---
title: Mass Spectrometry
module: Magnetic Field
moduleNumber: 6
lessonNumber: 5
order: 605
summary: >
  To weigh a single atom you cannot use a scale, so you use a magnetic field instead.
  A charged ion of unknown mass bends in a field by an amount that depends on its
  momentum and charge, so if every ion enters with the same velocity, its landing
  position reads off its mass-to-charge ratio directly. We build the instrument in
  two stages: crossed electric and magnetic fields that pass only ions with $v=E/B$,
  and a magnetic sector that bends the survivors along $r=mv/(|q|B)$. Then we ask what
  blurs a spectral line and how reference ions turn a position into a calibrated mass.
topics: [Magnetic Field]
draft: false
sources:
  - book: Tipler & Mosca
    ref: "Ch. 26 — The Magnetic Field; §26-2 Motion of a Point Charge in a Magnetic Field"
---

## Crossed fields and selector geometry

A velocity selector sets a transmitted speed. An electric field and a magnetic
field lie perpendicular to each other and to the nominal beam direction.
Particles with unequal transverse electric and magnetic forces miss the exit
aperture. A narrow speed band can therefore be passed from a source whose ions
have a broad initial energy distribution. Mass separation belongs to a later
dispersive stage.

Take a right-handed coordinate system with the beam entering along $+x$.
Let the electric field point along $-y$ and the magnetic field point along
$+z$. A positive ion then has an electric force toward $-y$ and a magnetic
force toward $+y$. The transverse force is

$$
F_y=q(vB-E).
$$

The sign reverses for a negative particle, but both electric and magnetic
terms reverse together. The condition for zero transverse force therefore has
the same speed for either sign of charge:

$$
v_s=\frac{E}{B}.
$$

Here $E$ and $B$ are magnitudes. The selected speed is independent of particle
mass and charge magnitude. An ion with that speed passes straight through even
when its charge state differs from another accepted ion.

> **Worked example (Setting a velocity selector).** A selector uses parallel plates
> $d=1.0\ \mathrm{cm}$ apart at $U=1.2\ \mathrm{kV}$, giving field
> $E=U/d=1.2\times10^5\ \mathrm{V\,m^{-1}}$. What magnetic field passes ions at
> $v=4.0\times10^5\ \mathrm{m\,s^{-1}}$? Balancing the transverse forces $qE=qvB$,
>
> $$
> B=\frac{E}{v}=\frac{1.2\times10^5}{4.0\times10^5}=0.30\ \mathrm{T}.
> $$
>
> Neither mass nor charge appears: every ion at $4.0\times10^5\ \mathrm{m\,s^{-1}}$
> passes regardless of species, which is why a dispersive stage must follow.

$$
% caption: Crossed-field velocity selector for a positive ion. With the beam moving right and the magnetic field out of the page, the electric force points down and the magnetic force up; only the ion whose speed makes the two forces equal, $v=E/B$, travels straight through.
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The physical plate voltage and plate spacing determine the electric field only
after the central gap is known. With an approximately uniform gap $d$ and a
plate potential difference $V_p$,

$$
E\approx\frac{V_p}{d},
\qquad
v_s\approx\frac{V_p}{dB}.
$$

The approximation excludes the fringing region near the plate ends. The
central-field value is often adequate for an instrument with a long plate
region and a beam that remains far from the edges. A short selector or a wide
beam samples nonuniform electric field, so the selected speed becomes
position dependent.

The selector response follows directly from the force balance. Let
$v=v_s+\delta v$ while the fields remain fixed. Since $E=v_sB$,

$$
F_y=qB\,\delta v.
$$

A faster positive ion curves in the magnetic-force direction. A slower positive
ion curves in the electric-force direction. Negative ions curve oppositely in
space, yet the magnitude of their departure from the central path is governed
by $|q|B|\delta v|$. The charge sign must be retained when predicting which
side aperture blocks the beam.

The mass dependence enters when a residual force has time to act. For selector
length $\ell$, a subsequent drift distance $D$, and a paraxial trajectory with
negligible change in $v_x$, the vertical coordinate at a downstream aperture is

$$
y=\frac{q(E-vB)}{mv^2}
\left(\frac{\ell^2}{2}+\ell D\right).
$$

The formula gives a first design estimate. It assumes uniform fields, small
deflection angle, and a particle entering at the central line with zero
transverse velocity. Light ions are rejected more strongly than heavy ions
with the same velocity offset because they acquire greater transverse
acceleration. A real selector therefore has an acceptance function that
depends on velocity, charge state, mass, initial angle, and aperture geometry.

An exit slit of width $w$ accepts the portion of phase space satisfying
$|y|<w/2$. Near the selected speed, replace $v$ in slowly varying factors by
$v_s$ and use $E-vB=-B\delta v$. The approximate velocity half-width becomes

$$
|\delta v|
\lesssim
\frac{m v_s^2w}
{2|q|B\left(\ell^2/2+\ell D\right)}.
$$

The design parameters impose a tradeoff. A longer selector, larger magnetic
field, longer drift, or narrower slit improves velocity discrimination and
reduces transmitted current while increasing alignment sensitivity. A design
report needs both selected speed and velocity acceptance; together they define
beam quality.

$$
% caption: Selector transmission versus speed offset from the selected value. The window width is set by the exit aperture and plate length; narrowing the slit passes a smaller speed band and less beam current together.
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$$

Beam alignment is checked with the magnetic field disabled and then with the
electric field disabled. Each single-field configuration should bend a test
beam in the predicted direction. Reversing the electric plate polarity and
reversing the magnetic field provide independent sign checks. A centered beam
with both fields present can otherwise conceal two wrong polarity assignments
that happen to compensate at one operating point.

## Beam deflection and charge-to-mass inference

An electric-deflection stage measures $q/m$ through transverse acceleration
and screen displacement. A collimated beam enters parallel plates of length
$\ell$ with speed $v$. A uniform transverse electric field $E_y$ acts only
between the plates.
The horizontal speed remains approximately $v$ while the transverse
acceleration is

$$
a_y=\frac{qE_y}{m}.
$$

The time spent between the plates is $\ell/v$. At the plate exit, the
transverse velocity and displacement are

$$
v_y=\frac{qE_y\ell}{mv},
\qquad
y_1=\frac{qE_y\ell^2}{2mv^2}.
$$

After the plates, the beam drifts a distance $D$ with that transverse velocity.
The total detector displacement is

$$
y=\frac{qE_y}{mv^2}
\left(\frac{\ell^2}{2}+\ell D\right).
$$

The sign of $y$ gives the sign of $q$ once the plate polarity and coordinate
system are known. A separate velocity selector sets $v=E_s/B_s$. Combining
the two measurements produces

$$
\frac{q}{m}
=\frac{y v^2}
{E_y\left(\ell^2/2+\ell D\right)}.
$$

The Thomson-style crossed-field measurement combines the two observables. The
selector determines speed, and electrostatic deflection determines
charge-to-mass ratio. The drift term $\ell D$ often dominates screen
displacement, so the plate-to-screen distance needs the same care as the plate
length.

$$
% caption: Electric deflection for charge-to-mass inference. The beam gains transverse displacement between the plates of length $\ell$, then travels straight over the drift distance $D$ to the screen; a separate velocity selector fixes the speed needed to solve for $q/m$.
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$$

The paraxial model fails when the deflection angle is large. In that case the
time within the plates differs from $\ell/v$ because longitudinal and
transverse motion couple through the actual path. Fringe fields extend the
effective plate length, and a finite beam width samples different electric
fields. These effects are reduced by operating at small angle, using long
uniform plates, mapping the field, and calibrating displacement with a
reference beam.

Detector response must also be separated from trajectory geometry. A
phosphor screen, position-sensitive detector, or swept collector converts an
impact coordinate into a readout coordinate. Screen distortion, pixel pitch,
point-spread width, and readout nonlinearity all affect the inferred $y$.
Known reference positions establish the pixel-to-distance relation, including
screen distortion, pixel pitch, and readout nonlinearity.

An independent magnetic-deflection run tests the same quantities by a different route.
A beam with known $q/m$ must have magnetic curvature consistent with the
selected velocity. A speed error, field-map error, electric-plate fringe
correction, detector calibration, or unrecognized charge state can produce a
disagreement. Reliability improves when each stage constrains a different
combination of the same physical quantities.

## Magnetic analyzers and mass-to-charge

A magnetic sector analyzer separates a beam by momentum-to-charge ratio. The
required circular-motion relation is used here as a measurement equation:

$$
p=|q|Br,
\qquad
\frac{p}{|q|}=Br.
$$

The radius $r$ is the fitted trajectory radius in the analyzing field. The
formula concerns the momentum component perpendicular to the field. An ion
with a substantial parallel velocity component follows a helical path outside
planar-sector geometry. Collimation and field alignment are therefore part of
the measurement definition.

A beam entering a uniform sector at known speed $v$ perpendicular to
$\vec B$,

$$
\frac{m}{|q|}=\frac{Br}{v}.
$$

In a selector–analyzer chain, $v=E_s/B_s$ at the selected speed. Let $B_a$ be
the analyzer field and $r$ the fitted sector radius. Then

$$
\frac{m}{|q|}
=\frac{B_aB_s r}{E_s}.
$$

The stages have separate measurement roles. Crossed fields set the speed. The
magnetic sector converts mass-to-charge ratio into position. With unknown
charge state, the reported observable is $m/|q|$.

$$
% caption: Semicircular ion path in a magnetic sector analyzer. An ion entering perpendicular to the field bends on a circle of radius $r=mv/(|q|B)$; at a common selected speed a larger mass-to-charge ratio traces a larger radius and lands farther along the detector plane.
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$$

Convert detector coordinate into a geometric radius. A sector with a nominal
centre and entrance angle has a position mapping that can be calculated from
the mechanical drawing, while mounting tolerances and field-edge geometry
shift the realized mapping. Reference ions with known $m/q$ establish the
actual radius-to-detector relation. A broad detector may require a polynomial
calibration; a narrow photographic plate can often be treated locally as
linear.

Acceleration-based mass analysis establishes ion energy with a source voltage,
then uses a magnetic sector. An ion accelerated from rest through a potential
magnitude $V$ has

$$
\frac12 mv^2=|q|V.
$$

Combining this energy equation with $r=mv/(|q|B)$ yields

$$
\frac{m}{|q|}
=\frac{B^2r^2}{2V}.
$$

The measured quantity is $m/q$. The acceleration voltage controls kinetic
energy per charge. Doubly charged ions gain twice the kinetic energy of singly
charged ions through the same voltage, and their curvature differs accordingly.

> **Worked example (Acceleration-based analyzer radius).** A singly charged ion of
> mass $20\ \mathrm{u}$ is accelerated from rest through $V=1.00\ \mathrm{kV}$ and
> enters a sector field $B=0.200\ \mathrm{T}$. With
> $m=20(1.66\times10^{-27})=3.32\times10^{-26}\ \mathrm{kg}$ and
> $q=1.602\times10^{-19}\ \mathrm{C}$, the speed after acceleration is
>
> $$
> v=\sqrt{\frac{2qV}{m}}
> =\sqrt{\frac{2(1.602\times10^{-19})(1000)}{3.32\times10^{-26}}}
> =9.8\times10^4\ \mathrm{m\,s^{-1}},
> $$
>
> and the sector radius is
>
> $$
> r=\frac{mv}{qB}=\frac{(3.32\times10^{-26})(9.8\times10^4)}{(1.602\times10^{-19})(0.200)}
> =0.102\ \mathrm{m}.
> $$
>
> A 10 cm radius. Because $r=\frac{1}{B}\sqrt{2Vm/q}$, a mass-$80\ \mathrm{u}$ ion at
> the same $V$ and $B$ lands at twice the radius, $\sqrt{4}$, and doubling $V$ spreads
> every radius by $\sqrt2$.

A velocity-selected beam has an analyzer radius that increases linearly with
$m/|q|$. For an acceleration-based beam, radius is proportional to
$\sqrt{m/|q|}$ at fixed $B$ and $V$. The geometry therefore sets the natural
detector scale. A detector with equal spatial bins has equal $m/q$ bins only
after the appropriate nonlinear conversion is applied.

The trajectory depends on the bending field sampled along its path. Field
variation across the mechanical sector and fringing at pole edges change the
effective sector angle and focusing. High-accuracy instruments map the field
or use reference masses across the detector range so that calibration captures
the realized magnetic geometry.

$$
% caption: Stages of a selected-beam mass spectrometer. The source and slit form the beam, crossed fields pass a single speed, the magnetic sector disperses by mass-to-charge, and the detector records position and count; each stage carries its own acceptance limit.
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Beam current is lost at every aperture. The source creates an emittance in
position and angle; the selector accepts a velocity interval; entrance and
exit slits accept a spatial interval; the sector accepts a momentum interval.
Reducing each interval raises resolution and reduces signal. Required
resolving power, detector noise floor, source intensity, and available
acquisition time determine the operating point.

## Charge state, energy, and beam identity

Ion charge is written $q=ze$, where $z$ is an integer charge state and $e$ is
the elementary-charge magnitude. A magnetic analyzer measures $m/z$ when
charge is expressed in units of $e$. A peak at a given $m/z$ can arise from a
light singly charged ion, a heavier multiply charged ion, or a molecular
fragment. Peak identity therefore combines mass analysis with source chemistry,
isotopic patterns, charge-state knowledge, and sometimes independent energy
measurements.

At fixed selected velocity, a sector radius satisfies

$$
r=\frac{m}{|q|}\frac{E_s}{B_sB_a}.
$$

Ions with equal $m/z$ follow the same ideal trajectory even when their masses
and charge states differ. A charge-state distribution can therefore produce
overlapping features. Source conditions, such as electron-impact energy or
ionization environment, influence the charge states and fragments present. A
mass spectrum records the response of an ion population; neutral-mass
assignments require charge-state and source information.

$$
% caption: Charge-state ambiguity in a sector analyzer. At fixed mass a higher charge state bends more tightly and a lower one more gently, so charge changes the landing radius; ions of equal mass-to-charge share one radius, and a charge-state assumption is needed before a position gives a neutral mass.
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An acceleration voltage fixes kinetic energy per charge.

$$
\frac{K}{z}=eV.
$$

Known charge state converts voltage into kinetic energy. An unknown charge
state leaves the instrument measurement as energy per charge.
Combining an electrostatic-energy stage with a magnetic momentum stage can
separate energy, momentum, and charge-state effects. The analysis must state
which quantity is inferred: kinetic energy $K$, energy per charge $K/q$,
momentum $p$, momentum per charge $p/q$, or mass-to-charge $m/q$.

An analyzer can infer charge sign from bend direction only after the magnetic
field orientation and detector coordinate system are calibrated. Reversing
$\vec B$ should reverse the dispersed pattern. Reversing the source
extraction polarity changes which charge sign enters the beamline. These
reversals are practical checks against a mirrored coordinate convention or a
detector readout that has been assigned the wrong direction.

Energy spread broadens a spectrum even when every ion has the same $m/z$.
In a magnetic sector, $r=p/(|q|B)$, so a fractional momentum spread produces
the same fractional radius spread:

$$
\frac{\delta r}{r}
=\frac{\delta p}{p}.
$$

For nonrelativistic ions at fixed mass, $\delta p/p\approx
\tfrac12\delta K/K$. A source with wide extraction-energy spread therefore
creates a wider detector feature. Finite selector aperture and angular
acceptance add their own width.

Multiple observables constrain charge state. The same
ion population may be measured at two acceleration voltages, two selector
settings, or with a detector capable of estimating kinetic energy. A genuine
$m/z$ assignment must predict the response between settings from the
instrument equations. A feature that remains at the same detector pixel while
$B$, $V$, or selector ratio changes in a way inconsistent with its proposed
identity is an artifact or an unmodeled beam component.

## Resolving power, peak width, and dispersion

Resolution compares the separation of measured responses with their widths.
Two ions with different mass-to-charge ratios can still reach a detector as one
unresolved feature. The relevant coordinate is usually the detector coordinate
$x$, measured along a focal plane or along a curved detector. Let
$\mu=m/|q|$. Local mass dispersion is

$$
\mathcal D_\mu=\frac{\d x}{d\mu}.
$$

An ion group with detector width $w_x$ corresponds to an approximate
mass-to-charge width

$$
\Delta\mu=\frac{w_x}{|\mathcal D_\mu|}.
$$

The definition applies whether $x$ happens to equal a radius, an arc length,
or a pixel number after calibration. It separates two instrument properties:
dispersion converts a physical change in $\mu$ into detector distance, while
the image width sets how much detector distance is lost to blur. Large
dispersion improves separation only while the image remains narrow.

At fixed selected speed, the sector relation is linear.

$$
\mu=\frac{B_a r}{v_s},
\qquad
\frac{\delta\mu}{\mu}
=
\frac{\delta B_a}{B_a}
+\frac{\delta r}{r}
-\frac{\delta v_s}{v_s}.
$$

Here a small fractional change in radius produces the same fractional change
in $\mu$ when $B_a$ and $v_s$ are held constant. An acceleration-based
analyzer has a different scaling:

$$
\mu=\frac{B_a^2r^2}{2V},
\qquad
\frac{\delta\mu}{\mu}
=
2\frac{\delta B_a}{B_a}
+2\frac{\delta r}{r}
-\frac{\delta V}{V}.
$$

The factor of two in the radius term matters during design. A detector blur
of one part in a thousand becomes a two-part-in-a-thousand $\mu$ blur in the
acceleration-based arrangement. Quoting a radius resolution without naming
the analyzer mode therefore leaves the analytical resolution incomplete.

Mass-spectrometry work often reports resolving power

$$
R=\frac{\mu}{\Delta\mu}.
$$

The width convention must accompany $R$. Full width at half maximum,
standard deviation, and a specified valley criterion give different numerical
values for the same pair of peaks. A report that states $R=1000$ without
the peak-width convention cannot be compared reliably with another
instrument. Equal-height peaks separated by one full width may look distinct
on a plot, whereas a weak peak next to a strong peak can require much larger
separation because the strong peak's tail raises the local background.

$$
% caption: Two mass-to-charge peaks on a position-sensitive detector. Whether they are resolved depends on the centroid gap measured against the peak widths; the ideal orbit-radius difference sets the nominal separation.
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Several independent widths add to the final spot. The entrance slit has
finite width, so ions begin at different transverse positions. The source
emits a finite angular range, which turns a point-like entrance image into a
fan of sector trajectories. A selector accepts a finite speed interval. The
magnetic field differs slightly from its nominal value across the beam
envelope. Collisions with residual gas and detector charge spreading can add
further broadening. When the mechanisms are independent and close to
Gaussian, their rms contributions combine approximately as

$$
w_x^2\approx
w_{\mathrm{source}}^2+
w_{\mathrm{angle}}^2+
w_{\mathrm{speed}}^2+
w_{\mathrm{field}}^2+
w_{\mathrm{det}}^2.
$$

The rms combination assumes independent, near-Gaussian contributions. A
clipped aperture produces shoulders and sharp edges. Multiple charge states
create asymmetric composite peaks. Detector saturation can flatten a maximum.
Residuals against a fitted peak model expose these departures more clearly than
a single quoted width.

Set slit width from resolution, count rate, detector linear range, and
available acquisition time. A rectangular aperture of width $a$ transmits
approximately in proportion to $a$ when incoming beam density is uniform
across the aperture. Reducing $a$ sharpens the geometric image and lowers the
count rate. An integrated peak area $N$ has a random counting scale of order
$\sqrt N$.

Source angular width requires separate treatment from source position. An
entrance slit can remove positional spread while leaving a large range of
directions. A collimator pair limits both, at the cost of transmission. Sector
instruments with focusing geometry arrange selected angular deviations to
converge near a focal surface. The focusing condition depends on sector angle
and field shape. A uniform sector focuses only at the relevant focal surface.
Bench alignment must verify the actual focal plane with a narrow calibration
beam.

Peak width also changes across a detector. A planar detector may have a
constant pixel pitch while the conversion from pixel position to $\mu$ changes
with position. Use the local dispersion $\mathcal D_\mu$ at each peak. A
single resolving-power number commonly describes a central detector region.
Calibration peaks distributed across the accepted range expose variation over
the mass range.

Instrument settings can favor either resolution or sensitivity. Stronger
collimation, narrower selector apertures, slower scans, and lower detector
gain can improve peak separability under particular limits. Each setting
changes a different term in the observed width or noise model. Record the
settings with the spectrum because a mass-to-charge axis omits the conditions
under which a claimed separation was achieved.

Source strength, detector background, and the response model set the shapes of
the two curves. Very narrow apertures can place the signal below a stable
background subtraction. A bright source can permit narrow slits and high
resolving power. A weak transient beam may require a wider aperture and a
lower resolution claim. The relevant figure of merit is the uncertainty of
the requested mass-to-charge distinction during the available measurement
time.

## Calibration, field integrals, and uncertainty control

An analysis formula connects ideal quantities. A working beam instrument has
electrode edges, finite apertures, detector pixels, supply drift, and
mechanical tolerances. Calibration establishes the connection between those
real components and the parameters in the formula. A spectrum should retain
the calibration records needed to reconstruct its horizontal scale, its peak
widths, and its stated uncertainty.

The selector relation $v_s=E_s/B_s$ assumes uniform transverse fields over
the entire ion path. Near the entrance and exit, both fields have fringe
regions. The transverse impulse provides the more general condition. An ion
that remains on the central line has

$$
\Delta p_y
=q\int\left(E_y-vB_z\right)\d t=0.
$$

Writing $\d t=\d x/v$ along an almost horizontal path gives

$$
v_{\mathrm{eff}}
=\frac{\int E_y\,\d x}{\int B_z\,\d x}.
$$

Uniform fields reduce this expression to $E_s/B_s$. Finite fringing changes
the effective path lengths and can shift the central transmitted speed even
when the plate voltage and central magnetic-field reading are correct. The
shift can be measured by scanning the selector ratio with a reference beam of
known speed or by comparing the selector setting against a downstream
acceleration-and-sector measurement.

The same issue arises in a sector analyzer. The scalar $B_a$ in
$p=|q|B_ar$ represents the magnetic field sampled by the orbit. Pole-face
edges, field gradients, and a displaced entrance beam change the sampled
average. Mapping the usable aperture with a calibrated probe documents the
spatial variation. A reference ion carried through the same aperture tests
the combined effect of the map, mechanical radius scale, and fringing. That
measurement includes the actual beam path as well as the map and mechanical
radius scale.

A position-sensitive detector requires its own calibration. Pixel number,
mechanical carriage position, and physical detector distance can each be
called $x$ in informal notes, although they may differ by an offset, scale
factor, and weak nonlinearity. Reference ions with known $\mu$ values provide
paired data $(x_i,\mu_i)$. A local calibration can be written

$$
\mu(x)=c_0+c_1x+c_2x^2+\cdots.
$$

Only terms supported by residuals should remain in the model. A high-order
polynomial can pass through every point in a small calibration set while
oscillating between points. A physically constrained sector geometry or a
piecewise local calibration is usually preferable when the detector spans a
broad range.

Calibration residuals test the coordinate model after the reference values
have been assigned. For every reference ion, calculate

$$
e_i=\mu_i-\mu(x_i).
$$

Plot $e_i$ against detector coordinate, nominal $m/q$, magnetic-field setting,
scan time, and scan direction. A constant nonzero residual indicates an
offset. A linear trend indicates an incorrect scale factor. Smooth curvature
indicates that the selected calibration function is too simple over that
range. Alternating residuals at successive standards can arise from a
high-order interpolation that follows calibration points too closely. A
time-dependent residual points toward supply drift, source-energy change, or
detector motion.

Compare residual size with both the required mass-to-charge separation and the
scatter of repeated readings. A residual of
$2\times10^{-4}$ in relative $\mu$ is harmless for a broad molecular survey
and decisive when adjacent isotope features differ by a few parts in
$10^4$. Reference peaks near the unknown feature carry the strongest local
constraint. References at the detector ends expose global scale curvature and
guard against extrapolation. Repeated measurements of one reference at fixed
settings estimate short-term repeatability; measurements after a scan estimate
the combined effect of drift and scan history. Keep both records because they
answer different calibration questions.

Calibration points must bracket the unknown peaks whenever possible.
Extrapolation outside the nearest standards transfers small curvature errors
into a systematic mass-scale error. Repeating the calibration before and
after a scan separates a stable offset from a time-dependent drift. A
temperature change in a magnet supply, electrode contamination, detector
gain drift, or a moved slit can alter the response without producing an
obvious discontinuity in the spectrum.

The selector-sector arrangement gives a direct uncertainty model.

$$
\mu=\frac{B_aB_sr}{E_s}.
$$

Independent standard uncertainties combine as

$$
\left(\frac{u_\mu}{\mu}\right)^2
=
\left(\frac{u_{B_a}}{B_a}\right)^2
+\left(\frac{u_{B_s}}{B_s}\right)^2
+\left(\frac{u_r}{r}\right)^2
+\left(\frac{u_{E_s}}{E_s}\right)^2.
$$

The equation applies to random components after known biases have been
corrected. A shared current supply can correlate $B_a$ and $B_s$; then a
covariance term belongs in the uncertainty calculation. A common systematic
scale error also fails to average away when many spectra are collected. State
whether each quoted term represents repeatability, calibration uncertainty, a
bound on an uncorrected bias, or a deliberately conservative allowance.

An accelerated-sector instrument has a different set of exponents.

$$
\mu=\frac{B_a^2r^2}{2V},
\qquad
\left(\frac{u_\mu}{\mu}\right)^2
=
\left(2\frac{u_{B_a}}{B_a}\right)^2
+\left(2\frac{u_r}{r}\right)^2
+\left(\frac{u_V}{V}\right)^2.
$$

The voltage term enters with a negative differential sign but a positive
variance contribution. A precision voltage readout can still be misleading
when the ion source loses part of the extraction voltage in a space-charge
region. Reference ions accelerated under the same source conditions test the
effective energy more directly than a supply display.

Reversal tests identify sign and coordinate mistakes. Reversing the analyzer
field reverses the bend for a beam of fixed charge. Use a documented prediction
when reversing both extraction polarity and detector coordinate convention. A
selector scan should have a central transmission maximum at the calibrated
$E_s/B_s$ ratio. A systematic displacement between the predicted and observed
maximum indicates a polarity error, a fringe correction, or a geometric offset
that must be resolved before mass assignments are reported.

Reproducibility requires a measurement sequence. Record zero settings,
aperture widths, magnet currents, plate voltages, detector bias, source
settings, scan direction, and acquisition time. Alternate unknown and
reference runs when drift is plausible. Retain raw detector coordinates as
well as the converted $\mu$ axis. Those records allow later recalibration if
the field map, voltage correction, or reference value is revised.

## Worked selector-sector analysis

> **Worked example (Mass-to-charge from a selector-sector chain).** A positive-ion
> beam passes a velocity selector with $E_s=2.40\times10^4\ \mathrm{V\,m^{-1}}$ and
> $B_s=0.0800\ \mathrm{T}$, then a sector analyzer with $B_a=0.2500\ \mathrm{T}$. A
> detector feature sits at radius $r=0.1000\ \mathrm{m}$. Work from speed toward mass.
> The selector passes only
>
> $$
> v_s=\frac{E_s}{B_s}=\frac{2.40\times10^4}{0.0800}=3.00\times10^5\ \mathrm{m\,s^{-1}},
> $$
>
> nonrelativistic for atomic ions. The analyzer radius fixes momentum-per-charge,
>
> $$
> \frac{p}{|q|}=B_ar=(0.2500)(0.1000)=2.500\times10^{-2}\ \mathrm{kg\,m\,s^{-1}\,C^{-1}},
> $$
>
> and dividing by the selected speed gives the mass-to-charge ratio,
>
> $$
> \frac{m}{|q|}=\frac{B_ar}{v_s}=\frac{B_aB_sr}{E_s}=8.33\times10^{-8}\ \mathrm{kg\,C^{-1}}.
> $$
>
> This is $m/|q|$, not $m$. Assigning a singly charged ion,
> $|q|=e=1.602\times10^{-19}\ \mathrm{C}$, gives
>
> $$
> m=(8.33\times10^{-8})\,e=1.34\times10^{-26}\ \mathrm{kg}\approx8.04\ \mathrm{u}.
> $$
>
> A doubly charged ion at the same spot would read $16.1\ \mathrm{u}$; the sector alone
> cannot choose. Charge state must come from the source, isotope structure, or a second
> measurement.

Uncertainty enters before the charge-state assignment. Suppose each magnetic
field calibration and the selector electric-field calibration has relative
standard uncertainty $0.050\%$, while the fitted radius has uncertainty
$0.150\%$. Treating these terms as independent gives

$$
\frac{u_\mu}{\mu}
=\sqrt{
(0.00050)^2+
(0.00050)^2+
(0.00150)^2+
(0.00050)^2}
=0.00173.
$$

The standard uncertainty in the measured ratio is therefore

$$
u_\mu
=(8.33\times10^{-8})(0.00173)
=1.44\times10^{-10}\ \mathrm{kg\,C^{-1}}.
$$

The radius term dominates this example. Reducing detector-position uncertainty
by half would improve the combined result more than reducing one of the
already small field-calibration terms by half. The actual error budget
determines the priority. Instrument changes should target the largest validated
contribution.

Peak resolution can be evaluated with the same geometry. A neighboring
feature separated by $0.200\%$ in $\mu$ has, under fixed selected speed, an
ideal radial separation

$$
\Delta r
=r\frac{\Delta\mu}{\mu}
=(0.1000\ \mathrm m)(0.00200)
=0.200\ \mathrm{mm}.
$$

An observed full width of $0.150\ \mathrm{mm}$ may allow two equal-height
features to be distinguished under a stated width convention. A width of
$0.300\ \mathrm{mm}$ produces substantial overlap. The result also depends
on intensity ratio and background. A numerical resolution claim must state
both the peak separation rule and the calculated value of $\Delta r$.

An acceleration-based cross-check can use the same target radius. Setting
$V=3.75\ \mathrm{kV}$ gives

$$
\frac{m}{|q|}
=\frac{B_a^2r^2}{2V}
=\frac{(0.2500\ \mathrm T)^2(0.1000\ \mathrm m)^2}
{2(3.75\times10^3\ \mathrm V)}
=8.33\times10^{-8}\ \mathrm{kg\,C^{-1}}.
$$

Agreement constrains selector calibration, analyzer field scale, radius
calibration, and extraction-energy interpretation together. A selector fringe
correction, a voltage loss near the source, an incorrect effective radius, or
a charge-state mixture can produce the same mismatch. Isolate the cause by
changing one control at a time and comparing the observed shift with the
relevant dependence on $E_s$, $B_s$, $B_a$, $V$, or $r$.

## Measurement sequence, data reduction, and reporting

Beam analysis begins with a stable reference state. Set the source
extraction voltage, source current, aperture positions, selector ratio,
analyzer current, detector bias, and vacuum condition before interpreting a
peak position. A spectrum recorded while any of these settings drifts is a
mixture of instrument states. The raw data should retain a time coordinate,
the unconverted detector coordinate, and every scanned control value.

The scan variable determines the form of the calibration. A fixed detector
array can collect an entire dispersed range at one magnet current. A scanning
instrument may move a detector, vary the analyzer magnetic field, or vary
the acceleration voltage. Magnetic-field scans follow the relation

$$
\mu\propto B_a
\quad\text{at fixed }r\text{ and }v_s,
$$

for a selector-sector layout, whereas an acceleration-sector layout at fixed
radius has

$$
\mu\propto \frac{B_a^2}{V}.
$$

Use the control setting recorded for each datum in the axis conversion. A
field scan also requires a current-to-field calibration; direct proportionality
between coil current and $B_a$ can fail near magnetic saturation or after an
incomplete hysteresis cycle.

Reference measurements should bracket an unknown run in time. A reference
peak before the run establishes the initial coordinate scale. A second
reference after the run detects drift. Interleaved references are needed when
the target precision approaches the observed drift rate. If the two
references disagree, report the disagreement and interpolate only when the
time dependence is supported by additional reference points. A single
before-and-after pair detects a net change but cannot establish that drift was
linear.

Peak reduction begins with separate background, detector-response, and fit checks.

| check | control measurement | invalid result signature |
|---|---|---|
| background | source blocked or ion-excluding setting | drifting baseline or structured residual |
| detector linearity | known attenuation or source-current change | peak height or area no longer proportional |
| peak model | baseline plus neighboring features | patterned centroid or width residual |
| reproducibility | repeated complete scans | between-scan shift beyond fit uncertainty |

- **Background.** Record a trace with the source blocked or with a setting that
  prevents ions from reaching the detector. Dark counts, electronic pickup,
  residual-gas ions, and scattered particles can all contribute. Check baseline
  stability before subtraction; model a changing background explicitly rather than
  treating it as a constant offset.
- **Detector response.** Gain sets the vertical scale and can change apparent peak
  shape. A counting detector can lose close arrivals through dead time; an analogue
  detector can saturate near a tall peak. Both suppress strong features more than
  weak ones and can corrupt isotope ratios or charge-state fractions despite a
  correct horizontal mass scale. Keep height or area comparisons inside the validated
  detector range.
- **Peak fit and repetition.** Extract centroid, width, area, and uncertainty from a
  model that includes baseline, peak shape, and overlapping neighbors. An asymmetric
  tail, flat top, or shoulder requires a different model or a narrower claim.
  Partially resolved groups require simultaneous fitting; a fixed integration window
  transfers area between groups as their positions change. Separate within-scan fit
  uncertainty from between-scan scatter caused by source instability, magnet drift,
  mechanical motion, or changing background.
Retain the following in the reduction record.

- **Raw trace**: detector coordinate, counts, time, and the complete control
  sequence before conversion to a mass-to-charge axis.
- **Reference set**: assigned reference values, their detector positions,
  calibration residuals, and the time at which each reference was measured.
- **Peak model**: baseline form, peak-shape function, fitting interval,
  centroid, width convention, integrated area, and residual plot.
- **Instrument configuration**: slit settings, selector voltage and magnetic
  field, analyzer magnetic field, acceleration voltage, source condition, and
  detector bias.
- **Uncertainty statement**: random repeatability, calibration terms, any
  common systematic scale term, and the stated confidence convention.

Detector position and magnetic-field scan direction should be recorded. A
magnet can follow different field-current paths while increasing and
decreasing current because of hysteresis. The consequence is a peak position
that shifts with scan direction even when the current readout returns to the
same number. Precycling the magnet through a documented range and approaching
each measurement from the same direction reduces this ambiguity. Alternating
upward and downward scans exposes a residual direction dependence.

Instrument artifacts have recognizable parameter dependences. A genuine
magnetic-sector peak moves with $B_a$ according to the analyzer relation.
A feature caused by detector electronics may remain at one detector channel
while the expected mass coordinate shifts. A source-space-charge effect often
changes with beam current and extraction voltage. A residual-gas feature may
track chamber pressure or source temperature. Stray electric fields can
displace the beam in a way that reverses with charge sign. Each diagnostic
uses an explicit control change and a predicted response. Identity evidence
comes from the observed response to that control change.

Charge-state assignments require an extra statement beyond a measured
$m/z$. An observed $m/z=14$ peak can represent a singly charged
approximately-14-unit ion, a doubly charged approximately-28-unit ion, or a
fragment whose neutral precursor was heavier. Isotopic spacing, source
chemistry, known extraction polarity, and energy-per-charge measurements can
reduce the alternatives. Ambiguous charge-state evidence requires the peak to
be reported as $m/z$, with the alternative particle assignments listed.

The final result should state the observable and the conditions. A concise
technical report gives the measured $m/|q|$, its uncertainty and width
convention, the calibration standards, the selector and analyzer settings,
the detector-coordinate model, the charge-state evidence, and unresolved
alternatives. Include raw or minimally processed data when the conclusion
depends on a line-shape choice, background subtraction, or a drift correction.
That level of record keeps later recalibration possible and separates a
measured trajectory property from an inferred particle identity.

## Model limits and independent closure checks

The preceding analyzer equations use nonrelativistic momentum,
$p=mv$ and kinetic energy $K=\tfrac12mv^2$. Their accuracy depends on the
ratio of beam speed to the speed of light. A velocity selector retains the
transverse balance $E=vB$ for perpendicular fields, because the electric and
magnetic force magnitudes still balance at the selected speed. The conversion
from radius and speed into mass changes once $v$ is large enough that
relativistic momentum differs appreciably from $mv$:

$$
p=\gamma mv,
\qquad
\gamma=\frac{1}{\sqrt{1-v^2/c^2}}.
$$

The sector measurement remains a measurement of momentum per charge.

$$
\frac{p}{|q|}=B_ar,
$$

Relativistic mass inference uses $\gamma mv$. Acceleration through voltage
obeys

$$
K=(\gamma-1)mc^2=|q|V
$$

when the extraction energy is dominated by the applied voltage. A
nonrelativistic reduction at high speed shifts the mass scale systematically.
Independent calibration is required because repeatability cannot expose this
common scale error.

The nonrelativistic source-energy relation provides an independent comparison.
If an ion begins with negligible kinetic energy and
gains $|q|V$, then

$$
\frac12mv_s^2=|q|V,
\qquad
\frac{m}{|q|}=\frac{2V}{v_s^2}.
$$

The selector measures $v_s=E_s/B_s$. The sector measures
$m/|q|=B_ar/v_s$. The source-voltage relation gives a third estimate:

$$
\frac{m}{|q|}
=\frac{2V B_s^2}{E_s^2}.
$$

All three estimates should agree within their stated uncertainty when the
source energy, selector ratio, and analyzer geometry are described correctly.
The comparison is especially sensitive to an extraction-voltage loss or an
incorrect selector effective-field integral. It also identifies a source
whose ions leave with substantial initial energy, since the simple
$|q|V$ energy gain no longer accounts for the selected speed.

The source-energy relation also has a charge-state consequence. A source at
fixed extraction voltage gives a larger kinetic energy to an ion with larger
$|q|$. At fixed mass, a multiply charged ion therefore enters the selector
with a higher speed. A separate source or selector setting can compensate.
The selector removes most of that speed variation by transmitting a narrow
band. Its transmitted intensities can still be strongly charge-state
dependent. Source and transmission corrections are required before peak height
is used as a neutral-abundance measurement.

Neutral particles travel undeflected through ideal crossed and magnetic fields.
A neutral contribution can reach a detector through a direct line of sight,
scattering, secondary ionization, or a detector response unrelated to the
analyzed trajectory. Beam stops and apertures should block the straight neutral
path before the detector. A persistent straight-through signal during
magnetic-field reversal is a practical indication of such a contribution.

Residual gas affects both trajectory and intensity. A collision can scatter
an ion out of the accepted angle range, change its charge state, produce a
fragment, or create a broad background. Increasing pressure generally lowers
the unscattered beam current and increases these nonideal components. The
effect is strongest for long flight paths and wide energy distributions.
Vacuum pressure belongs in the instrument record when weak peaks or
charge-state fractions are interpreted.

Space charge limits the single-particle picture at high beam current. A dense
positive ion beam has its own electric field. The resulting transverse
defocusing changes the source emittance, selector acceptance, and detector
spot width. A current scan at unchanged nominal fields distinguishes this
effect from a static geometric error: a space-charge contribution changes
with beam current, whereas a fixed mechanical offset remains approximately
constant. Reduced source current, wider source extraction spacing, or
additional focusing electrodes can reduce the beam-density contribution. Each
adjustment requires a fresh calibration of transmission and mass scale.

Assign a particle mass after the checks agree. Verify that field and voltage
units give the expected dimensions, reference peaks occur at calibrated
coordinates, field reversal yields the predicted bend reversal, a control scan
follows the correct dependence, and source-energy, selector, and sector
estimates agree where their assumptions apply. Report a remaining discrepancy
as an unresolved systematic effect. An accurate mass scale requires these
checks in addition to a narrow spectrum.
