1.6.3

Commercial Application

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Batteries

Electrochemical cells are used as batteries.

Batteries

Batteries

  • Batteries come in two forms:
    • Rechargeable.
    • Non-rechargeable.
  • Rechargeable batteries can have their reaction reversed by applying an electrical current.
    • This needs more sophisticated cells and is more expensive. But this process can be cheaper overall as you only need to buy one.
Lithium cobalt oxide batteries

Lithium cobalt oxide batteries

  • LiCoO2 batteries were the first lithium ion batteries invented.
  • The have one electrode made of LiCoO2 and one made of graphite.
  • The two half equations are:
    • Li+ + e- ⇌ Li(s), Eθ = −3.04V
    • Li+ + CoO2 + e- ⇌ LiCoO2, Eθ = 0.56V
The reactions

The reactions

  • The Li+/Li(s) cell has a more negative Eθ so is reversed.
  • The overall cell potential is: Eθcell = 0.56 − (−3.04) = 3.6V.
    • To reverse the reaction, you apply an external current of at least 3.6V to push the reactions in the opposite directions.

Fuel Cells

Fuel cells can be used to make electricity. They store the chemicals outside of the cell and put them in when we want electricity.

The hydrogen-oxygen fuel cell

The hydrogen-oxygen fuel cell

  • The most important fuel cell is the alkaline hydrogen-oxygen fuel cell.
    • Hydrogen and oxygen are the fuel.
    • The electrodes are platinum electrodes.
Anion exchange membranes

Anion exchange membranes

  • The anion exchange membranes do NOT allow the gases through.
  • These membranes do allow hydroxide ions (OH-) and water to pass through.
At the electrodes

At the electrodes

  • The hydrogen gas is delivered to the negative electrode where it reacts with the hydroxide ions. The half equation for this reaction is:
    • 2H2(g) + 4OH-(aq) → 4H2O(l) + 4e-
  • The oxygen gas is delivered to the positive electrode where it reacts with water and electrons. The half equation for this reaction is:
    • O2(g) + 2H2O(l) + 4e- → 4OH-(aq)
Overall reaction

Overall reaction

  • The overall reaction for the hydrogen-oxygen fuel cell is:
    • 2H2(g) + O2(g) → 2H2O(g)

Advantages and Disadvantages of Fuel Cells

Fuel cells can be better electricity-generating devices than the internal combustion engines that are found in cars.

Advantages of fuel cells

Advantages of fuel cells

  • Fuel cells have a high efficiency.
    • This means that they get more energy out of the same amount of fuel than less efficient devices.
  • Their only by-product is water (no CO2(g) is produced).
  • They don’t need to be recharged - they will work as long as the fuel is supplied.
Disadvantages of fuel cells

Disadvantages of fuel cells

  • Hydrogen is flammable and so must be stored very carefully.
  • Energy is needed to produce the reactants of hydrogen and oxygen.
    • This energy usually comes from fossil fuels, so there are some CO2(g) emissions.
Jump to other topics
1

Physical Chemistry

1.1

Atoms, Molecules & Stoichiometry

1.1.1Relative Masses1.1.2The Mole1.1.3Mass Spectrometry1.1.4Empirical & Molecular Formulae1.1.5Balanced Equations1.1.6Molar Volume1.1.7End of Topic Test - Amount of Substance
1.2

Atomic Structure

1.2.1Fundamental Particles1.2.2Isotopes & Mass Number1.2.3Electron Shells, Sub-Shells & Orbitals1.2.4Electron Configuration1.2.5Ionisation Energy1.2.6Factors Affecting Ionisation Energies1.2.7Trends of Ionisation1.2.8Specific Impacts on Ionisation Energies1.2.9Electron Affinity1.2.10End of Topic Test - Atomic Structure1.2.11A-A* (AO2/3) - Atomic Structure
1.3

Chemical Bonding

1.3.1Ionic Bonding1.3.2Covalent & Dative Bonding1.3.3Shapes of Molecules1.3.4Intermolecular Forces1.3.5Intermolecular Forces 21.3.6Electronegativity1.3.7Bond Length, Bond Energy, & Bond Polarity1.3.8Metallic Bonding1.3.9Physical Properties1.3.10End of Topic Test - Bonding1.3.11A-A* (AO2/3) - Bonding
1.4

States of Matter

1.4.1Simple Covalent Molecules1.4.2The Ideal Gas Equation1.4.3States of Matter1.4.4Particle Diagrams1.4.5The Liquid State1.4.6Giant Ionic Lattices1.4.7Giant Metallic Lattices1.4.8Giant Covalent Structures1.4.9Graphene & Fullerene1.4.10Recycling
1.5

Chemical Energetics

1.5.1Calorimetry1.5.2Bond Enthalpies1.5.3Enthalpy Changes1.5.4Hess' Law1.5.5Born-Haber Cycles1.5.6Born-Haber Cycle Calculations1.5.7Entropy1.5.8Free Energy1.5.9End of Topic Test - Energetics
1.6

Electrochemistry

1.6.1Electrochemical Cells1.6.2Electrochemical Series1.6.3Commercial Application1.6.4Nernst Equation1.6.5Redox
1.7

Equilibria

1.7.1Dynamic Equilibrium & Le Chatelier1.7.2Kc1.7.3Kp1.7.4pH1.7.5The Ionic Product of Water1.7.6Weak Acids & Bases1.7.7Introduction to Solubility Equilibria1.7.8Solubility Equilibria Calculations1.7.9Free Energy of Dissolution1.7.10pH and Solubility1.7.11Common-Ion Effect1.7.12End of Topic Test - Kp & Electrochemistry1.7.13A-A* (AO2/3) - Electrochemical Cells
1.8

Partition Coefficient

1.8.1Kpc
1.9

Reaction Kinetics

1.9.1Collision Theory1.9.2Orders, Rate Constants & Equations1.9.3Rate Graphs1.9.4Rate Determining Step1.9.5Maxwell-Boltzmann Distribution1.9.6Catalysts1.9.7Homogeneous Catalysts1.9.8Heterogeneous Catalysts1.9.9End of Topic Test - Kinetics1.9.10End of Topic Test - Rate Equations1.9.11A-A* (AO2/3) - Rate Equations
2

Inorganic Chemistry

2.1

The Periodic Table

2.1.1The Periodic Table2.1.2Trends in the Periodic Table2.1.3End of Topic Test - Periodicity & Trends2.1.4Ceramics2.1.5Period 3 Elements & Oxides2.1.6Period 3 Oxides2.1.7End of Topic Test - Period 3
2.2

Group 2

2.2.1Group 2 Chemistry
2.3

Group 17

2.3.1Introduction to Halogens2.3.2Reactions of Halogens2.3.3Chlorine & Chlorate(I)2.3.4End of Topic Test - Group 172.3.5A-A* (AO2/3) - Periodicity, Group 2 & 17
2.4

Transition Metals

2.4.1General Properties2.4.2Titrations2.4.3Shapes of Complex Ions2.4.4Variable Oxidation States2.4.5Ligands2.4.6Colours of Ions2.4.7Stereoisomerism of Complex Ions2.4.8Cisplatin2.4.9Ligand Substitutions & Kstab2.4.10End of Topic Test - Transition Metals2.4.11A-A* (AO2/3) - Transition Metals
2.5

Nitrogen & Sulfur

2.5.1Nitrogen & Ammonia2.5.2Formulated vs Manure Fertilisers2.5.3Nitrogen Containing Fertilisers2.5.4Fertilizers & Eutrophication2.5.5Common Atmospheric Pollutants & Their Properties2.5.6Catalytic Converters2.5.7Atmospheric Oxides
3

Organic Chemistry & Analysis

3.1

Introduction to Organic Chemistry

3.1.1Naming Conventions3.1.2Mechanism3.1.3Isomerism3.1.4End of Topic Test - Introduction to Organic Chem
3.2

Hydrocarbons

3.2.1Fractional Distillation3.2.2Cracking3.2.3Combustion3.2.4Chlorination3.2.5End of Topic Test - Alkanes3.2.6Introduction to Alkenes3.2.7Reactions of Alkenes3.2.8Polymerisation Reactions3.2.9End of Topic Test - Alkenes3.2.10Arenes3.2.11Evidence for Structure of Arenes3.2.12Reactions of Benzene3.2.13End of Topic Test -Arenes
3.3

Halogen Derivatives

3.3.1Properties of Haloalkanes3.3.2Substitution Reactions of Haloalkanes3.3.3Environmental Impacts of Haloalkanes3.3.4End of Topic Test - Halogenoalkanes
3.4

Hydroxy Compounds

3.4.1Types of Alcohol3.4.2Oxidation 13.4.3Oxidation 23.4.4Elimination3.4.5Acids & Esters3.4.6Acyl Chlorides & Acylation3.4.7Phenols & Their Reactions3.4.8End of Topic Test - Alcohols
3.5

Carbonyl Compounds

3.5.1Carbonyls3.5.2Hydrogen Bonding & Carbonyls3.5.3Aldehydes & Ketones3.5.4Tri-Iodomethane Reaction3.5.5End of Topic Test -Carbonyls
3.6

Carboxylic Acids & Derivatives

3.6.1Properties of Carboxylic Acids3.6.2Esters3.6.3Acyl Chlorides3.6.4End of Topic Test - Carboxylic Acids
3.7

Nitrogen Compounds

3.7.1Nature & Preparation of Amines3.7.2Basicity & Nucleophilicity3.7.3Amides3.7.4Reactions of Amino Acids3.7.5Amino Acids
3.8

Polymerisation

3.8.1Properties of Addition Polymers3.8.2Condensation Polymerisation3.8.3Effects of Side-Chains on Polymers3.8.4Hydrolysis of Ester & Amide Groups3.8.5Proteins3.8.6DNA3.8.7Adhesive & Conducting Polymers3.8.8End of Topic Test - Amines & Proteins
3.9

Analytical Techniques

3.9.1Chromatography3.9.2High-Performance Liquid Chromatography3.9.3Gas Chromatography3.9.4IR Spectroscopy3.9.5Uses of IR Spectroscopy3.9.6Mass Spectrometry3.9.7Mass Spectrometry Analysis3.9.8Nuclear Magnetic Resonance3.9.9Carbon-13 NMR3.9.10Proton NMR I3.9.11Proton NMR II3.9.12End of Topic Test - Analytical Techniques3.9.13A-A* (AO2/3) - Analytical Techniques
3.10

Organic Synthesis

3.10.1Chirality & Drug Synthesis3.10.2Organic Synthesis3.10.3Examples of Synthetic Routes3.10.4End of Topic Test - Organic Synthesis

Practice questions on Commercial Application

Can you answer these? Test yourself with free interactive practice on Seneca — used by over 10 million students.

  1. 1
    What's the downside to rechargeable batteries?Multiple choice
  2. 2
    In a lithium cobalt battery:Fill in the list
  3. 3
    Which of these accurately describes what a fuel cell does?Multiple choice
  4. 4
    What is the overall reaction for the alkaline hydrogen-oxygen fuel cell?Multiple choice
  5. 5
    Advantages of fuel cells:Fill in the list
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Electrochemical Series

Nernst Equation