/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Problem 127 An experimental fuel cell has be... [FREE SOLUTION] | 91影视

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An experimental fuel cell has been designed that uses carbon monoxide as fuel. The overall reaction is $$ 2 \mathrm{CO}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{CO}_{2}(g) $$ The two half-cell reactions are $$ \begin{array}{c} \mathrm{CO}+\mathrm{O}^{2-} \longrightarrow \mathrm{CO}_{2}+2 \mathrm{e}^{-} \\\ \mathrm{O}_{2}+4 \mathrm{e}^{-} \longrightarrow 2 \mathrm{O}^{2-} \end{array} $$ The two half-reactions are carried out in separate compartments connected with a solid mixture of \(\mathrm{CeO}_{2}\) and \(\mathrm{Gd}_{2} \mathrm{O}_{3}\). \(\mathrm{Ox}\) ide ions can move through this solid at high temperatures (about \(800^{\circ} \mathrm{C}\) ). \(\Delta G\) for the overall reaction at \(800^{\circ} \mathrm{C}\) under certain concentration conditions is -380 kJ. Calculate the cell potential for this fuel cell at the same temperature and concentration conditions.

Short Answer

Expert verified
The cell potential for this fuel cell at 800掳C and under certain concentration conditions is approximately 0.983 V.

Step by step solution

01

Convert 鈭咷 to Joules

We are given that the Gibbs free energy change 鈭咷 = -380 kJ. To work with the equation mentioned in the analysis, we need to convert this value to Joules. 1 kJ = 1000 J So, 鈭咷 = -380 * 1000 J = -380,000 J
02

Determine the number of transferred electrons (n)

To find the number of transferred electrons (n), we need to look at the two half-cell reactions: - CO + O虏鈦 鈫 CO鈧 + 2 e鈦 - O鈧 + 4 e鈦 鈫 2 O虏鈦 By multiplying the first half-cell reaction by 2, we will achieve the same number of transferred electrons as in the second half-cell reaction (4): - 2(CO + O虏鈦 鈫 CO鈧 + 2 e鈦) This gives us: - 2 CO + 2 O虏鈦 鈫 2 CO鈧 + 4 e鈦 Now, add the second half-cell reaction: - 2 CO + 2 O虏鈦 鈫 2 CO鈧 + 4 e鈦 - O鈧 + 4 e鈦 鈫 2 O虏鈦 We get the overall reaction: - 2 CO + O鈧 鈫 2 CO鈧 Therefore, the number of transferred electrons, n = 4.
03

Calculate the cell potential (E)

Now that we have the values of 鈭咷 (-380,000 J) and n (4), we can calculate the cell potential (E) using the relationship between 鈭咷, n, F (Faraday's constant), and E: $$ \Delta G = -nFE $$ Rearrange the equation to isolate E: $$ E = -\frac{\Delta G}{nF} $$ Plugging in the values, 鈭咷 = -380,000 J, n = 4, and F = 96,485 C/mol (Faraday's constant), we get: $$ E = -\frac{-380,000 \text{ J}}{4 \times 96,485 \text{ C/mol}} $$ Calculating this expression, we find: $$ E = \frac{380,000}{4 \times 96,485} = 0.983 \text{ V} $$ So, the cell potential for this fuel cell at the same temperature and concentration conditions is approximately 0.983 V.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Gibbs Free Energy
Gibbs Free Energy (\( \Delta G \)) is a vital concept in electrochemistry and thermodynamics. It measures the maximum reversible work that a thermodynamic system can perform. In the context of fuel cells, Gibbs Free Energy helps us determine whether a reaction is spontaneous. A negative \( \Delta G \), as in this case where \( \Delta G = -380\, \text{kJ} \), indicates that the reaction is spontaneous.
This means the fuel cell can potentially generate electricity without needing additional energy sources to drive the chemical reaction.
To connect Gibbs Free Energy to the fuel cell's voltage or cell potential, we use it with other concepts like Redox Reactions and Faraday's Constant. By converting \( \Delta G \) into Joules (since \( 1\, \text{kJ} = 1000\, \text{J} \)), we obtain a value that is convenient for our calculations. This conversion is crucial because it aligns the units for use in further electrochemical formulas.
Redox Reactions
Redox reactions, short for reduction-oxidation reactions, are processes where electrons are transferred between substances. In fuel cells, these reactions are split between two separate compartments, known as half-cells. Each half-cell contains one half-reaction.
  • Oxidation: This occurs when a substance loses electrons. For example, in the CO half-reaction, CO loses electrons to form CO鈧 (CO 鈫 CO鈧 + 2e鈦).
  • Reduction: This involves a substance gaining electrons. For instance, in the O鈧 half-reaction, O鈧 gains electrons to form O虏鈦 (O鈧 + 4e鈦 鈫 2O虏鈦).
To achieve a balanced overall reaction, it's necessary to ensure that the number of electrons lost in the oxidation matches the number gained in the reduction. By multiplying the first half-reaction by 2, both half-reactions transfer 4 electrons, which allows us to sum them up to get the overall reaction: 2 CO + O鈧 鈫 2 CO鈧.
Understanding redox reactions in fuel cells is crucial as it explains how chemical energy is converted into electrical energy, which is the primary goal of these cells.
Faraday's Constant
Faraday's Constant, denoted as \( F \), is quintessential in electrochemical calculations. It represents the charge of one mole of electrons, which is approximately \( 96,485 \text{ C/mol} \). This constant allows us to relate electrical charge to the amount of substance via Avogadro's number.
In the context of fuel cells, Faraday's Constant is used to calculate the cell potential from Gibbs Free Energy. When we assess how many moles of electrons (\( n \)) participate in the reaction, this constant helps translate the thermodynamic properties of Gibbs Free Energy into easily measurable electrical potentials, or voltage, of the fuel cell.
Using Faraday's Constant correctly simplifies the step of translating chemical energy into electrical terms, allowing scientists to predict how efficiently a fuel cell can operate.
Electrochemistry Calculations
Electrochemistry calculations are an essential part of understanding how fuel cells function. They tie together thermodynamic and kinetic aspects of the reactions involved. Armed with key parameters like Gibbs Free Energy, the number of electrons transferred (\( n \)), and Faraday's Constant (\( F \)), we compute the cell potential (\( E \)) of a fuel cell using the formula:\[E = -\frac{\Delta G}{nF}\]
This formula tells us how efficiently the fuel cell converts chemical energy into electrical energy.
  • By plugging in the numbers: \( \Delta G = -380,000 \text{ J} \), \( n = 4 \), \( F = 96,485 \text{ C/mol} \)
  • We get a calculated cell potential of about 0.983 V, indicating the voltage across the fuel cell electrodes when operating under the given conditions.
These calculations help not only in designing effective fuel cells but also in predicting their performance, optimizing their operation, and ensuring they meet energy and environmental goals.

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Most popular questions from this chapter

Consider the cell described below: $$ \mathrm{Al}\left|\mathrm{Al}^{3+}(1.00 M)\right|\left|\mathrm{Pb}^{2+}(1.00 M)\right| \mathrm{Pb} $$ Calculate the cell potential after the reaction has operated long enough for the \(\left[\mathrm{Al}^{3+}\right]\) to have changed by \(0.60 \mathrm{mol} / \mathrm{L}\). (Assume \(\left.T=25^{\circ} \mathrm{C} .\right)\)

Consider the following galvanic cell: a. Label the reducing agent and the oxidizing agent, and describe the direction of the electron flow. b. Determine the standard cell potential. c. Which electrode increases in mass as the reaction proceeds, and which electrode decreases in mass?

A galvanic cell is based on the following half-reactions: $$\begin{array}{ll} \mathrm{Cu}^{2+}(a q)+2 \mathrm{e}^{-} \longrightarrow \mathrm{Cu}(s) & \mathscr{E}^{\circ}=0.34 \mathrm{V} \\ \mathrm{V}^{2+}(a q)+2 \mathrm{e}^{-} \longrightarrow \mathrm{V}(s) & \mathscr{E}^{\circ}=-1.20 \mathrm{V} \end{array}$$ In this cell, the copper compartment contains a copper electrode and \(\left[\mathrm{Cu}^{2+}\right]=1.00 \mathrm{M},\) and the vanadium compartment contains a vanadium electrode and \(V^{2+}\) at an unknown concentration. The compartment containing the vanadium \((1.00 \mathrm{L}\) of solution) was titrated with \(0.0800 M \space \mathrm{H}_{2} \mathrm{EDTA}^{2-},\) resulting in the reaction $$\mathrm{H}_{2} \mathrm{EDTA}^{2-}(a q)+\mathrm{V}^{2+}(a q) \rightleftharpoons \mathrm{VEDTA}^{2-}(a q)+2 \mathrm{H}^{+}(a q) \space \mathrm{K=?}$$ The potential of the cell was monitored to determine the stoichiometric point for the process, which occurred at a volume of \(500.0 \mathrm{mL} \space \mathrm{H}_{2} \mathrm{EDTA}^{2-}\) solution added. At the stoichiometric point, \(\mathscr{E}_{\text {cell }}\) was observed to be \(1.98 \mathrm{V}\). The solution was buffered at a pH of \(10.00 .\) a. Calculate \(\mathscr{E}_{\text {cell }}\) before the titration was carried out. b. Calculate the value of the equilibrium constant, \(K,\) for the titration reaction. c. Calculate \(\mathscr{E}_{\text {cell }}\) at the halfway point in the titration.

An aqueous solution of an unknown salt of ruthenium is electrolyzed by a current of 2.50 A passing for 50.0 min. If 2.618 g Ru is produced at the cathode, what is the charge on the ruthenium ions in solution?

A chemist wishes to determine the concentration of \(\mathrm{CrO}_{4}^{2-}\) electrochemically. A cell is constructed consisting of a saturated calomel electrode (SCE; see Exercise 115 ) and a silver wire coated with \(\mathrm{Ag}_{2} \mathrm{CrO}_{4} .\) The \(8^{\circ}\) value for the following half-reaction is \(0.446 \mathrm{V}\) relative to the standard hydrogen electrode: $$\mathrm{Ag}_{2} \mathrm{CrO}_{4}+2 \mathrm{e}^{-} \longrightarrow 2 \mathrm{Ag}+\mathrm{CrO}_{4}^{2-}$$ a. Calculate \(\mathscr{C}_{\text {cell }}\) and \(\Delta G\) at \(25^{\circ} \mathrm{C}\) for the cell reaction when \(\left[\mathrm{CrO}_{4}^{2-}\right]=1.00 \mathrm{mol} / \mathrm{L}\) b. Write the Nernst equation for the cell. Assume that the SCE concentrations are constant. c. If the coated silver wire is placed in a solution (at \(25^{\circ} \mathrm{C}\) ) in which \(\left[\mathrm{CrO}_{4}^{2-}\right]=1.00 \times 10^{-5} \mathrm{M},\) what is the expected cell potential? d. The measured cell potential at \(25^{\circ} \mathrm{C}\) is \(0.504 \mathrm{V}\) when the coated wire is dipped into a solution of unknown \(\left[\mathrm{CrO}_{4}^{2-}\right] .\) What is \(\left[\mathrm{CrO}_{4}^{2-}\right]\) for this solution? e. Using data from this problem and from Table \(17-1,\) calculate the solubility product \(\left(K_{\mathrm{sp}}\right)\) for \(\mathrm{Ag}_{2} \mathrm{CrO}_{4}\)

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