Friday, December 24, 2010
Wednesday, December 22, 2010
Cell Potential
CELL POTENTIAL (Ecell)
- Difference in electrical potential of electrodes.
- Also called voltage or electromotive force (emf).
- Cell emf depends on the concentration of ions in the cell, the temperature of solutions and pressure of gasses involved.
· Unit : Volt (V).
Ecell > 0 | Ecell = 0 | Ecell < 0 |
Spontaneous cell reaction. | Reaction has reach equilibrium. | Non spontaneous cell reaction. |
STANDARD CELL POTENTIAL (EOcell)
- Difference in electrical potential of electrodes measured at specified temperature (usually 298 K) with all components in their standard state which are :
- 1 atm (for gases)
- 1M for solutions
- Pure solid for electrodes
Eocell = Eocathode - Eoanode
· STANDARD ELECTRODE (HALF-CELL) POTENTIAL (EOhalf-cell)
- Potential associated with a given half reaction (electrode compartment) when all components are in their standard states.
- Also called standard reduction potential.
- Changing the balancing coefficients of a half-reaction does not change Eo value because electrode potentials are intensive properties.
- Eg. :
Oxidation (anode) : Zn(s) → Zn2+(aq) + 2e- Eoanode = -0.76 V
Reduction (cathode) : Cu2+(aq) + 2e- → Cu(s) Eocathode = +0.34 V
Overall : Zn(s) + Cu2+(aq) → Zn2+(aq) + Cu(s)
Eocell = Eocathode - Eoanode
= Eocopper - Eozinc
= +0.34 V – (-0.76 V)
= +1.10 V
STANDARD HYDROGEN ELECTRODE (SHE)
- SHE is the standard reference electrode to measure the electrode potentials of other half-cell.
- SHE is assign as zero potential (0 V)SHE consists of H2 gas at 1 atm,25°C bubbling around a platinum electrode which is immersed in 1 M of solution H+.
- The electric potential of the half reaction is due to the reduction of H+ to H2 (g).
2H+ (aq) +2e-→H2 (g) E° =0.00V
STANDARD REDUCTION POTENTIAL TABLE
From the table,
- The element with more +ve E° becomes cathode.
- The element with more -ve E° becomes anode.
- The more +ve Eo favours reaction to the right.
- The more -ve Eo favours reaction to the left.
- The more +ve E° , the stronger the oxidising agent.
- The more -ve E° , the stronger the reducing agent.
Half-Cell Equation
HALF-CELL EQUATION
Oxidation (anode) : Zn(s) → Zn2+(aq) + 2e-
Reduction (cathode) : Cu2+(aq) + 2e- → Cu(s)
Overall : Zn(s) + Cu2+(aq) → Zn2+(aq) + Cu(s)
Salt Bridge
- Contains a solution of non reacting ions (KCl, KNO3, Na2SO4).
- It functions is to maintain electrical neutrality while redox reactions proceed at the electrodes.
OXIDATION HALF-CELL (ANODE) | REDUCTION HALF-CELL (CATHODE) |
Zn (s) → Zn2+(aq) + 2e- | Cu2+(aq) + 2e- → cu (s) |
· Zn2+ ions enter the solution causing an overall excess of positive charge. · Anode loses mass/erode · Cl- ions from salt bridge move into anode (Zn) half-cell. | · Cu2+ ions leave the solution causing an overall excess of negative charge. · Cathode gain mass/deposit · K+ ions from salt bridge move into cathode (Cu) half-cell. |
Comparison: Galvanic Cell and Electrolytic Cell
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Comparison between galvanic cell and electrolytic cell
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Electrochemical Cells:
1) Galvanic Cells
2) Electrolytic Cells
Similarities |
· They consist of an electrolyte each. Ø Electrolyte is mixture of ions (usually in aqueous solution) that are involve in reaction or that carry charge. · They consist of two electrodes. Ø Electrodes are objects that conduct electricity between cell and surroundings. Ø Electrodes consist of : I. Anode – Oxidation half-reaction takes place II. Cathode – Reduction half-reaction takes place · The process of donation of electrons occurs at the anode while the process of acceptance of electrons occurs at the cathode. · Electrons flow from the anode to the cathode in the external circuit. |
Galvanic Cells | Differences | Electrolytic Cells |
Converts electrical energy to chemical energy | Conversion of energy | Converts chemical energy to electrical energy |
a) The anode (positive terminal) is positively charged. b) The cathode (negative terminal) is negatively charged. | Charge of a) Anode b) Cathode | a) The anode (negative terminal) is negatively charged. b) The cathode (positive terminal) is positively charged. |
Carbon of two same metals or two different metals. | Type of electrodes | Two different metals. |
Spontaneous reaction. -Reaction that has a natural tendency to occur and does not require an energy input for it to occur. -eg : rusting of iron nails | Type of reaction | Non-spontaneous reaction. -Reaction that cannot occur naturally and needs energy input to help it to occur. -eg : photosynthesis |
Redox Reaction
REDOX REACTION
- A process in which there is a net movement of electrons from one reactant (reducing agent) to another (oxidizing agent).
- Chemical reaction involving oxidation and reduction occurs simultaneously.
- Also called oxidation-reduction reaction.
COMPARISON BETWEEN OXIDIZING & REDUCING AGENT
OXIDIZING AGENT | REDUCING AGENT |
Substance that undergoes reduction | Substance that undergoes oxidation |
Substance that accepts electrons in a redox reaction | Substance that loss electrons in a redox reaction |
Substance that undergoes a decrease in oxidation number | Substance that undergoes an increase in oxidation number |
Electrochemistry
Electrochemistry is a study of relationship between chemical change and electrical work.
OXIDATION | REDUCTION |
Loss of electron | Gain of electron |
Gain of oxygen | Loss of oxygen |
Loss of hydrogen | Gain of hydrogen |
Increase in oxidation number | Decrease in oxidation number |
Eg. : Zn(s) → Zn2+ (aq) + 2e- Oxidation no. : 0 +2 | Eg. : 2H+(aq) + 2e- → H2 (g) Oxidation no. : +1 0 |
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