Energy converted to light per second:
Power = 150 W = 150 J/s
Light energy = 8% of 150 = (8/100) × 150 = 12 J/s
Number of photons per second:
n = Total light energy / Energy per photon
n = 12 / (4·42 × 10⁻¹⁹)
n = (12 / 4·42) × 10¹⁹
n = 2·714... × 10¹⁹ ≈ 2·71 × 10¹⁹
Light energy/sec = 8% × 150 W = 12 J/s
n = 12 / (4·42×10⁻¹⁹) = 2·71 × 10¹⁹ photons/sec
Max Planck (1900) proposed that energy is emitted or absorbed in discrete packets called quanta (singular: quantum). For electromagnetic radiation, each quantum is called a photon. Energy of one photon: E = hν = hc/λ, where h = Planck's constant = 6·626 × 10⁻³⁴ J·s, ν = frequency (Hz), c = speed of light = 3 × 10⁸ m/s, λ = wavelength (m). Higher frequency → higher energy per photon. X-rays have much more energy per photon than radio waves. Visible light: ~2–3 eV per photon.
Einstein (1905, Nobel Prize 1921) explained the photoelectric effect using Planck's quantum concept. When light hits a metal surface, electrons are ejected only if photon energy ≥ work function (Φ) of the metal. KE of ejected electron = hν − Φ. If hν < Φ: no electron ejected regardless of intensity. If hν ≥ Φ: electrons ejected — more intensity means more photons → more electrons, but not faster ones. Threshold frequency ν₀ = Φ/h. Work function Φ = hν₀. This proved light has particle (photon) nature.
📌 E = hν (energy-frequency relation)
📌 E = hc/λ (energy-wavelength relation: higher λ → lower E)
📌 E = hcν̃ where ν̃ = wavenumber = 1/λ
📌 1 eV = 1·6 × 10⁻¹⁹ J (electron volt conversion)
📌 Energy of n photons = n × hν
📌 Number of photons n = Total energy / Energy per photon = E_total/hν
📌 In this problem: E per photon = 4·42×10⁻¹⁹ J corresponds to violet/UV light
Bohr (1913) proposed: (1) Electrons revolve in fixed circular orbits (stationary states) without losing energy. (2) Only orbits where mvr = nℏ (n = 1, 2, 3...) are allowed (angular momentum quantisation). (3) Energy is emitted/absorbed only when electron jumps between orbits: ΔE = E₂ − E₁ = hν. For hydrogen: Eₙ = −13·6/n² eV. Radius rₙ = 0·529n² Å (Bohr radius a₀ = 0·529 Å for n=1). Velocity vₙ = 2·18×10⁶/n m/s. Bohr model works only for hydrogen and hydrogen-like ions (He⁺, Li²⁺, etc.).
📌 Lyman series: n→1, UV region (1→1 to ∞→1)
📌 Balmer series: n→2, visible region (3→2 to ∞→2) — Hα(red), Hβ(blue-green), Hγ(violet)
📌 Paschen series: n→3, infrared region
📌 Brackett series: n→4, infrared region
📌 Pfund series: n→5, far infrared
📌 Rydberg formula: 1/λ = R_H(1/n₁² − 1/n₂²), R_H = 1·097×10⁷ m⁻¹
de Broglie (1924) proposed that all matter has wave properties. Wavelength λ = h/mv = h/p, where m = mass, v = velocity, p = momentum. For electrons: λ is significant (comparable to atomic dimensions). For macroscopic objects (cricket ball): λ is negligibly small (undetectable). Confirmed by electron diffraction experiments (Davisson-Germer, 1927). For accelerated electron: λ = h/√(2mKE) = h/√(2meV) where V = accelerating voltage. Heavier particles → shorter wavelength (e.g., proton has much shorter λ than electron at same KE).
It is impossible to simultaneously determine the exact position and exact momentum (or velocity) of a particle: Δx × Δp ≥ h/4π. This is not a limitation of instruments — it's a fundamental property of quantum systems. A particle with definite momentum has completely indefinite position (spread over all space) and vice versa. Consequences: electrons cannot have defined circular orbits (as in Bohr model). Instead, we use probability distributions (orbitals — regions of 90% probability). Uncertainty in energy and time: ΔE × Δt ≥ h/4π.
Principal quantum number n (1, 2, 3...): energy level, shell size. Azimuthal/angular quantum number l (0 to n−1): subshell shape (0=s, 1=p, 2=d, 3=f). Magnetic quantum number m_l (−l to +l): orbital orientation in space. Spin quantum number m_s (+½ or −½): electron spin (up ↑ or down ↓). Pauli exclusion principle: no two electrons in an atom can have all four quantum numbers identical. Maximum electrons in a shell: 2n². Maximum in a subshell: 2(2l+1). Aufbau principle + Hund's rule determine filling order.