Atomic Spectra and Atomic Energy States
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Transcript Atomic Spectra and Atomic Energy States
Atomic Spectra and
Atomic Energy States
Reminder: A.S. 13.1.5-13.1.7 due Monday 3/23/15
A.S. 13.1.8-13.1.13 due Tuesday 3/24/15
WebAssign Quantum #3 due Tuesday 3/24/15
Emission Spectra
When a gas is heated to a high temperature, or
exposed to a large electric field
Electrons in the atoms absorb the energy
When the electrons fall back down to the
original electron energy the energy is
emitted as Electromagnetic radiation
To the right: hydrogen gas, exposed to high
electrical potential
How do we see spectral lines?
Direct light through a diffraction grating, or a prism
Light at different wavelengths will diffract or refract different
amounts
The wavelengths that combine to give us the color we see
emitted can be separated in this way
Hydrogen, for example, is composed of 4 main wavelengths of
light:
Absorption Spectra
Sometimes, we see spectra showing us which
wavelengths were absorbed by a sample of gas:
Interestingly, the wavelengths of light ABSORBED by
the gas are the SAME as those EMITTED by the gas…
“Balmer Series”
Curiously (at the time!), the spectral lines always
occurred at very specific (discrete) wavelengths
In 1885, Johann Balmer determined that the spectral
lines for Hydrogen always followed this pattern:
1
1 1
=𝑅
− 2
𝜆
4 𝑛
(n an integer value ≥ 3)
But he couldn’t explain WHY this worked!
Review: Planetary Model
Rutherford came up with the planetary model of the
atom:
There is a central, dense, positively charged nucleus
Electrons occupy a large space outside the nucleus
Electrons occupy “orbits”, much like planets orbit the
sun (our center of the solar system)
WHY doesn’t this work?
Electron Energy Levels
Combining the ideas of Balmer and Rutherford, Niels
Bohr made an attempt to “correct” the fundamental
flaw of the planetary model using the following
assumption:
Electrons exist with discrete energy in each orbit
(energy level)
In order to move between energy levels, a discrete
amount of energy must be absorbed by or released
from the electron
Bohr Model of the Atom
Electrons exist at specific radii
from the nucleus—energy
levels
Quantitatively, the energy of
the electron in that energy
level can be determined using
the following relationship:
13.6
𝐸=− 2
𝑛
Characteristics of Electron Energy Levels
As n increases, the energy levels become closer together (unlike
the diagram on the previous slide)
As n approaches infinity, the total energy of the electron
approaches 0
As E approaches zero, the force keeping the electrons bound to
the nucleus decreases
Ionization Energy: The energy that must be added to an electron
in order to release it from the atom
Ways of ionizing an atom:
Significantly increasing the temperature
Bombarding it with additional electrons (high velocity
collisions)
Subjecting it to a very high electric potential
Causing photons to fall on the atoms
Limitations to Bohr’s Model
Describes the behavior of the electron in a Hydrogen
atom really well…however:
Does NOT treat any atom with more than one electron
Assumes circular orbits
Cannot predict INTENSITIES of emitted light—only
wavelength
Does not predict the division of energy levels (i.e. the p,
d, f orbitals all have subdivisions)
So…now what?
Schrodinger Theory:
Assumptions:
Electrons in the atom can be described by wave
functions
Wave functions fit boundary conditions in 3
dimensions, allowing for multiple “modes” that have a
discrete energy state
Electron has an undefined position, but there is a
probability that the electron exists in a position
Electron Wavefunctions
Wavefunction (ψ): a function of position and time
Mathematically the probability that an electron will
be in a particular position at a particular time can be
determined by the square of the absolute value of the
wavefunction at that time.
In other words, there are places where electrons are
most likely to be found…not just circular orbits!
Hydrogen electron probability
For each energy
level for
Hydrogen, there is
a probability curve
describing how
likely it is that an
electron can exist
in that position.
Uncertainty Principle
Fundamental idea: wave-particle duality
Since particles sometimes act like waves, and waves
sometimes act like particles, there isn’t a perfect,
clean way to divide physical objects into one category
or the other.
Misconception alert! This has nothing to do with
experimental uncertainties!
It’s all about measuring things with an indefinite
precision (remember those distribution graphs we
just saw? )
Heisenberg’s Uncertainty Principle
It is not possible to simultaneously measure both the
position and the momentum of a particle.
The more sure we are about the position of a particle,
the less certain we are about its momentum, and viceversa.
ℎ
∆𝑥∆𝑝 ≥
4𝜋
Another variation…
We can also describe the uncertainty principle in
terms of Energy and Time:
ℎ
∆𝐸∆𝑡 ≥
4𝜋