Hydration layer structures on calcite facets and their roles in selective adsorptions of biomolecules: A molecular dynamics study

作者：Zhu, Beibei; Xu, Xurong; Tang, Ruikang^*

来源：Journal of Chemical Physics, 2013, 139(23): 234705.

DOI：10.1063/1.4848696

• THIN-FILM FORMATION
• ATOMISTIC SIMULATION
• GROWTH MODIFICATION
• WATER INTERFACE
• SEEDED CALCITE
• FORCE-FIELD
• FREE-ENERGY
• CARBONATE
• SURFACE
• ACID

The selective adsorptions of biomolecules onto crystal faces are the key issues in the studies of biomineralization. Frequently, the adsorption processes are understood by using the direct binding model between organic compounds and inorganic crystals during the molecular dynamic studies. However, water molecules near crystals always exhibit intense ordering and preferential orientation to form structured hydration layer. By using the adsorption of poly acrylic acid oligomer, acrylic acid (AA) dimer, onto calcite as an example, we demonstrate that the induced hydration layers contribute significant effects on the organic-inorganic interactions. In particular, on calcite (104) plane, two carboxyl groups of AA dimer both interact with the crystal but the molecule has to compete with water due to the well-structured hydration layer. On (110) plane, although only one carboxyl group of AA dimer interacts with this surface, the water layer is relatively loose so that the molecule can easily replace water. With a consideration of the hydration layer, our free energy analysis indicates that AA dimer has a stronger interaction with (110) face than with (104) face, which is consistent with the experimental observations. The study follows that the attachment of organic additive onto inorganic crystal facet is greatly mediated by near-surface hydration layers, and therefore, the critical role of structured water layers must be taken into account in the understanding of biomineralization interfaces.

• 出版日期2013-12-21
• 单位浙江大学