Physics/Lessons/Nuclear Radiation/Radioactive Decay & Half-Life
Physics · Nuclear Radiation · A2 Level

Radioactive Decay & Half-Life

No one can say when a particular unstable nucleus will decay — but a large enough sample lets you predict, with real precision, what fraction remains after an hour, a year, or a millennium. This lesson turns that statistical regularity into the exponential decay law, and shows how it's measured using a Geiger–Müller tube.

15 min read

Radioactive decay is random and spontaneous

Radioactive decay is random: it's impossible to predict which individual nucleus in a sample will decay next, or exactly when. It's also spontaneous: decay is completely unaffected by external conditions — temperature, pressure, chemical bonding, or nearby nuclei all leave the decay rate unchanged, unlike a chemical reaction, whose rate depends strongly on these factors.

What can be predicted, with high precision, is the behaviour of a large sample. Each nucleus has the same fixed probability of decaying in any given interval, and with enough nuclei, this translates into a smooth, statistical decline in the number remaining over time.

Activity and the decay constant

The activity, $A$, of a sample is the number of nuclear decays occurring per unit time, measured in becquerels (Bq), where $1\,\text{Bq} = 1$ decay per second. Activity is directly proportional to the number of undecayed nuclei present, $N$:

$A = \lambda N$

where $\lambda$ is the decay constant, a fixed probability per unit time that any one nucleus of that isotope will decay, with units of $\text{s}^{-1}$. A larger $\lambda$ means a higher probability of decay per second, and so — for the same $N$ — a higher activity: $\lambda$ is a fixed property of the isotope, unlike $N$, which continuously falls as the sample decays.

The exponential decay law

Because activity ($A=\lambda N$, the rate at which nuclei are lost) is itself proportional to the number of nuclei remaining, the rate of decrease of $N$ is proportional to $N$ itself — precisely the condition that produces exponential decay.

DerivationN = N₀e^(−λt), from dN/dt = −λN
1
The rate of change of the number of undecayed nuclei is proportional to the number remaining: $\dfrac{dN}{dt} = -\lambda N$.
The minus sign shows $N$ is decreasing; $\lambda$ is the same decay constant as in $A=\lambda N$.
2
Separating variables: $\dfrac{dN}{N} = -\lambda \, dt$.
3
Integrating both sides, from $N_0$ at $t=0$ to $N$ at time $t$: $\displaystyle\int_{N_0}^{N}\dfrac{1}{N}\,dN = \int_0^t -\lambda\,dt$, giving $\ln N - \ln N_0 = -\lambda t$.
4
Combining the logarithms: $\ln\left(\dfrac{N}{N_0}\right) = -\lambda t$.
5
Exponentiating both sides: $\dfrac{N}{N_0} = e^{-\lambda t}$, so $N = N_0e^{-\lambda t}$.
$N_0$ is the number of undecayed nuclei at $t=0$; $N$ is the number remaining at time $t$.
▪ derived

The same exponential form applies to activity and to any measured count rate, since both are proportional to $N$: $A = A_0 e^{-\lambda t}$, where $A_0$ is the initial activity. This is convenient, since activity (or count rate, which is proportional to it) can be measured directly, whereas the number of undecayed nuclei usually can't.

Half-life

The half-life, $T_{1/2}$, is the time for the number of undecayed nuclei (or the activity) of a sample to fall to half its initial value — a fixed property of a given isotope, related directly to the decay constant.

DerivationT½ = ln 2 / λ
1
By definition, at $t=T_{1/2}$, $N = \dfrac{N_0}{2}$.
2
Substituting into $N=N_0e^{-\lambda t}$: $\dfrac{N_0}{2} = N_0 e^{-\lambda T_{1/2}}$.
3
Dividing both sides by $N_0$: $\dfrac{1}{2} = e^{-\lambda T_{1/2}}$.
4
Taking $\ln$ of both sides: $\ln\left(\dfrac{1}{2}\right) = -\lambda T_{1/2}$, i.e. $-\ln 2 = -\lambda T_{1/2}$.
$\ln(1/2) = -\ln 2$, a standard logarithm identity.
5
Rearranging: $T_{1/2} = \dfrac{\ln 2}{\lambda}$.
A larger decay constant $\lambda$ (higher probability of decay per second) always corresponds to a shorter half-life, and vice versa — the two describe the same underlying decay rate from different angles.
▪ derived

Worked example: using the decay law

Worked exampleActivity after a given time, from half-life
1
A source has half-life $T_{1/2} = 8.0$ days and initial activity $A_0 = 4.0\times10^{6}\,\text{Bq}$. Find its activity after 24 days.
2
Find $\lambda$: $\lambda = \dfrac{\ln 2}{T_{1/2}} = \dfrac{0.693}{8.0} = 0.0866\,\text{day}^{-1}$.
3
Apply $A = A_0 e^{-\lambda t}$ with $t=24$ days: $A = 4.0\times10^6 \times e^{-0.0866\times24} = 4.0\times10^6\times e^{-2.079}$.
4
$e^{-2.079} \approx 0.125$, so $A \approx 4.0\times10^6\times0.125 = 5.0\times10^5\,\text{Bq}$.
24 days is exactly three half-lives ($3\times8=24$), so this can be checked quickly: $4.0\times10^6 \times \left(\tfrac12\right)^3 = 5.0\times10^5\,\text{Bq}$ — matching, as it should.
▪ solved

Choosing a half-life for the job

Half-life isn't just an abstract number to calculate — in practice, an application is only workable if the isotope used has a half-life suited to it. A source decaying too quickly is gone before it's useful; one decaying too slowly stays hazardous for far longer than necessary. The two cases below show how deliberately short and deliberately long half-lives are each put to use, and why a very long half-life brings its own distinct danger.

Short half-lives: medical diagnosis

A radioactive tracer used to image an organ needs to be active for long enough to complete the scan, but should then decay away quickly, so the patient isn't left carrying a source of radiation dose for any longer than necessary. This means diagnostic tracers are deliberately chosen to have short half-lives — long enough (typically several hours) to inject the tracer, let it accumulate in the target organ, and take the images, but short enough that the patient's activity has fallen to a small fraction of its starting value within a day or two.

Case studyThe molybdenum–technetium generator
1
Technetium-99m (Tc-99m) is the radionuclide used in the great majority of medical scans: it's a pure gamma emitter, so it delivers no unnecessary particle dose, and its half-life of about 6 hours is ideal — long enough for a scan, short enough to clear quickly.
2
That same 6-hour half-life is a problem for supply: Tc-99m can't be manufactured centrally and transported to a hospital, since a large fraction would decay away in transit before it could ever be used.
A source with $T_{1/2}=6$ hours loses half its activity in the time it might take just to deliver it.
3
The solution is to generate Tc-99m on-site, exactly when it's needed, from its parent isotope molybdenum-99 (Mo-99) — itself formed in an excited state of technetium-99 by beta-minus decay, which happens to be the metastable Tc-99m state (see the previous lesson).
4
Mo-99 has a much longer half-life, around 66 hours, so a sealed generator unit supplied to a hospital keeps producing fresh Tc-99m for well over a week.
5
Hospital staff periodically "milk" the generator — chemically extracting (eluting) the Tc-99m that has accumulated, for immediate clinical use — while the remaining Mo-99 continues decaying and replenishing the supply of Tc-99m for the next extraction.
Only the longer-lived, more manageable Mo-99 ever needs to be transported; the short-lived Tc-99m is always made fresh at the point of use.
▪ case study

Long half-lives: dating and long-term standards

The opposite choice is needed when an isotope's decay is used to measure how much time has passed since some fixed starting point — this requires a half-life comparable to, or longer than, the age being measured, or the sample would have decayed away completely long ago. Radiocarbon dating of organic archaeological material relies on carbon-14, with a half-life of about 5,730 years, well matched to timescales of thousands of years; dating much older rock relies on isotopes with half-lives of billions of years, such as uranium-238.

The danger of very long half-lives

Because $A=\lambda N$ and $\lambda = \dfrac{\ln 2}{T_{1/2}}$, a longer half-life means a smaller decay constant, and so — for the same number of nuclei — a lower activity. This can seem reassuring, but it's exactly what makes very long half-lives hazardous in a different way: the low activity doesn't fall away on any useful timescale. A highly active, short-half-life source is dangerous now but safe soon; a long-half-life source stays dangerous for a very long time, since its activity barely decreases from one human lifetime to the next.

This is precisely the problem posed by high-level radioactive waste from nuclear reactors, some of which contains isotopes with half-lives of thousands to millions of years. Such waste can't simply be left to decay away in storage on any practical timescale, and if it escapes containment, it can enter the environment and the food chain — where, once absorbed into a living organism, it continues irradiating that organism from within for as long as it remains present. This is why long-half-life waste requires deep geological storage, engineered to remain sealed for timescales far beyond any human institution's normal lifespan.

Activity and hazard timescale are not the same thing

It's tempting to think a lower activity always means "safer", but activity only tells you the rate of decay right now — it says nothing about how long that rate will persist. A short half-life gives high activity that disappears quickly; a long half-life gives low activity that persists for a very long time. Judging real hazard means considering both the activity and the half-life together, not the activity alone.

Measuring count rate with a Geiger–Müller tube

A Geiger–Müller (GM) tube detects individual ionising particles: each one entering the tube triggers a brief pulse of current, registered as one "count" by a connected counter. Because only a fraction of the radiation emitted by a source enters the tube (radiation is emitted in all directions, and the tube covers only a small solid angle), the tube's count rate is proportional to, but numerically smaller than, the source's true activity.

A GM tube also detects background radiation — the small, steady rate of ionising events from cosmic rays, naturally occurring isotopes in rocks and building materials, and trace radioactivity in the body, present everywhere regardless of the source studied. Before measuring with a source present, background count rate must be measured separately (with no source nearby) and subtracted from every reading, to obtain the corrected count rate due to the source alone:

$\text{corrected count rate} = \text{measured count rate} - \text{background count rate}$
Always correct for background before using count rate as a proxy for activity

Every count-rate measurement in this topic — decay-constant experiments, half-life determinations, the inverse-square-law practical below — depends on the corrected count rate, not the raw reading. Skipping the subtraction systematically overestimates the true source count rate, and the error grows the weaker or more distant the source is, since background then makes up a larger fraction of the raw reading.

Required Practical: Inverse Square Law for Gamma Radiation

AQA Required Practical

This is AQA's Required Practical 12: investigating how radiation intensity varies with distance.

A gamma source radiates energy uniformly in all directions from a point, so the same total energy spreads over the surface of an ever-larger sphere as distance from the source increases. Since a sphere's surface area is proportional to $x^2$ ($x$ = distance from the source), gamma intensity follows an inverse square law:

$I \propto \dfrac{1}{x^2}$

and since a GM tube's corrected count rate is proportional to the intensity reaching it, count rate should also obey $\text{count rate} \propto \dfrac{1}{x^2}$.

Equipment

EquipmentPurpose
Gamma radioactive source (sealed, low-activity)Provides a known point source of gamma radiation
TongsHandles the source without direct contact
Geiger-Müller (GM) tube and counterDetects and counts incident gamma radiation
Metre rulerMeasures the distance $x$ between source and tube
Source-holder standHolds the source securely in line with the ruler and tube
Lead-lined storage containerSafely stores the source when not in use

Method

MethodCorrected count rate against 1/x²
1
Set up the GM tube on a stand, aligned along a metre ruler with the source holder, so the distance $x$ between source and the tube's window can be read directly.
2
With no source present, record the count over a suitably long time interval (e.g. several minutes) and calculate the background count rate.
3
Using tongs — never bare hands — place the gamma source in its holder at a measured distance $x$ from the GM tube.
4
Record the count over a fixed time interval (e.g. 60 seconds) and calculate the raw count rate.
5
Subtract the background count rate (from step 2) to find the corrected count rate at this distance.
6
Repeat steps 3–5 for a range of different distances $x$, keeping the counting time and orientation consistent throughout.
7
Plot corrected count rate against $\dfrac{1}{x^2}$ — a straight line through the origin confirms the inverse square relationship. Alternatively, plot $\ln(\text{count rate})$ against $\ln(x)$; a gradient of $-2$ confirms the power directly, without assuming it in advance.
▪ method

Sources of error and how to minimise them

Background radiation

Background must be measured and subtracted at every distance, not just once — a poorly corrected background disproportionately distorts readings far from the source, where the true count rate is smallest and background makes up the largest fraction of the reading.

Random statistical fluctuation in count rate

Radioactive decay is random, so a short counting interval gives a count rate with large statistical scatter. Count for a sufficiently long time at each distance (and/or repeat and average) to reduce the percentage uncertainty.

GM tube dead time at high count rates

A brief interval after each detected particle, during which the tube can't register a further count, causes under-recording — significant close to the source, where count rates are highest. Avoid working too close to a strong source, or apply a dead-time correction if known.

Measuring distance from the wrong reference point

Distance should be measured from the actual point of emission inside the source to the active detecting volume inside the tube, not from either outer casing — both typically add a few millimetres to a centimetre, introducing a systematic error that matters most at the smallest distances.

Safety

Handle sources with tongs at all times, minimise time near the source, maximise distance when not taking a reading, store in a lead-lined container between uses, and never point it toward another person.

Key takeaways

  • Radioactive decay is random (unpredictable for any one nucleus) and spontaneous (unaffected by external physical or chemical conditions).
  • Activity $A=\lambda N$, where $\lambda$ is the decay constant — a fixed probability of decay per unit time for a given isotope.
  • The decay law, from $\dfrac{dN}{dt}=-\lambda N$: $N=N_0e^{-\lambda t}$, and equivalently $A=A_0e^{-\lambda t}$ for activity or count rate.
  • Half-life $T_{1/2} = \dfrac{\ln 2}{\lambda}$: the time for $N$ or $A$ to halve, fixed for a given isotope.
  • Applications need a half-life matched to their timescale: short half-lives (e.g. Tc-99m, ≈6 hours) suit medical diagnosis, since activity clears quickly after use; long half-lives (e.g. carbon-14, uranium-238) suit dating, since the isotope must survive over the age being measured.
  • The molybdenum–technetium generator solves Tc-99m's supply problem: longer-lived Mo-99 (≈66 hours) is transported to the hospital, then "milked" to extract fresh, short-lived Tc-99m on-site as it's needed.
  • A very long half-life means low activity now, but that activity barely decreases over practical timescales — the danger of long-lived radioactive waste, requiring long-term (often deep geological) storage.
  • A GM tube's raw count rate must be corrected for background radiation (measured separately, with no source present) before it can be used as a proxy for source activity.
  • RP12: corrected GM-tube count rate from a gamma source plotted against $1/x^2$ gives a straight line through the origin, confirming $I \propto 1/x^2$; sources of error include background correction, GM tube dead time at high count rates, and measuring distance from the true point of emission, not the outer casings.