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A linear sweep voltammetry was obtained as follows from an electrode of porous carbon with an aqueous solution of sulfuric acid. The potential was swept

A linear sweep voltammetry was obtained as follows from an electrode of porous carbon with
an aqueous solution of sulfuric acid. The potential was swept at 100mVsec-1 in the range
where there were no faradaic reactions. The governing equation is described by: I=vC[1-
exp(-t) with v= scan rate, C= capacitance and t= time constant.
time (msec)
(a)[10 points] Calculate the values of electric double layer capacitance, solution resistance and
time constant of the non-faradaic reaction.
(b)[5 points] Calculate the % portion of current at time = time constant versus a saturated
current that can be obtained at an infinite time.
(c)[5 points] Think about the same non-faradaic process with a solution resistance at twice the
value of the above system. Indicate the point at time = time constant for this new
electrochemical system in the above figure.
(d)[10 points] Draw a plot of potential versus time when a fixed current is applied for the
system of (a) at 1mA and 2mA. Use the following empty graph.
ideal gas constant (R)=8.314JmolK
RTF at room temperature =26mV
M=molL=10-3molcm3
Faraday constant (F)=96500Cmole
ln(0.05)=-3,log(e)=0.434. EC2b EAnal.Overview [30 points]A linear sweep voltammetry was obtained as follows from an electrode of porous carbon withan aqueous solution of sulfuric acid. The potential was swept at 100 mV sec-1 in the rangewhere there were no faradaic reactions. The governing equation is described by: I = v C [1-exp(-t/)] with v = scan rate, C = capacitance and t = time constant.(a)[10 points] Calculate the values of electric double layer capacitance, solution resistance andtime constant of the non-faradaic reaction.unit valueCapacitanceResistanceTime constant(b)[5 points] Calculate the % portion of current at tim e = time constant versus a saturatedcurrent that can be obtained at an infinite time.
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