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Estimate the probability that a hydrogen atom at room temperature is in one of its first excited states (relative to the probability of being in the ground state). Don't forget to take degeneracy into account. Then repeat the calculation for a hydrogen atom in the atmosphere of the starγ UMa, whose surface temperature is approximately 9500 K.

Short Answer

Expert verified

As a result, no Hydrogen atoms can be found in the first excited state.

On this star, there is one atom in the first excited state out of 64500 hydrogen atoms.


Step by step solution

01

Given information

A hydrogen atom at room temperature is in one of its first excited states (relative to the probability of being in the ground state).

02

Explanation

With n = 2, assuming E1 is ground state energy and E2 is first excited state energy, the chance of finding the atom in either of the first excited states is:

Ps2=1Ze-E2/kT

The partition function is equal to the sum of the Boltzmann factors, but because the initial state has the greatest energy magnitude, we can approximate it as follows:

Z=∑se-E(s)/kT≈e-E1/kT

Substitute in the above equation

Ps2=eE1/kTe-E2/kTPs2=e-E2-E1/kT

There are four such states, therefore the probability of E2 equals Ps2multiplied by 4, so:

PE2=4e-E2-E1/kT

Substitute the energies and Boltzmann constant in eV (k = 8.617 x 10-5 eV/K) at room temperature T = 300 K for the energy of the ground state E1=-13.6 eV and the energy of the first excited state B2 =-3.4 eV.

PE2=4e-(-3.4eV-(-13.6eV))/8.617×10-5eV/K(300K)PE2=1.75×10-171

As a result, no Hydrogen atoms can be found in the first excited state.

03

Explanation

We must now calculate this probability for the star γUMa, which has a surface temperature of 9500 K, as follows:

PE2=4e-(-3.4eV-(-13.6eV))/8.617×10-5eV/K(9500K)PE2=1.55×10-5

On this star, there is one atom in the first excited state out of 64500 hydrogen atoms.

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Most popular questions from this chapter

For a COmolecule, the constant €is approximately 0.00024eV.(This number is measured using microwave spectroscopy, that is, by measuring the microwave frequencies needed to excite the molecules into higher rotational states.) Calculate the rotational partition function for a COmolecule at room temperature (300K), first using the exact formula 6.30 and then using the approximate formula 6.31

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{a) Show that the average position of the particle is given by

x=∫xe-βuxdx∫e-βuxdx

where each integral is over the entire xaxis.

A one-dimensional potential well. The higher the temperature, the farther the particle will stray from the equilibrium point.

(b) If the temperature is reasonably low (but still high enough for classical mechanics to apply), the particle will spend most of its time near the bottom of the potential well. In that case we can expand u(z) in a Taylor series about the equilibrium point

ux=ux0+x-x0dudxx0+12x-x02d2udx2x0+13!x-x03d3udx3x0+........

Show that the linear term must be zero, and that truncating the series after the quadratic term results in the trivial prediction x=x0.

(c) If we keep the cubic term in the Taylor series as well, the integrals in the formula for xbecome difficult. To simplify them, assume that the cubic term is small, so its exponential can be expanded in a Taylor series (leaving the quadratic term in the exponent). Keeping only the smallest temperature-dependent term, show that in this limit x differs from by a term proportional to kT. Express the coefficient of this term in terms of the coefficients of the Taylor series ux

(d) The interaction of noble gas atoms can be modeled using the Lennard Jones potential,

ux=u0x0x12-2x0x6

Sketch this function, and show that the minimum of the potential well is at x=x0, with depth u0. For argon, x0=3.9A∘and u0=0.010eV. Expand the Lennard-Jones potential in a Taylor series about the equilibrium point, and use the result of part ( c) to predict the linear thermal expansion coefficient of a noble gas crystal in terms of u0. Evaluate the result numerically for argon, and compare to the measured value α=0.0007K-1

Some advances textbooks define entropy by the formula

S=-k∑sPslnPs

where the sum runs over all microstates accessible to the system and Psis the probability of the system being in microstate s.

(a) For an isolated system, role="math" localid="1647056883940" Ps=1Ωfor all accessible states s. Show that in this case the preceding formula reduces to our familiar definition of entropy.

(b) For a system in thermal equilibrium with a reservoir at temperatureT,role="math" localid="1647057328146" Ps=e-EskTZ. Show that in this case as well, the preceding formula agrees with what we already know about entropy.

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En≈ϵ1.03n-0.03n2,n=0,1,2,…

where ϵ is the spacing between the two lowest levels. Thus, the levels get closer together with increasing energy. (This formula is reasonably accurate only up to about n = 15; for slightly higher n it would say that En decreases with increasing n. In fact, the molecule dissociates and there are no more discrete levels beyond n ≈15.) Use a computer to calculate the partition function, average energy, and heat capacity of a system with this set of energy levels. Include all levels through n = 15, but check to see how the results change when you include fewer levels Plot the heat capacity as a function of kT/ϵ. Compare to the case of a perfectly harmonic oscillator with evenly spaced levels, and also to the vibrational portion of the graph in Figure 1.13.

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