Introduction to Quantum Physics

102 Probability: The Heisenberg Uncertainty Principle

Learning Objectives

  • Use both versions of Heisenberg’s uncertainty principle in calculations.
  • Explain the implications of Heisenberg’s uncertainty principle for measurements.

Probability Distribution

Matter and photons display wave properties, which means that their behavior is spread over a region of space rather than being confined to a single classical path. This raises an important question: what does it mean to describe the position of a particle such as an electron? Is the electron located at the center of its associated wave, or is it distributed throughout the wave? Experiments show that whenever an electron is detected, it is found at one definite location. A detector does not record part of an electron spread across several places. Instead, it records a single localized event, such as one point on a screen. In this sense, each individual detection is particle-like. However, suppose an experiment is prepared in exactly the same way and repeated many times. The electron will not necessarily be detected at the same location in every trial. It may appear at one location during the first trial, at another location during the next trial, and somewhere else during a later trial. These differences are not simply the result of poor instruments or ordinary experimental error. Even when the preparation and measurement are controlled as carefully as possible, quantum mechanics does not generally predict the exact location of an individual detection. Although the position of any one electron cannot be predicted precisely, the results of many repeated measurements form a regular and predictable statistical pattern. Some locations receive many electrons, while other locations receive few or none. The resulting distribution has the same form as the diffraction or interference pattern associated with a wave, as shown in Figure 102.1.

Successive stages in the formation of an electron diffraction pattern. Individual electrons appear as separate dots, but as more electrons are detected, the dots form alternating regions of high and low probability.
Figure 102.1. An electron diffraction pattern builds up one detection at a time. Each electron arrives at one definite location, but the location of an individual electron cannot be predicted precisely. After many electrons have been detected, their positions form a distribution that agrees with the diffraction pattern predicted for waves having the electrons’ de Broglie wavelength.

The distinction between an individual detection and the complete pattern is essential. Quantum mechanics predicts the probability that a particle will be detected within a particular region. It does not ordinarily predict the exact result of one individual measurement. A region in which many electrons are detected corresponds to a high probability, while a region in which few electrons are detected corresponds to a low probability. The overall spatial pattern describing these probabilities is called a probability distribution. A probability distribution does not mean that a fraction of the electron exists at every possible position. Rather, it describes the relative likelihood of obtaining each possible position when the same measurement is performed repeatedly on identically prepared particles. After de Broglie proposed that matter has wave properties, physicists including Erwin Schrödinger and Werner Heisenberg explored the consequences of this idea. One of the most important conclusions was that, because of its wave character, the precise trajectory and final destination of an individual particle generally cannot be predicted. Nevertheless, each measurement produces one definite result. After enough measurements have been collected, the results form a probability distribution related to the particle’s wavelength and its corresponding diffraction pattern.

Probability Is Not Experimental Error

The statistical character of quantum mechanics should not be confused with uncertainty caused by faulty equipment. Better instruments can reduce ordinary measurement error, but they cannot make every individual electron arrive at a predictable location. The probability distribution is a fundamental feature of the quantum system itself.

The relationship between wave behavior and probability becomes especially clear in a double-slit experiment. Figure 102.2 compares the interference patterns produced by two different types of particles. When the particles have equal wavelengths and pass through slits with the same separation, they produce identical interference patterns.

Comparison of double-slit interference patterns produced by electrons and protons with equal wavelengths and equal slit separations.
Figure 102.2. Double-slit interference for electrons (a) and protons (b). When the particles have equal wavelengths and encounter the same slit separation, they produce identical interference patterns. In both cases, the pattern is a probability distribution built from individual particle detections whose locations cannot be predicted separately.

The locations of the bright interference regions follow the double-slit constructive-interference condition

[latex]d\sin\theta=m\lambda,[/latex]

where [latex]d[/latex] is the separation between the slits, [latex]\theta[/latex] is the angle at which a bright region appears, [latex]m[/latex] is an integer, and [latex]\lambda[/latex] is the wavelength of the electron, proton, photon, or other particle. The interference pattern develops statistically as individual particles strike the detector. At first, the detected particles appear as isolated points with no obvious pattern. As more particles arrive, alternating regions of high and low detection probability gradually emerge. After a sufficiently large number of particles have been recorded, the familiar interference pattern becomes clear. It might initially seem that electrons produce this pattern by interfering with other electrons in the beam. This possibility can be tested by reducing the beam intensity until only one electron at a time is present between the source and the detector. Under these conditions, no electron can interact with another electron while passing through the apparatus. Nevertheless, the same interference pattern gradually develops. This result shows that the pattern is not caused by collisions or interactions between different electrons. Instead, the quantum state associated with each electron has wave-like properties and extends through the experimental arrangement. The possible alternatives represented by the two slits combine according to the rules of wave interference. This behavior is often described by saying that the electron’s probability distribution interferes with itself. This does not mean that an electron divides into two smaller pieces. An electron is detected as one complete particle at one location. The wave-like aspect describes the possible outcomes and their probabilities, while the detector records a localized particle-like event. We might try to determine which slit the electron passes through by placing detectors near the openings. When a measurement is made that identifies the path, each electron is found to pass through one slit or the other. However, there is an important consequence: once which-path information is obtained, the double-slit interference pattern disappears. The resulting distribution is instead consistent with the patterns produced by the two slits acting independently. This outcome does not depend on the particular device used to determine the path. Any measurement that makes it possible to distinguish which slit the particle used changes the experimental situation. When the two paths remain indistinguishable, their probability amplitudes interfere. When the paths become distinguishable through measurement, the interference between them is lost.

Making Connections: From Interference to Atomic Structure

The same probability-based description used in the double-slit experiment also applies to electrons in atoms and molecules. Electrons do not travel around a nucleus along sharply defined planetary orbits. Instead, quantum mechanics predicts probability distributions that describe where an electron is likely to be detected. These distributions form the basis of the atomic orbitals used in chemistry and biochemistry.

Heisenberg Uncertainty

Why does obtaining information about an electron’s path change the observed pattern? The answer reflects a central feature of quantum mechanics: measurement is a physical interaction with the system being measured. To determine the position of a moving electron, something must interact with it. For example, a photon may scatter from the electron and then travel to a detector, or another particle may collide with it. The measuring probe carries momentum and energy. During the interaction, some momentum or energy is exchanged with the electron, altering its state. This effect is especially important for microscopic particles because the momentum carried by the measuring probe may be comparable to the momentum of the particle being observed. The measurement therefore cannot be treated as an entirely passive act. Information about one property may be obtained only at the cost of losing precision in another property. This limitation is not merely a practical problem caused by imperfect instruments. Quantum mechanics places a fundamental limit on the simultaneous precision with which certain pairs of physical quantities can be specified. Position and momentum are one such pair.

Portrait of physicist Werner Heisenberg as a young man.
Figure 102.3. Werner Heisenberg made foundational contributions to the development of quantum mechanics and formulated the uncertainty principle. His work changed both the mathematical description of microscopic systems and our understanding of the limits of physical knowledge. He received the Nobel Prize in Physics in 1932. Heisenberg remained in Germany during World War II and participated in Germany’s nuclear research program, a decision that damaged many of his relationships within the international scientific community. (Credit: author unknown, via Wikimedia Commons)

Werner Heisenberg formulated this limit in 1927 while developing quantum mechanics and studying the wave properties of particles. Consider the simultaneous measurement of the position and momentum of an electron. The same reasoning applies to any quantum particle. Because a wave extends over a region of space rather than occupying one geometric point, a particle described by a wavelength [latex]\lambda[/latex] cannot be localized much more precisely than approximately one wavelength. We may therefore estimate the uncertainty in position as

[latex]\Delta x\approx\lambda.[/latex]

Here, [latex]\Delta x[/latex] represents the spread in possible position measurements. If the position measurement is repeated using identically prepared particles, the measured locations will occupy a range rather than producing one identical result every time. To detect the particle, it must interact with a measuring device. During this interaction, momentum is exchanged. The amount of momentum transferred may vary from nearly zero to an amount comparable to the particle’s original momentum. Because the exact momentum transfer cannot be known simultaneously with a precise position measurement, the particle also has an uncertainty in momentum, represented by [latex]\Delta p[/latex]. Using the de Broglie relationship

[latex]p=\frac{h}{\lambda},[/latex]

we can estimate the momentum uncertainty as

[latex]\Delta p\approx\frac{h}{\lambda}.[/latex]

These two approximate relationships reveal an unavoidable trade-off. A shorter wavelength allows the particle to be localized within a smaller region, reducing [latex]\Delta x[/latex]. However, the shorter wavelength corresponds to a larger momentum and therefore to a larger uncertainty in momentum. Conversely, using a longer wavelength reduces the momentum uncertainty but spreads the wave over a larger region of space, increasing the uncertainty in position. Multiplying the two approximate uncertainty relationships gives

[latex]\Delta x\Delta p \approx \lambda\left(\frac{h}{\lambda}\right).[/latex]

The wavelength cancels, leaving

[latex]\Delta x\Delta p\approx h.[/latex]

This approximate result shows that reducing one uncertainty necessarily increases the other. More advanced quantum-mechanical analysis gives the precise lower limit

[latex]\Delta x\Delta p\geq\frac{h}{4\pi}.[/latex]

This relationship is known as the Heisenberg uncertainty principle. It states that position and momentum cannot simultaneously be known with uncertainties whose product is smaller than [latex]h/(4\pi)[/latex]. Neither uncertainty can be zero. A particle cannot possess both an exactly defined position and an exactly defined momentum at the same time. If the position is specified with greater precision, the range of possible momentum values must increase. If the momentum is specified with greater precision, the range of possible positions must increase.

Common Misconception: Uncertainty Is Not Instrument Error

The Heisenberg uncertainty principle does not say that scientists need better microscopes or more sensitive detectors. It describes a fundamental property of quantum systems. Even an ideal instrument cannot assign both an exact position and an exact momentum to the same particle at the same time. Measurement can disturb a microscopic system, but the uncertainty principle is deeper than ordinary disturbance. The quantum state itself does not contain simultaneously exact values of position and momentum.

A short-wavelength probe can provide precise position information because it can resolve a small region of space. However, a short wavelength corresponds to a large momentum. When such a probe interacts with a particle, the momentum exchange can substantially alter the particle’s motion. For example, suppose an electron is used to investigate another electron within an atom. To resolve distances comparable to the size of the atom, the probing electron must have a very short wavelength and therefore substantial momentum. Its interaction with the atomic electron may transfer enough energy and momentum to remove that electron from the atom. The measurement may reveal a position, but it destroys the original state whose motion we hoped to observe. For this reason, it is not physically meaningful to imagine following an electron as it travels around the nucleus along a precise classical orbit. An electron in an atom does not possess both a sharply defined trajectory and a sharply defined position at every instant. If the position of an electron is measured, one definite location is obtained. However, repeated measurements performed on many identically prepared atoms produce a spatial probability distribution. These distributions are called electron clouds or atomic orbitals. An orbital should not be interpreted as a path traveled by an electron. Instead, it represents the probability of detecting the electron in different regions surrounding the nucleus. Regions of greater probability are often drawn more densely or enclosed by surfaces that contain a chosen percentage of the total probability. These orbital probability distributions are central to chemistry and the health sciences. Their shapes and energies help explain chemical bonding, molecular geometry, electron transfer, and the interactions that determine the structures and functions of biological molecules.

Example 102.1: Heisenberg Uncertainty Principle in Position and Momentum for an Atom

  1. If the position of an electron in an atom is measured to an accuracy of 0.0100 nm, what is the electron’s uncertainty in velocity?
  2. If the electron has this velocity, what is its kinetic energy in eV?

Strategy

The accuracy of the position measurement gives the uncertainty in position:

[latex]\Delta x=0.0100\,\text{nm}=1.00\times10^{-11}\,\text{m}.[/latex]

The Heisenberg uncertainty principle relates the uncertainty in position to the uncertainty in momentum:

[latex]\Delta x\Delta p\geq\frac{h}{4\pi}.[/latex]

To calculate the smallest possible uncertainty in momentum, we use the equality. Once [latex]\Delta p[/latex] is known, the corresponding uncertainty in velocity can be found from

[latex]\Delta p=m\Delta v.[/latex]

For part (b), we interpret the uncertainty in velocity as a representative velocity scale and use it to estimate the electron’s kinetic energy.

Solution for (a)

Using the equality to represent the minimum uncertainty gives

[latex]\Delta x\Delta p=\frac{h}{4\pi}.[/latex]

Solving for the uncertainty in momentum,

[latex]\Delta p=\frac{h}{4\pi\Delta x}.[/latex]

Substituting the known values gives

[latex]\Delta p= \frac{6.63\times10^{-34}\,\text{J}\cdot\text{s}} {4\pi\left(1.00\times10^{-11}\,\text{m}\right)} =5.28\times10^{-24}\,\text{kg}\cdot\text{m/s}.[/latex]

Because

[latex]\Delta p=m\Delta v,[/latex]

the uncertainty in velocity is

[latex]\Delta v=\frac{\Delta p}{m}.[/latex]

Using the mass of an electron,

[latex]\Delta v= \frac{5.28\times10^{-24}\,\text{kg}\cdot\text{m/s}} {9.11\times10^{-31}\,\text{kg}} =5.79\times10^{6}\,\text{m/s}.[/latex]

Therefore, the minimum uncertainty in the electron’s velocity is

[latex]\boxed{\Delta v=5.79\times10^{6}\,\text{m/s}}.[/latex]

Solution for (b)

This velocity is about 1.9% of the speed of light, so the nonrelativistic kinetic-energy equation provides an adequate approximation:

[latex]\mathrm{KE}_e=\frac{1}{2}mv^2.[/latex]

Substituting the electron’s mass and taking the velocity to be equal to the calculated uncertainty gives

[latex]\mathrm{KE}_e= \frac{1}{2} \left(9.11\times10^{-31}\,\text{kg}\right) \left(5.79\times10^6\,\text{m/s}\right)^2.[/latex]
[latex]\mathrm{KE}_e=1.53\times10^{-17}\,\text{J}.[/latex]

Converting from joules to electron volts,

[latex]\mathrm{KE}_e= \left(1.53\times10^{-17}\,\text{J}\right) \left( \frac{1\,\text{eV}} {1.60\times10^{-19}\,\text{J}} \right) =95.5\,\text{eV}.[/latex]

Thus,

[latex]\boxed{\mathrm{KE}_e=95.5\,\text{eV}}.[/latex]

Discussion

An atom is typically about 0.1 nm across. Measuring an electron’s position to within 0.0100 nm therefore localizes it to a region about one-tenth the size of the atom. This is a relatively precise position measurement on the atomic scale. However, the price of this localization is a very large uncertainty in velocity. The value [latex]5.79\times10^6\,\text{m/s}[/latex] is not the exact velocity of the electron. It is the minimum spread in possible velocity values that is consistent with such a precise position measurement. To understand the size of this uncertainty, we treated it as a representative velocity and calculated a kinetic energy of 95.5 eV. This is much larger than the energy differences between many atomic energy levels, which are commonly on the order of a few electron volts. The calculation therefore shows that localizing an electron very precisely makes its momentum and kinetic energy highly uncertain. This result is one reason electrons in atoms cannot be described as tiny particles moving along precisely known circular orbits. Atomic orbitals instead represent probability distributions for where electrons may be detected.

Why do we not notice the Heisenberg uncertainty principle in everyday life? The reason is that Planck’s constant is extremely small:

[latex]h=6.63\times10^{-34}\,\text{J}\cdot\text{s}.[/latex]

Because the lower bound in the uncertainty relation contains this very small constant, quantum uncertainty is most significant for microscopic particles with small masses and momenta. For macroscopic objects, the minimum uncertainty is usually far too small to detect. For example, sunlight reflected from Jupiter allows astronomers to determine the planet’s position and follow its orbit. The photons that strike and leave Jupiter transfer some momentum to the planet, but Jupiter’s mass and momentum are so enormous that the resulting change and uncertainty are negligible. The same is true for ordinary biological and medical objects. A cell, organ, patient, surgical instrument, or imaging detector contains an immense number of particles and has a mass that is enormous compared with the mass of an electron. Its quantum uncertainty in position or momentum is therefore negligible on the scale of ordinary measurements. This agreement between quantum mechanics and classical physics for large systems is an example of the correspondence principle. Quantum mechanics remains valid, but its predictions become effectively indistinguishable from classical physics when applied to sufficiently large objects.

Heisenberg Uncertainty for Energy and Time

There is another important form of Heisenberg’s uncertainty principle that relates energy and time:

[latex]\Delta E\Delta t\geq\frac{h}{4\pi}.[/latex]

Here, [latex]\Delta E[/latex] is the uncertainty or spread in energy, and [latex]\Delta t[/latex] is a characteristic time interval. Depending on the situation, [latex]\Delta t[/latex] may represent the duration of a measurement or the lifetime of a particular quantum state. The relationship means that determining an energy very precisely requires observing the system for a sufficiently long time. A short observation time is associated with a larger possible spread in the measured energy. Conversely, a state that persists for a long time can have a more sharply defined energy. This form of the uncertainty principle is especially useful for unstable or short-lived states. An atom in an excited state, for example, remains in that state only briefly before emitting a photon and moving to a lower-energy state. Because the excited state has a finite lifetime, its energy cannot be perfectly sharp. Instead, repeated measurements reveal a small range of energies. The energy-time uncertainty relation is often written using the reduced Planck constant, [latex]\hbar=h/(2\pi)[/latex], as

[latex]\Delta E\Delta t\geq\frac{\hbar}{2}.[/latex]

This is mathematically equivalent to the form written with [latex]h[/latex>.

Connection to Spectroscopy and Medical Science

When an excited atom or molecule emits a photon, the photon energy corresponds to the difference between two energy levels. If the excited state exists for only a short time, the emitted photons have a small spread of energies rather than one perfectly exact energy. This produces a corresponding spread in wavelength or frequency known as natural line broadening. Spectral line widths are important in atomic spectroscopy, molecular identification, laser physics, and several biomedical imaging and sensing techniques. Although many other effects can also broaden spectral lines, the finite lifetime of an excited state creates a fundamental minimum width.

Example 102.2: Heisenberg Uncertainty Principle for Energy and Time for an Atom

An atom in an excited state temporarily stores energy. If the lifetime of this excited state is measured to be [latex]1.0\times10^{-10}\,\text{s}[/latex], what is the minimum uncertainty in the energy of the state in eV?

Strategy

The lifetime of the excited state provides the characteristic time interval:

[latex]\Delta t=1.0\times10^{-10}\,\text{s}.[/latex]

The minimum uncertainty in energy is found by using the equality in the energy-time uncertainty principle:

[latex]\Delta E\Delta t=\frac{h}{4\pi}.[/latex]

We first calculate [latex]\Delta E[/latex] in joules and then convert the result to electron volts.

Solution

Solving the uncertainty relation for [latex]\Delta E[/latex] gives

[latex]\Delta E=\frac{h}{4\pi\Delta t}.[/latex]

Substituting the known values,

[latex]\Delta E= \frac{6.63\times10^{-34}\,\text{J}\cdot\text{s}} {4\pi\left(1.0\times10^{-10}\,\text{s}\right)} =5.3\times10^{-25}\,\text{J}.[/latex]

Converting to electron volts,

[latex]\Delta E= \left(5.3\times10^{-25}\,\text{J}\right) \left( \frac{1\,\text{eV}} {1.6\times10^{-19}\,\text{J}} \right).[/latex]
[latex]\Delta E=3.3\times10^{-6}\,\text{eV}.[/latex]

Therefore, the minimum uncertainty in the energy of the excited state is

[latex]\boxed{\Delta E=3.3\times10^{-6}\,\text{eV}}.[/latex]

Discussion

A lifetime of [latex]10^{-10}\,\text{s}[/latex] is typical for many atomic excited states. Although this interval is extremely short by human standards, it is long enough on the atomic scale to produce only a small energy uncertainty. The calculated uncertainty is a few millionths of an electron volt, whereas typical atomic excitation energies are on the order of 1 eV. The energy spread is therefore very small compared with the total excitation energy. Nevertheless, the uncertainty is physically meaningful. It means that repeated measurements of photons emitted from identical excited atoms will not all produce exactly the same energy. Instead, the photon energies will be distributed over a narrow range. This energy spread contributes to the finite width of the associated spectral line. The example also demonstrates the inverse relationship between lifetime and energy uncertainty. A longer-lived state has a smaller energy spread, while a shorter-lived state has a larger energy spread.

The energy-time uncertainty principle becomes especially important for systems that exist only briefly. If the lifetime of a quantum state is very short, then [latex]\Delta t[/latex] is small, and the corresponding uncertainty in energy [latex]\Delta E[/latex] is relatively large. Some unstable nuclei and elementary particles have lifetimes as short as [latex]10^{-25}\,\text{s}[/latex], producing energy uncertainties of several GeV. Because mass and energy are related through Einstein's equation, [latex]E=mc^2[/latex], a spread in energy also corresponds to a spread in the measured mass of a short-lived particle. When many identical particles are produced and measured, they do not all appear to have exactly the same mass. Instead, the measured masses form a narrow distribution whose width is directly related to the particle's lifetime. This relationship is extremely useful in experimental particle and nuclear physics. Some unstable particles decay so rapidly that their lifetimes cannot be measured directly. Instead, physicists measure the spread in the observed decay energies or masses and use the energy-time uncertainty principle to determine the particle's lifetime.

Modern Perspective

The energy-time uncertainty principle is sometimes described by saying that energy may be "borrowed" for a short time. Although this picture can be useful as a qualitative visualization, it should not be taken literally. Modern quantum mechanics does not interpret the uncertainty principle as allowing violations of energy conservation. Instead, short-lived quantum states naturally possess an intrinsic spread in energy, while total energy remains conserved.

Throughout this chapter we have seen that individual quantum measurements always produce definite outcomes. An electron, for example, is detected at one specific location each time it is measured. However, when many identical experiments are repeated, those individual results build up a probability distribution whose shape reflects the wave nature of matter. The physicist Richard Feynman summarized this idea by remarking, "What there are, are particles." Individual observations always detect particles, yet the collection of many observations reveals the statistical wave behavior predicted by quantum mechanics. Exactly how a quantum system evolves between measurements cannot be described using the same classical concepts of trajectories that work for everyday objects.

Section Summary

  • Matter exhibits wave behavior and produces interference patterns similar to those produced by electromagnetic waves.
  • Individual measurements detect particles at definite locations, but repeated measurements form probability distributions that reflect the wave nature of matter.
  • The Heisenberg uncertainty principle places a fundamental limit on the simultaneous precision with which certain pairs of physical quantities can be known.
  • For position and momentum, the uncertainty principle is
    [latex]\Delta x\Delta p\ge\frac{h}{4\pi}.[/latex]
  • For energy and time, the uncertainty principle is
    [latex]\Delta E\Delta t\ge\frac{h}{4\pi}.[/latex]
  • These quantum limits become important for atoms, molecules, nuclei, and elementary particles but are negligible for ordinary macroscopic objects, explaining why classical physics accurately describes everyday life.

Conceptual Questions

  1. What is the Heisenberg uncertainty principle? Does it place limits on what can be known?

Problems & Exercises

  1. (a) If the position of an electron in a membrane is measured to an accuracy of [latex]1\text{.}\text{00 μm}[/latex], what is the electron’s minimum uncertainty in velocity? (b) If the electron has this velocity, what is its kinetic energy in eV? (c) What are the implications of this energy, comparing it to typical molecular binding energies?
  2. (a) If the position of a chlorine ion in a membrane is measured to an accuracy of [latex]1\text{.}\text{00 μm}[/latex], what is its minimum uncertainty in velocity, given its mass is [latex]5\text{.}\text{86}×{\text{10}}^{-\text{26}}\phantom{\rule{0.25em}{0ex}}\text{kg}[/latex]? (b) If the ion has this velocity, what is its kinetic energy in eV, and how does this compare with typical molecular binding energies?
  3. Suppose the velocity of an electron in an atom is known to an accuracy of [latex]2\text{.}0×{\text{10}}^{3}\phantom{\rule{0.25em}{0ex}}\text{m/s}[/latex] (reasonably accurate compared with orbital velocities). What is the electron’s minimum uncertainty in position, and how does this compare with the approximate 0.1-nm size of the atom?
  4. The velocity of a proton in an accelerator is known to an accuracy of 0.250% of the speed of light. (This could be small compared with its velocity.) What is the smallest possible uncertainty in its position?
  5. A relatively long-lived excited state of an atom has a lifetime of 3.00 ms. What is the minimum uncertainty in its energy?
  6. (a) The lifetime of a highly unstable nucleus is [latex]{\text{10}}^{-\text{20}}\phantom{\rule{0.25em}{0ex}}\text{s}[/latex]. What is the smallest uncertainty in its decay energy? (b) Compare this with the rest energy of an electron.
  7. The decay energy of a short-lived particle has an uncertainty of 1.0 MeV due to its short lifetime. What is the smallest lifetime it can have?
  8. The decay energy of a short-lived nuclear excited state has an uncertainty of 2.0 eV due to its short lifetime. What is the smallest lifetime it can have?
  9. What is the approximate uncertainty in the mass of a muon, as determined from its decay lifetime?
  10. Derive the approximate form of Heisenberg’s uncertainty principle for energy and time, [latex]\Delta E\Delta t\approx h[/latex], using the following arguments: Since the position of a particle is uncertain by [latex]\Delta x\approx\lambda[/latex], where [latex]\lambda[/latex] is the wavelength of the photon used to examine it, there is an uncertainty in the time the photon takes to traverse [latex]\Delta x[/latex]. Furthermore, the photon has an energy related to its wavelength, and it can transfer some or all of this energy to the object being examined. Thus the uncertainty in the energy of the object is also related to [latex]\lambda[/latex]. Find [latex]\Delta t[/latex] and [latex]\Delta E[/latex]; then multiply them to give the approximate uncertainty principle.

Glossary

Heisenberg’s uncertainty principle
a fundamental limit to the precision with which pairs of quantities (momentum and position, and energy and time) can be measured
uncertainty in energy
lack of precision or lack of knowledge of precise results in measurements of energy
uncertainty in time
lack of precision or lack of knowledge of precise results in measurements of time
uncertainty in momentum
lack of precision or lack of knowledge of precise results in measurements of momentum
uncertainty in position
lack of precision or lack of knowledge of precise results in measurements of position
probability distribution
the overall spatial distribution of probabilities to find a particle at a given location
definition

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