The Journal of Physical Chemistry B · 1997 · 130 citations · 27 references
Natural SciencesChemistryMaterials SciencePhysical ChemistrySurface ChemistrySurface ScienceAcid-base ChemistryChemical BondingElectrolyte SolutionsIntermolecular ForcesScanning Probe MicroscopySurface PhysicsAdhesion MechanicsDebye LengthElectric Double LayerHydrogen Bonding InteractionsIonizable Surface GroupsIonizationLateral Force MicroscopySurface Functional Groups
The study uses scanning force microscopy to investigate electrostatic and hydrogen‑bonding interactions between chemically modified probes and surface functional groups. The authors determine local ionization and surface pK values by measuring adhesion force titration curves with SFM, which resemble conventional solution pH titration curves. pH‑dependent adhesion and lateral force measurements reveal that adhesion forces vary with the ionization state of surface groups, the electric double layer follows theoretical Debye lengths in 1:1 electrolyte, and lateral force imaging can directly map the ionization state.
In this paper we present a scanning force microscopy (SFM) study on electrostatic and hydrogen-bonding interactions between chemically modified SFM probes and surface functional groups. pH-dependent adhesion force measurements in aqueous media between various ionizable functional groups showed a dependency of the adhesion force on the state of ionization (acid−base properties) of these surface-bound groups. The local degree of ionization and surface pK values can be determined from the obtained "adhesion force titration curves", which resemble conventional solution pH titration curves. In the presence of a 1:1 electrolyte, the electric double layer was probed and the measured Debye lengths were found to agree with theoretical predictions. pH-dependent lateral force imaging was found to directly map the ionization state of surface-bound functional groups.
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Calibration of atomic-force microscope tips
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