Quantum Mechanics Lecture Notes PDF
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This document is a set of lecture notes on quantum mechanics. It covers topics including De Broglie's hypothesis, wave functions, the Heisenberg uncertainty principle, postulates and consequences, linear superposition, simple harmonic oscillators, and conjugated systems. The notes also include the time-dependent Schrodinger equation and concepts of stationary states and expectation values.
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# Quantum Mechanics ## DeBroglie's Hypothesis - λ = h/p - λ is the wavelength of a particle - p is the momentum of a particle - deBroglie's hypothesis states that all matter has wave-like properties ## Wave Function - ψ = A cos(kx) - A is the amplitude of the wave - k is the wave number = 2π/λ -...
# Quantum Mechanics ## DeBroglie's Hypothesis - λ = h/p - λ is the wavelength of a particle - p is the momentum of a particle - deBroglie's hypothesis states that all matter has wave-like properties ## Wave Function - ψ = A cos(kx) - A is the amplitude of the wave - k is the wave number = 2π/λ - kħ = p - ħ is the reduced Planck constant - kħ = 2πħ /λ = h/λ = p - Wave vector; k = 2π/λ ## Heisenberg's Uncertainty Principle - Δx Δp >= ħ/2 - Δx is the uncertainty in position - Δp is the uncertainty in momentum - Heisenberg's uncertainty principle states that it is impossible to know both the position and momentum of a particle with perfect accuracy. ## Quantum Mechanics: Postulates ### Postulate 1 - The state of a system is fully specified by the **state function** or **wave function**: ψ(x, y,... t) - ψ(x, y,... t) is a function of space and time - The probability of finding a particle in a small volume dxdydz is: |ψ(x, y, z, t)|² dxdydz - Probability density = |ψ(x, y, z, t)|² - Total probability = ∫ |ψ(x, y, z, t)|² dxdydz = 1 - In order for the wave function to be physically meaningful, it must be **square integrable**. ### Postulate 2 - Corresponding to every observable, there is one **linear operator**. - **Linear operator:** An operator A is linear if: A(c₁f₁ + c₂f₂) = c₁Af₁ + c₂Af₂ - **Examples of linear operators:** - Position: x - Momentum: p = -iħ(d/dx) - Kinetic energy: K.E. =-ħ²/2m(d²/dx²) - Potential energy: V(x) ### Postulate 3 - Measurement of an observable gives one of the **eigenvalues** of the corresponding **operator**. - An **eigenvalue equation** is an equation of the form: Aψ(x, y, z, t) = a ψ(x, y, z, t) - In this equation, **a** is the eigenvalue, and **ψ(x, y, z, t)** is the eigenfunction. ### Postulate 4 - The **wave function** obeys the **time-dependent Schrödinger equation**: iħ(∂/∂t)ψ(x, y,... t) = Ĥψ(x, y,... t) - This equation describes the evolution of the wave function over time. ### Consequences of Postulate 4: - If the potential energy V(x) is time-independent: - **Stationary state**: ψ(x, t) = ψ(x)e^(-iEt/ħ) - **Standing waves**: ψ(x, t) = ψ(x)e^(-iEt/ħ) ## Linear Superposition - A general wave function in space can be written as a linear combination of the eigenfunctions: ψ(x) = Σc₁ψ₁(x) - The coefficients c₁ are complex numbers - The eigenfunctions are orthonormal: ∫ψᵢ(x)ψⱼ(x)dx = δᵢⱼ ## Time-Dependent Schrodinger Equation - The time-dependent Schrodinger equation (TDSE) describes the time evolution of a quantum system. - The solution to the time-dependent Schrodinger equation is the wave function ψ(x, t) - In the case of a time-independent potential: - The wave function can be separated into a product of a time-independent part ψ(x) and a time-dependent part T(t): ψ(x, t) = ψ(x)T(t). - The time-independent part of the wave function ψ(x) is called the **stationary state**. ## Simple Harmonic Oscillator (SHO) - The simple harmonic oscillator (SHO) is a fundamental system in quantum mechanics - The Hamiltonian of the SHO is: - H = -ħ²/2m(d²/dx²) + 1/2kx² - The energy eigenvalues of the SHO are: - E = (n + 1/2) ħω - The energy eigenstates of the SHO can be expressed as a combination of the Hermite polynomials and the Gaussian function. ## Expectation Value - The expectation value of an observable A is given by: - <A> = ∫ψ*(x)Aψ(x)dx ## Conjugated Systems - Conjugated systems are molecules that have alternating single and double bonds. - The π electrons in these systems are delocalized over the entire molecule. - The potential energy of the π electrons in a conjugated system can be approximated by a box potential model. - The energy levels of the π electrons are quantized. - The number of energy levels is equal to the number of π electrons. - In the limit of an infinite box, the energy levels become continuous. This provides a good approximation for large conjugated systems. **Please note that I have excluded images from this document. You can refer to the original image for the illustrations.**