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Electron Affinity

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Periodic TrendsIon Formation from Electron TransferIonic Bonding: Electron Transfer and Electrostatic Forces
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

Understanding ZeroThe Number ZeroCounting to FiveCounting to 10Counting to 20Counting a Set of Objects Up to 20Cardinality: The Last Number CountedMatching Numerals to QuantitiesSubitizing Small QuantitiesAddition Within 10Number Bonds to 10Addition Within 20Doubles and Near DoublesDoubles Facts Within 10Near Doubles Facts Within 20Mental Math Strategies for AdditionMental Math: Adding and Subtracting TensAddition Within 100Repeated Addition as MultiplicationMultiplication as Equal GroupsMultiplication: ArraysBasic Multiplication Facts (0s, 1s, 2s, 5s, 10s)Multiplication 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 100Multiplication and Division Fact FamiliesRelationship Between Multiplication and DivisionDivision Facts as Inverse of MultiplicationRemainders and Quotients in DivisionDivision Word ProblemsMulti-Step Word ProblemsSolving Multi-Step Word ProblemsMultiplication Word ProblemsDivision Word ProblemsIntroduction to Long DivisionFactors and MultiplesPrime and Composite NumbersEquivalent FractionsRelating Fractions and DecimalsDecimal Place ValueIntegers and the Number LineComparing and Ordering IntegersAbsolute ValueAdding IntegersSubtracting IntegersMultiplying IntegersDividing IntegersUnit RatesProportionsPercent ConceptConverting Between Fractions, Decimals, and PercentsOperations with Rational NumbersTwo-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 IntroductionSine, Cosine, and Tangent RatiosTrigonometric Ratios ReviewRadian MeasureConverting Between Degrees and RadiansThe Unit CircleGraphing Sine and CosineGraphing Tangent and Reciprocal Trigonometric FunctionsDerivatives of Trigonometric FunctionsAntiderivativesIndefinite IntegralsBasic Integration RulesRiemann SumsDefinite Integral DefinitionDouble 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 FieldsWork and CirculationLine Integrals of Scalar and Vector FunctionsFundamental Theorem for Line IntegralsConservative Vector FieldsConservative Vector Fields and Potential FunctionsCurl and Divergence of Vector FieldsCurl and DivergenceDivergence TheoremElectric Flux and Divergence TheoremGauss's Law: Integral Form and MeaningSolving Problems with Gauss'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 WavesPostulates of Special RelativityTime DilationLength ContractionLorentz TransformationRelativistic Velocity AdditionRelativistic Momentum and EnergyMass-Energy Equivalence and E=mc²Photons as Particles with Energy and MomentumPlanck-Einstein Relation: Energy and FrequencyPhotoelectric EffectThe Photon: Light as QuantaCompton ScatteringWave-Particle Dualityde Broglie WavelengthThe Schrödinger EquationState Vectors and WavefunctionsQuantum SuperpositionQuantum EntanglementBell Theorem and Bell InequalitiesPostulates of Quantum MechanicsObservables and Quantum OperatorsCommutators and Commutation RelationsQuantum Angular MomentumQuantum Mechanical Treatment of HydrogenSolving the Schrödinger Equation for Hydrogen AtomQuantum NumbersElectron ConfigurationPeriodic TrendsElectron Affinity

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