Tuesday, April 23, 2019

thermodynamics - Current and reversible heat in battery reaction


In the book Battery Technology Handbook by Kiehne [1] (Google Books) on page 21, equation (32):




The reversible heat effect per time unit can be related to current flow, because each multiple of the cell reaction requires the current amount nF:"


dQrevdt=QrevnFi


with n: number of exchanged electrons; F: Faraday constant (96485 As/equivalent); i: current in A.



Two questions:




  1. How is the current related to nF? current and nF have different dimensions?





  2. How can one derive equation (32)?




References



  1. Battery Technology Handbook, 2nd ed.; Kiehne, H. A., Ed.; Electrical engineering and electronics; Marcel Dekker: New York, 2003. ISBN 978-0-8247-4249-2.


Update in order to respond to comments


I know that ΔG is connected with a reversible process and in principle, your derivation makes sense. My problem lies in the formula:



ΔS=QrevT is a basic thermodynamic relation and the Gibbs Energy is defined as ΔG=ΔHTΔS. So, following your derivation ΔH would be zero. Since this problem is connected with my other question, which is linked in the comments, I would expect two different heat terms, a reversible one and a irreversible one. And from the formulas there, I expect Qrev to be connected only with entropy. Therefore, Qrev=TdGdT rather than Qrev=ΔG as the combination of your equations (2) and (4) implies.


I is quite hard to explain my problem...


There is another way to get to the equation in question, but this seems to be too simple:


Since, ΔGnF=Voltage, TΔSnF=formal Voltage. And VoltageI=P=˙Q=dQdt, equation (32) seems perfectly valid, but this is a kind of a weak derivation.



Answer




How is the current related to nF? current and nF have different dimensions?



nF is the charge C transferred during the reaction, while current i is the rate of charge transfer (dC/dt).


The following is a derivation, now edited to be more rigorous. The equation you provide is an expression for electrical Joule heating, which follows in the steady-state from the expression for the power (rate of work) generated by the battery. From Ohm's law



P=(dwrevdt)=i2R=iE0


where E0 is the (open-circuit) electric potential, i the current, wrev is the reversible electrical work. Note that E0 is the potential when reversible work is done.


Now assume a steady state, with constant P and T constraints, with work done and heat generated cancelling (so that the internal energy U=constant), that is


Qrev=wrev


and therefore also power and rate of heat dissipation equal:


(dQrevdt)=(dwrevdt)=iE0


Now according to the Nernst equation,


ΔG=wrev=nFE0


In the steady-state the dissipated heat is equal to the electrical work, so that, combining (2) and (4), we have that


QrevnF=wrevnF=E0



which leads, combined with (3), to the equation in the book:


(dQrevdt)=iQrevnF




Aside


Note I apply the opposite sign convention for work from that in the OP (apologies) - in the convention I use work is positive when performed on the system (charging a battery is positive work, discharging negative work). This does not affect the result of the derivation, since I apply the same sign convention for heat (for an exothermal process heat is negative).




On ΔH and an alternative (longer) derivation


For a process at constant p, it is common to encounter the expression


ΔH=Qp


However if there is non-PV work, the more general form of this equation is



ΔH=Qp+wnonpV


This expression is general and applies when the process is carried out either reversibly or irreversibly. In differential form,


dΔH=dQp+dwnonpV


Note also that in the preceding derivation non-pV work is electrical.


When the process is carried out reversibly a maximum amount of work is done and


wnonpV,rev=ΔG=ΔHTΔS=ΔHQrev


This leads to the following expression at constant T, equal to that in the linked problem (but note the different work sign convention here):


dΔH=dQrev+dwrev=dΔG+TdΔS


where I dropped the "non-pV" subscript since the work is assumed to be electrical.


Since H is a state function it must be equal for reversible and irreversible processes, and we can equate (a1) and (a2), leading to the following general expression:



dΔH=dQp+dwele=dΔG+TdΔS


which leads finally to


dQp=dwele+dΔG+TdΔS


Taking the time derivative of this equation results in the final expression in the linked problem (making sure to account for differences in the work sign convention):


˙Q=˙Qrev+˙Qirrev=ITdE0dT+I(EE0)


To obtain the equation in this problem it is only necessary to apply the reversibility condition starting from either (a3) or (a4). Starting from (a3),


dQrev=dwele,rev+dΔG+TdΔS


But dwele,rev=dΔG which leads to (somewhat trivially)


dQrev=TdΔS


Taking the time derivative and inserting the Nernst expression for ΔS (twice!) gives



˙Qrev=(dQrevdt)=ITdE0dT=IQrevnF


which is the desired expression. The same result can be arrived at by applying the reversibility condition to equation (a4).


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