Boltzmann Factor in QM Language

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The discussion centers on the Boltzmann Factor in quantum mechanics, specifically the probability of measuring a system with energy E, expressed as P(E) = 1/Z * e^-E/kT. The participant, Andrew, questions why this probability does not depend on the quantum state |psi>. The resolution lies in understanding the distinction between pure and mixed states, where the Boltzmann factors emerge from the thermal density matrix of an ensemble of systems at non-zero temperature, indicating interaction with a heat bath.

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  • Quantum Mechanics (QM) fundamentals
  • Statistical Mechanics principles
  • Understanding of pure and mixed states in quantum systems
  • Familiarity with thermal density matrices
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  • Study the derivation of the Boltzmann Factor in statistical mechanics
  • Explore the concept of thermal density matrices in quantum systems
  • Learn about the implications of non-zero temperature on quantum states
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Students and researchers in quantum mechanics, physicists exploring statistical mechanics, and anyone interested in the foundational concepts of the Boltzmann Factor and its implications in quantum systems.

andrewm
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Hi,

I'm stuck on "the summit of statistical mechanics" (as Feynman calls it): the definition of the Boltzmann Factor.

The probability of measuring the system with energy E is P(E) = 1/Z * e^-E/kT.

I've taken courses in QM and can't understand why P(E) does not depend on the ket of the system |psi>.

From QM, I want to write down P(Ei) = <psi|Ei><Ei|psi>. So why doesn't 1/Z * e^-E/kT depend on |psi>? Is it a hidden assumption about the nature of the system that all |psi> in the Hilbert Space have P(Ei) equal?

Thanks in advance,
Andrew
 
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The issue lies in the difference between a pure state, which represents an ensemble of identical systems, and a mixed state, which represents an ensemble of systems in different states. So you might want to consider an ensemble of systems in different energy eigenstates, represented by a thermal density matrix. The diagonal components are then the Boltzmann factors.
 
What if I consider a system in a single energy eigenstate?

If the system is prepared in an energy eigenstate, say E1, then surely a measurement of E1 has probability 1 and not 1/Z * e^-E1/kT ?

Or can I not prepare a system that has a definite energy?
 
The "problem" is that you are at non-zero temperature (otrhwise the Boltzmann factor would be 1), meaning you are implicitly assuming that your system is actually interacting with a heat bath of some sort.
 

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