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Showing 1321–1350 of 1709 reference entries
Aeppli and collaborators' archived 2025/2026 report compares 27Al⁺, 171Yb and 87Sr optical clocks with reported total fractional ratio uncertainties at or below 3.2×10⁻¹⁸.
Empirical findingMeasurementNetwork covariance and common reference limitsFor linear observations z=Aθ+ε with known positive-definite covariance Σ and full-column-rank A, generalized least squares yields θ̂=(AᵀΣ⁻¹A)⁻¹AᵀΣ⁻¹z.
MethodMeasurementHierarchical drift and excess scatterA network model can include per-instrument offsets, temporal drift, shared-reference effects and between-day variability alongside statistical noise.
MethodMeasurementModel discrepancy, calibration and predictive uncertaintyA discrepancy term δ(x) represents inadequacy of the physical response model, distinct from repeatability noise and uncertain calibration parameters.
MethodMeasurementCertified, reference and research-grade materialsReference-material value assignments have distinct status.
DefinitionMeasurementSRM 1947a · Property-specific certification (May 2026)The 12 May 2026 NIST certificate for Great Lakes Fish Tissue certifies total mercury and selected PCB, pesticide and PBDE values on a wet-mass basis.
Empirical findingMeasurementHigh-temperature radiometry and transfer uncertaintyDetector-based radiation thermometry infers thermodynamic temperature from calibrated spectral radiance, while transfer thermometers and blackbody realizations disseminate a scale.
MethodPhysicsA mixing-layer benchmark and observable dependenceNichols' worked compressible mixing-layer comparison specifies two streams, geometry, initial transients and statistical sampling before comparing RANS, LES and hybrid predictions with measurements downstream.
MethodChemistryVariational bounds and their limitsFor a normalized trial state of the same Hermitian, lower-bounded Hamiltonian, the Rayleigh energy cannot be below its ground-state energy.
Mathematical statementChemistryBasis convergence and extrapolationBasis convergence must be tested separately for SCF and correlation contributions.
MethodChemistrySCF convergence versus electronic stabilitySmall energy and orbital-gradient residuals identify a stationary SCF solution, which may be unstable to allowed orbital rotations.
MethodChemistryFunctional and dispersion errorA larger orbital basis does not remove exchange-correlation functional error.
ApproximationChemistryCounterpoise and fragment interaction energiesCounterpoise compares the complex energy with fragment energies evaluated in the complex basis, including partner basis functions without partner nuclei.
MethodChemistryFailure of a single electronic surfaceNear electronic degeneracy, nuclear motion can couple electronic states through derivative couplings, so a single Born–Oppenheimer potential surface can fail.
ModelChemistryFrom electronic excitation energies to spectraA computed vertical electronic excitation is not automatically a measured spectral maximum.
MethodChemistryTransmission coefficient and recrossingIn classical transition-state trajectory counting, recrossing the dividing surface reduces the fraction of nominal crossings that contributes to net reaction; this recrossing transmission coefficient is bounded by one.
ModelChemistryDiffusive barrier crossing and frictionIn an overdamped diffusive reaction-coordinate model, the flux contains both potential-driven drift and concentration spreading.
ModelChemistryMarcus reorganization and competing rate regimesThe classical harmonic reorganization model gives an electron-transfer barrier depending jointly on driving force and reorganization energy.
ModelChemistryActivity and electrochemical potential gradientsSpecies transport is driven by chemical and electrical contributions to electrochemical potential.
Mathematical statementChemistryDilute Nernst–Planck transportA dilute-solution Nernst–Planck flux combines diffusion, electric migration and convection.
ModelChemistryConcentrated electrolyte cross-transportStefan–Maxwell transport represents friction between different species rather than independent dilute diffusion through an inert solvent.
ModelChemistrySeparating electrode kinetics from transportCurrent–potential data can reflect charge transfer, bulk migration/diffusion, homogeneous reactions and evolving surface structure.
MethodChemistryDispersity as a distribution ratioMolar-mass dispersity is the ratio of mass-average to number-average molar mass.
DefinitionChemistrySize-exclusion calibration and molar massSize-exclusion results depend on column, solvent and calibration, so retention-based molar masses are not intrinsically absolute.
MethodChemistryNetwork gelation beyond linear step growthBranching models locate gelation when continuing connections become self-sustaining.
ModelChemistryMaxwell viscoelastic constitutive responseA Maxwell spring and dashpot in series predicts exponential stress relaxation with a characteristic time.
ModelChemistryStorage and loss moduliFor linear harmonic loading, the complex modulus separates in-phase elastic storage from quadrature viscous loss.
DefinitionChemistryDiffraction intensities and the phase problemCorrected diffraction intensities constrain squared structure-factor amplitudes, while phases remain essential for reconstructing electron density.
MethodChemistryPhasing and independent structural checksPhase probabilities and map weighting affect reconstructed density, and model-derived phases can bias the apparent support for that same model.
MethodChemistryVibronic coherence: a Br2+ case studyThe Br2+ attosecond study reports coherent vibronic signals and interprets their evolution using electronic/nuclear modeling with anharmonic and spin–orbit contributions.
Empirical finding