Difference between revisions of "Electron Spin Resonance"

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==Experimental setup==
==Operating instructions==
==ESR measurements==
==Desired and future ESR setup==

Revision as of 00:01, 22 November 2014

Electron Spin Resonance (ESR) is a phenomenon, usefull for the investigation of materials which contain unpaired spins. Those are caused by various sources. One are not completely filled atomic shells, however, the more interesting ESR signals arise from different circumstances combined in the term defect. For instance, a important one is impurities of semiconductors or isolators which can trap electron or holes. Therefore this measuring technique is very powerfull evaluation of material properties and is used in lots of research fields in physics, chemistry and biology.

Physical background

Precession of the two Quantum Vectors  \vec{S} and  \vec{\mu_S} around the magnetic field  \vec{B_Z}

As the term Electron Spin Resonance already implies, the most essential part of the entire topic is the Spin, an intrinsic angular momentum of the electron. In an atom most of the electron are paired regarding spin. That is, each electron has a partner with an opposite spin, creating a zero net spin. Depending on the electron configuration of an atom or one step above in molecules and solids respectively, it is possible that there are a few or even many single electrons, being up to material.

Generally the magnetic moment of an electron is given by

 \vec{\mu}=-\mu_B\left(\vec{L}+g_e\,\vec{S}\right) ,

where  \mu_B is the Bohr's magneton and  g_e the magnetogyric ratio, for a free electron it is  g_e=2.0023\approx 2 . This quantity is a measure for the quantitive relation of an angular momentum and its corresponding magnetic momentum. The latter formula includes the orbital angular momentum as well. With ESR it is only possible to detect and investigate the spin component of the total magnetic moment. Hence, in the further deviation we will look at the pure magnetic moment originating from the spin  \vec{S} .

If the spin  \vec{S} and its magnetic moment  \vec{\mu_S} is placed in a externally applied magnetic field, the magnetic moment of the spin starts to precess around the axis of the magnetic field due to the torque

 \vec{M}=\vec{\mu_S}\times\vec{B_Z} .

As always in Quantum Physics the chosen axis of the magnetic field points in  z direction.

The two allowed projections of  \vec{S} onto the z axis:  \pm m_S

In generell, the energy  E of a magnetic moment  \vec{\mu} is defined as

 E=-\vec{\mu}\cdot\vec{B_Z} .

The magnetic moment  \vec{\mu} is related to the spin  \vec{S} , which is a so called Quantum Vector with special properties:

  1. Absolute value:  |S|=\sqrt{s\left(s+1\right)}
  2. Projection onto the z-axis:  m_S=\pm\frac{\hbar}{2}

Incedentally, those two quantities are the best way to distinguish the state of the electron, because only their operator commute and hence, are mesasurable at the same time. For instance, it is not possible to measure two of the three cartesian components of the spin vector simultaneously.

The split of one energy state into two, once a magnetic field gets applied.

The equation for the energy of the electron's spin in an applied magnetic field contains a dot product between the magnetic moment and the B-field:


It may seem to complicate the situation, but acutally it simplifies it a lot. We have chosen our magnetic field to point into the  z direction. Since the spin is characterized by the projection onto the  z axis, depicted by the Quantum number  m_S , the dot product cancels to



 m_S=\pm\frac{\hbar}{2} .

Bohr's magneton  \mu_B and the magnetogyric ratio  g_e are both natural constants at this point. If a external magnetic field  B_Z is applied (positive value, because we picked the  z orientation of our coordinate system in such a way), the electron's energy is reduced or raised, depending whether  m_S is negative or positive, respectively. The original single energy state, which we still get out of the equation for  B_Z=0 , is split into two different energy states. Moreover, the energy difference

 \Delta E=E_{+1/2}-E_{-1/2}=+\frac{1}{2}\,\mu_B\,g_e\,B_Z-(-\frac{1}{2}\,\mu_B\,g_e\,B_Z)=\mu_B\,g_e\,B_Z

is proportional to the strength of the applied magnetic field. Therefore that difference can be tuned very precisely by the experimental setup, which is very important for the latter detection of the ESR signal.

For typical laboratory B-fields the energy difference  \Delta E ranges in the microwave photon band, if you convert the energy to wavelength or rather frequency. This is the point, where the name of the entire phenomenon originates. Namely, if one irradiates the unpaired spin, which normally sits in the lower energy state (due to general energy minimization of nature), with the correct frequency, the energy gets absorbed, combined with a transition to the upper level. In this case, the energy of the photons match exactly the energy difference between both states. Physicist call this situation Electron Spin Resonance.

In formula language the following becomes true:

 h\,\nu=\mu_B\,g_e\,B_Z ,

where  h is Planck's constant and  \nu the frequency of the incident light.

Other than the magnetogyric ratio  g_e are all quantities either natural constants or measured values. Above I claimed that this value is a natural constant, too. Well, technically it is one, however, depends on the material and its compounds and especially spin stucture. Taking the previous equation as well as transferring it to an expression for the magnetogyric ratio


yields material properties with regard to the spin configuration. For example, the comparison to the definite value of a free electron is an good indicator for various substances' features.

Experimental setup

Operating instructions

ESR measurements

Desired and future ESR setup