Understanding the Origin of Energy Gap in Kittel's Book

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Homework Help Overview

The discussion revolves around understanding the origin of the energy gap as presented in Kittel's Solid-state Physics book, specifically in relation to the expectation values of wave functions and their implications for potential energy calculations.

Discussion Character

  • Conceptual clarification, Mathematical reasoning

Approaches and Questions Raised

  • Participants explore the relationship between the expectation values of different wave functions and question how phase shifts affect these values. There is an attempt to clarify the calculation of potential energy expectation values in relation to the wave functions.

Discussion Status

Some participants have provided insights into the differences in potential energy associated with the wave functions, suggesting that the average energies lead to the understanding of the band gap. The conversation indicates a productive exploration of the topic, though no explicit consensus has been reached.

Contextual Notes

Participants are navigating the complexities of wave function behavior in relation to potential energy, with references to specific figures in the textbook. There is an acknowledgment of the need for careful consideration of the potential energy landscape in these calculations.

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[SOLVED] kittel page 166

Homework Statement


In Figure 3 of Chapter 7 of Kittel's Solid-state physics book, it says that this is the key to understanding the origin of the energy gap. However I do not understand why. It seems like if you take the expectation value of either [tex]|\psi(-)|^2[/tex] or [tex]|\psi(+)|^2[/tex], you will get exactly the same value. How can shifting the phase of the wave change its expectation value? There is absolutely no reason why the expectation value of sine squared should be different than the expectation value of cosine squared!

Homework Equations


The Attempt at a Solution

 
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I can not see where he his saying that the expacation values of the two wave functions in space are equal. He states: "When we caclulate the expectation values of the POTENTIAL ENERGY over the the ..:"

Look at the potential!... and do a quick head calculation.

psi(+) has its peaks right "above" the ion cores, i.e where the potential energy is max (see fig a). So psi(+) has larger probability to be located where the pot E is small ( = minus infinity). And psi(-) have its peakes "between" the ion cores, where the pot E is max ( = 0).

So the average energy of the the psi(+) is shifted down in comparison with psi(-), and that gives you the band gap.
 
That makes sense! You are calculating [tex]\int |\psi(x)|^2 V(x) dx[/tex] not [tex]\int |\psi(x)|^2 dx[/tex] since the latter is just 1.
 
exactly :)
 

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