For the full derivations these questions poke at, keep the parent note open, plus
Density of states, Partition function, Bose-Einstein statistics, Equipartition theorem,
Rayleigh-Jeans law, Wien's law and Stefan-Boltzmann law.
The three figures below are the visual backbone — glance at them before answering.
Every answer must give the reason, not just the verdict. (Look at figure s01 for the shape of the curves.)
TF1. "The ultraviolet catastrophe is caused by there being too many low-frequency modes."
False. The mode count g(ν)=8πν2/c3 grows without bound at highν; it is the pile-up of high-frequency modes each holding kBT that makes the classical integral diverge.
TF2. "Planck's quantization changes how many modes exist in the cavity."
False. Quantization only changes the average energy per mode⟨ϵ⟩. The density of states g(ν)=8πν2/c3 is purely geometric and is identical in the classical and quantum treatments.
TF3. "At very low frequency the Planck curve and the Rayleigh–Jeans curve agree."
True. For hν≪kBT (i.e. x→0) we expand ex−1≈x, giving ⟨ϵ⟩→kBT, which is exactly the classical (Rayleigh–Jeans) result — see how the curves hug on the left of figure s01.
TF4. "Because more modes exist at high ν, a hot body radiates most strongly at the highest frequencies."
False. The ν2 mode growth is beaten by the exponential factor e−hν/kBT in ⟨ϵ⟩, so the spectrum turns over at a finite peak νmax≈2.82kBT/h and falls off afterward.
TF5. "The Bose–Einstein occupation number nˉ=1/(ehν/kBT−1) can exceed 1."
True. Photons are bosons with no exclusion; for hν≪kBT (cheap, low-frequency modes) nˉ becomes very large, meaning many photons pile into the same mode.
TF6. "Doubling the temperature doubles the total radiated energy density."
False. Stefan–Boltzmann gives U∝T4, so doubling T multiplies U by 24=16, not 2.
TF7. "The peak of u(ν) and the peak of u(λ) point to the same frequency/wavelength pair."
False. Writing the dimensionless ratios xν=hν/kBT (frequency form) and xλ=hc/λkBT (wavelength form), the Jacobian ∣dν/dλ∣=c/λ2 shifts the maximum: xν≈2.82 but xλ≈4.97. Same physics, different peak location.
TF8. "A perfect blackbody is black because it never emits any light."
False. "Black" means it absorbs all incident radiation; in thermal equilibrium it also emits the full Planck spectrum. A hot blackbody glows brightly.
TF9. "The zero-point energy 21hν matters for the shape of the thermal radiation spectrum."
False. The equilibrium photon picture uses ⟨ϵ⟩=hνnˉ with no zero-point term; the constant 21hν per mode is T-independent and drops out of the observable radiated spectrum.
Each statement below hides one flaw. Name it and correct it. (Figure s02 shows the n-space octant for SE1.)
SE1. "We count modes as a full sphere of radius n in n-space, volume 34πn3."
The octant error. Since each ni=1,2,3… is positive, only 1/8 of the sphere is physical: N=81⋅34πn3=6πn3.
SE2. "Each wavevector k contributes one mode, so g(ν)=4πν2/c3."
The polarization factor is missing. Every k carries two independent transverse polarizations, so multiply by 2: g(ν)=8πν2/c3.
SE3. "By equipartition each oscillator carries 21kBT, so u=c34πν2kBT."
Each 1-D oscillator has two quadratic degrees of freedom (kinetic + potential), giving 2×21kBT=kBT, not 21kBT. And equipartition itself is invalid once levels are discrete: the theorem is derived by integrating over a continuous energy that appears quadratically; with allowed energies stuck at 0,hν,2hν,… that integral is replaced by a sum, and when the gap hν≫kBT the mode cannot even reach its first excited level, so it carries far less than kBT.
SE4. "The partition function is Z=∑ne−nhνβ=1−e−x1 (with β=1/kBT and x=βhν), so ⟨ϵ⟩=−∂x∂lnZ."
The energy average is ⟨ϵ⟩=−∂lnZ/∂β, differentiating with respect to β, not x=βhν. Getting the variable wrong drops the factor of hν (since ∂x/∂β=hν).
SE5. "Since ⟨ϵ⟩=hν/(ehν/kBT−1), at high ν each mode holds about hν."
At high ν, ehν/kBT≫1 so ⟨ϵ⟩≈hνe−hν/kBT→0. High-frequency modes hold almost nothing, not hν.
SE6. "In the Stefan–Boltzmann integral, substituting x=hν/kBT leaves a T-dependent integral."
The whole point of that substitution is to make the integral ∫0∞ex−1x3dx=π4/15 a pure number with no T; all T dependence is pulled out front as T4.
SE7. "Wien's law comes from setting ⟨ϵ⟩ maximum."
You maximize the full spectral density u(ν)∝ν3/(ex−1) (density of states × energy), not ⟨ϵ⟩ alone. This gives 3(1−e−x)=x, i.e. x≈2.821.
WQ1. Why does the classical result diverge but the quantum result stay finite?
Classically every mode gets kBT, so ∫ν2kBTdν diverges. Quantization makes ⟨ϵ⟩ decay like e−hν/kBT at large ν, and exponential decay overwhelms the ν2 growth, so the integral converges.
WQ2. Why is energy quantized in lumps of hν (proportional to frequency) the specific fix, rather than just any discreteness?
The lump size hν scaling with frequency is exactly what makes high-frequency modes expensive: a fixed thermal budget kBT can excite cheap low-ν lumps but not costly high-ν ones, freezing them out. Frequency-independent lumps would not selectively suppress the UV modes.
WQ3. Why can we treat each standing-wave mode as an independent harmonic oscillator?
In a linear cavity the EM field decomposes into normal modes that do not exchange energy directly; each mode's amplitude oscillates sinusoidally in time exactly like a 1-D harmonic oscillator, so its energy levels are those of a quantum oscillator.
WQ4. Why does a hotter star look bluer?
Wien displacement gives νmax∝T, so raising T pushes the spectral peak to higher frequency (shorter wavelength), shifting the perceived color from red toward blue-white.
WQ5. Why does the density of states depend on ν2 and not ν or ν3?
Modes fill a shell in 3-D k-space; the number in a shell of radius ∝ν scales with its surface area ∝ν2. In 2-D it would be ∝ν, in 1-D constant — the exponent tracks spatial dimension minus one.
WQ6. Why is the factor a geometric series in the partition function, and why must the ratio be less than 1?
The allowed energies nhν are equally spaced, so Z=∑n(e−x)n is geometric with ratio e−x. Since x=hν/kBT>0 we have e−x<1, so the sum converges to 1/(1−e−x); a ratio ≥1 would mean an unphysical infinite Z. (The geometric decay of these Boltzmann weights is drawn in figure s03.)
WQ7. Why does the photon picture have a chemical potential μ=0 (unlike a gas of atoms)?
Recall μ is the energy cost of adding one particle. For atoms particle number is fixed, so μ adjusts to enforce it and can be positive or negative. But photon number is not conserved — the walls freely create and destroy photons — so the system minimizes free energy with respect to number itself, which forces μ=0. That is exactly why Bose–Einstein gives nˉ=1/(ehν/kBT−1) with no e−βμ factor.
EC1. What is ⟨ϵ⟩ in the strict limit T→0 for a fixed ν>0?
x=hν/kBT→∞, so nˉ→0 and ⟨ϵ⟩→0. Every mode falls into its ground state; the cold cavity radiates nothing.
EC2. What happens to ⟨ϵ⟩ as ν→0 at fixed T?
x→0 gives ⟨ϵ⟩→kBT, the classical equipartition value — the very low-frequency corner is where quantum and classical predictions merge.
EC3. Does the total energy density U stay finite even though g(ν) diverges at large ν?
Yes. Although g(ν)→∞, the product g⟨ϵ⟩ decays exponentially at large ν, so U=∫0∞g⟨ϵ⟩dν converges to 15c3h38π5kB4T4.
EC4. Is there a mode with exactly ν=0?
No physical standing wave has zero frequency in the cavity (that would need nx=ny=nz=0, i.e. no wave). ν→0 is a limit, not an actual mode, and it contributes negligibly because g(ν)→0 there.
EC5. In the limit h→0 (imagining Planck's constant shrinking), what spectrum do we recover?
With h→0, x=hν/kBT→0 for allν, so ⟨ϵ⟩→kBT everywhere and we recover the divergent Rayleigh–Jeans law — the classical catastrophe returns, confirming h is what tames it.
EC6. What is the occupation of a mode when hν=kBT exactly (x=1)?
nˉ=1/(e1−1)≈0.58, i.e. on average about half a photon per mode — the crossover region between the "cheap, populated" and "expensive, frozen" regimes sits near x∼1.
Recall One-line summary of every trap
The count g∼ν2 is classical geometry; the energy⟨ϵ⟩ is where quantum
mechanics enters and where the catastrophe dies. Watch the factor of 2 (polarization), the octant (1/8),
the β-vs-x derivative, the T4 (not T) scaling, and the ν-peak vs λ-peak Jacobian.