Question: You are a research engineer at a start - up company focused on commercializing ultrasensitive silicon nanoscale field - effect transistors ( NanoFETs ) for
You are a research engineer at a startup company focused on commercializing ultrasensitive silicon nanoscale fieldeffect transistors NanoFETs for ion sensing in cells and tissue. Knowing that yourNanoFET devices utilize ntype silicon nanowires that show a k electrical resistance and ohmic metalsemiconductor contacts ie no electronic energy barrier at the metalsemiconductor interface complete the following.
a You have engineered NanoFETs sensitive to pH by chemically modifying the silicon surface with amine groups that have an isoelectric point of ie the pH when the surface is neutral Knowing that each pH the NanoFETs show a change in the
nanowires electrical resistance, plot out using MATLAB or another plotting program you are familiar with a representative current vs time trace as one of your NanoFET devices moves from outside a cell pH to inside a cell pH and then back to outside over a s measurement time. Assume that the sourcedrain voltage is held
constant at V
You have now engineered NanoFETs unmodified silicon surface capable of detecting individual viral nanoparticles. Knowing that the surface of viral nanoparticles is predominantly capped by lysine groups isoelectric point plot using MATLAB or another plotting program you are familiar with a representative current vs time trace for viral nanoparticles binding to the surface of the NanoFET in two different solutions one at a pH of the other at Assume i that at pH and a single viral nanoparticle causes an and change, respectively, in the nanowires electrical resistance when bound to the nanowire surface, ii the sourcedrain voltage is held
constant at V and iii the NanoFET detects binding events cumulatively over a second sampling time at each pHNote: you will be generating different current vs time traces, one for each pH; they can both be plotted on the same graph.
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