# OPT - Optical Pumping

## Contents |

## Optical Pumping Description (OPT)

**Note that there is NO eating or drinking in the 111-Lab anywhere, except in rooms 282 & 286 LeConte on the bench with the BLUE stripe around it.**Thank You, the Staff.

This experiment is quantum mechanics in action. When a sample of gaseous atoms is placed in a static magnetic field, the electronic states undergo Zeeman splitting in addition to fine-structure and hyperfine-structure splittings. By applying polarized light at the proper frequency, we can induce transitions from ground state levels to excited state energy levels. The atoms then decay to higher ground state levels until we have "pumped" all of them into the same (highest) ground state energy level. At this point we can see an increase in light passing through the sample because no more can be absorbed. However, when we apply a radiofrequency signal of just the right energy to stimulate transitions to a lower level, we see a sudden decrease in the radiation signal as the system is again pumped to the higher level. By determining the frequency of the RF signal we gain information about the atomic energy levels.

You will need to use your knowledge of fine, hyperfine, and Zeeman splitting to find the energy levels of two isotopes of rubidium. You will determine the nuclear spins of the isotopes, and the strength of the earth's magnetic field in the laboratory.

- Pre-requisites: Physics 137B (may be taken concurrently)
- Days alloted for the Experiment:

This lab will be graded 20% on theory, 30% on technique, and 50% on analysis. For more information, see the **Advanced Lab Syllabus.**

Comments: E-mail **Don Orlando**

# Optical Pumping Pictures

Optical Pumping setup Click here to see larger picture |
Optical Pumping Equipment & Coil Click here to see larger picture |
Optical Pumping coils assembly Click here to see larger picture |

# Before the 1st day of Lab

**Complete the following before your experiment's scheduled start date:**

- View the
**Optical Pumping**video.

**Note: **While the OPT video has been a great resource for the students helping them to quickly orient in the lab, it has become apparent that some common misconceptions regarding the experiment stem from some minor inconsistencies in the video. To remedy this, I have compiled an (incomplete) list of corrections below labeled by the time in the video. On a personal note, I am sad that Prof. Sumner Davis, a wonderful warm person, a colleague of many years, and a 111 lab enthusiast is no longer with us to call upon to tweak the video…

**Time code in Minutes for video in Bold:**

**05:26** The ^{2}P_{3/2} state splits into F=3,2,1, and 0 (because J=I=3/2 for ^{87}Rb).

**06:30** The order of the M_{F} sublevels of the F=1 state has to be reversed (because g_{F}=-1/2).

**12:34** The ratio of probabilities is not generally 50:50 (it depends on the specific sublevels involved), but this does not make too much of a difference for the discussion.

**13:05** In the OPT experiment, the atoms are actually pumped into an |M_{F}|=2 sublevel of the F=2 state (in the case of ^{87}Rb).

**14:53** I would say it is wrong to call radio-frequency radiation “light”.

**18:02** It is incorrect to label the horizontal axis “t”.

**20:22** The filter that removes the D2 radiation is not there to get rid of noise. In fact, if one removes the filter, while the same ground state will be pumped, the pumping, however, will not result in the rubidium vapor becoming transparent. This is a finer point of the experiment (of which there are many, most of them being glossed over).

2. **Check points****are examination points that are placed in this lab where you must STOP and call a GSI or professor to make sure you understand what's expected. There could be multiple check points throughout your lab so make sure you don't skip them since there is a sign off sheet that must be turned in with your lab report. There are 3 Checkpoints in this lab.**

3. Complete the **OPT Pre Lab and Evaluation** sheets. Print, fill out with the answers and turn it in with your report. The Pre-Lab must be printed separately. Discuss the experiment and pre-lab questions with any faculty member or GSI and get it signed off by that faculty member or GSI. Turn in the signed pre-lab sheet with your lab report.

4. View the **Error Analysis video **and **Error Analysis Notes**.

**Last day of the experiment please fill out the Experiment Evaluation**

**Suggested Reading: Read carefully Reference; 1, 2, 3, & 4**

- †R.L. De Zafra, “
**Optical Pumping**”, Amer. Journ. of Phys.**28**, 646 (1960). #QC1.A4**Searchable Page** - Reference Rubidium Diagrams
**Rb Energy Levels** - †A.L. Bloom, “
**Optical Pumping**”, Scientific American, October 1960, p.72. #T1.S5 - Experiment 7 report on Optical Pumping
- †N.F. Ramsey,
**Nuclear Moments**, Wiley, 1953. #QC174.1.R31. Advanced treatment. - C.E. Moore. "
**Rubidium**." Atomic Energy Levels Vol. II, National Bureau of Standards, 1952. #QC453.M6 - Detailed description of an experiment on Electron Spin Resonance using optical pumping [
**Experiment setup**]. Must read if you want to work out the first problem in the prelab. - All Optical Pumping References on Library Site
**Physics 111-Lab Library site**

More **References**

You should keep a laboratory notebook. The notebook should contain a detailed record of everything that was done and how/why it was done, as well as all of the data and analysis, also with plenty of how/why entries. This will aid you when you write your report.

## Objectives

- Optical Pumping of Rubidium Atoms, Rb
^{85}and Rb^{87; measurement of the nuclear spins} - Explore Magnetic Hyperfine Interactions of Rubidium
- Observe Zero-Field Transitions
- Confirm Breit-Rabi Equation
- Observe Double Quantum Transitions
- Study Rabi Oscillations
- Measure Optical Pumping pump up and pump down Times
- Study Temperature Dependence of Atomic Parameters
- Navigate through the DS345 Function Generator
- Measure the Energy Differences and Find Resonance Between Zeeman Splitting of Atomic Systems
- Determine the Nuclear Spins of Isotopes
- measure the value of the earth's magnetic field at UC Berkeley and angle at the Lab.
**Spectral Line Shape**

# Introduction

Measuring the energy levels of atomic, molecular, nuclear, and particle systems is a large part of experimental physics. The technique of optical pumping is used to measure the difference between the atomic energy levels with great precision. This experiment uses optical pumping to measure the splitting of the rubidium atomic energy levels when the Rb atoms are placed in a magnetic field. It is relatively simple to make these measurements, so it would be wise to use the opportunity to consolidate what you know and understand about atomic physics and quantum mechanics. You can get a solid appreciation of the physics and how elegant it is from this simple experiment. It also gives you an idea of how congested an actual laboratory set up is compared to how clean and organized the physics looks in a textbook.

Your goal in this lab is to find the resonance frequencies, and thereby measure the Zeeman splitting, of $^{85}Rb$ and $^{87}Rb$ for various magnetic field strengths. From this, you will then determine the nuclear spins of these isotopes and the strength of the Earth’s magnetic field.

# Preparation Before The Lab

Starting with the articles by **Bloom **and **D****e Zafra**, read through the Optical Pumping Reprints. The reprints for this lab are all theoretical, and should be understood before coming to lab. Note, however, that not all of the diagrams or discussions are correct for our experiment: some of the articles discuss only transitions between hyperfine levels, while we have Zeeman splitting as well. Try to keep clear which splittings are which, and which are important for our transitions. See, for example, De Zafra (p.647). (You will also find that there is some variation in notation between the various reprint articles; parsing these differences can be challenging, but it is an important skill to have. Let the consistency of the underlying physics guide you.)

**Definitions**

**As you study, here are some terms to understand (You can find all of the definitions to these terms and how they relate to the lab under the references tab or by clicking here): **

Absorption | Electron configuration | Linear and circular polarizers | Radiative lifetime |

Atomic energy levels | Equilibrium distribution | LS coupling | Relaxation |

Atomic orientation | Fine structure | Magnetic dipole moment | Resonance |

Buffer gas | Helmholtz coil | Maxwell-Boltzmann distribution | Selection rules |

Breit-Rabi equation | Hyperfine structure | Modulation | Spontaneous emission |

Degeneracy | Interference filter | Nuclear spin | Stimulated emission |

Discharge lamp | Larmor frequency | Paschen Bach effect | Spectroscopic notation |

Electric dipole transition | Line width | Quantum numbers | Zeeman effect |

**A. Starting with the Hamiltonian**

$\Large H = - \overrightarrow {\mu_I} \cdot \left ( \overrightarrow {B_J} + \overrightarrow {B_{ext}} \right ) - \overrightarrow {\mu_J} \cdot \overrightarrow {B_{ext}} $ (eq. 1)

where $ \overrightarrow {\mu_I} $ is the nuclear magnetic moment, $ \overrightarrow {\mu_J} $ is the electronic magnetic moment, $ \overrightarrow {B_J} $ is the magnetic field at the nucleus arising from the rest of the atom, and $ \overrightarrow {B_{ext}} $ is an externally applied field, derive the Breit-Rabi law in the low-field case:

$\Large \frac {\nu} {B_{ext}} = \left ( \frac {2.799} {2I + 1} \right ) \quad MHz / gauss $ (eq. 2)

(See Ramsey, for example. [Again, look for any notational differences that may exist; Ramsey lays out his conventions in the text, but some analysis may be required nonetheless.])

Also work out the numerical values of the g-factor associated with the split hyperfine states for ^{85}Rb and ^{87}Rb.

You will be asked to demonstrate this in the Pre-lab discussion, but you should not include it in your lab write up.

**B. Derive the expression for the magnetic field at the rubidium bulb due to the Helmholtz coils:**

$\Large 0.9 \times 10^{-6} \left ( \frac {tesla \cdot meter} {ampere} \right ) \frac {Ni} {a} $ (eq. 3)

where N is the number of turns of the coils, i is the current, and a is the radius of the coils. (Recall that there are $10^4$ Gauss in a Tesla.) Discuss the Helmholtz coil. Why is the field so uniform at the center, both laterally and longitudinally? How inhomogeneous is the magnetic field at the bulb? What are the qualitative and quantitative effects of this inhomogeneity? Are they important in this experiment?

You will be asked to demonstrate this in the Pre-lab discussion, but you should not include it in your lab write up.

**C. What are the effects of Earth’s magnetic field? What would happen if the Helmholtz coils were not perfectly aligned with the earth’s field?**

# Experimental Procedure

Taking data for this experiment is more straightforward than for any other lab in this course. But the experiment deserves more time and thought than most because it illustrates fundamental ideas about quantum mechanics which you probably have only vague notions. Take the time to think about what’s going on, and answer any questions that occur to you. You should know the equipment and how this experiment is connected to make things work. If you understand the signal flow for this experiment then it will be easy to complete.

1. Look over the block diagram (* Figure 1*) and check the connections of the equipment carefully. Make sure you understand what each unit does and that you know the limitations of the equipment (e.g. don’t run the current of the coil higher than 3 A; be sure to understand how the voltmeter and shunt gives you precise current measurements; don’t drive the RF at more than 5 V; don’t heat the bulb over 50

^{o}C; etc.). Inspect and open carefully the Rb light box to see its construction. You can get a better understanding of how the bulb works through the tutorial video and the definitions page. Be particularly careful of the D1 pass filter. It is expensive to replace! All pieces in this unit are already in their proper places.

You will find a large glass bulb in the light box, placed between the Rb lamp and the photodetector. The glass bulb is a Rubidium ABS Cell, Pyrex 80 mm OD sphere filled with Rb + 20 Torr N2 (filled with a thin atomic gas of rubidium in both its naturally abundant isotopes (^{85}Rb and ^{87}Rb)). Rb also resides on the walls of the glass bulb, whence it can be released by heating the glass cell, thereby giving a stronger optical pumping signal. The bulb also contains an inert buffer gas (e.g. helium, neon, or molecular nitrogen). The buffer gas keeps the Rb atoms localized within the volume of the bulb for long times before they diffuse onto the glass walls of the bulb. The bulb may or may not be coated with a thin wax layer (paraffin). The wax keeps the Rb atoms from hitting the glass surface, allowing them to retain their spin polarization for longer, and thereby leading to a longer relaxation time from the optically pumped state.

**The glass bulbs are fragile, expensive, and hard to replace. You should not need to handle the bulb or remove it from the light box. If you feel you need to do this, then please ask one of the laboratory teaching staff for help.**

2. Warning: **Never turn off the plug strip if any of the equipment is powered up.** Turn on all the equipment, starting with the Main switch (lower right-hand corner of the Rubidium Lamp Supply/Coil Driver Panel). Set the Rubidium Supply Output Current for the Rb lamp to approximately 25 milliamperes using the Adjust Knob. (Like much of the experimental apparatus, the Rb lamps at the two Optical Pumping stations are not identical; one may require a higher current to light the lamp [perhaps 30 mA].)

3. When you turn on the [SR560 Voltage PRE-AMP] make sure that the INPUT ‘A’ is selected, the DC/GND/AC button is set to the AC position. To start, set the Gain to 500, LF Roll-off to 0.1 Hz, and the HF Roll-off to 10 KHz. You may have to change some settings to make your signal clear. Also note that if you suddenly lose your signal, i.e. if your scope trace goes to a flat-line, you should press the OL REC (OverLoad RECovery) button. The SR560 requires you to adjust the dynamic reserve and the filter roll-off; set the gain mode to low noise and the roll off to 6 dB per octave for both the high and low pass filters.

4. We will be using a DS 345 synthesized function generator to drive the RF coils in this experiment (see * Figure 1*). Before you begin taking data, it would be wise to familiarize yourself with its capabilities, its limitations, and its interface (see

*and the [DS345 Manual]).*

**Figure 3**# DS345 generator **video on DS345**

**video on DS345**- Try experimenting with the signal modulation capabilities of the DS 345. Connect the modulation output
**(Do Not Terminate)**of the DS345 (on the back panel, see figure 3) to the Ch. 1 (X) input of the oscilloscope and connect the terminated function output of the DS 345 to the Ch. 2 (Y) input of the scope. Set the oscilloscope to trigger off of channel 1 in the “Norm” mode. Set the scope to “Alt” rather than “Chop”. Experiment with different amplitude modulation waveforms, span, and rate settings. You might also try using the X-Y mode of the scope to observe the output of the DS 345 (Function output against Modulation output) but don’t let it confuse you. It is important to have a clear understanding of what the X-Y mode represents and when to use it (the display is called a Lissajous figure).

- Now try frequency modulation. Note that you can’t set the span to twice the carrier frequency or more (the DS345 has trouble making oscillations with zero or negative frequencies). Try different modulation waveforms; look at sine, triangle and ramp modulations. Again, start with the oscilloscope in the linear, time sweep mode. The X-Y mode can also be revealing if you keep in mind what the modulation output represents. (As with AM, in FM, the modulation output gives a 0-5 V representation of the modulation function. Again, zero volts corresponds to the minimum frequency [the carrier frequency minus half the span] and 5 volts corresponds to the maximum frequency [the carrier frequency plus half the span], and so forth.) You should now have familiarized with the DS345 enough for this experiment.

$\checkmark$ __This is a Checkpoint:__**Once you feel you are familiar with the DS345, call over a GSI or Professor and explain what you will be using it for in this lab and show them you are cable of navigating the device. **

__The Effect of Temperature on Signal Strength__

__The Effect of Temperature on Signal Strength__

The temperature controller provides a DC signal to copper wires located inside the apparatus next to the rubidium bulb. The electrical current will radiate in the form of heat from the wires due to the friction of electron interaction ($\frac{dQ}{dt}= I^2R = I^2\frac{\rho l}{A}$) . The greater the current the hotter the wires will get, as the electrons traveling down the wire will feel more of a frictional force. You will notice that the "DC microamp" display of the controller runs both ways. In order to increase the heat you will want to turn the black knob clockwise, shifting the red needle to the left. The greater the displacement of the needle the faster the temperature will rise, you will be able to keep your signal at roughly a constant temperature by adjusting this knob.

Heat the sample to 48 ^{o}C, then turn the heater off to reduce noise, but remember that you want the temperature between 38 ^{o}C and 45 ^{o}C for good data (You will explore this temperature dependence in the following section and the noise associated with it**)**. A reading from the temperature sensor is output to an LED display labeled 'Oven Temperature'. **Make sure the temperature does not go above 55 ^{o}C**; if you start to approach this temperature, turn down the thermostat. The heater has an over-temperature shutoff switch in the heater box. If you over heat the box it will need time to rest and you should call one of the staff.

**Note: If the heater temperature stops, You have over heated the oven.**

**To reset get some cool spray and spray it on the temperature over temperature switch, black in color seen below.**

As mentioned before, heating the glass cell will release more rubidium atoms off the walls of the cell and into the buffer gas in the volume of the cell. The higher vapor density will attenuate the Rb lamp more when it is not optically pumped, and so your detected signal -- the difference in optical transmission through the cell in the presence and the absence of optical pumping -- will be larger. However, as the cell heats up and the vapor density increases, there may be effects, such as Rb-Rb collisions, that reduce the lifetime of the optically pumped electronic state, having the effect of decreasing the strength of your signal.

Take an experimentalist's approach: once you have identified the optical pumping resonance of each of the two isotopes in the following section, explore the variations of the signal with the changing temperature of the cell over the allowed range (from room temperature up to about 55 C as shown below). See what effect this has on the resonance strength and whether or not the value of resonance changes with temperature. The effect may be different for the two rubidium isotopes.

Note: Temperatures for ^{87}Rb may be different. Why? (Note that ^{87}Rb signal peaks at 42^{o}C). Explore these differences.

__Finding Resonance__

**Using the Function Generator to Find Resonance:**

The setup will need to be slightly tuned to find the resonance frequencies of the two isotopes. Initially we will want to induce the Zeeman splitting by driving a DC current through the magnetic coil, power the coils with roughly 1.0 Amp to start with. The strength of the coils will change the spacing between Zeeman levels and will ultimately dictate the resonance frequency needed to induce stimulated emission of the Rb. Next the RF coils shold be set to create the electromagnetic radiation required to induce these emissions. They can be driven using the function output of the DS345. The variation in the opacity of Rubidium gas that occurs when it is optically pumped and then hit by the resonance frequency electromagnetic radiation can be observed through the photodiode. In order to read the signal generated inside the bulb the photo diode's output will need to be connected to the PRE-AMP as the signal of radiation will be very low. It is important to make sure the PRE-AMP settings are as specified before or you will not receive a proper signal. Finally run the output of the PRE-AMP (the amplified photo diode output, see **[Photodiode Data Sheet] **for photo detector operation) to Ch.2 (Y) of the oscilloscope and keep Ch.1 (X) connected to the DS 345’s modulation output. It will be best to observe the results in the X-Y mode of the oscilloscope.

Use the Current knob on the Power Supply to adjust the current and the 10m$\Omega $** shunt**** **to measure it. **Current shunt resistors** are low resistance precision resistors used to measure AC or DC electrical currents by the voltage drop those currents create across the resistance. The **shunt** is a calibrated resistor and is temperature compensated so that its resistance value does not change with a change in temperature (On average the shunt's resistance changes less than 0.002% (or 20 ppm = parts per million) per °C of temperature change). The voltage that develops across the shunt is 10 mV per Amp of current through the coils. The Digital Volt meter reads the millivolt reading. (Note that there is a button on the front of the Digital Volt meter that changes the connections from front to rear of the unit.) This button should be in the front position. A circuit diagram of the set up can be found here. Make a note of the current value that the Multimeter and the power supply give you (the Multimeter displays voltage drop and will have to be converted to current using ohms law).

On the oscilloscope, with the modulation connected to ch1 and the amplified signal connected to ch2, you should see something like what is shown in figure 4. You may see some 60 Hz noise in your signal; adjusting the connections may help minimize the problem. The fault may simply be related to the electronics and not the settings. It is important to recognize the source of this noise if it arises (60 Hz noise is a commonly recurring theme in experimental physics). The function of the modulated signal will ultimately dictate how the oscilloscopes depicts what is happening. Since the frequency modulation serves to sweep a range set by the span of the function generator and output frequencies ranging from $Out_F - \frac{Span}{2}$ to $Out_F + \frac{Span}{2} $ the oscilloscope in XY mode will divide this frequency range amongst roughly 10 divisions along the axis where the Modulation output of the function generator is plugged in starting (with the minimum frequency on the left hand side of the display). Based on this information it should be noted that the span can not be equal to or greater than twice the carrier frequency of the function output [In case the reasoning behind this isn't so obvious see the FM Modulation section in the DS345 Manual]. This, in combination with understanding what the perpendicular axis represents in the XY plot, is useful for determining what the resonance frequencies of the isotopes are. Center the output of the function generator to a frequency close to one that would correspond to the energy difference between two Zeeman levels (You can calculate what this energy difference would be by using the Breit-Rabi equation you found in the prelab), thus inducing spontaneous emission. The signal should be a sine wave with a 10 Hz modulation. Sweep a range you believe will hold the resonance frequencies for the two isotopes, if you have hit the resonance frequency then the figure should look like figure 4. Once you have found the proper range it will be possible to better resolve the image to extract a better estimate of the resonance frequency value. You should ebe able to determine which peak corresponds to which isotope by examining the natural abundance of the two isotopes.

**Using the Helmholtz Coils to Induce a Modulating Frequency to Find Resonance:**

As explained in the introduction video, modulating the magnetic field of the Helmholtz coils is a quicker and more accurate way of finding what the resonance frequency is. That is, we will modulate the coil current and not the RF. The magnetic modulation does not cover as much as the RF modulation did so change the frequency of the carrier so it is closer to the resonance. Turn on field modulation by flipping the “Field” switch on the Coil Driver panel, and turn on the “Phase Out” output with the “Phase Switch”.

__Familiarize yourself with the Coil Driver panel:__ The PHASE ADJUST control on Coil Driver panel changes the phase of the modulation signal seen by the scope (the Phase Out signal) relative to the modulation signal that the rubidium sample experiences (which is the actual modulation in the coil current that changes the phase of the photo-detected signal). Connect the Phase out signal to Ch 1 (X) of the oscilloscope and the amplified photodetector signal to Ch 2 (Y). With the scope in Dual Trace Mode (Both Channels), trigger on EXT/Line Source (60 Hz PG&E power line) and set the time scale to around 2 msec/DIV. You may have to adjust the trigger Level knob to get a stable trace. Now change the phase with the Adjust knob: the modulation signal (Ch. 1) moves because we are changing its phase relative to the 60 Hz line signal that we are triggering on the oscilloscope. Seeing as the oscilloscope is powered by a 60 Hz signal and the detected signal is an effect caused by the rubidium bulb, the Adjust knob does not change the phase of the signal that the sample sees. It is simply a visual effect experienced by the electronics of the system.

After swapping the modulation output from the function generator with the modulation output from the Helmholtz coils (phase out), put the scope in X-Y mode. You should now see the detected signal (Ch. 2) displayed on the y-axis versus the field modulation signal (Ch. 1) on the x-axis.

$\checkmark $**This is a checkpoint and a great time to stop and think about the physics. Discuss the following questions with you partner and once you feel you have a better understanding of what is happening, call over a GSI to sign you off:**

**How you can tell when you have found the resonance condition in this mode? Should there be any symmetry? If so, how should it be symmetrical? Along what axis should the symmetry be found? It is up to you to determine which of the modes (Time Trace or X-Y) gives a more precise determination of the resonance condition–you might consider using both. Try them for repeatability. Discuss your reasoning with the GSI. These values will all be useful when you are estimate your errors using each method. **

**Once you have a good understanding of what is going on, here are some things to explore:**

- Temperature variation of the signal and intensity dependence;
- Signal variation with different voltages (ranging from 0V - 9 V) applied across the Helmholtz coils (Including reverse polarity). How does the resonance change with voltage/current supplied to the Helmholtz coils;
- Refining the resonance frequency measurements:
- This can be achieved using either of the two techniques: fixing the RF frequency and modulating the Helmholtz Coils while varying the current or fixing the current to the Helmholtz coils and modulating the RF signal;
- Pro Tip: It is much easier to fix the RF signal and vary the current of the Modulated Helmholtz coils while looking at the XY mode. It should be possible to get fairly accurate and precise resonance measurements using small span RF frequency modulation; if you have time, you might try retaking your points with this alternate methodology.

- Adjusting the span, rate, phase, carrier frequency, and using a triangle modulation rather than a ramp modulation:
- How sensitive are your resonance measurements to changing these variables? Record the qualitative behavior, and explain it. You should also get a quantitative estimate of the statistical error in you measurement technique; try making several independent measurements of the resonance frequency and see how they vary (See the
**Error Analysis Notes**for further discussion of errors). Are there any possible sources of systematic error? You may want to check that the field is properly aligned; find the field direction meter (vertical compass) and place it close to the center of the Helmholtz coils. See what happens to the magnetized “needle” when you reverse the current or turn off the power supply. You should also get a sense of what effects 60 cycle pick up might have on your measurements. - $\checkmark$
__This is a checkpoint:__**Derive a method for determining this error with your lab partner utilizing the Error Analysis Notes. Discuss this method with a GSI Before Taking Data. You should get a representative sample that at least includes both isotopes (the isotopes have different intensities, so one might expect different error values.**

- How sensitive are your resonance measurements to changing these variables? Record the qualitative behavior, and explain it. You should also get a quantitative estimate of the statistical error in you measurement technique; try making several independent measurements of the resonance frequency and see how they vary (See the
- Turn off the RF generator, and vary the current while looking for a resonance. The field should be on with reverse polarity. Set the field modulation to 100. Set the oscilloscope for a linear internal sweep in the x-direction. The resonance should be found around 0.08 A.( This is known as the Zero Field Resonance.)
- Measure the pumping time at resonance with a square wave amplitude modulation. Apply a DC Current of 1 Amp to the Helmholtz coils and apply the resonance frequency for the more abundant isotope through the RF coils. The PRE-AMP should run to Ch.2 and the modulation output from the function generator to Ch.1. Once the temperature is within optimal range turn off the heater. Apply an AM signal through the signal generator so that the gas reaches equilibrium before each shift in RF amplitude. Measure the rate of change in the signal height when the RF is gated on or off (that is, when the modulation signal goes from low to high or from high to low). Look for the time it takes for the signal to change by 1/e. Which corresponds to the pumping time and which to the relaxation time?
- Remember to take advantage of the scope’s magnification capabilities. The horizontal mode can be set to Mag, with magnifications of x5, x10, and x50. If you observe the relaxation process with a high enough magnification you will see small oscillations in the signal even after you eliminate 60 cycle noise. These are real, physical effects in the relaxation process known as Rabi oscillations. (You should be able to distinguish them from noise by modulating the frequency by small increments, [less than 1 Hz, say]; if they continue to track with the modulation, they’re probably real.)
- Be mindful of the effects the PRE-AMP’s filters and source coupling can have on your signal; adjust them to make sure that your values are real.
- Examine the time constant of the other isotope.

# Analysis

(See **Error Analysis Notes** for further discussion.)

- Make plots of frequency vs. current to help you analyze your data. You should have four sets of data and four lines when you plot them. The individual points, the slopes of the curves, and their axial intercepts have an interrelated significance.
- You have two equations to work with; one is the Breit-Rabi equation (eq. 2), and the other is the field of Helmholtz coils as a function of current (eq. 3). Write down the equations, rearrange them, see how the two isotopes fit in, see how additions or subtractions can help, use both + and – currents. Keep in mind that the B-field in the Breit-Rabi equation is the sum or difference of the field of the Helmholtz coils and the Earth’s field. From equation (2) we have a relation between ν
_{1}and I_{1}, and ν_{2}and I_{2}where the subscripts refer to the 85-Rb and 87-Rb isotopes. From your data determine the best ratio$\frac{\nu_1}{\nu_2}$ and from this deduce the values of $I_1$and $I_2$. Their true values are exactly half-integral. (Are the ratio, and this half-integral expectation, sufficient to determine both nuclear moments?) - Having now determined the values of $I_1$and $ I_2$use equation (2) to determine the value of B at the bulb for one positive and one negative value of the current in the coil. Compare these values with those calculated from the coil dimensions and current. Which values are more accurate? Why? Once you have determined the nuclear spins, the Breit-Rabi equation is as accurate as the numerical constant 2.799, since the nuclear spins must be odd half-integers exactly. The field of the Helmholtz coils is not as accurate as the numerical constant $0.9\times10^{-6}$ since the radii of the copper wire turns are not all exactly the same, and the separation of the coils is not exact. By using the Breit-Rabi equation, you can determine this constant more accurately. Try drawing a line parallel to the frequency axis at a particular current, both plus and minus. What can you learn from the intersections with the curves? Do the same with a line parallel to the current or B axis.
- Perform a line fit on each of your four data sets. For each, find the slope and intercept and there respective errors using the theory and techniques of error analysis as illustrated in Lyons, Data Analysis for Physical Science Students, Section 2.9, page 63ff. (Also see Error Analysis Notes). Show clearly how you do this, with a sample calculation. If you use Excel you must show that you know what the program is doing. In particular, what is R and what influences its value? Don’t just use a data reduction code blindly – you don’t learn anything that way. You might also try a Chi-Square analysis to check whether your data and error estimates are consistent (again, see Lyons). Also, check to see that their slopes are consistent with the values of nuclear spins that you found.
- From the intercepts calculate the earth’s field, and its errors. Ultimately you can have four values for the earth’s field for each isotope. Check to see that all eight values fall within the range of your statistical errors. If they don’t, what might be wrong? Say something about which values you think are the most accurate, and why.
- Explain why there is a resonance at zero field, i.e. the magnetic field generated by the Helmholtz coils and the Earth magnetic field sum up to zero.
- What do you need to know and to take account of, in order to make a rough estimate or calculation of the pumping time to compare with your experimentally measured value?
- Go to the page on data analysis and complete the steps.

**Data Analysis**

**Overview**

**The purpose of the experiment is t**o determine the nuclear spins of the two isotopes $^{85}Rb$ and $^{87}Rb$ [It is known that both spins are odd half-integral values, like 1/2, 3/2, 5/2, etc.] and to measure B_{e}, the Earth’s magnetic field.

We have two rubidium isotopes in gaseous form inside a bulb placed in a magnetic field and subject to electromagnetic radiation. The Earth’s magnetic field also affects the rubidium energy levels and their populations. We set the current in the coil producing the magnetic field, and adjust the radio frequency to produce a resonance condition. The parameters that we either want to change, vary, or to measure are the current, the field produced by the current, and the frequency of the applied RF radiation at resonance. The relevant equations are:

$\Large 0.9 \times 10^{-6} \left ( \frac {tesla \cdot meter} {ampere} \right ) \frac {Ni} {a} $

B_{H}, magnetic field from the Helmholtz coils

i, current in the coils

a, radius of the coils

The value 0.9 is approximate because the radius a is not exactly the same for each of the N windings and we have no simpler way of incorporating this fact.

$\Large \frac {\nu}{B_{ext}} = \frac {2.799} {2I + 1} \quad MHz / gauss $

ν, frequency of applied em radiation

I, nuclear spin of Rb

B = B_{H} + B_{e}, the total magnetic field from the Helmholtz coil and the Earth

This equation is called the “Breit-Rabi” [bright-robby] equation.

**Nuclear Spins**

**Nuclear Spins**

Using the results from the four tables of Resonance Frequency vs. Current, determine the values of the nuclear spins (I) of both the isotopes. This can be accomplished by looking at the same current value, and thus same external magnetic field, and rearranging the Breit-Rabi equation to get a linear equation with a slope dependence of 2I + 1, and an intercept dependent only on the earth’s field. [Sketch 4 straight lines]

Another way of determining the spins is to set the current and take the ratio of the resonance frequencies for the two isotopes, at the same current.

In both methods there will be some errors, but it does not matter because we know that the spins have exact half-integral values. This is a case in which the use of error analysis is unwarranted because the results are unambiguous.

**Earth’s Magnetic Field**

**Earth’s Magnetic Field**

To determine the value of the earth’s magnetic field, we need to find a way to determine $B_H$ exactly, or to eliminate it from the equations. $B_H$ can be eliminated by setting i = 0 and using the frequency intercepts and the Breit-Rabi equation. Recall that the equation for $B_H$ as a function of i is not exact.

There is yet another way to determine the earth’s field. There is a reversing switch on the coil current, to reverse the direction of the field. For the same absolute value of the current, the field must have the same strength, except for possible hysteresis effects. Check for hysteresis by measuring the resonant frequency at a particular current, when the value of current is reached from above (run the current to a max, and then come down to the desired value), and from below (run the current to zero, and then come up to the desired value).

So, at a particular current, measure the resonance frequencies for both positive and negative values of current. Add and subtract the two equations, and get exact expressions for $B_e$ and for the more exact parameter for the relation between current and $B_H$

.

**Errors in the Field**

How do we treat the errors in the value of the earth’s field? Step back a little, and see what data you have and how you can arrange it to make error computation the simplest. Here are several approaches.

- Look at plots of your data. You should have 4 lines, two for each isotope, one with positive current and one with negative current. You can do a least-square fit of each line, calculate the position of the zero-current intercepts, and obtain values for the field. Then you can calculate “errors of adjusted coefficients” using the methods given in Lyons and other references.
- But, by changing negative current points to negative frequencies as well, each isotope has only one plot line and presumably the zero crossing is more accurate. Then there are only two lines to fit, one for each isotope, and the errors can be calculated as described above for adjusted coefficients.
- A still easier method is to use pairs of points with the same absolute values of current, and add the two resulting equations. We then have values of the earth’s field without adjusting any coefficients, and the errors can be calculated as an error of a single parameter, rather than as an error of an adjusted coefficient. We have

$\Large \nu^+ = \frac{ 2.799 \left(|\overrightarrow {B_H}| + |\overrightarrow {B_E}|\right)}{2I + 1}$, | $\Large \nu^- = \frac{ 2.799 \left(|\overrightarrow {B_H}| - |\overrightarrow {B_E}|\right)}{2I + 1}$, | $ \Large \overrightarrow{B_E}| = \frac {1}{2} \left ( \frac { |\nu^+ - \nu^-|}{2.799} \right ) \left ( 2I + 1 \right ) $ |

The standard deviation is calculated as described above in Error of a Single Parameter: Measurement Statistics. Compute the average; compute the differences, square them, add, divide by N(N - 1) and take the square root. Then step back, look at the results, and see if they look reasonable. If not, you’ve goofed somewhere, and must try again.

# Notes and advice from Prof. Budker

- Nov. 19, 2007. The Physics-111 Optical Pumping experiment utilizes radio-frequency transitions between Zeeman sublevels split in energy in an external magnetic field (for example, the field of the Earth). The experiment illustrates how an optical-pumping device can be used as a magnetometer. Another interesting and very important application of optical pumping is atomic clocks. The clocks are based on microwave (rather than rf) transitions which are between the two ground-state hyperfine-structure levels (i.e., the levels with different total angular momentum F). A nice discussion appropriate for the Physics-111 students (particularly those who have mastered the Optical Pumping experiment) is given in an article by James Camparo, "The Rubidium Atomic Clock and Basic Research," Physics Today -- November 2007.
**Last day of the experiment please fill out the Experiment Evaluation**

# References

- J.R. Taylor, Taylor Book 2ed "An Introduction to Error Analysis", Oxford,
- L. Lyons, "A Practical Guide to Data Analysis for Physical Science Students", Cambridge, 1991. #QC33.L9
- James Camparo, “The Rubidium Atomic Clock and Basic Research”, Physics Today -- November 2007
- Carver, Thomas R. "Optical Pumping"; Science: vol. 141, Aug 16, 1963, pp. 599-608.
- Corney, Alan, "The Hanle Effect and The Theory of Resonance Fluorescence Experiments"; Atomic and Laser Spectroscopy, (1977). Pp. 473-533.
- Diagrams of the electronics [Diagrams]
- Check out all the Reprints for this experiment;

Other reprints and reference materials can be found on the Physics 111 Library Site