Quantum Mechanics and Hydrogen Atom - Vocabulary
Hydrogen Energy Levels and Transitions
- Hydrogen energy levels: En=−n213.6 eV
- Ground state: E1=−13.6 eV=−2.178×10−18 J
- As n → ∞, En→0− (levels approach zero from below)
- Ionization energy (to remove the electron completely): E<em>ion=13.6 eV per atom; per mole: E</em>ionmol≈1.3×103 kJ/mol
- Energy change for a transition: ΔE=E<em>f−E</em>i
- If \Delta E > 0: absorption (electron goes to higher n)
- If \Delta E < 0: emission (photon emitted; electron goes to lower n)
- Photon energy relations: Eph=hν=λhc
- Wavelength from transition: λ=∣ΔE∣hc
- Example: ground to n=4
- ΔE=E<em>4−E</em>1=−1613.6−(−13.6)=12.75 eV
- Eph=12.75 eV=2.04×10−18 J
- λ≈2.04×10−18hc≈97 nm
- Balmer series (transitions to nf=2) yield visible lines (red ~656 nm, blue ~486 nm, etc.).
- Absorption vs emission visual cue: absorption raises energy level; emission lowers it; energy gaps smaller for some transitions than others.
- Wave-particle duality (brief context): light can behave as waves or particles depending on the experiment; matter also shows wave-like behavior (De Broglie).
Photon Energy and Wavelength (General)
- Photon energy: Eph=hν=λhc
- Wavelength from energy: λ=Ehc
- Common scale: 1 eV≈1.602×10−19 J⇒λ≈1240 nm per eV (conversion examples vary with E in eV or J)
- Units reminder: for exam, give wavelength in nanometers (nm); 1 m = 109 nm
Absorption vs Emission (Energy Changes)
- Absorption: \Delta E = Ef - Ei > 0 (photon absorbed)
- Emission: \Delta E = Ef - Ei < 0 (photon emitted; take absolute value for photon energy)
- Photon energy magnitude: ∣ΔE∣=Eph=hν=λhc
- Practical note: on exam, compute final minus initial energy in joules, take absolute value for wavelength or frequency
De Broglie Wavelength and Matter Waves
- De Broglie relation: λ=mvh
- Electron example: me=9.11×10−31 kg, v≈1×106 m/s
- λ≈9.11×10−31×1066.626×10−34≈7×10−10 m≈0.7 nm
- Macroscopic object (e.g., baseball): wavelength ~10−34 m (undetectable)
- TEM and diffraction demonstrate electron waves; orbitals arise from wavefunctions solving Schrödinger equation
Schrödinger Equation and Atomic Orbitals (Hydrogen-like)
- Core equation: H^ψ=Eψ
- H^=T+V (kinetic + potential energy)
- ψ is the wavefunction; |\psi|^2 gives probability density
- Principal quantum number: n (and angular quantum number l, magnetic ml) label orbitals
- Orbitals (solutions):
- s orbital: spherical probability cloud
- p orbitals: dumbbell shape (3 orientations)
- Key conceptual point: orbitals arise from solving the Schrödinger equation; electrons described by wavefunctions rather than precise orbits; nodes are regions with zero probability
- Hydrogen energy depends primarily on n (non-rel, single-electron model)
Quick Exam Context and Practice Tips
- Core task: given a transition, find the wavelength (nm) or energy (J) using
- ΔE=E<em>f−E</em>i=−n<em>f213.6+n</em>i213.6(in eV)
- ∣ΔE∣=hν=λhc
- λ=∣ΔE∣hc
- Use the correct unit: report wavelength in nanometers (nm)
- Example reminder: ionization energy per atom = 13.6 eV; per mole ≈ 1.3×103 kJ/mol
- Remember conversions: 1 m = 109 nm; 1 eV = 1.602×10−19 J
- On the exam, you may be asked to apply the Balmer-serving idea or interpret an orbital diagram in energy terms
- Tools: calculator is allowed; phones or laptops prohibited; periodic table reference may be allowed depending on instructor