Topic 6 of 6
How transition-metal catalysts work
Follow a surface cycle and an electron-transfer cycle.
A-Level 9476 (2026-2027)
Catalysis uses accessible bonding and oxidation states
A catalyst participates in steps and is regenerated overall.
Transition metals and their compounds can offer a pathway with lower activation energy. Their ability to interact with reactant electron density helps surface catalysis; accessible oxidation states help electron-transfer cycles. These are chemical reasons for catalytic activity, not a claim that every transition metal catalyses every reaction.
- Adsorb
N2 and H2 attach to active sites on solid iron. Interactions with the surface weaken their bonds.
- React
Surface species are brought together and react through steps with lower activation barriers than the uncatalysed route.
- Desorb
NH3 leaves, freeing sites for another cycle. Iron is regenerated; N2 + 3H2 ⇌ 2NH3.
In a catalytic converter, transition-metal surfaces also help CO react with NO: 2CO(g) + 2NO(g) → 2CO2(g) + N2(g). Adsorption holds reactants near each other and facilitates bond changes. The catalyst does not change the reaction enthalpy or equilibrium constant.
Worked example
An iron-ion cycle transfers electrons in solution
Explain how Fe2+ can catalyse S2O82- + 2I- → 2SO42- + I2. All reactants and the catalyst are aqueous.
- First: S2O82- + 2Fe2+ → 2SO42- + 2Fe3+. Iron(II) donates electrons.
- Next: 2Fe3+ + 2I- → 2Fe2+ + I2. Iron(III) accepts electrons.
- Adding the steps cancels both iron species and gives the required overall reaction. Fe2+ is regenerated.
- Oppositely charged reactants can meet in each catalysed step, replacing the direct encounter between two anions with a lower-barrier route.
This is homogeneous catalysis using the Fe(II)/Fe(III) pair. A positive overall cell potential establishes feasibility, while the catalyst addresses the kinetic barrier.