In the early twentieth century, physicists found themselves surrounded by many physical observations that could not be explained by Classical Mechanics – including the optical spectra emitted by atoms and molecules, blackbody radiation, and the photoelectric effect. It was a time in which the models proposed by theorists (like Einstein, Bohr, and Plank) influenced the tests carried out by experimentalists (like Franck and Hertz)… and vice versa.
Only through this back and forth (observation, modeling, testing, revision, etc.) did Quantum Mechanics emerge as the explanation of the universe that we rely on today.
The Franck-Hertz Critical Potential experiment is the first direct measurement of electron transition energies in atoms. Though there had been significant previous work measuring the discrete wavelengths of light emitted by hot gases and models for the quantization of light into photons, it was not until these results (and, in fact, not until the reinterpretation of these results, since Franck and Hertz initially drew the wrong conclusions) that physicists had clear evidence of the connection between wavelength, frequency, and energy in light: $E = hf = hc/\lambda$.
By the end of this experiment, students are expected to be able to do the following:
Technical:
Data Collection:
Analysis:
Students will gain exposure to and practice with the following topics:
Experimental topics covered:
Physics topics covered:
To prepare for each lab this year, you will be asked to read over some preliminary information (theory, background, motivation, etc.) and answer some questions. This prelab assignment will be included on all experiments, but the questions and readings will be tailored to each experiment to make sure you are prepared to start working as soon as you get to lab.
Before coming to lab, read the information below and complete the exercises that follow in a separate document. You will not be graded on whether you get every question correct, but you will be evaluated on whether you made a satisfactory effort to complete these questions before lab.
The prelab assignment is due before lab begins and should be submitted to Canvas. There are no exceptions. (For example, if your lab begins at 1:30 pm and you submit at 1:31 pm, you will receive zero credit.)
In 1900, Max Planck attempted to establish a firm theoretical foundation for understanding the blackbody radiation spectrum. In order to do so, he reluctantly introduced the idea that electrons in the walls of a black body cavity emitted energy (in the form of light) that was quantized in multiples of some elementary unit. Despite this quantization of energy, Planck still believed that the light traveled outward in a continuous wave.
In 1905, in his study of the photoelectric effect, Albert Einstein found that more generally any traveling light wave (not just that emitted by blackbody radiation) is composed of these discrete chunks. Together, their work established that photons of light carry energy $E=hf = hc/\lambda$, where $f$ is the frequency of the light, $\lambda$ is the wavelength, $c$ is the speed of light, and $h$ is now called Planck's constant.
In 1913, Niels Bohr introduced his model of the hydrogen atom, which included the concept of discrete (quantized) energy states. In Bohr’s model, transitions from one energy state to another would help explain the discrete lines observed in the emission spectra of the elements. However, when measuring spectral lines with a diffraction grating spectrometer (assuming a wave nature of light), one is measuring wavelengths, not energies. Therefore, the relationship between energy and wavelength (or frequency) still remained only theoretical, not tested by experiment.
In 1914, James Franck and Gustav Hertz demonstrated that atoms in a gas may absorb energy due to collisions with electrons and that this transfer of energy always occurs in discrete, measurable amounts. At the time of their work, Franck and Hertz were apparently unaware of Bohr's findings, and the only mechanism known to them for such energy transfer was ionization (i.e., the complete removal of an electron from the atom). As a result, their initial interpretation of the results was incorrect.
With time, however, the correct interpretation emerged. If atoms absorb energy from the electrons in discrete and measurable chunks, and the wavelength of the subsequently emitted light can be measured, then the relation between the energy and wavelength of photons can be determined. Thus, the Franck-Hertz experiment is a crucial link which lends credibility to the Bohr atomic model and the Planck-Einstein quantum hypothesis. For this work, Franck and Hertz were awarded the 1925 Nobel Prize in Physics.
In the version of the Franck-Hertz experiment presented here, electrons with charge $e$ are boiled off a hot cathode and accelerated by a potential difference, $V_a$. From classical physics, with no radical (quantum) assumptions, these electrons have energy $E=eV_a$. These electrons pass through helium gas (mercury gas in the original apparatus). If the electrons have sufficient energy to excite the helium atoms, the electrons lose energy and are attracted to a collector ring, where they are detected as a current. Thus, we expect certain energies to cause increases in current. We shall see!
The original Franck-Hertz apparatus was a vacuum tube containing a drop of mercury in equilibrium with mercury vapor. The mercury vapor pressure was controlled by an oven.
In our setup, we instead will use a vacuum tube containing low-pressure helium gas. The geometry of the modified Franck-Hertz tube is shown in Fig. 1. This apparatus eliminates the need for a temperature-controlling oven.
Mounted within the vacuum tube are the following:
The anode is held at a potential, $V_a$, which is more positive than the cathode. Thus, electrons generated at the cathode are accelerated to a kinetic energy of $K = eV_a$ by the time they reach the anode can. In the absence of any collector ring potential and with no helium atoms present, the electrons would continue, undeflected, to the inside of the glass tube. However, since the collector ring is held at a potential 1.5 V more positive than its surroundings, the electrons are attracted toward the collector ring as they pass it. The aperture of the anode cylinder is such that these electrons would miss the collector ring.
In our experiment, we will increase $V_a$ linearly with time. Thus, the electron energy will also increase with time. Collisions between electrons and helium atoms will occur, but as long as the electron energy is less than an atomic excitation energy, these collisions will not result in significant energy absorption by the atom. Electrons scattered in this manner (elastically) are relatively unlikely to reach the collector ring, since they will have energies nearly equal $V_a$.
An electron whose energy is reduced to less than 1.5 eV by exciting a helium atom will be attracted to the collector ring, and will contribute to a measured negative current. On the other hand, electrons not exciting atoms will miss the ring and continue to the anode on the inner surface of the tube.
A note on mean free path:
The helium pressure and the geometry of the tube play a linked role in the design of the apparatus. The mean free path is defined as the average distance an electron must travel between collisions with helium atoms. Thus, the mean free path is determined by the helium pressure.
In this tube, the helium pressure has been set so that there is a small probability of collision in the region between the cathode and the cylindrical anode (where the electrons are being accelerated), but a large probability for a collision thereafter (where the electrons are traveling at constant speed). Thus, when the collisions take place, the electron energy is well known.
A note on the work function and contact potential difference:
As electrons leave or enter a metal surface, they are subject to electric field gradients due to the charges present in the metals. The potential barrier caused by these field gradients is called the work function of the metal. Work functions differ for different metals. In our tube, electrons leave the cathode and enter the anode, and will experience field gradients at both interfaces. The net effect of these gradients is called contact potential difference (CPD). The CPD will effectively increase or reduce the accelerating voltage, depending upon their signs and magnitudes.
Table 1 gives the wavelengths emitted by transitions from the lower excited states to the ground state of helium. It is important to note that these wavelengths were measured spectroscopically. Only later were they converted to energies using the Planck relation, $E = hc/\lambda$.
Recall that, at the time of the Franck-Hertz experiment in 1914, the Planck relation was only an assumption, used to “fudge” the black-body theory. An independent method to measure energies was needed to verify the Planck relation. You are here to measure those energies!
For the hypothetical atom in the prelab, we ignored the spin of the electron. Here, it will be important to keep track of the spin because the orientation of one electron (relative to the other) adds an additional small separation in the energy levels.
In Table 1 below, we are using the expanded spectroscopic notation $n^{2S+1}L$, where $n$ is the principle quantum number, $S$ is the total spin, and $L$ is the angular momentum quantum number (such that S is L = 0, P is L = 1, and D is L = 2). In this notation, an excited state $n^3L$ is an orthohelium state and $n^1L$ is a parahelium state.
Excited state ($n^{2S+1}L$) | Wavelength (measured by spectroscopy), $\lambda$ (nm) | Energy (calculated), $E = hc/\lambda$ (ev) |
---|---|---|
$2^3S$ | 62.559 | 19.82 |
$2^1S$ | 60.143 | 20.62 |
$2^3P$ | 59.144 | 20.97 |
$2^1P$ | 58.435 | 21.22 |
$3^3S$ | 54.576 | 22.72 |
$3^1S$ | 54.095 | 22.92 |
$3^3P$ | 53.891 | 23.01 |
$3^3D$ | 53.740 | 23.07 |
$3^1D$ | 53.740 | 23.07 |
$3^1P$ | 53.706 | 23.09 |
$4^3S$ | 52.551 | 23.59 |
$4^1S$ | 52.375 | 23.67 |
Ionization ($\infty$) | – | 24.587 |
Table 1: Energy levels and resonance energies of helium. |
These wavelength measurements were taken originally from the book A.R. Striganov, N. S. Sventitskii, Tables of Spectral Lines of Neutral and Ionized Atoms, 1968 (a.r._striganov_n._s._sventitskii_-_tables_of_spectral_lines_of_neutral_and_ionized_atoms_-_1968a.pdf), and are quoted (along with energy calculations) in N. Taylor et. al., “Energy levels in helium and neon atoms by an electron-impact method”, Am J Phys 49(3), March 1981 (franck-hertz-ajp.pdf).
The ionization energy is taken from the NIST Atomic Spectra Database and truncated to three decimals. That measurement is from a 2011 paper(Extreme Ultraviolet Frequency Comb Metrology) and is precise down to better than than 1 part in 1,000,000,000.
Consider a hypothetical atom that has the following electron energy diagram.
Recall that when designating an energy level as nL, n represents the principal quantum number and L represents the orbital angular momentum quantum number. For historical reasons, L is not written as a number but as a letter following the convention $S$ for $L = 0$, $P$ for $L = 1$, $D$ for $L = 2$, and $F$ for $L = 3$. These electron clouds have different shapes (or distributions) which mean that different L orbitals have slightly different energies, even within the same principal energy level.
In order for an electron in the ground state (1S) to be excited to one of the higher energy states, it must receive an amount of energy $\Delta E$ equal to the difference between its initial (ground) and final (excited) state.
Now suppose that our critical potential tube (as illustrated in Fig. 1) is filled with this hypothetical gas (instead of helium). You collect the following data.
You are expected to keep a record of your work in a permanent lab notebook. There is no exact formula for what should go into a lab notebook. A good rule of thumb is to record everything which you would need to refer back to if you wanted to exactly reproduce your experiment at a later time, or that you might need to know when writing a paper on your results or explaining to a colleague what you did and how you did it.
For this experiment, you will need to first make sketches of the wiring and apparatus setup, and record voltages and equipment settings while you test that the apparatus is functioning correctly. Once you are concentrating on collecting data, you will need to make sketches of your scope traces, record the accelerating voltage ranges and scope settings, and keep track of scope readings and/or saved files. After you leave the lab and sit down to do your analysis, you likely will not remember all of these details, so it it critical to record them.
We recommend (highly!) that while you are in the lab collecting data you should be doing calculations and making quick plots of the data in order to evaluate how things are going and ascertain any corrections you may need to make. These calculations and plots should all go into your lab notebook.
The Hertz tube console is used to control the accelerating potential, $V_a$, and read the current from the collector ring. The accelerating voltage is supplied as a sawtooth ramp of frequency 20 Hz.
Note that a few control consoles have a design difference where outputs 3 and 4 have a proportionality constant of 1/2000 instead of 1/1000 such that $V_3 = V_{a, max}/2000$ and $V_4 = V_{a, min}/2000$. These devices are clearly marked with this difference.
A separate DC power supply provides current to the filament and a 1.5 V battery supplies a small potential to attract electrons to the collecting ring. A digital oscilloscope is used to view and measure the current in the collector ring and the accelerating voltage, $V_a$.
A full wiring diagram is shown in Fig. 2. However, rather than connect everything at once, it will be more instructive to work through the logic of the connections step-by-step.
Multimeters
To begin, connect the two digital voltmeters that monitor the $V_{a,min}$ and $V_{a,max}$ values produced by the console.
If everything is connected correctly, you should be reading voltage values from the two outputs in the range from 0 to 60 mV. Adjust the MAX and MIN control knobs and observe how the voltages change.
Oscilloscope
Next, connect the FAST Outputs 1 and 2 to oscilloscope Channels 1 and 2 in order to monitor the $V_a$ ramp voltage and the ring collector voltage, respectively. (We will not use the SLOW outputs on the console.)
At the moment, Channel 2 should be a flat signal at 0 V (as the collector ring is not yet attached to the console). However, Channel 1 should display a sawtooth voltage signal with a frequency of 20 Hz (or period of 1/20 Hz = 50 ms).
You may notice that the voltages displayed on the oscilloscope at the maximum and minimum of the ramp do not match the voltages you read on your meters ($V_3$ and $V_4$), nor do they match the actual $V_a$ maximum and minimum values. As a result, you will need to calibrate; when you collect data, you will record scope voltage measurements $V_{scope}$, but you will need to determine a conversion formula between those values and the actual $V_a$.
You may want to discuss your results with a TA before moving on.
Now connect the tube to the console.
With the filament power supply OFF, connect the supply to the tube base.
Do not turn the power supply on yet. It is possible to damage or destroy the filament by running too much current.
Do not connect any wires to the ground (green) jack on the power supply. The ground of the power supply (which is connected to the third prong in the wall outlet) is different from the ground potential of the console.
Next, connect the anode and cathode to the $V_a$ ramp…
In order to maintain the ring collector at +1.5 V relative to the anode, connect a AA battery between the anode and ground.
Finally, connect the ring collector to the console.
With the ring current now connected to the console, you should observe a signal on Channel 2 of the oscilloscope. (Zoom in if the signal still appears flat.) The signal will likely be noisy (and may also have a periodic component with a frequency of 60 Hz) because the ring is collecting any stray electrons from the room which pass through the tube near the ring. In order to suppress this background noise, we can use a grounded shield which will intercept these electrons and direct them to ground (instead letting them pass through the tube to be picked up by the ring).
With the shield in place, the signal on the scope should now be much less noisy (though likely still not quite flat).
Before turning on the filament, we need to make one more adjustment to the oscilloscope. Under the Channel 2 menu, select Invert: On. This will multiply the voltage measured on Channel 2 by -1 (thus inverting the signal). By the manufacturer's conventions, the collector ring current circuit is outputs a negative voltage (proportional to current), though it will be more intuitive to look at and interpret the signal as a positive voltage (current).
It is now time to turn on the tube and begin to look for critical potential dips.
If the observed signal is already smooth, it may be possible to make out all the details already. However, if the signal is noisy, you may want to implement averaging. (To turn averaging on, select Acquire: Average: N where N is the number of trigger events the scope will average over. You may need to select N = 16 or 64 if your signal is especially noisy.)
A light on the front of the power supply will indicate whether the power supply is in constant voltage (CV) or constant current (CC) mode.
If you have no need to limit a voltage or current, then you can turn one of the knobs up to maximum and control the power supply by the other knob. (Typically this means CV mode… so turning current to max and using the voltage knob to adjust.)
If, however, you wish to limit a voltage or current (for example to prevent a fuse from blowing or to protect a sensitive circuit), then you can turn the corresponding knob down to a lower lower level.
In this experiment – where we wish to make sure we never exceed about 1.2 A of current – we can set this limit by slowly turning up the voltage knob until we reach a reading of about 1.2 A. Then, we can slowly turn down the current knob until the light on the front of the supply changes from CV to CC. At that point, the supply is now limited to about 1.2 A and you should not be able to exceed that amount no matter what the voltage setting.
You should notice that there are two or three groups of small peaks superimposed on the positively increasing collector ring signal. These peaks represent increases in the collector ring current that occur when the accelerated electrons have just enough kinetic energy to excite an electron in a helium atom from the ground state up to one of the excited electronic levels. After colliding with the atom and giving up this energy, the electron (now with $K=0$) is attracted to the ring.
First, the flux of electrons emitted by the filament wire increases as the accelerating potential increases. The electron current density, $J$, (in units of current/area) is given by a formula known as Child's Law,
$J = k V_A^{3/2}$, |
where $k$ is a proportionality constant that depends on the mass of the electron, the charge of the electron, and the separation distance between the anode and cathode.
Child's law is a consequence of the space charge limiting effect. The first electrons to be emitted from the filament when it is heated form a “cloud” around around the wire known as space charge. The negative electric potential created by this cloud makes it harder for future electrons to be ejected. However, as the potential between anode and cathode is increased, this repulsive effect is reduced, leading to the increase in the flux of electrons emitted.
Second, even though the trajectories of the accelerated electrons form a cone that does not intersect with the collection ring (see Fig. 1), it is always possible that an electron undergoes an elastic scatter off a helium atom and changes direction. As the flux of electrons increases, the number of electrons that are randomly scattered into the collection ring increases proportionally.
Therefore, since the electron flux increases as $V_A^{3/2}$, the background upon which the peaks appear also should increase as $V_A^{3/2}$.
As was the case in the prelab question, the first set of peaks corresponds to the minimum energies required to excite an electron from the ground state of helium up to one of the possible excited states. As there are many possible excited states, there are many possible excitation energy peaks… though just as in the prelab, some of these energies may be so closely spaced that we can't distinguish them as separate and they instead merge together into one peak.
We will spend more time on Day 2 investigating these individual dips, but for now let's focus just on the first dip (as the mark of the beginning of these possible excitations).
For the second set of peaks, the interpretation is a bit more complicated. Here, electrons have enough energy to excite two different atoms.
Given the complexity of this spectrum, we won't try to identify each peak. Again, for now let's focus just on the first dip (as the mark of the beginning of these possible two-atom excitations).
Adjust $V_{a,min}$ and $V_{a,max}$ so as to zoom in on the group of peaks at the lowest $V_a$ on the scope. (You may have to adjust the scope trigger level to keep the peaks centered on the display.) If the peaks are weak, adjust the filament voltage – without exceeding 1.2 A – to maximize the number of peaks visible in this group. Adjust the voltage scale on Channel 2 so that the peaks fill as much of the display as possible. If needed, average over trigger events to capture a spectrum of peaks and the accelerating voltage ramp.
As you will have to interpret your signal for the analysis, you should stop and make sure you can answer the following questions.
Speak with a TA if you aren't sure. Save screenshots of your signals (by using the scope transfer or USB thumb drive procedures introduced in the Scope Exercises lab). You may also want to save the raw scope data csv files (t vs. V for channels 1 and 2). Make sure to capture at least the three following scenarios:
In your analysis, you will need to visually identify features in the signal. Make sure you have what files you need before leaving the lab.
Recall from the note in the introductory material that “as electrons leave or enter a metal surface, they are subject to electric field gradients due to the charges present in the metals. The potential barrier caused by these field gradients is called the work function of the metal. Work functions differ for different metals. In our tube, electrons leave the cathode and enter the anode, and will experience field gradients at both interfaces. The net effect of these gradients is called contact potential difference (CPD). The CPD will effectively increase or reduce the accelerating voltage, depending upon their signs and magnitudes.”
This means that the voltage corresponding to the first peak in the first set of peaks does not actually correspond to the true accelerating voltage for that electron; it instead is the true potential plus the CPD (which may be positive or negative). If we designate the measured voltage of the first peak in the first set as $V_0$, the contact potential difference as $V_{CPD}$, and the true voltage of the first transition as $V_{0,true}$, we have the relation
$V_0 = V_{0,true} + V_{CPD}$. | (1) |
Thinking now about the second set of peaks, the measured voltage of the first peak in that group is (using the same subscript conventions)
$V_0^{\prime} = 2V_{0,true} + V_{CPD}$. | (2) |
Putting Eqs. (1) and (2) together, we can solve for the true voltage required for the transition as
$V_{0,true} = V_0^{\prime} - V_0$, | (3) |
and then solve for the CPD as
$V_{CPD} = V_0 - V_{0,true}$. | (4) |
or in terms of measured quantities,
$V_{CPD} = 2V_0 - V_0^{\prime}$. | (4.5) |
Once the CPD is known, you can now correct the systematic offset in the measurement of the peak positions in the first group.
Collect data from both the first and second sets of peaks as needed to compute the contact potential difference (as described above).
Check with a TA if you need help with these tasks.
You now have some preliminary data to explore. Just as in a professional research lab, your work is not done yet. Analyze what you have (keeping in mind that we are not looking for the right answer… or even the complete answer yet.) The results of your analysis will likely generate new questions, and you will be able to use Day 2 to make improvements, repeat measurements, extend your experiment, or… do all of the above.
Complete the following set of analysis exercises and submit by 11:59 pm the day before you are due back in lab. Do not respond in bullet points or isolated text; respond in full sentences and paragraphs, and format your responses appropriately. Because this is your first analysis for the class, we have tried to be very explicit in what we are looking for and have provided prompting questions.
For each item below, include whatever data, plots, calculations, etc. you used in your determination. (If something is used in more than one item, you do not need to present it each time; you may reference plots, data, equations, etc. that you provided earlier in the analysis if that is appropriate.)
When we ask you to do something for your analysis that you have not done before, we will try to provide you with more explicit guidance so that you understand what we are looking for (and so we can model how a professional physicist thinks through the discussion of different types of results).
For this analysis, the item most likely to be new to you is the requested “discussion of your calibration”. In discussing a particular experimental procedure like calibration, the goal is to make clear to the reader both why you performed a calibration and how you performed it.
Some things to consider include the following:
The above is not a bullet point checklist to be filled out; we are looking for you to articulate clearly and concisely the what, why and how of your calibration. The better you understand what you were doing, why you were doing it, and how you did it… the easier this task will be.
More generally, whenever describing procedure or attempting to justify or explain a technique, keep the following in mind:
On Day 2, you will repeat your data collection, implementing any changes you want to make based on the results of your previous analysis. In addition, you will dig down into the details of signal in order to measure individual peak positions and try to identify the different possible excitation energies.
You may wish to remind yourself of the expected helium electron transitions shown in Table 1 (in the “Helium transition energies” dropdown in the “Before you come to lab…” section) before beginning.
You will collect a fresh set of data. Are there any changes you want to make from how you collected data on Day 1? For example…
Even if you are completely happy with your data and data collection strategy from Day 1, you should collect a fresh set of data. If nothing else, it will give you a feeling for how reproducible the results are or how results may fluctuate from day to day (or from apparatus to apparatus).
Rewire your apparatus and adjust your settings to recover the helium excitation signal you saw on Day 1. Once you have a clear signal, zoom in on the first set of dips and optimize your signal.
You likely noticed on Day 1 (and if not, you can look at your trace now) that the peaks are not sharp delta functions, but instead have some “width” to them. This limits how close together two features can be before the cease to be resolvable (i.e. distinguishable as two separate features instead of one single feature).
There are several valid definitions of resolution, but for this experiment we will define is as the full width at half-maximum (FWHM) of that peak. It is useful to measure (or otherwise predict) the resolution of your measurement apparatus so that you know the limitations of what data you can collect.
To determine resolution…
NOTE: Since the FWHM value is small, the voltage ramp difference will also be small. You will likely need to to zoom in quite a lot on Channel 2 (the $V_a$ voltage ramp) so that it covers more of the height of the scope screen. If you attempt to make a measurement without zooming in, the voltage difference may appear to be zero).
Now consider the following:
Next we wish to identify as many helium excitation energies as we can.
In addition, we can make a (somewhat crude) estimate of the helium ionization energy. (This is the energy required to eject an electron completely from the atom instead of exciting it from ground to some intermediate state. You may find it helpful to think of the ionization energy as the energy required to excite the electron from its ground state to the $n = \infty$ state.)
Look at the end of the first set of peaks. Where does the series of peaks end? Does there appear to be a slight “kink” in the background at this point (where the background appears to increase slope)? This marks the onset of ionization (where we begin to collect some of the low-energy electrons ejected by helium in addition to electrons randomly scattered into the collection ring).
Collect data (and save scope traces or screenshots) as needed to complete the following:
Check with a TA if you need help with these tasks.
While we are able to get a crude estimate of the ionization energy from the signal we have been looking at, there is another trick we can use. If the 1.5 V potential between the anode and the collecting ring is reversed – so that the collecting ring is now 1.5 V negative relative to the anode – the apparatus will collect positively charged ions instead of low energy electrons. When $V_a$ reaches the ionization potential (i.e., accelerated electrons have enough energy to eject an electron completely from a helium atom), the resulting positively-charged helium ions will be collected by the negatively biased collector ring.
To measure the ionization potential, reverse the 1.5 V battery in its holder so that the positive terminal is now connected to the tube anode. Observe the signal on the scope and adjust $V_{a,min}$, $V_{a,max}$, and the filament voltage until you obtain a signal from the collector ring with the features shown in Fig. 4.
NOTE: Because the particles collected by the ring have opposite sign from earlier (positive ions instead of negative electrons), the current produced by the ring also has an opposite sign. You may wish to undo the inversion of your Channel 2 signal (i.e., select Invert:Off in the Channel 2 menu) so that your current signal is again a positive-definite value.
At accelerating voltages below $V_0$ (the energy corresponding to the lowest electron excitation energy), your current signal will likely be flat or nearly flat. As $V_a$ increases from $V_0$ to $V_{ion}$, the signal will increase as some helium atoms are ionized in the following two collision process: the first collision puts the atom in a metastable excited state and then – before the atom can decay back to the ground state – a second collision knocks the electron out of the excited state, ionizing the atom. (This ionization of the metastable state is not what we are trying to measure.) The abrupt change in slope that occurs at $V_{ion}$ represents the onset of ionization from the ground state.
Collect data as needed to determine the ionization potential. You may need to adjust $V_{a,min}$ and $V_{a,max}$ in order to get close to the ionization point to observe the “kink” in the slope of the current.
Check with a TA if you need help with these tasks.
For your Day 2 analysis, complete the following set of analysis exercises and submit by 11:59 pm the day before you are due back in lab. Note that some of the tasks are identical to Day 1, but you should use your Day 2 data here (and any improved data collection or analysis methods you wish to apply).
For each item below, include whatever data, plots, calculations, etc. you used in your determination. (If something is used in more than one item, you do not need to present it each time; you may reference plots, data, equations, etc. that you provided earlier in the analysis if that is appropriate.)