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Hi, I'm Steve, a graduate student in physics at Berkeley.
Here's my personal website
Boxes!
RSI | This user made a miraculous recovery from RSI using the treatment method of John Sarno. |
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Licensing!
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Released into public domain
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I agree to release my text and image contributions, unless otherwise stated, into the public domain. Please be aware that other contributors might not do the same, so if you want to use my contributions under public domain terms, please check the multi-licensing guide.
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Please keep in mind: My text and images for Wikipedia are public domain. If you use them without giving any credit or attribution or link to their author (me) and/or source (wikipedia), you are not behaving illegally...but you are behaving unethically!
Images I made!
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The
exponential function ez can be defined as the
limit of (1+
z/N)
N, as N approaches infinity. Here, we take
z=iπ, and take N to be various increasing values from 1 to 100. The computation of (1+
iπ / N)
N is displayed as N repeated multiplications in the
complex plane, with the final point being the actual value of (1+
iπ / N)
N. As N gets larger, it can be seen that (1+
iπ / N)
N approaches a limit of -1. Therefore
eiπ=-1.
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A broad probability distribution on a log scale. The total area in blue and red are the relative probabilities that the first digit of a number drawn from this distribution starts with 8 and 1, respectively. This distribution follows Benford's law to a reasonably good accuracy: The ratio of the blue and red areas is nearly the same as the ratio of the blue and red widths.
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A narrow probability distribution on a log scale. The total area in blue and red are the relative probabilities that the first digit of a number drawn from this distribution starts with 8 and 1, respectively. This distribution does not follow Benford's law: The ratio of the blue and red areas is very different from the ratio of blue and red widths.
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A loop of wire (black), carrying a
current, creates a
magnetic field (blue). When the wire is
reflected in a mirror (dotted line), the magnetic field it generates is
not reflected in the mirror: Instead, it is reflected
and reversed. The position of the wire and its current are (polar) vectors, but the magnetic field is a pseudovector.
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Diffusion from a microscopic and macroscopic point of view. Initially, there are
solute molecules on the left side of a barrier (purple line) and none on the right. The barrier is removed, and the solute diffuses to fill the whole container.
Top: A single molecule moves around randomly.
Middle: With more molecules, there is a clear trend where the solute fills the container more and more uniformly.
Bottom: With an enormous number of solute molecules, all randomness is gone: The solute appears to move smoothly and systematically from high-concentration areas to low-concentration areas, following
Fick's laws.
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Simulation of many identical atoms undergoing
radioactive decay, starting with either 4 atoms (left) or 400 (right). The number at the top is how many half-lives have elapsed. Note the
Law of Large Numbers: With more atoms, the overall decay is less random.
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Simulation illustrating the Law of Large Numbers. Each frame, you flip a coin that is red on one side and blue on the other, and put a dot in the corresponding column. A pie chart shows the proportion of red and blue so far. Notice that the proportion varies a lot at first, but gradually approaches 50%.
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Two
current-carrying
wires can attract or repel each other magnetically, as described by
Ampère's force law. Here, the bottom wire has current
I1, which creates magnetic field
B1. The top wire carries a current
I2 through this magnetic field, so the wire experiences a
Lorentz force F
12. Simultaneously (not shown), the top wire makes a magnetic field which results in an
equal and opposite force on the bottom wire.
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Angular frequency
ω (in radians per second), is larger than frequency
ν (in cycles per second, also called
Hz), by a factor of 2π.
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Three flashing lights, from lowest frequency (top) to highest frequency (bottom). f is the frequency in
Hertz ("Hz"), meaning the number of flashes per second. T is the period in seconds ("s"), meaning the number of seconds per flash. T and f are
reciprocals.
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The Shockley-Queisser limit for the maximum possible efficiency of a solar cell. (Under certain assumptions.)
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The Shockley-Queisser limit for the maximum possible efficiency of a solar cell. (Under certain assumptions.) (Zoomed in near maximum-efficiency region.)
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The Shockley-Queisser limit for the maximum possible short-circuit current density of a solar cell. (Under certain assumptions.)
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Black curve: The Shockley-Queisser limit for the maximum possible open-circuit voltage of a solar cell. (Under certain assumptions.) Red dotted line is "y=x", showing that the open-circuit voltage is lower than the bandgap voltage.
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A
homogeneous function is not necessarily
continuous, as shown by this example. This is the function
f defined by
if
or
if
. This function is homogeneous of order 1, i.e.
for any real numbers
. It is discontinuous at
.
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A
harmonic oscillator in
classical mechanics (A-B) and
quantum mechanics (C-H). In (A-B), a ball, attached to a spring (gray line), oscillates back and forth. In (C-H),
wavefunction solutions to the
Time-Dependent Schrödinger Equation are shown for the same potential. The horizontal axis is position, the vertical axis is the real part (blue) or imaginary part (red) of the wavefunction. (C,D,E,F) are stationary states (energy eigenstates), which come from solutions to the
Time-Independent Schrödinger Equation. (G-H) are non-stationary states, solutions to the Time-Dependent but not Time-Independent Schrödinger Equation. (G) is a randomly-generated
quantum superposition of the four states (C-F). (H) is a "
coherent state" ("Glauber state") which somewhat resembles the classical state B.
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Three wavefunction solutions to the Time-Dependent Schrödinger equation for a
harmonic oscillator. Left: The real part (blue) and imaginary part (red) of the wavefunction. Right: The probability of finding the particle at a certain position. The top two rows are two stationary states, and the bottom is the
superposition state , which is not a stationary state. The right column illustrates why stationary states are called "stationary".
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Electron
wavefunctions for the
1s orbital of the hydrogen atom (left and right) and the corresponding bonding (bottom) and antibonding (top) molecular orbitals of the H
2 molecule. The
real part of the wavefunction is the blue curve, and the
imaginary part is the red curve. The red dots mark the locations of the protons. The electron wavefunction oscillates according to the
Schrödinger wave equation, and orbitals are the
standing waves. The standing wave frequency is proportional to the orbital's energy. (This plot is a one-dimensional slice through the three-dimensional system.)
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It is impossible to make
magnetic monopoles from a
bar magnet. If a bar magnet is cut in half, it is
not the case that one half has the north pole and the other half has the south pole. Instead, each piece has its own north and south poles. A magnetic monopole cannot be created from normal matter such as
atoms and
electrons, but would instead be a new
elementary particle.
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An FTIR interferogram. This is the "raw data" which can be
Fourier transformed into the FTIR spectrum. The peak at the center is the ZPD position ("Zero Path Difference"), where the two mirrors in the FTIR's
interferometer are equidistant from the
beamsplitter.
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Why do crystals have smooth, flat faces? As a
halite crystal is growing, new atoms can very easily attach to the parts of the surface with rough atomic-scale structure and many
dangling bonds. Therefore these parts of the crystal grow out very quickly (orange arrows). Eventually, the whole surface consists of smooth,
stable faces, where new atoms cannot as easily attach themselves. (After
this webpage.)
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Relationship between the (continuous)
Fourier transform and the discrete Fourier transform.
Left column: A continuous function (top) and its Fourier transform (bottom).
Center-left column: If the function is periodically repeated, its Fourier transform becomes zero except at discrete points.
Center-right column: Conversely, if the function is discretized (multiplied by a
Dirac comb), its Fourier transform becomes periodic.
Right column: If a function is both discrete and periodic, then so is its Fourier transform. The situation in the right column is mathematically identical to the discrete Fourier transform.
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Example of how the
polarization density in a bulk crystal is ambiguous. (a) A solid crystal. (b) By pairing the positive and negative charges in a certain way, the crystal appears to have an upward polarization. (c) By pairing the charges differently, the crystal appears to have a downward polarization.
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The
hydraulic analogy compares electric current flowing through circuits to water flowing through pipes. When a pipe (left) is filled with hair (right), it takes a larger pressure to achieve the same flow of water. Pushing electric current through a large resistance is like pushing water through a pipe clogged with hair: It requires a larger voltage drop to drive the same current.
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The
IV curve of a non-ohmic device (purple). Point A represents the current and voltage right now. The
chordal resistance (
static resistance) is the
inverse slope of line B through the origin. The
differential resistance is the inverse slope of
tangent line C.
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In the
hydraulic analogy, a capacitor is analogous to a rubber membrane sealed inside a pipe. This animation illustrates a membrane being repeatedly stretched and un-stretched by the flow of water, which is analogous to a capacitor being repeatedly charged and discharged by the flow of current.
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The different types of
rotation operators.
Top: Two particles, with
spin states indicated schematically by the arrows.
(A) The operator
R, related to
J, rotates the entire system.
(B) The operator
Rspatial, related to
L, rotates the particle positions without altering their internal
spin states.
(C) The operator
Rinternal, related to
S, rotates the particles' internal spin states without changing their positions.