Electron Affinity

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electron affinity periodic trends anions

Core Idea

Electron affinity is the energy change when an atom gains an electron. Nonmetals generally have higher electron affinity than metals, reflecting their tendency to gain electrons.

Explainer

From your study of periodic trends, you know that atomic properties like atomic radius and ionization energy change systematically across periods and down groups because of how nuclear charge and electron shielding interact. Electron affinity adds another dimension to this picture: instead of asking how hard it is to *remove* an electron (ionization energy), it asks how much energy is released or absorbed when a neutral atom *gains* an electron to form an anion. Specifically, it is the energy change for the process X(g) + e⁻ → X⁻(g).

For most nonmetals, this process releases energy — the atom is more stable with the extra electron than without it. By convention, a negative electron affinity value means energy is released (exothermic), and a more negative value means the atom has a stronger "desire" to gain that electron. Think of it this way: a chlorine atom is one electron short of a filled valence shell. When it gains that electron, it achieves the stable electron configuration of argon, and the system drops to a lower energy state, releasing 349 kJ/mol. This is one of the highest electron affinities in the periodic table, which explains why chlorine so readily forms Cl⁻ ions.

The periodic trend generally mirrors what you saw with ionization energy but in reverse perspective. Electron affinity becomes more negative (stronger) as you move from left to right across a period, because increasing nuclear charge pulls the incoming electron more strongly while atomic radius shrinks. Moving down a group, electron affinity generally becomes less negative (weaker) because the incoming electron is added to a shell farther from the nucleus, where it feels less nuclear attraction and more shielding from inner electrons. However, this trend has notable exceptions. The noble gases have essentially zero or positive electron affinities because their valence shells are already full — adding an electron would mean starting a new, higher-energy shell with no stabilization. Nitrogen, with its half-filled 2p subshell, also has a surprisingly low electron affinity because the incoming electron must pair with an existing electron, introducing repulsion.

Understanding electron affinity alongside ionization energy gives you a complete picture of an element's tendency to form ions. Elements with high ionization energies *and* strongly negative electron affinities (like the halogens) are eager electron acceptors — they form anions easily. Elements with low ionization energies *and* weak electron affinities (like the alkali metals) are eager electron donors — they form cations easily. This complementary relationship is what drives ionic bond formation and underpins the concept of electronegativity that you will encounter next.

Practice Questions 5 questions

Prerequisite Chain

Counting to 10Counting to 20Understanding ZeroThe Number ZeroCounting to FiveOne-to-One CorrespondenceCombining Small Groups Within 5Addition Within 10Addition Within 20Two-Digit Addition Without RegroupingTwo-Digit Addition with RegroupingAddition Within 100Repeated Addition as MultiplicationMultiplication Facts Within 100Division as Equal SharingDivision as Grouping (Measurement Division)Division: Grouping (Repeated Subtraction) ModelDivision: Fair Sharing ModelDivision as Equal SharingDivision as GroupingBasic Division FactsDivision Facts Within 100Two-Digit by One-Digit DivisionDivision with RemaindersRemainders and Quotients in DivisionDivision Word ProblemsIntroduction to Long DivisionFactors and MultiplesPrime and Composite NumbersEquivalent FractionsRelating Fractions and DecimalsDecimal Place ValueReading and Writing DecimalsComparing and Ordering DecimalsAdding and Subtracting DecimalsMultiplying DecimalsDividing DecimalsDividing FractionsMixed Number ArithmeticOrder of OperationsInteger Order of OperationsVariable ExpressionsCombining Like TermsOne-Step EquationsTwo-Step EquationsSolving Multi-Step EquationsEquations with Variables on Both SidesAngle Pairs: Complementary, Supplementary, and VerticalParallel Lines and TransversalsCorresponding AnglesAlternate Interior AnglesTriangle Angle Sum TheoremExterior Angle TheoremTriangle Inequality TheoremSimilar Triangles: AA SimilaritySimilar Triangles: SSS and SAS SimilarityProportions in Similar TrianglesRight Triangle Trigonometry IntroductionTrigonometric Ratios ReviewRadian MeasureConverting Between Degrees and RadiansThe Unit CircleGraphing Sine and CosineGraphing Tangent and Reciprocal Trigonometric FunctionsDerivatives of Trigonometric FunctionsAntiderivativesIterated Integrals and Fubini's TheoremDouble Integrals in Cartesian CoordinatesDouble Integrals over Rectangular RegionsDouble Integrals in Polar CoordinatesDouble Integrals: Definition and SetupIterated Integrals and Fubini's TheoremDouble Integrals over Rectangular RegionsDouble Integrals over General RegionsApplications of Double Integrals: Area, Mass, and MomentsTriple Integrals in Cartesian CoordinatesTriple Integrals in Cylindrical and Spherical CoordinatesChange of Variables and the Jacobian DeterminantApplications of Triple Integrals: Volume and MassVector Fields and Their RepresentationsLine Integrals of Vector FieldsGreen's TheoremSurface Integrals and Flux of Vector FieldsSurface Integrals and Flux of Vector FieldsDivergence Theorem: Flux and OutflowDivergence TheoremElectric FluxGauss's LawConductors in Electrostatic EquilibriumCapacitance and CapacitorsDielectricsDielectric Constant and Relative PermittivityElectric Field Inside Dielectric MaterialsDielectric Materials and PolarizationDielectric Susceptibility and PermittivityEnergy Density in Electric FieldsElectric Current and Current DensityElectrical Resistance and ResistivityOhm's Law and Circuit ElementsElectromotive Force (EMF) and BatteriesKirchhoff's Circuit Laws: Voltage and CurrentDC Circuit Network Analysis MethodsTransient Response in RC CircuitsRC CircuitsLC and RLC CircuitsAC Circuits: FundamentalsImpedance and ReactanceAC Power and ResonanceElectromagnetic WavesThe Electromagnetic SpectrumBlackbody Radiation and Planck's LawPhotoelectric EffectThe Photon: Light as QuantaCompton ScatteringWave-Particle Dualityde Broglie WavelengthHeisenberg Uncertainty PrincipleWavefunction and the Born RuleThe Schrödinger EquationState Vectors and WavefunctionsQuantum SuperpositionQuantum EntanglementBell Theorem and Bell InequalitiesPostulates of Quantum MechanicsScattering TheoryIntroduction to Scattering TheoryPartial Wave Analysis in ScatteringSpin Angular MomentumElectron Spin and Intrinsic Magnetic MomentStern-Gerlach Experiment: Spin Quantization and MeasurementElectron Diffraction and Matter Wave PropertiesDavisson-Germer Experiment: Crystal Diffraction of ElectronsElectron Diffraction and Matter Wave InterferenceWavefunctions and Probability Density InterpretationQuantum Superposition and Linear Combinations of StatesQuantum Operators and ObservablesCanonical Commutation Relations and UncertaintyHeisenberg Uncertainty Principle and Measurement LimitsTime-Independent Schrödinger Equation and EigenvaluesHydrogen Atom in Quantum MechanicsSpectral Lines and Energy TransitionsSelection Rules for Atomic TransitionsLS and jj Coupling Schemes in Multi-Electron AtomsPauli Exclusion Principle and Antisymmetric WavefunctionsElectron Configuration and the Aufbau PrincipleThe Periodic Table and Atomic Electronic StructureThe Periodic TableElectron ConfigurationPeriodic TrendsElectron Affinity

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