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Classical Mechanics
-studies motion and behavior of objects on a bigger scale, predicts a precise trajectory for particles,allows
translational,vibrational and rotational to be excited
Classical physics: light-electromagnetic radiation
Quantum Mechanics-behavior of sub-atomic particles
Electromagnetic field
An oscillating electric and magnetic disturbance that spreads as a harmonic wave through empty space, the vacuum.
Has two components: Electric Field & Magnetic Field
*The wave travels at a constant speed called the speed of light, c, which is about 3 108 m s1
Wavelength is the distance bet the neighboring peaks of the curves
Frequency (v) - # of times per second at which its displacement at fixed point return to its original value
# of cycle a wave complete its one second
Measured in Hertz: 1 Hz= 1 s-1
*Wavelength is inversely proportional to frequency but directly proportional to velocity
Wave number- spatial wavelength, inversely proportional to the wavelength, usually in cm-1
Electromagnetic Spectrum- description and classification of electromagnetic field according to its frequency and wavelength
Einstein Temperature
-expressing frequencies of oscillation of atoms as a temperature
-high frequency corresponds to high Einstein temperature
Debye Formula
Physical Chemistry 2
Debye Temperature- they oscillate over a range of frequencies from 0 up to maximum value
- Max Planck explains blackbody radiation in the context of quantized energy emission: Quantum theory is born.
- Albert Einstein proposes that light, which has wavelike properties, also consists of discrete, quantized bundles of energy,
which are later called photons.
1911
- Ernest Rutherford proposes the nuclear model of the atom.
1913
- Niels Bohr proposes his planetary model of the atom, along with the concept of stationary energy states, and accounts
for the spectrum of hydrogen.
1914
- James Franck and Gustav Hertz confirm the existence of stationary states through an electron-scattering experiment.
1923
- Louis de Broglie generalizes wave-particle duality by suggesting that particles of matter are also wavelike.
1924
- Satyendra Nath Bose and Albert Einstein find a new way to count quantum particles, later called Bose-Einstein statistics,
and they predict that extremely cold atoms should condense into a single quantum state, later known as a Bose-Einstein
condensate.
1925
- Wolfgang Pauli enunciates the exclusion principle.
Werner Heisenberg, Max Born, and Pascual Jordan develop matrix mechanics, the first version of quantum
mechanics, and make an initial step toward quantum field theory.
1926
- Erwin Schrdinger develops a second description of quantum physics, called wave mechanics. It includes what
becomes one of the most famous formulas of science, which is later known as the Schrdinger equation.
- Enrico Fermi and Paul A.M. Dirac find that quantum mechanics requires a second way to count particles, Fermi-Dirac
statistics, opening the way to solid-state physics.
- Dirac publishes a seminal paper on the quantum theory of light.
1927
- Heisenberg states his Uncertainty Principle, that it is impossible to exactly measure the position and momentum of a
particle at the same time.
1928
- Dirac presents a relativistic theory of the electron that includes the prediction of antimatter
1932
- Carl David Anderson discovers antimatter, an antielectron called the positron.
1948
- Richard Feynman, Julian Schwinger, and Sin-Itiro Tomonaga develop the first complete theory of the interaction of
photons and electrons, quantum electrodynamics, which accounts for the discrepancies in the Dirac theory.
1957
- John Bardeen, Leon Cooper, and J. Robert Schrieffer show that electrons can form pairs whose quantum properties
allow them to travel without resistance, providing an explanation for the zero electrical resistance of superconductors. This
theory was later termed the BCS theory (after the surname initials of the three physicists).
1959
- Yakir Aharonov and David Bohm predict that a magnetic field affects the quantum properties of an electron in a way that
is forbidden by classical physics. The Aharonov-Bohm effect is observed in 1960 and hints at a wealth of unexpected
macroscopic effects.
1960
- Building on work by Charles Townes, Arthur Schawlow, and others, Theodore Maiman builds the first practical laser.
1964
- John S. Bell proposes an experimental test, "Bell's inequalities," of whether quantum mechanics provides the most
complete possible description of a system.
1970
- Foundations are laid for the standard model of particle physics, in which matter is said to be built
of quarks and leptons that interact via the four physical forces.
1982
- Alain Aspect carries out an experimental test of Bell's inequalities and confirms the completeness of quantum
mechanics.
1991 - Richard R. Ernst develops two-dimensional nuclear magnetic resonance spectroscopy (2D-FT NMRS) for small molecules in
solution and is awarded the Nobel Prize in Chemistry in 1991 "for his contributions to the development of the methodology
of high resolution nuclear magnetic resonance (NMR) spectroscopy."
2000
- Scientists at European Organization for Nuclear Research (CERN) publish experimental results in which they claim to
have observed indirect evidence of the existence of a quarkgluon plasma, which they call a "new state of matter.
2009 - Aaron D. O'Connell invents the first quantum machine, applying quantum mechanics to a macroscopic object just large
enough to be seen by the naked eye, which is able to vibrate a small amount and large amount simultaneously.
2014 - Scientists transfer data by quantum teleportation over a distance of 10 feet with zero percent error rate, a vital step towards a
quantum internet.
ELECTROMAGNETIC RADIATION
-produced by oscillating electric and magnetic disturbances
-electric and magnetic fields come at right angles and the combined wave moves perpendicular
James Clerk Maxwell
-first to predict the existence of electromagnetic waves
-proposed that a light-including various forms of radiant energy-is an electromagnetic distribution in the form of waves
-proposed a unified theory of electromagnetism
Physical Chemistry 2
Electromagnetism- how electrically charged particles interact with each other and with magnetic fields
Electromagnetic theory
There are four main electromagnetic interactions:
1. The force of attraction or repulsion between electric charges is inversely proportional to the square of the
distance between them.
2. Magnetic poles come in pairs that attract and repel each other, much as electric charges do.
3. An electric current in a wire produces a magnetic field whose direction depends on the direction of the current.
4. A moving electric field produces a magnetic field, and vice versa.
Heinrich Hertz
-provide an experimental confirmation of Maxwells prediction by producing the first man-made electromagnetic waves
General Properties of all electromagnetic radiation:
Electromagnetic radiation can travel through empty space.
The speed of light is always a constant. (Speed of light : 2.99792458 x 108 m/s)
Wavelengths are measured between the distances of either crests or troughs.
Electromagnetic wave- is the radiation consisting of waves, of energy associated with electric and magnetic fields, resulting from the
acceleration of an electric charge
Properties of Electromagnetic Waves
1. The energy of electromagnetic radiation is directly proportional to the frequency.
2. Electromagnetic radiation with higher frequency than visible light has higher energy. This is why ultraviolet light can burn
your skin and X-rays and gamma rays can damage tissues.
3. Electromagnetic radiation with a lower frequency than visible light has less energy
4. Higher frequency electromagnetic waves have shorter wavelengths
5. Wavelengths vary greatly from long wavelengths (many meters) to very short wavelengths (the size of atomic nuclei).
Electromagnetic spectrum- number of different radiations.
Radiation is energy that travels and spreads out as it goes.
Radio waves
the lowest frequency which is about 30 billion hertz, or 30 gigahertz (GHz),
longest wavelength greater than about 10 millimeters (0.4 inches),
Ionosphere is a set of ionized layers in the upper portions of the atmosphere
Radio pulses travel more slowly within the ionosphere than in free space,
Radio is used primarily for communications including voice, data and entertainment media.
Microwaves
fall in the range of the EM spectrum between radio and IR
used for high-bandwidth communications, radar and as a heat source for microwave ovens and industrial applications.
Infrared
Infrared is in the range of the EM spectrum between microwaves and visible light.
IR light is invisible to human eyes, but we can feel it as heat if the intensity is sufficient.
Visible light
found in the middle of the EM spectrum, between IR and UV.
visible to most human eyes.
Ultraviolet
Ultraviolet light is in the range of the EM spectrum between visible light and X-rays
UV light is a component of sunlight; however, it is invisible to the human eye.
It has numerous medical and industrial applications, but it can damage living tissue.
X-rays
Soft X-rays comprise the range of the EM spectrum between UV and gamma rays.
Hard X-rays occupy the same region of the EM spectrum as gamma rays.
The only difference between them is their source: X-rays are produced by accelerating electrons, while gamma rays are
produced by atomic nuclei.
Gamma-rays
range of the spectrum above soft X-rays.
Gamma radiation causes damage to living tissue, which makes it useful for killing cancer cells
BOHR ATOMIC THEORY
A.
BOHR ATOMIC MODEL
An atom is made up of three particles, electrons, protons and neutrons. Electrons have a negative charge and protons
have a positive charge whereas neutrons have no charge. They are neutral. Due to the presence of equal number of negative
electrons and positive protons, the atom as a whole is electrically neutral.
The protons and electrons are located in a small nucleus at the centre of the atom. Due to the presence of protons, the
nucleus is positively charged.
The electrons revolve rapidly around the nucleus in fixed circular paths called energy levels or shells. The 'energy
levels' or 'shells' or 'orbits' are represented in two ways: either by the numbers 1, 2, 3, 4, 5 and 6 or by letters K, L, M, N, O and
P. The energy levels are counted from centre outwards.
Each energy level is associated with a fixed amount of energy. The shell nearest to the nucleus has minimum energy
and the shell farthest from the nucleus has maximum energy.
There is no change in the energy of electrons as long as they keep revolving with the same energy level. But, when an electron
jumps from a lower energy level to a higher one, some energy is absorbed while some energy is emitted.
When an electron jumps from a higher energy level to a lower one, the amount of energy absorbed or emitted is given
by the difference of energies associated with the two levels. Thus, if an electron jumps from orbit 1 (energy E 1) to orbit 2 (energy
E2), the change in energy is given by E2 - E1.
The energy change is accompanied by absorption of radiation energy of E = E 2 E1 = h where, h is a constant
called 'Planck's constant' and is the frequency of radiation absorbed or emitted. The value of h is 6.626 x 10 -34 J-s. The
absorption and emission of light due to electron jumps are measured by use of spectrometers.
B.
Physical Chemistry 2
Electrons revolve round the nucleus with definite velocities in concentric circular orbits situated at definite distances
from the nucleus. The energy of an electron in a certain orbit remains constant. As long as it remains in that orbit, it neither emits
nor absorbs energy. These are termed stationary states or main energy states.
Bohr proposed that the angular momentum of an electron is quantized. Thus, the motion of an electron is restricted to
those orbits where its angular momentum is an integral multiple of h/2, where h is Plancks constant.
Thus we have the relationship mvr = nh/2, where m is mass of electron, v is velocity of electron of said orbit, r is radius
of that orbit, n is a simple integer.
The stationary states or allowed energy levels are only those where n = 1, 2, 3. This is called Bohr quantum condition.
The energy of an electron changes only when it moves from one orbit to another. An electronic transition from an inner
orbit to outer orbit involves absorption of energy. Similarly, when an electron jumps from an outer orbit to inner orbit it releases
energy, which is equal to the difference between the two energy levels.
Based on the Bohr theory, Bohr calculated the radii of the various orbits and the energies associated with the electrons
present in those shells.
Operators act on a wave function from the left, and the order of operations is important (much as in the case of multiplying by
matrices - commutatively is important).
Physical Chemistry 2
III.
Individual Measurements
Postulate 3: For a single measurement of an observable corresponding to a quantum mechanical operator, only values
that are eigenvalues of the operator will be measured.
If measuring energy: one obtains eigenvalues of the time-independent Schrdinger equation:
n (x,t) = Enn(x,t)
Note: The total wave function defining a given state of a particle need not be an eigenfunction of the operator (but one
can expand the wave function in terms of the eigenfunctions of the operator as a complete basis).
IV.
<a>=
This is a general form for the expectation value expression. If the wavefunction is normalized, then the denominator
is identically 1 (this is assumed to be the case since every valid wavefunction must be normalized).
Consider the following cases:
A. The wavefunction represents an eigenfuntion of the operator of interest. The expectation value of a
measurable is:
<a> =
= aj
Now consider that the wavefunction itself is not an eigenfunction of the operator . However, since the
wavefunction belongs to the space of functions that are eigenfunctions of the operator, we can construct
(expand) the wavefunction from the basis of eigenfunctions of . Thus:
(x,t) = bnn (x,t)
Where the bnn (x,t) are eigenfunctions of the operator . Consider:
<a> =
=
=
=
The only terms that survive m =n terms (orthogonality of eigenfunctions of Hermitian operators). Thus,
<a> =
=
The average value of the observable is a weighted average of the possible eigenvalues (i.e., possible measurement
outcomes).The weighting factor is the square of the expansion coefficient, bn for the n'th eigenfunction with eigenvalue an.
Thus, the expansion coefficients, bn represent the degree to which the full wavefunction possesses the character of
the eigenfunction n. By anology to vector space, the coefficients can be thought of as projections of the wavefunction on to the
basis functions (i.e., the eigenfunctions of the operator).
Identically prepared quantum systems can have different outcomes with regard to measure observables. (super
position of states)
Initial measurement of a quantum mechanical system is probabilistic. Subsequent measurements will yield the same
value of the observable. This is a transition from a probabilistic to a deterministic outcome. Collapse of the wavefunction.
V.
Time Evolution
Postulate 5: The time-dependent Schrdinger equation governs the time evolution of a quantum mechanical system:
(x,t) =
The Hamiltonian operator contains the kinetic and potential operators. This equation reflects the deterministic
(Newtonian) nature of particles/waves. It appears to be in contrast to Postulate 4 (many observations lead to different
measured observables, each weighted differently, i.e., a probabilistic view of the particle/wave). The reconciliation is in the fact
that Postulate 4 pertains to the outcomes of measurements at 5 a specific instant in time.
Postulate 5 allows us to propagate the wavefunction in time (we propagate a probabilistic entity). Then, at some
future time, if we make another measurement, we are again faced with the implications of Postulate 4.
In dealing stationary quantum mechanical states, we do not need to have an explicit knowledge of the time
dependent wavefunction, particularly if the operator of interest is independent of time. Consider:
(x) n (x,t) = ann (x,t)
Recalling that the time dependent wavefunction can be written as the product of time-independent and timedependent components:
n (x,t) = n (x)
Thus:
Physical Chemistry 2
(x) n
(x) n (x) =
ann (x)
There is no restriction on the value of k. Thus a free particle, even in quantum mechanics, can have any non-negative
value of the energy and the energy spectrum is continuous.
Particle in 1D Box
This is the simplest non-trivial application of the Schrdinger equation, but one which illustrates many of the fundamental
concepts of quantum mechanics. For a particle moving in one dimension (again along the x- axis), the Schrdinger equation can be
written
These are the only values of the energy which allows solutions of the Schrdinger
equation consistent with the boundary conditions. The integer n, called a quantum
number, is appended as a subscript on E to label the allowed energy levels. The
normalized eigenfunctions is
The normalized solutions X(x), Y (y), Z(z) can therefore be written down as
Three quantum numbers are required to specify the state of the three-dimensional system. The corresponding eigenfunctions are
Physical Chemistry 2
Where t is the time necessary for the wave to reach a position x. The solution of this equation can be obtained in the form
(Eq. 26)
Where f1(x) is a function only of x and f2(t) can be written as (Eq. 27)
If we differentiate
Physical Chemistry 2
And hence on substitution of Eq. (29) and Eq. (30) into Eq. (25) we get (Eq. 31)
But wave length =ux/v. Making this substitution, (Eq. 31) becomes (Eq. 32)
Equation (32) applies to a wave moving in the x direction only. If we consider a wave moving in three dimensions, then
f1(x) can be replaced by , where = (x,y,z), and Eq.(32) is transformed to Eq.(33)
Or Eq. (34)
Again according to de Broglies hypothesis a wave of length can be considered to be a particle of mass m moving with a
velocity v, namely = h/mv . Substituting the latter into Eq. (34), we obtain Eq. (36)
Finally, the total energy of the particle, E, is the sum of its potential energy, U, and its kinetic energy Ek = (1/2) mv2.
Consequently,
And
Substitution of the latter expression to Eq. (36) thus yields Eq. (37)
which is the Schrodingers wave equation, and the postulated basis of all quantum mechanical behavior of matter.
TIME-INDEPENDENT SCHRODINGER EQUATION
Where:
V(x) = the potential energy of the particle at the point x
E = sum of potential and kinetic energies
= convenient modification of Plancks constant
Physical Chemistry 2
Js
In general case, Schrodinger equation is written
Where is the Hamiltonian operator for the system:
For the evolution of a system with time, it is necessary to solve the time-dependent Schrodinger equation:
Although the Schrodinger equation should be regarded as a postulate, like Newtons equations of motion, it can be seen
to be plausible by noting that it implies the de Broglie relation for a freely moving particle in a region with constant potential energy
V:
General strategies for solving differential equations of this and other types that occur frequently in physical chemistry, we
note that a solution is:
Where
In quantum mechanics, a wave function that describes the spatial distribution of a particle (a spatial wave function) is
complex if the particle it describes has a net motion. In the present case, we can use the relation
to
write
.
The real and imaginary parts of can be shown as
Source: Atkins
and we see that the imaginary component
real and imaginary parts of the wave function are real, in the sense of being present, and we express as a complex function
simply to help the visualization of the motion of the particle the wave function describes.
harmonic wave,
implies that
is a wave of wavelength
). The quantity
Because
, which
it follows that
Therefore, the linear momentum is related to the wavelength of the wave function by
Physical Chemistry 2
APPROXIMATION METHOD
Techniques of Approximation
Many problems and almost all the problems of interest in chemistry do not have exact solutions. To make progress with
these problems we need to develop techniques of approximation.
There are two major approaches:
Variation theory
Perturbation theory
Variation theory
It is one way of finding approximations to the lowest energy eigenstate or ground state, and some excited states. This
allows calculating approximate wave functions such as molecular orbital.
Perturbation theory
The Hamiltonian for the problem we are trying to solve, , can be expressed as the sum of a simple Hamiltonian, (0),
which has known eigenvalues and eigenfunctions, and a contribution, (1), which represents the extent to which the true Hamiltonian
differs from the model Hamiltonian:
= (0) + (1)
Time-independent perturbation theory
Perturbation is always present and unvarying.
It might represent a dip in the potential energy of a particle in a box in some region along the length of the box.
the true energy of the system differs from the energy of the simple system
E = E(0) + E(1) + E(2) + . . .
where E(1) is the first-order correction to the energy, a contribution proportional to (1)E(2) is the second-order correction
to the energy, a contribution proportional to (1)2
The true wave function also differs from the simple wave function
= (0) + (1) + (2) + . . .
(1) is the first-order correction to the wave function
First-order corrections to the energy of the ground state with the wave functions 0 and energy E0
E(1) as the average value of the perturbation
Second-order corrections to the energy of the ground state with the wave function 0 and energy E0
Analogy
shift in energy of vibration of a violin string when small weights are hung along its length
We should note the following three features of Second-order corrections to the energy of the ground state:
1. Because En (0) >E0 (0), all the terms in the denominator are negative and, because the numerators are all positive,
the second-order correction is negative, which represents a lowering of the energy of the ground state.
2. The perturbation appears (as its square) in the numerator; so, the stronger the perturbation, the greater the lowering
of the ground-state energy.
3. If the energy levels of the system are widely spaced, all the denominators are large, so the sum is likely to be small;
in which case the perturbation has little effect on the energy of the system: the system is stiff, and unresponsive to
perturbations. The opposite is true when the energy levels lie close together.
Example 9.5 Using perturbation theory
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Physical Chemistry 2
Find the first-order correction to the ground-state energy for a particle in a well with a variation in the potential of the form
V = sin(x/L), as in Fig. 9.43.
Method
Identify the first-order perturbation hamiltonian and evaluate E 0(1) from
First-order corrections to the energy of the ground state.
We can expect a small lowering of the energy because the average potential
energy of the particle is lower in the distorted box.
Answer:
The perturbation hamiltonian is
(1) = sin(x/L)
Therefore, the first-order correction to the energy is
Because in our case the perturbation is that of the interaction of the electromagnetic field with a molecule (eqn 9.67), we
conclude that
Therefore, the rate of transition, and hence the intensity of absorption of the incident radiation, is proportional to the
square of the transition dipole moment:
The size of the transition dipole can be regarded as a measure of the charge redistribution that accompanies a transition.
The rate of transition is also proportional to E2, and therefore the intensity of the incident radiation (because the intensity is
proportional to E2).
Example Problems
(a) Involving Variational Method
Using the variational method approximation, find the ground state energy of a particle in a box using this trial function:
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Physical Chemistry 2
Where
b. A quartic oscillator that arises from only using a quartic term cx4 and compare the results.
Solution:
A.) The Hamiltonian for this problem is
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Physical Chemistry 2
B.)
The
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