of 1.1 volt, when [Zn2+] and [Cu2+] are unity. State the direction of flow of current on applying external potential of 1.1 volt.
›Reveal solutionSolution
An external potential exactly equal and opposite to the cell's own EMF brings the system to balance, so no net current flows in either direction — this is the basis of potentiometric EMF measurement.
The Daniell-type cell Zn(s)∣Zn2+(aq)∥Cu2+(aq)∣Cu(s) spontaneously drives current in the galvanic direction (electrons flow from Zn anode to Cu cathode through the external circuit) with an EMF of 1.1 V under standard conditions.
If an external opposing potential is applied, it works against this spontaneous cell reaction:
- If the external potential is less than 1.1 V, the cell's own EMF still dominates, and current continues to flow in the original (galvanic) direction, though at a reduced magnitude.
- If the external potential is greater than 1.1 V, it overpowers the cell's own EMF, and current is forced to flow in the reverse direction (the cell now behaves as an electrolytic cell, being charged/driven backward). …
- CBSE 2025Set ANNUAL1 markMCQQ.The correct statement in a cell of zinc and copper is(a) zinc acts as cathode and copper as anode(b) zinc acts as anode and copper as cathode(c) the standard reduction potential of zinc is more than that of copper(d) the flow of electrons is from copper to zinc
›Reveal solutionSolution
Zinc has a lower (more negative) standard reduction potential than copper, so it is oxidized (anode) while copper is reduced (cathode).
In a Daniell-type zinc–copper cell, E°(Zn²⁺/Zn) = −0.76 V is lower than E°(Cu²⁺/Cu) = +0.34 V. The electrode with the lower (more negative) reduction potential is oxidized — zinc loses electrons and acts as the anode (Zn → Zn²⁺ + 2e⁻) — while the electrode with the higher reduction potential is reduced — copper gains electrons and acts as the cathode (Cu²⁺ + 2e⁻ → Cu). Electrons flow …
- CBSE 2024Set D1 markMCQQ.The electromotive force of the cell Zn | ZnSO4 || CuSO4 | Cu is 1.1 volt. Its cathode is(a) Zn(b) Cu(c) ZnSO4(d) CuSO4
›Reveal solutionSolution
Reduction happens at the cathode; Cu2+ is reduced to Cu, so Cu is the cathode.
In the Daniell cell Zn | ZnSO4 || CuSO4 | Cu:
- Anode (oxidation, left): Zn -> Zn2+ + 2e-
- Cathode (reduction, right): Cu2+ + 2e- -> Cu …
- CBSE 2024Set ANNUAL1 markMCQQ.An electrochemical cell can behave like an electrolytic cell when _______.(a) Ecell = 0(b) Ecell > Eext(c) Eext > Ecell(d) Ecell = Eext
›Reveal solutionSolution
A galvanic (electrochemical) cell starts behaving like an electrolytic cell when an external potential greater than the cell's own emf is applied against it, reversing the direction of current flow.
Consider a Daniell cell: Zn(s) | Zn2+(aq) || Cu2+(aq) | Cu(s), which normally works as a galvanic cell producing a cell potential Ecell, with electrons flowing from Zn (anode) to Cu (cathode) through the external circuit.
If an external opposing emf (Eext) is applied to this cell:
- When Eext < Ecell, the cell continues to work as a galvanic cell, but the current decreases.
- When Eext = Ecell, no current flows through the cell (this is used to measure the cell's emf accurately, e.g. using a potentiometer). …
- CBSE 2024Set ANNUAL1 markQ.Write True/False: A hydrogen bridge is used to maintain continuity of ion flow in a Daniell cell.
›Reveal solutionSolution
This statement is FALSE. A Daniell cell uses a salt bridge (e.g. containing KCl or KNO3 in agar-agar gel), not any "hydrogen bridge", to complete the internal circuit.
A Daniell cell consists of a Zn electrode dipped in ZnSO4 solution (anode) and a Cu electrode dipped in CuSO4 solution (cathode), connected externally by a wire and internally by a salt bridge. The salt bridge allows ions to migrate between the two half-cells, maintaining electrical neutrality in each compartment as the cell reaction proceeds, and completes the internal circuit …
- CBSE 2023Set 56/1/11 markMCQQ.The correct cell to represent the following reaction is : Zn+2Ag+→Zn2++2Ag (A) 2Ag∣Ag+∣∣Zn∣Zn2+ (B) Ag+∣Ag∣∣Zn2+∣Zn (C) Ag∣Ag+∣∣Zn∣Zn2+ (D) Zn∣Zn2+∣∣Ag+∣Ag
›Reveal solutionSolution
By convention the anode (oxidation) is written on the left and the cathode (reduction) on the right. Zinc is oxidised and silver ions are reduced, so the cell is Zn∣Zn2+∥Ag+∣Ag — option (D).
A cell diagram is written anode (left) ∥ cathode (right), with each half-cell running from the electrode metal outward and the double bar ∥ marking the salt bridge.
For the reaction
Zn+2Ag+→Zn2++2Ag
- Zinc loses electrons: Zn→Zn2++2e− (oxidation, anode, left).
- Silver ions gain electrons: Ag++e−→Ag (reduction, cathode, right).
Writing the anode as metal ∣ ion and the cathode as ion ∣ metal gives
Zn∣Zn2+∥Ag+∣Ag
Checking the options: …
- CBSE 2022Set E1 markMCQQ.The standard electrode potentials for the following reactions are given ( At 25°C ): Ag+(aq) + e- -> Ag(s), E° Ag+/Ag = +0.80 V ; Sn2+(aq) + 2e -> Sn(s), E° Sn2+/Sn = -0.14 V. The electromotive force (EMF) of the given cell Sn | Sn2+ (1M) || Ag+ (1M) | Ag is(a) 0.66 V(b) 0.80 V(c) 1.08 V(d) 0.94 V
›Reveal solutionSolution
For Sn | Sn2+ || Ag+ | Ag, EMF = E°(Ag+/Ag) - E°(Sn2+/Sn) = 0.80 - (-0.14) = 0.94 V.
In the cell notation the left electrode is the anode (oxidation) and the right is the cathode (reduction):
- Cathode (reduction): Ag+ + e- -> Ag, E° = +0.80 V
- Anode (oxidation): Sn -> Sn2+ + 2e-, E°(Sn2+/Sn) = -0.14 V
E°cell = E°cathode - E°anode = (+0.80) - (-0.14) = +0.94 V.
…
- CBSE 2022Set ANNUAL1 markMCQQ.Which one of the following statements is incorrect for a voltaic cell ?(a) It converts chemical energy to electrical energy.(b) It uses electrical energy to carry out chemical changes.(c) It is based on a redox reaction.(d) It has −ΔG.
›Reveal solutionSolution
A voltaic cell produces electricity from a spontaneous redox reaction — it does not consume electrical energy, so statement (b) describes an electrolytic cell instead.
Checking each option against what a voltaic (galvanic) cell actually does:
- (a) True — a voltaic cell converts chemical energy into electrical energy.
- (b) False — this describes an electrolytic cell, which uses externally supplied electrical energy to force a non-spontaneous chemical change. A voltaic cell does the opposite. …
- CBSE 2022Set ANNUAL1 markMCQQ.For the given cell reaction Mg∣Mg2+∣∣Cu2+∣Cu:(a) Mg as cathode(b) Cu as cathode(c) Cu is oxidizing agent(d) None of the above
›Reveal solutionSolution
By IUPAC convention the electrode written on the LEFT of a cell is the anode and the one on the RIGHT is the cathode. Here Mg is the anode and Cu is the cathode. Option (B).
The cell is written as Mg∣Mg2+∣∣Cu2+∣Cu.
Convention: anode (negative, oxidation) is written on the left; cathode (positive, reduction) is written on the right.
The electrode reactions are:
- Anode (Mg, oxidation): Mg→Mg2++2e−
- Cathode (Cu, reduction): Cu2++2e−→Cu …
- CBSE 2021Set A1 markMCQQ.Zn(s) | Zn2+(aq) || Cu2+(aq) | Cu(s) is(a) Weston cell(b) Daniel cell(c) Calomel cell(d) None of these
›Reveal solutionSolution
A zinc-copper galvanic cell with this notation is the Daniell cell.
The cell Zn(s) | Zn2+(aq) || Cu2+(aq) | Cu(s) is the Daniell cell, a galvanic (voltaic) cell.
- At the anode (LHS): Zn(s) → Zn2+ + 2e- (oxidation).
- At the cathode (RHS): Cu2+ + 2e- → Cu(s) (reduction). …
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