Class 12 · Notes

Dual Nature of Radiation & Matter— Notes, Formulas & Revision

Complete revision notes and formulas for Dual Nature of Radiation & Matter (Class 12). Curated for JEE, NEET, AP Physics, SAT, and CUET. Tap any topic to open the live simulation and full PYQ set.

Photoelectric Effect

Animated photons knock electrons out of metals — Einstein's KE_max = hf − φ with 4 metal choices.

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When light of sufficient frequency strikes a metal surface, electrons are ejected — the photoelectric effect, discovered by Hertz (1887) and explained by Einstein (1905).

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Einstein's photon hypothesis: light comes in quanta of energy E = hf. Each photon interacts with ONE electron.

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Einstein's equation: K_max = hf − φ, where φ is the work function (minimum energy to release an electron from the metal surface).

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Below the threshold frequency f₀ = φ/h, NO electrons are emitted, regardless of intensity. Above, electrons emerge instantaneously.

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Maximum KE depends on the frequency, NOT intensity. Intensity affects only the NUMBER of photoelectrons per second.

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Stopping potential V_s is the retarding voltage that just stops the most energetic photoelectrons: eV_s = K_max = hf − φ.

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Quantum nature: classical wave theory cannot explain (i) threshold frequency, (ii) zero time-delay, (iii) K_max independent of intensity.

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Result: light has particle-like (photon) behaviour even though it's a wave — laid the foundation for quantum mechanics.

Einstein photoelectric equation

φ = work function (eV). Below f₀ = φ/h, no emission.

Threshold frequency

Minimum frequency for photoemission.

Stopping potential

V_s measured directly in experiments → V_s vs f gives slope h/e.

Photon energy

h = 6.626 × 10⁻³⁴ J·s = 4.136 × 10⁻¹⁵ eV·s.

Photon momentum

Used in radiation pressure and Compton scattering.

PHOTON model explains every fact wave theory cannot: threshold, instantaneity, KE vs f, KE independent of I.

Plot of V_s vs f is a straight line; slope = h/e, x-intercept = f₀, y-intercept = −φ/e.

Same metal: brighter (higher intensity) light → MORE electrons but SAME K_max.

Intensity also determines the saturation current — once all emitted electrons reach the anode.

Work function φ depends only on the metal (not on light). Alkali metals (Cs, K, Na) have low φ (~2 eV) → visible light suffices.

Compton effect (X-rays scattered by electrons changing wavelength) is the other key confirmation of photon momentum.

Threshold Frequency

KE_max vs f plot — zero below f₀ = φ/h, linear slope h above. Compare 4 metals.

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Threshold frequency f₀ is the minimum frequency of light below which no photoemission occurs, regardless of intensity.

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Defined by the work function: hf₀ = φ ⇒ f₀ = φ/h.

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Equivalently, threshold wavelength λ₀ = hc/φ. Below f₀ (or above λ₀): no photoelectrons.

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Threshold is metal-specific. Cesium (φ ≈ 2.14 eV) responds to visible red. Copper (φ ≈ 4.7 eV) needs UV.

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Above f₀: any non-zero intensity produces photoelectrons instantaneously (no measurable delay even at extremely low intensities — classical theory predicted ~minutes of delay).

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Threshold is sharp — there is no 'gradual onset'. It's a step function in classical experiments.

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Threshold frequency was a primary mystery for classical physics — solved by Einstein's photon model.

Threshold frequency

Set entirely by the material's work function.

Threshold wavelength

Useful shortcut: λ₀[nm] = 1240/φ[eV].

Einstein equation at f₀

Photoelectrons emerge with zero KE.

Threshold is INDEPENDENT of intensity. A very dim source above f₀ still emits; a very bright source below f₀ does not.

Different metals have different f₀. The same light may emit from one metal but not from another.

Long-wavelength (red, IR) light has lower energy per photon — explains why most metals need UV.

The existence of a sharp threshold was experimental evidence that classical wave physics could not be the full story.

Useful threshold wavelengths: Cs ≈ 580 nm (yellow), K ≈ 540 nm (green), Na ≈ 540 nm. All alkali metals work with visible light.

λ₀ = 1240/φ is the most efficient calculation shortcut.

KE vs Frequency

Parallel lines of slope h/e = 4.14 × 10⁻¹⁵ V·s — same slope, different intercepts per metal.

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Maximum KE of photoelectrons varies LINEARLY with frequency: K_max = hf − φ.

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Slope = h (Planck's constant). x-intercept = f₀ = φ/h. y-intercept (at f=0) = −φ.

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Below threshold (f < f₀): K_max would be negative — physically means no emission.

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Crucially: K_max does NOT depend on intensity. Same f and metal ⇒ same K_max regardless of how bright the light is.

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This linearity was a key prediction of Einstein's photon theory — confirmed by Millikan's experiments.

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Different metals: parallel lines (same slope h) but different intercepts (different φ).

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Photon picture: each photon transfers its full energy hf to ONE electron. The electron uses φ to escape, keeps the rest as KE.

K_max vs f (Einstein)

Linear in f; slope = h, intercept = −φ.

K_max in terms of V_s

Stopping potential gives K_max directly.

Threshold (K_max = 0)

Below this frequency, no photoemission.

K_max depends on frequency, NOT on intensity. Bright dim red light gives no emission from a metal that responds only above blue.

Slope of K_max vs f is UNIVERSAL — Planck's constant h, independent of metal.

Doubling f doesn't usually double K_max — only if you start far above φ. The contribution −φ shifts everything.

Photoelectrons can have a RANGE of KEs (from 0 to K_max), depending on how deep in the metal they were and energy losses on the way out.

K_max measurable via stopping potential: V_s × e = K_max.

Linear K vs f and zero-time-delay together killed the classical wave-theory of photoemission.

Intensity vs Current

Higher intensity → more photoelectrons → higher saturation current. Same V_s across intensities.

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Photoelectric current (number of electrons per unit time × charge) is DIRECTLY proportional to intensity, for given frequency above threshold.

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Doubling intensity doubles the rate of photons hitting the surface ⇒ doubles the rate of photoelectron emission ⇒ doubles the saturation current.

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Intensity does NOT affect: K_max, threshold frequency, stopping potential.

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This proportionality is exact in the photon picture: I = (photon rate)·hf. Doubling I doubles photon rate, hence emission rate.

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Saturation current: at high anode voltage, every photoelectron is collected. Saturation level scales with I.

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Below saturation (low voltage), some electrons return to the cathode without crossing — current is sub-saturation.

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Photodetectors, solar cells, light meters — all rely on the intensity-current proportionality.

Photocurrent (saturation)

η = quantum efficiency; N_photons = photons/sec arriving.

Photon flux from intensity

I = intensity (W/m²); A = area; hf = energy per photon.

Intensity dependence

Linear, for given f > f₀.

Intensity controls QUANTITY (number of electrons). Frequency controls QUALITY (energy per electron).

Doubling intensity at the same f doubles the photocurrent. Doubling intensity below f₀ still produces ZERO current.

Saturation occurs when anode voltage is high enough to collect every electron — current then becomes I_max independent of V.

Below saturation, some photoelectrons turn back due to space-charge or low anode-attraction.

Solar cells exploit this: more sunlight (higher I) → more photoelectrons → more current.

Quantum efficiency η is < 1 in reality — not every photon ejects an electron (reflection, deeper absorption losses).

Stopping Potential

eV_s = hf − φ — split view: I–V curve + V_s vs f plot with live point.

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Stopping potential V_s is the retarding voltage (anode held NEGATIVE w.r.t. cathode) at which photoelectric current drops to ZERO.

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At V = V_s, even the MOST energetic photoelectron (K = K_max) is just barely stopped: eV_s = K_max.

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Stopping-potential equation: eV_s = hf − φ.

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V_s is INDEPENDENT of intensity — depends only on frequency and metal.

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Plotting V_s vs f: straight line with slope h/e and x-intercept f₀.

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Slope h/e ≈ 4.136 × 10⁻¹⁵ V·s — same for all metals. Y-intercept (at f = 0): −φ/e — depends on metal.

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Millikan's 1914 experiment measured V_s vs f for several metals — confirmed Einstein's equation and gave a precise value of h.

Stopping potential

Maximum KE of photoelectrons = retarding work done by V_s.

Slope of V_s vs f

Universal — same for every metal.

Intercept on V_s axis (f = 0)

Negative — graph crosses below x-axis.

Threshold from intercept

x-intercept of V_s vs f line.

V_s is what's MEASURED — K_max is INFERRED via eV_s.

V_s does not depend on the intensity of incident light. This was a key surprise to classical physicists.

All metals give parallel V_s-vs-f lines (same slope h/e, different intercepts).

The slope h/e from Millikan's data gave one of the most precise early measurements of Planck's constant.

If V is REVERSED to positive (anode + w.r.t. cathode), saturation current is observed.

Lab-trick: extrapolate the V_s-vs-f line — its x-intercept gives f₀, y-intercept gives −φ/e.

Wave-Particle Duality

Double-slit with wave, particle, and both modes — see interference fringes build from discrete hits.

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Wave-particle duality: light and matter both exhibit wave-like AND particle-like properties depending on the experiment.

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Light: behaves as wave in interference, diffraction, polarisation. Behaves as particle (photon) in photoelectric effect, Compton scattering, pair production.

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Matter: behaves as particle in collision/Newtonian experiments. Behaves as wave in electron diffraction (Davisson-Germer, 1927), neutron interferometry, etc.

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The two pictures are COMPLEMENTARY — you can't see both at once. Bohr's complementarity principle.

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Photon energy E = hf, momentum p = h/λ. Matter wavelength λ_dB = h/p (de Broglie).

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For everyday objects (e.g., a thrown ball), de Broglie wavelength is fantastically tiny (~10⁻³⁴ m) — wave nature is undetectable.

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Wave-particle duality is a foundational pillar of quantum mechanics — it eventually led to the Schrödinger equation, where particles are described by wavefunctions.

Photon (light as particle)

Particle properties: discrete energy and momentum.

de Broglie (matter as wave)

Wave properties: every moving particle has an associated wavelength.

Energy-momentum relation (massive)

Relativistic — important for fast electrons.

Wave and particle pictures are not contradictory — they describe DIFFERENT EXPERIMENTAL OUTCOMES.

Same experiment cannot show both pictures simultaneously (e.g., 'which-slit' detection destroys interference).

For massive objects, λ_dB = h/(mv) is extremely small ⇒ classical (particle) behaviour dominates.

For electrons at typical accelerating voltages (50–100 V), λ_dB ~ 0.1 nm — comparable to atomic spacing ⇒ diffraction observable.

Double-slit experiments with single photons / electrons show interference builds up dot-by-dot — proving wave + particle simultaneity.

All matter has wave nature; the question is whether λ_dB is large enough to detect.

de Broglie Wavelength

λ = h/(mv) — Gaussian wavepacket across 4 particle types from electron to dust.

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Louis de Broglie (1924): every moving particle of momentum p has an associated wave of wavelength λ = h/p.

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For a particle of mass m and speed v (non-relativistic): λ = h/(mv).

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For an electron accelerated through V volts: λ = h/√(2meV) = 12.27/√(V[volts]) Å.

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Larger momentum (heavier or faster) ⇒ smaller wavelength.

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Matter waves were experimentally verified by Davisson-Germer (electron diffraction off Ni crystal, 1927) and G.P. Thomson (electron diffraction through thin foils).

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Atom-interference experiments now confirm de Broglie waves for atoms and even C₆₀ buckyballs.

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de Broglie's hypothesis led directly to Schrödinger's wave equation and modern quantum mechanics.

de Broglie wavelength

Universal — any particle, any speed (non-rel).

Electron via potential difference V

V in volts; very useful shortcut for V < 1 kV.

Through kinetic energy

K = ½mv² = eV for accelerated electrons.

Relativistic correction

Becomes important for K ≳ mc² (e.g., > 0.5 MeV for electrons).

Smaller mass / smaller speed ⇒ LONGER wavelength ⇒ wave nature more apparent.

An electron at 100 V acceleration has λ ≈ 1.23 Å — comparable to atomic spacings ⇒ diffraction works.

A proton at 100 V has λ ≈ 0.029 Å — needs much higher KE to do crystallography.

Heat-of-Schrödinger 'matter wave' is the wavefunction ψ — its modulus squared |ψ|² is the probability density.

Useful shortcut: For electron, λ[Å] = 12.27/√V (V in volts).

Atom interferometers use cold atoms (slow) to make λ_dB ~ μm — large enough to make wave phenomena practically engineerable.

Electron Diffraction

Bragg diffraction 2d sinθ = nλ — Ni crystal lattice + I vs θ plot with n=1,2,3 peaks.

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Electrons can diffract off crystal lattices — Davisson and Germer's 1927 experiment was the first direct evidence of matter waves.

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An electron beam incident on a single-crystal nickel target produces a diffraction pattern, analogous to X-ray diffraction.

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Bragg's law applies: 2d·sin θ = nλ — the same as for X-rays — but here λ = h/p (de Broglie).

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G.P. Thomson independently showed electron diffraction through THIN foils, getting Debye-Scherrer rings.

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Confirmed de Broglie's hypothesis quantitatively: the measured λ matched h/p for the electron's KE.

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Modern applications: electron microscopy (resolution depends on small λ), low-energy electron diffraction (LEED) for surface analysis.

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Neutrons also diffract — used in neutron crystallography (better for light atoms like H than X-rays).

Bragg's law

d = crystal-plane spacing; θ = glancing angle; n = order; λ = wavelength.

Electron wavelength (NR)

V = accelerating voltage in volts.

Davisson-Germer 54 V check

Matches the measured Ni-crystal diffraction angle precisely.

Davisson-Germer (1927) experiment is THE classical confirmation of matter waves and earned the Nobel Prize (1937).

The diffraction pattern from a crystal is sharp because the crystal acts as a 3D grating with periodic d ~ Å.

Higher acceleration voltage ⇒ smaller λ ⇒ smaller diffraction angles (finer pattern).

Electron microscope's resolution is limited by λ — high-V accelerators give λ ~ pm, allowing atomic-scale imaging.

Electron diffraction is destructive testing for biological samples; X-rays are usually preferred for non-conducting crystals.

G.P. Thomson (son of J.J. Thomson, who discovered the electron as a particle) demonstrated its wave nature — father vs son, particle vs wave.

Matter Wave Visualization

Traveling Gaussian ψ(x,t) in position + |φ(k)|² in momentum — two reciprocal views.

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All matter has wave-like properties: every moving particle has a de Broglie wave λ = h/p.

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Quantum mechanics replaces the classical concept of trajectory with the wave function ψ(x,t) — |ψ|² is the probability density.

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Bound states (atoms, nuclei) are described by standing matter waves — explains discrete energy levels.

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Matter waves can interfere and diffract like light. Experimental demos: electron diffraction (Davisson-Germer), neutron interferometry, atom interferometers.

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Matter waves do NOT travel at v_particle in general — phase velocity v_p = E/p, group velocity v_g = dE/dp = v_particle.

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For a relativistic particle: v_p · v_g = c² (so v_p > c for massive particles — but this carries no information).

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Macroscopic objects have λ_dB so small that wave behaviour is hidden — but it is THERE, in principle.

de Broglie wave

Defines matter wavelength.

Phase / group velocity

v_p × v_g = c² (relativistic).

Schrödinger wave equation

Equation governing matter waves; ψ encodes wave nature.

Matter wave is a PROBABILITY wave: |ψ|² gives the chance of finding the particle at a location, NOT a real classical wave.

Standing matter waves in a box give DISCRETE allowed wavelengths ⇒ quantization of energy levels.

Electron diffraction confirms electrons have wave nature — Davisson-Germer (1927) saw Ni-crystal diffraction.

Even C₆₀ buckyballs show interference fringes when sent through gratings.

Matter waves are ALWAYS present, but for macroscopic objects λ_dB is far smaller than any aperture — no fringes appear.

Group velocity = particle velocity is why a wavepacket 'tracks' the classical motion in the limit.

Heisenberg Uncertainty

Δx · Δp ≥ ℏ/2 — tune position spread; momentum spread responds inversely. Live product.

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Heisenberg's uncertainty principle (1927): you cannot simultaneously know a particle's position and momentum to arbitrary precision.

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Quantitatively: Δx · Δp_x ≥ ℏ/2, where ℏ = h/(2π).

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Similarly for energy and time: ΔE · Δt ≥ ℏ/2 — has implications for line widths and short-lived excited states.

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NOT a statement about measurement disturbance — it's a fundamental property of wave packets.

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Smaller Δx requires a sharper wave packet, which has a broader range of k (= 2π/λ) — and therefore a broader range of momentum.

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Macroscopic objects: ℏ is so small that Δx·Δp can be far below any measurable scale ⇒ classical mechanics is recovered.

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Implications: there is NO classical 'orbit' for electrons in atoms — only probability clouds.

Position-momentum (1D)

ℏ = h/(2π) ≈ 1.054 × 10⁻³⁴ J·s.

Energy-time

Short-lived states have broader natural line widths.

Approximate (with h)

Loose form often used in JEE — factor differs by 4π.

Equality case (Gaussian)

Achieved by a coherent state (Gaussian wave packet).

Uncertainty is a property of QUANTUM STATES, not an artifact of measurement — even an ideal apparatus cannot beat it.

Sharper position localisation requires a wave packet built from a wider range of wavelengths ⇒ wider spread in p.

Why electrons don't crash into nuclei: confined to a tiny Δx, they must have huge Δp ⇒ huge KE ⇒ would escape. Atoms are stable BECAUSE of uncertainty.

ΔE·Δt: a state living only for Δt has energy uncertain by ~ℏ/Δt — explains natural line broadening in spectroscopy.

Uncertainty does NOT mean 'we just don't know' — quantum states genuinely lack precise simultaneous values for incompatible observables.

Macroscopic: a bullet (m = 0.01 kg) localised to 0.1 mm has Δp ≥ ℏ/(2·10⁻⁴) ~ 5×10⁻³¹ kg·m/s — completely negligible compared to classical p.

Dual Nature of Radiation & Matter on sciphylab (also known as SciPhy, SciPhy Lab, SciPhy Labs). Free physics revision for Class 12, JEE Mains, JEE Advanced, NEET UG, AP Physics 1/2/C, SAT Subject Physics, and CUET-UG.