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A half reaction is obtained by considering the change in oxidation states of individual substances involved in the redox reaction. Often, the concept of half reactions is used to describe what occurs in an electrochemical cell, such as a Galvanic cell battery. Half reactions can be written to describe both the metal undergoing oxidation (known ...
In electrochemistry, the Nernst equation is a chemical thermodynamical relationship that permits the calculation of the reduction potential of a reaction (half-cell or full cell reaction) from the standard electrode potential, absolute temperature, the number of electrons involved in the redox reaction, and activities (often approximated by concentrations) of the chemical species undergoing ...
In electrochemistry, overpotential is the potential difference between a half-reaction's thermodynamically determined reduction potential and the potential at which the redox event is experimentally observed. [1] The term is directly related to a cell's voltage efficiency.
In the reaction between hydrogen and fluorine, hydrogen is being oxidized and fluorine is being reduced: H 2 + F 2 → 2 HF. This spontaneous reaction releases 542 kJ per 2 g of hydrogen because the H-F bond is much stronger than the F-F bond. This reaction can be analyzed as two half-reactions. The oxidation reaction converts hydrogen to protons:
For example, half the water oxidation reaction is the reduction of protons to hydrogen, the subsequent half reaction. 2 H + + 2 e − H 2 {\displaystyle {\ce {2H+ + 2e- -> H2}}} This reaction requires some form of catalyst to avoid a large overpotential in the delivery of electrons.
The half reaction, balanced with acid, is: 2 H + + 2e − → H 2. At the positively charged anode, an oxidation reaction occurs, generating oxygen gas and releasing electrons to the anode to complete the circuit: 2 H 2 O → O 2 + 4 H + + 4e −. Combining either half reaction pair yields the same overall decomposition of water into oxygen and ...
In other words, it assumes that the electrode mass transfer rate is much greater than the reaction rate, and that the reaction is dominated by the slower chemical reaction rate ". [7] [circular reference] Also, at a given electrode the Tafel equation assumes that the reverse half reaction rate is negligible compared to the forward reaction rate.
Using the Eyring equation, there is a straightforward relationship between ΔG ‡, first-order rate constants, and reaction half-life at a given temperature. At 298 K, a reaction with ΔG ‡ = 23 kcal/mol has a rate constant of k ≈ 8.4 × 10 −5 s −1 and a half life of t 1/2 ≈ 2.3 hours, figures that are often rounded to k ~ 10 −4 s ...