0000000000323648

AUTHOR

Martin Nalbach

0000-0003-0045-7548

showing 6 related works from this author

Stabilization of Polar Step Edges on Calcite (10.4) by the Adsorption of Congo Red

2015

In this work, we present the stabilization of polar step edges along the [010] direction of calcite (10.4) by the presence of a water-soluble organic molecule, namely Congo Red. While characteristic etch pits are observed on the surface in the absence of the additive, no etch pits can be found in the presence of the additive. Using atomic force microscopy, we can directly follow the restructuring of the surface. Upon addition of Congo Red, the charge-neutral step edges confining the characteristic etch pits vanish, while polar step edges along the [010] direction appear on the surface, which are entirely decorated by well-ordered molecular islands of the additive. After the restructuring ha…

CalciteChemistryDirect evidenceAtomic force microscopyMineralogySurfaces and InterfacesCondensed Matter Physics530Congo redchemistry.chemical_compoundAdsorptionChemical physicsElectrochemistryPolarStep edgesMoleculeGeneral Materials ScienceSpectroscopy
researchProduct

How deprotonation changes molecular self-assembly – an AFM study in liquid environment

2013

We study the influence of Alizarin Red S deprotonation on molecular self-assembly at the solid-liquid interface of the natural cleavage plane of calcite immersed in aqueous solution. To elucidate the adsorption details, we perform pH dependent high-resolution atomic force microscopy measurements. When Alizarin Red S is deposited onto calcite(10.4) in a liquid environment at an acidic pH of 5, weakly bound, ordered islands with a (3 x 3) superstructure are observed. A sharp structural transition is revealed when increasing the pH above 8. Above this pH, stable needle-like structures oriented along the [01.0] direction form on the surface. Comparing these results with potentiometric titration…

SuperstructureAqueous solutionChemistryPotentiometric titrationInorganic chemistryALIZARIN REDProtonationGeneral ChemistryCondensed Matter Physics530CrystallographyDeprotonationAdsorptionMolecular self-assemblySoft Matter
researchProduct

Three-dimensional atomic force microscopy mapping at the solid-liquid interface with fast and flexible data acquisition

2016

We present the implementation of a three-dimensional mapping routine for probing solid-liquid interfaces using frequency modulation atomic force microscopy. Our implementation enables fast and flexible data acquisition of up to 20 channels simultaneously. The acquired data can be directly synchronized with commercial atomic force microscope controllers, making our routine easily extendable for related techniques that require additional data channels, e.g., Kelvin probe force microscopy. Moreover, the closest approach of the tip to the sample is limited by a user-defined threshold, providing the possibility to prevent potential damage to the tip. The performance of our setup is demonstrated …

Kelvin probe force microscopeMaterials sciencebusiness.industryInterface (computing)Nanotechnology02 engineering and technologyConductive atomic force microscopy010402 general chemistry021001 nanoscience & nanotechnology53001 natural sciencesSample (graphics)0104 chemical sciencesOpticsData acquisitionChemical force microscopyMicroscopy0210 nano-technologybusinessInstrumentationFrequency modulationReview of Scientific Instruments
researchProduct

Molecular Self-Assembly Versus Surface Restructuring During Calcite Dissolution.

2016

Organic additives are known to alter the mineral-water interface in various ways. On the one hand, organic molecules can self assemble into ordered structures wetting the surface. On the other hand, their presence can affect the interfacial morphology, referred to as surface restructuring. Here, we investigate the impact, of a class of calcium-complexing azo dyes on the dissolution of calcite (10.4) using high-resolution atomic force microscopy operated in aqueous solution, with a focus on the two constitutional isomers Eriochrome Black T and Eriochrome Black A. A very pronounced surface restructuring is observed in the presence of the dye solution, irrespective of the specific dye used and…

CalciteAqueous solutionMorphology (linguistics)Chemistry02 engineering and technologySurfaces and Interfaces010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences5300104 chemical sciencesEriochrome Black Tchemistry.chemical_compoundChemical engineeringElectrochemistryMolecular self-assemblyOrganic chemistryMoleculeGeneral Materials ScienceWetting0210 nano-technologyDissolutionSpectroscopyLangmuir : the ACS journal of surfaces and colloids
researchProduct

Structure-Dependent Dissolution and Restructuring of Calcite Surfaces by Organophosphonates

2017

Organophosphonates are well-known to strongly interact with the surfaces of various minerals, such as brucite, gypsum, and barite. In this work, we study the influence of six systematically varied organophosphonate molecules (tetraphosphonates and diphosphonates) on the dissolution process of the (10.4) surface of calcite. In order to pursue a systematic study, we have selected organophosphonates that exhibit similar structural features, but also systematic architectural differences. The effect of this class of additives on the dissolution process of the calcite (10.4) surface is evaluated using in situ dynamic atomic force microscopy. For all of the six organophosphonate derivatives, we ob…

CalciteGypsumAtomic force microscopyBruciteDiphosphonates02 engineering and technologyGeneral Chemistryengineering.material010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics53001 natural sciences0104 chemical scienceschemistry.chemical_compoundCrystallographychemistryChemical engineeringengineeringMoleculeGeneral Materials ScienceOrganophosphonates0210 nano-technologyDissolutionCrystal Growth & Design
researchProduct

Where Is the Most Hydrophobic Region? Benzopurpurine Self-Assembly at the Calcite–Water Interface

2017

Control of molecular self-assembly at solid–liquid interfaces is challenging due to the complex interplay between molecule–molecule, molecule–surface, molecule–solvent, surface–solvent, and solvent–solvent interactions. Here, we use in-situ dynamic atomic force microscopy to study the self-assembly of Benzopurpurine 4B into oblong islands with a highly ordered inner structure yet incommensurate with the underlying calcite (10.4) surface. Molecular dynamics and free energy calculations provide insights by showing that Benzopurpurine 4B molecules do not anchor to the surface directly but instead assemble on top of the second hydration layer. This seemingly peculiar behavior was then rationali…

CalciteChemistryAtomic force microscopy02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology53001 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsHydrophobeMolecular dynamicschemistry.chemical_compoundCrystallographyGeneral EnergyAdsorptionChemical physicsMoleculeSelf-assemblyPhysical and Theoretical Chemistry0210 nano-technologyLayer (electronics)The Journal of Physical Chemistry C
researchProduct