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An electron carrier cycles between oxidation and reduction. Ubiquinone carries two electrons, while cytochrome c carries one at a time.^[ref]

For example, transferring the two electrons supplied by one NADH requires two one-electron deliveries by cytochrome c. It does not require two permanently consumed cytochrome c molecules: an available electron carrier can unload, return and reload. Electron carriers recycle material while the net redox conversion supplies free energy.

An electron configuration records the occupation of electron shells and electron subshells by electrons. For neutral sodium in its ground state, $1s^{2}2s^{2}2p^{6}3s^1$ gives $2+2+6+1=11$ electrons; adding the occupations within each electron shell gives $(2,8,1)$. A superscript counts electrons, rather than multiplying the preceding labels. Removing the outer electron gives the sodium ion ${\mathrm{Na}}^{+}$ with $1s^{2}2s^{2}2p^6$, or $(2,8)$. See Flowers et al., Chemistry 2e, electron configurations of atoms and ions.

Electron counting records metal valence electrons plus ligand donations using a declared convention. In ionic counting, subtract metal oxidation state from its group number, then add donor electrons; in neutral counting, combine neutral metal and ligand fragments consistently. An Fe–Fe single bond contributes one electron to the count at each metal.

The electron density describes the expected number of electrons per unit volume at position $\mathbf{r}$. For a system with a fixed number $N$ of electrons, $\int n(\mathbf{r})d^3\mathbf{r}=N$. A Lewis structure allocates electron counts without specifying this spatial density.

Electron diffraction is interference between scattered electron probability amplitudes. It connects the de Broglie wavelength of the incident beam to the arrangement of the scattering material. In elastic scattering from a fixed crystal, $|{\mathbf{k}}_{\mathrm{out}}|=|{\mathbf{k}}_{\mathrm{in}}|=2\pi /\lambda$, and constructive crystal scattering selects wavevector transfers $\mathbf{Q}={\mathbf{k}}_{\mathrm{out}}-{\mathbf{k}}_{\mathrm{in}}$ in the reciprocal lattice. The physical momentum transfer to the electron is $\hslash \mathbf{Q}$ in this convention.

Bragg's law expresses the same condition as $2d\sin {\theta }_B=n\lambda$, where $d$ is the spacing of the chosen lattice planes, $n$ the diffraction order, and ${\theta }_B$ the angle to those planes. The angle between incoming and outgoing propagation directions is $\chi =2{\theta }_B$ for that reflection geometry. In normal-incidence backscattering, a detector's angle $\varphi$ from the outward surface normal instead gives $\chi =\pi -\varphi$; neither detector colatitude nor angle to the surface normal should silently replace ${\theta }_B$. A finite-row electron diffraction model uses a different spacing, the spacing between sites along a surface row, and makes that distinction explicit.

A substituent that increases electron density in a specified molecular region through induction or chemical resonance. Donation into an arene can affect an attached metal and its other coordination ligands.

An electron donor supplies electrons to an electron acceptor in a redox conversion.

The mean velocity of the electron population associated with a net electric current, distinct from random thermal or Fermi motion. Its sign is opposite to conventional current for negative charge carriers. Its usually small magnitude is not the propagation speed of an electromagnetic signal in a transmission line.

Electronegativity describes a chemical atom's tendency to attract electron density towards itself in a chemical bond. It helps answer a useful question: when two different chemical atoms share electrons, which end of the chemical bond tends to be richer in electron density? For hydrogen chloride, the answer is chlorine: the covalent bond is a polar covalent bond, conventionally written ${\mathrm{H}}^{\delta +}-{\mathrm{Cl}}^{\delta -}$. The symbols indicate partial atomic charges, not isolated ions carrying whole elementary electric charges.^[ref]

Electronegativity is a comparison scheme, not the number of electrons on a chemical atom. A partial atomic charge depends on how the electron density is partitioned; formal charge instead follows an integer allocation in a Lewis structure. Neither is numerically equal to electronegativity. Nor is electronegativity identical to electron affinity, which concerns adding an electron to an isolated species. Different electronegativity scales use different measured inputs and conventions; compare numbers only after specifying the scale.^[ref]

For a concrete comparison, the Royal Society of Chemistry lists Pauling electronegativities ${\chi }_{\mathrm{P}}(\mathrm{H})=2.20$ and ${\chi }_{\mathrm{P}}(\mathrm{Cl})=3.16$. Their difference is $0.96$, so the electronegativity rule predicts bond polarization towards chlorine in hydrogen chloride. An isolated molecular hydrogen molecule has identical ends and zero electronegativity difference. These examples explain a direction of unequal sharing, not a quantitative partial atomic charge.^[ref][ref]

A larger electronegativity difference often suggests stronger bond polarization, but there is no universal numerical boundary where a covalent bond suddenly becomes ionic bonding. Tables of cutoffs are classification aids with exceptions. Hydrogen fluoride, for example, is described by a polar covalent bond even when its electronegativity difference exceeds a textbook's nominal ionic threshold. The actual electron density, physical setting, and chemical substance's structure matter.^[ref]

The distinction from ionization energy is equally useful: an ionization energy measures the cost of removing an electron from a specified isolated species, whereas electronegativity compares attraction for electron density in a bonded environment. Neither the removal cost alone nor the attachment release alone supplies a unique bonded-atom electronegativity. A scale combines selected measured inputs with a model and a convention.^[ref]

For an original relative comparison, stipulate fictitious bonded sites $A,B,C$ on one chosen dimensionless electronegativity scale:The electronegativity heuristic predicts bond polarization towards $B$ in $A-B$, towards $C$ in $B-C$, and towards $C$ in $A-C$. Shifting ${\chi }_0$ leaves every comparison unchanged. Although the $A-C$ difference is twice the $A-B$ difference, this does not make its partial atomic charge or bond dipole twice as large: those require additional information about electron density and bond length. These symbols describe a stipulated ordering, not a table of measured chemical elements.

Keep the chemical context attached to that ordering. A chemical atom in a molecule has neighbours and an electron configuration; an isolated-atom energy scale and a bonded-atom comparison are different constructions. The chemical environment dependence of electronegativity explains why a table is a useful approximation rather than an immutable property of every site. Furthermore, an applied electric field can induce bond polarization even between identical chemical atoms, through electric polarizability; equal tabulated electronegativity does not forbid that response.

For external electrons on shell, factor out signed electric charge in the parity-preserving interaction vertex:The $u$ are Dirac spinors; ${\gamma }^{\mu }$ are gamma matrices. With on-shell renormalization scheme normalization $F_1(0)=1$, the Gordon identity gives $g_s/2=F_1(0)+F_2(0)$ and $a_e=F_2(0)$.^[ref]

This explains a subtlety: the Dirac equation already predicts a spin magnetic dipole moment with $F_2=0$. Rewriting its Dirac electromagnetic current with the Gordon identity produces a spin-dependent term even before any loop order correction. $F_2$ measures the additional response after that baseline is included. The limit $q\to 0$ is taken after extracting its coefficient; setting $q=0$ in the interaction vertex at the outset would hide it. This electromagnetic anomalous magnetic moment is not a failure of gauge invariance of the kind called a quantum anomaly.

An electron energy analyzer selects electrons by kinetic energy, allowing their count rate to be recorded as an energy scan.

Measurement of the energy lost by transmitted electrons to electronic, vibrational or other excitations.

The kinetic electron Fermi temperature is $T_F=[\sqrt{m_e^2{c}^4+p_F^2{c}^2}-m_e{c}^2]/k_B$, where the Fermi momentum $p_F=\hslash (3{\pi }^2{n}_e{)}^{1/3}$ counts the net electrons. Strong degeneracy requires $T\ll T_F$. With mean molecular weight per electron ${\mu }_e$ and $n_e=\rho /({\mu }_e{m}_u)$, $T_F=(m_e{c}^2/k_B)[\sqrt{1+(\rho /{\rho }_{\ast }{)}^{2/3}}-1]$. Its nonrelativistic and ultrarelativistic limits scale as ${\rho }^{2/3}$ and ${\rho }^{1/3}$, respectively.

For classical nondegenerate electrons, the free-particle Boltzmann occupancy has the form $z_e\exp [-p^2/(2mkT)]$, with chemical potential measured relative to its rest energy. Counting the two spin states in phase space gives $n_e=2z_e(2\pi mkT/h^2{)}^{3/2}$. A bound level of energy $-I_n$ has relative occupancy $(g_n/g_{+})z_e{e}^{I_n/kT}$ against its parent ion. Eliminating $z_e$ gives the level-specific Saha ionization equation.

A collection of mobile electrons treated statistically. A dense electron gas in a metal generally requires Fermi-Dirac statistics.

A device that produces and accelerates a directed beam of electrons.

The contribution of electrons to heat capacity. For a uniform noninteracting three-dimensional Fermi gas at fixed particle number and volume, its low-temperature value is $C_V\simeq ({\pi }^2/2)N{k}_{B}T/T_F$; only states near the Fermi surface can change occupation readily.

An electron hole is an unoccupied electron quantum state in an otherwise nearly full energy band, often the valence band. “Filled” refers to occupation of the allowed quantum states, not to filling all space with a continuous fluid of electrons. Each state, including its spin label, can hold at most one electron by the Pauli exclusion principle. The almost full energy band and its few missing occupants are therefore simpler to describe as a background plus a few electron holes. The electron hole is a quasiparticle, not a Positron inserted into the crystal.

Removing an electron of electric charge $-e$ changes the background's electric charge by $+e$. Thus an electron hole carries positive electric charge relative to that background. Promoting an electron into the conduction band creates an electron hole without changing the whole crystal's electric charge: $(-e)+(+e)=0$. An unbound pair still consists of two separate charge carriers; only a bound state of their relative motion is an exciton.

The local cartoon explains why a vacancy can move: when a neighboring electron fills it, another vacancy appears where that electron was. The vacancy has moved opposite to that particular transfer of an electron. In an extended Bloch state, use crystal momentum instead of imagining a permanently empty atomic site. For a completely filled energy band the summed electric current vanishes. Omitting one electron with group velocity ${\mathbf{v}}_v$ removes its contribution $-e{\mathbf{v}}_v$, leaving a contribution $+e{\mathbf{v}}_v$. This fixes both the positive electric charge and the velocity convention of the electron hole.

More precisely, near a parabolic valence band maximum, set its energy $E_v(0)$ as reference and define the electron hole wave vector by ${\mathbf{k}}_h=-{\mathbf{k}}_v$. ThenThe occupied electron branch has negative curvature there, while the electron hole branch has positive effective mass $m_h^{\ast }$. The velocity equality compares the electron hole with the missing Bloch state's group velocity; it does not contradict the opposite vacancy motion in a local transfer cartoon. The sign conventions are listed in Phys 460 Lecture 17.

The attractive electrostatic interaction between an electron and an electron hole. In a screened effective-mass approximation its potential has the displayed form. It can bind an exciton and reduce its optical excitation energy below the corresponding unbound-pair threshold.

An electron-hole pair consists of an excited electron and the unoccupied valence state described as an electron hole. Promoting a valence electron across a semiconductor band gap creates such a pair without changing the total electric charge. The carriers can separate under an electric field, or undergo electron-hole recombination. A bound electron-hole pair is an exciton; an arbitrary unbound pair need not be an exciton.